REFERENCE TO A SEQUENCE LISTING
This application contains a Sequence Listing that has been submitted in .XML format via PatentCenter and is hereby incorporated by reference in its entirety. The .XML is named Sequence_Listing.xml, and is 255 kilobytes in size.
BACKGROUND
Insect pests are detrimental to crop production and human health throughout the world and insect control can in some instances consume between 10-25% of a country's gross national product (GNP). (http World Wide Web internet site “fao.org/3/a-av013e.pdf”). In the U.S., annual loss due to crop pests is estimated to exceed $120 billion USD/year. (Polaszek A. (1998) Wallingford, UK: CABI. 530 pp.).
Within crop pests, Lepidoptera are the most detrimental insect pests of cereal crop cultivation. Chemical control is often expensive, inefficient, and can be associated with negative environmental consequences. Host plant resistance is an attractive option but impeded by lack of robust Lepidoptera resistant germplasm (http World Wide Web internet site “cnbc.com/2015/05/08/insects-feast-on-plants-endangering-crops-and-costing-billions.html”).
Since 1996, commercialization of crop plants genetically engineered to produce Bacillus thuringiensis (Bt) insecticidal proteins have resulted in efficient pest control, increased yield, reduced insecticidal use, and enhanced farmer profits. (Khan Z R, et al. (2014). Philos. Trans. R Soc. Lond Biol Sci. 369: 1639).
Consequently, the cumulative area planted with Bt crops worldwide reached greater than 1 billion acres during 2011. Within the U.S., Bt Corn, Bt Soybean, and Bt Cotton accounted for 90% of all the total corn, soybean and cotton acres during 2013 (Tabashnik B E, et al. (2013). Nat. Biotech. 31: 510-521). However, evolution of field resistance against Bt in lepidopteran pests raises potential concerns about the sustainability of this approach. (Campagne P., et al. (2013) PLoS ONE 8(7): e69675. Doi:10.1371). That is further exacerbated by loss of resistance against pyramided Bt traits as well (https World Wide Web internet site dt npf.com/agriculture/web/ag/news/article/2016/08/10/rootworm-resistance-pyramided-bt.html).
SUMMARY
Provided herein is an isolated double stranded RNA (dsRNA) molecule comprising a nucleic acid sequence complementary to about 200 to 1000 contiguous nucleotides of a target gene sequence—wherein the target gene is a MIGGS-IRTG as defined herein-involved in gut microbe clearance and/or containment induced by microbes ingested during feeding and/or active feeding. In certain aspects, the target gene is critical for insect immune responses and certain aspects provide that it is abundantly expressed in the midgut. In certain aspects, the target gene sequence includes at least one of the protein coding region, the 5′ UTR region, the 3′ UTR region, and any combination thereof, of a target gene. Further, certain aspects provide that the dsRNA molecule silences the target gene when ingested by an insect. In certain aspects, the target gene is a type 1 MIGGS RNAi target or a type 2 MIGGS RNAi target as defined elsewhere herein. In certain aspects, the target gene is a pattern recognition receptor (PRR) class gene or an insect midgut structural component gene. In certain aspects, the target gene is expressed abundantly in a midgut specific manner during active feeding.
In certain aspects, a dsRNA molecule disclosed anywhere herein comprises two annealed complementary RNA strands. In certain aspects, said dsRNA molecule comprises a single RNA strand comprising an inversely repeated sequence with a spacer in between, wherein the single RNA strand can anneal to itself to form a hairpin loop structure.
In certain aspects, a dsRNA molecule disclosed anywhere herein comprises a nucleic acid sequence complementary to about 200 to 1000 contiguous nucleotides of the protein coding region of the target gene sequence. In certain aspects, said dsRNA molecule comprises a nucleic acid sequence complementary to about 200 to 1000 contiguous nucleotides of the 5′ UTR region or the 3′ UTR region of the target gene sequence. In certain aspects, said dsRNA molecule comprises a nucleic acid sequence complementary to a contiguous region comprising at least about 50%, 60%, 70%, 80%, 90%, 95%, 98%, 99%, or 100% of the length of the target gene sequence protein coding region, 5′ UTR region, or 3′ UTR region. In certain aspects, said dsRNA molecule comprises a nucleic acid sequence complementary to about 200 to 650 contiguous nucleotides of a target gene sequence.
Certain aspects of this disclosure are drawn to a target gene selected from the group consisting of M. sexta-Hemolin (MsHEM), M. sexta-Serine proteinase homolog 3 (MsSPH-3), M. sexta-Peptidoglycan recognition protein 2 (MsPGRP2), M. sexta-Beta-1, 3-glycan-recognition protein 2 (MsβGRP2), M. sexta-Relish family protein 2A (MsREL2A), M. sexta-Dorsal (MsDor), M. sexta-Spatzle (MsSPZ1A), M. sexta-Toll receptor (MsTOLL), M. sexta-Scolexin A (MsSCA1), M. sexta-Hemolymph proteinase 18 (MsHP18), M. sexta-Transferrin (MsTRN), M. sexta-Arylphorin beta subunit (MsARP), M. sexta-Chymotrypsinogen-like protein 1 (MsCTL1), M. sexta-Valine Rich Midgut Protein (MsVMP1), M. sexta-Imd (MsImd), M. sexta-FADD (MsFADD), M. sexta-Dredd (MsDRD), M. sexta-Relish F (MsReIF), M. sexta-Cdc42 (MsCdc42), M. sexta-Dsor1 (MsDsor1), M. sexta-Fos (MsFos), M. sexta-Jra (MsJra), M. sexta-Caudal (MsCAD1), M. sexta-Atg8 (MsAtg8), M. sexta-Atg13 (MsAtg13), M. sexta-IAP1 (MsIAP1), M. sexta-Chitin synthase 2 (MsChs2), M. sexta-Beta-1 tubulin (MspTub), M. sexta-Beta fructofuranosidase 1 (MsSuc1), and orthologs thereof. In certain aspects, the target gene is selected from the group consisting of M. sexta-Hemolin (MsHEM), M. sexta-Serine proteinase homolog 3 (MsSPH-3), M. sexta-Peptidoglycan recognition protein 2 (MsPGRP2), M. sexta-Beta-1, 3-glycan-recognition protein 2 (MsβGRP2), M. sexta-Relish family protein 2A (MsREL2A), M. sexta-Dorsal (MsDor), M. sexta-Spatzle (MsSPZ1A), M. sexta-Toll receptor (MsTOLL), M. sexta-Scolexin A (MsSCA1), M. sexta-Hemolymph proteinase 18 (MsHP18), M. sexta-Transferrin (MsTRN), M. sexta-Arylphorin beta subunit (MsARP), M. sexta-Chymotrypsinogen-like protein 1 (MsCTL1), M. sexta-Valine Rich Midgut Protein (MsVMP1), M. sexta-Imd (MsImd), M. sexta-FADD (MsFADD), M. sexta-Dredd (MsDRD), M. sexta-Relish F (MsReIF), M. sexta-Cdc42 (MsCdc42), M. sexta-Dsor1 (MsDsor1), M. sexta-Fos (MsFos), M. sexta-Jra (MsJra), M. sexta-Caudal (MsCAD1), M. sexta-Atg8 (MsAtg8), M. sexta-Atg13 (MsAtg13), M. sexta-IAP1 (MsIAP1), M. sexta-Chitin synthase 2 (MsChs2), M. sexta-Beta-1 tubulin (MspTub) and M. sexta-Beta fructofuranosidase 1 (MsSuc1).
Also provided herein is an isolated double stranded RNA (dsRNA) molecule comprising a nucleic acid sequence complementary to about 200 to 1000 contiguous nucleotides of a target gene sequence, wherein the target gene comprises a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-14, 16-29, 31-70, 71-75, 76-88, 89-105, and 106-110. In certain aspects, the target gene sequence includes at least one of the protein coding region, the 5′ UTR region, the 3′ UTR region, and any combination thereof, of a target gene. Further, certain aspects provide that the dsRNA molecule silences the target gene when ingested by an insect.
In certain aspects disclosed herein, the target gene is sequence selected from the group consisting of: i) SEQ ID NOs: 1-9, 11, 14, 31, 39, 43, 44, and 71-75.
In certain aspects disclosed herein, the target gene is sequence selected from the group consisting of: ii) SEQ ID NOs: 3, 4, and 43. In certain aspects, the dsRNA molecule causes impeded growth, developmental progression, and/or mortality and the like of TH, DMB, and FAW in an orthologous manner.
In certain aspects disclosed herein, the target gene is sequence selected from the group consisting of: iii) SEQ ID NOs: 76, 77, 80, 81, 85, 87, and 88. In certain aspects, the dsRNA molecule causes impeded growth, developmental progression, and/or mortality and the like of DBM. Further, in certain aspects, the DBM is a Bt resistant strain.
In certain aspects disclosed herein, the target gene is sequence selected from the group consisting of: iv) SEQ ID NOs: 89, 92, 96, 101, 103, and 105. In certain aspects, the dsRNA molecule causes impeded growth, developmental progression, and/or mortality and the like of FAW.
In certain aspects disclosed herein, the target gene is sequence selected from the group consisting of: v) SEQ ID NOs: 107-110. In certain aspects, the dsRNA molecule caused impeded growth, developmental progression, and/or mortality and the like of RFB.
In certain aspects of the dsRNA molecule disclosed above, the dsRNA molecule comprises two annealed complementary RNA stands. In certain aspects, the dsRNA molecule comprises a single RNA strand comprising an inversely repeated sequence with a spacer in between and where the single RNA strand can anneal to itself to form a hairpin loop structure.
In certain of the dsRNA molecule disclosed above, the dsRNA molecule comprises a nucleic acid sequence complementary to about 200 to 1000 contiguous nucleotides of the protein coding region of the target gene sequence. In certain aspects, the dsRNA molecule comprises a nucleic acid sequence complementary to a contiguous region comprising at least about 50%, 60%, 70%, 80%, 90%, 95%, 98%, 99%, or 100% of the length of a sequence selected from the group consisting of SEQ ID NOs: 1-14, 16-29, 31-70, 71-75, 76-88, 89-105, and 106-110. In certain aspects, the dsRNA molecule comprises a nucleic acid sequence complementary to a contiguous region comprising at least about 50%, 60%, 70%, 80%, 90%, 95%, 98%, 99%, or 100% of the length of the target gene sequence protein coding region, 5′ UTR region, or 3′ UTR region.
In certain aspects disclosed herein the dsRNA molecule comprises a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 111-119, 120-126, 127-135, and 136-139. In certain aspects, the dsRNA is a fragment of at least about 200 nucleotides thereof. In certain aspects, i) the isolated dsRNA molecule comprising a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 110-119, or the fragment thereof, causes impeded growth, developmental progression, and/or mortality and the like of TH; ii) the isolated dsRNA molecule comprising a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 120-126, or the fragment thereof, causes impeded growth, developmental progression, and/or mortality and the like of DBM; iii) the isolated dsRNA molecule comprising a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 127-135, or the fragment thereof, causes impeded growth, developmental progression, and/or mortality and the like of FAW; or iv) the isolated dsRNA molecule comprising a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 136-139, or the fragment thereof, causes impeded growth, developmental progression, and/or mortality and the like of RFB.
In certain of any of the above aspects, the dsRNA molecule can form siRNA. Certain aspects provide for an isolated siRNA molecule derived from the processing of said dsRNA molecule.
Certain further aspects provide of an insecticidal composition comprising an isolated dsRNA molecule or an siRNA molecule disclosed anywhere herein, and a synthetic carrier or microbial conduit. In certain aspects, a microorganism has a natural capacity or is engineered to produce and/or deliver dsRNA to increase its bioavailability and/or biostability for causing RNA interference including but not restricted to plant growth promoting organisms, normal commensal and/or symbiotic microorganisms associated with the target insect pest or parasites and/or natural enemies of the target pest or pest target host or host cultivation range etc. from an insect or parasite and/or natural enemies of the target pest engineered or identified from natural populations containing microbial conduit to produce and/or deliver dsRNA and/or drive the transmission of such microbial conduits into natural populations of insect pests as a control option. In certain aspects of an insecticidal composition disclosed herein, the dsRNA molecule is conjugated with the synthetic carrier.
Certain aspects are also drawn to a recombinant DNA construct encoding a dsRNA molecule disclose anywhere herein. In certain aspects, the recombinant DNA construct comprising a gene silencing sequence comprising about 200 to 1000 contiguous nucleotides of a target gene sequence. In certain aspects, the target gene is a MIGGS-IRTG, as defined herein, involved in gut microbe clearance and/or containment induced by microbes ingested during feeding and/or active feeding. In certain aspects, the target gene is critical for insect immune responses. In certain aspects, the target gene is abundantly expressed in the midgut. In certain aspects, said target gene sequence includes at least one of the protein coding region, the 5′ UTR region, the 3′ UTR region, and any combination thereof, of a target gene. In certain aspects, the target gene is a type I MIGGS RNAi target or a type 2 MIGGS RNAi target as described elsewhere herein. In certain aspects, the target gene is a pattern recognition receptor (PRR) class gene or an insect midgut structural component gene. In certain aspects, the target gene is expressed abundantly in a midgut specific manner during active feeding.
In any of the above aspects of a recombinant DNA construct, the gene silencing sequence comprises about 200 to 1000 contiguous nucleotides of the protein coding region of the target gene sequence. In certain aspects, the gene silencing sequence comprises about 200 to 1000 contiguous nucleotides of the 5′ UTR region or the 3′ UTR region of the target gene sequence. In certain aspects, the gene silencing sequence comprises at least 50%, 60%, 70%, 80%, 90%, 95%, 98%, 99%, or 100% contiguously of the length of target gene sequence protein coding region, 5′ UTR region, or 3′ UTR region. In certain aspects, the gene silencing sequence comprises about 200 to 650 contiguous nucleotides of the target gene sequence.
In any of the above aspects of a recombinant DNA construct, and as noted throughout this disclosure, in certain aspects, a target gene can be selected from the group consisting of M. sexta-Hemolin (MsHEM), M. sexta-Serine proteinase homolog 3 (MsSPH-3), M. sexta-Peptidoglycan recognition protein 2 (MsPGRP2), M. sexta-Beta-1, 3-glycan-recognition protein 2 (MsβGRP2), M. sexta-Relish family protein 2A (MsREL2A), M. sexta-Dorsal (MsDor), M. sexta-Spatzle (MsSPZ1A), M. sexta-Toll receptor (MsTOLL), M. sexta-Scolexin A (MsSCA1), M. sexta-Hemolymph proteinase 18 (MsHP18), M. sexta-Transferrin (MsTRN), M. sexta-Arylphorin beta subunit (MsARP), M. sexta-Chymotrypsinogen-like protein 1 (MsCTL1), M. sexta-Valine Rich Midgut Protein (MsVMP1), M. sexta-Imd (MsImd), M. sexta-FADD (MsFADD), M. sexta-Dredd (MsDRD), M. sexta-Relish F (MsReIF), M. sexta-Cdc42 (MsCdc42), M. sexta-Dsor1 (MsDsor1), M. sexta-Fos (MsFos), M. sexta-Jra (MsJra), M. sexta-Caudal (MsCAD1), M. sexta-Atg8 (MsAtg8), M. sexta-Atg13 (MsAtg13), M. sexta-IAP1 (MsIAP1), M. sexta-Chitin synthase 2 (MsChs2), M. sexta-Beta-1 tubulin (MspTub), M. sexta-Beta fructofuranosidase 1 (MsSuc1), and orthologs thereof. In certain aspects a target gene can be selected from the group consisting of M. sexta-Hemolin (MsHEM), M. sexta-Serine proteinase homolog 3 (MsSPH-3), M. sexta-Peptidoglycan recognition protein 2 (MsPGRP2), M. sexta-Beta-1, 3-glycan-recognition protein 2 (MsβGRP2), M. sexta-Relish family protein 2A (MsREL2A), M. sexta-Dorsal (MsDor), M. sexta-Spatzle (MsSPZ1A), M. sexta-Toll receptor (MsTOLL), M. sexta-Scolexin A (MsSCA1), M. sexta-Hemolymph proteinase 18 (MsHP18), M. sexta-Transferrin (MsTRN), M. sexta-Arylphorin beta subunit (MsARP), M. sexta-Chymotrypsinogen-like protein 1 (MsCTL1), M. sexta-Valine Rich Midgut Protein (MsVMP1), M. sexta-Imd (MsImd), M. sexta-FADD (MsFADD), M. sexta-Dredd (MsDRD), M. sexta-Relish F (MsReIF), M. sexta-Cdc42 (MsCdc42), M. sexta-Dsor1 (MsDsor1), M. sexta-Fos (MsFos), M. sexta-Jra (MsJra), M. sexta-Caudal (MsCAD1), M. sexta-Atg8 (MsAtg8), M. sexta-Atg13 (MsAtg13), M. sexta-IAP1 (MsIAP1), M. sexta-Chitin synthase 2 (MsChs2), M. sexta-Beta-1 tubulin (MspTub) and M. sexta-Beta fructofuranosidase 1 (MsSuc1).
Further aspects provide for a recombinant DNA construct comprising a gene silencing sequence comprising about 200 to 1000 contiguous nucleotides of a target gene sequence, wherein the target gene comprises a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-14, 16-29, 31-70, 71-75, 76-88, 89-105, and 106-110. In certain aspects, the target gene sequence includes at least one of the protein coding region, the 5′ UTR region, the 3′ UTR region, and any combination thereof, of a target gene.
In any of the above aspects of a recombinant DNA construct, the target gene sequence is selected from the group consisting of: i) SEQ ID NOs: 1-9, 11, 14, 31, 39, 43, 44, and 71-75; ii) SEQ ID NOs: 3, 4, and 43; iii) SEQ ID NOs: 76, 77, 80, 81, 85, 87, and 88; iv) SEQ ID NOs: 89, 92, 96, 101, 103, and 105; and v) SEQ ID NOs: 107-109, and 110. In certain aspects, the gene silencing sequence comprises about 200 to 1000 contiguous nucleotides of a sequence selected from the group consisting of SEQ ID NOs: 1-14, 16-29, 31-70, 71-75, 76-88, 89-105, and 106-110. In certain aspects, the gene silencing sequence comprises at least 50%, 60%, 70%, 80%, 90%, 95%, 98%, 99%, or 100% contiguously of a sequence selected from the group consisting of SEQ ID Nos: 1-14, 16-29, 31-70, 71-75, 76-88, 89-105, and 106-110. In certain aspects, the gene silencing sequence comprises about 200 to 650 contiguous nucleotides of a sequence selected from the group consisting of SEQ ID NOs: 1-14, 16-29, 31-70, 71-75, 76-88, 89-105, and 106-110. In certain aspects, the gene silencing sequence is operably linked to one or more promoters for the expression of a dsRNA molecule that silences the target gene when ingested by an insect. In certain aspects, the construct is an expression vector. And, in certain aspects, the expression vector can target single or multiple insect RNAi target genes or chimeric RNAi target genes.
Certain aspects of the disclosure also provide for a host cell comprising the dsRNA molecule, the siRNA molecule, a polynucleotide encoding a dsRNA molecule, and/or the construct or a dsRNA encoding segment thereof disclose anywhere herein. In certain aspects, the host cell is a bacterial or plant cell or organelle. In certain aspects, the organelle is a plastid. In certain aspects, the host cell is a transgenic and/or transplastomic plant cell. In certain aspects, the hose cell expresses a dsRNA and/or produces an siRNA disclosed anywhere herein.
Certain aspects also provide for a transgenic and/or transplastomic plant comprising a dsRNA molecule, an siRNA molecule, a polynucleotide encoding the dsRNA, and/or a construct or a dsRNA encoding segment disclosed anywhere herein. In certain aspects, at least one cell of the plant expresses the dsRNA molecule and/or produces the siRNA molecule. Further, certain aspects provide for a seed, part, tissue, cell, or organelle of the above transgenic and/or transplastomic plant. In certain aspects, the seed, part, tissue, cell, or organelle comprises the dsRNA molecule and/or the siRNA molecule. In certain aspects, the organelle is a plastid.
Certain aspects provide for a method of silencing: (i) an insect immune response gene and/or (ii) an insect gene encoding for structural components of the insect midgut. In certain aspects, the method comprises providing for ingesting an isolated dsRNA molecule, an siRNA molecule, an insecticidal composition, a host cell, a transgenic and/or transplastomic plant, transplastomic plant and/or a seed, part, tissue, cell, or organelle as disclosed anywhere herein, to an insect.
Certain aspects provide for a method of protecting a plant from an insect pest of the plant. In certain aspects, the method comprises topically applying to a plant an isolated dsRNA molecule, an siRNA molecule, and/or an insecticidal composition disclosed anywhere herein, and providing the plant in the diet of the insect pest. In certain aspects, the dsRNA is topically applied by expressing the dsRNA in a microbe and topically applying the microbe onto the plant.
Certain aspects provide for a method of producing a plant resistance to a pest insect of said plant. In certain aspects, the method comprises transforming a plant with a polynucleotide encoding the dsRNA molecule and/or a construct or a dsRNA encoding segment thereof as disclosed anywhere herein, wherein the plant expresses a dsRNA molecule and/or produces an siRNA disclose anywhere herein.
Certain aspects provide for a method of improving crop yield. In certain aspects, the method comprises growing a population of crop plants transformed with a polynucleotide encoding a dsRNA molecule and/or a construct or a dsRNA encoding segment thereof wherein the plant expresses a dsRNA molecule and/or produces an siRNA molecule as discloses anywhere herein. In certain aspects, the population of transformed plants produces higher yields in the presence of pest insect infestation than a control population of untransformed plants.
Certain aspects provide for a method for producing a plant resistant against a pest insect of said plant. In certain aspects, the method comprises: a) transforming a plant cell and/or organelle with a polynucleotide encoding a dsRNA molecule and/or a construct or a dsRNA encoding segment thereof as disclosed anywhere herein; b) regenerating a plant from the transformed plant cell and/or organelle; and c) growing the transformed plant under conditions suitable for the expression of said double stranded RNA molecule, wherein said transformed plant of (c) is resistant to the plant pest insect compared to an untransformed plant.
In certain of any of the aforementioned aspects, the method the dsRNA is ingested by an actively feeding stage of the insect. In certain aspects, the ingestion of the dsRNA induces a melanotic response in the insect larvae. In certain aspects, the ingestion of the dsRNA results in perturbation of gut microbial homeostasis. In certain aspects, the ingestion of the dsRNA results in defective clearance of opportunistic microbes. In certain aspects, the ingestion of the dsRNA results in defective containment of gut microbes.
In certain of any of the aforementioned aspects, the silencing of the target gene results in reduced appetite and/or developmental defects resulting in incomplete development and/or mortality and/or decrease the reproductive success of the insect. In certain aspects, the reduced appetite and/or developmental defects and/or mortality and/or reduced reproductive fitness of the insect is observed after sustained feeding for at least 72 hours.
In certain of any of the aforementioned aspects, the insect is of the order Lepidoptera, Coleoptera, Hemiptera, Blattodea, or Diptera. In certain aspects, the insect is Manduca sexta (M. sexta) (tobacco hornworm), Spodoptera frugiperda (fall armyworm), Ostrinia nubilalis (European corn borer), Plutella xylostella (Diamondback moth), Leptinotarsa decemlineata Say (Colorado potato beetle), Diabrotica spp. (Corn rootworm complex), Tribolium castaneum (Red flour beetle), Popillia japonica (Japanese beetle), Agrilus planipennis (Emerald ash borer), Diaphorina citri (Asian citrus psyllid), Cimex lectularius (Bed bug), a cockroach or termite, or insect pests such as mosquitoes and flies.
In certain of any of the aforementioned aspects, the plant host is selected from the group consisting of Zea mays L (corn), Sorghum bicolor (sorghum), Setaria italica (fox tail millet), Pennisetum glaucum (Pearl millet), Solanum tuberosum (potato), Oryza sativa (rice), Lycopersicon esculentum (tomato), Solanum melongena (eggplant), cultivars of the Brassica oleracea family, Citrus sinensis (Orange), trees of the Oleaceae family, and crops of Rosaceae.
One aspect of the instant disclosure encompasses a method of silencing an insect immune response gene, an insect gene encoding structural components of an insect midgut, or both. The method comprising providing for ingestion (a) an isolated double stranded RNA (dsRNA) molecule, or a dsRNA molecule in a host cell, in a transgenic or transplastomic plant or cell, organelle, or part thereof, in a microbial conduit, or in an insecticidal composition, wherein the dsRNA molecule comprises a nucleic acid sequence complementary to about 21 to 2000 contiguous nucleotides of a target gene sequence comprising a nucleic acid sequence of SEQ ID NO: 76, wherein the dsRNA molecule silences the target gene when ingested by an insect; (b) an siRNA molecule derived from the processing of the dsRNA molecule; (c) a polynucleotide, a construct, or a dsRNA encoding segment encoding the dsRNA molecule; or (d) a combination of (a)-(d).
The microbial conduit can comprise plant growth promoting organisms, normal commensal and/or symbiotic microorganisms associated with a target insect pest or parasite, and/or natural enemies of the target pest or pest target host or host cultivation range etc. from an insect or parasite, and/or natural enemies of the target pest engineered or identified from natural populations containing microbial conduit to produce and/or deliver dsRNA and/or drive transmission of such microbial conduits into natural populations of insect pests as a control option.
In some aspects, the dsRNA molecule is bound to a synthetic carrier. In some aspects, the synthetic carrier comprises chitosan, liposomes, carbon quantum dots, biodegradable particles of plant, or soil.
Ingestion of the dsRNA, the siRNA molecule, the polynucleotide, construct, or dsRNA encoding segment encoding the dsRNA molecule, or any combination thereof can silence the target gene to thereby induce (a) a melanotic response; (b) results in perturbation of gut microbial homeostasis; (c) results in defective clearance of opportunistic microbes; (d) results in defective containment of gut microbes, or any combination of (a) to (d).
The host cell can be a bacterial cell, a yeast cell, or a fungal cell. The target gene sequence can include at least one of a protein coding region, a 5′ untranslated region (UTR), a 3′ UTR, or any combination thereof.
The dsRNA molecule can comprise a single RNA strand comprising an inversely repeated sequence with a spacer in between and where the single RNA strand can anneal to itself to form a hairpin loop structure; or wherein the dsRNA molecule comprises two separate complementary RNA stands annealed together.
The target gene can be selected from the group consisting of Manduca sexta-Peptidoglycan recognition protein 2 (MsPGRP2), Plutella xylostella PGRP2, and Tribolium castaneum PGRP2.
In some aspects, the dsRNA comprises a nucleic acid sequence of SEQ ID NO: 76, or a fragment of at least about 21 nucleotides thereof, optionally.
In some aspects, the construct encoding the dsRNA comprises a gene silencing sequence operably linked to one or more promoters for expression of a dsRNA molecule that silences the target gene when ingested by an insect, optionally wherein the construct further comprises an additional transcription regulatory region or an additional transcriptional regulatory element. The construct can be an expression vector, and the expression vector can target single or multiple insect RNAi target genes or chimeric RNAi target genes.
The dsRNA molecule can cause impeded growth, developmental progression, and/or mortality and the like of DBM, optionally wherein the DBM is a Bt resistant strain. In some aspects, the silencing of the target gene results in reduced appetite and/or developmental defects resulting in incomplete development and/or mortality and/or decreased reproductive success of the insect, optionally wherein the reduced appetite and/or developmental defects and/or mortality and/or reduced reproductive fitness of the insect is observed after sustained feeding for at least 24 hours.
In some aspects, the insect is of the order Lepidoptera, Coleoptera, Hemiptera, Blattodea, or Diptera. In some aspects, the insect is Manduca sexta (M. sexta) (tobacco hornworm), Spodoptera frugiperda (fall armyworm), Ostrinia nubilalis (European corn borer), Plutella xylostella (Diamondback moth), Leptinotarsa decemlineata Say (Colorado potato beetle), Diabrotica spp. (Corn rootworm complex), Tribolium castaneum (Red flour beetle), Popillia japonica (Japanese beetle), Agrilus planipennis (Emerald ash borer), Diaphorina citri (Asian citrus psyllid), Cimex lectularius (Bed bug), a cockroach or termite, or insect pests such as mosquitoes and flies. In some aspects, the plant is selected from the group consisting of Zea mays L (corn), Sorghum bicolor (sorghum), Setaria italica (fox tail millet), Pennisetum glaucum (Pearl millet), Solanum tuberosum (potato), Oryza sativa (rice), Lycopersicon esculentum (tomato), Solanum melongena (eggplant), cultivars of the Brassica oleracea family, Citrus sinensis (Orange), trees of the Oleaceae family, and crops of Rosaceae.
Another aspect of the instant disclosure encompasses a method of protecting a plant from an insect pest of the plant. The method comprises topically applying to the plant (a) an isolated double stranded RNA (dsRNA) molecule, or a dsRNA in a host cell, in a transgenic or transplastomic plant or cell, organelle, or part thereof, in a microbial conduit, or in an insecticidal composition, and providing the plant in the diet of the insect pest, wherein the dsRNA molecule comprises a nucleic acid sequence complementary to about 21 to 2000 contiguous nucleotides of a target gene sequence comprising a nucleic acid sequence of SEQ ID NO: 76, and wherein the double stranded RNA molecule silences the target gene when ingested by an insect; (b) an siRNA molecule derived from processing of the dsRNA molecule; (c) a polynucleotide, a construct, or a dsRNA encoding segment encoding the dsRNA molecule; or a combination of (a)-(c).
Yet another aspect of the instant disclosure encompasses a method of producing a transgenic or transplastomic plant. The method comprises (a) transforming the plant with a polynucleotide encoding a dsRNA, a construct or a dsRNA encoding segment encoding the dsRNA, or both to generate a transformed plant cell; (b) regenerating a plant from the transformed plant cell and/or organelle to generate a transformed plant; and (c) growing the transformed plant under conditions suitable for expression of said dsRNA. The transformed plant of (c) is resistant to a plant pest insect compared to an untransformed plant and wherein the dsRNA molecule comprises a nucleic acid sequence complementary to about 21 to 2000 contiguous nucleotides of a target gene sequence comprising a nucleic acid sequence of SEQ ID NO: 76.
One aspect of the instant disclosure encompasses a method of improving crop yield. The method comprises growing a population of transgenic or transplastomic plants comprising a polynucleotide encoding a dsRNA, a construct or a dsRNA encoding segment encoding the dsRNA molecule, wherein the dsRNA comprises a nucleic acid sequence complementary to about 21 to 2000 contiguous nucleotides of a target gene sequence comprising a nucleic acid sequence of SEQ ID NO: 76 and wherein the population of transformed plants produces higher yields in the presence of pest insect infestation than a control population of untransformed plants.
BRIEF DESCRIPTION OF THE DRAWINGS
The application file contains at least one photograph executed in color. Copies of this patent application publication with color photographs will be provided by the Office upon request and payment of the necessary fee.
FIG. 1 shows schematic representation of bacterially ingestible dsRNA assay. (Kamath R S, et al. (2000) Genome Biol. 2: 1-10; Newmark et al. (2003) Proc. Natl. Acad. Sci. USA 100: 11861-11865).
FIG. 2A-C shows representative phenotypes of TH larvae. TH larvae exposed to bacterially (HT115 (DE3)) expressed dsRNA against MIGGS RNAi targets MsPGRP2 (A); MsVMP1(B); and negative control dsRNA against Cassava plant specific gene MeCAT1 (C).
FIG. 3A,B shows feeding activity of TH larvae exposed to dsRNA against negative control MeCAT1 (A) and MIGGS RNAi target MsPGRP2 (B) containing bacterial (HT115 (DE3)) plates.
FIG. 4 shows survival rates of healthy conventionally-reared (CR) and germ-free (GF) first instar TH larvae exposed to bacterially (HT115 (DE3)) expressed dsRNA against MIGGS RNAi targets MsPGRP2; MsVMP1 and negative control dsRNA against Cassava plant specific gene MeCAT1. The differences observed using 4 replicates/treatment were statistically significant across all time points at a P value between P<0.001 to P<0.05.
FIG. 5 shows percentage melanotic reaction of healthy conventionally-reared (CR) and germ-free (GF) first instar TH larvae exposed to bacterially (HT115 (DE3)) expressed dsRNA against MIGGS RNAi targets MsPGRP2; MsVMP1 and negative control dsRNA against Cassava plant specific gene MeCAT1. The differences observed using 4 replicates/treatment were statistically significant across all time points at a P value between P<0.001 to P<0.05.
FIG. 6 shows schematic representation of dsRNA producing L4440 vector containing coding sequence of Cassava CAT1 (MeCAT1) and TH MIGGS RNAi targets MsPGRP2 and MsVMP1.
FIG. 7 shows midgut-preferred expression of two TH MIGGS RNAi target genes MsHEM and MsSPH3 in comparison to the control gene RPS3. The control cDNA libraries were derived from conventionally reared larvae and treatment cDNA libraries were derived from TH larvae injected with 75 CFU of E. coli. The control and treatment larvae were used to isolate hemolymph fraction (HL), dissect midgut (MDG) to obtain rest of the body (RB). The HL, MDG and RB were used for RNA isolation and cDNA synthesis.
FIG. 8 shows schematic representation of oral induction procedure for MIGGS RNAi target genes. The insect larvae were reared on induction media containing live gram-negative bacteria E. coli and lyophilized cell wall signatures from gram-positive bacteria and fungi, following a previously published protocol (Wang et al. (2006). J Biol. Chem. 281(14): 9271-9278).
FIG. 9A,B shows expression of MIGGS RNAi target genes in TH larvae in response to feeding on induction media. Genes with immunity function (A,B) are induced (I) between 24-48 hours post larval exposure to induction media and mostly not detected in the absence of induction (UI).
FIG. 9C,D also shows expression of MIGGS RNAi target genes in TH larvae in response to feeding on induction media. Genes with immunity function (C) are induced (I) between 24-48 hours post larval exposure to induction media and mostly not detected in the absence of induction (UI). While, the genes essential for midgut structural integrity (D) are expressed under both conditions.
FIG. 10A-F shows representative phenotypes of TH larvae (initial size shown in A) exposed to bacterially expressed dsRNA against insecticidal MIGGS-RNAi target genes MsToll2, MsSuc1, and MspTub in comparison to negative (B) and positive (C) control treatment. The insecticidal activity is manifested as stunted growth and development, loss of appetite and melanotic reaction (D-F) in comparison to regular growth and development observed with negative control treatment (B).
FIG. 11 shows percentage mortality of TH larvae feeding on bacterially expressed dsRNA against insecticidal MIGGS RNAi targets MsToll2, MsSuc1, and MspTub. The insecticidal MIGGS candidates confer statistically significant mortality that is comparable to positive control treatment (MsVATPaseE). Data is average of 3-replicates/treatment±SEM at p≤0.001(***).
FIG. 12A-C shows the induction of MIGGS-IRTGS in DBM larvae feeding on induction media. The genes with immunity function (A-B) are induced (I) between 24-48 hours post larval exposure to induction media and mostly not detected in the absence of induction (UI). While, the genes essential for midgut structural integrity (C) are expressed under both conditions.
FIG. 13A-H shows representative phenotypes of Bt resistant DBM larvae (initial size shown in A) exposed to bacterially expressed dsRNA against insecticidal DBM MIGGS RNAi targets PxPGRP2 (D), PxIMD (E), PxβGRP2 (F), PxCAC (G), and PxCHS1 (H) in comparison to positive (C) and negative control (B) treatment. The insecticidal activity is manifested as stunted growth and development, loss of appetite and melanotic reaction (D-H) in comparison to regular growth and development observed with negative control treatment (B).
FIG. 14 shows percentage mortality of DBM larvae feeding on bacterially expressed dsRNA against insecticidal MIGGS RNAi targets PxPGRP2, PxIMD, PxβGRP2, PxCAC, and PxCHS1. The insecticidal MIGGS candidates confer statistically significant mortality that is comparable to positive control treatment (MsVATPaseE). Data is average of 3-replicates/treatment±SEM at p≤0.001(***) p≤0.01(**).
FIG. 15A,B illustrates a sprayable RNAi set up using dsRNA against TH MIGGS targets MsPGRP2, Ms βGRP2, MsCHS2, and MsVMP1. One cm2 leaf discs from field soil grown tobacco plants (A) were drop inoculated with various concentrations of purified dsRNA against TH MIGGS RNAi targets (B). The bioassays were carried out for 5 days with 3 first instar larvae per well and leaf discs changed at the end of every 24 hours.
FIG. 16 shows percentage mortality of TH larvae feeding on various concentrations of dsRNA against the core set of TH MIGGS RNAi targets MsPGPRP2, MsβGRP2, MsCHS2, and MsVMP1. The leaf disc coated dsRNA causes significant mortality at 8 and 16 μg of dsRNA concentration. The leaf disc coated dsRNA against three core MIGGS targets confers statistically significant mortality that is comparable to positive control treatment (MsVATPaseE). Data is average of 3-replicates/treatment±SEM at p≤0.001(***); p≤0.01(**) and p≤0.05(***).
FIG. 17A-H shows representative phenotypes of TH larvae (initial size shown in A and E) exposed to 8 and 16 μg of dsRNA against the core set of MIGGS RNAi targets MsPGPRP2 (D), MsβGRP2 (F), MsCHS2 (G), and MsVMP1 (H). The insecticidal activity is comparable to the positive control treatment (C) and manifested as stunted growth and development, loss of appetite and melanotic reaction (D,F-G) in contrast to the regular growth and development observed with negative control treatment (B).
FIG. 18A-D shows representative phenotypes of TH larvae feeding on leaves from transplastomic plants expressing dsRNA against core MIGGS targets MsPGRP2 (PTS-28-10 and PTS-28-7-B), MsβGRP2 (PTS-26-19 and PTS-26-4-C), and dsCHS2 (PTS-27-3-1 and PTS-27-13-1-D). The TH larvae feeding on leaves expressing dsRNA against MIGGS targets MsPGRP2 (B), MsβGRP (C), and MsCHS2 (D) display stunted growth, development, loss of appetite and melanotic reaction in comparison to negative control PTS-27-13-2 (A).
FIG. 18E shows that the insecticidal activity of transplastomic lines is manifested as significant reduction in mean weights in comparison to negative control.
FIG. 18F shows that the transplastomic events confer significant mortality in comparison to negative control. The mortality rate was scored on a 0-3 score were 0, 1, 2 and 3 indicated ≤0, 25, 50 or ≥50 mortality respectively. Data is average of 6 replicates/treatment (N=24)±SEM at p≤0.001(***); p≤0.01(**) and p≤0.05(*).
FIG. 19 shows percentage mortality of Bt resistant DBM larvae feeding on various concentrations of dsRNA against the DBM orthologs of TH core MIGGS RNAi targets PxPGPRP2, PxβGRP2, PxβTUB, and PxCHS1. The leaf disc coated dsRNA causes significant mortality at 0.5-1 μg of dsRNA concentration. The leaf disc coated dsRNA against all core MIGGS targets confers statistically significant mortality between 0.5 μg and 1 μg dsRNA dosage that is comparable to positive control treatment (MsVATPaseE). Data is average of 3-replicates/treatment±SEM at p≤0.01(**) and p≤0.05(*).
FIG. 20A-H shows representative phenotypes of Bt resistant DBM larvae (initial size shown in A and E) exposed to 0.5-1 μg of dsRNA against the DBM orthologs of TH core MIGGS RNAi targets PxPGPRP2(D), PxβGRP2(F), PxβTUB(G), and PxCHS1(H). The insecticidal activity is comparable to the positive control treatment (C) and manifested as stunted growth and development, loss of appetite and melanotic reaction (D,F-H) in contrast to the regular growth and development observed with negative control treatment (B).
FIG. 21A-D illustrates MIGGS-IRTG induction procedure in FAW feeding on wheat plants grown microbe rich field soil (A) and microbe depleted sterile surface (B). Ten first instar FAW larvae (C) were infested into each pot containing five wheat seedlings and contained using porous netting material (D). The larval samples were collected at various time points after infestation and used for pooled RNA-Seq approach to identify differential expressed transcripts in response to induction by the microbes in the filed soil.
FIG. 22A,B shows bi-clustering comparison of differential gene expression in FAW larvae feeding on microbe-depleted plants (A) in comparison to larvae feeding on microbe rich plants (B). RNA-Seq data indicated that plants growing on field soil caused preferential up-regulation of MIGGS pathway genes in FAW. In total, 100 differential expressed genes were identified, 30 of which were associated with MIGGS pathways. Notably, FAW orthologs of TH insecticidal targets including PGRP2, βGRP2 and IMD were captured in the data set, indicating clearly that MIGGS pathway genes are up regulated in response to insect feeding on plants exposed to soil microbiome.
FIG. 23A-F shows representative phenotypes of FAW larvae exposed to pure dsRNA against FAW orthologs of TH core MIGGS RNAi targets SFCHS2 (B), SFβGRP2 (C), SFPGRP2 (D), and two novel MIGGS RNAi targets from RNA-Seq study SFRC (un-annotated-E) and C-type lectin-6 (SFCTL-F). Leaf discs coated with dsRNA causes reduced growth, development and loss of appetite in comparison to negative control treatment (A) when supplied at 8 and 16 μg of dsRNA concentration per leaf disc.
FIG. 23G,H illustrates from FIG. 23A-F significant weight reduction (G) and mortality (H). The rates of mortality was scored on a 0-3 scale where 0, 1, 2 and 3 indicated ≤0, 25, 50 or ≥50 mortality respectively. The dsRNA treatments imposed caused statistically significant reduction in mean weights (G) that translated into significant rates of mortality (H) in comparison to negative control. Data is average of 3 replicates/treatment±SEM at p≤0.001(***); p≤0.01(**) and p≤0.05(*).
FIG. 24 shows mean weights (A) of FAW larvae exposed to 16 μg of pure dsRNA against newly discovered MIGGS RNAi targets from the RNA-Seq data. The rates of mortality was scored on a 0-3 score were 0, 1, 2 and 3 indicated ≤0, 25, 50 or ≥50 mortality respectively. The dsRNA treatments imposed caused statistically significant reduction in mean weights (A) that also translated into significant rates of mortality (B) in comparison to negative control. Data is average of 3 replicates/treatment±SEM at p≤0.001(***); p≤0.01(**) and p≤0.05(*).
FIG. 25 shows representative phenotypes of RFB beetles feeding on rice flour mixed with 1 μg of pure dsRNA against core MIGGS targets in RFB TcPGRP2, MsβGRP2, dsCHS2, and a previously discovered target MDGP. The RFB beetles feeding on dsRNA against all MIGGS targets displayed significant mortalities at the end of 72 hours of feeding in comparison to negative control treatment (TE). The rates of mortality were significantly higher than negative control treatment and were comparable to the positive control treatment TcvATPaseE. Mortality rate was scored on a 0-3 scale were 0, 1, 2 and 3 indicated ≤0, 25, 50 or ≥50 mortality respectively. Data is average of 6 replicates/treatment (N=18)±SEM at p≤0.001(***); p≤0.01(**) and p≤0.05(*).
FIG. 26A,B shows imageJ analyzed RT-PCR data correlating TH larval phenotypes observed when exposed to 8-16 μg pure dsRNA against a positive control (A) and a core insecticidal MIGGS RNAi target MsβGRP2 (B). The transcript down regulation is correlated with the larval phenotypes observed in FIG. 17. For each pair of vertical bars, 8 μg pure dsRNA is the left bar and 16 μg pure dsRNA is the right bar.
FIG. 26C,D shows imageJ analyzed RT-PCR data correlating TH larval phenotypes observed when exposed to 8-16 μg pure dsRNA against core set of insecticidal MIGGS RNAi targets MsPGPRP2 (C) and MsCHS2 (D). The transcript down regulation is correlated with the larval phenotypes observed in FIG. 17. For each pair of vertical bars, 8 μg pure dsRNA is the left bar and 16 μg pure dsRNA is the right bar.
DETAILED DESCRIPTION
Overview
RNAi-mediated gene-silencing offers a sustainable alternative approach to insect control. Most of the successful RNAi-based pest control strategies thus far employ homology dependent silencing of essential gene functions. Despite this, effective RNAi-based crop protection is lacking for Lepidopteran pests, due to their variable sensitivity to ingested double stranded RNA (dsRNA). (Terenius O, et al. (2011). J Insect Physiol. 57(2): 231-245).
Plant pests are in constant contact with, and ingest significant amount of microbes during herbivory. (Gayatri Priya N. et al. (2012). 7(1), PLos ONE. E30768; Peñuelas and Terradas (2014). 19(5): Trends Plant Sci. 278-280; Engel and Moran (2013). FEMS microbiol. rev. 37(5): 699-735). This interaction between ingested microbes and insect midgut is often considered passive. Recent studies suggest, however, an active role of midgut specific immune responses in reducing variation of core microbial communities during insect herbivory through the activation of pattern recognition receptors (PRR). (Casanova-Torres and Goodrich-Blair (2013). Insects. 4: 320-338; Tang X, et al. (2012) 7(7) PLoS ONE:e36978; Ryu J H. et al. (2008). Science. 37(5): 777-82; Shrestha S. et al. (2009). J Asia Pac. Entomol. 12: 277-283; Buchon, N. et al. (2013). Front. Cell. Infect. Microbiol. 11: 615-626). Further, maintenance of core gut microbial communities via active immune responses and/or their containment in the midgut is key to successful herbivory.
Although, the core innate immune response pathways are conserved, their specific components are under strong selection for diversification. (Casanova-Torres and Goodrich-Blair (2013). Insects. 4: 320-338). Therefore, it is contemplated herein that these pathways provide novel and specific targets for devising sustainable pesticidal RNAi biotechnologies against insect pests. Although gut immune responses have been studied from an immunological perspective, their active manipulation via genetic engineering for pest protection is currently lacking.
Provided herein is the identification of “insect RNAi target genes” (IRTGs) involved in gut microbial clearance and/or containment induced by microbes ingested during feeding and/or active feeding (referred to herein as microbe-induced gut specific genes (MIGGS)) and examples of a novel biotechnology for insect protection via inter-specific silencing of MIGGS-IRTGs. In certain aspects, the MIGGS-IRTGs are Lepidoptera-specific. For example, in certain aspects detailed below, the insect is Manduca sexta (M. sexta; Lepidoptera) (tobacco hornworm (TH)). For example, in certain aspects detailed below, the insect is Spodoptera frugiperda (fall armyworm (FAW)). For example, in certain aspects detailed below, the insect is Plutella xylostella (Diamondback moth (DBM). For example, in certain aspects detailed below, the insect is Ostrinia nubilalis (European corn borer). Still, it is also considered understood that successful, feeding-induced loss of appetite, developmental defects, and/or lethality has the potential to provide protection beyond the order Lepidoptera in an orthologous manner. For example, protection against coleopteran pests such as Leptinotarsa decemlineata (Say) (Colorado potato beetle), Diabrotica spp. (Corn rootworm complex), and Tribolium castaneum (Red Flour Beetle (RFB)). Additionally, this MIGGS-RNAi technique may allow containment of disease transmitting insect vectors and/or enable further manipulation of the plant-microbe-insect interactions for devising pesticidal RNAi for crop protection.
In certain aspects detailed below, silencing of a target gene can result in reduced appetite and/or developmental defects and/or mortality and/or reduced fitness of the insect. In certain aspects these effects are observed after sustained feeding for at least about 24, 36, 48, or 72 hours, or any time inbetween.
Definitions
To the extent necessary to provide descriptive support, the subject matter and/or text of the appended claims is incorporated herein by reference in their entirety.
It will be understood by all readers of this written description that the exemplary embodiments described and claimed herein may be suitably practiced in the absence of any recited feature, element or step that is, or is not, specifically disclosed herein.
It is to be noted that the term “a” or “an” entity refers to one or more of that entity; for example, “a dsRNA molecule,” is understood to represent one or more dsRNA molecules. As such, the terms “a” (or “an”), “one or more,” and “at least one” can be used interchangeably herein.
Furthermore, “and/or” where used herein is to be taken as specific disclosure of each of the specified features or components with or without the other. Thus, the term and/or” as used in a phrase such as “A and/or B” herein is intended to include “A and B,” “A or B,” “A” (alone), and “B” (alone). Likewise, the term “and/or” as used in a phrase such as “A, B, and/or C” is intended to encompass each of the following embodiments: A, B, and C; A, B, or C; A or C; A or B; B or C; A and C; A and B; B and C; A (alone); B (alone); and C (alone).
It is understood that wherever aspects are described herein with the language “comprising,” otherwise analogous aspects described in terms of “consisting of” and/or “consisting essentially of” are also provided.
Unless defined otherwise, technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure is related. Numeric ranges are inclusive of the numbers defining the range. Even when not explicitly identified by “and any range in between,” or the like, where a list of values is recited, e.g., 1, 2, 3, or 4, unless otherwise stated, the disclosure specifically includes any range in between the values, e.g., 1 to 3, 1 to 4, 2 to 4, etc.
The headings provided herein are solely for ease of reference and are not limitations of the various aspects or aspects of the disclosure, which can be had by reference to the specification as a whole.
As used herein, the term “non-naturally occurring” condition, substance, polypeptide, polynucleotide, composition, entity, plant, organism, individual, and/or any combination thereof, or any grammatical variants thereof and the like, is a conditional term that explicitly excludes, but only excludes, those forms that are well-understood by persons of ordinary skill in the art as being “naturally-occurring,” or that are, or might be at any time, determined or interpreted by a judge or an administrative or judicial body to be, “naturally-occurring.”
As used herein, the term “identity,” e.g., “percent identity” to an amino acid sequence or to a nucleotide sequence disclosed herein refers to a relationship between two or more amino acid sequences or between two or more nucleotide sequences. When a position in one sequence is occupied by the same nucleic acid base or amino acid in the corresponding position of the comparator sequence, the sequences are said to be “identical” at that position. The percentage of “sequence identity” is calculated by determining the number of positions at which the identical nucleic acid base or amino acid occurs in both sequences to yield the number of “identical” positions. The number of “identical” positions is then divided by the total number of positions in the comparison window and multiplied by 100 to yield the percentage of “sequence identity.” Percentage of “sequence identity” is determined by comparing two optimally aligned sequences over a comparison window. In order to optimally align sequences for comparison, the portion of a nucleotide or amino acid sequence in the comparison window can comprise additions or deletions termed gaps while the reference sequence is kept constant. An optimal alignment is that alignment which, even with gaps, produces the greatest possible number of “identical” positions between the reference and comparator sequences. Percentage “sequence identity” between two sequences can be determined using, e.g., the program “BLAST” which is available from the National Center for Biotechnology Information, and which program incorporates the programs BLASTN (for nucleotide sequence comparison) and BLASTP (for amino acid sequence comparison), which programs are based on the algorithm of Karlin and Altschul ((1993). Proc. Nat. Acad. Sci. USA. 90(12): 5873-5877).
As used herein, the term “complementary” refers to the ability of polynucleotides to form base pairs with one another. Base pairs are typically formed by hydrogen bonds between nucleotide units in antiparallel polynucleotide strands. Complementary polynucleotide strands can base pair in the Watson-Crick manner (e.g., A to T, A to U, C to G), or in any other manner that allows for the formation of duplexes. When using RNA as opposed to DNA, uracil (U) rather than thymine (T) is the base that is considered to be complementary to adenosine. However; when a U is denoted in the context of the present invention, the ability to substitute a T is implied, unless otherwise stated.
As used herein, the term “polypeptide” is intended to encompass a singular “polypeptide” as well as plural “polypeptides,” and refers to a molecule composed of monomers (amino acids) linearly linked by peptide bonds (also known as amide bonds). The term “polypeptide” refers to any chain or chains of two or more amino acids, and does not refer to a specific length of the product. Thus, peptides, dipeptides, tripeptides, oligopeptides, “protein,” “amino acid chain,” or any other term used to refer to a chain or chains of two or more amino acids are included within the definition of “polypeptide,” and unless specifically stated otherwise the term “polypeptide” can be used instead of, or interchangeably with any of these terms. The term “polypeptide” is also intended to refer to the products of post-expression modifications of the polypeptide, including without limitation glycosylation, acetylation, phosphorylation, amidation, derivatization by known protecting/blocking groups, proteolytic cleavage, or modification by non-standard amino acids. A polypeptide can be derived from a natural biological source or produced by recombinant technology, but is not necessarily translated from a designated nucleic acid sequence. Thus, it can be generated in any manner, including by chemical synthesis.
As used herein, the term “protein” refers to a single polypeptide, i.e., a single amino acid chain as defined above, but can also refer to two or more polypeptides that are associated, e.g., by disulfide bonds, hydrogen bonds, or hydrophobic interactions, to produce a multimeric protein.
As used herein, the term “nucleotide” refers to a ribonucleotide or a deoxyribonucleotide or modified form thereof, as well as an analog thereof. Nucleotides include species that comprise purines, e.g., adenine, hypoxanthine, guanine, and their derivatives and analogs, as well as pyrimidines, e.g., cytosine, uracil, thymine, and their derivatives and analogs. Further, the term nucleotide also includes those species that have a detectable label, such as for example a radioactive or fluorescent moiety, or mass label attached to the nucleotide.
As used herein, the term “polynucleotide” refers to polymers of nucleotides, and includes but is not limited to DNA, RNA, DNA/RNA hybrids including polynucleotide chains of regularly and/or irregularly alternating deoxyribosyl moieties and ribosyl moieties (i.e., wherein alternate nucleotide units have an —OH, then and —H, then an —OH, then an —H, and so on at the 2′ position of a sugar moiety), and modifications of these kinds of polynucleotides, wherein the attachment of various entities or moieties to the nucleotide units at any position are included. The term “polynucleotide” is also intended to encompass a singular nucleic acid as well as plural nucleic acids, and refers to an isolated nucleic acid molecule or construct, e.g., messenger RNA (mRNA) or plasmid DNA (pDNA). A polynucleotide can comprise a conventional phosphodiester bond or a non-conventional bond (e.g., an amide bond, such as found in peptide nucleic acids (PNA)). A polynucleotide can be single stranded or double stranded.
As used herein, the term “nucleic acid” refers to any one or more nucleic acid segments, e.g., DNA or RNA fragments, present in a polynucleotide. By “isolated” nucleic acid or polynucleotide is intended a nucleic acid molecule, DNA or RNA, which has been removed from its native environment. For example, a recombinant polynucleotide encoding a polypeptide subunit contained in a vector is considered isolated as disclosed herein. Further examples of an isolated polynucleotide include recombinant polynucleotides maintained in heterologous host cells or purified (partially or substantially) polynucleotides in solution. Isolated RNA molecules include in vivo or in vitro RNA transcripts of polynucleotides. Isolated polynucleotides or nucleic acids further include such molecules produced synthetically. In addition, polynucleotide or a nucleic acid can be or can include a regulatory element such as a promoter, ribosome binding site, or a transcription terminator.
As used herein, a “coding region” is a portion of nucleic acid comprising codons translatable into amino acids. Although a “stop codon” (TAG, TGA, or TAA) is not translated into an amino acid, it can be considered to be part of a coding region, but any flanking sequences, for example 5′ untranslated regions (5′ UTRs; also known as a leader sequence), 3′ untranslated regions (3′ UTRs; also known as a trailer sequence), promoters, ribosome binding sites, transcriptional terminators, introns, and the like, are not part of a coding region. Two or more coding regions can be present in a single polynucleotide construct, e.g., on a single vector, or in separate polynucleotide constructs, e.g., on separate (different) vectors. Furthermore, any vector can contain a single coding region, or can comprise two or more coding regions, e.g., a single vector can separately encode a selection marker gene and a gene of interest. In addition, a vector, polynucleotide, or nucleic acid can encode heterologous coding regions, either fused or unfused to a nucleic acid encoding a polypeptide subunit or fusion protein as provided herein. Heterologous coding regions include without limitation specialized elements or motifs, such as a secretory signal peptide or a heterologous functional domain.
A variety of transcription regulatory regions are known to those skilled in the art. These include, without limitation, transcription regulatory regions that function in vertebrate cells, such as, but not limited to, promoter and enhancer segments from cytomegaloviruses (the immediate early promoter, in conjunction with intron-A), simian virus 40 (the early promoter), and retroviruses (such as Rous sarcoma virus). Other transcription regulatory regions include those derived from vertebrate genes such as actin, heat shock protein, bovine growth hormone and rabbit 0-globin, as well as other sequences capable of controlling gene expression in eukaryotic cells. Additional suitable transcription regulatory regions include tissue-specific promoters and enhancers.
Similarly, a variety of translation regulatory elements are known to those of ordinary skill in the art. These include, but are not limited to ribosome binding sites, translation initiation and termination codons, and elements derived from picornaviruses (particularly an internal ribosome entry site, or IRES).
As used herein, the term “vector” is nucleic acid molecule as introduced into a host cell or organelle, thereby producing a transformed host cell or organelle. A vector can include nucleic acid sequences that permit it to replicate in a host cell, such as an origin of replication. A vector can also include one or more selectable marker gene and other genetic elements known in the art. Illustrative types of vectors include plasmids, phages, viruses and retroviruses.
As used herein, the term “transformed” cell or organelle, or a “host” cell organelle, is a cell or organelle into which a nucleic acid molecule has been introduced by molecular biology techniques. As used herein, the term transformation encompasses those techniques by which a nucleic acid molecule can be introduced into such a cell or organelle, including transfection with viral vectors, transformation with plasmid vectors, and introduction of naked DNA by electroporation, lipofection, and particle gun acceleration. A transformed cell or a host cell can be a bacterial cell or a eukaryotic cell.
As used herein, the term “expression” refers to a process by which a gene produces a biochemical, for example, a polynucleotide or a polypeptide. The process includes any manifestation of the functional presence of the gene within the cell including, without limitation, gene knockdown as well as both transient expression and stable expression. It includes without limitation transcription of the gene into messenger RNA (mRNA), and the translation of such mRNA into polypeptide(s). It also includes without limitation transcription of the gene into an RNA molecule that is not translated into a polypeptide but is capable of being processed by cellular RNAi mechanisms. If the final desired product is a biochemical, expression includes the creation of that biochemical and any precursors. Expression of a gene produces a “gene product.” As used herein, a gene product can be either a nucleic acid, e.g., an RNA produced by transcription of a gene or a polypeptide that is translated from a mRNA transcript. Gene products described herein further include nucleic acids with post transcriptional modifications, e.g., polyadenylation, or polypeptides with post translational modifications, e.g., methylation, glycosylation, the addition of lipids, association with other protein subunits, proteolytic cleavage, and the like.
As used herein the term “engineered” includes manipulation of nucleic acid or polypeptide molecules by synthetic means (e.g. by recombinant techniques, in vitro peptide synthesis, by enzymatic or chemical coupling of peptides or some combination of these techniques).
As used herein, the term “hpRNA” refers to hairpin RNA comprising a single-stranded loop region and a base-paired stem of an inversely repeated sequence. hpRNA can be generated from an hpRNA construct (or vector) and/or an hpRNA transgene comprising an inversely-repeated sequence of the RNAi target gene with a spacer region between the repeats. The RNA transcribed from such a sequence self-hybridizes to form a hairpin structure. The stem can be used as a substrate for the generation of siRNAs, but few or none are generated from the loop. Since a spacer region is needed for the stability of the transgene construct, but is not involved in siRNA production, an intron sequence is often used in this position. (Watson J M, et al. (2005). FEBS Letters. 579: 5982-8987).
As used herein, the term “siRNA” refers to small (or short) interfering RNA (or alternatively, silencing RNA) duplexes that are capable of inducing the RNA interference (RNAi) pathway. These molecules can vary in length (generally between 18-30 base pairs) and contain varying degrees of complementarity to their target mRNA in the antisense strand. Some, but not all, siRNA have unpaired overhanging bases on the 5′ or 3′ end of the sense strand and/or the antisense strand. The term “siRNA” includes duplexes of two separate strands, as well as single strands that can form hairpin structures comprising a duplex region.
As used herein, the phrase “duplex region” refers to the region in two complementary or substantially complementary polynucleotides that form base pairs with one another, either by Watson-Crick base pairing or any other manner that allows for a stabilized duplex between polynucleotide strands that are complementary or substantially complementary. For example, a polynucleotide strand having 21 nucleotide units can base pair with another polynucleotide of 21 nucleotide units, yet only 19 bases on each strand are complementary or substantially complementary, such that the “duplex region” has 19 base pairs. The remaining bases may, for example, exist as 5′ and 3′ overhangs. Further, within the duplex region, 100% complementarity is not required; substantial complementarity is allowable within a duplex region. Substantial complementarity as used herein refers to 79% or greater complementarity. For example, a mismatch in a duplex region consisting of 19 base pairs results in 94.7% complementarity, rendering the duplex region substantially complementary.
As used herein, the phrase “gene silencing” refers to a process by which the expression of a specific gene product is lessened or attenuated. Silencing of a gene does not require that the expression or presence of the gene product is completely absent, but that in the context (e.g., comparing expression of a target gene in a plant expressing a gene silencing nucleic acid compared to a control plant or the health of an insect feeding on a gene silencing nucleic acid compared to a control insect), an observable effect in comparison to a control is observed. While gene silencing can take place by a variety of pathways, unless specified otherwise, as used herein, gene silencing refers to decreases in gene product expression that results from RNA interference (RNAi) as understood by one of ordinary skill in the art. The level of gene silencing can be measured by a variety of means, including, but not limited to, measurement of transcript levels by Reverse transcription polymerase chain reaction (PCR), Northern Blot Analysis, B-DNA techniques, transcription-sensitive reporter constructs, expression profiling (e.g. DNA chips), and related technologies. Alternatively, the level of silencing can be measured by assessing the level of the protein encoded by a specific gene. This can be accomplished by performing a number of studies including Western Analysis, measuring the levels of expression of a reporter protein that has e.g. fluorescent properties (e.g. GFP) or enzymatic activity (e.g. alkaline phosphatases), or several other well-known procedures. Further, gene silencing can be assessed by its effect on a pest insect such as resulting in reduced appetite and/or developmental defects and/or mortality of an insect.
As used herein, the term “control” is consistent with its well-established scientific use that refers to a standard of comparison recognized by one of ordinary skill in the art as having a representative level of expression, phenotype, resistance, feeding, mortality, development, etc. Further, one of ordinary skill in the art will recognize, for example, that a statistical outlier and/or non-representative result produced by chance, abnormal environmental condition, manipulation, or other reason, that varies from a standard representation, would not be an appropriate control.
As used herein, “microbe-induced gut specific genes (MIGGS)” refers to a gene or group of genes expressed in the insect midgut in response to microbes ingested during normal process of insect feeding and primarily functioning to clear or respond to the ingested microbes and/or contain the microbes to insect gut via maintenance of midgut structural integrity.
As used herein, “actively feeding stage of the insect” refers to all feeding stages of insects with both complete and incomplete metamorphosis.
Nucleic Acids for Gene Silencing
Provided herein are nucleic acid molecules for use in, among other things, crop protection from insect pests. In certain aspects disclosed herein, the nucleic acid molecules are isolated. The nucleic acid molecules specifically target certain insect genes (referred to herein interchangeably as “target genes,” “RNAi target genes,” “insect RNAi target genes,” and “IRTGs”), in insects for gene silencing. For example, in certain aspects, the nucleic acid molecules target certain insect microbe-induced gut gene (MIGGS) RNAi targets. In certain aspects, the silencing of a target gene occurs when a nucleic acid molecule of this disclosure is ingested by an insect. In certain aspects, the target gene is an insect gene that is implicated in insect immune responses (type 1 MIGGS RNAi target). A critical immune response gene is a genetically tractable nuclear or cytoplasmic loci that is important for providing cellular and/or humoral defense in insects against internal microorganisms, external microorganisms, and/or other insect parasites. In certain aspects, the immune response genes (type 1 MIGGS RNAi target) can also be a pattern recognition receptor (PRR) gene (Casanova-Torres and Goodrich-Blair (2013). Insects. 4:320-338). A PPR gene is a genetically tractable loci of an insect that encodes soluble or membrane bound proteins that recognize signatures associated with and/or released by microorganisms. PRR genes can activate or be activated by the immune response pathways to minimize microbial infection and can be co-regulated by the immune deficiency (IMD) pathway (Tang X, et al. (2012) 7(7) PLoS ONE:e36978; Ryu J H. et al. (2008). Science. 37(5): 777-82; Shrestha S. et al. (2009). In certain aspects the PRR type genes are co-regulated by the immune deficiency (IMD) pathway in TH were identified, these genes having been recently summarized. (Casanova-Torres and Goodrich-Blair (2013). Insects (4): 320-338; Zhong X, et al. (2012). Insect Biochem. Mol. Biol. 42(7): 514-524); Zhang X, et al. (2015). Insect Biochem. Mol. Biol. 62:38-50; Cao X, et al. (2015). Insect Biochem. Mol. Biol. 62:64-74; Kanost M R, et al. (2016). Insect Biochem. Mol. Biol 76:118-147). In certain aspects, the target gene is an insect gene that is necessary for structural integrity of insect organs including the mid-gut and also facilitates the containment of the ingested microbes to the insect gut. (type 2 MIGGS RNAi target). In certain aspects, the target gene is an insect midgut structural component gene (type 2) (Odman-Naresh et al. (2013). PLoS ONE 8:e82015. 10.1371/journal.pone.0082015). A midgut structural component gene is a genetically tractable loci in an insect that encodes chitin fibrils, proteins, or glycoproteins that form a protective sac-like structure called peritrophic matrix enveloping the insect food bolus/midgut also functioning to contain the ingested microbes in the gut (Engel and Moran (2013). FEMS Microbiol Rev. 37 699-735). In certain aspects, the target genes (type 1 and 2 MIGGS RNAi targets) are predominantly expressed in the insect midgut, for example, abundantly and/or exclusively expressed in the larval and/or adult insect midgut in response to active feeding and/or microbial infection and/or responding to microbes ingested during feeding. In certain aspects, the target gene is induced predominantly in a midgut specific manner during active feeding (type 1 and type 2 MIGGS RNAi targets). The midgut abundance of both type 1 and 2 MIGGS RNAi target genes may mitigate problems associated with reduced amounts of bioavailability.
Representative examples of insect MIGGS RNAi target genes and their nucleic acid sequences identified from published literature are provided herein. In certain aspects, the target gene is one or more of M. sexta-Hemolin (MsHEM), M. sexta-Serine proteinase homolog 3 (MsSPH-3), M. sexta-Peptidoglycan recognition protein 2 (MsPGRP2), M. sexta-Beta-1, 3-glycan-recognition protein 2 (MsβGRP2), M. sexta-Relish family protein 2A (MsREL2A), M. sexta-Dorsal (MsDor), M. sexta-Spatzle (MsSPZ1A), M. sexta-Toll receptor (MsTOLL), M. sexta-Scolexin A (MsSCA1), M. sexta-Hemolymph proteinase 18 (MsHP18), M. sexta-Transferrin (MsTRN), M. sexta-Arylphorin beta subunit (MsARP), M. sexta-Chymotrypsinogen-like protein 1 (MsCTL1), M. sexta-Valine Rich Midgut Protein (MsVMP1), M. sexta-Imd (MsImd), M. sexta-FADD (MsFADD), M. sexta-Dredd (MsDRD), M. sexta-Relish F (MsReIF), M. sexta-Cdc42 (MsCdc42), M. sexta-Dsor1 (MsDsor1), M. sexta-Fos (MsFos), M. sexta-Jra (MsJra), M. sexta-Caudal (MsCAD1), M. sexta-Atg8 (MsAtg8), M. sexta-Atg13 (MsAtg13), M. sexta-IAP1 (MsIAP1), M. sexta-Chitin synthase 2 (MsChs2), M. sexta-Beta fructofuranosidase 1 (MsSuc1), and orthologs thereof.
In certain aspects, the target gene is one or more of M. sexta-Hemolin (MsHEM), M. sexta-Serine proteinase homolog 3 (MsSPH-3), M. sexta-Peptidoglycan recognition protein 2 (MsPGRP2), M. sexta-Beta-1, 3-glycan-recognition protein 2 (MsβGRP2), M. sexta-Relish family protein 2A (MsREL2A), M. sexta-Dorsal (MsDor), M. sexta-Spatzle (MsSPZ1A), M. sexta-Toll receptor (MsTOLL), M. sexta-Scolexin A (MsSCA1), M. sexta-Hemolymph proteinase 18 (MsHP18), M. sexta-Transferrin (MsTRN), M. sexta-Arylphorin beta subunit (MsARP), M. sexta-Chymotrypsinogen-like protein 1 (MsCTL1), M. sexta-Valine Rich Midgut Protein (MsVMP1), M. sexta-Imd (MsImd), M. sexta-FADD (MsFADD), M. sexta-Dredd (MsDRD), M. sexta-Relish F (MsReIF), M. sexta-Cdc42 (MsCdc42), M. sexta-Dsor1 (MsDsor1), M. sexta-Fos (MsFos), M. sexta-Jra (MsJra), M. sexta-Caudal (MsCAD1), M. sexta-Atg8 (MsAtg8), M. sexta-Atg13 (MsAtg13), M. sexta-IAP1 (MsIAP1), M. sexta-Chitin synthase 2 (MsChs2), and M. sexta-Beta fructofuranosidase 1 (MsSuc1), M. sexta-Sickie (MsSck), M. sexta-Akirin (MsAki), M. sexta-Cactus (MsCac), M. sexta-Gloverin (MsGlv) and M. sexta-Beta-1-tubulin (MspTub).
In certain aspects, the target gene is an ortholog of one or more of M. sexta-Hemolin (MsHEM), M. sexta-Serine proteinase homolog 3 (MsSPH-3), M. sexta-Peptidoglycan recognition protein 2 (MsPGRP2), M. sexta-Beta-1, 3-glycan-recognition protein 2 (MsβGRP2), M. sexta-Relish family protein 2A (MsREL2A), M. sexta-Dorsal (MsDor), M. sexta-Spatzle (MsSPZ1A), M. sexta-Toll receptor (MsTOLL), M. sexta-Scolexin A (MsSCA1), M. sexta-Hemolymph proteinase 18 (MsHP18), M. sexta-Transferrin (MsTRN), M. sexta-Arylphorin beta subunit (MsARP), M. sexta-Chymotrypsinogen-like protein 1 (MsCTL1), M. sexta-Valine Rich Midgut Protein (MsVMP1), M. sexta-Imd (MsImd), M. sexta-FADD (MsFADD), M. sexta-Dredd (MsDRD), M. sexta-Relish F (MsReIF), M. sexta-Cdc42 (MsCdc42), M. sexta-Dsor1 (MsDsor1), M. sexta-Fos (MsFos), M. sexta-Jra (MsJra), M. sexta-Caudal (MsCAD1), M. sexta-Atg8 (MsAtg8), M. sexta-Atg13 (MsAtg13), M. sexta-IAP1 (MsIAP1), M. sexta-Chitin synthase 2 (MsChs2), M. sexta-Beta fructofuranosidase 1 (MsSuc1), and other IMD pathway or structural integrity genes.
One of ordinary skill in the art would understand that nucleic acid molecules can be, for example, deoxyribonucleic acid (DNA) or ribonucleic acid (RNA). In certain aspects of any target gene silencing nucleic acid molecule described anywhere herein, the nucleic acid molecule is a DNA molecule. In certain aspects of any target gene silencing nucleic acid molecule described anywhere herein, the nucleic acid molecule is a RNA molecule. In certain aspects of any target gene silencing nucleic acid molecule described anywhere herein, the RNA molecule is a double stranded molecule (dsRNA), for example, for use in the RNA interference (RNAi) process. As used herein, a dsRNA molecule is a RNA molecule comprising at least one annealed, double stranded region. In certain aspects, the double stranded region comprises two separate RNA strands annealed together. In certain aspects, the double stranded region comprises one RNA strand annealed to itself, for example, as can be formed when a single RNA strand contains an inversely repeated sequences with a spacer in between. One of ordinary skill in the art will understand that complementary nucleic acid sequences are able to anneal to each other but that two sequences need not be 100% complementary to anneal. The amount of complementarity needed for annealing can be influenced by the annealing conditions such as temperature, pH, and ionic condition. In certain aspects, the annealed RNA sequences are 100% complementary across the annealed region. In certain aspects, the annealed RNA sequences are less than 100% complementary across the annealed region but have enough complementarity to anneal within their environment, such as in a host cell or the gut of an insect. In certain aspects, the annealed RNA sequences are substantial complementarity as defined elsewhere herein.
It is contemplated that the nucleic acid molecules disclosed anywhere herein for the silencing of target genes derive their specificity from comprising a nucleic acid sequence that is complementary or substantially complementary to at least a portion of a target gene sequence. Substantially complementary sequences, however, may be more likely to have reduced specificity and produce off-target effects. As referred to anywhere herein, a target gene sequence can include at least the target gene protein coding region, the 5′ untranslated region (5′ UTR), and/or the 3′ untranslated region (3′ UTR) and any portion or combination thereof. For example, predicted UTR regions can be identified using previously established criteria (Siepel, et al. (2005). Genome Res. 15: 1034-1050) when corresponding genomic sequences are available.
In certain aspects, an isolated double stranded RNA (dsRNA) molecule comprises a nucleic acid sequence complementary to about 21 to 2000 contiguous nucleotides of a target gene sequence discloses anywhere herein. For example, in certain aspects, an isolated double stranded RNA (dsRNA) molecule comprises a nucleic acid sequence complementary to about any of 21, 22, 23, 24, 25, 30, 40, 50, 60, 100, 120, 200, 240, 300, 400, 500, 600, 650, 750, 1000 to about any of 23, 24, 25, 30, 40, 50, 100, 200, 300, 400, 500, 600, 650, 750, 1000, or 2000 contiguous nucleotides of a target gene sequence. For example, in certain aspects, an isolated dsRNA molecule comprises a nucleic acid sequence complementary to about 100 to 1000 or about 200 to 1000 contiguous nucleotides of a target gene sequence. For example, in certain aspects, an isolated dsRNA molecule comprises a nucleic acid sequence complementary to about 100 to 1000 or about 200 to 1000 contiguous nucleotides of the protein coding region of a target gene sequence. For example, in certain aspects, an isolated dsRNA molecule comprises a nucleic acid sequence complementary to about 100 to 1000 or about 200 to 1000 contiguous nucleotides of the 5′ UTR region or the 3′ UTR region of a target gene sequence. In certain aspects, the isolated dsRNA molecule comprises a nucleic acid sequence complementary to a contiguous region comprising at least about 50%, 60%, 70%, 80%, 90%, 95%, 98%, 99%, or 100% of the length of the target gene sequence protein coding region, the target gene sequence 5′ UTR region, the target gene 3′ UTR region, and/or any combination thereof. For example, if a target gene sequence protein coding region is determined to be 200 nucleotides long, then an isolated dsRNA molecule comprising a nucleic acid sequence complementary to a contiguous region comprising 95% of the length of the target gene sequence protein coding region would be complementary to a contiguous region 190 nucleotides long.
In certain aspects of any target gene silencing nucleic acid molecule described anywhere herein, including dsRNA molecules for RNAi, the target gene comprises one or more of the nucleic acid sequence of SEQ ID NO: 1-14, 16-29, 31-69, 70-75, 76-88, 89-105, and 106-110. In certain aspects, the target gene comprises the nucleic acid sequence of SEQ ID NO: 3 or 14. Thus, in certain aspects, the isolated dsRNA molecule comprises a nucleic acid sequence complementary to about any of 21, 22, 23, 24, 25, 30, 40, 50, 100, 200, 300, 400, 500, 600, 650, 750, 1000 to about any of 23, 24, 25, 30, 40, 50, 100, 200, 300, 400, 500, 600, 650, 750, 1000, or 2000 contiguous nucleotides of a target gene sequence comprising a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-14, 16-29, 31-69, 70-75, 76-88, 89-105, and 106-110. For example, in certain aspects, the isolated dsRNA molecule comprises a nucleic acid sequence complementary to about 100 to 1000 or about 200 to 1000 contiguous nucleotides of a target gene sequence comprising a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-14, 16-29, 31-69, 70-75, 76-88, 89-105, and 106-110. In certain aspects, the isolated dsRNA comprises a nucleic acid sequence complementary to about 200 to 1000 contiguous nucleotides of the protein coding region of a target gene sequence comprising a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-14, 16-29, 31-69, 70-75, 76-88, 89-105, and 106-110. In certain aspects, the isolated dsRNA molecule comprises a nucleic acid sequence complementary to a contiguous region comprising at least about 50%, 60%, 70%, 80%, 90%, 95%, 98%, 99%, or 100% of the length of the target gene sequence protein coding region, the target gene 5′ UTR region, and/or the target gene 3′ UTR region. In certain aspects, the isolated dsRNA molecule comprises a nucleic acid sequence complementary to a contiguous region comprising at least about 50%, 60%, 70%, 80%, 90%, 95%, 98%, 99%, or 100% of the length of a sequence selected from the group consisting of SEQ ID NOs: 1-14, 16-29, 31-69, 70-75, 76-88, 89-105, and 106-110.
In certain aspects of any target gene silencing nucleic acid molecule described anywhere herein, the nucleic acid molecule can form siRNA. Thus, certain aspects provide for an siRNA molecule derived from the processing of a dsRNA molecule for silencing a target gene disclosed herein.
Insecticidal Compositions
Certain aspects of the disclosure provide for an insecticidal composition comprising a nucleic acid molecule disclosed anywhere herein for silencing a target gene, including long dsRNA, hpRNA, and siRNA. In certain aspects, the insecticidal composition also comprises a synthetic carrier or a microbial conduit. For example, a microbial conduit can be a microorganism that has a natural capacity or is engineered to produce and/or deliver dsRNA to increase its bioavailability and/or biostability for causing RNA interference. Representative examples include plant growth promoting organisms, normal commensal and/or symbiotic microorganisms associated with the target insect pest or pest target host or host cultivation range etc. from an insect engineered or identified from natural populations to produce and/or deliver dsRNA. In certain aspects a microbial conduit can be used as a direct topical application on a whole plant or coated onto a seed or mixed with growth media or transmitted through fertilizer or irrigation, etc. In certain aspects, the nucleic acid molecule of the insecticidal composition is conjugated to the synthetic carrier. For example, a synthetic carrier can be an inert chemical compound with a natural or engineered affinity to bind (conjugate) a dsRNA molecule to increase its biostability and/or bioavailability for causing RNA interference. In certain aspects, a synthetic carrier comprises a combination of inert chemicals or nanoparticles that upon combining and/or individually have a net positive charge or general affinity to bind to negatively charged dsRNA. Representative examples include chitosan, liposomes, carbon quantum dots, biodegradable particles of plant (e.g. coconut coir or grain flour, etc.) or soil (e.g. calcified clay) origin etc. In certain aspects, the dsRNA conjugated with a synthetic carrier can be used as a direct topical application directly and/or after aerosolization on a whole plant or coated onto a seed or mixed with growth media or transmitted through fertilizer or irrigation, etc. In certain aspects, dsRNA or a composition comprising dsRNA can be used as a direct topical spray on application to whole plant, coated onto a seed or mixed with growth media or transmitted through fertilizer or irrigation or combined with plant growth promoting microbes etc.
Recombinant Constructs
Certain aspects of this disclosure provide for a recombinant nucleic acid construct, such as a DNA vector, comprising and/or encoding a nucleic acid molecule disclosed anywhere herein for silencing a target gene, including long dsRNA, hpRNA, and siRNA. Certain aspects provide for recombinant nucleic acid constructs comprising and/or encoding an RNAi precursor of a nucleic acid molecule disclosed anywhere herein for silencing a target gene, including long dsRNA, hpRNA, and siRNA.
Certain aspects of this disclosure provide for a recombinant nucleic acid construct, such as a DNA vector, comprising a target gene silencing sequence for silencing a target gene described anywhere herein. In certain aspects, a recombinant DNA construct comprises a gene silencing sequence comprising about any of 21, 22, 23, 24, 25, 30, 40, 50, 60, 100, 120, 200, 240, 300, 400, 500, 600, 650, 750, 1000 to about any of 23, 24, 25, 30, 40, 50, 100, 200, 300, 400, 500, 600, 650, 750, 1000, or 2000 contiguous nucleotides of a target gene sequence disclosed anywhere herein. In certain aspects, a recombinant DNA construct comprises a gene silencing sequence comprising about 100 to 1000 or about 200 to 1000 contiguous nucleotides of a target gene sequence. In certain aspects, the gene silencing sequence comprises about 100 to 1000 or about 200 to 1000 contiguous nucleotides of the protein coding region of the target gene sequence. In certain aspects, the gene silencing sequence comprises about 100 to 1000 or about 200 to 1000 contiguous nucleotides of the 5′ UTR region or the 3′ UTR region of the target gene sequence. In certain aspects, the gene silencing sequence comprises at least 50%, 60%, 70%, 80%, 90%, 95%, 98%, 99%, or 100% contiguously of the length of target gene sequence protein coding region, the target gene sequence 5′ UTR region, target gene sequence 3′ UTR region and/or any combination thereof.
In certain aspects, the target gene comprises a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1-14, 16-29, 31-69, 70-75, 76-88, 89-105, and 106-110. In certain aspects, the gene silencing sequence comprises about 100 to 1000 or about 200 to 1000 contiguous nucleotides of a sequence selected from the group consisting of SEQ ID NOs: 1-14, 16-29, 31-69, 70-75, 76-88, 89-105, and 106-110. In certain aspects, the gene silencing sequence comprises at least 50%, 60%, 70%, 80%, 90%, 95%, 98%, 99%, or 100% contiguously of the length of a sequence selected from the group consisting of SEQ ID NOs: 1-14, 16-29, 31-69, 70-75, 76-88, 89-105, and 106-110.
In certain aspects, the recombinant DNA construct has a gene silencing sequence operably linked to one or more promoters for the expression of a dsRNA molecule that silences the target gene when ingested by an insect. Thus, in certain aspects, the construct is an expression vector. Representative promoters for use in expressing a dsRNA molecule include, but are not limited to, CaMV35S or ZmUbil promoters etc. In certain aspects, the expression vector can target single or multiple insect RNAi target genes, for example, the vector could comprise one or more gene silencing sequences or could employ multiple vectors to target multiple insect RNAi target genes or chimeric dsRNA molecules.
Host Cells and Plants
Provided herein are host cells, plants, and plants parts comprising, expressing, processing, and the like a dsRNA as described anywhere herein for inducing RNAi in an insect. In certain aspects, a host cell comprises a dsRNA molecule, siRNA molecule, a polynucleotide encoding a dsRNA molecule, and/or a construct or a dsRNA encoding segment thereof described anywhere herein. Representative examples of host cells include bacterial cells, fungal cells, yeast cells, plant cells, plant organelles (e.g., including plastids), and mammalian cells. In certain aspects, the host cell is a bacterial or plant cell. In certain aspects, the host cell is a transgenic and/or transplastomic plant cell. One of ordinary skill will understand that there are many well-known methods for introducing a nucleic acid, such as a vector, into a host cell including well-known methods for generating transgenic and/or transplastomic plant cells. In certain aspects, the hose cell expresses a dsRNA molecules and/or produces siRNA to silence a target gene. In certain aspects, a transgenic and/or transplastomic plant can comprise a dsRNA molecule, siRNA, a polynucleotide encoding a dsRNA, and/or a construct or a dsRNA encoding segment thereof. In certain aspects, at least one cell of a transgenic and/or transplastomic plant expresses a dsRNA molecule and/or produces a siRNA for silencing a target gene. Certain aspects provide for a seed, part, tissue, cell, or organelle of a plant described herein, wherein said seed, part, tissue, cell, or organelle comprises a dsRNA molecule and/or the siRNA for silencing a target gene.
Methods of Insect Control
Also provided for herein are various methods of using a dsRNA molecule or vector encoding such dsRNA described anywhere herein for inducing RNAi in an insect and/or silencing a target gene. In certain aspects, this provides for control of insect pests.
Certain aspects provide for a method of silencing an insect immune response gene and/or an insect gene encoding for structural components of the insect midgut. In certain aspects, a method provides for the silencing an insect MIGGS-IRTG. Such method comprises providing for ingestion through spray, drenches, granules, seed coating or plant-incorporated protectant, or the like, to an insect an isolated dsRNA (pure or crude extract), siRNA, insecticidal composition, host cell, transgenic and/or transplastomic plant, and/or the seed, part, tissue, cell, or organelle thereof described anywhere herein.
Certain aspects provide for a method of silencing an insect immune response gene and/or an insect gene encoding for structural components of the insect midgut. In certain aspects, a method provides for the silencing an insect MIGGS-IRTG. Such method comprises providing for ingestion through spray, drenches, granules, seed coating or plant-incorporated protectant, or the like, to an insect an isolated dsRNA, siRNA, insecticidal composition, host cell, transgenic and/or transplastomic plant, and/or the seed, part, tissue, cell, or organelle thereof described anywhere herein.
Certain aspects provide for protecting a plant, such as a crop plant, from an insect pest including but not limited to pests of the order Lepidoptera like Manduca sexta (tobacco hornworm), Spodoptera frugiperda (fall armyworm), Ostrinia nubilalis (European corn borer), Plutella xylostella (Diamondback moth) or pests of the order Coleoptera like Leptinotarsa decemlineata Say (Colorado potato beetle), Diabrotica spp. (Corn rootworm complex), Tribolium castaneum (Red flour beetle), Popillia japonica (Japanese beetle), Agrilus planipennis (Emerald ash borer) or pests of the order Hemiptera like Diaphorina citri (Asian citrus psyllid), Cimex lectularius (Bed bug) or pests of the order Blattodea like all species of cockroaches and termites or insect pests of the order Diptera like all species of Mosquitoes and flies etc. Representative examples of plant hosts include, but are not restricted to, Zea mays L (corn), Sorghum bicolor (sorghum), Setaria italica (fox tail millet), Pennisetum glaucum (Pearl millet), Solanum tuberosum (potato), Oryza sativa (rice), Lycopersicon esculentum (tomato), Solanum melongena (eggplant), all cultivars of Brassica oleracea family, Citrus sinensis (Orange), trees of Oleaceae family and crops of Rosaceae etc. Such methods comprise, for example, topically applying to the plant the isolated dsRNA (pure or crude extract), the siRNA, and/or the insecticidal composition described anywhere herein, and providing the plant in the diet of the insect pest. In certain aspects the dsRNA molecule is topically applied by expressing the dsRNA in a microbe followed by topically applying the microbe onto the plant and/or seed.
Certain aspects provide for producing a plant resistance to a pest insect of said plant. Such methods comprises transforming the plant with a polynucleotide encoding a dsRNA and/or a construct or a dsRNA encoding segment describe anywhere herein, wherein the plant expresses a dsRNA and/or siRNA and/or the plant comprises a dsRNA and/or siRNA containing insecticidal compositions described anywhere herein, for silencing a target gene. In certain aspects, the transformed plant is more resistant to a pest insect of said plant than untransformed plants.
Certain aspects provide for improving crop yield. Such methods comprise growing a population of crop plants transformed with a polynucleotide encoding a dsRNA and/or the construct or a dsRNA encoding segment thereof described anywhere herein, wherein the plant expresses a dsRNA and/or siRNA and/or the plant comprises a dsRNA and/or siRNA containing insecticidal compositions described anywhere herein, for silencing a target gene. In certain aspects, a population of transformed plants produces higher yields in the presence of pest insect infestation than a control population of untransformed plants.
Certain aspects of the disclosure provide for an insecticidal composition comprising a nucleic acid molecule disclosed anywhere herein for silencing a target gene, including long dsRNA, hpRNA, and siRNA. In certain aspects, the insecticidal composition also comprises a synthetic carrier or a microbial conduit. For example, a microbial conduit can be a microorganism that has a natural capacity or is engineered to produce and/or deliver dsRNA to increase its bioavailability and/or biostability for causing RNA interference. Representative examples include plant growth promoting organisms, normal commensal and/or symbiotic microorganisms associated with the target insect pest or parasites and/or natural enemies of the target pest or pest target host or host cultivation range etc. from an insect or parasite and/or natural enemies of the target pest engineered or identified from natural populations containing microbial conduit to produce and/or deliver dsRNA and/or drive the transmission of such microbial conduits into natural populations of insect pests as a control option. In certain aspects a microbial conduit can be used as a direct topical application on a whole plant or coated onto a seed or mixed with growth media or transmitted through fertilizer or irrigation, etc. In certain aspects, the nucleic acid molecule of the insecticidal composition is conjugated to the synthetic carrier. For example, a synthetic carrier can be an inert chemical compound with a natural or engineered affinity to bind (conjugate) a dsRNA molecule to increase its biostability and/or bioavailability for causing RNA interference. In certain aspects, a synthetic carrier comprises a combination of inert chemicals or nanoparticles that upon combining and/or individually have a net positive charge or general affinity to bind to negatively charged dsRNA. Representative examples include chitosan, liposomes, carbon quantum dots, biodegradable particles of plant (e.g. coconut coir or grain flour, etc.) or soil (e.g. calcified clay) origin etc. In certain aspects, the dsRNA conjugated with a synthetic carrier can be used as a direct topical application directly and/or after aerosolization on a whole plant or coated onto a seed or mixed with growth media or transmitted through fertilizer or irrigation, etc. In certain aspects dsRNA or composition comprising the dsRNA can be used as a direct topical spray on application to whole plant, coated onto a seed or mixed with growth media or transmitted through fertilizer or irrigation or combined with plant growth promoting microbes etc.
Certain aspects provide for producing a plant resistant against a pest insect of said plant. Such methods comprise first transforming a plant cell with a polynucleotide encoding the dsRNA and/or the construct or a dsRNA encoding segment described anywhere herein. Next, a plant is regenerated from the transformed plant cell. The plant is then grown under conditions suitable for the expression of the dsRNA. In certain aspects, the transformed plant confers genetically tractable (maternal and/or paternal inherited) gain of function phenotypically manifested as an ability to impair the normal feeding and/or growth and/or development and/or reproductive success of the target plant pest and is consequently resistant to the plant pest insect compared to a control untransformed plant.
In certain aspects of any of the aforementioned methods, the insect larvae ingest the dsRNA. In certain aspects of any of the aforementioned methods, ingestion of the dsRNA induces a melanotic response in the insect larvae. In certain aspects of any of the aforementioned methods, ingestion of the dsRNA results in perturbation of gut microbial homeostasis. In certain aspects of any of the aforementioned methods, ingestion of the dsRNA results in defective clearance of opportunistic microbes. In certain aspects of any of the aforementioned methods, ingestion of the dsRNA results in defective containment of gut microbes.
One of ordinary skill in the art will recognize that, the inventors have demonstrated midgut specific expression of a representative number of MIGGS-IRTGS in TH in response to their feeding on a lab strain of Escherichia coli (E. coli) bacteria. For example, a set of 20 MIGGS-IRTGS (SEQ ID NOs: 1-9, 11, 14, 31, 39, 43, 44, 71-75) that are induced in TH larvae feeding on an induction medium (Wang et al. (2006). J. Biol. Chem. 281(14): 9271-9278) is disclosed herein. It was previously reported that these twenty genes are expressed abundantly in the gut (Table 1). The gut specific expression of 2/20 genes were tested and validated the same (FIG. 7).
Orthologs of the representative TH MIGGS-IRTG (SEQ ID NOs: 76-88) set were identified from transcriptomic resources of an economically important Bt. resistant lepidopteran pest DBM using a combination of reciprocal best Blast analysis (Ward et al. (2014). PLoS ONE 9(7): e101850) and literature curation. Most of these MIGGS-IRTGS were induced in response to the feeding of DBM larvae on induction medium (Wang et al. (2006). J. Biol. Chem. 281(14): 9271-9278), similar to observations with TH larvae.
It was also demonstrated that most of the MIGGS-IRTGS were induced in another economically important lepidopteran pest, FAW, feeding on plants grown on representative field soil, using a RNA-Seq approach.
The RNA-Seq approach also identified additional RNAi candidates (SEQ ID NOs: 89-105) belonging to the MIGGS category. Further, orthologs of the expanded representative TH MIGGS-IRTG set (SEQ ID NO: 106-110) were identified from transcriptomic resources of an economically important Coleopteran pest RFB. It was demonstrated that most of the MIGGS-IRTGS were induced in response to the feeding of RFB beetles on induction medium (Wang et al. (2006). J. Biol. Chem. 281(14): 9271-9278), similar to observations with the order lepidoptera.
It was demonstrated that the targeted silencing of 9 out of 20 MIGGS-IRTGS employing bacterially expressed dsRNA protocol (Timmons L. et al. (2001). Gene. 263:103-112.) is insecticidal to TH larvae. Insecticidal activity against TH larvae correlated with the down regulation of target transcripts. It was demonstrated that the targeted silencing of 7 out of 14 MIGGS-IRTGS using bacterially expressed dsRNA protocol (Timmons L. et al. (2001). Gene. 263:103-112.) is insecticidal to DBM larvae. It was demonstrated that targeted silencing of 9 MIGGS-IRTGS are insecticidal to FAW larvae using bacterially expressed dsRNA protocol (Timmons L. et al. (2001). Gene. 263:103-112.). A core set of three MIGGS-IRTGS (SEQ ID NO: 3, 4, and 43) was identified that are efficacious against all three lepidopteran pests TH, DBM and FAW in an orthologous manner and that leaf discs coated with dsRNA against the core MIGGS-IRTGS are insecticidal against TH, DBM and FAW larvae. Further, plastidal expressed dsRNA against the core MIGGS-IRTGS impacted larval growth and survival.
The following examples are included to demonstrate certain embodiments of the disclosure. It should be appreciated by those of skill in the art that the techniques disclosed in the examples which follow represent techniques discovered by the inventor to function well in the practice of the disclosure. However, those of skill in the art should, in light of the present disclosure, appreciate that many changes can be made in the specific embodiments which are disclosed and still obtain a like or similar result without departing from the spirit and scope of the disclosure.
EXAMPLES
In certain aspects, work was performed towards the identification, induction, isolation and cloning of the selected M. sexta (tobacco hornworm (TH)) MIGGS-IRTGS into a bacterial expression system capable of enabling the cloned genes to produce dsRNA (Timmons L. et al. (2001). Gene. 263:103-112.). Upon ingestion by M. sexta larvae, the bacterially expressed dsRNA is intended to silence, or at least knock-down, reduce, and the like the corresponding MIGGS-IRTG in order to curtail the feeding behavior and/or cause lethal effects in the insect pests. Based upon these results, additional testing was done on other representative insect species to demonstrate and establish for purposes of support wide applicability of the compositions and approaches of the disclosure.
For MIGGS-IRTG selection, PRR type genes co-regulated by the immune deficiency (IMD) pathway in TH were identified, these genes having been recently summarized (Casanova-Torres and Goodrich-Blair (2013). Insects (4): 320-338; Zhong X, et al. (2012). Insect Biochem. Mol. Biol. 42(7): 514-524); Zhang X, et al. (2015). Insect Biochem. Mol. Biol. 62:38-50; Cao X, et al. (2015). Insect Biochem. Mol. Biol. 62:64-74; Kanost M R, et al. (2016). Insect Biochem. Mol. Biol 76:118-147). Notably, most of the PRR genes selected for this study are abundantly induced or predicted to express in a midgut specific manner (Pauchet Y, et al. (2010). Insect. Mol. Biol. 19: 61-75; Kim and Lee (2014). Front. Cell. Infect. Microbiol. 3: 116; Lee and Hase (2014). Nat. Chem. Biol., 10: 416-424).
The TH-Transferrin, Arylphorin β subunit, chymotrypsinogen-like protein 1 and few other immunity related genes do not belong to the conventional PRR type immune responsive genes. However, these genes were included as they potentially contribute to the midgut microbial homeostasis through IMD co-regulation (Pauchet Y, et al. (2010). Insect. Mol. Biol. 19: 61-75). Additionally identified were a TH gene indicated to be a valine rich midgut protein critical for the formation of midgut peritrophic matrix and related genes critical for maintaining the structural integrity of the midgut, which are possibly involved, in the gut microbial containment. (Odman-Naresh et al. (2013). PLoS ONE 8:e82015. 10.1371/journal.pone.0082015; Engel and Moran (2013). FEMS Microbiol Rev. 37 699-735). A non-insect gene that encodes for catalase 1 from cassava (Manihot esculanta) was used as a control.
Materials and Methods
TH larvae required for isolation of IRTG genes and subsequent bioassays were reared as follows: Eggs were procured from Carolina Biological Sciences (Burlington, NC, USA). The eggs were not surface sterilized and used directly for conventional rearing (CR). The larval colony establishment and maintenance was performed employing a Phytatray II (Sigma, MO, USA) unit containing Gypsy Moth diet. (Gunaratna R T and Jiang H (2013). Dev. Comp. Immunol. 39: 388-398).
Bt.-resistant DBM eggs were procured from Benzon Research (Carlisle, PA, USA) and reared conventionally, as described above.
FAW eggs were procured from Benzon Research (Carlisle, PA, USA) and reared conventionally, as described above.
For germ free (GF) rearing procedure, all eggs were surface sterilized with a solution of Tween-80 (polyoxyethylene sorbitan monooleate), bleach, and distilled water as described previously. (Broderick N A, et al. (2009). Environ. Entomol. 29:101-107). The surface sterilized eggs were transferred to Phytatray II (Sigma, MO, USA) unit containing Gypsy Moth diet augmented with antibiotics (500 mg/l each of penicillin, gentamicin, rifampicin, streptomycin). (Broderick N A, et al. (2009). Environ. Entomol. 29:101-107; Gregory R. Richards (2008). Journal of Bacteriology. 190, 4870-4879).
Both CR and GF larvae were reared in an environmental chamber with a 16:8 hours (light:dark) photoperiod at 25° C., until use. For the induction of a representative set of MIGGS-IRTGS of PRR category, 75 colony forming units (CFU) of DH5α competent cells (Invitrogen, CA, USA) re-suspended in PBS buffer were injected into healthy 2-3 instar M. sexta larvae. The larvae were snap frozen in liquid nitrogen and processed for RNA isolation and cDNA synthesis described herein.
For testing the up-regulation of MIGGS-IRTGS by oral feeding on induction media, first instar larvae were reared on Luria broth agar media plated with a mixture of live E. coli (3×107 cells), M. luteus (30 μg), and curdlan (30 μg) in 50 μl of H2O (Wang et al. (2006). J. Biol. Chem. 281(14): 9271-9278).
Total RNA was isolated using RNeasy Mini Kit reagent (QIAGEN, NY, USA) and treated with TURBO DNase (Ambion-Life Technologies, NY, USA) using manufacturer's protocols. One μg of DNase treated RNA was used for cDNA synthesis using iScript cDNA synthesis kit (Bio-Rad, CA, USA). The cDNA was used as a template for amplifying near full-length transcripts of the IRTG. Similarly, a control gene from cassava was also amplified. For tissue specific cDNA synthesis the control and treatment larvae were squeezed to isolate hemolymph fraction (HL), dissect midgut (MDG) to obtain rest of the body as described in Pauchet et al. (2010). Insect. Mol. Biol. 19: 61-75). The cDNA template was used for RT-PCR reactions were appropriate using the SuperScript III One-Step RT-PCR system following manufacturers protocol (Thermo Scientific; USA).
Transcripts of TH, DBM, and FAW MIGGS-IRTGS and non-insect control genes were PCR amplified using PrimeSTAR GXL DNA Polymerase (Clontech Laboratories, CA, USA). The PCR reactions were conducted using the following conditions: denaturation at 98° C. for 30 s, annealing at 55/60° C. for 30 s and elongation at 72° C. for 45 s, for 35 cycles. The PCR products were resolved by agarose gel electrophoresis and stained with ethidium bromide. The transcripts were gel eluted using QIAquick gel extraction kit (QIAGEN, NY, USA).
Sequence confirmed transcripts were cloned into pCR8/GW vector (Invitrogen, CA, USA) using manufacturer's protocol. The sequence confirmed recombinant pCR8 clones were cloned into L4440gtwy using LR clonase enzyme (Inivtrogen, CA, USA). The L4440gtwy is a modified version of Timmons and Fire feeding Vector and was a kind gift from Guy Caldwell (Addgene plasmid #11344). (Timmons & Fire (1998). Nature, 395: 854).
For ingestible RNAi bioassays, sequence confirmed MIGGS-IRTG were cloned into an L4440 feeding vector between two T7 promoters in inverted orientation and transformed into an E. coli bacterial strain carrying IPTG-inducible expression of T7 polymerase, HT115 (DE3). (Timmons & Fire (1998). Nature, 395: 854). Modification of IRTG in this manner was previously demonstrated to induce the expression of dsRNA. (Timmons L, et al. (2001). Gene, 263, 103-112; Kamath R S, et al. (2000). Genome Biol. 2: 1-10.).
The HT115 (DE3) strain is an RNase III-deficient E. coli strain whose T7 polymerase activity is IPTG-inducible. The HT115 (DE3) genotype is as follows: F—, mcrA, mcrB, IN (rinD-rrnE) 1, lambda -, mc14::Tn10 (DE3 lysogen: lavUV5 promoter-T7 polymerase) (IPTG-inducible T7 polymerase) (RNase III minus), with tetracycline as a selectable marker. (Kamath R S, et al. (2000). Genome Biol. 2:1-10). The standard heat shock protocol for transformation of L4440::IRTG and control construct was used.
Single colonies of HT115 bacteria containing cloned L4440 plasmids were picked and grown in a 5 mL LB culture with 50 mg/ml ampicillin (Amp). One mL of the liquid culture was saved for plasmid isolation followed by sequence confirmation of the L4440::IRTG clone. The recombinant bacterial clones were grown for 8 hours in liquid culture and were seeded directly on LB plates containing 1 mM IPTG and 50 mg/ml Amp for inducing the dsRNA. (Kamath R S, et al. (2000). Genome Biol. 2: 1-10). Seeded plates were allowed to dry under laminar airflow chamber and incubated at 37° C. temperature overnight.
For larval bioassay three to five 1-2-instar TH, DBM, and FAW larvae were placed on induced plates containing HT115 (DE3) cells containing the desired L4440::IRTG. Bioassays were conducted testing the TH larvae against MIGGS-IRTGS and controls listed in Table 1.
TABLE 1
|
|
List of total MIGGS-IRTGS from TH tested.
|
Manduca sexta MIGGS
NCBI
Insect Biological
Midgut
Insecticidal
|
RNAI Target Genes
Acession Number
Function
Expression
Activity
|
|
Ms_PGRP2 (SEQ ID NO: 3)
GQ293365.1
Immunity
Yes*
Yes
|
Ms_IMD (SEQ ID NO: 31)
Msex2.05477-RA
Immunity
Yes{circumflex over ( )}
No
|
Ms_Toll2 (SEQ ID NO: 8)
EF442782.1
Immunity
Yes{circumflex over ( )}
Yes
|
Ms_Sck (SEQ ID NO: 71)
Msex2.03324-RA
Immunity
Yes{circumflex over ( )}
No
|
Ms_Akl (SEQ ID NO: 72)
Msex2.12479-RA
Immunity
Yes{circumflex over ( )}{circumflex over ( )}
No
|
Ms_Rel2A (SEQ ID NO: 5)
HM363513.1
Immunity
Yes{circumflex over ( )}
Yes
|
Ms_Spz1A (SEQ ID NO: 47)
GQ249944.1
Immunity
Yes{circumflex over ( )}
Yes
|
Ms_Cac (SEQ ID NO: 73)
Msex2.02793-RA
Immunity
Yes{circumflex over ( )}
No
|
Ms_Dorsal (SEQ ID NO: 6)
HM363515.1
Immunity
Yes{circumflex over ( )}{circumflex over ( )}
No
|
Ms_Cad1 (SEQ ID NO: 39)
Msex2.04570-RA
Immunity
Yes{circumflex over ( )}
No
|
Ms_Hemolin1 (SEQ ID NO: 1)
M64346.1
Immunity
Yes++
No
|
Ms_SPH3 (SEQ ID NO: 2)
AF413067.1
Immunity
DNA
No
|
Ms_Transferrin1 (SEQ ID NO: 11)
M62802.1
Immunity
Yes+++
No
|
Ms_Gloverin1 (SEQ ID NO: 74)
Gl110649240
Immunity
Yes{circumflex over ( )}{circumflex over ( )}{circumflex over ( )}
No
|
Ms_HPA18 (SEQ ID NO: 9)
AY672794.1
Immunity
No
No
|
Ms_βGRP2 (SEQ ID NO: 4)
AY135522.1
Immunity
Yes*
Yes
|
Ms_CHS2 (SEQ ID NO: 43)
AY821560.1
Structural Integrity
Yes*
Yes
|
Ms_βTub (SEQ ID NO: 75)
AF030547
Structural Integrity
Yes+
Yes
|
Ms_Suc1 (SEQ ID N: 44)
GQ293363.1
Structural Integrity
Yes*
Yes
|
Ms_VMP1 (SEQ ID NO: 14)
NA
Structural Integrity
Yes+
Yes
|
Ms_vATPaseE (Positive Control)
X67131
ATP Hydrolysis
Yes
Yes
|
Me_Catalase 1 (Negative Control)
AF170272
None
No
No
|
|
Phenotypic differences in the larval development on L4440::IRTG containing HT115 (DE3) plates were documented and compared with the larval growth on negative and positive controls containing HT115 (DE3) plates. The larval phenotypes for a given treatment with appropriate controls were only considered true and documented if they were reproducibly observed in ⅔ or ⅘ larvae, in at least two independent feeding experiments.
For sprayable RNAi, a 24-well plate-based bioassay system was developed using a modified cetyl trimethylammonium bromide method of MEGAscript RNAi kit following manufacturer's protocol (Thermo Scientific, USA) for large-scale purification of dsRNA against a given MIGGS-IRTG. Integrity of the dsRNA was determined by electrophoresis on 1% agarose gel and its concentration determined using NanoDrop UV-VIS spectrometer. Leaf discs of 1 cm2 diameter were detached from Nicotiana benthamiana (for TH) or Arabidopsis Col-WT (for DBM) or wheat cultivar Bobwhite (for FAW) plants grown on field soil were drop inoculated with 0, 4, 8 or 16 μg of purified dsRNA in TE buffer. Air-dried dsRNA coated leaf discs were placed in the bioassay plate containing 1 mL of 1% Murashige and Skoog agar medium per well. Each well contained one leaf disc and was infested with conventionally reared three first instar TH or DBM or FAW larvae. dsRNA coated leaf discs were replaced once every 24 hours and insecticidal activity of each dsRNA measured as a function of larval mortality after five days continuous feeding. The RFB bioassays were conducted using a previously published flour disc assay protocol (Cao et al. (2018). Int. J. Mol. Sci. 19, 1079) with adult beetles.
For RNA-Seq analysis to test if the MIGGS pathway genes are induced by soil microbiome in FAW, wheat (Triticum aestivum) seeds were surface sterilized and planted in 4.5″ pots containing field soil or filled with 4:1 sterile turface:sand mix. Seedlings were grown a growth chamber at for 20 days and infested with ten first-instar FAW larvae per pot. Vigorous larval feeding activity was confirmed and larval samples collected for RNA-Seq analysis. A “pooled RNA-Seq” approach (Rajkumar et al. (2015). BMC Genomics. 16(1): 548) was used to obtain a snap shot of differential FAW gene expression in response to feeding on plants grown on microbe rich (field soil) and microbe depleted (sterile surface) substrate.
In order to demonstrate additional dsRNA delivery methods a plastidal dsRNA expression system was employed. Since high concentrations of long dsRNAs can be stably produced in plastids (Zhang et al. (2015). Science. 347(6225): 991-994), three of the most potent insecticidal TH MIGGS-IRTGS (SEQ ID NO: 3, 4, and 43) dsRNAs (dsMsPGRP2; dsMsβGRP2 and dsMsCHS2) were expressed by plastid transformation in tobacco plants in collaboration with Plastomics Inc. following a previously published protocol (Zhang et al. (2015). Science. 347(6225): 991-994). Detached leaves of stable transplastomic lines expressing dsRNA against MIGGS targets were fed to TH larvae and assessed for insecticidal activity.
Results
Bioassays (FIG. 1) indicated that the oral feeding activity of TH larvae on L4440::MsPGRP2 and L4440::MsVMP1 containing HT115 (DE3) plates resulted in growth impediment and/or mortality. Contrawise, the larvae growing on L4440::MeCAT1 containing HT115 (DE3) plates developed normally without any aberrant phenotypes.
The representative phenotypes of TH larvae at 192 hours post exposure (HPE) to larvae exposed to bacterially (HT115 (DE3)) expressed dsRNA against MIGGS RNAi targets MsPGRP2 (FIG. 2A); MsVMP1 (FIG. 2B) and negative control dsRNA against Cassava plant specific gene MeCAT1 (FIG. 2C). The phenotypic effects leading to larval mortality were usually associated with the development of melanotic reaction, reduced appetite, growth and development (FIGS. 2A and B).
Consistent with above, the TH larvae exposed to bacterially expressed negative control MeCAT1 dsRNA displayed vigorous feeding (area between the arrowheads FIG. 3A). In contrast, the TH larvae exposed to bacterially expressed dsRNA against the MIGGS RNAi target MsPGRP2 displayed a curtailed feeding (representative picture, area between arrowheads FIG. 3B).
In general, melanization is a highly conserved immune response and is often associated with microbial infection of insects. (Kim S R, et al. (2005). Insect molecular biology, 14(2): 185-194. doi:10.1111/j.1365-2583.2004.00547). The intensification of melanotic response in TH larvae upon continued exposure to bacterially expressed dsRNA against the MIGGS RNAi targets MsPGRP2 and MsVMP1 containing HT115 (DE3) plates strongly indicates an infection, possibly due to the defective clearance of opportunistic microbes ingested during feeding. Such defective clearance has been previously associated with the perturbation of gut microbial homeostasis. (Packey and Sartor (2009). Curr. Opin. Infect. Dis. 22(3): 292-301).
Closer observation indicated that the CR larvae feeding on bacterially expressed dsRNA against the MIGGS RNAi targets MsPGRP2 and MsVMP1 displayed discernable mortality starting at day 5, reaching up to 100% and 80% mortality respectively, by day 8 (FIG. 4).
To test if both the incidence and intensity of the observed phenotype could be delayed by clearing gut microbiotas, a GF set of TH larvae were also subjected to the above treatment with appropriate controls, in parallel. Interestingly, that the incidence of larval mortality was not only delayed, but also lower in GF larvae in comparison to CR larvae (FIG. 4) was observed.
The incidence of larval mortality on bacterially expressed dsRNA against MIGGS RNAi targets MsPGRP2 and MsVMP1 plates also correlated with the development of melanotic reaction (FIG. 5). Most notably, there was a concomitant delay in the development of melanotic reaction in GF larvae in comparison to CR larvae (FIG. 5). All the phenotypes observed were statistically significant at a p-value between 0.001 and 0.05. No significant development of mortality or melanotic reaction was observed in larvae exposed to the bacterially expressed negative control MeCAT1 dsRNA (FIGS. 4 and 5).
Although MsVMP1 is not directly involved in immune responses, down regulation may abrogate microbial containment, resulting in an infectious phenotype (FIG. 2B). Alternatively or in addition, down regulation of MsVMP1 may have resulted in wounding of the peritrophic matrix (the protective lining of the larval midgut) that also may have contributed to a sepsis mediated infectious phenotype (FIG. 2B); this is further substantiated by delayed onset of infectious symptoms in the larvae (CR or GF) exposed to dsRNA against MsVMP1 in comparison with larvae exposed to dsRNA against MsPGRP2 (FIGS. 4 and 5). Both defective clearance and defective containment of opportunistic microbes have been previously associated with lethal phenotypes. (Packey and Sartor (2009). Curr. Opin. Infect. Dis. 22(3): 292-301). The schematic representation of dsRNA delivery vectors used for above study is indicated in FIG. 6.
Most of the TH MIGGS RNAi targets disclosed herein (e.g., Table 1) are inducible and have been identified from open access midgut specific immunotranscriptome and/or other datasets (Pauchet Y, et al. (2010) Insect. Mol. Biol. 19:61-75; Odman-Naresh et al. (2013) PLoS ONE 8:e82015; Kanost M R, et al. (2016) Insect Biochem. Mol. Biol 76:118-147; Brummett et al. (2017) Insect Biochem Mol Biol. 81: 1-9; Cao X, et al. (2015) Insect Biochem. Mol. Biol. 62:64-74); Zhong X, et al. (2012) Insect Biochem. Mol. Biol. 42(7): 514-524; Xia Xu et al (2012). Dev Comp Immunol. 38(2): 275-284). A validation study targeting two MIGGS RNAi targets MsHEM and MsSPH3 confirmed their preferential midgut specific manner (FIG. 7) when injected with 75 CFU of gram negative E. coli. Further, literature curation confirmed the abundant expression of these MIGGS targets in the insects gut (Table 1).
Oral feeding of TH larvae on induction media containing a mixture of live E. coli and lyophilized cell wall signatures from gram positive bacteria and fungi (FIG. 8) successfully induced (FIG. 9) the MIGGS RNAi target genes listed in Table 1. The genes with immunity related function were induced between 24-48 hours post larval exposure to induction media and mostly not detected in the absence of induction (FIG. 9A-C). While, the genes essential for midgut structural integrity are expressed under both conditions (FIG. 9D). This, clearly suggests that the MIGGS RNAi targets are induced in response to microbes ingested during feeding.
High-throughput screening of microbe induced MIGGS RNAi targets (FIG. 9) using bacterially delivered dsRNA screen identified 3 insecticidal candidates (FIG. 10). These MIGGS RNAi targets include Toll receptor (MsToll2), Beta fructofuranosidase 1 (MsSuc1) and Beta tubulin (MspTub) genes (FIG. 10D-F). The insecticidal activity was manifested as stunted growth and development, loss of appetite and melanotic reaction (FIG. 10D-F) as observed with the positive control MsVATPaseE treatment (FIG. 10C) in comparison to the negative control treatment (FIG. 10B). The developmental defects due to the bacterially expressed dsRNA exposure resulted in lethality ranging from 60-70% (FIG. 11), with MsSuc1 being the most effective target for killing TH larvae. Mortality rates were statistically significant and comparable to the MsVATPaseE positive control.
Additionally, a combination of reciprocal best BLAST analysis and literature curation was used to identify the orthologs of TH MIGGS RNAi targets from the DBM transcriptomic resources (Table 2).
TABLE 2
|
|
List of MIGGS-IRTGS identified from DBM transcriptome resources.
|
|
|
Midgut
Insecticidal
|
Expression
Activity in
|
Manduca sexta MIGGS RNAi
Insect Biological
Putative Plutella
in Plutella
Plutella
|
Target Genes
Function
Xylostella Orthologs
Xylostella
Xylostella
|
|
Ms_PGRP2
Immunity
Px_PGRP2 (SEQ ID NO: 76)
Yes*
Yes
|
Ms_IMD
Immunity
Px_IMD (SEQ ID NO: 77)
Yes*
Yes
|
Ms_Rel2A
Immunity
Px_Rel (SEQ ID NO: 78)
Yes*
No
|
Ms_Tol2
Immunity
Px_Toll2 (SEQ ID NO: 79)
Yes*
No
|
Ms_Cac
Immunity
Px_Cac (SEQ ID NO: 80)
Yes*
Yes
|
Ms_Dorsal
Immunity
Px_Dorsal (SEQ ID NO: 81)
Yes*
Yes
|
Ms_Hemolin1
Immunity
Px_Hemolin1 (SEQ ID NO: 82)
Yes*
No
|
Ms_SPH3
Immunity
Px_SPH3 (SEQ ID NO: 83)
DNA*
No
|
Ms_Transferrin1
Immunity
Px_Transferrin1 (SEQ ID NO: 84)
Yes*
No
|
Ms_βGRP2
Immunity
Px_βGRP2 (SEQ ID NO: 85)
Yes*
Yes
|
Ms_Gloverin1
Immunity
Px_Geoverin (SEQ ID NO: 86)
Yes*
No
|
Ms_CHS2
Structural Integrity
Px_CHS1 (SEQ ID NO: 87)
Yes*
Yes
|
Ms_βTub
Structural Integrity
Px_βTUB (SEQ ID NO: 88)
Yes*
Yes
|
Ms_vATPaseE (Positive Control)
ATP Hydrolysis
Px_vATPaseE
Yes*
Yes
|
Me_Catalase 1 (Negative Control)
None
Ne_Catalase 1
No*
No
|
|
Manduca sexta MIGGS RNAi
NCBI Accession
NCBI Acession
|
Target Genes
Number
Putative Plutella Xylostella Orthologs
Number
|
|
Ms_PGRP2
GQ293365.1
Px_PGRP2 (SEQ ID NO: 76)
AFV15800.1
|
Ms_IMD
Msex2.05477-RA
Px_IMD (SEQ ID NO: 77)
Px103008
|
Ms_Rel2A
HM363511.1
Px_Rel (SEQ ID NO: 78)
Px102858
|
Ms_Tol2
EF442782.1
Px_Toll2 (SEQ ID NO: 79)
Px106338
|
Ms_Cac
Msex2.02793-RA
Px_Cac (SEQ ID NO: 80)
Px116565
|
Ms_Dorsal
HM363515.1
Px_Dorsal (SEQ ID NO: 81)
Px100110
|
Ms_Hemolin1
M64346.1
Px_Hemolin1 (SEQ ID NO: 82)
ACN53154.1
|
Ms_SPH3
AF413067.1
Px_ SPH3 (SEQ ID NO: 83)
XP_004322155.1
|
Ms_Transferrin1
M62802.1
Px_Transferrin1 (SEQ ID NO: 84)
BAF36818.1
|
Ms_βGRP2
AY135522.1
Px_βGRP2 (SEQ ID NO: 85)
QβVIJ95.1
|
Ms_Gloverin1
G1110649240
Px_Geoverin (SEQ ID NO: 86)
ACN69342.1
|
Ms_CHS2
AY821560.1
Px_CHS1 (SEQ ID NO: 87)
KX420588.1
|
Ms_βTub
AF030547
Px_βTUB (SEQ ID NO: 88)
EU1Z7912.2
|
Ms_vATPaseE (Positive Control)
X67131
Px_vATPaseE
AB189032
|
Me_Catalase 1 (Negative Control)
AF170272
Ne_Catalase 1
AF170272
|
|
It was demonstrated that 14 MIGGS RNAi target genes identified could also be induced in Bt resistant strain of DBM feeding on the induction media (FIG. 12), thus suggesting that oral induction of microbe associated cell wall signatures could induce the MIGGS RNAi target genes in economically important DBM.
High throughput screening of microbe induced DBM MIGGS RNAi target genes (FIG. 12) using bacterially delivered dsRNA screen indicated that 7/15 MIGGS RNAi targets tested showed insecticidal activity against a Bt resistant strain of DBM (FIG. 13). The DBM insecticidal targets included PxPGRP2 (SEQ ID NO. 76), PxβGRP2 (SEQ ID NO. 85), PxCHS2 (SEQ ID NO. 87), PxCAC (SEQ ID No. 80), PxIMD1 (SEQ ID No. 77), PxDor (SEQ ID No. 81) and PxβTub (SEQ ID NO. 88). The insecticidal activity was manifested as stunted growth and development, loss of appetite and melanotic reaction (FIG. 13D-H) as observed with the positive control MsVATPaseE treatment (FIG. 13C) in comparison to the negative control treatment (FIG. 13B). The developmental defects due to the bacterially expressed dsRNA exposure resulted in lethality ranging from 53-70% (FIG. 14), with PxPGRP2 the most effective target for killing DBM larvae (FIG. 14). Mortality rates were statistically significant and comparable to the PxVATPaseE positive control (FIG. 14).
In order to test if our MIGGS RNAi technology could work using multiple dsRNA delivery platforms we tested if dsRNA against the four TH MIGGS insecticidal targets could work in a sprayable format. We used dsRNA against MsPGRP2, MsβGRP2, MsCHS2 and MsVMP1 for sprayable RNAi assays (FIG. 15) at a concentration of 0, 4, 8 or 16 μg of purified dsRNA in TE buffer. Most efficacious leaf disc coated dsRNA was 16 μg of dsRNA against MsCHS2 that caused 58% mortality. Similar, but slightly reduced, mortality was observed when insects were fed 8 μg of leaf disc coated dsRNA against the same MIGGS targets. Observed mortality rates were statistically significant and comparable to those observed in TH larvae exposed to dsRNA against a known positive control target MsVATPaseE (FIG. 16). No statistically significant larvae death was observed when feeding on 4 μg dsRNA (FIG. 16), indicating that 8-16 μg dsRNA per leaf disc was required to cause mortality in this assay. In addition to death, TH larvae feeding on dsRNA were characterized by developmental defects, loss of appetite, melanotic reaction and reduced growth compared to negative controls, indicating significant detrimental impact of MIGGs targeting on insect health (FIG. 17). The insecticidal TH MIGGS targets MsPGRP2, MsβGRP2 and MsCHS2 will be henceforth referred to as core set.
Similarly, in order to test an additional delivery platform, the core insecticidal MIGGS RNAi targets MsPGRP2; MsβGRP2 and MsCHS2 were expressed by plastid transformation in tobacco plants in collaboration with Plastomics Inc. Detached leaves of stable transplastomic lines (FIG. 18) expressing dsRNA against MIGGS targets indicated that the TH larvae feeding on leaves expressing dsRNA against MIGGS targets MsPGRP2 (B); MsβGRP (C) and MsCHS2 (D) display stunted growth, development, loss of appetite and melanotic reaction in comparison to negative control (A). The insecticidal activity is manifested as significant reduction in mean weights in comparison to negative control (E). The mortality rate was scored on a 0-3 score were 0, 1, 2 and 3 indicated ≤0, 25, 50 or ≥50 mortality respectively. The transplastomic events confer significant mortality in comparison to negative control (F). Data is average of 6 replicates/treatment (N=24)±SEM at p≤0.001(***); p≤0.01(**) and p≤0.05(*). Clearly suggesting that the stably expressed dsRNA against the core MIGGS RNAi targets also impacts larval growth and development.
Next, we tested if our MIGGS RNAi technology can also work in a sprayable format against Bt resistant strain of DBM. We used the DBM orthologs of insecticidal TH MIGGS core set (PxPGRP2, PxβGRP2 and PxCHS2) and two newly discovered insecticidal DBM MIGGS targets (PxCAC and PxIMD1) for sprayable RNAi assays at a concentration of 0.1, 0.5 and 0.25 μg. We observed lethality ranging from 53-67%, with PxPGRP2 being the most effective target for killing DBM larvae (FIG. 19). Mortality rates were statistically significant and comparable to the PxVATPaseE positive control (FIG. 19). In a manner similar to that seen for sprayable dsRNA against TH, in addition to death, DBM larvae exposed dsRNA treatments were characterized by developmental defects, loss of appetite, melanotic reaction and arrested growth (FIG. 20). Clearly suggesting that dsRNA against the insecticidal MIGGS RNAi targets identified herein when used in sprayable format is also effective against Bt resistant strain of DBM.
Most of our MIGGS RNAi target gene induction procedures thus far relied upon either direct injection or oral feeding of extraneously supplied microbial signatures. To determine if our MIGGS RNAI target genes are induced under field conditions, we exposed the larvae of economically important lepidopteran pest FAW to wheat seedlings grown on microbe rich and microbe depleted plants (FIG. 21). Pooled RNA-Seq analysis indicated that plants growing on field soil caused preferential up-regulation of MIGGS pathway genes in FAW. In total, 100 differential expressed genes were identified, thirty of which were MIGGS pathway related genes (FIG. 22).
TABLE 3
|
|
List of MIGGS-IRTGS identified from using RNA-Seq approach in FAW.
|
Spodoptera fruglperda MIGGS RNAI
Putative Insect
Midgut
Insecticidal
|
Target Genes
Query_Contigs_ID*
Biological Function
Expression*
Activity
|
|
Sf_PGRP1 (SEQ ID NO: 89)
rep_c7951
Immunity
Yes
Yes
|
Sf Attacin (SEQ ID NO: 90)
rep_c9395
Immunity
Yes
Yes
|
Sf_Ctypelectin15 (SEQ ID NO: 91)
joint2_rep_c488
Immunity
Yes
No
|
Sf_Galectin4 (SEQ ID NO: 92)
rep_c25253
Immunity
Yes
No
|
Sf_Lysozyme (SEQ ID NO: 93)
rep_c18992
Immunity
Yes
No
|
Sf_Hemolymph proteinase 10
c12881
Immunity
No
Yes
|
(SEQ ID NO: 94)
|
Sf_Trypsin like Serine protease
rep_c48453
Immunity
Yes
Yes
|
(SEQ ID NO: 95)
|
Sf-C type Lectin 6 (SEQ ID NO: 96)
joint2_rep_c448
Immunity
Yes
Yes
|
Sf_Serine protease 13 (SEQ ID NO: 97)
rep_c1904
Immunity
Yes
No
|
Sf_Cecropin (SEQ ID NO: 98)
rep_c42380
Immunity
Yes
Yes
|
Sf_Relish (SEQ ID NO: 99)
c13122
Immunity
Yes
No
|
Sf_Toll2 (SEQ ID NO: 100)
joint2_c3284
Immunity
Yes
No
|
Ms_βBGRP2 (SEQ ID NO: 101)
EF641300
Immunity
Yes
Yes
|
Sf_c20042 (SEQ ID NO: 102)
c20042
Immunity
Yes
No
|
Sf_rc16438 (SEQ ID NO: 103)
rc16438
Immunity
Yes
Yes
|
Sf_L2rC2367 (SEQ ID NO: 104)
joint2_rep_C2367
Immunity
Yes
No
|
Sf_CHSB (SEQ ID NO: 105)
AY525599
Structural Integrity
Yes
Yes
|
|
Most notably, FAW orthologs of TH insecticidal targets including PGRP2, PGRP2 and IMD were captured in the data set. This discovery indicated that MIGGS pathway genes are up regulated in response to insect feeding on plants exposed to microbes in the field soil.
Preliminary experiments were performed to screen the insecticidal activity of 17 FAW MIGGS RNAi targets discovered during RNA-Seq (Table 3, above) in which dsRNA against the FAW orthologs of insecticidal TH MIGGS core set (SfPGRP2 (SEQ ID NO. 89), SfβGRP2 (SEQ ID NO. 101) and SfCHS2 (SEQ ID NO. 105) and three newly discovered MIGGS targets SfCTL (SEQ ID NO. 96), SfRC (SEQ ID NO. 103) and SfGAL (SEQ ID NO. 92) from RNA-Seq were fed to FAW larvae at 0, 4, 8 or 16 μg-purified dsRNA in TE buffer. FAW 1st instar larvae were allowed to feed on dsRNA coated leaves following the bioassay described for TH above. Data indicated that FAW larvae (FIG. 23) exposed to pure dsRNA against SFCHS2 (B); SFβGRP2 (C); SFPGRP2 (D), SFRC (E), and SFCTL (F) causes reduced growth, development and loss of appetite in comparison to negative control treatment (A) resulting in significant weight reduction (G) and mortality (H) at 8 and 16 μg of dsRNA concentration. The rates of mortality was scored on a 0-3 score were 0, 1, 2 and 3 indicated ≤0, 25, 50 or ≥50 mortality respectively. The dsRNA treatments imposed caused statistically significant reduction in mean weights (G) that also translated into significant rates of mortality (H) in comparison to negative control (FIG. 23). Screening of insecticidal activity of additional MIGGS RNAi target genes identified from the RNA-Seq dataset indicated that 16 μg of leaf disc coated dsRNA against MIGGS RNAi targets SfTSP (SEQ ID NO. 95), SfAtta (SEQ ID NO. 90), SfCec (SEQ ID NO. 98) and SfHp10 (SEQ ID NO. 94) caused statistically significant reduction (FIG. 24) in mean weights (A) that also translated into significant rates of mortality (B) in comparison to negative control. Data is average of 3 replicates/treatment±SEM at p≤0.001(***); p≤0.01(**) and p≤0.05(*).
Experiments with an economically important coleopteran pest RFB were also conducted to test if MIGGS-IRTGS targets identified by a combination of reciprocal best BLAST analysis and literature curation (Table 4) are insecticidal against the order coleoptera.
Preliminary feeding trails with 1 μg of purified indicated that dsRNA against RFB MIGG RNAi targets TcPGRP2 (SEQ ID NO. 107), TcβGRP2 (SEQ ID NO. 108), TcMDGP (SEQ ID NO. 109) and TcCHS2 (SEQ ID NO. 110) is insecticidal to the adult RFB beetles. Significant rates of RFB mortalities were observed (Figure. 25) when scored on a 0-3 scale were 0, 1, 2 and 3 indicated ≤0, 25, 50 or ≥50 mortality respectively in comparison to the negative control treatment. Data is average of 3 replicates/treatment±SEM at p≤0.001(***); p≤0.01(**) and p≤0.05(*).
TABLE 4
|
|
List of MIGGS-IRTGS identified from RFB transcriptome resources.
|
Spodoptera frugiperda
|
MIGG RNAI Target Genes
Query_Contigs_
Putative Insect
Midgut
Insecticidal
|
(SEQ ID NO)
ID
Biological Function
Expression
Activity
|
|
TcPGRPL0
DT786101.1
Immunity
Yes*
No
|
(SEQ ID NOL: 106)
|
TcPGRP2
XM_965754.3
Immunity
Yes*
Yes
|
(SEQ ID NO: 107)
|
TcβGRP2
XM_966587.4
Immunity
DNA
Yes
|
(SEQ ID NO: 108)
|
TcMDGP
XM_971351
Structural Integrity
Yes**
Yes
|
(SEQ ID NO: 109)
|
TcCHS2
EFA 10719.1
Structural Integrity
Yes***
Yes
|
(SEQ ID NO: 110)
|
|
One possible reason for larval mortality could involve down regulation of MIGGS-IRTGS transcripts upon feeding on exogenously supplied dsRNA against the target genes. Preliminary RT-PCR data indicated that the larval phenotypes (FIG. 17) also correlated with down regulation of target transcripts (FIG. 26).
Importantly RNA-Seq analysis indicated that the MIGGS-IRTG pathway targets are induced by soil microbiome indicating that our novel RNAi approach could be effective even under field conditions.
Given the ease of identification, high specificity, and applicability to diverse pests and delivery platforms, RNAi silencing of the MIGGS-IRTG pathway genes identified, this approach offers an unprecedented potential as a novel pesticidal strategy.
The translation of these preliminary findings into a pesticidal RNAi technology against economically important pests might lead to sustainable alternatives including but not restricted to the methods described anywhere herein.
Additionally, the proposed approach will shed more light into understanding the tri-trophic interaction between plants-microbe-insect interactions as it pertains to sustainable insect pest protection.
Sequences
SEQ ID NOs: 1-14 and 31-44 are representative examples of M. sexta-RNAi target gene sequences.
SEQ ID NO: 15 is non-insect gene sequence that encodes for catalase 1 from cassava (Manihot esculanta).
SEQ ID NOs: 16-29 are coding region sequences of representative M. sexta-RNAi target genes.
SEQ ID NO: 30 is the coding region sequence of catalase 1 from cassava (Manihot esculanta).
SEQ ID NOs: 45-70 are 5′UTR and 3′UTR region sequences of representative M. sexta-RNAi target genes.
SEQ ID NOs: 71-75 are the coding region sequences of additional representative M. sexta-RNAi target genes.
SEQ ID NOs: 76-88 are the coding region sequences of representative P. xylostella-RNAi target genes.
SEQ ID NOs: 89-105 are the coding region sequences of representative S. frugiperda-RNAi target genes.
SEQ ID NOs: 106-110 are the coding region sequences of representative T. castaneum-RNAi target genes.
SEQ ID NOs: 111-119 are representative examples of Manduca sexta insecticidal dsRNA sequences.
SEQ ID NOs: 120-126 are representative examples of Plutella xylostella insecticidal dsRNA sequences.
SEQ ID NOs: 127-135 are representative examples of Spodoptera frugiperda insecticidal dsRNA sequences.
SEQ ID NOs: 136-139 are representative examples of Tribolium castaneum insecticidal dsRNA sequences.
>M. sexta-Hemolin (MsHEM); M64346.1
|
(SEQ ID NO: 1)
|
ATGGTTTCAAAAAGTATCGTCGCTTTGGCTGCGTGCGTCGCAATGTGCGTAGCCCAGCCA
|
|
GTGGAGAAGATGCCTGTGCTGAAGGACCAACCCGCTGAAGTCCTCTTCCGGGAGTCTCAG
|
|
GCCACCGTTCTCGAATGTGTTACCGAGAATGGCGATAAAGATGTCAAATATTCTTGGCAA
|
|
AAAGACGGCAAAGAATTCAAATGGCAGGAACACAATATCGCCCAGCGCAAAGACGAAGGC
|
|
AGCCTGGTCTTCCTCAAGCCCGAGGCTAAAGATGAAGGCCAATACAGATGTTTCGCTGAG
|
|
TCGGCCGCCGGAGTCGCCACCTCCCACATCATCTCCTTTAGAAGGACCTACATGGTCGTA
|
|
CCTACTACTTTTAAGACTGTAGAAAAGAAACCGGTAGAAGGGTCATGGCTCAAACTTGAG
|
|
TGCAGCATCCCCGAAGGTTATCCTAAACCTACTATTGTATGGAGAAAGCAGCTTGGTGAA
|
|
GACGAAAGTATAGCAGATTCTATACTGGCACGTCGTATTACACAATCTCCAGAGGGAGAC
|
|
CTGTACTTCACGAGCGTCGAGAAAGAAGACGTAAGCGAAAGCTATAAATACGTTTGCGCT
|
|
GCTAAGTCACCGGCTATTGATGGGGATGTCCCTCTTGTTGGATACACTATTAAAAGCTTA
|
|
GAAAAGAATACAAATCAGAAAAACGGTGAGCTGGTCCCGATGTACGTCAGTAATGATATG
|
|
ATAGCTAAGGCCGGAGACGTTACTATGATCTACTGCATGTATGGTGGAGTCCCAATGGCT
|
|
TACCCCAACTGGTTCAAAGACGGTAAGGACGTGAACGGCAAACCGAGCGACCGCATCACC
|
|
CGCCACAACAGAACCTCCGGCAAAAGACTGTTCATCAAGGAGACGCTGCTCGAAGATCAG
|
|
GGCACTTTTACTTGCGACGTGAACAACGAAGTCGGCAAGCCACAGAAACATTCCGTCAAA
|
|
CTTACCGTAGTCAGTGGACCCAGATTTACGAAGAAACCAGAAAAGCAAGTCATCGCTAAG
|
|
CAGGGCCAGGACTTTGTAATCCCCTGTGAAGTATCCGCCTTACCGGCCGCCCCTGTCTCC
|
|
TGGACGTTCAACGCCAAGCCCATCAGCGGCAGCCGCGTGGTAGCCAGCCCGAGCGGACTG
|
|
ACCATCAAGGGCATCCAGAAGTCTGACAAGGGTTATTATGGCTGCCAGGCCCACAACGAG
|
|
CACGGAGATGCCTACGCTGAGACGCTCGTGATTGTTGCTTAA
|
|
>M. sexta-Serine proteinase homolog 3 (MsSPH-3); AF413067.1
|
(SEQ ID NO: 2)
|
ATGTTGTTGCTTCTGTATTGTCTTGTGGCGGCCTCCGCGCCGTTCTTTATTGCAGCGGAC
|
|
CAAGGCAGCCCTGACCTGCCTTTAGCTACCGAACCACCAACAGAATGCGGAACAATAGCA
|
|
CCTGATGATAGCTTAGTATTAGATGGGTCCGTTGGTAAAAGTGACAAATTACCTTGGTAT
|
|
GCTATTATCTACACAACCACCACCCGGCCATACAAGCAGATCGGTGGAGGAACCCTCATC
|
|
ACTCCTTCAGTAGTAATCTCAGCCGCTCACTGTTTCTGGCGCAATGGTGAGGTTCCATCT
|
|
AAGGATAATTACGCCGTGGCGCTCGGCAAGACCCATAGTGCTTGGAATAGCCATGCCGAT
|
|
GTAAACGCTCACAAGTCTGATGTAAAAGAAATACACATACCACCGCAGTTTAAGGGAAGG
|
|
AACACTAATTATCGGAATGATATAGCAATCGTGGTCATGTCAGACCCTGTGACCTACAAA
|
|
GTGGACATCCGCCCTATCTGTTTGAACTTCGATGTACAATTTGAAAGACTGCAATTAAAA
|
|
GACGGCATTATGGGGAAGATCGGCACATGGAATGTAAGTCGTGAGACACTGAAACTATCG
|
|
AAAACATTAAAAGTGGTGGAGAATCCATACATTGACGCAGCGACTTGTATTAGTGAGTCT
|
|
CCGGCAAGCTTCAGAAATTCCATCACTGCGGACAAAATATGCATCGGATACGTTAACGGC
|
|
ACCGGGCTATGTAGAGGTGATGGCGGCGCTGGGGTGGCTTTCCCTAGCCAGGAACAAGGA
|
|
GTGCAACGTTACTACCTCAGAGGTGTTATATCTACAGCCCATACCAGCGATGATGGCAAC
|
|
TTATGTGCAGATGGATTTGTAACTGCCACTGCTATAGGCCATCACGAACATTTTATCAAA
|
|
CAGTTTATAAGCGTTTAG
|
|
>M. sexta-Peptidoglycan recognition protein 2 (MsPGRP2); GQ293365.1
|
(SEQ ID NO: 3)
|
ATGGCGAGCTTCGCTTTAATAGTTATCCTTAGCGTAATTGGCTTTATATCGGCCTATCCT
|
|
AGTCCTGAAGGTTACAGTTCTGCCTTCAACTTTCCATTCGTAACCAAGGAGCAGTGGGGC
|
|
GGCAGGGAGGCACGCACGTCGACGCCACTCAACCACCCAGTGCAGTTCGTGGTGATCCAC
|
|
CACAGTTACATTCCCGGCGTGTGCCTCAGCCGGGACGAGTGCGCGCGCAGCATGCGCTCC
|
|
ATGCAGAACTTCCACATGAACAGTAACGGGTGGAGTGATATTGGATACAACTTCGCTGTC
|
|
GGCGGTGAAGGGTCGGTGTACGAGGGCCGCGGCTGGGACGCGGTCGGCGCACACGCAGCT
|
|
GGCTATAACAGTAACAGTATCGGCATCGTGCTCATCGGCGATTTTGTTTCAAACCTCCCG
|
|
CCGGCGGTGCAAATGCAAACCACACAAGAATTGATCGCAGCGGGCGTGCGACTCGGTTAC
|
|
ATCAGGCCCAACTACATGCTCATCGGGCATCGTCAGGTCTCCGCCACTGAGTGCCCAGGA
|
|
ACCAGACTCTTCAACGAAATCACCAACTGGAACAACTTCGTGAGGATATGA
|
|
>M. sexta-Beta-1, 3-glucan-recognition protein 2 (MsßGRP2); AY135522.1
|
(SEQ ID NO: 4)
|
ATGTGGATCAAGAGCGTCTGTTTGTTCGCAACCATTGCGGGCTGCTTGGGCCAGCGAGGG
|
|
GGTCCATACAAGGTGCCTGATGCGAAACTCGAAGCTATCTACCCCAAAGGCTTGAGAGTC
|
|
TCTGTGCCAGATGATGGCTACTCCCTATTTGCCTTCCACGGCAAGCTCAATGAGGAGATG
|
|
GAAGGTTTAGAGGCTGGCCATTGGTCCAGAGACATCACCAAAGCGAAGCAGGGCAGATGG
|
|
ATATTCAGAGATAGGAATGCTGAGCTGAAGCTTGGAGACAAAATTTACTTCTGGACTTAC
|
|
GTTATTAAGGATGGATTGGGATACAGGCAGGACAATGGAGAATGGACTGTTACAGAATTC
|
|
GTCAATGAGAACGGTACAGTGGTGGACACTAGTACAGCGCCGCCACCAGTAGCACCCGCC
|
|
GTTTCAGAGGAAGATCAATCGCCAGGTCCTCAGTGGAGACCTTGCGAAAGATCCCTGACT
|
|
GAGTCCTTGGCCCGCGAACGCGTTTGCAAAGGCAGCCTTGTCTTTAGCGAGGACTTTGAT
|
|
GGTTCCAGTTTGGCCGACTTGGGCAATTGGACCGCTGAAGTCAGATTCCCTGGCGAACCG
|
|
GACTACCCGTACAACTTGTACACTACGGACGGCACTGTGGGATTCGAAAGTGGGTCTCTG
|
|
GTGGTGAGACCCGTCATGACCGAGTCCAAATACCACGAGGGCATCATATACGACCGCCTC
|
|
GACCTTGAGAGATGTACAGGACAGCTGGGTACGCTGGAATGCAGGCGAGAGAGCAGCGGC
|
|
GGTCAGATTGTACCACCTGTGATGACAGCTAAACTGGCCACTCGACGCAGCTTCGCGTTC
|
|
AAGTTCGGCAGGATCGATATAAAGGCGAAGATGCCGCGCGGGGACTGGTTGATACCAGAA
|
|
CTCAACCTCGAACCTTTAGATAACATATACGGCAACCAGCGATACGCTTCGGGTCTCATG
|
|
CGGGTCGCGTTCGTGAGAGGAAACGATGTATACGCCAAGAAGCTCTACGGAGGTCCGATA
|
|
ATGTCCGACGCGGACCCGTTCAGGTCCATGCTGTTGAAGGACAAGCAAGGGTTGGCCAAC
|
|
TGGAATAATGATTACCACGTCTACTCGCTGCTGTGGAAGCCTAACGGTTTAGAGCTGATG
|
|
GTGGACGGTGAAGTGTACGGCACCATCGACGCTGGCGATGGCTTCTACCAGATTGCGAAG
|
|
AACAACCTCGTGAGCCACGCCTCGCAGTGGCTCAAGGGCACCGTCATGGCGCCGTTTGAT
|
|
GAAAAGTTCTTCATCACTCTGGGTCTTCGCGTGGCGGGTATCCACGACTTCACGGACGGT
|
|
CCGGGCAAACCTTGGGAGAACAAGGGCACCAAGGCCATGATCAACTTCTGGAACAATCGG
|
|
TTCCGCTGGTTCCCCACGTGGCACGACACCAGTCTTAAAGTCGACTACGTCAGAGTCTAT
|
|
GCTCTTTAG
|
|
>M. sexta-Relish family protein 2A (MsREL2A); HM363513.1
|
(SEQ ID NO: 5)
|
ATGTCCTCTTGTCCAAGCGACTATGATCCCAGTGAATCGTCCAAATCTCCACAAAGTATT
|
|
TGGGAGTCAGGAGGATACAGTTCTCCGTCGCAACAAGTTCCTCAATTGACTTCTAACTTA
|
|
ACAGAATTGTCTGTTGATCACAGCTATAGATACAATGGAAATGGACCATATCTACAGATC
|
|
ACAGAGCAACCACAGAAATACTTTCGGTTCCGTTATGTTAGCGAGATGGTGGGAACACAT
|
|
GGATGTTTGCTTGGCAAATCTTATACAACAAACAAAGTTAAAACTCATCCGACAGTTGAA
|
|
CTCGTGAATTACACCGGTCGAGCCCTGATAAAGTGCCAACTATCGCAAAACAAGAGCGAA
|
|
GACGAACACCCGCACAAACTGCTCGATGAACAAGACAGAGACATGAGCCACCACGTTCCC
|
|
GAGCACGGCAGTTATAGAGTGGTATTTGCTGGTATGGGTATAATTCATGCTGCCAAAAAG
|
|
GAAGTTGCGGGGTGGCTCTATAGAAAATATATACAGCAGAACAAGAATGAAAAGTTTAAT
|
|
AAGAAAGAGCTCGAAGCGCATTGTGAGAGGATGTCCAAAGAGATCGATTTAAATATAGTT
|
|
AGACTGAAGTTTAGCGCTCACGATATTGACACTGGCATTGAAATTTGCCGGCCAGTGTTC
|
|
TCTGAACCCATTTATAATTTGAAGTGTGCGTCTACGAATGATTTGAAAATATGCCGCATA
|
|
AGCCGTTGTTACGGTAGACCGAGAGGCGGCGAAGATATCTTCATATTTGTCGAAAAGGTC
|
|
AACAAGAAAAACATCCAAGTTCGGTTCTTTAGACTGGAAAACGGGGAGCGCACCTGGTCA
|
|
GCGATGGCGAACTTTCTGCTAAGCGATGTTCACCACCAATACGCTATCGCTTTTAGAACG
|
|
CCACCGTACGTCAATCACCAAATTTCTGAAGACGTGCAAGTTTTTATAGAACTCGTACGC
|
|
CCTTCAGACGGTAGGACGAGCGCTCCCATGGAGTTCACATACAAGGCTGAGCAAATCTAT
|
|
AAACAGAACAAGAAACGTAAAACTACTTCGTCGTACTCGTCGCTCGACAGCTCCTCAGGT
|
|
TCGGCCGGTTCAATTAAAAGCATCAGCGAACTGCCCGCGCCCGTTGTTTTTGCTGAAAAC
|
|
GTAAGTTTTTTCTATGACACATTACTCATTCTTCAACCCATGACGAATCTATAA
|
|
>M. sexta-Dorsal (MsDor); HM363515.1
|
(SEQ ID NO: 6)
|
ATGCTTGTGACGTTATGCGGCGGGAACTATAGTGGATTGTCGTTAACAAAAACTAATCAT
|
|
TATATGTCACCAAAATCATATGTGCCAGGAAATGGTTATGACGCCGCCGTAATCCTAGGT
|
|
ACCACGGAGCAGAATGACAGCGAACCCTCAAACTTGAATATTAGTGATGTTTTTGAAGCC
|
|
ATCACGCTCGCTGATCCGTCGTTCGGCGCGGGCGTGCCGTCGGTAGAGGAGACGATGGCG
|
|
CACACGCAGCCCCAGCCGCTGCAAATGCCGTACGTGGTCGTCGTGCAGCAGCCCGCCAGC
|
|
AAAGCGCTCAGATTTCGATATGAGTGCGAGGGCAGATCAGCCGGTTCGATTCCCGGCGCG
|
|
TCGAGCACGCCCGAGAACCGAACCTTCCCCGCCATCAAGATAATCGGCTACACCGGCACC
|
|
GTCTCCATCGTAGTGTCGTGTGTCACCAAAGATGAGCCTTGCAGGCCGCACCCACACAAC
|
|
CTGGTCGGGCGCGACCACTGCGACCGCGGCGTGTTCTCCGTCCGCATCGAGATCACCGAC
|
|
GAGAATAACGAATACCAGTTTCGGAACCTGGGCATACAGTGCGTCAAGCGGCGCGACATC
|
|
GGCGAGGCGCTGCGGATCCGAGAGGACCTGCGCGTCGATCCGTTCAAAACCGGCTTCACC
|
|
CACCGGAACCACCCGCAAGGCATCGATCTGAATGCAGTGCGGCTCGCGTTCCAAGTGTTC
|
|
CTGCCGCACTCCAGCGGCAAGATGCGGCGCACGCTCGCGCCCGTCGTGTCCGACGTCATC
|
|
TACGACAAGAAGGCCATGAGCGACCTGCTCATCGTGCGCGCGAGCCACTGCGCCGGCCCG
|
|
GCGCGCGGCGGCACGCAGGTCGTACTGCTCTGTGAAAAGGTGACTCGCGAGGACACCGTG
|
|
GTGGTGTTCTACCAGGAGGACAACAACCGCGTGCTGTGGGAGGAGATGGCGATCATCATC
|
|
GTGGTGCACAAACAGTATGCCATAGCGTTCGAGACGCCGCCATACAAGAACCCAAACATT
|
|
ACTGATAATGTCAATGTACGATTCCAGCTGAGAAGGCTCTCCGACAAGATGACGAGCAAC
|
|
TCGCTGCCGTTCGAGTACATTCCCGAATACCAAGATTACCCTAGTTACAGGCAGGATAAC
|
|
TCAGAAAGAAATCCCCAATCGCAGCCAATTACGCACAAGGTAACGGTGGAGGACTTTGAA
|
|
TCGACAACTAAAAGATATTTTACGCGAAGCACTGACAACAGTAATTACGGTTGGGATGCG
|
|
GTTCCGGTCACGTACAATGGAAGAAAGAAGGTTTGCTATTGCCCCAAGAGGAGCTAA
|
|
>M. sexta-Spatzle (MsSPZ1A); GQ249944.1
|
(SEQ ID NO: 7)
|
ATGGCCTGGATCCAGCATTTACTCGTTTGGCTCTTCGTTATGTCAACATCAGCATACAAA
|
|
TGCAAAGACTGCTTCAGTTTCGCATCACAATATCCGTCGTACGATAGTCAAGTATACGAA
|
|
CAACCTGACAGACGGATAGCGGGACGGTCAGCACAATACGAACATTTAAGAACAAACGAG
|
|
AGGTCTCTCCCGGTCTACAGCGAGACCCAGAGGATACAAGCAGAAGAGAGAAGAAGACAC
|
|
AGTTCGAGACTAGAAGAACCGAGACAACGTGCTGAGAATGGTTCATATAAGATATTGAAT
|
|
AACCCTCCGAAACCCTGTATTACTAATAGGAGAAGTCAAATTGATTCGTCGAATGATAGG
|
|
GTAGTGTTCCCCGGTCCGACTTCAGAAAGGTCGTACGTACCCGAAGTGCCAGAGGAATGC
|
|
AAGAAAATCGGCATATGCGACAGTATACCGAATTACCCAGAAGAACACGTAGCTAATATT
|
|
ATATCTCGACTTGGAGACAAAGGAAAAGTATTACAAATAGACGAACTGGACGTATCAGAC
|
|
ACTCCAGATATCGCCCAGAGGTTGGGTCCGCAGGAGGACAACATGGAACTATGTAGCTTT
|
|
AGAGAAAAGATTTTTTACCCCAAGGCAGCGCCAGACAAAGATGGAAATTGGTTCTTCGTT
|
|
GTGAATTCAAAAGAAAACCCAGTACAGGGTTATAAAGTTGAAATTTGCGACCGTCAGCAA
|
|
TTACCATGCGCGGAGTTCGCGAGCTTCCAACAGGGATATGAAGCGAGGTGCATCCAGAAA
|
|
TACGTTCGCCGGACCATGTTGGCGTTGGATCCCAAGGGTCAGATGACCGACATGCCCCTT
|
|
AAAGTGCCCAGCTGTTGCTCATGCGTGGCCAAATTGACAATCATATGA
|
|
>M. sexta-Toll receptor (MsTOLL); EF442782.1
|
(SEQ ID NO: 8)
|
ATGCAGGCTCGGCGGTGGTGCGCGGCACTGCTATTAATGCAGATGCTGAGCTGGCTCGGA
|
|
GTCAGTGGACACTTACCGCGTCCCGAGTGCGCGCCAGCCGCAGATTGCCAACTTATACGA
|
|
GACAACATAATCGATGGATATGCACAATTCTACTTCAACGTATCAGGACATGAAGTGAAA
|
|
TTTGAACATTACATCGGAAACGACTTCGATGTCGAATTGTCATGCAATTACATCGCCATG
|
|
GACAACGCAATGCTGCCGCGGTTCTCAACGACCTTTTCAGTCAACGTAATAGTGGTTAAA
|
|
GAATGTGCTTTGCCAAGAAGTGGGTCAATCGATGCCGCTGTCGCTGCACTTAATATCAAC
|
|
GTTTTGACGGAGCTGACTCTGGACAAATTCCTAGAGCCGGCGGTGATCACGCGCGCACAT
|
|
CTTACCAGTTTACAACGACTAGAGAGGCTGGAGCTACACGGTAACTCAAACACAAGCCTC
|
|
GCCCCCGGCGCACTGGCCGCGCTCTCCGCCGCGTCCGCACTGAAATGTCTTGTATTGCAT
|
|
GCAGTACGCGTGCCCGCCGCTGACCTGGCGCGCTTGCCGTCGTCACTGCAAGAACTAGCG
|
|
TTGTTGGATGTGGGCGCTGCGAGTATGCATTTAGATTCATCGGTTAATTTGACGTCACTC
|
|
TTCGTAATCGATACACATTATCCTGTCGTCGTGAATGTGAGCAACGCCGTTGCGCTCAGA
|
|
GACTTGCACATAAATACCCCAAGTACTGTGTTGACCGAAGACGTGCTCCCGTCGTCACTC
|
|
AACTCACTTGAACTAGAGGGGTGGAACGAAACGCATCCGGTGCCTAAGACACGTTGTGTA
|
|
CTACTTAAGGAACTTAATGTAATCGGCACCGACAATGATGCCTATCCGGTGACTCTCCCG
|
|
GACGAGTGGCTGTCCAACTGCGGACAGCTGAGGGATCTTGAAATGATCTCCGTGCCGATT
|
|
AGCGCCGTACTTCCGGCGCGGATGCTGGCTAACGCAATTAGGCTTGAAACGATTACTATC
|
|
TGGAACTGTAACCTGACCGCGTTGCCGTCGGGCCTGTTAGACGACACGCTGAACCTCGCC
|
|
ACACTCGACTTGTCCAACAATCAACTTGCATCGTTGCCCAGAAAATTATTTGAGCACACG
|
|
AAGTTACTACGCAGTCTCATACTATCGAACAATCAGCTGACGAGCGAGGTAGTGTGGACG
|
|
CTGTCGACCGTCACCTCGCTTGTTGAACTAAAGCTCAGCAATAATAACCGCATAGGCGAC
|
|
TTATGTTCCCACGACTCAGTGTCAGCAGGTCCCTCACCACTGAGTTCACTGACGGGGCTA
|
|
AACTATCTCCATCTGAGCAACACAGGAGTATCACACGTGTGCTCCGACTGGCGAGAAAAG
|
|
CTAACCTACCTCACGAATCTCAACTTAAGGGACAACCCCATCACTCTCTACAATTTGGCG
|
|
GATCTACAGTTTCGTCGAATCTGGGTGGACGCTCGTGTGTATTTAGGACATTTCAAGCAG
|
|
CAGTTTACGCGCACAGATTACGAACTCGCCAGTAATAATAACACTGAGGCGGTCGTAACT
|
|
TTATCCGGTTCGTTAGAATGCGACTGCAATTCATACTGGGCAGCACAGGTGTTCCGTATG
|
|
AAAGCTTGGCAGGCATCCAGCTCCATGATATATTGTGAAAAAAAACCGGTCATTGAGGTG
|
|
GATCCCGACACCTTTACCTGCCTTGAGCCAGCGAAGTGTGCTGCGCTGGCGGATAGTTGT
|
|
ACGTGCCGTATCCGCGACGACATTCAGTACAAACAAGTGGTCGTTGTGCACTGCACCGGA
|
|
CTCGCCGAGTTCCCGCGCCTGCCACTAACCACGGACAAGTGGATCCTGCACCTGCCCCAC
|
|
AACAACATATCATACCTCGCCGCGGCCGACGTATCGCCGAACATCGTGGAACTCGATCTA
|
|
AGAAACAATTCAATCAAGAATATCGACGTACAGGCATCAGCAAAACTAGCCTTCGTCCGG
|
|
CTGCAATTGGGTGGTAACCCGATCGAGTGTGACTGCGAGGCGTTGAAGCTGCTGGCGCCG
|
|
CTGCTCAAACCTGACTCAAAGCTGCTTGACAGAAAGGACGTGAAATGTGAGAACGACGCG
|
|
CAGATTACCTTGGCGATGCTGAAATTATGTACTAAGTCATCCAATGGGCTGATGTACTTG
|
|
CTGTTCCTGTTGCTGTTACTCGCATTTGTCGTAACCGGACTGCTCGCACGAACCGCAATT
|
|
CGCCTGCGCATCAAAATGATCCTCATGAGACTGGGTTGGATGTCGAGACTACTGGAGCCC
|
|
GCGGACGACGATCGCCCGTACGACGCGTTTGTGTCTTTCGCACACGAGGATGAGGAGCTG
|
|
GTGATGGAGCAGCTGGCGGCACGGCTCGAGAGCGGCTCGCGGCCGTACCGACTGTGTCTG
|
|
CACTACCGCGATTGGGCGCCAGGCGAGTGGATCCCGGCGCAAATAGCGGCTTCGGTGCGG
|
|
GCCTCTCGGCGCACGGTGGCGGTTGTGTCGGCGCACTACTTACAGTCGGGCTGGGCGCTT
|
|
GCCGAGATCCGGGAGGCGACCGCAGCCTCGCTGCAGGAAGGCATGCCACGTCTCATCATC
|
|
GTGCTGCTCGACGAGACCGACCGGTTGATGCTCGATATAGACCCTGAGTTGCACGCCTAT
|
|
GTGCGCAACAATACCTACGTGCGCTGGCATGATCCATGGTTTTGGGAGAAGCTGAAGCAG
|
|
GCGCTGCCTCCACCGCGGGAACAACGGTCGCCAATAGCTCCGTCGCTACCAGCGCTGGCG
|
|
CTGTCCCATGACAGCCTAACTCTGCGCACGTACTCTCCCAGAGAAAGTGACCCAGCGCCC
|
|
GCTGCTAAGCCGGCGCACACTCCGCACGAGACGGACGAGCCAGCGCCGGGCGCGAGTCCT
|
|
TGCTACAAATGA
|
|
>M. sexta-Scolexin A (MsSCA1); AF087004.1
|
(SEQ ID NO: 9)
|
CGGCAGTCGGTTGTGTTGGCAGTGGCGGCGGTGCTCTTCGGGTGCGCGTGCGCAGCGCCC
|
|
AATCCTGGCGCCAACGACATACAACTTAATCAAAAATTAAGTATCGAAGCTAAGGGGGCA
|
|
AAGCAGCCAATTGATACGAGGGCAGTGAAGGAACGGTATCCATACGCAGTTCGGAGTTTC
|
|
GGAGGCTTCTGCGGAGGAACCATTATCAGTCCCACCTGGATCCTGACCGCCGGCCACTGC
|
|
TCGATACTCTATGCGGGGAGCGGCCTACCGGCCGGCACCAACATTACCGAGGTATCTAGC
|
|
TTGTACCGCTTCCCCAAGCGGCTCGTCATACACCCGCTCTTCTCCATAGGACCCGTCTGG
|
|
CTCAACGCTACGGAGTTCAACCTCAAACAGGCGGCTGCACGATGGGACTTCTTGTTGATA
|
|
GAACTGGAGGAACCGCTGCCGTTGGACGGCAAGATCCTGGCGGCTGCGAAGCTCGACGAC
|
|
CAGCCCGACCTCCCCGCAGGCCTCGACGTGGGCTATCCGAGCTACAGCACCGACACCTAC
|
|
GAGGCTAAGATACAAAGCGAGATGCACGGAAAGAAGCTTTCGGTTCAATCTAACGAGGTG
|
|
TGCTCGAAGCTAGAGCAGTTCAAGGCGGAGGACATGTTGTGCGCCAAGGGACGTCCACCG
|
|
CGATACGACTTCGTCTGCTTCAGCGACAGTGGCAGTGGGCTAGTAGACAACAATGGTCGC
|
|
CTAGTCGGCGTGGTGTCGTGGGCCGAGAACAACGCTTTCGAGTGCCGCAACGGCAACCTG
|
|
GCGGTCTTCTCGCGAGTGTCCAGCGTACGCGAGTGGATCCGACAAGTCACCAACATATAA
|
|
>M. sexta-Hemolymph proteinase 18 (MsHP18); AY672794.1
|
(SEQ ID NO: 10)
|
ATGGTTTATATTTTAATAATTTTAGTGATTTGCAATTTTAGTTGTATTAGTTGTCAGTCC
|
|
GGGACAGTGGAAAGCAGGATTCATTTTAAAGATGAAGGGCCGGAATGTTATGATGCAAAT
|
|
AAAAAGGGCACCTGTGTTAGTGCTCACAGATGCCTTGATGTAGTTAGAAAACTTAAAGAC
|
|
GGAGAGAAACCCACGATATGTGGCTACCAAGGCACGGAACCAATGGTGTGTTGCACAGAC
|
|
TGTACTCTGGTTGATAATATTAGTAATTTGGTCGTAAGTTCCATATCCGGGTACCTGTGG
|
|
AAGGATGGTCAGAAAGCGTGGGACAAATGTCTGGAATACGTTGACAAGCTGTCGTACCCA
|
|
TGCGCTTCAACCTACTCCCACTACCTCAGCTCCGTTTGGGAGAAAGATAAGGAGTGCAGT
|
|
ATGGTTCAGTTTGTTGGCGTGAGGCGATTCGCCTCGTATAACGGACAACCGGCGAAACGG
|
|
AACGAGTACCCTCACATGGCTCTGCTCGGCTACGGCGACGACCAGGAGACGGCGCAGTGG
|
|
CTCTGCGGCGGCTCAGTGATCAGTGATCAATTCATCCTCACGGCTGCACACTGCATCTTT
|
|
ACAAATCTATTGGGTCCAGTACGTTTCGCAGCGCTAGGAATACTGCAGCGATCGGATCCA
|
|
GTAGAGTTATGGCAAGTTTACAAGATCGGCGGCATAGTTCCCCATCCGCAGTATAAGTCA
|
|
CCTATCAAGTACCACGACATTGCTCTCCTGAAGACTGAAAACAAAATAAAGTTTAATGAG
|
|
AACGTGCTGCCAGCGTGTTTGTTCATAGAGGGCAGAGTGGGTGGGAGTGAGCAGGCTAAA
|
|
GCGACCGGTTGGGGCGCGCTTGGACATAAACAGACGGCAGCTGACGTACTGCAAGTGGTT
|
|
GACCTTCAAAAGTTCAGTGACGAAGAGTGCGGAAGTACCTACCGTCCTTACCGGCATTTG
|
|
CCTCAAGGCTACGACAGCGCCACGCAGATGTGCTACGGCGACAAGGGAAAACTGAATATG
|
|
GACACCTGTGAGGGCGACAGCGGCGGTCCTCTACAGTTCCAAAACTCCTCGCTCCTCTGC
|
|
ATACACATAGTAGCGGGAGTGACGTCATTCGGCGACGCGTGCGGGTTTGCGGGCGGCGCC
|
|
GGGATGTACACACGAGTGTCGTACTATATTCCCTGGATCGAGAGCGTTGTATGGCCGTGA
|
|
>M. sexta-Transferrin (MsTRN); M62802.1
|
(SEQ ID NO: 11)
|
ATGGCTTTGAAACTTTTAACTTTGATAGCCCTGACTTGTGCGGCTGCGAATGCAGCTAAA
|
|
TCTTCATACAAACTATGCGTGCCAGCAGCATACATGAAGGACTGCGAGCAGATGCTTGAA
|
|
GTACCCACGAAGTCTAAAGTGGCCTTGGAATGTGTACCGGCTAGAGACAGGGTGGAATGC
|
|
CTCAGCTTTGTTCAGCAGCGACAGGCGGACTTCGTCCCCGTCGACCCTGAGGACATGTAC
|
|
GTGGCCTCCAAGATCCCCAACCAGGACTTCGTCGTCTTCCAGGAGTACAGGACTGATGAA
|
|
GAGCCTGATGCGCCATTCCGTTATGAAGCCGTTATTGTGGTTCACAAAGACCTACCCATC
|
|
AACAACTTGGATCAGCTGAAGGGACTGAGGTCTTGCCACACCGGAGTCAATCGTAACGTC
|
|
GGGTACAAGATCCCACTAACGATGTTGATGAAACGTGCCGTGTTCCCGAAAATGAACGAC
|
|
CACAGCATTTCGCCGAAAGAGAACGAACTGAAAGCGCTATCGACGTTCTTCGCAAAGTCG
|
|
TGCATCGTCGGCAAATGGTCGCCTGACCCCAAAACCAACTCGGCTTGGAAATCACAATAC
|
|
AGCCATTTGTGTTCAATGTGCGAACACCCGGAGCGTTGTGACTATCCCGACAATTACAGC
|
|
GGGTACGAGGGCGCGTTGAGATGCCTCGCCCACAACAACGGGGAGGTCGCGTTCACCAAA
|
|
GTCATATTCACACGTAAATTCTTTGGGCTTCCAGTAGGTACCACTCCAGCGAGTCCATCA
|
|
AACGAAAATCCCGAAGAGTTCAGATATCTCTGCGTGGACGGATCTAAAGCCCCCATCACT
|
|
GGCAAGGCTTGTTCATGGGCTGCCAGACCTTGGCAAGGACTGATCGGTCACAATGACGTA
|
|
CTTGCCAAACTCGCTCCGCTCAGAGAGAAGGTTAAGCAACTTGCTGATTCTGGTGCAGCT
|
|
GACAAACCGGAGTGGTTCACCAAAGTCCTTGGTCTATCAGAGAAGATCCACCATGTCGCT
|
|
GACAATATCCCAATCAAGCCCATCGACTACCTGAACAAGGCTAACTACACGGAGGTCATT
|
|
GAAAGAGGACATGGAGCTCCCGAGCTGGTCGTCAGGCTATGTGTGACGTCAAACGTGGCA
|
|
TTATCTAAGTGCCGGGCTATGTCCGTGTTCGCATTCAGTAGAGACATCAGGCCGATCCTA
|
|
GACTGTGTTCAAGAAAACAGCGAAGATGCCTGTCTTAAGAGCGTCCAAGACAACGGTTCA
|
|
GATCTTGCCTCAGTAGACGATATGAGAGTAGCTGCAGCGGCTAAGAAGTACAACTTACAT
|
|
CCAGTTTTCCACGAAGTGTATGGAGAGCTAAAGACGCCCAACTACGCAGTGGCTGTTGTC
|
|
AAGAAGGGCACTGCCTACAACAAGATCGACGACTTAAGGGGAAAGAAATCTTGCCACAGC
|
|
TCTTACAGTACTTTCAGCGGTCTGCACGCGCCTCTCTTCTACCTTATTAACAAGAGGGCC
|
|
ATTCAATCTGACCACTGCGTGAAGAACTTGGGAGAATTCTTCTCAGGCGGATCTTGCTTG
|
|
CCTGGTGTCGACAAACCCGAAAACAACCCAAGCGGTGATGATGTGTCTAAATTGAAGAAG
|
|
CAATGTGGATCCGACAGCAGCGCTTGGAAGTGCTTGGAAGAGGACAGAGGAGACGTCGCA
|
|
TTTGTTTCAAGTGCCGATCTGTCCCACTTCGACGCCAACCAATACGAGCTGCTCTGCCTG
|
|
AACCGCGACGCTGGCGGTAGAGATGTTCTCTCCAGTTTCGCCACTTGCAACGTCGCCATG
|
|
GCCCCGTCCAGGACCTGGGTGGCTGCGAAGGACTTCCTGTCTGACGTATCTATCGCCCAC
|
|
ACACCATTGAGCCTCGCCCAAATGCTCGCTACGAGACCTGACCTCTTCAACATTTACGGA
|
|
GAGTTCTTGAAGAACAACAATGTTATTTTCAATAATGCCGCTAAAGGCTTAGCAACAACT
|
|
GAGAAACTTGACTTCGAGAAGTTCAAGACCATCCACGACGTCATCTCTTCATGTGGTCTC
|
|
GCCTAA
|
|
>M. sexta-Arylphorin ß subunit (MsARP); M28397.1
|
(SEQ ID NO: 12)
|
ATGAAGACTGTCATAATCCTAGCGGGGTTGGTGGCCCTGGCCCTCGGCAGCGAAGTGCCT
|
|
GTCAAGCACTCCTTCAAAGTTAAGGATGTTGATGCGGCTTTCGTCGAACGTCAAAAGAAG
|
|
GTCTTAGATCTTTTCCAAGATGTCGACCAAGTAAATCCTAACGATGAGTACTACAAGATT
|
|
GGCAAGGAATACAACATCGAGGCTAACATCGACAATTACTCGAACAAGAAGGCCGTCGAA
|
|
GAATTCTTGCAGTTATACAGGACAGGTTTCTTGCCTAAGTACTATGAATTTTCACCCTTC
|
|
TATGACAGACTAAGGGACGAGGCCATTGGTGTTTTCCACCTCTTTTACTACGCTAAAGAT
|
|
TTTGATACGTTCTACAAATCTGCCGCATGGGCGCGTGTGTACCTCAACGAAGGACAGTTC
|
|
TTATACGCCTACTACATTGCTGTGATTCAGCGTAAAGATACTCAGGGCTTCGTTGTACCA
|
|
GCACCGTATGAAGTCTACCCTCAATTCTTCGCAAACTTGAACACTATGCTCAAAGTCTAC
|
|
CGTACCAAAATGCAGGATGGAGTTGTTAGTGCCGATTTAGCTGCACAACACGGCATCGTA
|
|
AAGGAGAAAAACTACTACGTATACTATGCCAATTACTCCAACTCATTAGTGTACAACAAC
|
|
GAGGAACAGAGACTGTCGTACTTCACTGAGGACATCGGCTTGAATTCGTACTACTACTAC
|
|
TTCCACTCTCACTTGCCTTTCTGGTGGAATTCTGAGAGATACGGAGCACTAAAATCGCGC
|
|
CGTGGTGAAATCTACTATTACTTCTATCAGCAATTAATTGCACGTTATTACTTTGAACGT
|
|
CTCTCGAACGGCCTGGGTGACATTCCCGAATTCTCATGGTACTCACCAGTCAAGTCTGGC
|
|
TACTATCCACTGATGTCTTCTTATTACTACCCCTTCGCTCAAAGGCCCAACTACTGGAAC
|
|
GTGCACAGCGAAGAAAACTACGAGAAAGTACGATTCTTGGACACGTATGAAATGTCATTC
|
|
CTTCAGTTCCTCCAAAACGGACACTTCAAAGCGTTTGACCAGAAGATTGACTTCCACGAT
|
|
TTCAAAGCTATCAACTTTGTTGGAAACTACTGGCAAGATAATGCTGACCTGTACGGTGAG
|
|
GAAGTTACTAAGGACTACCAACGTTCATATGAAATTATAGCCCGCCAAGTGCTTGGTGCT
|
|
GCACCTAAACCATTCGACAAGTACACATTCATGCCCAGCGCTTTAGACTTCTACCAGACG
|
|
TCTCTGCGTGACCCAATGTTCTACCAACTTTACAACAGAATTCTGAAGTACATATATGAG
|
|
TACAAGCAGTACCTGCAACCGTACTCTTCAGAAAAACTGGCATTCAAGGGTGTCAAGGTG
|
|
GTCGATGTTGTAGTAGACAAACTGGTTACCTTCTTCGAGTACTACGACTTTGATGCGTCC
|
|
AACAGCGTTTTCTGGAGCAAAGAGGAGGTTAAATCTAGCTACCCCCATGATTTCAAGATC
|
|
CGTCAGCCACGCCTTAACCACAAGCCATTCTCTGTCTCTATCGACATCAAATCTGAAGCT
|
|
GCCGTTGATGCCGTTGTCAAGATATTCATGGCACCTAAATACGACGATAATGGATTCCCT
|
|
CTGAAATTAGAAAACAACTGGAACAAATTCTTCGAGCTGGACTGGTTCACATACAAATTT
|
|
GTTGCTGGTGACAACAAAATCGTGAGGAACTCAAACGACTTCTTGATCTTCAAGGACGAC
|
|
TCTGTTCCCATGACTGAGTTGTACAAATTATTAGAACAAAATAAGGTTCCACACGACATG
|
|
TCCGAGGATTACGGCTACCTGCCTAAAAGACTGATGCTGCCAAGAGGTACTGAGGGTGGT
|
|
TTCCCATTCCAGTTCTTCGTTTTCGTATATCCATTCAACGCTGACAGCAAAGATCTTGCA
|
|
CCGTTCGAGGCCTTCATCCAGGACAACAAACCTTTGGGCTATCCATTCGACCGTCCCGTT
|
|
GTTGACGCTTACTTCAAGCAACACAACATGTTCTTCAAGGACGTCTTCGTATACCATGAC
|
|
GGCGAGTACTTCCCGTACAAGTTCAATGTTCCTTCCCATGTGATGCACTCAAACGTTGTT
|
|
CCTAAACACTGA
|
|
>M. sexta-Chymotrypsinogen-like protein 1 (MsCTL1); AM419170.1
|
(SEQ ID NO: 13)
|
ATGTACGTGAAAGTAGCACTTCTGTTGGTAGCCCTCATTGCTGGGAGCTGGGCCTTCCCA
|
|
AAGCTCGAAGATGAGCAGGACATGTCCATCTTCTTCACGCAGCTCGATTCGAGCGCGCGT
|
|
ATCGTGGGTGGTACCCAGGCCCCCAGCGGAAGTCACCCTCACATGGTGGCGATGACCACC
|
|
GGTACCTTCATCAGGAGCTTCAGCTGTGGAGGCTCAGTTGTCGGTAGACGTTCCGTTCTG
|
|
ACTGCGGCTCATTGCATCGCTGCTGTTTTCAGTTTCGGTTCCCTCGCCAGTACCCTCCGC
|
|
TTGACGGTCGGCACCAACTTCTGGAACCAGGGAGGCACCATGTACACCGTCGCTCGCAAC
|
|
ATAACCCACCCCCACTACGTCTCTGCGACCATCAAGAACGACATCGGTCTGTTCATCACT
|
|
CACAACAACATCATCGACACGACTGTCGTCCGCAGCATCCCTCTTAACTTTGACTATGTG
|
|
CCCGGTGGTGTTCTCACTAGAGTCGCCGGATGGGGCAGGATCAGGACCGGCGGTGCCATC
|
|
TCTCCCTCTCTGCTGGAGATCATTGTGCCTACTATCAGTGGAAGCGCATGCGTAGCCAGT
|
|
GCAATCCAAGCTGGCATCGATCTGAACATGAGACCACCTCCCGTCGAGCCTCACATCGAG
|
|
CTGTGCACCTTCCACGGTCCTAACGTAGGCACTTGTAATGGTGACTCCGGCAGCGCTCTT
|
|
GCCCGCCTAGACAACGGCCAGCAGATCGGTGTGGTATCGTGGGGCTTCCCGTGCGCACGC
|
|
GGCGGTCCCGACATGTTCGTCAGGGTCAGCGCCTACCAATCCTGGCTGCAGCAGAGCATC
|
|
GTATAA
|
|
>M. sexta-Valine Rich Midgut Protein (MsVMP1); NCBI accession number not assigned
|
as yet
|
(SEQ ID NO: 14)
|
ATCATTGACGGACCTTCCGTTGGACCNGCCATCATCGGCGCTGGAGACATCGCTGTCGGC
|
|
CCTGCTATCGTCGACTTCCCTTTCCCCGACGGCGGTGCCGTGTCTGCCCCCGTTGAGCCT
|
|
TCCCCCATCGCCATCGGACCCGCTATCGTCGGTGAATCCCCTATCTCCGTCGGACCTGCC
|
|
ATCGTTGAGGCCGGAGACATCGCTGTTGGACCCGCTATCATCGACTTCCCCCTTCCCGAC
|
|
GGTGGCGCCGTGTCCGCCCCCGTTGAGGTTTCTCCCGTCGACTCCGTCGTCGTCGGCCCT
|
|
GCCGCCGGCTCTCAGAGCTCTCCCCTCGTCCAGATCATCATCAACGTTAAGGCCCCCGCT
|
|
GGTGCCGGCCCCGTTGTCGATGCCGTCGCTGACAAGCCCATGGACATCATTGATGTTATG
|
|
CCCGTCGTCGACCCTGCTGATTTCGTGGACCTCACCCCCGTTGTAGAGCCTGTAGAAGTC
|
|
GTCGACATTGTCGATGTCATGCCCGTGGTTGACCCCATCAACATCATCGATGTTATGCCT
|
|
GTTGTTAAGCCCGTAAACCCCCTTGCCCGTTCTTAAGGG
|
|
>M. esculanta-Catalase 1 (MeCAT1); AF170272
|
(SEQ ID NO: 15)
|
ATGGATCCTTGCAAGTTCCGTCCATCAAGCTCAAACAATACCCCCTTCTGGACCACCGAT
|
|
GCTGGTGCTCCAGTATGGAACAACAATTCCTCCATGACTGTTGGAACCAGAGGTCCAATC
|
|
CTTTTGGAGGACTATCATATGATAGAGAAACTTGCCAACTTTACCAGAGAGAGGATTCCA
|
|
GAGCGTGTCGTCCATGCTAGGGGAATGAGTGCAAAGGGCTTCTTTGAAGTCACCCACGAT
|
|
GTCTCTCACCTTACTTGTGCTGATTTCCTTCGAGCCCCTGGAGTTCAAACCCCTGTCATC
|
|
GTCCGTTTCTCCACTGTTATCCACGAGCGTGGCAGCCCTGAAACACTCAGGGATCCTCGA
|
|
GGTTTTGCGACTAAGTTCTACACCAGAGAGGGCAACTTTGATATTGTGGGAAACAACTTC
|
|
CCTGTCTTCTTCATCCGTGATGGAATAAAATTCCCAGATGTGATACACGCTTTTAAGCCC
|
|
AATCCCAAGTCTCACATCCAAGAATACTGGAGGATCTTTGACTTCTTATCACACCATCCT
|
|
GAGAGCTTGAGCACCTTCGCCTGGTTCTTCGATGATGTTGGAATTCCCCAAGATTACAGA
|
|
CACATGGAAGGTTTCGGTGTTCACACCTTTACTTTCATCAACAAGGCTGGAAAAGTAACC
|
|
TACGTGAAATTTCACTGGAAACCCACTTGCGGGGTCAAGTGTTTGATGGATGATGAGGCA
|
|
CTTAAGATCGGAGGTGCCAACCACAGCCATGCTACGCAGGATTTATACGACTCCATTGCC
|
|
GCTGGCAACTATCCTGAGTGGAGACTCTTCATCCAGACAATGGATCCAGCTGATGAAGAC
|
|
AAATTCGACTTTGATCCACTTGATATGACCAAGATCTGGCCTGAGGATATTTTTCCTCTA
|
|
CAGCAAATTGGCCGTTTGGTCTTGAACAGGAACATCGATAACTGGTTTGCTGAGAATGAA
|
|
ATGCTCGCATTCGACCCTGGTCATATTGTTCCTGGCATTCACTATTCAAACGACAAGTTG
|
|
TTTCAGCTCAGAACCTTTGCATATGCTGACACTCAGAGGCACCGTCTCGGACCCAACTAT
|
|
AAGATGCTCCCTGTTAATGCTCCCAAGTGTGCTTATCACAACAATCATTACGATGGTTTC
|
|
ATGAATTTCATGCACAGGGATGAGGAGGTGGATTACTTCCCATCCAGGTATGATCCAGTT
|
|
CGCCATGCTGAGAGAAGCCCCATTCCTAACGCTATCTGTAGTGGAAGGCGTGAAAAGTGC
|
|
GTCATTGAAAAGGAGAACAATTTCAAGCAACCTGGAGAGAGATATCGATCCTGGGCACCT
|
|
GATAGACAAGAAAGATTCCTGTGCAGATTGGTTAACGCCTTATCAGAGCCACGTATCACC
|
|
TTTGAGATTCGCAGTATCTGGGTCTCTTACTGGTCTAAGTGCGACGCGTCTCTGGGTCAA
|
|
AAGCTGGCTTCTCGTCTCAACGTGAGGCCAAATATATGA
|
|
>M. sexta-Hemolin (MsHEM); M64346.1
|
(SEQ ID NO: 16)
|
GGCAAAGAATTCAAATGGCAGGAACACAATATCGCCCAGCGCAAAGACGAAGGCAGCCTG
|
|
GTCTTCCTCAAGCCCGAGGCTAAAGATGAAGGCCAATACAGATGTTTCGCTGAGTCGGCC
|
|
GCCGGAGTCGCCACCTCCCACATCATCTCCTTTAGAAGGACCTACATGGTCGTACCTACT
|
|
ACTTTTAAGACTGTAGAAAAGAAACCGGTAGAAGGGTCATGGCTCAAACTTGAGTGCAGC
|
|
ATCCCCGAAGGTTATCCTAAACCTACTATTGTATGGAGAAAGCAGCTTGGTGAAGACGAA
|
|
AGTATAGCAGATTCTATACTGGCACGTCGTATTACACAATCTCCAGAGGGAGACCTGTAC
|
|
TTCACGAGCGTCGAGAAAGAAGACGTAAGCGAAAGCTATAAATACGTTTGCGCTGCTAAG
|
|
TCACCGGCTATTGATGGGGATGTCCCTCTTGTTGGATACACTATTAAAAGCTTAGAAAAG
|
|
AATACAAATCAGAAAAACGGTGAGCTGGTCCCGATGTACGTCAGTAATGATATGATAGCT
|
|
AAGGCCGGAGACGTTACTATGATCTACTGCATGTATGGTGGAGTCCCAATGGCTTACCCC
|
|
AACTGGTTCAA
|
|
>M. sexta-Serine Proteinase homolog 3 (MsSPH-3); AF413067.1
|
(SEQ ID NO: 17)
|
ATGTTGTTGCTTCTGTATTGTCTTGTGGCGGCCTCCGCGCCGTTCTTTATTGCAGCGGAC
|
|
CAAGGCAGCCCTGACCTGCCTTTAGCTACCGAACCACCAACAGAATGCGGAACAATAGCA
|
|
CCTGATGATAGCTTAGTATTAGATGGGTCCGTTGGTAAAAGTGACAAATTACCTTGGTAT
|
|
GCTATTATCTACACAACCACCACCCGGCCATACAAGCAGATCGGTGGAGGAACCCTCATC
|
|
ACTCCTTCAGTAGTAATCTCAGCCGCTCACTGTTTCTGGCGCAATGGTGAGGTTCCATCT
|
|
AAGGATAATTACGCCGTGGCGCTCGGCAAGACCCATAGTGCTTGGAATAGCCATGCCGAT
|
|
GTAAACGCTCACAAGTCTGATGTAAAAGAAATACACATACCACCGCAGTTTAAGGGAAGG
|
|
AACACTAATTATCGGAATGATATAGCAATCGTGGTCATGTCAGACCCTGTGACCTACAAA
|
|
GTGGACATCCGCCCTATCTGTTTGAACTTCGATGTACAATTTGAAAGACTGCAATTAAAA
|
|
GACGGCATTATGGGGAAGATCGGCACATGGAATGTAAGTCGTGAGACACTGAAACTATCG
|
|
AAAACATTAAAAGTGGTGGAGAATCCATACATTGACGCAGCGACT
|
|
>M. sexta-Peptidoglycan recognition protein 2 (MsPGRP2); GQ293365.1
|
(SEQ ID NO: 18)
|
ATGGCGAGCTTCGCTTTAATAGTTATCCTTAGCGTAATTGGCTTTATATCGGCCTATCCT
|
|
AGTCCTGAAGGTTACAGTTCTGCCTTCAACTTTCCATTCGTAACCAAGGAGCAGTGGGGC
|
|
GGCAGGGAGGCACGCACGTCGACGCCACTCAACCACCCAGTGCAGTTCGTGGTGATCCAC
|
|
CACAGTTACATTCCCGGCGTGTGCCTCAGCCGGGACGAGTGCGCGCGCAGCATGCGCTCC
|
|
ATGCAGAACTTCCACATGAACAGTAACGGGTGGAGTGATATTGGATACAACTTCGCTGTC
|
|
GGCGGTGAAGGGTCGGTGTACGAGGGCCGCGGCTGGGACGCGGTCGGCGCACACGCAGCT
|
|
GGCTATAACAGTAACAGTATCGGCATCGTGCTCATCGGCGATTTTGTTTCAAACCTCCCG
|
|
CCGGCGGTGCAAATGCAAACCACACAAGAATTGATCGCAGCGGGCGTGCGACTCGGTTAC
|
|
ATCAGGCCCAACTACATGCTCATCGGGCATCGTCAGGTCTCCGCCACTGAGTGCCCAGGA
|
|
ACCAGACTCTTCAACGAAATCACCAACTGGAACAACTTCGTGAG
|
|
>M. sexta-Beta-1, 3-glucan-recognition protein 2 (MsßGRP2); AY135522.1
|
(SEQ ID NO: 19)
|
GCGTCTGTTTGTTCGCAACCATTGCGGGCTGCTTGGGCCAGCGAGGGGGTCCATACAAGG
|
|
TGCCTGATGCGAAACTCGAAGCTATCTACCCCAAAGGCTTGAGAGTCTCTGTGCCAGATG
|
|
ATGGCTACTCCCTATTTGCCTTCCACGGCAAGCTCAATGAGGAGATGGAAGGTTTAGAGG
|
|
CTGGCCATTGGTCCAGAGACATCACCAAAGCGAAGCAGGGCAGATGGATATTCAGAGATA
|
|
GGAATGCTGAGCTGAAGCTTGGAGACAAAATTTACTTCTGGACTTACGTTATTAAGGATG
|
|
GATTGGGATACAGGCAGGACAATGGAGAATGGACTGTTACAGAATTCGTCAATGAGAACG
|
|
GTACAGTGGTGGACACTAGTACAGCGCCGCCACCAGTAGCACCCGCCGTTTCAGAGGAAG
|
|
ATCAATCGCCAGGTCCTCAGTGGAGACCTTGCGAAAGATCCCTGACTGAGTCCTTGGCCC
|
|
GCGAACGCGTTTGCAAAGGCAGCCTTGTCTTTAGCGAGGACTTTGATGGTTCCAGTTTGG
|
|
CCGACTTGGGCAATTGGACCGCTGAAGTCAGATTCCCTGGCGAACCGGACTACCCGTACA
|
|
ACTTGTACACTACGGACGGCACTGTGGGATTCGAAAGTGGGTCTCTGGTGGTGAGACCCG
|
|
TCATGACCGAGTCCAAATACCACGAGGGCATCATATACGACCGCCTCGACCTTGAGAGAT
|
|
GTACAGGACAGCTGGGTACGCTGGAATGCAGGCGAGAGAGCAGCGGCGGTCAGATTGTAC
|
|
CACCTGTGATGACAGCTAAACTGGCCACTCGACGCAGCTTCGCGTTCAAGTTCGGCAGGA
|
|
TCGATATAAAGGCGAAGATGCCGCGCGGGGACTGGTTGATACCAGAACTCAACCTCGAAC
|
|
CTTTAGATAACATATACGGCAACCAGCGATACGCTTCGGGTCTCATGCGGGTCGCGTTCG
|
|
TGAGAGGAAACGATGTATACGCCAAGAAGCTCTACGGAGGTCCGATAATGTCCGACGCGG
|
|
ACCCGTTCAGGTCCATGCTGTTGAAGGACAAGCAAGGGTTGGCCAACTGGAATAATGATT
|
|
ACCACGTCTACTCGCTGCTGTGGAAGCCTAACGGTTTAGAGCTGATGGTGGACGGTGAAG
|
|
TGTACGGCACCATCGACGCTGGCGATGGCTTCTACCAGATTGCGAAGAACAACCTCGTGA
|
|
GCCACGCCTCGCAGTGGCTCAAGGGCACCGTCATGGCGCCGTTTGATGAAAAGTTCTTCA
|
|
TCACTCTGGGTCTTCGCGTGGCGGGTATCCACGACTTCACGGACGGTCCGGGCAAACCTT
|
|
GGGAGAACAAGGGC
|
|
>M. sexta-Relish family protein 2A (MsREL2A); HM363513.1
|
(SEQ ID NO: 20)
|
AGTGTGCGTCTACGAATGATTTGAAAATATGCCGCATAAGCCGTTGTTACGGTAGACCGA
|
|
GAGGCGGCGAAGATATCTTCATATTTGTCGAAAAGGTCAACAAGAAAAACATCCAAGTTC
|
|
GGTTCTTTAGACTGGAAAACGGGGAGCGCACCTGGTCAGCGATGGCGAACTTTCTGCTAA
|
|
GCGATGTTCACCACCAATACGCTATCGCTTTTAGAACGCCACCGTACGTCAATCACCAAA
|
|
TTTCTGAAGACGTGCAAGTTTTTATAGAACTCGTACGCCCTTCAGACGGTAGGACGAGCG
|
|
CTCCCATGGAGTTCACATACAAGGCTGAGCAAATCTATAAACAGAACAAGAAACGTAAAA
|
|
CTACTTCGTCGTACTCGTCGCTCGACAGCTCCTCAGGTTCGGCCGGTTCAATTAAAAGCA
|
|
TCAGCGAACTGCCCGCGCCCGTTGTTTTTGCTGAAAACGTAAGTTTTTTCTATGACACAT
|
|
TACTCATTCTTCAACCCATGACGAATCTATAA
|
|
>M. sexta-Dorsal (MsDor); HM363515.1
|
(SEQ ID NO: 21)
|
ATGCTTGTGACGTTATGCGGCGGGAACTATAGTGGATTGTCGTTAACAAAAACTAATCAT
|
|
TATATGTCACCAAAATCATATGTGCCAGGAAATGGTTATGACGCCGCCGTAATCCTAGGT
|
|
ACCACGGAGCAGAATGACAGCGAACCCTCAAACTTGAATATTAGTGATGTTTTTGAAGCC
|
|
ATCACGCTCGCTGATCCGTCGTTCGGCGCGGGCGTGCCGTCGGTAGAGGAGACGATGGCG
|
|
CACACGCAGCCCCAGCCGCTGCAAATGCCGTACGTGGTCGTCGTGCAGCAGCCCGCCAGC
|
|
AAAGCGCTCAGATTTCGATATGAGTGCGAGGGCAGATCAGCCGGTTCGATTCCCGGCGCG
|
|
TCGAGCACGCCCGAGAACCGAACCTTCCCCGCCATCAAGATAATCGGCTACACCGGCACC
|
|
GTCTCCATCGTAGTGTCGTGTGTCACCAAAGATGAGCCTTGCAGGCCGCACCCACACAAC
|
|
CTGGTCGGGCGCGACCACTGCGACCGCGGCGTGTTCTCCGTCCGCATCGAGATCACCGAC
|
|
GAGAATAACGAATACCAGTTTCGGAACCTGGGCATACAGTGCGTCAAGCGGCGCGACATC
|
|
GGCGAGGCGCTGCGGATCCGAGAGGACCTGCGCGTCGATCCGTTCAAAACCGGCTTCACC
|
|
CACCGGAACCACCCGCAAGGCATCGATCTGAATGCAGTGCGGCTCGCGTTCCAAGTGTTC
|
|
CTGCCGCACTCCAGCGGCAAGATGCGGCGCACGCTCGCGCCCGTCGTGTCCGACGTCATC
|
|
TACGACAAG
|
|
>M. sexta-Spatzle (MsSPZ1A); GQ249944.1
|
(SEQ ID NO: 22)
|
CGAACAACCTGACAGACGGATAGCGGGACGGTCAGCACAATACGAACATTTAAGAACAAA
|
|
CGAGAGGTCTCTCCCGGTCTACAGCGAGACCCAGAGGATACAAGCAGAAGAGAGAAGAAG
|
|
ACACAGTTCGAGACTAGAAGAACCGAGACAACGTGCTGAGAATGGTTCATATAAGATATT
|
|
GAATAACCCTCCGAAACCCTGTATTACTAATAGGAGAAGTCAAATTGATTCGTCGAATGA
|
|
TAGGGTAGTGTTCCCCGGTCCGACTTCAGAAAGGTCGTACGTACCCGAAGTGCCAGAGGA
|
|
ATGCAAGAAAATCGGCATATGCGACAGTATACCGAATTACCCAGAAGAACACGTAGCTAA
|
|
TATTATATCTCGACTTGGAGACAAAGGAAAAGTATTACAAATAGACGAACTGGACGTATC
|
|
AGACACTCCAGATATCGCCCAGAGGTTGGGTCCGCAGGAGGACAACATGGAACTATGTAG
|
|
CTTTAGAGAAAAGATTTTTTACCCCAAGGCAGCGCCAGACAAAGATGGAAATTGGTTCTT
|
|
CGTTGTGAATTCAAAAGAAAACCCAGTACAGGGTTATAAAGTTGAAATTTGCGACCGTCA
|
|
GCAATTACCATGCGCGGAGTTCGCGAGCTTCCAACAGGGATATGAAGCGAGGTGCATCCA
|
|
GAAATACGTTCGCCGGACCATGTTGGCGTTGGATCCCAAGGGTCAGATGACCGACATGCC
|
|
CCTTAAAGTGCCCAGCTGTTGCT
|
|
>M. sexta-Toll receptor (MsTOLL); EF442782.1
|
(SEQ ID NO: 23)
|
CAAGTGGTCGTTGTGCACTGCACCGGACTCGCCGAGTTCCCGCGCCTGCCACTAACCACG
|
|
GACAAGTGGATCCTGCACCTGCCCCACAACAACATATCATACCTCGCCGCGGCCGACGTA
|
|
TCGCCGAACATCGTGGAACTCGATCTAAGAAACAATTCAATCAAGAATATCGACGTACAG
|
|
GCATCAGCAAAACTAGCCTTCGTCCGGCTGCAATTGGGTGGTAACCCGATCGAGTGTGAC
|
|
TGCGAGGCGTTGAAGCTGCTGGCGCCGCTGCTCAAACCTGACTCAAAGCTGCTTGACAGA
|
|
AAGGACGTGAAATGTGAGAACGACGCGCAGATTACCTTGGCGATGCTGAAATTATGTACT
|
|
AAGTCATCCAATGGGCTGATGTACTTGCTGTTCCTGTTGCTGTTACTCGCATTTGTCGTA
|
|
ACCGGACTGCTCGCACGAACCGCAATTCGCCTGCGCATCAAAATGATCCTCATGAGACTG
|
|
GGTTGGATGTCGAGACTACTGGAGCCCGCGGACGACGATCGCCCGTACGACGCGTTTGTG
|
|
TCTTTCGCACACGAGGATGAGGAGCTGGTGATGGAGCAGCTGGCGGCACGGCTCGAGAGC
|
|
GGCTCGCGGCCGTACCGACTGTGTCTGCACTACCGCGATTGGGCGCCAGGCGAGTGGATC
|
|
CCGGCGCAAATAGCGGCTTCGGTGCGGGCCTCTCGGCGCACGGTGGCGGTTGTGTCGGCG
|
|
CACTACTTACAGTCGGGCTGGGCGCTTGCCGAGATCCGGGAGGCGACCGCAGCCTCGCTG
|
|
CAGGAAGGCATGCCACGTCTCATCATCGTGCTGCTCGACGAGACCGACCGGTTGATGCTC
|
|
GATATAGACCCTGAGTTGCACGCCTATGTGCGCAACAATACCTACGTGCG
|
|
>M. sexta-Scolexin A (MsSCA1); AF087004.1
|
(SEQ ID NO: 24)
|
TCGAAGCTAAGGGGGCAAAGCAGCCAATTGATACGAGGGCAGTGAAGGAACGGTATCCAT
|
|
ACGCAGTTCGGAGTTTCGGAGGCTTCTGCGGAGGAACCATTATCAGTCCCACCTGGATCC
|
|
TGACCGCCGGCCACTGCTCGATACTCTATGCGGGGAGCGGCCTACCGGCCGGCACCAACA
|
|
TTACCGAGGTATCTAGCTTGTACCGCTTCCCCAAGCGGCTCGTCATACACCCGCTCTTCT
|
|
CCATAGGACCCGTCTGGCTCAACGCTACGGAGTTCAACCTCAAACAGGCGGCTGCACGAT
|
|
GGGACTTCTTGTTGATAGAACTGGAGGAACCGCTGCCGTTGGACGGCAAGATCCTGGCGG
|
|
CTGCGAAGCTCGACGACCAGCCCGACCTCCCCGCAGGCCTCGACGTGGGCTATCCGAGCT
|
|
ACAGCACCGACACCTACGAGGCTAAGATACAAAGCGAGATGCACGGAAAGAAGCTTTCGG
|
|
TTCAATCTAACGAGGTGTGCTCGAAGCTAGAGCAGTTCAAGGCGGAGGACATGTTGTGCG
|
|
CCAAGGGACGTCCACCGCGATACGACTTCGTCTGCTTCAGCGACAGTGGCAGTGGGCTAG
|
|
TAGACAACAATGGTCGCCTAGTCGGCGTGGTGTCGTGGGCCGAGAACAACGCTTTCGAGT
|
|
GCCGCAACGGCAACCTGGCGGTCTTCTCGCGAGTGTCCAGCGTACGCGAGTGGATCCGAC
|
|
AAGTC
|
|
>M. sexta-Hemolymph proteinase 18 (MsHP18); AY672794.1
|
(SEQ ID NO: 25)
|
GATGGTCAGAAAGCGTGGGACAAATGTCTGGAATACGTTGACAAGCTGTCGTACCCATGC
|
|
GCTTCAACCTACTCCCACTACCTCAGCTCCGTTTGGGAGAAAGATAAGGAGTGCAGTATG
|
|
GTTCAGTTTGTTGGCGTGAGGCGATTCGCCTCGTATAACGGACAACCGGCGAAACGGAAC
|
|
GAGTACCCTCACATGGCTCTGCTCGGCTACGGCGACGACCAGGAGACGGCGCAGTGGCTC
|
|
TGCGGCGGCTCAGTGATCAGTGATCAATTCATCCTCACGGCTGCACACTGCATCTTTACA
|
|
AATCTATTGGGTCCAGTACGTTTCGCAGCGCTAGGAATACTGCAGCGATCGGATCCAGTA
|
|
GAGTTATGGCAAGTTTACAAGATCGGCGGCATAGTTCCCCATCCGCAGTATAAGTCACCT
|
|
ATCAAGTACCACGACATTGCTCTCCTGAAGACTGAAAACAAAATAAAGTTTAATGAGAAC
|
|
GTGCTGCCAGCGTGTTTGTTCATAGAGGGCAGAGTGGGTGGGAGTGAGCAGGCTAAAGCG
|
|
ACCGGTTGGGGCGCGCTTGGACATAAACAGACGGCAGCTGACGTACTGCAAGTGGTTGAC
|
|
CTTCAAAAGTTCAGTGACGAAGAGTGCGGAAGTACCTACCGTCCTTACCGGCATTTGCCT
|
|
CAAGGCTACGACAGCGCCACGCAGATGTGCTACGGCGACAAGGGAAAACTGAATATGGAC
|
|
ACCTGTGAGGGCGACAGCGGCGGTCCTCTACAGTTCCAAAACTCCTCGCTCCTCTGC
|
|
>M. sexta-Transferrin (MsTRN); M62802.1
|
(SEQ ID NO: 26)
|
ATGGCTTTGAAACTTTTAACTTTGATAGCCCTGACTTGTGCGGCTGCGAATGCAGCTAAA
|
|
TCTTCATACAAACTATGCGTGCCAGCAGCATACATGAAGGACTGCGAGCAGATGCTTGAA
|
|
GTACCCACGAAGTCTAAAGTGGCCTTGGAATGTGTACCGGCTAGAGACAGGGTGGAATGC
|
|
CTCAGCTTTGTTCAGCAGCGACAGGCGGACTTCGTCCCCGTCGACCCTGAGGACATGTAC
|
|
GTGGCCTCCAAGATCCCCAACCAGGACTTCGTCGTCTTCCAGGAGTACAGGACTGATGAA
|
|
GAGCCTGATGCGCCATTCCGTTATGAAGCCGTTATTGTGGTTCACAAAGACCTACCCATC
|
|
AACAACTTGGATCAGCTGAAGGGACTGAGGTCTTGCCACACCGGAGTCAATCGTAACGTC
|
|
GGGTACAAGATCCCACTAACGATGTTGATGAAACGTGCCGTGTTCCCGAAAATGAACGAC
|
|
CACAGCATTTCGCCGAAAGAGAACGAACTGAAAGCGCTATCGACGTTCTTCGCAAAGTCG
|
|
TGCATCGTCGGCAAATGGTCGCCTGACCCCAAAACCAACTCGGCTTGGAAATCACAATAC
|
|
AGCCATTTGTGTTCAATGTGCGAACACCCGGAGCGTTGTGACTATCCCGACAATTACAGC
|
|
GGGTACGAGGGCGCGTTGAGATGCCTCGCCCACAACAACGGGGAGGTCGCGTTCACCAAA
|
|
GTCATATTCACACGTAAATTCTTTGGGCTTCCAGTAGGTACCACTCCAGCGAGTCCATCA
|
|
AACGAAAATCCCGAAGAGTTCAGATATCTCTGCGTGGACGGATCTAAAGCCCCCATCACT
|
|
GGCAAGGCTTGTTCATGGGCTGCCAGACCTTGGCAAGGACTGATCGGTCACAATGACGTA
|
|
CTTGCCAAACTCGCTCCGCTCAGAGAGAAGGTTAAGCAACTTGCTGATTCTGGTGCAGCT
|
|
GACAAACCGGAGTGGTTCACCAAAGTCCTTGGTCTATCAGAGAAGATCCACCATGTCGCT
|
|
GACAATATCCCAATCAAGCCCATCGACTACCTGAACAAGGCTAACTACACGGAGGTCATT
|
|
GAAAGAGGACATGGAGCTCCCGAGCTGGTCGTCAGGCTATGTGTGACGTCAAACGTGGCA
|
|
TTATCTAAGTGCCGGGCTATGTCCGTGTTCGCATTCAGTAGAGACATCAGGCCGATCCTA
|
|
GACTGTGTTCAAGAAAACAGCGAAGATGCCTGTCTTAAGAGCGTCCAAGACAACGGTTCA
|
|
GATCTTGCCTCAGTAGACGATATGAGAGTAGCTGCAGC
|
|
>M. sexta-Arylphorin ß subunit (MsARP); M28397.1
|
(SEQ ID NO: 27)
|
CTGTCATAATCCTAGCGGGGTTGGTGGCCCTGGCCCTCGGCAGCGAAGTGCCTGTCAAGC
|
|
ACTCCTTCAAAGTTAAGGATGTTGATGCGGCTTTCGTCGAACGTCAAAAGAAGGTCTTAG
|
|
ATCTTTTCCAAGATGTCGACCAAGTAAATCCTAACGATGAGTACTACAAGATTGGCAAGG
|
|
AATACAACATCGAGGCTAACATCGACAATTACTCGAACAAGAAGGCCGTCGAAGAATTCT
|
|
TGCAGTTATACAGGACAGGTTTCTTGCCTAAGTACTATGAATTTTCACCCTTCTATGACA
|
|
GACTAAGGGACGAGGCCATTGGTGTTTTCCACCTCTTTTACTACGCTAAAGATTTTGATA
|
|
CGTTCTACAAATCTGCCGCATGGGCGCGTGTGTACCTCAACGAAGGACAGTTCTTATACG
|
|
CCTACTACATTGCTGTGATTCAGCGTAAAGATACTCAGGGCTTCGTTGTACCAGCACCGT
|
|
ATGAAGTCTACCCTCAATTCTTCGCAAACTTGAACACTATGCTCAAAGTCTACCGTACCA
|
|
AAATGCAGGATGGAGTTGTTAGTGCCGATTTAGCTGCACAACACGGCATCGTAAAGGAGA
|
|
AAAACTACTACGTATACTATGCCAATTACTCCAACTCATTAGTGTACAACAACGAGGAAC
|
|
AGAGACTGTCGTACTTCACTGAGGACATCGGCTTGAATTCGTACTACTACTACTTCCACT
|
|
CTCACTTGCCTTTCTGGTGGAATTCTGAGAGATACGGAGCACTAAAATCGCGCCGTGGTG
|
|
AAATCTACTATTACTTCTATCAGCAATTAATTGCACGTTATTACTTTGAACGTCTCTCGA
|
|
ACGGCCTGGGTGACATTCCCGAATTCTCATGGTACTCACCAGTCAAGTCTGGCTACTATC
|
|
CACTGATGTCTTCTTATTACTACCCCTTCGCTCAAAGGCCCAACTACTGGAACGTGCACA
|
|
GCGAAGAAAACTACGAGAAAGTACGATTCTTGGACACGTATGAAATGTCATTCCTTCAGT
|
|
TCCTCCAAAACGGACACTTCAAAGCGTTTGACCAGAAGATTGACTTCCACGATTTCAAAG
|
|
CTATCAACTTTGTTGGAAACTACTGGCAAGATAATGCTGACCTGTACGGTGAGGAAGTTA
|
|
CTAAGGACTACCAACGTTCATATGAAATTATAGCCCGCCAAGTGCTTGGTGCTGCACCTA
|
|
AACCATTCGACAAGTACACATTCATGCCCAGCGCTTTAGACTTCTACCAGACGTCTCTGC
|
|
GTGACCCAATGTTCTACCAACTTTACAACAGAATTCTGAAGTACATATATGAGTACAAGC
|
|
AGTACCTGCAACCGTACTCTTCAGAAAAACTGGCATTCAAGGGTGTCAAGG
|
|
>M. sexta-Chymotrypsinogen-like protein 1 (MsCTL1); AM419170.1
|
(SEQ ID NO: 28)
|
ATGTACGTGAAAGTAGCACTTCTGTTGGTAGCCCTCATTGCTGGGAGCTGGGCCTTCCCA
|
|
AAGCTCGAAGATGAGCAGGACATGTCCATCTTCTTCACGCAGCTCGATTCGAGCGCGCGT
|
|
ATCGTGGGTGGTACCCAGGCCCCCAGCGGAAGTCACCCTCACATGGTGGCGATGACCACC
|
|
GGTACCTTCATCAGGAGCTTCAGCTGTGGAGGCTCAGTTGTCGGTAGACGTTCCGTTCTG
|
|
ACTGCGGCTCATTGCATCGCTGCTGTTTTCAGTTTCGGTTCCCTCGCCAGTACCCTCCGC
|
|
TTGACGGTCGGCACCAACTTCTGGAACCAGGGAGGCACCATGTACACCGTCGCTCGCAAC
|
|
ATAACCCACCCCCACTACGTCTCTGCGACCATCAAGAACGACATCGGTCTGTTCATCACT
|
|
CACAACAACATCATCGACACGACTGTCGTCCGCAGCATCCCTCTTAACTTTGACTATGTG
|
|
CCCGGTGGTGTTCTCACTAGAGTCGCCGGATGGGGCAGGATCAGGACCGGCGGTGCCATC
|
|
TCTCCCTCTCTGCTGGAGATCATTGTGCCTACTATCAGTGGAAGCGCATGCGTAGCCAGT
|
|
GCAATCCAAGCTGGCATCGATCTGAACATGAGACCACCTCCCGTCGAGCCTCACATCGAG
|
|
CTGTGCACCTTCCACGGTCCTAACGTAGGCACTTGTAATGGTGACTCCGGCAGCGCTCTT
|
|
GCCCGCCTAGACAACGGCCAGCAGATCGGTGTGGTATCGTGGGGCTTCCCGTGCGCACGC
|
|
GGCGGTCCCGACATGTTCGTCAGGGTCAGCGCCTACCAATCCTGGCTGCAG
|
|
>M. sexta-Valine Rich Midgut Protein (MsVMP1); NCBI accession number not assigned
|
as yet
|
(SEQ ID NO: 29)
|
ATCATTGACGGACCTTCCGTTGGACCNGCCATCATCGGCGCTGGAGACATCGCTGTCGGC
|
|
CCTGCTATCGTCGACTTCCCTTTCCCCGACGGCGGTGCCGTGTCTGCCCCCGTTGAGCCT
|
|
TCCCCCATCGCCATCGGACCCGCTATCGTCGGTGAATCCCCTATCTCCGTCGGACCTGCC
|
|
ATCGTTGAGGCCGGAGACATCGCTGTTGGACCCGCTATCATCGACTTCCCCCTTCCCGAC
|
|
GGTGGCGCCGTGTCCGCCCCCGTTGAGGTTTCTCCCGTCGACTCCGTCGTCGTCGGCCCT
|
|
GCCGCCGGCTCTCAGAGCTCTCCCCTCGTCCAGATCATCATCAACGTTAAGGCCCCCGCT
|
|
GGTGCCGGCCCCGTTGTCGATGCCGTCGCTGACAAGCCCATGGACATCATTGATGTTATG
|
|
CCCGTCGTCGACCCTGCTGATTTCGTGGACCTCACCCCCGTTGTAGAGCCTGTAGAAGTC
|
|
GTCGACATTGTCGATGTCATGCCCGTGGTTGACCCCATCAACATCATCGATGTTATGCCT
|
|
GTTGTTAAGCCCGTAAACCCCCTTGCCCGTT
|
|
>M. esculanta-Catalase 1 (MsCAT1) AF170272
|
(SEQ ID NO: 30)
|
ATGGATCCTTGCAAGTTCCGTCCATCAAGCTCAAACAATACCCCCTTCTGGACCACCGAT
|
|
GCTGGTGCTCCAGTATGGAACAACAATTCCTCCATGACTGTTGGAACCAGAGGTCCAATC
|
|
CTTTTGGAGGACTATCATATGATAGAGAAACTTGCCAACTTTACCAGAGAGAGGATTCCA
|
|
GAGCGTGTCGTCCATGCTAGGGGAATGAGTGCAAAGGGCTTCTTTGAAGTCACCCACGAT
|
|
GTCTCTCACCTTACTTGTGCTGATTTCCTTCGAGCCCCTGGAGTTCAAACCCCTGTCATC
|
|
GTCCGTTTCTCCACTGTTATCCACGAGCGTGGCAGCCCTGAAACACTCAGGGATCCTCGA
|
|
GGTTTTGCGACTAAGTTCTACACCAGAGAGGGCAACTTTGATATTGTGGGAAACAACTTC
|
|
CCTGTCTTCTTCATCCGTGATGGAATAAAATTCCCAGATGTGATACACGCTTTTAAGCCC
|
|
AATCCCAAGTCTCACATCCAAGAATACTGGAGGATCTTTGACTTCTTATCACACCATCCT
|
|
GAGAGCTTGAGCACCTTCGCCTGGTTCTTCGATGATGTTGGAATTCCCCAAGATTACAGA
|
|
CACATGGAAGGTTTCGGTGTTCACACCTTTACTTTCATCAACAAGGCTGGAAAAGTAACC
|
|
TACGTGAAATTTCACTGGAAACCCACTTGCGGGGTCAAGTGTTTGATGGA
|
|
>M. sexta-IMD (MsIMD); Msex2.05477-RA
|
(SEQ ID NO: 31)
|
ATGACTTCTTTGAAAAGCAAATTAGCAGAATTCTTGAAGGGGTTAAAATCAGATGCAACC
|
|
CCAAGCCCCGAGGCCATCGACAGAACCCAGGGTAAATCCACAAACTGAGCAATGAAAATG
|
|
ACGCACCCTCGGATAGTGAACCTGAAGAAATCATTATAGAAGATATGACGATACGAAGAA
|
|
AAAGAAAAAGGCAAGTTACAAGAAACCGTTCTTTAGCTCCAAACCTGGTGCATTCCCCGA
|
|
AAAGAAAAAAGACAAGAATACCAAAGACGATTACAGCAACTTTGTGAATACTCAAGCCAC
|
|
TGGTGATGTCATCAATATTGTAGGCTGTAACAATTTCCGCTGGGGTAATAATTATTATTT
|
|
GGGAAATACCAAGAAACAGGCTCCTCCTAAGAAATATTTCCAAGAAGAGGAAGACAGTGA
|
|
ACCAGAAGATGATATTCAGAAATGCAACTTAATCAAACTGCTATTTGAAGCTGAAAATAA
|
|
GCCAGAACATGAGTACCTGGACTACATTTCCCAGAACATGAATGAAAAGTGGCACAGATT
|
|
CTTTGTGAAACTAGGTTTTACACCAGGAAGGATCAAAACATCCATCATAGATAATGCCAG
|
|
TTATGGTATTTCAGAGGCTCGATACGCATTGCTACTTGAGTGGGTGAATAAAAAACGGGA
|
|
CTCTAATCTTGGACAGCTATCGAATTTATTGTGGAAACACGGCGAGAGGCGAATTGTCAA
|
|
AGAATTAGCCATTATGTACTCTGCAAGCAAGGCCAAATCTGATGATGAATAG
|
|
>M. sexta-FADD (MsFADD); Msex2.03129-RB
|
(SEQ ID NO: 32)
|
ATGACTCTATCGGAATCAAAATTTAAACAATTAAAAGAACAAATTATTTTACATGCAAGT
|
|
GCAACTGAAAGACATGCTCAAATTTTGAACTCATTAAAGGATTTGTTTAAAGAAGATATT
|
|
AATTCTGTTCGAAGATTTGAACAAATCAGCAATATAGCACAATTATTAAAAGTTTTAGAA
|
|
ATAAGAGATGTGTTGTCAGAGGATGATGTTGCTCCTTTGAAAGATGTGGCACGCCAACTA
|
|
CCAAATAGCTCAGAAATGCTGCGGAAAATTGCTGAATATGAAGAAAATCACAAGTGTGGA
|
|
GAGTTTATTTCTGTTCCTAAGTCACCTCCAAAACAAAAAGAACATAGTCATTCTGGATGG
|
|
GATATTAACAGCATACAGAATTCTGAATATTCTGTAAAAAAGGAAAGGATATTTGAAGTT
|
|
ATTTCTGAAGAAATTGGCACCCATTGGAGAAATCTAGCGAGATATTTGAAAACAAGGGAA
|
|
TGTACAATAATTGAAATTGACAGTAAAAACATACCACTTTCAAGTAAAGCTATGGAGATT
|
|
TTGAAATTGCATTGTAAAAAAGCAAATCCACAAAAGTGGTTTTTTGACTTGTGTAATGCA
|
|
TTGGACAAAGTGCATAGGACTGACATAGTGTTATCACTGCAAGAAATTATGTCTATGAAT
|
|
ATTTAG
|
|
>M. sexta-Dredd (MsDRD); Msex2.04297-RC
|
(SEQ ID NO: 33)
|
ATGTTGTCTTCCGATGCCAGAAGTTCCCTAAATTCCAAGAGTGATAATGAAACGTTTATA
|
|
TTAAACTTGGATTCGATTTCAAAGATTGAAAAACAATTACAAGATAATCCTTATGATATG
|
|
ATCTCTTTAGTGTTCCTGTTGTACGACGTGCCGGATACGGCGCTGCAGAGATTGATGGTG
|
|
TATCAACGAGTGACGAGTGACGTCAGTGGAACAAATATTAATTTGTTGCAAGAATGGTAC
|
|
TGTCACGCCAGCAGTCGCCCTGACTGGCAACATGAATTATTAGAAGCATTAATGATATGC
|
|
CAATTGAACTCCATTGTGAAGAGCCTTGGTTTCCATATACCCACTATGAGAGTATTTTAC
|
|
CAATCAAATGATCCCTTCAGCAGCAAGTACATAAATCCCGTAAAGAAAGTCCTTTATCAT
|
|
GCCTGTGAAAATATAAACTCAACTAATCTTTTGAAATTAAAAAAATCACTTCTTTCATAT
|
|
GATATAAATGTAATGGAATATACAACTTGTGAGCTTATATTTTTAGAGCTCCTGTCCAAT
|
|
AAATTTATTACTATTAATAATATTGGCCAAAAGATTAAAACAAACCAGAACTGCATATGT
|
|
AATGTAGAAAACCTTGTGAAGATCTTAGACAACTTAAATGGATTGAAAAAAGTGGCTATG
|
|
AATTTGAGATATTTTCAAAGTAAATTCAATGATGAAGAGGTGGATTCATTCGCGTCTGTC
|
|
AATGGAAGCAGCTCACCATCACTTCCAGTGCCTCCTCTTGATGGTACAAAATTAAAGCAA
|
|
GATGACAAGAATTATGGAGCTGAAGATTTCTCAGAGCTATTCGACATAATAAATAATATG
|
|
CCAGAACCGCTTGAAAACAATTTTAAATCTGATACAATGTCAACTAAACAGAATAGATAT
|
|
GAGATAAAAAATCCGGAACAACTAGGTGTTTGCATAGTTATAAACCAAGAGAATTTTTAT
|
|
CCATCCAAAAATAGTATTGAAGACCACCAAATTGTTCCATTAGAAGAGAGAAAAGGATCT
|
|
AGTGTGGATAAAAGGACTTTGGAAAGAACCATGACATCATTAAAATTTCAAGTTCACAGT
|
|
TGCTCTGATTTAGATCATGATGAAATGATAGAATTCATCAAAAAGAAAATTAATAAACAT
|
|
GTTACATCAAATGACAGTATTTTTATGTTGTGTATACTGTCACATGGTGTAAGGGACCAT
|
|
GTGTATGCTGCTGACTCTGTGAAAATTAAAGTAGAGTCTATACAAAATCTGTTGGATTCA
|
|
GATGAAATGAGCCACTTGAGAGGCATACCGAAGGTGTTTATTATACAAGCTTGCCAAGTT
|
|
GAGGATACACCTCATCCTACATTTGCTGCTGACAATGTCCAAACAAATTACTACTTGGGA
|
|
AAATTAGACTTCCTTATTTACTGGGCCACTGCACCTGAATATGAAGCCTTCAGACATGAG
|
|
CAGACGGGGTCATTATTCATTCAAGCTCTTTGTAAACTGTTGCGTCAAAGAGCTAAACAT
|
|
GATCACTTACATGAAATCTTTACACAAGTAAATAACAATGTTACCAATCTGTGCACTAAG
|
|
TTGCAGCGTGCACAAGTACCTCTCTTCAAAAGTACTCTGAGGAAAAATTTATATTTACAA
|
|
GTGCCAGAATAA
|
|
>M. sexta-Relish F (MsRelF); Msex2.08004-RE
|
(SEQ ID NO: 34)
|
ATGTCCTCTTGTCCAAGCGACTATGATCCCAGTGAATCGTCCAAATCTCCACAAAGTATT
|
|
TGGGAGTCAGGAGGATACAGTTCTCCGTCGCAACAAGTTCCTCAATTGACTTCTAACTTA
|
|
ACAGAATTGTCTGTTGATCACAGCTATAGATACAATGGAAATGGACCATATCTACAGATC
|
|
ACAGAGCAACCACAGAAATACTTTCGGTTCCGTTATGTTAGCGAGATGGTGGGAACACAT
|
|
GGATGTTTGCTTGGCAAATCTTATACAACAAACAAAGTTAAAACTCATCCGACAGTTGAA
|
|
CTCGTGAATTACACCGGTCGAGCCCTGATAAAGTGCCAACTGTCGCAAAACAAGAGCGAA
|
|
GACGAACACCCGCACAAACTGCTCGATGAACAAGACAGAGACATGAGCCACCACGTTCCC
|
|
GAGCACGGCAGTTATAGAGTGGTATTTGCCGGTATGGGTATAATTCATACTGCCAAAAAG
|
|
GAAGTTGCAGGGTGGCTCTATAGAAAATATATACAGCAGAACAAGAATGAAAAGTTTAAT
|
|
AAGAAAGAGCTCGAAGCGCATTGTGAGAGGATGTCCAAAGAGATCGATTTAAACATAGTT
|
|
AGACTGAAGTTTAGCGCTCACGATATTGACACTGGCATTGAAATTTGCCGGCCAGTGTTC
|
|
TCTGAACCCATTTATAATTTGAAGTGTGCGTCTACGAATGATTTGAAAATATGCCGCATA
|
|
AGCCGTTGTTACGGTAGGCCGAGAGGCGGCGAAGATATCTTCATATTTGTCGAAAAGGTC
|
|
AACAAGAAAAACATCCAAGTTCGGTTCTTTAGACTGGAAAACGGGGAGCGCACCTGGTCA
|
|
GCGATGGCGAACTTTCTGCTAAGCGATGTTCACCACCAATACGCTATCGCTTTTAGAACG
|
|
CCACCGTACGTCAATCACCAAATTTCTGAAGACGTGCAAGTTTTTATAGAACTCGTACGC
|
|
CCTTCAGACGGTAGGACGAGCGCTCCCATGGAGTTCACATACAAGGCTGAGCAAATCTAT
|
|
AAACAGAACAAGAAACGTAAAACTACTTCGTCGTACTCGTCGCTCGACAGCTCCTCAGGT
|
|
TCGGCCGGTTCAATTAAAAGCATCAGCGAACTGCCCGCACCCGTTGTTTTTGCTGAAAAC
|
|
TTACCTGAAAACAATGAGCGTATTATAGATATACCCGTACAACAGAATATGCTGTACCAG
|
|
GTTCTGCCAAGTCAATGTGATTTAGCCGACGCGTTCATGGAGGTGGACAGCAAGGGAAGT
|
|
CCGGCCAGCGTCGTGGACCCGATGTGGGCCGGCGCCGACGTCGGGCTGCAGATGGCGTCG
|
|
AGCCTGCCCGCCATCAAACTCGGCTCCACCGAACTAGAGAGCTTGGCGCACCGCAGCCGG
|
|
GACGGAGTGCCCATGGACAAAGAATTCCTTGACAATTATCTCAGCTCTCTCAACTCGCTT
|
|
GGTGAACTTAACGACGATGATGAGATCAATCATATGCAATATGTGCGCTCGTTACAGATG
|
|
GTCCACGCCGACTCGGCACGACGAAAGGCTGAACCGCAACCCAAAGACACTGTAACCAAA
|
|
CCGACTCAATCTTCCCCGAAGGACACAGACTATGGCGCCCAGTCGGGACGCCCCACTGAA
|
|
TATTCTGCTTATTATAAAATGGAAGACGGCGTGGAAGTCAAAAAACTGGTGAAAGAATTG
|
|
TGTAGTATCATACAGAACAAAGCGGGATATAAAAAACAAGAAGTGAGAAACAAATTGGAG
|
|
AGGCTGTTCACCTACCGTCTGTCCAACGGAGATACATTCCTTCATATGACATTGTGCAGC
|
|
AATCAAAGTAGTTTTGAATACATCGTCAAAATCATACATAGCGTGAAAATGACACATCTA
|
|
TTGGACTATTGTAATAATAAACAGCAAACCATATTACACATGGCTATTGTAAACGACCTG
|
|
CCTCGAATGGTCTCTTTACTTATTGCAAAAGGTTGCAATCCAATGAATAAAGACAGCGAG
|
|
GGCGACAATGCGGTGCACTACGCTGTGAGGAGCGAATGTTGTTTAGAAGCATTATTGGAC
|
|
GCCATCAAAAATAACAATGTTCGGTGCGATTTGAACGACTGCAATAACGAGAAGCAGACG
|
|
GCGCTGCACCTGTCGACGAGCGGCGCGAGCGCGCGGCAGCTGGCGGCGCGCGGCGCCGAC
|
|
CCGCGCGTGCGCGACGCGCAGGGCCGCACGCCGCTGCACCTCGCCGCCTACGACGACAAC
|
|
TGCGACGTCGTCAGGGCGCTGCTCGAGTTCGTGTCGCCCTCGGAAATAGACGTTGTGGAC
|
|
GGCTGTGGCAACACTGCGTTACAGATCGTCTGCGGCGGCTCCGTTAAGAAGAACACTTTG
|
|
GAAATAGTAAAACTGTTGCTCCAAAAAAAGGCTGATCCGTTGAAGCAAGATGGGCACAAC
|
|
ATATCGGCGTGGAAGATGGCGCGCGAACACTCCGAAATACGGGACGCGATGAAGGACTAT
|
|
GTCCCCGCCGCCGCGTACGAGGAGGACACCAAGTCGGAAATGGACGATGAGTTCGAATCC
|
|
GCTGATGAGGAGGACTACCGGATGGGTTCCGGATCGGGCGCTGTGAGTCTGCCGGAGCTG
|
|
GGCGCATACGTGGAGGCGCTGAGCGCGGCGCTGGAGGCGCGCGGCGCGTGGCGCGCGCTC
|
|
GCGCACCGCCTCGGCCTCGCCGCCGCGCTCGACTGGTGCGCGCGACAGCACGCGCCCGCG
|
|
CGCACGCTGCTGCTGCACCTCAAGGAATGCAGAAACGACATATCCTCGAAAACGTTGGCT
|
|
GTAATTCTAGAAGATATGGGAGAATTAGAGGCTGCTTCAATTATAAGGAGACACATAGAG
|
|
TGA
|
|
>M. sexta-Cdc42 (MsCdc42); Msex2.04668-RA
|
(SEQ ID NO: 35)
|
ATGCAGGCGATCAAGTGTGTCGTCGTCGGAGACGGTGCCGTCGGTAAAACATGTCTGCTC
|
|
ATCAGCTACACGACAAATGCCTTCCCCGGAGAATACATACCTACAGTATTCGACAATTAT
|
|
TCAGCGAATGTGATGGTGGACGGGAAGCCGATCAACCTGGGCCTGTGGGATACGGCGGGG
|
|
CAGGAGGACTACGACCGGCTGCGGCCGCTGTCCTACCCACAGACCGACGTGTTCCTTATA
|
|
TGCTTCTCGCTCGTCAACCCGGCTTCGTTCGAGAACGTTCGGGCTAAGTGGTACCCAGAA
|
|
GTGCGGCATCACTGCCCGTCGACGCCCATCATCCTCGTCGGTACCAAGCTGGACTTGCGC
|
|
GAAGACAAAGACACCATAGAGAAACTTAAGGACAAGAAGCTCGCGCCTATCACTTACACA
|
|
CAGGGTCTGGGCATGTCGAAGGAGATCAACGCGGTGAAGTACCTCGAGTGCTCTGCGCTG
|
|
ACGCAGAAGGGTCTGAAGACGGTGTTCGACGAGGCCATCCGCGCCGTGCTGTGTCCCGTG
|
|
CCGCCCCCCAAACAGAGCCGGAAGTGCACGCTGCTGTAA
|
|
>M. sexta-DSor1 (MsDSor1); Msex2.00725-RB
|
(SEQ ID NO: 36)
|
ATGAGTAAGATGTCAAAGAATAAATTAAACTTGACCCTGCCACCAGGGTCAATAGACACA
|
|
GCACCAGCCATCACACCATCCAATATGACACCACAGCTGAAGTCCGCAACAGCTACGGAG
|
|
CGTCAGGGCTTGGCTGGTAAATCGAAAACCAGCATCGAAGCCCTGACAGAGAGGTTGGAG
|
|
CAAATCGAGATGGACGACACACAGAGACGGAGAATAGAAGTGTTTCTGTGTCAGAAGGAG
|
|
AAGATCGGGGAGCTTAGTGATGATGATTTTGAAAAGCTTGGAGAGTTAGGCCAAGGCAAC
|
|
GGTGGCGTTGTAATGAAAGTCCGTCACAAGTCAACCGGTCTGATAATGGCGCGAAAGTTA
|
|
ATCCATCTGGAAGTCAAGCCGGCAATAAAGAAGCAAATCATCAGGGAGTTGAAAGTCTTA
|
|
CACGAATGTAACTTTGCGCATATCGTCGGCTTCTACGGGGCCTTTTATAGCGACGGCGAG
|
|
ATCTCGATTTGTATGGAGTACATGGACGGTGGGTCCTTAGACCTTATACTGAAGAAGGCC
|
|
GGCAAGATTCCTGAATCTATTCTAGGAACAATAACATCCGCCGTGCTGAAAGGTCTGAGC
|
|
TACCTCCGGGACAAGCACGCCATCATGCATCGCGACGTGAAACCATCAAACATTCTGGTG
|
|
AACAGCAACGGCGAGATCAAGATATGCGATTTCGGCGTGTCCGGTCAGCTGATCGATTCC
|
|
ATGGCCAACTCTTTTGTCGGCACTAGGAGTTATATGTCTCCCGAACGTCTCCAAGGCACG
|
|
CACTATTCAGTCCAATCTGACATATGGTCGCTCGGGCTGTCGTTGGTAGAGATGGCAATC
|
|
GGAATGTATCCCATACCGCCGCCGGACGCGAAGACCCTGGCTGCCATCTTCGGTGGACAG
|
|
AATGAAGATCATTCTCCTGGTCAGGCGCCGAACTCGCCCCGTCCGATGGCCATATTCGAG
|
|
TTGCTGGACTACATCGTGAACGAGCCGCCGCCGAAGCTGCCCGCCGGAATATTCTCCGAC
|
|
GAGTTCAAGGACTTCGTCGACCGCTGCTTGAAGAAGAATCCAGACGAACGAGCCGACTTG
|
|
AAGACTTTGATGAATCACGAATGGATACGCAAAGCGGACGCAGAAAAGGTGGACATAGCG
|
|
GGGTGGGTGTGCAAGACAATGGACCTCATGCCTTCCACTCCAAACTCTAACGTGTCTCCT
|
|
TTTTCTTCATAA
|
|
>M. sexta-FOS (MsFOS); Msex2.09858-RA
|
(SEQ ID NO: 37)
|
ATGCAGAACATCGATCCTCTGGAGATCGCCAACTTCCTCGCCACGGAGCTGTGGTGCCAG
|
|
CAGTTGGCGAACCTCGAGGGCCTCCAGTCGGGGGTCCCGACTCGCACAACGGCCACCATC
|
|
ACGCCGACGCAACTGCGCAACTTCGAGCAGACTTACATCGAGCTGACCAACTGCCGCAGC
|
|
GAGCCCACCACGCACGCCGGCTTCGTGCCGCCGTCAGTCACGCACGCCAACAACTACGGC
|
|
ATCCTGAATCCGACGGCGTATTGTGATTCGGGCCCGACGACGGCGCTGCACGTGTCGCCG
|
|
GGCCCGCTCTCCGCCAGCGGCGACAGCAGCAGCAGCCCCGGCCTGCCCACGCCCAAGCGG
|
|
CGCAACATGGGCGGCCGCCGGCCCAACAAGGCGCCGCAAGAACTCACGCCCGAGGAAGAA
|
|
GAGCGCAGGAAGATCCGCCGCGAGCGAAACAAAATGGCCGCCGCCCGTTGTCGCAAGCGC
|
|
AGACTCGACCACACCAACGAGCTGCAAGAGGAAACCGACAAATTAGAGGAAAAGAAGCAT
|
|
GCGCTCCAGGAGGAAATCCGCAAACTGAACGCTGACCGGGAGCAGCTGCAAGTGATCCTT
|
|
CAGAACCATATGGTATCATGCCGGCTCAACAAGAGATCCATCAGCCCGCCCGATGTGAAG
|
|
CCCTTCCAGGACCCGTACGCCTACCCTGAGATACCCGAGGATGGCGTCCGTGTCAAGGTG
|
|
GAAGTGGTCGACCCCTCAGTAGACACGGTCTTAGTGTTGGACAATATTTACTCAACGCCG
|
|
CCGACTGACAAAAAAATTATGCTGTCGTCGGCCAACCCAGCCGTGGTGACGAGTGGGTCG
|
|
CCCGCCGCCCTGGAGACCCCGCCGGCGATAGTGCGTCCCAACAGACCCAACTCCCTCCAG
|
|
GTGCCGCTCAGCCTCACACCAGCACAGTTACACAACAACAAGGCGCTGGGAAACAACAAA
|
|
ATAGCCGGCATAGAGATAAGCACGCCGAGCAACGGCATCCCGTTCAACTTCGAGAGCCTG
|
|
ATGGAGGGCGGCACGGGGCTGACGCCGGTGCACGGCCACGCGCTGCCGCTGCCGCACCCG
|
|
TGCGCGCAGCAGCAGCGCGCCGCGCCCGACGCCTCGCCCGCCGAGCCGGCGCCGAGCTCG
|
|
CTGGTGAGCCTCTGA
|
|
>M. sexta-Jra (MsJra); Msex2.12422-RB
|
(SEQ ID NO: 38)
|
ATGGTTCGGCACTCCGGCCACGGCATGGAGACCACTTTCTATGACGAGCAGTATCCCATC
|
|
AGCGGCCCCGTGGAGAACCTGAAGCGGCCCCTCACGTTAGACGTGGGGCGCGGCGTGAAG
|
|
CGCGCCAGGCTCGGCGGGGCACCCGTACTCTCATCTCCAGACCTACAGATGCTGAAGCTC
|
|
GGCTCGCCAGAGCTCGAGAAACTGATCATCCAGAACGGCTTGGTGACGACGGCCACCCCC
|
|
ACTCCAGGTGCGCCGGTGCTGTTCCCCGCGGTCGCGCCTACCGAAGAGCAAGAGATGTAC
|
|
GCGCGGCCATTCGTCGAGGCGCTAGACAAGCTGCACCACGGCGAGGTGACCCCGATCGGG
|
|
CGGCGAGTGTACGCCGACCTGGACCGGCCGCTCGAGCGGTACCCCACGCCCGTGGTGAAG
|
|
GACGAGCCGCAGACGGTGCCCAGCGCCGCCAGCTCGCCTCCACTTTCCCCTATTGACATG
|
|
GACACGCAGGAGCGGATCAAACTGGAGCGCAAGCGACAGAGGAATCGAGTGGCCGCTTCC
|
|
AAATGCAGGCGGCGCAAGCTCGAACGCATCTCCAAGCTGGAGGACAAGGTGAAGATCCTG
|
|
AAGGGCGAGAACGCGGAGCTGGCGCAAATGGTGGTGAAGCTAAAAGAGCACGTACACCGA
|
|
CTGAAGGAGCAAGTGCTGGAGCACGCCAACGGCGGCTGCCACATCGAGTCGCACTTCTGA
|
|
>M. sexta-Caudal (MsCAD1); Msex2.04570-RA
|
(SEQ ID NO: 39)
|
ATGGTGAATTACGTTAATCCCCTCGCCATGTACCAAGGCAAGGGCGGGCAATACGGCGGC
|
|
GGGTGGTACGGCTGGCAGCATCAGAACTTTGAAGAACAACAATGGTGTGCTTGGAACGGT
|
|
GCGCCGGCGGGTGGCGAGTGGGCGCCAGATCCACATCATTTTCCCAAAAGAGAACCTGGA
|
|
GAGAGAGAAATAGCAGACATGCCATCACCGGCACGAGGAGACTTGGCAAGTCCAGCAGAA
|
|
GGTTCGCCGAGCTCGGGGTCGAGGCCGTCGCAGCCGCCAGCACCGCCGCGTTCCCCATAC
|
|
GAATGGATGAAAAAACCCAACTACCAGACACAACCTAACCCAGGTAAAACGCGCACAAAA
|
|
GACAAATACAGGGTGGTGTACAGTGATCATCAGAGGCTGGAGTTAGAGAAGGAGTTCCAC
|
|
TACAGCAGGTACATCACTATTCGTCGCAAGGCAGAACTCGCCGTCAGCCTTGGCCTTTCC
|
|
GAACGACAGGTCAAAATTTGGTTTCAAAATAGACGAGCCAAGGAAAGGAAACAGGTGAAG
|
|
AAACGCGAAGAAGTGGTGATGAAAGAGAAAGGCGACCATGCATCTCTACAGCACGCGCAG
|
|
CTGCACCATGCCACCATGCTGCATCACCAGCAGATGATGAACGGCATGATGCACCACCAC
|
|
CACTACCACCAAGGCGTGTTGCAAGGCGTGCCGGAGCCGCTGGTGCCGGGCGTGCCGCCC
|
|
GTGCCGCTGCTGTGA
|
|
>M. sexta-Atg8 (MsAtg8); Msex2.12227-RA
|
(SEQ ID NO: 40)
|
ATGAAATTCCAATACAAAGAAGAACATTCTTTCGAAAAGAGGAAGACTGAAGGCGAAAAG
|
|
ATTCGCAGGAAATACCCGGATCGCGTTCCAGTAATTGTAGAGAAAGCCCCGAAGGCTAGA
|
|
TTGGGAGACCTCGATAAGAAGAAGTATTTGGTGCCGTCTGATTTGACTGTCGGACAATTT
|
|
TATTTCCTAATTAGGAAACGCATCCATCTTCGGCCTGAGGACGCATTGTTCTTTTTCGTG
|
|
AACAATGTTATTCCACCAACATCCGCCACCATGGGCTCTCTGTACCAGGAACATCATGAC
|
|
GAAGATTTCTTCCTCTACATTGCATTTTCTGATGAAAATGTTTATGGATTTTAA
|
|
>M. sexta-Atg13 (MsAtg13); Msex2.06273-RA
|
(SEQ ID NO: 41)
|
ATGGCACCCGAAGTGGCTTTTTCTAACATAAATGACAAGAATGAATTTACTAAATTCACA
|
|
AAATTCTTAGCTTATAAAGGCGTTCAAGTTATTGTAGAATCGAGGAAGGGTGTAAAAATA
|
|
GATCCTAATAGTAAACCAAGATCATCAGACACTGATTGGTTCAATCTTCAAATACCAGAC
|
|
TCTCCAGAGGTTAACCAGGCAACTAAGAATGCATTGCCTTCAGACAAGGTGTTAGAGATT
|
|
ATCAAAGCCCAACTGCACGTGGAAATATCAGTACAAACCGAGGATGGCGATGAAATGGTT
|
|
TTGGAGTTGTGGACCCTTGAACTTGACGAAACTCAGTTTGACACTTCTGTTAAAGCCACG
|
|
AACACAGTTTACTTCAGAATGGGAATATTACTTAAGTCGCTTATAACTATAACAAGAATT
|
|
ACTCCAGCGTACCACTTGTCGAGGAAGCAAAGAACAGAGTCGTTCACAATATTCTACAGA
|
|
GTATACAATGGCGAACCGAAAGTAAAAGCGCTTGGAGAATCAGTGAAGAAAATTCAAGCT
|
|
GGAATGCTCAAAACTCCACTTGGAGGGATAATATTCTCCGTGGCCTACCGCACAAACTTC
|
|
TCCATTTCGCCAAACAGATCGGAGAAGGACAAAACATTGCTTTTGAAGAGTGATCATTTC
|
|
GAACTGAGTCCAAAACATGTGATATTTGAATCCAAGAAAAAGAAAGACGAGAAAAAAGAA
|
|
TACAAGCCTCTGAAACCTGTTGATTTGAATAAGCCACTTCGATTAGCCGCATTTGTAGAC
|
|
GAGGATGTTGTAAAAAAGGCCTTTGATGACTTCATGGAGAAGATGCCGATTCCCAAATAC
|
|
CGAGTGATACGTAGGGAGAGAAGTCCAGAGAGCGACAAGCCTATAGTATCCAAAAGTACT
|
|
CAGGATTTGGACGCTTCTGTGACGTCAAAGAGTCCGACGTCAATGGAAATGCCACCTAAA
|
|
AAGTTCACAGGCTTTCGCAATGAGAACGAACCTCCATTAAAACTTCTCCATTTCCCATTC
|
|
GCTGATAACCATCCGATAAGAGAACTGGCCGAGTTTTACAAAGAGTTCTTCAACGCCCCC
|
|
CATTTGAAGTTAGCTGATGACGTTAGCCTGAAATCGGGCAGTGCTGAATCGGTAAAAGAG
|
|
GTGATAGAGATTACAACTGAAGATTTGTCGAAAGATCTCGAATTGTATGAGAACTCGGTG
|
|
TTGGAGTTTGATGAGCTCTTGGCAGATATGTGCCGATCGGCTGAGTGGAGTGGGAACTAG
|
|
>M. sexta-IAP1 (MsIAP1); Msex2.05607-RA
|
(SEQ ID NO: 42)
|
ATGGCATCAGCTGGCGCCGTACCGAATATTCTAGTGTCGTCGTCGCTTTTCAAGACCACT
|
|
CCTCGGGATCCTAAAATTCGTCGAAAAACAAGCCCTTTGAAGTTACCACCTTGTGACACA
|
|
CATATAGGCTCGCCTCCACCATCATCCTCTCCGACCTCCTCGTCAACTGATAAAACCGAT
|
|
AATCATGATACTTTTGGTTTCCTTCCTGACATGCGtgatatgcgCCGCGAAGAAGAACGA
|
|
CTGAAAACTTTCGATAAGTGGCCTAGCACGTACGTGACACCTGAAGAGTTAGCTCGTAAT
|
|
GGTTTCTACTACCTTGGGCGCGGTGATGAAGTTCGCTGTGCATTCTGTAAAGTAGAAATT
|
|
ATGCGATGGGCGGAAGGAGACGACCCTGCGAAAGATCACAAACGATGGGCGCCCCAATGT
|
|
CCGTTTTTACGTAATCTTTCGAACGGTACTAATGGCAGCGGAGAAGGTAGTTCGGAAGGT
|
|
CGCGACGAGTGTGGTGCGCGAGCAGCGACGCGGGAGCCTGTGCGTATGCCCGGACCTGTG
|
|
CATCCCCGCTATGCAACAGAGTTATCGCGTCTCGCCAGTTTCAAGGATTGGCCGCGTTGC
|
|
ATGCGCCAAAAACCAGAGGAACTCGCGGAAGCAGGATTTTTCTACACCGGCCAAGGGGAT
|
|
AAAACGAAATGTTTCTATTGCGATGGAGGTCTCAAAGATTGGGAAAACGACGATGTTCCA
|
|
TGGGAACAGCATGCCCGTTGGTTCGATCGTTGTGCGTATGTGCAACTTGTTAAAGGCCGT
|
|
GATTATGTCCAGAGGGTATTATCGGAAGCGTGTGTTATACGTGCCACCGACGAAAAGCCT
|
|
GCGCCTGCACCTCAACCGTCCCAACCAAATGTCTCAGTTGTATCAGAAGAAAAACCTGTC
|
|
GAAGAGGCTAAGATATGCAAAATATGTTATTCCGAAGAACGAAACATATGCTTTGTGCCG
|
|
TGCGGTCATGTGGTCGCTTGTGCAAAGTGTGCCTTATCTACTGATAAATGCCCAATGTGC
|
|
CGGAGGGCTTTCACAACTGCACTGCGACTCTATTTTTCGTGA
|
|
>M. sexta-Chitin synthase 2 (MSCHS2); AY821560.1
|
(SEQ ID NO: 43)
|
ATGGCCGCAACTACACCAGGTTTTAAGAAGTTAGCAGACGATTCTGAGGATTCAGATACA
|
|
GAATACACCCCGCTGTATGATGACGGTGATGAAATAGATCAAAGAACTGCACAAGAAACA
|
|
AAAGGATGGAATCTATTTCGAGAGATTCCGGTGAAAAAGGAGAGTGGATCTATGGCCACA
|
|
AAAAATTGGATAGAAACAAGCGTAAAAATCATAAAAGTGCTTGCCTACATATTGGTTTTT
|
|
TGTGCTGTACTGGGTTCCGCAGTCATAGCTAAAGGAACTCTTCTATTTATTACGTCACAA
|
|
CTGAAGAAAGACAGACAAATTACTCACTGCAATAGACGACTTGCTTTAGACCAACAGTTC
|
|
ATAACGGTACACAGTTTAGAAGAAAGAATAACATGGCTATGGGCAGCACTTATTGTATTC
|
|
GGTGTGCCGGAGTTAGGGGTGTTTTTGAGATCCGTCAGGATATGCTTCTTCAAAACTGCC
|
|
AAGAAACCAACCAAAACACAGTTTATTATTGCTTTCATAACAGAGACACTACAAGCAATA
|
|
GGAATAGCAGCACTTGTATTAATAATTCTACCAGAATTAGACGCTGTGAAAGGAGCCATG
|
|
TTGATGAACGCCACGTGCGCTATCCCTGCATTGCTAAACATTTTCACGAGAGACCGAATG
|
|
GATTCTAAGTTTTCTATAAAATTGATATTGGATGTATTGGCGATATCGGCACAAGCCACG
|
|
GCGTTTGTTGTTTGGCCTCTTATGGAAAGAACGCCAGTTCTATGGACCATACCAGTTGCA
|
|
TGTGTGTTAGTGTCTCTAGGCTTCTGGGAGAATTTTGTTGACACCTACAATAAAAGTTAT
|
|
GTTTTTACGGTGCTGCAGGAACTACGCGACAACCTCAAGAGGACTCGGTACTACACTCAG
|
|
CGGGTGCTATCTGTTTGGAAGATTATAGTGTTTATGGCATGCATTTTAATATCGCTGCAT
|
|
ATGCAAAATGACAATCCGTTTACCTTTTTCACTCACGCCAGCAAAGCCTTTGGAGAGAGA
|
|
CAGTATGTCGTTAACGAGGTTCTAATAGTAGTCCGAGATGACGAAACCATAGGCTATGAC
|
|
GTCACCGGAGGTATATTCGAATTGGACGCGATATGGACCTCAGCATTGTGGGTCGCATTA
|
|
ATTCAAGTGGGAGCAGCCTACTTCTGTTTCGGAAGTGGCAAGTTTGCTTGCAAAATTCTT
|
|
ATACAAAATTTTAGTTTCACTTTAGCATTGACTCTCGTCGGGCCCGTGGCAATCAACCTC
|
|
CTTATTGCTTTCTGCGGAATGAGAAATGCAGACCCTTGCGCTTTCCATAGAACTATACCT
|
|
GACAATTTGTTTTACGAGATACCACCTGTGTACTTCTTGCGGGAGTACGTGGGCCACGAG
|
|
ATGGCGTGGGTGTGGTTATTGTGGCTCATATCTCAAGCGTGGATCGTGTTTCACACGTGG
|
|
CAGCCGCGATGCGAGCGCCTCTCCGCAACTGACAAACTGTTTGCCAAACCGTGGTACATC
|
|
GGACCGCTAATCGACCAATCGTTGCTGCTAAACAGGACTAAGGATTTGGATAATGATTGC
|
|
CAGGTTGAGGATTTGAAGGGTCTTGGCGACGATTCGTCGGTTGGAAGCGATCTTGCCATC
|
|
GTAAAAGATATCAAACCGTTCGATTCGATAACCAGAATACAAGTGTGTGCGACAATGTGG
|
|
CACGAGACCAATGAGGAGATGATCGAGTTCTTGAAGTCGATATTCCGCCTCGACGAGGAC
|
|
CAGAGCGCGCGCCGCGTGGCGCAGAAGTACCTCGGCATCGTCGACCCCGACTACTACGAA
|
|
CTCGAGTGTCATATTTTCATGGATGACGCTTTTGAAATATCCGATCACAGTGCCGAAGAC
|
|
TCGCAGGTGAATCGCTTCGTGAAGTGCCTAGTGGATGCGGTGGACGAAGCGGCTTCCGAA
|
|
GTGCATCTGACTAACGTGAGGTTAAGGCCCCCCAAGAAATACCCCACCCCGTACGGCGGA
|
|
AAACTAATTTGGACCATGCCAGGGAAAAATAAGTTGATTTGCCATTTGAAAGATAAATCC
|
|
AAGATTCGGCACAGAAAGAGATGGTCGCAGGTTATGTACATGTACTATTTCCTGGGGCAT
|
|
CGCTTGATGGACCTGCCAATATCCGTGGATCGTAAGGAAGTGATTGCCGAGAACACGTAC
|
|
CTATTAGCTTTGGATGGAGACATCGACTTCAAGCCGAGCGCTGTGACGTTGCTGGTCGAT
|
|
CTTATGAAGAAGGATAAGAACTTGGGCGCCGCTTGCGGTCGCATTCATCCTGTCGGCTCT
|
|
GGTTTCATGGCCTGGTACCAGATGTTCGAGTATGCTATTGGTCATTGGCTGCAAAAGGCG
|
|
ACTGAACACATGATCGGCTGCGTACTCTGTAGTCCGGGATGCTTCTCCCTCTTCAGAGGA
|
|
AAGGCGCTTATGGACGACAACGTCATGAAGAAATACACACTCACTTCTAACGAGGCTCGA
|
|
CATTACGTGCAATACGATCAAGGCGAGGACCGTTGGCTGTGTACGTTGCTGCTGCAGCGC
|
|
GGGTACCGCGTGGAGTACTCGGCGGCGTCGGACGCCTACACGCACTGCCCCGAGCGGTTC
|
|
GACGAGTTCTTCAACCAGCGCCGCCGCTGGGTGCCCTCCACCATGGCCAACATATTCGAT
|
|
CTGCTCGCGGACTCCAAACGCACCGTGCAAGTCAACGACAACATTTCCACTCTGTATATC
|
|
GTCTATCAGTGCATGCTTATGATGGGTACGATTTTGGGTCCGGGAACAATCTTCCTGATG
|
|
ATGATTGGCGCAATAAACGCTATAACAGGCATGAGCAATATGCACGCACTTCTCTTTAAC
|
|
CTGGTGCCCGTGCTTACGTTTTTGGTTGTCTGTATGACATGCAAGTCCGAGACTCAGTTG
|
|
ATGCTCGCGAACCTCATTACCTGCTTTTATGCGATGGTAATGATGTTTGTGATCGTCAGT
|
|
ATCGTCCTACAAATATCACAAGATGGTTGGCTAGCGCCATCTAGTATGTTCACTGCGGCA
|
|
ACATTTGGAATATTCTTCGTAACAGCGGCTTTGCATCCACAAGAAATAATATGTTTGTTG
|
|
TACATTTCCATATATTACATCACAATTCCGAGCATGTATATGTTGTTGATTATCTACTCC
|
|
CTATGCAATTTGAACAACGTCTCGTGGGGAACTCGAGAGGTGGCTCAGAAGAAGACTGCA
|
|
AAGGAAATGGAAATGGATAAGAAAGCAGCGGAAGAAGCAAAGAAGAAGATGGATAATCAA
|
|
AGCATAATGAAATGGTTCGGCAAGTCGGACGAGACGAGCGGCTCGCTGGAGTTCAGCGTG
|
|
GCGGGACTGTTCCGCTGCATGTGCTGCACCAACCCTAAGGACCACAAGGACGACTTGCAT
|
|
CTCTTGCAGATCGCCAACTCCATCGAGAAGATCGAAAAGAGATTGTCGGCACTTGGCGCG
|
|
GAGGAGTCCGAGCCGGCGCAGGCGCAGACGCGGCGCCGCTCGTCGCTGGGGCTGCGGCGC
|
|
GACTCGCTCGCCACCATGCCCGAGTACGCCGACAGCGAGCTGTCCGGAGACATTCCTCGC
|
|
GAAGAAAGAGACGATCTTATAAACCCCTATTGGGTGGAGGATCCCAATCTGCAGAAAGGT
|
|
GAAGTAGACTTCTTGACGACGGCTGAAATCGAATTCTGGAAGGACTTGATTGATGTTTAT
|
|
TTGAGGCCTATCGATGAAAACAAGGAAGAGCAGGAACGTATCAAAACCGATCTAAAGAAC
|
|
TTGCGTGACACGATGGTGTTCGCGTTCGCCATGTTGAACTCGTTATTCGTGTTGGTGATA
|
|
TTCCTGCTGCAGTTCAACCAGGACCAGTTGCACATAAAGTGGCCGTTCGGGCAGGATGTC
|
|
GCGCTTTCTTATGACAAGGAAAGGAATGTTGTATTGGTGGAGCAGGAATTCCTTATGTTG
|
|
GAGCCTATAGGTTCCCTGTTCCTCGTGTTCTTCGGGTTTGTAATGTTGATACAGTTCGTG
|
|
GCGATGTTGTCCCATCGTTCGTATACTATTACGCATTTGCTCTCCACAACAGAGCTTCAC
|
|
TGGTATTTCAGCAGACGTCCGGACCAGATGTCAGATGAAAACCTCTTGGAAAGGAAGGTG
|
|
GTAGAAATAGCGAGAGAGTTGCAGAAGTTAAACACGGACGACCTAGACCGCCGCGCGGTC
|
|
GAAACTAACGACGTGTCGCGGCGAAAGACTCTACACAACCTAGAGAAGGCGCGAGACACC
|
|
AAGCACAGCGTGATGAACCTTGACGCTAACTTCAAGAGGCGACTGACTATACTACAGAGC
|
|
GGTGATCCTAACGTGATATCTCGGCTGTCATCGTTGGGCGGCGATGAGGTTACTCGTCGC
|
|
GCCACGATACGCGCATTAAAGACGAGGAGGGACTCACTGCTCGCTGAAAAACGACGCTCC
|
|
CAGCTGCAAGCGGCGGGCGACGCTACAGGCTACATGTATAACCTGTCAGGCACTGCGGTG
|
|
AACGACATGAGCGGCCGAGCTTCGACGGCCAGCGCCTACATTAATAAAGGATACGAACCC
|
|
GCTTTCGATAGCGACGACGACGAACCACCGCGTCCGCGCAGGAGCACTGTACGCTTCAGA
|
|
GAAAACTACACGTAA
|
|
>M. sexta-Beta-fructofuranosidase 1 (MsSuc1); GQ293363.1
|
(SEQ ID NO: 44)
|
ATGTACATTAAAACAGCAACATTTTTGCTGTGCGTTTTCCTTGGTAGTGTATCGTCATGT
|
|
TGCGTTAATGGGCGGTACTACCCGAGGTACCATTTGTCGCCACCGCATGGCTGGATGAAC
|
|
GACCCCAACGGATTCTGCTACTTCAAAGGTGAATACCATATGTTTTACCAGTACAATCCC
|
|
ATGTCAAGTTTGGAGGCTGGCATAGCTCATTGGGGTCATGCGAAAAGTAAAGATTTGTGC
|
|
CATTGGAAACACTTAGACCTCGCCATCTATCCTGATCAGTGGTACGATCAAACGGGAGTA
|
|
TTTTCTGGAAGTGCGCTAGTAGAGAATGACGTCATGTACCTTTATTATACTGGAAATGTA
|
|
AATCTTACTGATGAAATGCCATTTGAGGGACAATTCCAAGCTCTTGGTATCAGTACTGAC
|
|
GGTGTCCACGTAGAAAAGTATAAAGACAATCCAATAATGTACACGCCAAACCATCAACCT
|
|
CACATCCGAGACCCAAAAGTTTGGGAACACGACGGCTCTTATTATATGGTCTTAGGAAAC
|
|
GCATATGATGATTATACAAAGGGCCAAATAGTTATGTACGAATCATCAGACAAGATCAAC
|
|
TGGCAAGAAGTAACTATACTATATAAATCAAATGGATCTTTCGGTTACATGTGGGAGTGT
|
|
CCAGATTTATTCGAAATAGACGGCAAGTTTGTACTTCTGTTCTCTCCTCAAGGCGTGAAG
|
|
TCTGTGGGCGATATGTACCAGAATCTGTATCAAGCAGGATACATCGTCGGAGAATTCGAT
|
|
TACGATACTCATTCATTCACAATACTAACCGAATTCAGAGAATTGGATCACGGTCATGAT
|
|
TTTTACGCTACACAAACAATGAAAGATCCTAGTGGAAGAAGAATAGTCGTTGCTTGGGCA
|
|
AGTACTTGGGAGTATGCTTATCCTGAACGAGCAGATGGTTGGGCTGGCATGCTCACACTA
|
|
CCTAGAACTTTAACTTTGACAAAAGATTTAAGACTAATCCAAACTCCAATTAGAGAGATC
|
|
GATCAAGTTTTTAGAAGAAGACTATATTCAGGAAAAGCCTCAGCAGGCAAAACTGTCGCT
|
|
TTACCAGACAAAGCAGGGAAAGTAGAACTGAAATGGGATACACCAAGAAATATAAAGGTA
|
|
GTTATAGAATCTCAAAATGAGTGCCAAAACGTAGTAATCAGTTATGATCACGAGGATGGT
|
|
ACTATTACTTTGGACAGAGGAGGCGATGACGCAATCCGCCGCACTCACTGGGATCCTCGA
|
|
GGTCACCTCAAATGGACCATTTTTATTGACGCAAGCTCCATAGAACTCTCTTGTGGTGAT
|
|
GGAGAAGTATGGTTTACAAGCAGATTTTTCCCTGAAGGAGTCGTATCTGTTCGCCTTGGA
|
|
GAAGATACTTGTGTTGATAAGTTTACCGTGCATTCTATTCGCCGTACTACTCCAGACCCC
|
|
GAGGCTCATTGTCGTTGTGAATCAGAAGAATAA
|
|
>M. sexta-Hemolin (MsHEM); M64346.1-UTRs
|
5′UTR
|
(SEQ ID NO: 45)
|
TGTTACATTAATTATAAAAAAAAATACAAAAAAGAAATATATAAGTAAGTACTAATAATA
|
|
TGGTCTAGTTTATTATAAGTCTTAGAGACTAACGATAAATAATAAATTTCTCATGAACCA
|
|
CCTATTTATTTATTTGAAAAGCATTTTAAATATATTATAGATTTAAACGTAACGAAGTCT
|
|
TTAAACTCGCGGGTAAAAACGCATACTTACTTGACTCTACATCGGCGACACACGAAAAAC
|
|
TTATTCGTACTGTTTTTTCATTGAATATGTTATGAAAAAGAAAACTATATGTAATCGCAG
|
|
TCACATATATAAAACTTTATAAAAAAGTTAACAGAGATAAATAACTTGTTTGGTGTTCGT
|
|
CATAGCAATAGAGTAGCCGCGGCGCCTAAGGCTACGAAATAAGCTCATTGAACTGTAATG
|
|
GAGTGTGCCTAGTTGTTTCTCTTCTTACCAAGACTCAAGAGGGATTTGGAGCTTCATCTA
|
|
CGATTATTATACCTACCTACGTATAGACTATAATGGATAGTAAAAATAGAAAGTAATTTC
|
|
TTTTATATCAACTTTTGTATTCATATGTAAGTACTTACTTATAATTATTTATTTTTTTAG
|
|
GTGAAA
|
|
3′UTR
|
(SEQ ID NO: 46)
|
GTTAACAATAAACAATACTGTTAACCGTACGTAGTGTTAAATAATACAAATATATGTATT
|
|
TTACAATAAGATTTCCTGTTTTTAAATTATCCTCACGTAACGTATTGGGTATCTAAGCGG
|
|
TTGAGCAGTGAGATAAGTCTACCCCAAAGTAGTCCGTTCATCAAACGACATAACCATCTC
|
|
GTCATTTAGTTAAAACAAAAAAAGAATAATGATAAAAGATATAAAATTCTGTATAAGAAC
|
|
CAATACCTAGCACCTTTCTCACATTGCCAAACATACATTAAAAAACAGTATTATGCTTTT
|
|
TTCGCTCTTTTATTCTATATTTTATATTAAAAAATACCTATAGTAAATACTGTTTTCATC
|
|
GTCGCCGGTATTCATACACGTAGTATACGTACCTAACTCTGAAACTACTGGTTTGAATTG
|
|
AAAAA
|
|
>M. sexta-Serine Proteinase homolog 3 (MsSPH-3); AF413067.1
|
5′UTR
|
(SEQ ID NO: 47)
|
AGCGCTTTGGGAACGTTCCGTGGCACGATA
|
|
3′UTR
|
(SEQ ID NO: 48)
|
GATGGTGGAATGTTTAAAAATACAAGAGTGTGAGGCAGTGATTAATGGTCTGTAATATCC
|
|
GATTCTTGCTGGCTTCTGTTTCGTAATTAACGTAAAATCTAATTATCATTAGAATATTTT
|
|
GGAAAACCTTAGAGTTACCTTCGGAAAACTTCACCGTTTGCCGCTGGTGTGAAGATCTGT
|
|
TCCCCCCATAAACTGATGGGAAATTGTATGTAGGTACTCGAGTTATAATTTCTTTTTATA
|
|
CCTGCGTTTAAGTTCCATTACAACTTTCTAATTTTATGAATAAATATCTAATAAACGATT
|
|
AACAAAATTAAAAAAAAAAAAAAAAAA
|
|
>M. sexta-Peptidoglycan recognition protein 2 (MsPGRP2); GQ293365.1
|
5′UTR
|
(SEQ ID NO: 49)
|
|
ACGGCATAAATTGTTAGGTCGTCTGAGAGGCGAGTGTTGTATTTTTAATTGCCAAAGAGG
|
|
CTGCGAAGTTCGCAATAATCATTAGAAAA
|
|
3′UTR
|
(SEQ ID NO: 50)
|
AATGACCAAAGATAATACGACTGTTTTATAATTTTTGTTAATAAATGTTGTTGCATTATG
|
|
GAAAAAAA
|
|
>M. sexta-Beta-1, 3-glucan-recognition protein 2 (MsßGRP2); AY135522.1
|
3′UTR
|
(SEQ ID NO: 51)
|
ATTAAAACTAACGAAAAGACTCGTTTCCATAGTGGTATATTTTCAACTCGTCAATTTCAG
|
|
GTACAAGCATGTTTGGTGGAAGGATATTATCGGCCCGAATAGGCACTGTACACCAAGTAC
|
|
AACCATGACTCATCAAAGGTGTCGCGTTCTGGAATCACCTGTATTTCCAACAGGCCGGCA
|
|
TAATTGTGTCGTCTAGCGAGGGATAACTCAATAGTCTATTTGAACGCCATTCTACTTACC
|
|
ATTAGGTGTAGTGAAGATATTTGGGGCTAGACAAAATGGAAGGAAATTTATGAGTTGCAT
|
|
CGAATGATTATCACTAAGTATTCGAATGATTCATTTCGTTGTTGGTGCAATAGGATGTCA
|
|
AGGGTCAAATGGACATTAAAAGAGAGTTTAAGGTGTTTTTTTACAATTAACGTTGATCTA
|
|
TCACTTTACTTGCCTATTAAGTAAAGTATTATTTTGAAAAATACAAAATACTTGAGTTTA
|
|
TAGTATCTCTTGCGTTTATGGTACTGTCAAAAATATCAGTATTATTCATTTACAAAATTA
|
|
AAATTTAATAATCTAAATTATTCTTCATGTAAATGATCATTTATACCTCTGCCTTGATTA
|
|
TG
|
|
>M. sexta-Relish family protein 2A (MsREL2A); HM363513.1
|
5′UTR
|
(SEQ ID NO: 52)
|
AGAGTACGTTCGATGGCAGTCTGTCGAACATTGGTAGTTTCCCGTTTGAGTGTTGTTTAC
|
|
TCCCTTTGAGGGATTAGTTTATTCTCCACGAATATAAACATCGGAAAATCAAAAACTAAG
|
|
TTGATAAAAAGTTGTGTGCTCCGGTATAATTTTTTGGTATCAGTGACGGACAAAGGTGAT
|
|
ATAAAA
|
|
3′UTR
|
(SEQ ID NO: 53)
|
TATATTCATGAGAAGGGGACAACTAAGGATTGAATATCAGCAGAACTTGAGTTATGTTAA
|
|
TGAGGTATTTATATTAGCTTAATACTTAAAGGGGAAAATTCGATTAGCTTTTCAAATATA
|
|
CTTAAATTTTAGTTTTTGTCAAATATCGGTGTTTCCCATTTTGATATTTTTTTATCCATA
|
|
TTTTAATAATAAATATCTTGTCTTAGCAATTTTAATGGGTAATTATAAAGAAACTCACGC
|
|
ACCATAGTTGCACTAAACTACAAAATTACACAAAA
|
|
>M. sexta-Dorsal (MsDor); HM363515.1
|
5′UTR
|
(SEQ ID NO: 54)
|
ATACAACGATATCACAGGCGTCCGGGGACGGACCAGTTTAAACAAACATTACAGTGAATA
|
|
GCGATGTGATTATTTTCTTGCTTGTATAGAGTTAAATTTTTAAATTAGATTTAAATATTA
|
|
AAATATTTGCGAATAAAA
|
|
3′UTR
|
(SEQ ID NO: 55)
|
ACTTAACAATTACATCTATAAATCTCTCCTCTATCAACCTAGTGGGCGTCCTCTACAACT
|
|
ACCACGTCTGGTATACAAATAGTGACAACCTGAAATTGTGAGATTTAAATTGTGTAGTTA
|
|
TGATAAATAAACAATAAATCCAAAAAAAAAAAAAAAAAAAAAAAAAAA
|
|
>M. sexta-Toll receptor (MsTOLL); EF442782.1
|
5′UTR
|
(SEQ ID NO: 56)
|
GAAAAGTTATTCACAATATGACCCGAAGTGTCAGCGCCGCACATGCGCGGGAGCACTCGT
|
|
ACTTATACCAGACATTGTGACTAAATACCTAATTTTATGTTTTGCTCATCGCCCATTGCG
|
|
CGACATTAAGCAGTATCCAGTAGTCAGTGATCAGTGTTACTACACTATTTTGCTTCTCAG
|
|
CGATTAGTCAACACGCGCATATCGTTTACTTCAACAAACAATTATTACGCAAATCGTGAT
|
|
ATTTGAATGTAGAGACACGAATCAAAGATTATTCGTTTAACGTTATTTTCGCGGGATGTT
|
|
TCTCTGTTGGGGGGTACTGTTGCGTGGTGTGCAGTCAAAGGTTTATTTTATCGGGTATTG
|
|
TGCTCTTTAAGTGTTGACGCGGCGGATTATCGTCGGTTAGACTAATAAATCGTGTCGATT
|
|
TATGTGTGACCCACTACGGTGTCGTGCGACGTG
|
|
3′UTR
|
(SEQ ID NO: 57)
|
ATCCAGAACTTGCGTGTACCCTTCGATATACAGGGCTATTTTGACATCGTGTTACTAAAT
|
|
GAAACCACATTCTCGTCTTCACCTTTGCTGACATTGTGCCAAAAATCATCCATTAATAAC
|
|
GAATATTTCCACCAAAAAAAAAAAAAAAAA
|
|
>M. sexta-Scolexin A (MsSCA1); AF087004.1
|
3′UTR
|
(SEQ ID NO: 58)
|
TAGACCATACCGTTGTCATTTTGGGCTGTAGTGTATAGATAATAAATATAGACGCGTGTA
|
|
CTGGTGTGACGTACGGAAGTGGAGAGTTGGGAGCGACAGCTCACCGCTCACTCCACTCCC
|
|
GGCCGCCGCGCGAGTAGCAGTGTCAGTGATTGCAAAAAAAAAAAAAAAAAAAAAAAAAAA
|
|
AAAAAAAAAA
|
|
>M. sexta-Hemolymph proteinase 18 (MsHP18); AY672794.1
|
5′UTR
|
(SEQ ID NO: 59)
|
GCCAGACGTTTCAGTTTGTTTCGAACT
|
|
3′UTR
|
(SEQ ID NO: 60)
|
TTATGAATAAATACAATTTAATAAGCATTATTTATTAAAAAAAAAAAAAAAAAAAAAAAA
|
|
>M. sexta-Chymotrypsinogen-like protein 1 (MsCTL1); AM419170.1
|
5′UTR
|
(SEQ ID NO: 61)
|
TACTTCGGGCTACACAATGTACGTGAAAGTA
|
|
3′UTR
|
(SEQ ID NO: 62)
|
TCTCCGAACCGAACCTGATCTTAACTGTAAATAAAATAAGCGATACCCAAAAAAAAAAAA
|
|
AAAAAAAAAAAAAAAAA
|
|
>M. sexta-Dredd (MsDRD); Msex2.04297-RC; Currently annotated as Manduca sexta
|
Caspase-6; HM234679.1 in NCBI
|
5′UTR
|
(SEQ ID NO: 63)
|
TTGGTAACCCTGTGGGAAGTCCCAAAGTCGAAGCTCGAGAACAGTTTTAAGCAGAGGTT
|
|
TTAAGTCTAATTTATTGGTCTCTGGTTTTAAGTTAGTGTCATGTGTCAACAATAATAAA
|
|
GCTTTATTTTTGGCTCTATTTATAAGTAAGGTATCATCCTTTCAGCGTTAAAACAAAGG
|
|
GCGTAGCTCATGTTCATGTAGTTCTTTTAAATAAGTGTGAACTAAGTGTATATGTACAT
|
|
TTATTACTGGTGACA
|
|
3′UTR
|
(SEQ ID NO: 64)
|
CATAATATTTTTATTTAGATATATTGTAAGTACTAAGAATGAAGTGGTGATAGCTTAGTT
|
|
GGGAGTGGAATGGACAGCCAAGACAAATGTCAGCAAGTTCAAATCCAAAGGCATACACCT
|
|
CTGACTTTTAAAAAAAAATATGTGTGTATTCTTTGTAAATTATCACTTGCTTTACGGTGA
|
|
AGGAAAACATCATGAGGAAACTCTCAATAGTAAAGGTATCCCATTGCCCAGCAGTGGGAC
|
|
AGTATATTATACAGGGTTGATATTATTATTATTATATACTATGCTTTGCTCATGCGCTCA
|
|
TTCACTCCAGCATTAATGACCTTTCCTGGTATTGAAGTTCTGCTAAGTATTTTATGGGAT
|
|
AAAAATACCCTGAATGTTAATCCACACACATTCAGTATGTCAAATTTCATCTAAATCCAT
|
|
TTAGGTGTGTTCTATTTGATACTAAGTTCCAACAAAAATCTTCATAAACGTCAGGACCCC
|
|
TCAGGAGCAACATTATTAATAAGATTAATAATAAATTTTCAATGCATAATAATTTTAATA
|
|
TAATTTATATTACTTAATGTTGAAGTTGATATACTTAA
|
|
>M. sexta-Relish F (MsRelF); HM363513.1
|
5′UTR
|
(SEQ ID NO: 65)
|
AGAGTACGTTCGATGGCAGTCTGTCGAACATTGGTAGTTTCCCGTTTGAGTGTTGTTTAC
|
|
TCCCTTTGAGGGATTAGTTTATTCTCCACGAATATAAACATCGGAAAATCAAAAACTAAG
|
|
TTGATAAAAAGTTGTGTGCTCCGGTATAATTTTTTGGTATCAGTGACGGACAAAGGTGAT
|
|
ATAAAA
|
|
3′UTR
|
(SEQ ID NO: 66)
|
TATATTCATGAGAAGGGGACAACTAAGGATTGAATATCAGCAGAACTTGAGTTATGTTAA
|
|
TGAGGTATTTATATTAGCTTAATACTTAAAGGGGAAAATTCGATTAGCTTTTCAAATATA
|
|
CTTAAATTTTAGTTTTTGTCAAATATCGGTGTTTCCCATTTTGATATTTTTTTATCCATA
|
|
TTTTAATAATAAATATCTTGTCTTAGCAATTTTAATGGGTAATTATAAAGAAACTCACGC
|
|
ACCATAGTTGCACTAAACTACAAAATTACACAAAAAAAAAAAAAAAAAAAAAAAAAA
|
|
>M. sexta-Chitin synthase 2 (MSCHS2); AY821560.1
|
5′UTR
|
(SEQ ID NO: 67)
|
ATTACGCTTTGAGCAGCCACTTTGTAAACACTAGCCTATTAACTCCGTCACTGCTTCGGC
|
|
GATAACACTTCTGTATATCTGTTATTGTTTGTTAATTTTTGGCGCAAGGATATATTTAAT
|
|
ATGTGCTAAGTTTGTGGCTAATTTATATTATGTTTCTACATTAAAGGTATGTATTAGTGA
|
|
TTTTTTGTAACTTATTTAATTACAAACATTATAACATATTTTATTAGAAAAGGGTTTTGT
|
|
ATCCTATGTAGCGCCTGTTTCACGATGCCTCTTGAAGTATACTGAAATGGGTACCCGTCG
|
|
ATAGTGTTTGCTTTAATAGGCAACGCATAGTGAAAACTTTGTACTTTAACCTTTTCAAAA
|
|
GCATGAATAATTAAAAAAAAATATTAGAATAATGTGAAAAAGGTGTACAGTGTGATAAAT
|
|
ATGGAGTATACAATATTCTTGTTCCAGTTATAAGATAAGGCACA
|
|
3′UTR
|
(SEQ ID NO: 68)
|
TATTTGGCCAAAATTGTGAACTGTAAACATGCAATAAAATGATGAACG
|
|
>M. sexta-Beta-fructofuranosidase 1 (MsSuc1); GQ293363.1
|
5′UTR
|
(SEQ ID NO: 69)
|
TGAGAACAAAAACATTAGCTCCGCGTTTAAAA
|
|
3′UTR
|
(SEQ ID NO: 70)
|
TTATCGTGCTAAAGTAATAGTTATTGTTTCACATTATGTTCAAATAAAAAAGTAATTATT
|
|
TATGTTCAAATAAAAAAGTAATTATTTAAGTGTCTTGTAAATCTGCGAATAAATATACTT
|
|
AATGTATAAAAAAAAAAAAA
|
|
>M. sexta-Sickie (MsSck); Msex2.03324RA
|
(SEQ ID NO: 71)
|
ATGACGACGTTGACTGCAAATAGGCAAGTGTCGGTGTTGCAGACGTCGATCCCGCTGCCG
|
|
GCGTCGGCGGCGGCGGTGCGGCGCGCTCCGCCCGACAAACGACCGCTGCCCGCCACACCA
|
|
GTACATGCAGGTGGCAAGAGTGGTCTTTCTGCGAGTTCCAGCCGCTCCACCAGTCCATTA
|
|
GGACAGGGTGCAGTCAGTTTTATACCACGTGCGCCTAATTCATCATCTGGATCCCGGCCG
|
|
AACTCGTCCCTCCTTGCGCCCAGTAGCAAAATACCCTCCACCGCAACACAAGGGCAACAG
|
|
CATTCACAAACACCCACAGCCCAAAATGGAACACCCACAAAGCAGTCTATGCTTGACAAG
|
|
TTAAAGCTATTCAATAAAGACAAAATTAGCAATGAAAAACAAAACAGCAAAAGCACTGCA
|
|
GTATCAAAACGCACCAGTTCTTCCAGTGGTTTCTCATCGGCAAAGAGTGAGAGATCAGAC
|
|
TCGAGTTTAAGCCTTAATGAGTCTTCTAACATACCCAACACACATATCAAATCGTCTAAT
|
|
TTAATAGGACCTAAAACAATACGGCAACAAAGCGATACTTTATCAAAAGACAAATCTGGT
|
|
AAAAATTTAAAACCTAAGTTAGTTAATTCTAAATCTCCTAGAGATTCTACAACTAACTTG
|
|
AATAGGGCTAGTAGCAAAACAACTAATAATGATAAATCGAGGAATAGTCCAAAACTTCCT
|
|
GCTAGGGATAAGGAATCGAAACTAGCCACACCTAAAACCATGAGTAACACAAAACTAAAC
|
|
CAAGTTGAAGATCAACCGAGGGGTTCCAAAACTAAAGTGGAATCGAAAATGGTAAAGCTT
|
|
TCCGGTAGCCAAGTTAAGCTGAGTGAACAAAGATCCGATACTCCACAAGACTGTAAAGAA
|
|
AATGTAACTCCTAATGCGAAAAATCATCAGAGTCACTCTCAAACACCATGTGGAGGACAG
|
|
GGATTTGGAACTCCAAACCATACAGGAATACCTAAACCGACTGCCGCTGTCAAGGGAACT
|
|
TTTAAAATATCAAAAGACGATAGACATGTTATACAGAAAAGTACAAATAGTCAATTAAGT
|
|
CCTATACAAAGCAATTCTAGTTTAAATTCTACAAATAACATAAGTGCACTTCCATTCTGT
|
|
AGAGAACAATCTAATTTAAGTAAGGATATAACTCAAAAGCAGACACTAGCCGTATCCCCG
|
|
ATGCCGGTTATGAGCACAGGGAATCAAAATCATAGTTCGCAAATGTCTGAAAGTTCACAC
|
|
TCCAATTCTACGCACAGTACTACAGGCCAACATTCGAACTCTAGCGATAGCAGCGTTATA
|
|
TACCGTCCTTCTAGCGAATCAGGTTCTGAAATGTCGAAGACTGCTAGTCACAGTGTGGCA
|
|
TCAAATAAACGGCTAGACATGAATACTACTTATATAAATGACGTTATAAACGAAGCGGAG
|
|
ATATCAGAAAAGGAGGCAGCACAAAGACGTCACGTCGATAATTCAATCCCCAAGCAATCG
|
|
TTTGATCCCAATAAAACGTTAACCGAAATAAGTAGGAGGCTCGAAAGTGATAGTAGATCT
|
|
AGCACACCGTCGCATTGTCGTGATAATTCTTTAGGCGAAGACGAGAATCCAATGATGAAT
|
|
GTTTTACCAATGAGACCGTTACTTCGCGGATACAACAGTCATTTAACCTTGCCCATGAGA
|
|
ACTTCAGGTTTGGCACAGAAAAATATAAGCGTTTATCCACACCACGCAAATACTGTAAAA
|
|
GCAAACTTTGGACGGGAAAACATAGGTCTTCGCGATCGTATAAACTATGGGCCTGGTTTT
|
|
TCGAATCCTGATTATTGTGATCTGGAAATTGCTTCGGGATACATGTCTGATGGTGATTGT
|
|
TTGAGAAGAATTAATATCGGTGAGATGGAATGCGGGAGGAACAACGACATGATGGACGGC
|
|
TATATGTCCGAGGGTGGTGCTTCACTCTACGGTCGTCGGATGAACTACCAGCAACCACAA
|
|
TTTCAACAAATGGACGAAAGACGAAGTGGTGGTCGCAATAGAGGCATGGAGGGTGGTAGT
|
|
GGTGTAGTCTACAGAGTAGTGGGTCGCACACGCAGCAAAGCCGACTCCGGACAGCAGACC
|
|
GAGCGCCAGCCTCAGCCTTCCCGGCAGGACACCACGTGGAAGAAGTACACTGACTCGCCC
|
|
GGGAATCAGCCAGCACCCGCGCCTCCTAGTCCATCTCACTCGCGCAAGGGTGAGAGACGA
|
|
ACTGGCCATCATTCACCGCAGCACCACAAACGAGAAAAACTCACTGCAGCTCAGCAGCTT
|
|
GGGATCGCACCTCATCCTCAGTATGCCGCTCCAGCTCAAGCAGCTAACCCTGCTGGTCAG
|
|
CATTCCTCTAGAAACCCAGGCCCACAGCTCCAGTCTCCGAGTGGAGGGTCGCGTCCCTCC
|
|
AGCGTCTCTAGCGGTGGTAATGGCAGTGCCTGCTCGTCGAAGGCTAAAGTTCCTCAAAAT
|
|
TTTGGATATGTGAAAAGACAAAACGGTGTACAGCAGCCGGCACCTCAGGCCAACGGTCCA
|
|
CCGCCGCAACATGGAGGCCACACTGGAAGAACCGCCCAGGTGTCTGCAGTGCCAAGAACT
|
|
AAAGTCAAAGTTTCGGGAGGAACCCAGACATGCACACAGGATTTACAGATTCACAAAAAT
|
|
GGTATCGGACCTAAATCGTATTCTCTGGGCGGCACCGCGGCTGCCCAACTGTCAGCGTCA
|
|
GTGCGAGAGAGACTGCTCGGGTCACAATCACTACCAAAACCTGGAACACACGAATTCGCA
|
|
GCGTTATTCCATCACCACAGAATTGCACCCAGAGGCGGCATGAAGATCAGCGATGGCAGC
|
|
CTTTCTGACACACAGACATACTCTGAAGTGAAATCAGACTATGGGATACCCTACGCGCCC
|
|
TGGCTCAGGCATAGCAACACATACTCGGCGAGCGGGCGGTTGTCAGAGGGAGAGTCGATG
|
|
GAGTCGCTCACGTCGCTGCACTCGGCGCAGGCGCAGGCGCACAACCACACCTCCTCCCCT
|
|
AACTCCCACCGCAGCTCACTCACACACAATAAGCTCATCATGCACCGAGATGCACAGGGC
|
|
TCCAGGCTTAACAGGAGCAACAGCATTAGATCGACTAAGTCAGAAAAATTATATCCGTCG
|
|
ATGCTTCAAAGGTCTTCAGAGAGCGATTATGAACCGTATTATTGTTTACCTGTGCAGTAT
|
|
GGACCAACAGGTCAAGGTCTAAACTATGGTGTGTCGGAGCCGCCGTCGCCGTCGCCGCGC
|
|
TCGGCGCTGAGCCCGACGCACGCGCCCGGCAACGTCATGCACACGCCGCGCCACTCACAC
|
|
CACTACCCGAAAAAGAACGACGATGTGCACGGTTCGACGGCGTCGCTAGTGTCGACCGCC
|
|
TCCTCGCTGGCTGCCGGCGCAGGCGCAGAAGAGAGGCACGCCCATGAGGTGCGAAAGCTG
|
|
AGAAGAGAACTGGCCGATGCGAAAGAAAAAGTTCACACTTTAACAACGCAGTTAACAACC
|
|
AACGCGCACGTGGTGTCCGCATTCGAGCAGAGTCTGTCGAATATGACGCAGCGCCTGCAG
|
|
CAGCTCACCGCAACCGCCGAGAGAAAGGATTCGGAACTGACGGAGCTTCGTCAAACGATT
|
|
GAGTTGCTGCGGAAACAGTCGATTCAAGCTGGTCTGACTACTGCTCACATGCAGTCCATG
|
|
GGAATCCGTGCCGATGGCGTCAACGTCACTGGACAGCAGGACCCAACAACCCAAACGCAG
|
|
CAGTCATCACCACAACGTAACGCACAAACGGGCAACGGTGCGATCACGCGGCATCTATCG
|
|
ACCGACAGCGTGTCGAGCATCAACAGCCTGAGCAGCGGCTCCTCAGCGCCTCACGACAAA
|
|
AAACACAAGAAAAAAGGATGGCTACGCTCATCGTTCACGAAGGCATTCTCACGGAACGCG
|
|
AAGATATCTAAAACAGCGAAGCACTCGTCCCTCGGGCAGCTGTCGTCACAGGACAGCTCG
|
|
TCGGGCTCGCATCACTACGACGACCCGCACACGATACGAGAGGGCAGTAATGAGAACAGT
|
|
CTAGAACATTCCCACGAGGCTCTTCCTGATACTAAGGAGAAGCCGGCGCCTGTCAAGCCT
|
|
GAAGAACAAACCAAAGATAACAAAGAGGAATCTGTCTTGGTGGATGAGCTGAAGCGGCAA
|
|
CTGCGCGAGAAGGATCTCGTGTTGACCGACATCAGACTGGAGGCGCTCAGCTCCGCGCAT
|
|
CAGTTGGAGAGTCTCAAAGACACCGTTATAAAAATGAGAAACGAGATGTTGAACCTGAAG
|
|
CAAAACAACGAGCGTTTGCAGCGGCTGGTGACGTCACGCTCGCTCGCCGGCAGCCAGAGC
|
|
TCGCTCGGCACCGGCGGCTCCGCCGTCGAGGACCCGAGGCGGTTCAGCCTCGCGGACCAG
|
|
GCCACCATGCACCAGGCGGCGATCGACATTCACGCCCAGCCTCTCGACCTCGACTTCAAC
|
|
TGCATGTCAGCCACACCAACCATCGACTTCTCGAAGAAAGGTTCACCCAAGTCCGGCATG
|
|
GTGGAGCCCATATATGGGAATAAGGCTGCCTGCGAACTGAACGAGAACAATGAGACGCTG
|
|
CTAGGAGCGTTGAATGGGGCCAGCGATTTGTTCTCCAACGGACTCAATGCTGGAGAGCGG
|
|
CTGAGTGGAGATTACGATATAAACAGCGTGTTACCGCCGCCTAAAACACGCGAGCTTGCT
|
|
ATTGGTGAAAGCTACTCTGATATTGGTGTAGCAGACAGCCAGGGAGACACGACTGATGGA
|
|
AAGAAAATAGCGATAGCTGTATATTTAGGTCAACCCGAAACATTCCAAAGATATTTCGAA
|
|
GAGGTCCAAGACACATTGACGGAGTCCGAGTGCAGATTCTACGCGAAGCAATCGGCAAGC
|
|
GCGTACAATCATTTCGAGAAACAAGCCAGTTTCGAATCGCCGAGAATGTCCACGAATCAC
|
|
AGTCCAGAAGTGGAGACACAAGACTACCCGCAAATAAATAAGTCGAACACGAATAGCCTT
|
|
AAAAGCAACAAATCTACGCACAGTAGCTCGTATAAGAATGTTTATAATAGTGATTCGACA
|
|
ATAAACTGCAACGAGTACACTATAGCGTACACTTATATATCTGGCAAGACGACTTGGCAG
|
|
AATTTAGATTATATAGTTAGGAAGTCCTTTAAGGACTACTTGTCTAGGATAGATTTGGGC
|
|
ACGAATCTCGGTCTGAACACTGATTCTATAACGTCGTACCATTTGGGTGAAGCGACGCGT
|
|
GGGCCGGAGATCGGCTTCCCGGAGCTGTTGCCATGCGGGTACATCATAGGGACCGTGAAC
|
|
ACGCTGTACATCTGCTTGCAAGGAGTCGGCAGTCTGGCGTTCGATAGCCTTATACCAAAA
|
|
AATATTGTATATAGATACGTTTCTCTGCTATCGGAACACAGGCGAGTGATACTCTGTGGT
|
|
CCCAGCGGCACCGGCAAGTCATACTTAGCGGCGAAACTCGCTGAATTTTACGTCCAGAAA
|
|
ACACAAAGGCGCGGCAATCCCGCCGAAGCTGTAGCTACATTCAACGTGGACAGAAAGTCG
|
|
TGCAACGAGCTGCGCGCGTACCTGGCGAACATCGCGGAGCAGTGCGGCGCGGCGGCCGCG
|
|
GGCGAGGAGGCGCCGCTGCCGTCCGTCGTGGTGCTCGACAACCTGCAGCACGCCTCCGCG
|
|
CTCGGCGACGCCTTCGCGGGGCTGCTGCCGCCCGACAACAGGAACATGCCCGTTATTATC
|
|
GGTACCATGTCCCAAGCGACGTGCAACACCACGAATCTCCAACTACATCACAACTTCAGA
|
|
TGGCTCCTCACCGCTAACCACATGGAACCCGTCAAAGGATTCTTAGCTAGGTATCTCCGA
|
|
AGAAAGTTATTCTCGCTGGAGCTGCGGCTGGGTCGGCGCGAGCCGGCGCTGGCGGCGGTG
|
|
CTGGAGTGGCTGCCGGGCGTGTGGGCCGCGCTCAACGCCTTCCTCGAGGCGCACTCCTCC
|
|
AGCGACGTCACCGTCGGGCCGCGGCTCTTCCTCGCCTGCCCCATGGACTTGGAGGCCAGC
|
|
CAGGCATGGTTCGCAGACGTGTGGAACTACAGCATAGTGCCGTACGCTTCGGAGGCGGTG
|
|
CGCGAGGGCATCGCGCTGTACGGCAGGCGACGACACGCCGCCGTCGACCCGCTGCAGCAC
|
|
ATCAAGTCTACATACCCCTGGAGAGAACCCAATCACTCGCATACTTTGAGACCCATAACA
|
|
GTTGATGATGTTGGCATCGAAGAGTCAAGCCAAGACTCCGCCGTGAACAACAATCAAGAT
|
|
CCTCTGTTGAACATGCTGATGCGGCTACAAGAAGCGGCGAACTACAGCGGAAACCAAAGC
|
|
CAGGACTCTGACAACGCCAGCATGGACTCGAACCTCACACACGACAGCTCTGTAGGGAAC
|
|
GAGCTTTAA
|
|
>M. sexta-Akirin (MsAki); Msex2.12479-RA
|
(SEQ ID NO: 72)
|
ATGGCGTGTGCTACACTTAAAAGAAATTTGGATTGGGAATCCATGGCGCAATTGCCTGCT
|
|
AAAAGGCGAAGATGTTCGCCATTTGCTGCAAGTTCTAGCACAAGTCCTGGATTTAAAGTG
|
|
TCTGAAACCAAGCCATCTACATTCGGAGAGGCCGTTAGTGCACCTGTGAAAATGACCCCA
|
|
GAGCGCATGGCTCAAGAGATCTGCGACGAGATCAAGCGGCTGCAGCGGCGCCGGCAACTG
|
|
CGGCTGGCTGGCAGCTCCGCCGCTTCGTGCTCATCGTCGAGCGGCAGCGAGGGCGACTGC
|
|
TCGCCGCCACATCGCTCCTCGCACACTTCGCACAAGATGCACAACCGTGCGCTCTTCACT
|
|
TTCAAACAGGTGCGCATGATCTGCGAGCGGATGCTGCGCGAGCAGGAGGTGGCTCTGCGC
|
|
GCGGAGTACGAGTCGGCGCTCAGCACCAAGCTCGCCGAGCAGTACGAGGCGTTCGTGCGG
|
|
TTCAACCTTGATCAGGTGCAGCGCAGACCCCCGCCCAGCACGTGCATGCCCCTCGGCATG
|
|
GACGCCGAGCATCACATGCACCAGGACCTCGTACCTAGCTATCTGTCCTAA
|
|
>M. sexta-Cactus (MsCac); Msex2.02793-RA
|
(SEQ ID NO: 73)
|
ATGAGTGCCAAAAAAGGATATGAAACGAAGATTGTCGAGGAAGAAAACATGGATTCCGGA
|
|
ATTGTGTCTGGTGAATTGGAATCTTATGAGATTTCGGGTGAAGTGGATTCGGGCGTGATT
|
|
GATTGTGATAAGAAATACGAAGGGGTTCCAAGTGAGGTGTTGGAATTGACGGACAAGTTC
|
|
AAAAGTGTAAATGTGAGAGAGAAGAGCTGTCCTGATGTTCCACCACTGGCGGACCTGTTC
|
|
CACCCTGACAACGACGGAGATACACAACTACACATTGCATCGGTACACGGCTGCGAGAAA
|
|
TCAGTGAGCACGATCATCAGGGTGTGCCCTGACAAGGAGTGGCTGGACCTGCCCAACGAC
|
|
TACGGCCACACGCCCCTCCACCTCGCGGTGATGAGCGGCAATGCCGTGGTGACAAGGATG
|
|
CTGGTGATAGCCGGCGCTTCGCTCGCTATTCGCGACTTCATGGGAGAGACGCCCTTACAC
|
|
AAGGCGACCGCAGCGCGAAACCAGGAGTGTCTCAAAGCCCTGCTTGCCCCTGTACCGGAA
|
|
CAGCCCAATAGGAAATTGTCTTCAATACTCGACCAGAGGAACTATAACGGTCAATGTTGT
|
|
GTCCACCTGGCGGCGTCAATTGGAAGCGTAGAGACGCTACAGACCCTGGTCTACTACGGA
|
|
GCCGATATCAATGCCAGGGAGAACCTGGCGGGCTGGACGGCGCTGCACATCGCGGCGCGG
|
|
CGCGGCGACGTGCGCGTGGTGCAGTTCCTGCGGTCGCGCTGCGCCGGCGCGGCGACGCGG
|
|
CCGCGGGACTACGCCGGCCGCACGCCGCGCCGCCTCGCGCGCCGCACCAAGGCCGCCGCC
|
|
GCCTTCGACGACAAGGACGACAGCGACTCCGACTCCGACTCGGACGATGATGATATGTAC
|
|
GACAGTGATAGCGAGACGTTGTTCGAAAAACTCCGCGAGAGCCTGAGCACGTCGATCAAC
|
|
GTCGCCTGA
|
|
>M. sexta-Gloverin (MsGLV); GI110649240
|
(SEQ ID NO: 74)
|
CCACGACAACCACTGATGAAGTTATTTTTTATAGCAATTCTTTTCGCTGCCATCGTCGCT
|
|
TGCGCGTGCGCTCAAGTGTCGATGCCCCCGCAATACGCTCAGATATATCCAGAATATTAC
|
|
AAGTACTCCAAACAAGTCCGCCATCCCAGAGACGTGACCTGGGACAAGCAAGTCGGCAAC
|
|
AATGGGAAGGTCTTCGGAACTCTGGGACAGAATGACCAGGGTCTTTTCGGTAAAGGAGGC
|
|
TATCAACACCAATTCTTCGATGATCACCGCGGCAAACTGACAGGACAGGGTTACGGGTCC
|
|
AGGGTCCTCGGACCTTACGGAGACAGCACCAACTTCGGCGGCCGGCTTGACTGGGCCAAC
|
|
AAGAATGCTAACGCTGCTCTTGATGTGACCAAGAGCATTGGCGGTAGGACTGGGCTGACT
|
|
GCCAGTGGATCAGGCGTGTGGCAACTTGGGAAGAACACGGATTTATCTGCGGGAGGCACT
|
|
CTGTCTCAGACGCTTGGACATGGGAAGCCTGATGTCGGCTTCCAAGGTCTCTTCCAGCAT
|
|
AGATGGTGA
|
|
>M. sexta- Beta-1 tubulin (MsßTub); AF030547
|
(SEQ ID NO: 75)
|
ATGAGGGAAATCGTGCACATCCAGGCTGGCCAATGCGGCAACCAGATCGGAGCTAAGTTC
|
|
TGGGAGATCATCTCTGACGAGCATGGCATCGACCCCACCGGCGCTTACCATGGCGACTCG
|
|
GACCTGCAGCTGGAGCGCATCAACGTGTACTACAATGAGGCCTCCGGCGGCAAGTACGTG
|
|
CCGCGCGCCATCCTCGTGGACCTCGAGCCCGGCACCATGGACTCTGTCCGCTCCGGACCT
|
|
TTCGGACAGATCTTCCGCCCGGACAACTTCGTCTTCGGACAGTCCGGCGCCGGTAACAAC
|
|
TGGGCCAAGGGACACTACACAGAGGGCGCCGAGCTTGTCGACTCGGTCTTAGACGTCGTA
|
|
CGTAAGGAAGCAGAATCATGCGACTGCCTCCAGGGATTCCAACTCACACACTCGCTCGGC
|
|
GGCGGTACCGGTTCCGGAATGGGCACCCTCCTTATCTCCAAAATCAGGGAAGAATACCCC
|
|
GACAGAATTATGAACACATATTCAGTTGTACCATCACCCAAAGTGTCTGATACAGTAGTA
|
|
GAACCTTACAATGCAACACTGTCAGTCCACCAACTCGTAGAAAACACCGACGAAACCTAC
|
|
TGTATCGACAATGAGGCTCTCTATGACATCTGCTTCCGCACGCTCAAACTTTCCACACCC
|
|
ACATATGGCGACCTTAACCACCTGGTGTCGCTCACAATGTCCGGCGTGACCACCTGCCTC
|
|
AGGTTCCCCGGTCAGCTGAATGCGGATCTCCGCAAGCTGGCGGTGAACATGGTGCCCTTC
|
|
CCGCGTCTGCACTTCTTCATGCCGGGCTTCGCTCCGCTCACGTCGCGCGGCAGCCAGCAG
|
|
TACCGCGCCCTCACCGTGCCCGAACTCACCCAGCAGATGTTCGACGCTAAGAACATGATG
|
|
GCGGCGTGCGACCCGCGTCACGGCCGCTACCTCACCGTCGCCGCCATCTTCCGTGGTCGC
|
|
ATGTCCATGAAGGAGGTCGACGAGCAGATGCTCAACATCCAGAACAAGAACTCGTCGTAC
|
|
TTCGTTGAATGGATCCCCAACAACGTGAAGACCGCCGTGTGCGACATCCCGCCCCGTGGT
|
|
CTCAAGATGTCGGCCACTTTCATCGGCAACTCCACCGCTATCCAGGAGCTGTTCAAGCGC
|
|
ATCTCTGAACAGTTCACCGCTATGTTCAGGCGCAAGGCTTTCTTGCATTGGTACACCGGC
|
|
GAGGGCATGGACGAGATGGAGTTCACCGAGGCCGAGAGCAACATGAACGACCTGGTGTCC
|
|
GAGTACCAACAGTACCAGGAGGCCACCGCCGACGAGGACGCCGAGTTCGACGAGGAGCAA
|
|
GAGCAGGAGATCGAGGACAACTAG
|
|
>P. xylostella-Peptidoglycan recognition protein 2 (PxPGRP2); ACB32179.1
|
(SEQ ID NO: 76)
|
ATGACGTTGTCTTTTGGCGTGTTTCTGCTGATATCTTCAGTGTTTTGTTGTTGTGCTCAT
|
|
GCAGGGTGTGGCGTGGTGACCAGACAGCAGTGGGATGGGCTGGACCCGATACAGTTGGAG
|
|
TACCTGCCCCGGCCCCTGGGGCTGGTGGTGGTCCAGCACACCGCCACCCCCGCGTGTGAC
|
|
ACTGACGCCGCGTGTGTGGAGCTGGTGCAGAACATACAGACCAATCATATGGATGTGCTG
|
|
AAGTTTTGGGATATTGGACCGAACTTCCTGATTGGTGGGAACGGCAAGGTGTACGAGGGC
|
|
CCTGGTTGGCTGCACGTCGGCGCCCACACTTACGGCTACAACAGGAAGTCTATCGGGATC
|
|
TCTTTCATTAGGAATTTTAATGCTAAGACCCCAACAAAAGCAGCGTTGAATGCGGCTGAA
|
|
GCATTGCTGAAGTGTGGAGTGAGAGAAGGACACCTGTCTCACTCATACGCAGTGGTCGGC
|
|
CATAGACAACTGATCGCAACAGAGAGCCCAGGCAGGAAACTGTACCAAATCATCAGGCGC
|
|
TGGCCAAACTACCTCGAGGATATTGATAAGATTAAAAACAACAAGTAG
|
|
>P. xylostella-Immune Deficiency Protein (PxIMD); Px003008
|
(SEQ ID NO: 77)
|
ATGTCTATCCTAAAATCAAAGTTATTCGAAACTATTGCAAAAAGTTTCAAGTCTGATGCA
|
|
GTCCCGAAGCCACCTAGAGAACCGGTAGAGACTACAGAGACATCACAAAATAATACCGAA
|
|
AATCAACCTTACAATGTCGAAGAAGAGGAAATACCCGAACCAGAAAAGCCTAAGAAAGAA
|
|
AAAAAGAATCCCAAGCCTACCAAAAAAACTTTCTTTAATCGTGACAAAACTAACAAACAC
|
|
GACGATACCCGCAAACATACAAAATCCGGAAAGGACCAGACATCAATTAATACTCAAGGT
|
|
AACTTGAAAATTATACTTCCTGTAACTTAAACGGCCCGTTGACCCCAGTTTACCTTTCGC
|
|
CTTTCTTGATATATTTTTGTAATCCAGCCTTACTTTGGTAATACATACTTGCCCCACTTG
|
|
TATTTAGTTAATGGTGGCACTAGCTAGATAGTAATGTTAAATGATGATAAGCAGTAGTGA
|
|
TTCATCATTCAAATGTATCATTGTCCTTTAATGTTAAGCGCAAATAGATTTTCATTGTTC
|
|
TCCCATGTGCTTCATGTTTTATGTATTTATAGGTAGGTACTTAATGTTTTATAAATATTT
|
|
TTTTGTTAATTGGGAATCCCCAGTCCCCATTGTCTGGACCAGTTTATATATAATTGAACT
|
|
AACAAGAGTGTGCTTTAAATACTATTCTCTGCAATTATGATAATTAAACAACATGAATTT
|
|
CTCTTCACTTCCCTTCTCTTATTTAAATAATATTGTAGGAAACTGTAATAACTAATACAA
|
|
GATTATAAATTTCATTCTAGCAACTGGTGATGTAATCCATGTGGTAAATTCCAAAGATGT
|
|
GCAGGTCGGCCATCAGTATGTGTACAACATGGGAACTCCCGGAGCTAACTCACAGAAGAA
|
|
TAACCCATTTGATGATGAAGAAACAGTAGAAAAGACAAATCTAATAACTCTGGTCATGGA
|
|
AGCAAAAATTATGGTAATAACACATTTTTAACTAGGCATAAGGTCATAATTTAGCCAGAA
|
|
TCATCAGCTTGTCCTGTGGCTCTTGTTGAGCTGGTGGAAAGAATACATAGGTAATGAATA
|
|
TTTTGATCAATACTCATTGCAAAAATCACAATAATGCCATTGAAAATCTATAACATGTTC
|
|
CTTAAGTATCACTTATCATCAATCCAATTAAGTCATCACACAGATCAATCGGTTAGTTCT
|
|
GTTTATTTACTTCTTTCAGCTGGAACATGAATACATGGACTATGTCTCGAAGAACCTCGG
|
|
CAGGAACTGGCACAGCTTCTTCAGAACGCTCGGCTTCACGCGGGGGCGCATCGAGACTGT
|
|
GGAACTGGATGAGGGCAGAAATGGTGTTGCAGAGGTATGAAAAAAACATACATGTTAATT
|
|
TGTGTTGTTTGGCTGATGTGGCAACTAAGTTCGTAACTGCTATGATCAACTGTTTGTGTC
|
|
ATAGGTATTTTTTTTGCCCTTCCACACATCTGAGGTAACAAGGACACCTCCTGCACTCAA
|
|
AACACAACTGCTATGTCCTACTGATGAGTCCTAGGAAACTCAGAAACCATCTGTTTCCCC
|
|
CATTCTCAATTCCATAAAGCTAAAAAGTGGTAGTTACACAATTCACAATTCATAAACATG
|
|
CTTTGTCATAGTTAGAAAAGCAGCTCAGCTATGAGGCATCCACTCCACAGTCCACTCACG
|
|
AAAGCCCTCTTTAAAAACATAAAATCATCATCATCAGCCCTCAATTGCCCACTGTTGCAT
|
|
ATAGGCCTTCTTTTGATTATGCCAAGTTTTTCGTTTCTCTAGTCCACAGACTTGACATAG
|
|
TTGTCACAAATTTATTCTACGTACTTGTATTTCCAGGTGCGCTACAAGTTGCTCCTGGAG
|
|
TGGGCCCGCACCGACGAGGACCCCACGCTGGGGCGGCTCGCCACGCGGCTGTGGGACGAG
|
|
GGAGAGCGGCAGACCGTCAAGGAACTCGCCATCTTGTATAATAATAATTTCAAGCAACAA
|
|
TGTTGA
|
|
>P. xylostella-Relish (PxRel); Px002858
|
(SEQ ID NO: 78)
|
ATGGTAGTGGTGAAAAGCCAATTAAAAATGCAAAGTGACCAGGACACGGACTCGTCCACT
|
|
GCCGGTGCTTCGCCGCGCAGCTTCTACATCGAGTCGCCGCACAGCTCGCCGGGACAACAA
|
|
GTGCCTTATTTAACTAATTACATGACAGTACTGTCCTGTGCAGATAATAACTTAATGGAT
|
|
ACAGGAAGCAATGGACCATTCCTGAGCATCACGGAGCAGCCATGTGACCACTTCAGGTTC
|
|
CGCTACAAGAGCGAGATGGTCGGCACCCACGGCTGCATCGTCGGCAAGACCAGCGCCAGC
|
|
AACCGCACCAAGACATACCCTTCTGTTGTTCTGCTCAACTACAAAGGCCGCGCCACCATC
|
|
AAGTGCAGCCTCGCGCAGCACAACAACCGCAAGCAGCACCCGCACCAGCTGGTCGAGGAT
|
|
GACCAGGAGCGCGACCTGAGCGCCGAGGTCAACCCCGAGAAGGGCTATGAAGTTGGATTT
|
|
CGTGGCATGGGCATAATACATACAGCGAAGAAAGATGTTCCGGCACTCCTATACAAGAAA
|
|
TTGAGTGAGAGACTGCCACATTTCAATGCCCGTGAGCTGAAGGCCCAGTGTGAGAACGAG
|
|
GCGCGCAGTATAAACCTCAACATCGTGCGCCTCAAGTTCAGTGCGCACAATGTCGACACG
|
|
GACGAGGAGATATGCGCTCCGGTGTTCTCGGAACCTATCCACAACATGAAAAGCGCCGCG
|
|
ACGAACGACCTGAAGATCTGCCGCATGAGCCGCACGTCGGGGCGCCCGCGCGGCGGCGAC
|
|
GACGTCTACCTACTCACCGAGAAGGTTAACAAAAAGAACATCGACATTCGCTTCGTGCAA
|
|
CTGGAGCGCGGCGAGGTGTGCTGGACCGGCAAGGCCAGGTTCCTCATGAGCGACGTGCAC
|
|
CACCAGTACGCTATTGTGATCAGAACACCAGCATACAAGAACCCCGAGATTACGTCTGAC
|
|
GTAAAAGTGTACGTAGAACTATTCCGCCCGTCCGATGGCCGCTCCAGCGAACGCATAGAG
|
|
TTCACGTACAAGGCAGAAGAAGTCTACAAGCAAAGCAAGAAACGGAAGGCCAACTCTTAC
|
|
TCCTCTATCGGAAGTTCATCTAGCGGTAATTCTATCAAAAGCGTCAGTGATCTTCCAGCA
|
|
ACTGTTATTATGGCCAATGAAATGAATGCGGCTAACAACAACTTTAGTAAAATCTCTTCA
|
|
ATGCTGAGCCCAAACAATATACCAGAAATACCGACACAAACGACTGTGGGTCTATCAGAC
|
|
GCTCTCTACGACATAACAGTGACAGAAGACCACCAAATGCACATCAGTCCCATGCTATGC
|
|
CAACCAGTGGAAGAGTATCCCCTAAAGCTTAACTCGCAGGATATCATACAAGTGAATTTG
|
|
AACTCTAAGGACATCGACCAACTGCTCAAAGTCAACAGTGTGCCTGATACCGATAAAGAC
|
|
TTTGCTGACTTCAATTTTAGTGACTACTACAAGGCACTCGATAGCAACTTTTTAGCTGAT
|
|
GGTGGTGGTGATAGCTTCAGTCAGTGTATCTTCAACTCTATGCAACTGAGGCCTGACTCT
|
|
GGGAGAGGCACG
|
|
>P. xylostella-Toll receptor (PxToll2); Px006338
|
(SEQ ID NO: 79)
|
ATGCCTAAAGTAATAATCGCCAGTTTTGCTTATATAGTAGGTGTGTTTGTCCTGTGTGCT
|
|
GGGCTAGAAACAAGTCCAACCTGTTCCAGCATCGAAGGACCTACTCCAGGTGAATTCATA
|
|
ATACAAAGAGGTATCGTACCGGACAATGATTCAGCCACCACAGTAAGCTTCCGAGGCTGC
|
|
CGAATATCTGACATTCAGCCGAGAGCATTCCATGGGCTACCTTCCCTGCAATACATAGAC
|
|
TTATCAAGAAATAGCATTAAAAACCTGAAACTTGGCATTCTTAATGACGTCACTAGACTC
|
|
ACTCATCTGAACTTGTCTTATAACTTCATCAGCGATTTAGAAGAGAGTTTGTTCAACCAA
|
|
TCGTCAAGGTTGGAGGTGTTGGATCTCCGGTGGAATAAGATTGAAGTTATGAAAGTGGGC
|
|
GTTTTCAGTCCATTGAAGAGATTGAAGTATTTGGATCTGTCCGACAACGAAATAGTTGGG
|
|
GCCAGCCTGAGCCCCGCTATGTTTGATTCCTGTAAAGCTCTATCCACTATCAATTTTTCA
|
|
AGAAATGATATGTCTGGTGCTCCCACTGATTTGCTTCGAGCTGTGGAGGTACTGGACACA
|
|
CTGAAACTGGATGGGTGCTTTTTGAAACAAGTTCCGGAATTTGCTACGAGGAGCAATACC
|
|
GGCACAATGAAGAAACTTATTTTATCATCGAACCAAGTGAGCACTGTGAAACTTACTACG
|
|
TTCATCAGTTTAACAAACCTGGAGGAACTAGATTTGAGTTCAAATGTAATTTCAGAATTG
|
|
CATGAAGACGTATTCAAGCCATTAAAAAACTTGAAAATTATTATTTTACGCTCGAACCGA
|
|
CTGGAAAAAATTCCTGATAAGTTGTTTTATAATATGTTACGATTAAGGAAGGTAGATTTA
|
|
TCTTTTAATTCTTTGATGATAATACCTGTGAATGCCTTTCGTTTTACGACGATAGAAATG
|
|
TTGAATATATCGCATAATAAGTTCACATATTTAGTCGACAACTTTTGTTTGGAACTTAGA
|
|
AACTCGGGAGTGAAACTGAAAAAGTTTTACTTCAACAGTAATCCCTGGCAGTGTCCTTGC
|
|
TTGAGGGATTTATTAAAGGAAATGAAGACGTATAGAATATCGTACAATAATGCTAAATAC
|
|
GATGGTAAAAATGCAGTTTGTATTTCAGGAGACATTATTAATACTTGCTTGAGACAACCT
|
|
GATGTCAATGAACACTTCAATGATTTGTACTATTCTGACTAA
|
|
>P. xylostella-Cactus (PxCac); Px016665
|
(SEQ ID NO: 80)
|
ATGAGTTTCAAGAAGGATTTCGACACCTCAAAGAAGATCCAGGAGGATGAAAACACAGAC
|
|
TCTGGGTTCCTATCTGGGCCGATAAGTGAGCAGCTGACCTCGGAAGATTGTGATTTAGCG
|
|
GAGGAAAGTGAGCGTGCTCGCAGCAGGCTTAGTGAGGAAGATCCTGAGCCTGAGCTGCAG
|
|
TTGGACAGTGGGCTGGACCTCTCGGAGTGTCTGTCGAGTGTTAAGCTTAGTGATAGTGCA
|
|
GTGTACACACCCACCTCGCAGACCACCCCCACAGTCACTATAGGTGATGAGAAAACTCAT
|
|
GACATCCCACCCCTCGCCATCCTGTTCCAGCAGGATGACGATGGAGACACACAACTACAC
|
|
ATTGCAGCGGTACATGGGTGCGAAAAATCAGTAGGAACATTAGTAAGAGTTTGCCCTGAC
|
|
AAAGATTGGCTAAATGTACCAAATGACTTTGGACAGACCGCCTTACACTTAGCAGCCATG
|
|
AGTGGGCATGCAGTAGTCACACGCATGCTGGTGATGGCCGGTGCATCTCTTGGCATTCGA
|
|
GACCTTGTTGGCAACACACCTTTACATGTGGCAGCCGCAGCGGGCTACGTCGGCTGTCTC
|
|
CAAGCTTTACTGGCTCCTGCTCCAGAACAACAGCAGAGAAGGCTAGCATCCACGTTGAAC
|
|
CAGAAAAATTACAATGGTCAAACGTGCGTCCATGTGGCTGCGATGGCCGGCCACGTCGAC
|
|
GCGCTGCAGACATTGGTCTATTACGGAGCTAACATCAATGCTGCGGAGGGTCTATGCGGG
|
|
TGGACACCTCTACACGTAGCGGCGGCGCGAGGCGACGTCGACACGGCTCGCTACTTGCTC
|
|
GAGAAGTGCGCTGGCGTCGATCCCTCTGCCCTGGACTACGCCGGTCGTACGGCCAGGAAA
|
|
CTGGCGTTGAAGAATAAAGCGGCCGCCCTGTTTGACGGCAGTGAGGGCAGCGAGGAGGAG
|
|
GATAGTGACAGTGAGGATGAGATGCTTCTGGAAAGCGACCAGAGTCTGTTCGACCGGATC
|
|
CGTGACGGTATGAACGCCATCAACGTCGCCTGA
|
|
>P. xylostella-Dorsal (PxDor); Px000110
|
(SEQ ID NO: 81)
|
ATGAACGCGCCCGCCGACTCCGCCGTGGTGACGTTCACCAACCTGGGCATCCAGTGCGTG
|
|
AAGCGGAGAGACATCGAGGACGCCCTGGCTGTGAGAGAGGAGATGCGAGTTGACCCCTTC
|
|
AAGACCGGATTCAGCCACAAGAACTCCCCGCAAAGCATCGACCTGAACGCCGTCCGACTC
|
|
TGCTTCCAAGTGTTCCTGCCGGACGAGCGATCCGGCAAGATCCGCCACGCGCTGCCGCCG
|
|
GTCGTGTCCGATGTCATCTATGACAAGAAGGCCATGAGTGACCTGGTTATCACGAGGCTG
|
|
AGTCATTGTTCTGCGCCCGCGCAGGGCGGCAAGCAAGTTATATTGCTGTGTGAGAAGGTG
|
|
GCCCGCGAAGACATAACCGTAACCTTCTTCGAGAAGTCCGGCGAGCGCGTGACGTGGCAG
|
|
GCGGACGCGGCGGACGTGTTCGTGCACAAGCAGGTGGCCATCTGCTTCACCACGCCGCCT
|
|
TACCGCGACCCGCATGTGCAGGACCATGTGCAGGCGTACATCCAGCTGCGTCGTCCGACG
|
|
GACAACGCGACGAGCGAGCCGCTCCCCTTCGAGCTGCTCCCGTCCAGCGCAGATCCGAAT
|
|
TATCTGAAGCGAAAGCGACAGAAACCGATACAGAACTTCAGTCGGTACTTACAGCCGATC
|
|
GATAGCGACATGAAGCAGCAGCTGCCGGACTATTTCCAGGACAACATGGCGCTGTCCAGC
|
|
ATCCCCTCCGTGAAGCTGGAGCCCCGAGATAAGACTCCTCCTCACAACATGAGCAGCCCG
|
|
CCGCTGCTGTTCCCCCCCGCGCACGCCGCGCCCGCACACCATGACCCCTACGCGTGGAAC
|
|
ATGCAACTAGACAACATGCAGTCGGGTCTGACGGCGCCCGGGCCGAGCCGCCTGCCGCAG
|
|
TACAGCCAGGACATGGCCTGGACCAACCAGATGGGCCACGTGTCCCCTATGCACCAGGCC
|
|
ATGTCCCCTAACATGGGTCACGTCTCCCCCATGCATCAAGCCATGTCCCCAAATATGGGC
|
|
CATGTCTCTCCCATGCACCAAGCTATGTCTCCAAATATGGTCCAGTCACCTATGGGTCAT
|
|
GTGTCCCCTAACATGGGCCATGTATCCCCTAATATGGGTCATGTGTCCCCTAATTTGGGT
|
|
CATGTGTCACCTAACCTGTGCCAGCAACCAATGGCTCCTATGGCGCAGCAGCTGATGGAC
|
|
CCGTCCCCCAGCGACCCACCCTCCATCACGGGGCTGCTGATGGATCGCCCGGACCAGCCC
|
|
TACTCCGGGGAGCTGTCTGGACTCTCCGCCCTGCTGGCTGAGGCAGCCCCCGCAGAGATG
|
|
CTCAGCGATAGCCTCAACAGACTGTCTACGGGGGACTTGTTGAGACAAGTTGATATGTGA
|
|
>P. xylostella-Hemolin (PxHem); ACN69054.1
|
(SEQ ID NO: 82)
|
ATGACTTTAATTTTCAAGAGTGTTTTATTTTTGGGCTTAATATTGACTACTTTTATTGTT
|
|
TCCGCTCAGCCTGTGAAACAAGATGGCGGCTCAGCACACGAAGAAATATTGTTCCGTGAG
|
|
CACGGCCAGCCGGTGGTGTTGACCTGCGCGCGCGCAGACGACCCCAACCAAGGTGGCATT
|
|
AGAACGTGGTTGAGAAACGGGACGCCATTAGAAGACGGCAAAATGTCTCCCGAAATAAAA
|
|
TTCCTCGACGACAAATCACTCTGGTGTTGCAGCCCTCACCAGCCGTGGAAGGGGTCTACC
|
|
AATGCTTCACCGAAACCCATAAGGGCATTGCAACCTCCCCGAAATTCAGCGTGAAACAGA
|
|
CTTATCTCAAAGCTCCAGAGACTACGCCTTCAGTCAATATCAAACCAGCAAAAGGCCTTC
|
|
CCTTTAGCTTGGACTGTGACGTCCCTGAAGGATATCCGAAGCCTGAAGTGCAATGGTTCC
|
|
TACAACACGGGAAAGATCACACCCTGATTGAGGCAATTATCAATAAACGGATCACACAGG
|
|
CTCCGAACGGAGCTCTTTACTTCTCAAATGCTACAACCGAAGATGTGAATGTGGGAGACT
|
|
TTAGATACGTCTGTATGGCGAGGAATGATGCGGTAGACTTACCAGTGGTGGTGTCGGAAG
|
|
CTGTCATCACAGGTCTGAGCAGCGAGGGTGGTAAGGGTAGATTGGTGGAGCAGTACGTCA
|
|
GTAAAGAAGTTAGGGCGGTTGCGGGGGAGACCACAGCGCTATTTTGCATTTTCGGTGGCA
|
|
CCCCACTAGCCCACCCAGACTGGACGAAAGACGGCAAGAATGTGAACGGGGCGCCCGGCG
|
|
ACCGAGTGACCCGACACAACAGGAGCTCAGGAAGACGACTCATCATCAAGAACACCACTC
|
|
TAGAAGATGCTGGAACTTACCAGTGCGCCGTTGACAACGGCGTTGGGACTGAAATGCGTT
|
|
CTGTCAAGGTTACTGTTGAAGCGAAACCTTCAATAACGATTGTGAATGAAGTAGCAGCGA
|
|
AGCTTGGAGAAGAAGTCAAGATTTGCGAAGCGACCGGAGTCCCAACGCCAAAACTAACGA
|
|
TAACTCACAACGCTAAACCGTTGGTTGCGTCAAATAACGTTGTTATAACCAACGATGGAG
|
|
TTGTTATAAAGAATATTCAGGCTATTGATCGAGGGTATTATGGGTGTGATGCTGTCAACG
|
|
AGCTAGGAAGCGAATTTCGTGAAACTTATCTAAGTATTGCCTGA
|
|
>P. xylostella-Sph-3 (PxSph3); XP_004922188.1
|
(SEQ ID NO: 83)
|
ATGCAGCTTAATTTCTGTATCAATGTGATCGCGACCATATTGTTGATTGTGACTGGCGGG
|
|
GATTCCCAAAAACGAGTGGGTGACATTTGCATTGATCAATACACGAACACGTACGGAAGG
|
|
TGTGTTTTCTCGGATCGATGTCCATCAGCTTTACGTAATTATCAACAGAACGGCATTCGG
|
|
CCATCAATATGCACTTACAACTTCGACAATGCACTGGTGTGTTGTACTGAACGCGGAAAT
|
|
ATTCTTCAAACGGCGAGGCCCCCGCCACCGCCTGATCAGGAAGACAGATTTCAGTCCTCT
|
|
GCTGGAAACAACAACAACAACAATAAACCTAACATTAGAGTTAGCGAAAGAAAATGCCGC
|
|
GAGTACAGCAAATCAGTAACGTTCACGGTGAGCTTCAGCTCGCTGCTGCCGGAGCCCGAG
|
|
TTGCAGTCCATCTCGCGGCCGCGCTGCAGCCGGAGCGGCGTGGGGCTCGTGCTCGGCGGC
|
|
CGGGACGCCGCGCCGGAGGAGTTCCCGCACATGGCAGCGATCGGCTTCGCATCAGCGGAA
|
|
GGCTACGACTTCAAGTGCGGGGGGTCCCTCATCAGCGCGCGCTGGCCGCTGACCGCGCCC
|
|
TGCGCGCGCGCCCGCGCCTCCAGCCGGCCCGTGGTGGCGCGCTTAGGAGATAGGAATATC
|
|
AACCCGAAAGCGCAGGACGACGCCACGCCTGTCGACGTGCCAATCCGGAACATCATCGTG
|
|
GACGTGGACCTCAGCAACAGCATCCGCCCCGCGTGCCTGTGGCCCGGCGGACCCTTCCAC
|
|
GAGGATAAGGCTATAGCTACGGGCTGGGGGGTGGTGAACCAACGCACGCAAGAGAAAGCG
|
|
GACCTCCTCCAGAAGGTCTCGCTCACTCTGCTCGAGAACTCATACTGCGACCGTCTGCTG
|
|
AGGAACAACCGCAACCGACACTGGCAGGGCTTCCGCGACTCGCAGTTGTGCGCCGGCGAG
|
|
GTGCGCGGCGGCATGGACACGTGTCAGGGCGACTCCGGCGCACCGCTCCAGATCGTGTCC
|
|
AAGGAGAACCAGTGCATCTACCACCTCATCGGCCTGACCTCCTTCGGCTACAAGTGCGCG
|
|
GAGCAGAACAAGCCGTCGGTCTACACCAGGGTGTCGACTTACGTGGACTGGATAGAGTCT
|
|
GTGGTGTGGCCGGAGGAGTATGCGGCTTGGGCGGCGGGGAGGAGTAAATAA
|
|
>P. xylostella-Transferrin (PxTrs); BAF36848.1
|
(SEQ ID NO: 84)
|
ATGATAGTGAAAATAGCCATTTTGGTGATAGCAATAACGTTCAACGATGTGTCTGCGAAA
|
|
ACTTCGTACAAGATCTGCGTACCGTCTCAGTTCATGAAGGCATGTGAACAAATGCTTGAA
|
|
GTGGAAACGAAGAGCAAAGCGATACTGGAATGTTTGCCGGCCAGAGATCGAGTGGAATGC
|
|
CTGACCCTGGTGCAGCAACGGCAGGCGGACCTCGTCCCAGTGGACCCTGAAGACATGTAC
|
|
GTGGCGAGTAAGCTGCCCAACCAGGACTTTGTGCTTTTCCAGGAGTTCCGGACCGATGAA
|
|
GAGCCGGATGCGGAGTTCCGTTACGAGGCCGTCATAGTTGTTCACAAGGACCTTCCAGTT
|
|
ACCAACTTGGACCAGCTTAAGGGCTTGAAGTCATGCCATACTGGAATCAATAGAAATGTG
|
|
GGGTACAAGATACCACTAACGATGCTGATGAAGCGCTCCGTGTTCCCTGCGATGACAGAC
|
|
CGCAGCATCTCTCCTAAAGAGAACGAGCTGAAGGCTCTCTCGACGTTCTTCAGCAAGTCC
|
|
TGCATCGTCGGCCAGTGGTCGCCTGACCCGAAGACCAACACTTTCTGGAAGTCCCAATCC
|
|
AGCAAGCTATGCTCCATGTGCGAGGACCCTGCCAAGTGCGACTACCCCGACAACTACAGC
|
|
GGCTACGAGGGCGCGCTGCGCTGCCTGGCGCACAACGGCGGCGACGTGGCCTTCACTAAG
|
|
GTCATCTATGTGCGGAAGTTCTTTGGGCTCCCAGTAGGCACAAGCCCGGCGACTCCTTCT
|
|
TCTGAGAACCCGGACAACTTCGCGTACCTTTGCGCGGACGGGTCCAAGGTCCCTATCAGA
|
|
GGAAAGGCATGTTCTTGGGCCGCAAGACCGTGGCAGGGGTTGTTGGGACATCAGGACGTT
|
|
CTGGCCAAATTGTCGCCTTTGAGGGAGAAGATTAAGCAGCTGTCTAGAGCTGGAGCAGAA
|
|
TCGAAGCCGGAGTGGTTCACCAACGTTCTAGGCCTCTCTGAAAAGATCCACTTGGTCGCC
|
|
GACAACATTCCCATTCGTCCCGTCGACTATCTGCAGAAGGCCAACTACACTGAGGTCATC
|
|
GAGAGAGGGCACGGCCCGCCTGAACCTGTTGTGAGACTCTGCGTGACGAGCTCGGTGGCG
|
|
CTGGCGAAATGCCGCGCCATGTCCGTGTTCGCCTTCAGTAGAGACATCCGCCCCCGGCTG
|
|
GACTGTGTGCAAGAGGCTTCGGAAAGCGATTGCTTGAAAAGTGTCCAAGACAATGGCTCA
|
|
GACCTGGCGTCAGTAGACGACATGCGGGTAGCGTCAGCATCCAACAAGTACAACCTACAT
|
|
CCAGTATTCCACGAGGTATATGGAGTCAGCAAGACCCCTAACTATGCGGTAGCTGTCGTC
|
|
AAGAAGAATACTCAGTATGGAAAGATTGAGGATTTGAGGGGAAACGGTCCTGTCACAATC
|
|
CTTTATGGAAGCTTCAGTGGCTTTGATGCCCCTCTGTACTACCTTATTAATAAGAAAATC
|
|
ATAGGCACTGAACAGTGCCTGAAAAAGCTTGGAGAATTTTTCGCAGCCGGATCTTGCTTA
|
|
CCTGGAGTAGGCAAATTAGAGAACAACCCTACAGGAGATAATGTCGATAATCTGAAGAAA
|
|
CAATGTTCTGGAGACAACAGCCCAATAAAATGCTTACAAGAAGACAAAGGAGACATAGCA
|
|
TTTGTGTCAAGTGCTGACCTGAAAAACCTGGATGCCTCTCAATATGAGCTGCTCTGTCTA
|
|
AACAGAGAGAACGGTGGGCGAGACTCAATAACCAACTACGCTACATGCAACATTGCCATG
|
|
GCCCCATCCCGAACCTGGCTCTCAGCTAAAGACTTCCTGTCCGATGTGTCCATAGCACAC
|
|
ACTCCGCTGAGCTTAGCACAACTACTGGATACCAGAAAGGATCTGTTTAACATTTACGGA
|
|
GAGTTTTTGAAGAATAATAATGTTATTTTTAATAATGCTGCCACTGGACTGGCCACAACA
|
|
GAAAAGATGGACTTTGAAAAGTTCAAGGCAATCCATGATGTTATCTCATCTTGTGGTGTC
|
|
GCATAA
|
|
>P. xylostella-Transferrin (PxTrs); BAF36848.1
|
(SEQ ID NO: 85)
|
ATGCTGCTTAGGACGATACATTTGTTGTTAATTGTTTGTTGTGCGTGGTGCTATGAAGTG
|
|
CCTCCGGCTAAATTGGAAGCTATTTATCCAGCTGGCTTGCGAGTGTCAATACCCGACGAT
|
|
GGCTTCTCGCTATTCGCCTTCCACGGCAAGTTGAACGAGGAGATGGAGGGCCTGGAGGCG
|
|
GGCCACTGGTCCAGAGACATCACCAGACCCAAGAACAACCGCTGGGTCTTCAGCGATAAA
|
|
CAGGCCAGGCTCAAGATAGGGGACAAAGTGTTCTTCTGGACGTATGTTATCAAGAACGGA
|
|
CTCGGGTACCGACAGGATGACGGGGTGTGGACTGTTGAAGGATTCGTCGACGTCGAAGGC
|
|
AACCCGGTTGACCCCGCGAATGGACAACCCATCTCAGCGCCGACCAGACCTCCAACCCAA
|
|
CCAGGCCGGGTGCCAAATGTCCCCATGCCGTGTGACATCTCAGTCACCACGGCATCAGTG
|
|
CCAGGGTACATCTGCAAGGGACAGCTGCTCTTTGAAGACAACTTCAATGGGGCTCTGGAG
|
|
AAAGGAAAGATATGGACGCCGGAGATTATGATGCCTGATGAACCGGATTACCCGTTCAAC
|
|
ATCTACCTGAACGACAGGAACCTGCGCGTGAGGGACGGCCGGCTGTCTATCAAGCCCGTC
|
|
ACGCTCGAGTCCAAGTACGGGGAGGAGTTCCTGGCCAAACTAGACTTGTCTGCCAGGTGT
|
|
ACTGGTAACGTGGGTACTACCCAATGCAGCAGAGAGTCCATTGGGGCCCAGATCATACCT
|
|
CCGATAATCACAGCCAAGGTTACCACCAAGAACAAGTTCAGCTTCAAGTATGGAAGGATT
|
|
GAAGTGAGCGCCAGAATGCCGCGCGGTGATTGGTTGATTCCAGATATTCTGCTGGAGCCG
|
|
AAAGAAAACCTTTACGGAGTACGCAATTACGCGTCAGGTCTACTCAGCATAGCCTCAGTC
|
|
AGAGGAAACACTGCTTACTCGAAGACCCTCAAAGGAGGCCCCATACTGTGTGACAAGGAA
|
|
CCGCAGAGAAGTGCCAAGTTGAGCGAAAAAGTTGGATATGACCATTGGAATAAAGCCTTC
|
|
CATAACTACACCATGATTTGGGCACCAAGTGGCATCACCATGCTGGTGGACGGCGAGCAG
|
|
TACGGGGACATCCGTCCCGGCGACGGCTTCAGCCAGGACCCGGCGGTGAGCAGCGTGGTG
|
|
GCCGCGCCGCAGTGGCTGAAGGGCACCAGCATGGCGCCCTTTGATGTTATGTTCTACATA
|
|
TCCCTTGGTCTCCGCGTGGGCGGAGTGAACGACTTCCCCGACACTCCTGAGAAGCCGTGG
|
|
AAGAACAAGGCCACTAAAGCCATGCTGAATTTCTGGAACGCCCGGGAACAGTGGCAGAGC
|
|
AGCTGGTTTGAGGACACCACTGCACTCCTCATAGACTATGTCAGGGTTTATGCGCTGTGA
|
|
>P. xylostella-Gloverin (PxGlv); ACM69342.1
|
(SEQ ID NO: 86)
|
ATGTACCGATTTGCAGTTATTTTATCTGTAGTCGCCGCGTGTGCCGTGGCTCAAGTTTCT
|
|
CTACCTCCTGGATATAATGATAAATACCCAGGCTTCTACAAATACTCCAAGCTAGCCCGG
|
|
CATCCGCGACAAGTGACGTGGGACAAGAATGTCGGCCGTGGGAAGGTGTTCGGCACCCTC
|
|
GGCGGCACTGACGATAGTCTCTATGGTAAGGCGGGCTACCGTCAGGACATCTTCAACGAC
|
|
CACCGCGGCCACCTGCAGGGTGAGGCTTCTGGCACCAGGGTACTCAGTCCCTACGGAGAC
|
|
AGCAGTCACCTGGGCGGTAGACTCGACTATAGCAACAAGCACGCCAACGCCAACCTGGAT
|
|
GTCAGCAAGCGGATCGGAGGCGTCACTAGTTGGCAAGCAGAAGGCAAGGCTAGATGGCCG
|
|
ATTGGCAAGAACAGTGAGCTATCAGCCGGCGGAATGATCAGACAAGACCACTTCGGCCAC
|
|
GGGAGACCAGACTACGGAGTCGTCGGTGGGTTTAAATCTAGGTTTTAA
|
|
>P. xylostella-Chitin synthase 1 (PxCHS1); KX420688.1
|
(SEQ ID NO: 87)
|
ATGGCGACGTCGGGGGGAGTGCGGGGGCGGCGGGAGGAGGGCAGCGACAACTCGGACGAC
|
|
GAGCTGACCCCGCTCCAGCAGGAGATCTACGGCGGCAGCCAACGCACAGTACAAGAAACA
|
|
AAAGGATGGGATGTGTTCCGAGAGATCCCGCCGAAGCAGGACAGCGGGTCGATGGAGAGC
|
|
CAGCGCTGCCTGGAGATCACCGTGCGCATCATGAAGATCCTGGCCTACCTGGTGACCTTC
|
|
GTCGTGGTGCTGGGTTCAGGGGTGCTGGCCAAGGGGTCTGTGCTCTTCATGACCTCGCAG
|
|
CTGAAGAAAGATAGAAGACTGGCGTATTGTAATAAGAATTTAGGTAGAGATAAGCAGTTT
|
|
ATAGTGACGTTGCCGGACGAGGAGCGGGTGGCGTGGATGTGGGCGCTGTTCATCGCATTT
|
|
ATGGTCCCCGAGATCGGGACCCTTATCAGATCTGTCCGGATATGCTTCTTCAAGTCCTCC
|
|
AGAACTCCAAGCAGCGCTCAATTTATTGTGATTTTTGTATCGGAATCTCTCCACACCATC
|
|
GGATTGGCGCTTTTGATGTTCAAAGTGTTGCCAGAAATCGACGTGGTCAAAGGAGCTATG
|
|
ATAACGAATTGCCTCTGCATCATTCCAGCCATTCTGGGGCTATTGTCTAGAAACTCAAGG
|
|
GACTCGAAAAGGTTCATGAAAGTTATAGTAGACATGGCTGCGATTGGGGCTCAAGTCACA
|
|
GGATTCATATTATGGCCACTGCTGGAGAATAAGCCGGTCTTATGGCTGATACCGATCTCG
|
|
TCAATCTGCATATCACTAGGCTGGTGGGAGAACTATGTCACTCGGCAGAGTCCAATCGGT
|
|
ATAATCAAGAGCCTCGGCCGCCTCAAGGAGGAGCTGAACCACACGCGCTACTACACGTAC
|
|
CGCTTCATCTCCGTGTGGAAGATCCTGCTGTTCCTCATGTGCATCCTCACCAGCATCTGG
|
|
CTGGACGGCGACGAGCCCGGCATGTTCTTCCAGCTCTTCAGCGAGGGGTTCGGACCGCAT
|
|
AACATTGTTGTCGAAGAGATCCAACTCCAGACGGGAGGCACAATGATCCCGGACTTAGCC
|
|
AACGCCACACTAACCGGAGACTCAGTGGAGGTGGCAGCGGCCTACAACTCTGCCGTCTAC
|
|
GTCATCCTCATACAAGTGTTTGCCGCTTACTTCTGCTACATATTCGGGAAGTTCGCCAGC
|
|
AAGATCCTGATCCAAGGGTTCAGTTACGCCTTCCCGATCAACTTGGTCATACCGCTGGTC
|
|
GTGAACTTCTTGATTGCTGCTTGCGGTATCCGGAATGGTGATACGTGCTGGTTCCATGGG
|
|
ACTATTCCGGATTATCTGTTCTTTGAGAGCCCACCAGTGTACTCACTAAGCGACTTCATA
|
|
TCCCGCCAAATGGCATGGGTTTGGCTGCTATGGCTTCTGTCTCAGACGTGGATCACCATC
|
|
CACATCTGGACGCCCAAGGCCGAGCGTCTGGCGTCCACGGAGAAACTGTTCGTACTGCCC
|
|
ATGTATAACGGACTGCTCATCGACCAAAGCATGGCGCTAAATCGTAAGAGAGATGACCAG
|
|
AAGGATGTTAAGACTGAGGATCTGGCCGAAATCGAAAAGGAGAAGGGCGACGAGTACTAC
|
|
GAAACTATTTCTGTGCACACCGACAACACTGGGTCCTCTCCCAGAGCCGTAAAATCTTCC
|
|
GATCAGATCACAAGAATCTACGCATGCGCGACGATGTGGCACGAGACGAAGGACGAGATG
|
|
ATGGAGTTCCTCAAGTCCATCCTGCGGCCGGACGAGGACCAGTGCGCGCGCCGCGTCGCG
|
|
CAGAAGTACCTCAGAGTCGTGGACCCCGACTACTACGAGTTTGAAACCCACATATTCTTG
|
|
GACGACGCTTTCGAAATATCGGACCACAGTGACGACGATTCCCAGGTGAATCGATTCGTG
|
|
AAACTGTTGGTGGACACGATTGACGAGGCTGCGTCAGAGGTGCACCAGACTAATATTCGT
|
|
ATGAGGCCGCCGAAGAAATTACCTGCCCCGTACGGGGGACGGCTGACCTGGGTGCTGCCT
|
|
GGGAAGACCAAGATGATCTGCCACTTGAAGGACAAGGCCAAGATTCGACACAGGAAGCGA
|
|
TGGTCTCAGGTGATGTACATGTACTACCTGCTCGGCCACCGTCTCATGGAGCTGCCCATC
|
|
TCCGTGGACCGCAAGGAGGTGATGGCTGAGAACACGTACCTCCTGACACTGGACGGAGAC
|
|
ATCGACTTCCAACCGCACGCTGTCAGGCTGCTGATTGATTTGATGAAGAAGAACAAGAAC
|
|
CTGGGCGCTGCTTGCGGACGCATCCATCCTGTTGGCTCTGGGCCAATGGTGTGGTACCAG
|
|
ATGTTCGAGTACGCGATCGGTCATTGGCTGCAGAAGGCGACGGAACACATGATTGGCTGC
|
|
GTGCTGTGTAGCCCCGGATGCTTCTCGCTCTTCAGAGGGAAGGCTCTCATGGACGACAAC
|
|
GTCATGAAGAAATACACGCTGCGATCCGACGAGGCTAGGCATTACGTGCAGTACGATCAA
|
|
GGGGAGGATCGTTGGTTATGCACATTGCTGTTACAACGAGGATACCGAGTAGAGTACTCA
|
|
GCCGCCTCCGACGCCTACACGCACTGCCCTGAAGGTTTCAGCGAGTTCTATAACCAGCGT
|
|
CGTCGCTGGGTACCCTCCACTATCGCCAACATCATGGACTTGCTTGCCGACTACAAACAT
|
|
ACCATCAAAATCAACGACAATATCTCCACACCGTACATCGCTTACCAGATGATGTTGATT
|
|
GGCGGTACGATCTTGGGCCCCGGAACTATATTCCTTATGTTGGTGGGAGCCTTCGTGGCT
|
|
GCGTTTAGAATCGACAACTGGACTTCATTCGAATACAACCTCTACCCGATATTGATCTTC
|
|
ATGTTCGTTTGTTTCACGATGAAATCTGAGATACAGTTACTGGTGGCACAAATACTCTCT
|
|
ACGGCATATGCAATGATAATGATGGCGGTAATCGTGGGTACAGCTTTACAATTGGGCGAG
|
|
GACGGAATAGGTTCGCCATCGGCTATCTTCTTGATATCACTGTCAAGTTCATTCTTCATA
|
|
GCCGCTTGTTTGCATCCTCAAGAGTTTTGGTGTATCGTCCCCGGTATCATTTACCTTCTG
|
|
TCTATTCCTTCTATGTATCTCCTGTTGATTTTGTATTCGACTATAAATCTTAACGTCGTA
|
|
TCTTGGGGTACCCGAGAGGTGCAGGTTAAGAAAACTAAGAAGGAAATCGAGCAAGAAAAG
|
|
AAAGAAGCGGAAGACGCAAAGAAGAGTGCGAAACAGAAGTCTTTACTCGGGTTCTTGCAA
|
|
GGAGCAAACCAGAATGAGGATGAAGGGTCAATAGAGTTCTCATTCGCGGGTCTATTCAAG
|
|
TGCATGTTGTGCACACACCCTAAAGGCAACGAGGAAAAGGTGCAACTGTTGCATATCGCA
|
|
TCTACACTTGACAAGCTCGAGAAGAAACTGGAAACTGTTGAAAAGACCCTCGACCCTCAC
|
|
GGCCTCCACAGAGGTAGGAAGCTGTCGATAGGCCACCGCGGCAGTACCAACGGAGACCAC
|
|
GGGCTGGACGCCCTGGCTGAAGACAATGAGGACCACAACCTCGACTCTGACACCGACACT
|
|
CTATCCACGGCACCTAGAGAACAAAGAGACGAATTAATAAATCCATACTGGATTGAGGAC
|
|
CCAGAATTAAAGAAGGGAGAGGTAGACTTCTTGAGTCAGTCCGAGATTCACTTCTGGAAG
|
|
GATCTGATTGATAAGTATCTGTACCCGATCGATGCCAATAAGGAGGAGCAGGCCCGTATC
|
|
TCGCACGACCTGAAAGAGCTGCGAAACTCATCCGTCTTTTCCTTCTTTATGATCAATGCC
|
|
CTCTTTGTTCTCATCGTATTCTTGCTGCAACTGAACAAGGACAACCTCCACATAAAGTGG
|
|
CCCTTCGGAGTCAAAACTAACATTACGTATGATGAGGTGACGCAAGAGGTGCTGATCTCC
|
|
AAGGATACCTGCAACTAGAGCCTATTGGTCTGGTGTTCGTGTTCTTTTTCGCATTGATTT
|
|
TAGTCATCCAGTTCACTGCCATGTTGTTCCATCGATTCGGAACTTTGTCGCATATATTAT
|
|
CGTCTACGGAACTGAACTGGTTCTGCAATAAGAAGGCGGAAGACTTATCTCAAGACGCAC
|
|
TGCTAGATAAGAATGCGATAGCAATAGTGAAGGATCTCCAGAAACTAAACGGGCTCGATG
|
|
ACGGGTATGACAATGACTCGGGGTCGGGCCCGCACAATGTGGGAAGGAGAAAGACGATAC
|
|
ACAACCTGGAGAAAGCGAGACAGAAGAAGAGGAACATAGGAACGCTCGACGTCGCTTTCA
|
|
AGAAGCGATTCTTCAACATGAACGCTAATGAAGGACCAGGAACACCAGTTCTGAACCGCA
|
|
AGATGACGTTGCGAAGAGAGACGTTGAAGGCGTTGGAAACGAGGAGGAATTCTGTGATGG
|
|
CCGAACGAAGGAAGTCGCAAATGCAAACACTTGGAGCTAACAACGAATATGGAGTCACTG
|
|
GAATCTTAAACAACAACCCAGCGGTGATGCCGCGCCACCGGCCGTCGACAGCCAACATTT
|
|
CGGTCAAGGACGTCTTCGCGGAACCCAACGGGGGACAAGTGAACCGAGGGTACGAGACCA
|
|
CGCACGGCGACGAGGGAGACGGCAACTCCATCAGACTGCAGCCGAGAACCAACCAGGTC
|
|
TCCTTCCAGGGGAGATACCAATAA
|
|
>P. xylostella-Beta tubulin (PxBTUB); KX420688.1
|
(SEQ ID NO: 88)
|
GCGGCAGCCAGCAGTACCGCGCGCTGACCGTGCCCGAGCTCACACAGCAGATGTTCGACG
|
|
CCAAGAACATGATGGCGGCTTGCGACCCGCGCCACGGCCGCTACCTCACCGTGGCCGCCA
|
|
TCTTCCGCGGACGCATGTCCATGAAGGAGGTCGACGAGCAAATGTTGAACATCCAGAACA
|
|
AGAACAGCAGCTACTTCGTCGAATGGATCCCGAACAACGTCAAAACGGCCGTGTGCGACA
|
|
TACCGCCTCGTGGACTGAAGATGTCTGCCACCTTTATCGGGAACACGACAGCAATCCAAG
|
|
AGCTCTTCAAGAGGATTTCTGAGCAGTTCACTGCTATGTTCAGGAGGGAAGCGTTCCTCC
|
|
ACTGGTATACTGGTGAAGGCATGGACGAGATGGAGTTCACAGAGGCGGAGAGCAACATGA
|
|
ACGACCTGGTCTCCGAGTACCAGCAGTACCAGGACGCCACGGCTGAAGACGAGGGAGAAT
|
|
TCGACGAGGATATTGAAGACGAGTGA
|
|
>S. frugiperda-Peptidoglycan recognition protein 1 (SfPGRP1); rep_c7951
|
(SEQ ID NO: 89)
|
GCATTAACATCTCAGGATTTGATTCGAAAGTAAGGTCTGAATTTAGTCCTTACATTTACT
|
|
TAAAATTAGGTCCTTTTTGGTTTGTACTGAAATGAAAGTTTTTCTGTTCTTGGTCTTAAT
|
|
TGTGAAGATAATGGCTGAGGCAAAAGGAGATTGTGATGTGATCCCGATTACGCAGTGGGG
|
|
AGATTCACCTCTTAAAAGGGAGGATYCTCTTCCAAATCCAGTGAATATTGTTGTCGTCCA
|
|
AYACRCTGTGGTACCGGAGTGTAACAATGATGAAGAGTGTGAGAAAGCAGCCAMTGGAAT
|
|
CAGGAGCTACCACATTAACAAACGTGGATTCACTGATATAGGACAATCGTTCCTGATTGG
|
|
TGGAAACGGGAGAGTTTATGAAGGAGCCGGCTGGCATCACGTTGGGGCCCATACTTTGGG
|
|
ATACAATGCAAGATCTGTGGGGATCTCCTTCATTGGCGATTTTAGAACAAAATTACCAAC
|
|
ACCCGAAGCACTGAAAGCCTTCAACAGTCTCCTGGAATGTGGAGTCACGAACAATTATCT
|
|
GTCAAAGGACTATCACCTGGTGGCCCATAGTCAGCTCTCTATGACTGACAGTCCYGGAGA
|
|
CATGYTGAGGAAGCAGGTGGAATCGTGGCCTCMTTGGCTGGATAATGCCAAAGACATACT
|
|
TAAGTAGAARAAGACTAAACGCCGTACTTTGAGCCATTTAATGGTTACTTAACCCAGTCC
|
|
TTAGCAATTTGATACAAGGCCAATGTCTCTAAGGGCGGCAGTAAAGGTCAAAACACATTT
|
|
AATGAGTGTGTTTAAGATTTTGCTAGTGAAAATTGTTTTGAAGTACGTATTTGATGTAAG
|
|
TGATGATATCAGTACCCTTAGTATGAGTTTGCTTTACGTTCCACGAGATGGAAACGAGAG
|
|
CGCGTTCGGCGCTCTGATTGGTTCGTTCATTCATGCCGGCCAATCATAGCGCCGAATGGG
|
|
CTCTCATTTCGTTTTCGTTCAACGTAAAGTAAATTCGTACTAAGGGTACTGACTTTAAAA
|
|
TAAGTTACCAAAAAGAGTATTACCTATTTACATTATTTTATTTATTTTAGGTGTATTGTA
|
|
ATTCAAGTATTAAATTAATTAGTGTAGATTAATKSCATGCATTTTATATTTGATTTCATT
|
|
GAATAA
|
|
S. frugiperda-Attacin (SfAtta); rep_c9395
|
(SEQ ID NO: 90)
|
ATCATTCCAGATCCTCTCTCATACATCCAACACTTGAAGCAAACCAATCCACATACATTA
|
|
TAGCAACATGTTCGCTCTCAAGTTGGTACTAGCTGCAGTGCTGGTGGTCGCAAGCGCCAG
|
|
ACATCTACCACAGGACCACTCAACGTACGACCAAGTACAACTCCTCGGGTTCGACGAAGA
|
|
TGGACGACCAGTGTTTGAGCACGAAGACTTACTCCCAGAACTAGAGGAGTCCTACCAGCC
|
|
AGAGCACCTGGCGAGGACTCGCAGACAGGCGCAGGGCAGCGTCACCCTCAACTCCGACGG
|
|
CGGCATAGGCCTGGGCGCTAAGATCCCGCTCGCACACAACGACAAGAATGTGGTGAGCGC
|
|
CATCGGCTCCATGGACTTCAACAACAAGTTGCAGCCTGCTTCCAAGGGCTTCGGTCTGGC
|
|
TCTGGACAACGTCAACGGGCACGGACTGACGGTGATGAAGGAAAGTATCCCCGGGTTCGG
|
|
GGACAGGCTGTCGGGCGCTGGCAAGCTGAACGTGTTCCACAACGACAACCACAACGTGGC
|
|
CGTGACCGGCTCTCTCGCCAGGAACATGCCCAGCATCCCGAACGTGCCCAACTTCAACAC
|
|
GTACGGCGGGGGCGTCGACTACATGTACAAGAACAAGGTGGGAGCGTCTCTGGGCATGGC
|
|
CAGTACTCCGTTCTTGGACCGCAAGGACTACTCCGCGATGGGCAACCTGAACCTGTTCCG
|
|
CAGCCCGACCACTACCGTGGACTTCAGCGGCGGCTTTAAGAAGTTCGAATCTCCCTTCAT
|
|
GAGCAGCGGCTGGAAGCCTAACTTCGGCCTTACTTTCGGCAGATCTTTCTAGATATATTT
|
|
TGTAATCTAAATTTAACTTTAACTTTGTTGTATAATATTTTGTCGAATTAAGATCAGTAT
|
|
TGTTCATACTAATATTATATTATCAGTGTTTCTTATAAATTAA
|
|
S. frugiperda-CtypeLectin15 (SfCTL15); Joint2_rep_c488
|
(SEQ ID NO: 91)
|
AGTTTTCGTGCTTAGCACACAGAGCGCCGAACGCGCTCTCGTTTCAATTACTTTAAACGT
|
|
AAAGCAAACTCGCACTAAGGTTACTGTGACCTTTGTAAACATGTACAATGCAATACTATG
|
|
TTGTTATTTTCGATACAATCATATAAAAGACAACGTTTAAAAAAAAAGCATAGCACAGAC
|
|
CACAGTACAAGTATCGAGACCAAACTTTTGTTAAAACTTATTTCGTTCTGTGCAGCAACT
|
|
CTAATGCGAATAATGTGCAAATTATAATAAATATGTTTTGTATATAAACATGTGTTATCT
|
|
CAAGTTCAAGACATTCCGGCTCCTACAGTCAACAGATACAGTGCACAAAAATGTTAAAAA
|
|
TATATTTAATTTGTTTGTCTTACTTGTTCATGTTAAACTTAGACAGGGCACAATGCACCC
|
|
CCCAGTATTGGTTCAACATGGATGCGAATGGTTGGCTGAAAGTGCACACGATACCCGCCA
|
|
CGTGGGAGGAAGCATTCCTTCGGTGTCACTATGAAGGTGCGGTACTTGCGTCCCCCTTGA
|
|
CGCAACAACTGAGTAAGGCTCTTMAAAACAAGTTTGCAGKCWTCGGTAACCCATCAATCC
|
|
ACTTGGGGACACATGATTTGTACTCCASTGGTTACTACTTTTCTGTAGAAGGAGTACCAA
|
|
TGGACAGCTTGGTGCTGAAATGGAGTAATATCAGAGGTACGGGCGAYTGCCTGGCGATGT
|
|
CACGCGACGGGGAAGCATTTTTCACGAAATGCGAGCAACCTCGACCCTACATCTGCTACA
|
|
AGAAGCTGGACAATCTGACGATGAACATCTGTGGAACATTYGATGACGCKTATCAATTCT
|
|
ACGATAAGACTGGCAGCTGCTATAAGAGACACAACGYCTATCAGACATGGCCTGACGCGT
|
|
TCAAGATATGCGCTGCCGAGGGAGGSTACCTGGTGATCCTGAACGATGACACAGAGGCCG
|
|
CCATCATCAAGGATATGTTCCCCGTACGGCCAGGAAAGCCCAACGAATGGGAGAACTTCC
|
|
ACGTGGGKCTGCGGGCATGGGGACCGGAACGTACTTGGATCACTATTCATGGAGAAAAAA
|
|
TTGATGATGTATTCCATAATTGGAACCCGGGACAGCCGGACAACTACAAGGGAGTCCAGG
|
|
ACACTGGCGCTTTCCTTAGARMAGGCACTTTAGACGATCATGCCGCTGGTGACAAATGTA
|
|
TGTTTGTCTGTGAGAAGGATCCTAAAGTAAAACGCTTCGAAGAGYTACCCGAAGGATTGG
|
|
CMGAAGTTTTAGGACAATAGGCCGCTAGTCAAATATTGTTCATATACCTWAGTTTTAATT
|
|
ATGTAAAAATAATARTCGATTGCAGAATTTAATAAAATTTAAACTAAAAAAAAAAAAAAA
|
|
AAAAAGGTMAAAACATGTC
|
|
S. frugiperda-Galectin4 (SfGlc4); rep_c2653
|
(SEQ ID NO: 92)
|
GCCTTGTAGTTCGACAGTCAAATCCAACGGGTGTCAGAAACAATTTCCGTTTTTCCGGCT
|
|
ATTGATCGTCATATAAATAACTCCGAAGGAAAAATGACTACAATCGACAATCCGACAGTA
|
|
CCGTTCACGAGACCCATTCCTGGGCATCYGCTCCCCGGCCGCAAAATGGTCGTTAAGGGT
|
|
GCAATCTCTCCCAGATCAGATAGGTTCTCAATAAACTTGAAATGTGGTAGCGAGGACATC
|
|
GCTTTCCACTTCAACCCTCGCTTCAGTGAGCAGAAAATAGTTCGCAACTCTTATATTTCT
|
|
GGCAAGTGGGGTCATGAGGAGATCAGTGGAGGCATGCCGTTGGTAAGGGGAGAGCATTTT
|
|
GAAGCGCAATTTGAATGCAATGAAGATAATTTTTCGGTGGAGTTGAACGGGAAACATTTC
|
|
TGCAATTACTCTTATCGCATCCCAATCCATAAGATCACCCACGTCAACGTGGACGGTGAC
|
|
GTCACGATAAGTCAGATCACCTTCGTGGACGCCTGAGCCATCGCCCGATCTTACAATGGT
|
|
ACTTTTTTTTTACTTATGAACTAATGCTGGAAACCAAACTTCTTTATTCAAATATTTTTC
|
|
TTTTGTCTTTATGACTATCAGTGTTTTTATTGCAATAAAAAG
|
|
S. frugiperda-Lysozyme (SfLys); rep_c18992
|
(SEQ ID NO: 93)
|
ATCAGTGTGGTGTCTTCAACCCAAGTGCATTGTATTGCTTGGTAAATAATAACTGASAAC
|
|
AAAAATCTTGGTTATTGCTTGAACAGGTTTCGCCTATCAATTAGCCGAATATTGTTACCC
|
|
TTGACACGCAATAATTGGTTACTCGATTAAAGCTTGAAGAGGTAAAGTGCCGAAATGACG
|
|
CGCGCCATTCTGTTTGTTGTTGTTTTATGCTTTATTGCAAAATGCTATGGAAAAACATTC
|
|
ACKGAATGTGAATTAGTTCAGGAGCTAAGAAGGCAAGGATTTCCTGAACATGAGCTTAAA
|
|
GATTGGGTRTGYCTGATCGAAGCGGAGAGTTCCAAACGAACCAACGCCATTGGTAACGGC
|
|
AATTCAGATGGCTCTCTCGACTATGGCTTATTCCAAATCAAATAACCGCTACTGGTGCAG
|
|
CGAYGGTGACCATCCAGGCAAGGGATGCAACGATACCGCTAGTAAAGATCTGTTGCTGGA
|
|
TGACATCACAATAGCGTCTCAGTGCGCTAAGACCATTTTCGGTGTCCACGGATTTAACGC
|
|
CTGGGTCGCATGGGTGAACAAATGCAAAGGAAGGACCTTACCYAACCTTCACTGTTAGTT
|
|
ATTTATTGAGAAAATGTAACTAAGGTATATGGTTACTTTGTACCTAAATATAGGTATTAG
|
|
GCATATATTGTCCACTCTCATCAAATTTTTACTTTTATATCAGT
|
|
S. frugiperda-Hemolymph proteinase 10 (SfHP10); c12881
|
(SEQ ID NO: 94)
|
ATTCGCTGTACGCACCTCGGATTGTGCGGTCAACTWTACAAGGCTCGTACCTTGCAGTTG
|
|
AACCGACAATCTATTCCTAAAGCCTTTTTAAGGTCAGGAAAAATAGTTCCTACATCTAAA
|
|
TGCAGTAGAATTTGCGAAACGAATTTAAATAAAAATGGCGTCGATTGTGTTTGTGATTTT
|
|
GTGTGTTACCGTCGCTGCGGTGAAAAGCGCGATTTTAAACCCGTGGAGTAAAGTTGAGGC
|
|
CAACAAATGTGGTGTAGAAGCCAGTACTAACTTGGTCCATCACAATCCATGGTTGGTCTA
|
|
CATCGAGTATTGGCGTGGAAACTCAGATACTGAGATCCGATGCGCCGGTACTTTAATCGA
|
|
CAGCAAACATGTCGTCACAGCTGCCCACTGCGTTAGGACTCTGAAGTTTAGTCATTTGAT
|
|
CGCCCGTCTTGGCGAATACGACGTAAATTCTAAGGAGGACTGCGTTCAGGGCGTGTGTGC
|
|
CGATCCCATCGTCAGAATCAAGGTGGCTGAGATCATCGTGCATCCTAACTACAGCAACCG
|
|
GGAACATGACATTGCAATCTTAAGGCTGGAGGAGGAAGCTCCTTATACCGATTTCACTCC
|
|
GGCCCATCTGTCTGCCTTCTGGTGATCTCGCGGAAGACACCCAGTTCTTAGCAGCCGGCT
|
|
GGGGTGARATCCCCACGAAAGGCTTCTTCAGCCACGTGAAGAAAATCGTCCCCTACGTAC
|
|
TGGAATCGAGAGAGATGCCAAAAGGTGTACCAGTACAATTATATCCCGGAGAACGTGATC
|
|
TGTGCCGGT
|
|
S. frugiperda-Trypsin like serine protease (SfTSP); rep_c48453
|
(SEQ ID NO: 95)
|
CAAGTAGCAACAAAATGCGTGTCCTCGCTTGCTTGGCCCTTCTCTTAGCTGTGGTAGCAG
|
|
CCGTCCCCTCCAATCCCCAGAGGATTGTGGGTGGTTCGGTCACCACCATTGACCGGTACC
|
|
CCACCATTGCATCCCTGCTGTACTCGTGGAACTTGAGTTCCTACTGGCAGGCGTGCGGTG
|
|
GTTCCATCTTGAACAACCGTGCCATCCTTACTGCTGCCCACTGCACAGTTGGTGACGCCG
|
|
CCAACAGATGGAGAATCCGTCTTGGCTCCACCTGGGCCAACAGCGGTGGTGTCGTTCACA
|
|
ACGTCAACACTAACATCGTCCACCCCTCATACAACTCTGCAACTTTGAACAACGACATCG
|
|
CTATCCTCCGCTCCGCCACCACCTTCTCCTTCAACAACAATGTTCAGGCTGCCTCCATTG
|
|
CTGGTGCCAACTACTTGCCCGGTGACAACACCGCCGCCTGGGCCGCTGGATGGGGAACTA
|
|
CCTCCGCTGGTGGCTCTAGCTCTGAGCAGCTCCATCACGTTGAGCTGCGCATCATCAACC
|
|
AGGCTACTTGCAAAAACAATTACGCTACCCGCGGTATCACCATCACCTACAACATGTTGT
|
|
GCTCTGGCTGGCCCACCGGTGGTCGCGACCAGTGCCAGGGTGACTCTGGTGGTCCTCTCT
|
|
ACCACAACGGCATCGTTGTTGGTGTCTGCTCTTTCGGTATTGGCTGTGCTCAGGCTGCCT
|
|
TCCCCGGTGTCAACGCTCGTGTATCCCGCTACACTGCCTGGATCTCTTCCAACGCATAAG
|
|
ATGTTACTTGGTGCTAATAATATTTTTTTGTAATAAAATGTTACTTTTATCCTCC
|
|
S. frugiperda-C Type Lectin 6 (SfCTL6); Joint2_rep_c448
|
(SEQ ID NO: 96)
|
AACAGTTTTCTATTGGCAGTCAAAGACTTCAGTCGAAAAATAATCCTCATCAGAGTCGTG
|
|
AAGCAAGGTGCCCAAAATATAATGTAACCTAGATACCTATTAATAAATTATTTGTCAACC
|
|
AAAACGTTACGTTCAAAGTCCTTAAAATCAAAATATCTTATGATTAGTTTTGATTTAAAA
|
|
ATAGAGGTTCGAAATCGCCAACCCAAATAGGTTTAGTTTACGATTCAGGAAAAATCCTAA
|
|
CGTAGGGAAACATTATTTTACAAGACTTTTGGCTTAAAAACTTTGAGAACCAATGTCAAA
|
|
TTTGATAATAACTAATGAGGTATAAAAGCTTGATCCTATTAGGACTTATTTTCATAACAC
|
|
CATCGAGTTTGTATTTAATRRAGACGTGKGTTAACTAACAACATGAAGACCGGTGTAAAA
|
|
TATTCTGTTMTTTGGATATTCTCTCTATTYTGCTATATAGAGGCAACATTTCGTTGTGAC
|
|
TACACGTACAGCAAGGAAGCGAAGGGCTGGTTCAAACATGTGGTGATACCAGCTACTTGG
|
|
GCTGACGCACGWCTGCACTGCACGTTGGAAGGTGCAACGCTGGCTTCTCCACTCAACCAG
|
|
GCTATMAGTAATGAGATGCAGTCCMTCCTGGCRAACCTCTCGGCGCTGCAATCAGAAGTC
|
|
TTCACTGGAATTCACRCGACTKTTTCACGRMRCAACTTATATCATACYATYGAAGGTATA
|
|
CCTCTTAGTAAAATTCCATTAGATTGGGCAACAAATGAGCCAAATGGTGGGAGAGATGAA
|
|
AACTGTATCACGTTTAACTCCGATGGCCAAGCGGCAGACAGATCCTGTAARGAGACTCGA
|
|
CCTTACATCTGCTACCGACACACWACTAAAGTGACTGTGKCCAATGAATGTGGGACTGTA
|
|
GATCCTGAATACAATTTGGATAAAAGAACGGGCKCYTGCTATAAGTTCCACACRGTACCT
|
|
CGCACGTTCGAGCGTGCCAACTTCGCGTGTTCTGCTGAAGGTGGMCACCTTGCCATAATC
|
|
AACRGTGATRTCGAAGCTGCAGTACTGAAGGAACTCTTCGAAAGGAATCCACCTGCAAAG
|
|
ATGTTCGGTACTTTCTGGAAAGACGTTGCTTTCATTGGTTTCCATGACTGGGGTGAATAT
|
|
GGTGACTGGAGGACAATTCACGGTCAAACGCTAGTAGAGGCAGGATACAGCAAGTTTTCA
|
|
TCTGGAGAGCCAAATAATTCCTCGACGGGAGAATTCTGTGGTTCCATCTATCGGAATGGT
|
|
ATGCTCAACGACCTTTGGTGTGGGCATCCTAAACCATTCATCTGTGAGAAGGACCCGAAA
|
|
TATCCAGCCGTATGTTGTGTTACAGAATCAGAACCAGAATTGGACCCTACTCACTTCTTA
|
|
GAGTAATTCAAATTGGATCTTTTTTTATAATTCTACATCATTAGAAATATGATGTTTAGT
|
|
TGAATCTGCTTTTGAAGATTGATT
|
|
S. frugiperda-Serine protease homolog 13 (SfSph13); rep_c1904
|
(SEQ ID NO: 97)
|
GAAKAGTGTCAATTTATTTAATTGTCAAAATCGCGTTGAATGTAAGATTGCTATAGAAAT
|
|
TATTTGTAAAAACTTTCTCAAAAATTTAATTCTAAAATGTAAAGGAACCTAAAATCAGAT
|
|
ACCGATAACACATTTTGTAAATGGTTTAATATTGAAACGAAACTTCTAAACATTTTTGGT
|
|
GAAATACACATAATAATATAACTTCTTCGAAAACTAGGTAGATAGACTTCAACTCAGTTT
|
|
TTATTAGCGAGCTAGAAGATACAGAGATTATCTAAGATGGTGTGTGATGGTCCGGATCCT
|
|
CCAGAGAACAATCCTCACGAAATTGTTCCACCTCCTAGGAATGAATTGATAATGAATGGT
|
|
AATCAAGGGGATGACAGTGATGAAGAACATGAATATTTTGGCTATGAACCTTTGGCGCAA
|
|
GGTCCAGAACTAGCAGTCTCAGATCACGATAGTGATGATGACCCAGAGAGTGCTGAAACA
|
|
CCTCCAGCTGATGTTCCAAATATAGAGCCAATGGAAAATGTACTAAGCCGGGAAGTTTGG
|
|
AGTGCCCCGAGRCATACAGATGCTATACAAATGGATAATGAACGGGCTCAACAGGTGATG
|
|
AGAGCTATGGCAAATTTTGCTCTACCCCAGGCCTCAWTTCCAGAATGGGCTCAGAGCATC
|
|
TCTGAAGAACAATGGAAGCAAACTCTGAATGAACAAATAGAAAGATTGAAAAATAAAAGA
|
|
TAAACTAATTATATGTAGTATAATAATAATTAAGATTTAAGTGATAAAAATAACAATTAT
|
|
AACTTATATGTTTAAAAAATGTATATAAACTGTAAACTTTAAGCTTATTCACATTACTTT
|
|
AAATATAGAAAAAATATGTGTACCTATTTATTGTTTGGCTACATAATCCAATATAGATTA
|
|
AATTGCAAATGTTTAATGTAATTATTTAGTTGGATCAAAAATAACAGCACTAAAGGTCAC
|
|
TAGTTTAGTTCTTTCATTTCGAATGAAAAAGTAAAATGGAGAATCTGCATAGAAATTTTC
|
|
AGCTGACCGTGTTAATGTTCCACTTGTTGCGGCTACTGCTTCTGTTCCAAACTCATTAAT
|
|
TGTTAACTTTACATCATGAATTATGGAATCCACATGTATTCCAGGGTTGGGTAGACTGTC
|
|
CAAAATGTTTGTCCCATTTCCTTCGTTTTCTGAGTATCTGTCTGATTCTCCTTCAGATTT
|
|
ATTCACAAACTGATTGGTGTTATTTACCATAAGTGCGAAGTTTGCTTGGCCTGGTATAAA
|
|
CATACTTTGTATCCCAATAGATTGCAAGGTGCTCTCTAGCTTTGTGGTGCTTTTAATTTT
|
|
CATCTTAGGGAAACGAATAACACAATTTTTCACATGCATTTCATTGATGGTATCATCAAT
|
|
AACTTTGTTGTTAATATTTTCCATGAGTTCCAATAATGTTAATCGYTTATGAGATAATGG
|
|
TTTTAAAGCGTACATAAAAGTTTCACTGTCGTTATATGGCAATGCTATCATGTGGAAATC
|
|
ATGTTCCTCAGAAACCTTGTAACGAAACTCCCCAAAATTCAACATCATGTCAGCCATAAC
|
|
TTCATCTGTGGCCCTTTTGAATTCCATCTTTCTTGTGAATTGCGGTGCAAAAGGCTGTTT
|
|
CCATGTGCCACTAAAGTACAATGCAGTTAAAAGTACTACTTTAGTATGGGGAGGCAGAGA
|
|
ATCTTTCAAAAAATCGTCTATATTTCCTTCTGTGTGCTTGCTCACCCACTCATTGATGCT
|
|
GTTTTTAGATCCTTCGGTTTCTTGAAAATCAGTACGTAACACATCGCCTCCGTAAACACC
|
|
ATGCAGATAACTTCTGTACAACTCTCGCAATTCTACTTGGTTGTCTACAAATATCGCGTC
|
|
AGCGTACAAAGTTTTTGAAAACTCGTTCATATTTAAACTCTGTAGTAGTTCGCCGAACTG
|
|
TTCGTGGTTCTTGCGGTTTCGTAGAATATCTTGGGAAAATCCGAGTGTCTCTGCGATTTC
|
|
ATCATGTGTCATCCCAACACTTCCGAGTAATGTCATGGCAAGCAGACCAGCGACACCTAT
|
|
TGGTGATATCACGATGTTTTCGTTTTTCTTTTCGTTCATCATTTTGACTAGTAAATTATA
|
|
TCCAAAATTATTTATAGCTTTTGGTATCGAGTTATCTTTCGTATTTGTTGTTTCTAAGTT
|
|
ATCATTTTCAGCAGTTGTGGTTGGTATTATCGTGCTTGAAATCTGACTGTCCTCTTCATT
|
|
TTGTCCAGAATATTGAAAATATAATGTTGTTATAATTAAAAATAACAATGACTTGCTATC
|
|
CATGTTGTGGTGCTTAAATAAGGTATTAAACGTAAACTTCACACTAACAGGAACAGGTTC
|
|
CTATTATTTCCCACTTAAATCGTGAACTTACGGCATAGACACTATACACGTCTACTCGTT
|
|
TGACCAACTCTGAGAGCAACTCAAAAACAACCTTGTGTGTGTATGAATAACGAACTAAAA
|
|
T
|
|
S. frugiperda-Cecropin (SfCec); rep_c42380
|
(SEQ ID NO: 98)
|
TTCGTGTCGTATCACTAGAGTTCGAAATACAAAATAATAATACATTTATTATTTTGCCAT
|
|
AATTAATAATAAAGTTATTTTATTTCATAATAATAATGAATTTCACAAAGATATTTTGTT
|
|
TGTTTTTGTCTTGCTTTGTTTTGATGGCGACCGTGTCAGGAGCTCCTGAACCGAGGTGGA
|
|
AATTCTTCAAGAAAGTGGAGAAGTTGGGCCAAAACATCCGCKATGGTATCATAAAGGCAG
|
|
GACCCGCAGTGGCCGTGGTGGGATCAGCRGCAGCCATWGGAAAGTGAKCCCTACGACCTG
|
|
AGACATGAAGACTAATATCCAYTAAAATAASAATATTGAGGCKTATAATATTAATTTATT
|
|
RTRTTTGTAAATTAAATTATTTGTAAGATAA
|
|
S. frugiperda-Relish (SfRel); c13122
|
(SEQ ID NO: 99)
|
ATAATATGAAGAGTGCTGCGACTAACGATTTAAGAATCTGTCGTATAAGTCGGTCGTCCG
|
|
GAATTGCTTCTGGCGGCGAAGATGTCTTCATTCTGGTGGAAAAAGTTAATAAGAAAAACA
|
|
TAATGATTCGATTCTTCGAGTTGGATGAAAACGGAGAAAAGAGGTTGGACCAATGTTGGG
|
|
CGATTTGTGCAAAGCGATGTTCATCACCAATACGCAATCGTCTTTCGTACTCCTCCATAC
|
|
AAAAACCCTGAGACGCCAGTCGATGTGGAAGTGTATATCGAACTGGTTCGTCCATCGGAC
|
|
GGCCGTACCAGTGAACCGAAGCAATTCAAGTACAGAGCCAACCAAGCGTACAAACAGATC
|
|
AAGAAGAGGAAGACTGGATCTTCCTACTGTTCTATTGGCAGCTCATCTAGTGGATCGTTG
|
|
AAAAGTGGTTGCGACATTCCCATATCTGTTGTCAATCATCAACCAGAAGAAGTTCCCATG
|
|
GATCGCGAGCCACCGGTGCCGTCGTCGATGTATGTTTTACCCCAGGTGCATGATTCGACG
|
|
ACACCAAACCAATGCGATCTGGCCAGTGCTCTGTACTCTGCTCCTGGTTCGGAGACCAGC
|
|
CAGTCTCCTATATCGAGTCCGATGTGGAGTGAGCCTCACAGCGTGATGCTGCCGATGTCG
|
|
CCCATTGCCAACCTTCAGCTCAACTCCGCAGACTTCGAACAGATCACAGTACCCACT
|
|
S. frugiperda-Toll (SfToll);joint2_ c3284
|
(SEQ ID NO: 100)
|
AAAACCGAATAACCGGTATACCGGATAACTTCTTCAAGGATTTGAAGAATATAGAGCATT
|
|
TAGATTTGAGCTTCAATAAGATAACTAAATTGACCAGTGGAGTGTTGTCACCAATGAAAC
|
|
AATTGAAGTATTTGAACCTGAATCGAAAYCATTTGGAAGTTTTRCCTGAATTCCTCTTCG
|
|
CTGGCCTCAGRAAACTAGARAAWGTRWCAATMAACGAAAATCTACTCACTTCCATAGATT
|
|
CTTTAGCATTCCAAGGRGCWACGGCWTTGCATACAATATCTTTATACGGCAACAGATTAA
|
|
CATTGAAGTCCAATGAACACATCCAAGACTATATGGACTTAGATCTCTACTCACCCTTYA
|
|
ACACTTTGAGCGAATTAAAAAATTTGAACCTTAGTAAGAAYAAYATAAGCTCTATATTCG
|
|
ATGATTGGMGGATWGTGYTRCTCAATYTGGAGTTGCTGGATCTATCTTATAAYCATATTG
|
|
GAGAGTTATTGCCGGACACCTGYCAATTCCTAAGCAACAARRTYACAGTGGACCTGCAGC
|
|
ACAATGACATAAGTACTGTTATTTTATATCCTACGTCTCATATGGACTTCACAGAACCCA
|
|
GCATGCCATCAAACAATGTGTTTCTCTTAGACAACAACCCATTTAACTGTGATTGCCACA
|
|
TATATAACCTAGCTATGCGTCTACAAGGCAAAAAGCTGCCCTACGAACCTACTTTCAACG
|
|
TAGGCAAGGCCGAATGCAAATCCCCACGCCACTTAAGTGGGGATTTGTTGTCACATGTAT
|
|
CCCCACTCGACTTATACTGCGAAGAAATGTCGCCTGATGTTCGTTTTAATTGTAGTTCGG
|
|
TTAAAATGAGGCCTGCGTACAATGATTTGGCGTACGACTGTGATGATGTACCACCTTACT
|
|
TCTCTGATGACATTAAAAACTACTCTTTGAAATTACGACACCCACCAAAAGACTTACGCA
|
|
ACCTAACACTAAGTCTACTAAACCTAACCGGCATAGGATTACAAGAAATCCCMTTTACRC
|
|
CGTCAGAATCGGTAAAAGTAATCGATTTATCGAACAACAATCTCACAGAGATACCKATMM
|
|
GATTCTTAGAATCGAATACGACRTTGTWTTTATCGAATAATCCATTTGTTTGCGATTGTT
|
|
CTTCRAAAGATGATATTTTAGCTTTAMGRGCRAGTTAYAATGTGAATGATTTGGATATAG
|
|
TYAGCTGTTCAAACGGCGTTTTGGTAACAGATTTAGAAATATCATCGCTATGCTATACAA
|
|
GAACTTTAATAGCAGAAATAGGTGGTATAYTAATATTCTTAYTAATAATCTTAGTRTTTA
|
|
TAATAACATTYATATTTCCTAGACAAATGGTACTRTATTGTGGTCATAGGCTMTTTCCKT
|
|
GCTGGTATATCGACGATCCAGAAACTACGGCAAAAGAATATGACATATTCATATCTTATG
|
|
CTCATAAAGACCAAAAATATAGTGAATAAGCTACTCCCGTAAACTAGAAAATGATTTCAA
|
|
GTTAAAAGTCTGCGTTCATTACCGAGATTGGGAAGTCGGTGATTTCATTCCGGATCAGAT
|
|
CAATCGATCAGTATCGAATTCGAGAAAAACGATTATTCTTTTATCGAATAGCTTTCTCGA
|
|
TTCGACTTTCGCGAATTTGGAATTTCGTACCGCGCATAATTTAGCTTTGAAAGAGGGAAG
|
|
AGAGAGGGTCATTTTAATACTTTTAGAGGACGTTAGTAAACATGAGAAGTTATCTGAAGA
|
|
ATTAAAGTATCATATGAATATGAATACGTATCTTACATGGGATGATATTAGATTTGATGA
|
|
AAAGTTAAAACGAAGGACGATACCACAGAAATATAATAGAAAGAAATTCGTAGCGCCGGC
|
|
CATTTTAAAACCTATATTCAGACAGGCTACTGAGAATAATTTGAAAAAGGCACTCGATGT
|
|
ACACTTTGAATAGTGCAGGCCAATTGGTGAATTTAGCTCAAAATAAGAAGAATATTGATA
|
|
TGGTATAGCTTTTCCCAAATAAGGCTCTTTTAAACATGTTAAGCCCTCTCTCACCCGACC
|
|
TCTCTGACTACCGCACTCAGAGACATTTTAATGTATWTTTTTTTTTTAATTGGGTACAAG
|
|
CCCGCCACAACATCCCAGACCGCT
|
|
S. frugiperda-Beta 1, 3 glucanase recognition protein (SfBGRP2); EF641300
|
(SEQ ID NO: 101)
|
ATGTGGTCGGTGTTAGCCGGAGTATTGGCGATCGCGTCGCTAGGCGCGGCTTGCACCCCC
|
|
AGTTTGACCACCGTCAGTGGTACCCACGCACCGGTCACCGTCTGCTCTGGTGCTCTGATC
|
|
TTCGCTGATGGCTTCGACACTTTTGACCTCGAGAAATGGCAGCACGAGAATACTTTAGCT
|
|
GGTGGCGGTAACTGGGAGTTCCAATACTACGGCAACAATCGCACCAACTCTTTCGTGCGC
|
|
AGTGGAAGTTTGTTCATCCGTCCCTCTCTAACATCAGACGAGTTCGGAGAAGCTTTCCTC
|
|
TCATCTGGACACTGGAACGTCGAGGGTGGTGCTCCTGCTGATAGATGCACAAATCCACAA
|
|
TGGTGGGGTTGCGAGAGAACAGGCACGCCGACCAACATTTTGAACCCAATCAAGAGTGCT
|
|
CGTGTCCGTACCGTCAATTCCTTCAGCTTCCGTTACGGACGCCTCGAAGTCCGCGCTAAA
|
|
ATGCCCGCCGGAGATTGGATTTGGCCAGCTATCTGGTTGATGCCTGCGTACAACACTTAC
|
|
GGTACTTGGCCCGCATCAGGAGAGATTGACTTAGTTGAGTCCCGAGGCAACCGTAACATG
|
|
TTCCACAATGGTGTCCATATCGGTACACAGGAAGCAGGCTCGACCTTGCACTACGGACCT
|
|
TACCCAGCGATGAACGGTTGGGAGCGCGCCCATTGGGTCAGAAGGAACCCTGCTGGCTAC
|
|
AACAGCAACTTCCACCGTTACCAACTTGAATGGACACCAACTTACTTGCGATTCAGTATC
|
|
GACGACATGGAGCTTGGACGTGTAACCCCTGGCAATGGCGGCTTCTGGGAATACGGTGGT
|
|
TTCAACAGCAACCCTAACATTGAGAACCCATGGAGATTCGGAAGCAGAATGGCGCCTTTC
|
|
GATGAGAAGTTCTACCTTATCATGAATGTGGCTGTCGGTGGTACCAACGGATTCTTCCCT
|
|
GATGGCGTCAGCAACCCATCACCCAAACCCTGGTGGAACGGATCACCAACCGCCCCAAGA
|
|
GACTTCTGGAACGCGAGATCAGCTTGGTTGAACACCTGGAACCTGAATGTCAACGATGGA
|
|
CAGGACGCATCCATGCAAGTCGACTACGTCCGCATCTGGGCTTTGTAA
|
|
S. frugiperda-c20042 (Sfc20042); Un-annotated
|
(SEQ ID NO: 102)
|
ATCAGTCGTCCCTCGTACATCCAACACTTCAAACCAAATATCTCCATATACATAGTAACA
|
|
ACATGTTCGCCCTAAAGTTGGTACTAGCTGCAGTGCTGGTGGTCGCAAGCGCCAGACATC
|
|
TACCACAGGACCACTCAACGTACCGAACATGTACAGCTGCTCGGGTTCGACGAAGATGGA
|
|
CGGCCAGTGTTTGAGCACGAAGACCTGCTCGCAGAACCAGAGGAGTTCTATCAGCCAGAG
|
|
CACCTGGCGAGGACTCGCAGACAGGCACAGGGCAGCGTCACCCTCAACTCCGACGGCGGC
|
|
ATGGGCCTGGGCGCTAAGATCCCGCTCGCACACAACGACAAGAATGTGGTGAGCGCTATC
|
|
GGCTCCATGGACTTCAACAACAAGCTGCAGCCTGCTTCCAAGGGCTTCGGTCTGGCTCTG
|
|
GACAACGTCAACGGGCACGGACTGACGGTGATGAAGGAAAGTATCCCCGGGTTCGGGGAC
|
|
AGGCTGTCGGGCGCTGGCAAGCTGAACGTGTTCCACAACGACAACCACAACGTGGCCCTG
|
|
ACCGGCTCTCTTGCCAGGAACATGCCCAGCATCCCGAACGTGCCCAACTTCAACACGTAC
|
|
GGCGGGGGCGTCGACTACATGTACAAGAACAAGGTGGGAGCGACTCTGGGCATGGCCAGT
|
|
ACTCCGTTCTTGGACCGCAAGGACTACTCCGCGATGGGCAACCTGAACCTGTTCCGCAGC
|
|
CCGACCACTACCGTGGACTTCAGCGGCGGCTTCAAGAAGTTCGAATCTCCCTTCATGAGC
|
|
AGCGGCTGGAAGCCTAACTTCTCCTTTAATCTTGGCAGGTCATTCTAGAAATATTTTTAA
|
|
ACTCTTATTTAAAAATTAAATGTAAAAAATCCWGTTTGTTCATGATAATAAGAATAAATR
|
|
ACAGTATTGTTCGTACTATTTACTATGTAATCTATAAATTGTATTAATAAATGAAAATTA
|
|
A
|
|
S. frugiperda-rc16438 (Sfrc16438); Un-annotated
|
(SEQ ID NO: 103)
|
ATCAGTCGTCCCTCGTACATCCAACACTTCAAACCAAATATCTCCATATACATAGTAACA
|
|
ACATGTTCGCCCTAAAGTTGGTACTAGCTGCAGTGCTGGTGGTCGCAAGCGCCAGACATC
|
|
TACCACAGGACCACTCAACGTACCGAACATGTACAGCTGCTCGGGTTCGACGAAGATGGA
|
|
CGGCCAGTGTTTGAGCACGAAGACCTGCTCGCAGAACCAGAGGAGTTCTATCAGCCAGAG
|
|
CACCTGGCGAGGACTCGCAGACAGGCACAGGGCAGCGTCACCCTCAACTCCGACGGCGGC
|
|
ATGGGCCTGGGCGCTAAGATCCCGCTCGCACACAACGACAAGAATGTGGTGAGCGCTATC
|
|
GGCTCCATGGACTTCAACAACAAGCTGCAGCCTGCTTCCAAGGGCTTCGGTCTGGCTCTG
|
|
GACAACGTCAACGGGCACGGACTGACGGTGATGAAGGAAAGTATCCCCGGGTTCGGGGAC
|
|
AGGCTGTCGGGCGCTGGCAAGCTGAACGTGTTCCACAACGACAACCACAACGTGGCCCTG
|
|
ACCGGCTCTCTTGCCAGGAACATGCCCAGCATCCCGAACGTGCCCAACTTCAACACGTAC
|
|
GGCGGGGGCGTCGACTACATGTACAAGAACAAGGTGGGAGCGACTCTGGGCATGGCCAGT
|
|
ACTCCGTTCTTGGACCGCAAGGACTACTCCGCGATGGGCAACCTGAACCTGTTCCGCAGC
|
|
CCGACCACTACCGTGGACTTCAGCGGCGGCTTCAAGAAGTTCGAATCTCCCTTCATGAGC
|
|
AGCGGCTGGAAGCCTAACTTCTCCTTTAATCTTGGCAGGTCATTCTAGAAATATTTTTAA
|
|
ACTCTTATTTAAAAATTAAATGTAAAAAATCCWGTTTGTTCATGATAATAAGAATAAATR
|
|
ACAGTATTGTTCGTACTATTTACTATGTAATCTATAAATTGTATTAATAAATGAAAATTA
|
|
ACTATMTAAMWAAAAAAAAAAAAAAAAAAAAAAAAAACATGTC
|
|
S. frugiperda-j2rc2367 (Sfrc2367); Un-annotated
|
(SEQ ID NO: 104)
|
ATCAGTCGTCCCTCGTACATCCAACACTTCAAACCAAATATCTCCATATACATAGTAACA
|
|
ACATGTTCGCCCTAAAGTTGGTACTAGCTGCAGTGCTGGTGGTCGCAAGCGCCAGACATC
|
|
TACCACAGGACCACTCAACGTACCGAACATGTACAGCTGCTCGGGTTCGACGAAGATGGA
|
|
CGGCCAGTGTTTGAGCACGAAGACCTGCTCGCAGAACCAGAGGAGTTCTATCAGCCAGAG
|
|
CACCTGGCGAGGACTCGCAGACAGGCACAGGGCAGCGTCACCCTCAACTCCGACGGCGGC
|
|
ATGGGCCTGGGCGCTAAGATCCCGCTCGCACACAACGACAAGAATGTGGTGAGCGCTATC
|
|
GGCTCCATGGACTTCAACAACAAGCTGCAGCCTGCTTCCAAGGGCTTCGGTCTGGCTCTG
|
|
GACAACGTCAACGGGCACGGACTGACGGTGATGAAGGAAAGTATCCCCGGGTTCGGGGAC
|
|
AGGCTGTCGGGCGCTGGCAAGCTGAACGTGTTCCACAACGACAACCACAACGTGGCCCTG
|
|
ACCGGCTCTCTTGCCAGGAACATGCCCAGCATCCCGAACGTGCCCAACTTCAACACGTAC
|
|
GGCGGGGGCGTCGACTACATGTACAAGAACAAGGTGGGAGCGACTCTGGGCATGGCCAGT
|
|
ACTCCGTTCTTGGACCGCAAGGACTACTCCGCGATGGGCAACCTGAACCTGTTCCGCAGC
|
|
CCGACCACTACCGTGGACTTCAGCGGCGGCTTCAAGAAGTTCGAATCTCCCTTCATGAGC
|
|
AGCGGCTGGAAGCCTAACTTCTCCTTTAATCTTGGCAGGTCATTCTAGAAA
|
|
S. frugiperda-Chitin synthase B (SfChsB); AY52599)
|
(SEQ ID NO: 105)
|
ATGGCGAGACCAAGACCTTATGGTTTTAGGGCTTTAGATGAGGAGAGTGATGACAATTCG
|
|
GAGTTGACTCCGTTGCACGATGATAATGATGACCTAGGACAAAGAACAGCTCAAGAGGCA
|
|
AAAGGATGGAATCTGTTTCGAGAGATTCCGGTGAAGAAGGAGAGTGGGTCTATGGCCTCA
|
|
ACTGCCGGGATAGACTTCAGTGTAAAGATCCTTAAAGTCCTGGCGTATATTTTTATATTT
|
|
GGCATAGTGCTCGGATCTGCGGTTGTGTCTAAGGGTACGCTGCTTTTTATCACATCACAA
|
|
CTGAAAAAGGGCAAAGCAATCGTTCACTGTAATAGACAGTTAGAACTGGACAAGCAGTTT
|
|
ATAACAATCCATTCGTTGCAAGAGCGTGTGACGTGGCTATGGGCAGCCTTCATAGCATTC
|
|
AGTATTCCAGAAGTTGGCGTTTTCTTGAGATCAGTCAGAATATGCTTCTTCAAAACAGCA
|
|
CCGAAGCCTTCTGTTTTACAGTTTTTGACGGCCTTCGTAGTAGACACCCTTCATACAATA
|
|
GGCATTGGATTACTGGTGCTTTTCATCCTGCCAGAATTAGACGTGGTTAAAGGAACAATG
|
|
CTAATGAATGCTATGTGCTTCATGCCTGGAATACTAAACGCTGTGACCAGAGACCGCACG
|
|
GACTCTCGATACATGTTGAAAATGGCACTAGATGTACTAGCTATCTCCGCTCAAGCCACC
|
|
GCGTTCGTCGTCTGGCCTCTGCTAAAAGGCGTTAGTATGCTCTGGACGATTCCTGTCGCA
|
|
TGCGTATTCATCTCACTCGGATGGTGGGAAAATTTCGTCGGCGATATCGGAAAACAATGG
|
|
CCAGTCCTGGAACCTGTACAAGAACTTCGTGACAATTTAAAGAAGACTCGTTACTACACA
|
|
CAGAGGGTGTTGTCTTTGTGGAAGATATTCATATTCATGTGTTGCATCCTGATATCTTTG
|
|
GCGGCACAAGATGACAGCCCGCTTTCTTTCTTCACGGAGTTTGCTACTGGATTTGGTGAG
|
|
CGCTTCTACAAAGTTCATGAGGTTCGAGCGATACAGGACGAATTTGAAGGTTTTCTGGGC
|
|
TACAAAATTATGGACTTATACTTCGATCAAATGCCAGCGGCATGGGCCACCCCACTGTGG
|
|
GTGGTGCTGATCCAGGTCCTGGCTTCTTTAGTCTGTTTTATGGCAAGTTTGTCTGCCTGC
|
|
AAGATTCTGATACAAAACTTCAGCTTTACATTTGCGTTGAGTCTTGTTGGACCTGTCACC
|
|
ATCAACTTGTTGATTTGGCTTTGCGGCGAGAGGAACGCAGATCCCTGCGCATATAGTAAT
|
|
ACGATACCAGATTATCTGTTCTTCGACATACCACCGGTGTATTTCCTGAAGGAGTTTGTG
|
|
GTGAAAGAGATGTCGTGGATTTGGTTGCTGTGGCTGGTGTCGCAGGCGTGGGTGACGGCC
|
|
CACAACTGGCGCTCCCGGGCCGAGCGTCTCGCCGCCAGCGACAAGCTCTTCAACAGGCCT
|
|
TGGTACTGCAGCCCCGTCCTCGACGTCTCCATGCTGTTGAACAGAACCAAGAATGAAGAA
|
|
GCGGAAATAACGATAGAGGATCTAAAAGAAACAGAGAGTGAGGGTGGGTCTATGATGAGC
|
|
GGATTTGAAGCAAAGAAAGACATAAAGCCTTCTGACAACATTACGAGGATATATGTCTGC
|
|
GCGACTATGTGGCACGAAACGAAAGAAGAAATGATGGACTTCTTGAAGTCTATCCTGCGT
|
|
TTCGATGAGGATCAGAGCGCGCGTCGCGTCGCACAGAAGTACTTGGGCATTGTAGATCCT
|
|
GATTACTATGAACTCGAAGTACACATCTTCATGGACGATGCTTTCGAAGTGTCGGACCAC
|
|
AGCGCGGACGACTCGAAAGTGAATCCCTTCGTGACGTGTCTCGTGGAGACTGTCGACGAG
|
|
GCTGCTTCAGAGGTCCATCTCACCAACGTGAGGTTGAGGCCACCGAAGAAATTCCCCACA
|
|
CCGTACGGCGGCCGACTGGTCTGGACTCTCCCAGGAAAGAACAAAATGATATGCCACCTC
|
|
AAAGACAAGTCCAAAATACGACACAGGAAAAGATGGTCTCAAGTGATGTACATGTACTAC
|
|
CTATTGGGCCACCGCCTGATGGACGTGCCGATCTCAGTGGACCGCAAGGAAGTCATCGCA
|
|
GGGAACACCTACTTACTGGCTTTGGACGGCGACATTGACTTCAAACCGACAGCAGTCACG
|
|
TTACTAATCGATTTGATGAAGAAGGATAAGAATTTAGGAGCAGCGTGCGGGCGCATCCAT
|
|
CCTGTGGGCTCAGGCTTCATGGCATGGTATCAAATGTTCGAGTACGCTATTGGTCATTGG
|
|
CTGCAAAAGGCGACTGAACACATGATTGGCTGTGTACTCTGTAGCCCTGGATGCTTCTCC
|
|
CTCTTCAGAGGAAAGGCTTTGATGGACGACAACGTTATGAAGAAATATACCTTAACTTCC
|
|
CACGAGGCACGACACTATGTGCAATACGATCAAGGCGAGGACCGTTGGTGCACGCTACTG
|
|
CTGCAGCGCGGGTACCGCGTGGAGTACAGCGCGGTGTCGGACGCGTACACGCACTGCCCC
|
|
GAGCACTTCGACGAGTTCTTCAACCAGCGCCGCCGCTGGGTGCCCTCCACGCTCGCCAAC
|
|
ATCTTCGACCTGCTCGGCAGCGCCAAGCTCACCGTCAAGTCCAACGACAACATCTCCACC
|
|
CTCTATATAGTCTATCAGTTCATGTTGATAGTGGGTACGGTGTTGGGTCCCGGCACGATC
|
|
TTCCTGATGATGGGGGGAGCCATGAACGCCATCATTCAGATCAGCAACGCGTACGCGATG
|
|
ATGTTGAACCTCGTACCACTCGTCATCTTCCTTATAGTCTGTATGACTTGTCAGTCAAAG
|
|
ACGCAGCTCTTCCTCGCTAACCTCATAACATGCGCATACGCAATGGTGATGATGATCGTG
|
|
ATAGTGGGGATAGTTCTGCAGATAGTGGAGGATGGATGGCTGGCTCCGTCCAGTATGTTC
|
|
ACAGCTTTAATATTCGGTACATTCTTCGTCACCGCGGCACTACACCCGCAAGAGATCAAA
|
|
TGTTTGTTGTTCATAGCAGTGTACTATGTAACCATCCCTAGTATGTACATGTTGTTGATC
|
|
ATATACTCCATCTGTAATCTCAACAACGTATCCTGGGGTACCAGGGAGACACCGCAGAAG
|
|
AAAACTGCTAAGGAAATGGAAATGGAACAGAAGGAAGCAGAAGAAGCGAAGAAAAAAATG
|
|
GAGAGTCAGGGTTTGAAGAAGTTGTTTGCCAAGGGAGAAGAGAAGAGTGGTTCGTTAGAG
|
|
TTCAGTGTGGCGGGCCTGTTGCGATGTATGTGCTGCACCAATCCAGAGGATCATAAGGAC
|
|
GATCTCAACATGATGCAGATCTCACACGCGTTGGAGAAGATAAATAAGAGATTGGATCAA
|
|
CTCGATGTCCCTCCTGAGCCGACCCACCAGCCCTCGCATCCGCACACACACGTGGAGACG
|
|
GTCGGTGTTCGTGATTACGAAGACAGCGAGATTTCCACTGAAATTCCTAAGGAAGAACGA
|
|
GACGACCTGATTAACCCCTACTGGATCGAGGACGTGGAACTCCAGAAGGGCGAGGTAGAC
|
|
TTCCTCACCACCGCTGAGACCAACTTCTGGAAGGATGTCATCGATGAATACTTACTGCCT
|
|
ATTGATGAGGACAAGCGTGAAATTGAACGTATAAGAAAAGATTTGAAGAACTTGCGAGAT
|
|
AAGATGGTGTTTGCGTTCGTGATGTTGAACTCTCTGTTCGTGCTCGTCATCTTCCTGCTG
|
|
CAGCTCAGCCAGGACCAGCTGCACTTCAAGTGGCCATTCGGACAGAAGTCCAGCATGGAG
|
|
TACGATAATGATATGAATATGTTCATCATAACCCAAGACTACTTAACGCTGGAACCTATC
|
|
GGTTTCGTGTTCCTCCTGTTCTTCGGCTCCATCATCATGATCCAGTTCACCGCCATGTTG
|
|
TTCCATCGCCTGGACACGCTGGCCCATCTGCTGTCCACCACCAAGCTGGATTGGTATTTC
|
|
AGTAAGAZGCCGGACGACCTATCAGACGATGCGCTAATAGACTCTTGGGCGTTGACAATA
|
|
GCGAAGGATCTTCAACGTCTGAACACCGACGACTTGGATAAACGAAATAACAACGAACAC
|
|
GTGTCCAGGAGGAAGACCATATATAACTTGGAGAAAGGGAAGGAAACCAAACCGGCTGTT
|
|
ATCAACCTCGATGCCAACGCCAAGAGGAGATTGACTATCCTGCAGAATGAAGACTCAGAA
|
|
TTGATCTCCCGCCTGCCATCTCTGGGACCTAATTTGGCAACTCGTCGTGCCACGGTGCGT
|
|
GCAATAAACACTCGACGCGCATCTGTCATGGCGGAGCGACGCAGGTCTCAGTTCCAAGCG
|
|
CGACCTTCCGGGGGATCATACATGTATAATAACCCTCAAAACACGATTCAGCTGGACGAT
|
|
ATGGTCGGGGGGCCGTCGACGTCGGGAGTGTACGTGAACCGAGGGTACGAGCCCGCCCTG
|
|
GACAGCGACATCGAGGACACGCCCGTGCCCACCAGACGATCCGTTGTACACTTCACCGAC
|
|
CATTTCGCGTGATAACCACCAAAATCTGACTAACATCTCCATATTACATTTTCTACTCTG
|
|
TTACGAAACGATAAAGTTTAAAGTGTATTAAATAAATTGGACAGATTTGAGTAGGTTTCA
|
|
CGTTTGTGTTTAAATAATTTATGAAAATAACATACCTATTGCTTTATGACCGCTTTAATA
|
|
TTAAAAGAAACTCAATATATGCATTAA
|
|
T. castaneum-Peptidoglycan recognition protein LC (TcPGRPLC); DT786101.1
|
(SEQ ID NO: 106)
|
ATATAAAAAAAAAAAAATATTAGGCAATTTATTTACACAAATAGCACAATTTATCAATTC
|
|
ACAAGTTGTGTATTTTATTATAAATACTAAATCAACAATAGCGACTAACAATTAACACAA
|
|
TTTTATTTCACTTCCTGTCACTATCGCGAGTAATAAATTCCCGCATCAAAATGCGGCCAA
|
|
TTTTTGATCTCTTTGTAAACATTTGGCCCCGGACTTTCCGTTCTAAACGTCTGATTGTGA
|
|
GCTACCAGTTTATAATCCCTGGCCAATTTTCCACTCTTTACCCCCTCATCTAGCAATTTC
|
|
TTCGCCACGCTGATCATCTCCGTCGTCAAATGATCATGAAAAAAATTCCCAATAAAACTA
|
|
ATCCCGATCGAATCATCCATGTGAAAATTCCTGATATCCCAGCCTCGTCCAACATACGCA
|
|
TTCCCATCTCCACCAATTACGAAATTGTACCCAATATCGGGACTTTTCAAATTGCCCACA
|
|
TGGTAGTCCTGCATGGACTGCACCCTTTGCGAACATGCAGGAAAGTCGCTACAAGTCGGG
|
|
GTAACAGTGTGTGAAACGATGACAAAATGAGTGGGATGTGGCAGTGGTTTAGAGAAGTTT
|
|
AAGGTGGCACGGCCTCCCCAAATTTTTTTCTCGATGATGGCACCGGGGCCCAAAGGAAGT
|
|
CTTGGAGTCGCAGTGTTAGTGTCGGGAGTTTCGGGAGACTTTTCAGTTTTCCGTGGGAGT
|
|
ATTACAACGCAAGTIGTGGTGACGAGGATTACGATTACGACTAGAGAAATGCCCAAATAT
|
|
TTCACAGGTTTGGAGTATAAAAAGGAGTTTTTTTGGTTTTTCAGCGGGGGGGAGAGTCGG
|
|
AAACAGGGGCTTTTCAGACTTGACGAAGTTTACCAATGGAATCAGTTGAATTAACAAATC
|
|
CTTTTCCCTAAAGTCCTCTAAAAACAGATGATGGGGCCCCAT
|
|
T. castaneum-Peptidoglycan recognition protein 2 (TcPGRP2); XM_965754.3
|
(SEQ ID NO: 107)
|
ATGAGTGGCAGTGACCCTTTAACAAATACCCAACAATCCGATCAAGATTATTACCATCCA
|
|
CTCTGTTATTCAATTCAAGTGGACGACGAAAATGAACAATCAGCTCTCCTGCCCGCATTT
|
|
CATCAAAGGAAAAGTTTGCGAGTTCAGGATAAAATCTTTATTGTATTTTTATTTTCAATT
|
|
CTAATTACCGGACTAGCCATTGGCCTCTATCTCCTTGCAACTGAGGGACACGAATGGAAA
|
|
GCTGCAGGAGTCTATAATATTACAGTTCGGGAACAGTGGCAAGCTCACGTCCCTTCATCA
|
|
ACAATGCCAAAGTTGGAACTTCCCGTAAGAAGAGTTTTATTTCTTCCTGCAAATACCACT
|
|
AGCTGCGGCAGCAAATCCCACTGTGCCAAAGTCCTCCAGGAACTACAATTACAGCATATG
|
|
CTGCAGTGGAAAGAACCTGACATCTCCTACAATTTCATAATGACTGCAGATGGCAGAATT
|
|
TTCGAGGGGAGAGGATGGGACTTTGAAACTTCTGTTCAAAATTGTACGGTTAATGATACT
|
|
GTGACAGTTGCTTTTTTGGACGAATTAGATGCGAAAGCACCGACGTTTAGACAAGCTGAA
|
|
GCGGCAAAAATGTTCCTGGAAGTGGCAGTAACAGAGGGAAAATTAGAACGGTGTTTTAAT
|
|
ACCGCGGTCTGGGGAGGAAATAAATTCTTCATTGATTTGGCTCGAAATGTTCAAGACGTC
|
|
TTATCGGAATGCGAGGGAATTACTTAA
|
|
T. castaneum-Beta 1-3 glucan binding protein (TcßGRP2); XM_966587.4
|
(SEQ ID NO: 108)
|
ATGTGCGTTTGCAAGACTGTGCTATTAATCGTTGGGCTGGGGGGTTGTTTTGCGGGTCCG
|
|
GTCCGTAATTATGGGCCATTGAGACATTACAACGTTCCGCGACCCTCAATCCAAGCATTC
|
|
AGGCCCCGTGGCTTCAAAGTGAGCATCCCTCATACTGAAGGCATCCAATTATTCGCCTTT
|
|
CATGGAAATATTAATAAACCCCTGCACGGTCTCGAGGCCGGACAATTTTCCCAAGACGTC
|
|
CTCCAAAGGGAGGGAGACGAGTGGGTGTTCCAAGACTCCAGTGCCAAATTAAACGTGGGA
|
|
GATAAAATCTATTATTGGCTCTTTATCATTAAAGAAGACCTGGGCTACAGATACGATCAC
|
|
GGCGAGTACGAAGTGAAAGTTTTAGCCACCCGTGACTTCGATTCTCCTCAAACAACCTCT
|
|
GTGACGCCGAATCTTGCCCCCAATCTCGGCATTTGCGAAAAGGTGATGGTAAATCTCACG
|
|
CGGAAGCTGCTCGATTTGCAGCAAGAAATTGAGTCCCTTAGGGAGACGAACGATATTTTG
|
|
GAGGATATGGTTCAGAAGCACACTGATACGGCGACTACTCTCACTTTGGACGGCTTGATG
|
|
ATAAAGGATGACGACGAACTTGTTTCGGTGATTCAAGCAATTATTAAAGATAAACTTGGA
|
|
CTAAAAAGCAGGATTCAAAATGTGACGAGGCAGGAGAATGGAATGGTCAAGTTTCAAGTG
|
|
GCGAGTTTGAGAGAAAAGTTGGAGGTTGTCAAAGCGGCCAAAAGAAAACTCAAGTCGTCG
|
|
AGCTTTACGATCACGTATTAA
|
|
T. castaneum-midgut protein (TcMDGP); XM_971351
|
(SEQ ID NO: 109)
|
ATGTATCCGTTGAAGAGGATGCCCAGTGAAGAAATCAGTATCAGTGATCTGCCTAGCGAA
|
|
ATGAAAGAAGTTTTACTAGAAATTAGCCCGAACTTTGATGAAAATCTGAAACGGGCTTTC
|
|
AGGAACGAAGGAGTGAGGCTGCAGAGAGTGCAGAACAATGGACGATTTATTCATCAGCTG
|
|
GACGACGTTCTCTTATCCATAGACGATACCAAAATCGAGTTACGCAACCTGAAATTCCCC
|
|
TGGATCCCCGACTTCCGCATCGTGGACTTGTCCAGCGACCTGCCCATGTCATGCCTCGAC
|
|
CTAAACCTAAACCTGGGCAATTTGCGAATTGAGGGCGAGTACGAAGCCAACAACACCACA
|
|
CTCAGGCGATGGCTCCCGGTATCTCACATTGGTCGAATCGTGATCGGTTTTAACAACGTC
|
|
CGAGCGAACGGAAAAGTCGGACTCGTGCTCGAGCAGGATTCTTTCGTTCCGCAGAATTAT
|
|
GATATTAGATATGAGCCGACGGATGTTGTTATTAGGGTTAGCTATCACGTGGATGGCGAG
|
|
AATGAGGTGCAAAATGAGATTAGCAATTCAGATATTGAGGCCACGCTAGGCAAGACCGTG
|
|
TGGGTGCAGTTGACTGAGATATTGTCCAACCTGTTGCATAGGCAATTGGGCGAGGTTGTA
|
|
GTGGAGTTTTCCGTGACGGAACTCCTCGTCGATAGGGACGAGGAATACAGGGAATACGCC
|
|
AAGGGACAAGCAGCGCGCGCCAATAAACTCCTGGACTCGCTTTTGTGCTCAGCCAAGGAC
|
|
TATTTAGTCGCGAAGGACTTGAGGACGGTCAAAACGCCACCCTTCGACGTCGTCTTCAAA
|
|
GGGAAAGTCTCGGGGGTGCAGCAGGGGACCTTCAGCACGGGGGAAGGGTTCCTCCAAGAC
|
|
CTCGCCACTTTGACGCGGAGACACAGCTTTAGTTTGTACGAAGACAAACACAAACTCACG
|
|
ATATATGGGGGGATCAGGCTGAGGGAGTTTAAACTCGGGTATGGGGGCTACCAGGGCCAG
|
|
TACGAGGAAACGGCCGTCTCAGGCAGCATCAAAGGCTCGCTCTACAAGAACGAGATTTTC
|
|
GTCAAGATCACTGTGAAAAAAGAAGGCGAGCGGTGCTCGACTCAGTTAGATTCCGTCCAA
|
|
GTTGTTGTTGTAAAGTAA
|
|
T. castaneum-Chitin synthase 2 (TcCHS2); EFA 10719.1
|
(SEQ ID NO: 110)
|
ATGGCGGCGCGTCATCGCTTTGCCACAGGGAGCCCTGAGGAAACAGAGCCCCTGTATTCG
|
|
TCGACGCAAATGCCCGAAAAAGTCCGGGAAAAATGGAACGTCTTCGACGACCCCCCAAGA
|
|
GAGCCCACTTCGGTTCCGAAGTCAAAAGAACCTACATCGAGTGGGGGGTGAAGTTTTTGA
|
|
AAGTTGTGACAATCATAACTGTGTTTTTTGTGGTCCTTGGTGCTGCAGTGGTTTCGAAAG
|
|
GGACAACCTTGTTCATGACGTCACAAATAAAAAAGAATGTGACAAGGGCTTATTGCAACA
|
|
AAAAGATAGACCGCAACCTCCAATTCGTCGTCTCCCTCCCCGAAGTGGAGCGCGTGCAAT
|
|
GGATCTGGCTCCTCATTTTCGCTTACTTGATCCCCGAAGTGGGTACCTGGATCCGCGCCG
|
|
TCCGCAAATGCCTCTACAAGCTCTGGAAAATGCCCTCCCTCTCCGAATTCCTCTCCCTCT
|
|
TCGGCACGGAAACGTGCCCCGCCATCGGAAGCGCAATTTTGATATTCGTCGTCCTCCCCG
|
|
AGCTGGACGTCGTCAAAGGGGCGATGCTCACAAACGCGGTTTGTTTCGTGCCCGGAGTTG
|
|
TGGCAATGTTCTCGCGCAAACCGTGCTCCATAAACGAGAACCTGAAAATGGGGCTGGACA
|
|
TCGCCAGCATAACTGCACAGGCGTCAAGCTTCGTGGTGTGGCCCTTGGTTGAAAATAACC
|
|
CGACCTTGTACCTAATCCCCGTTTCCGTGATTTTGATTTCGGTGGGTTGGTGGGAGAATT
|
|
TCGTGTCGGAAACGTCCTACTTACCGTTTATCCGGGCTCTGGGCAAGAGCAAAAAGGAGT
|
|
TTAAGACAAGGACGTACTTCATTTACGCGTTCGTGGCCCCGGTTAAATGCCTGGCGTTTT
|
|
TTTGCACCGCTTTGGTCATTTTTTACTGCCAGGAGGGCAGTGTTGACTTTTTATTTGATA
|
|
ATTTTTCAGCCGCGTTTCAGGATCATAACATTGAAATTACCGAAGTCGCGCCCGTCTTGC
|
|
CGGGGAATTACGCAAATGCAGTTCGGTCGGGAGCCGAAACCCCATCCACACAAGCAGTTA
|
|
CATGACGGGGATTTGGGTTTGGTTGATTAACATTTCGGCGACTTATATTTGCTACGCGTT
|
|
TGGGAAATTCTCCTGCAAAGTCATGATCCAGAGCGTTAGCTTCGCTTTTCCGATCAATTT
|
|
GTCGGTCCCTGTCCTCTTATCCGGACTGATCGCAATGTGTGGCATGTACTACAGGGATGA
|
|
GTGTTCTTTCGCTGAGTCAATTCCTCCATATTTGTTTTTCGTTCCTCCACCTCTCATGTT
|
|
CCTACAAGATTTTCTCTCGCACCAACACGCCTGGATTTGGCTGGTTTGGTTGCTGTCACA
|
|
AGCCTGGATTTCGGTGCACATTTGGTCCCCAAACTGTGACAAACTTTCAAGCACCGAACA
|
|
GTTGTTTATTCGGCCCATGTATGACGCGTTTTTGATCGATCAAAGCCTGGCGTTAAACCG
|
|
GAGACGTGACGAAAATCCCAGAAATTACAGAAGCGACGAAGGGCCTCAAATTACAGAGCT
|
|
CGAGCCGGAAACGATCGAGAGTCAGGACGCCATAACCCGGATTTACGCCTGCGGGACAAT
|
|
GTGGCACGAAACTCCCGAAGAAATGATGGAATTTTTGAAATCGGTGTTCCGCTTGGACCA
|
|
AGACCAGTGTTCCCACAGGATTGTGAGGGAGCATTTGGGACTCAAGCATGACAATTACTA
|
|
CGAATTGGAGACTCATATATTTTTCGATGATGCGTTTATTCGGACCAGTGAAGACGATAA
|
|
TGATCCCCACGTCAACGAATACGTTGAGTCACTTGCGTCCATTATCGACGAGGCTGCGAC
|
|
TAAGGTTCACGGTACCACGGTGAGGGTGCGTCCGCCCAAAGTGTACCCCACGCCTTACGG
|
|
CGGACGCCTGGTCTGGACGCTCCCAGGGAAAACAAAAATGATCGCCCACTTGAAGGACAA
|
|
GAAGAAGATTAGGGCGAAAAAGCGCTGGTCTCAGTGCATGTACATGTACTTTTTGCTCGG
|
|
ATTCAGATTGCAAGCCAACGACGAACTCTCCGCCCACAGCAAGGAAATCCGCGGCGAAAA
|
|
CACCTACATCCTCGCCCTGGACGGCGACATCGATTTCCAACCCGAAGCCCTGCACCTCTT
|
|
GGTGGACTACATGAAGAAGAACAAAACGTTGGGGGCGGCCTGCGGCCGCATCCACCCCAT
|
|
CGGCAGCGGCGGCATGGTCTGGTACCAAATGTTCGAATACGCCGTCGGTCACTGGATGCA
|
|
AAAAGCCACCGAGCACGTCATAGGCTGCGTCCTCTGCAGCCCCGGCTGTTTCTCCCTGTT
|
|
CCGGGGAAAAGCCCTCATGGACAAAAGCGTCATGAAGAAGTACACCACTCGATCGACCCA
|
|
AGCCAAGCACTACGTGCAGTACGATCAAGGGGAGGACCGGTGGTTGTGCACTTTGTTACT
|
|
CCAGAGGGGCTACCGTGTGGAATACTCCGCAGCCTCGGACGCTTTCACGCACTGTCCGGA
|
|
AGGCTTCAACGAGTTTTACAACCAGCGGAGGCGCTGGATGCCGTCCACTATGGCCAACAT
|
|
TTTGGACCTTTTGATGGATTACGAGCACACGGTCAAAATCAACGAAAATATTTCCATGCT
|
|
GTACATCGGGTACCAAATTATTTTAATGATCGGTACGGTCATTGGCCCCGGTACTATTTT
|
|
CCTCATGTTGGTCGGCGCCTTCGTGGCTGCCTTTGGGCTCGACCAATGGAGCAGTTTCTA
|
|
CTGGAATTTACTACCAATCGCAGTTTTTATCCTAGTATGTGCCACTTGTAGCTCCGATAT
|
|
CCAATTATTTTTCGCCGGCCTTATCAGCGCCATTTACGGCCTGATAATGATGGCTGTTTT
|
|
CGTCGGTGTGATGCTCCAAATCAGCCAAGACGGCCCACTTGCGCCTTCCTCCCTTTTCTT
|
|
CTTCTGCATGGCTGCTGAATTTATAATCGCAGCACTGCTGCATCCGCAAGAATTCAACTG
|
|
TTTGAAATACGGGGTCATTTACTACGTCACGGTCCCCAGCATGTACCTCCTCCTAGTCAT
|
|
CTACTCGGTCTTCAATATGAACAACGTGTCCTGGGGGACGCGCGAAGTGACAGTCGTGCC
|
|
CAAGCCTGACCCCAACGCCGTCCAGAAAATCGAAGAGAAAAAACCGGAGAAGAAAGACAA
|
|
AGTTTTGACGTTTCTGGGCGCGAATGCCCAGGACGACGAAGGCGGGCTTGAATTTTCGGT
|
|
CAACAAACTTTTCAAATGCATGATTTGTACGTACAAGGCCGATAACAAGGAAAACGAGCA
|
|
GTTGAGGAAAATACAAGAGTCGTTGAGAGACTTGAATAGGAAAATCGAGTCGCTGGAAAA
|
|
AATGCAATATCCGGATTTGAGGTCTCCTGCCGTTAGCAACGTTACAACGTTCATGGAGGG
|
|
CTCAAAGGCGACGGTTAAGAACAACGTGGAGGATAACTACATGGAGGCTCCGCAAGACAA
|
|
TGTTTCGCAACCGTCGGATGAGGTCATGGAGAATAGTTGGTTCTACGATGGGCCTTTGAT
|
|
TAGGGGGGAAGTGCATTACTTGAATAGGAATGAGGAAACGTTTTGGAATGAACTGATAGA
|
|
GCAGTATTTACACCCGATTGAGGATGACAAGAAGAAGGTTTCGGCTGAATTGAAAGATTT
|
|
GAGGGACAAAATGGTGTTTACTTTCCTGATGTTGAATTCGCTCTACGTTATTGTGATTTT
|
|
TTTGCTCACTTTGAAGAAGGATTTGCTCCATCTGGACTGGCCGTTTGACCCCAAAGTGAA
|
|
CTTCACGTATTTCGAGGACAAAAATGAGATTGGCGTTTACATAACATACCTCCAGCTGGA
|
|
GCCCATCGGTTTCGTGTTCCTCATATTTTTCGCCCTGCTTATGGTGATCCAGTTCTTCGC
|
|
AATGATGATCCACCGCTTCGGCACCTTCTCCCAAATCATCACAAAAACACAATTAGACTT
|
|
CGATCTGTGCAGCAAACCAATCGACGAAATGACTGTGGACGAACTCAGGTCCCGCGACCC
|
|
TATAAAAATAGTCGCAGATTTACAAAAACTAAAAGGTATAAACAACGAATACGAGGACCA
|
|
AACGGAAGTTCCGGTCGAAATGCGAAAAACAGTAAGTAATTTGGCGCAAACGAGCGGTGG
|
|
TGGTGAGAACAAGCCCATATTTTATTTGGATGAAGCGTTCCAAAGGCGAGTCACTCAAAT
|
|
AGGGAGCACTTCAAGCAACAACCCGAGCATTAGCGCCTTTAGGAAGAAAAGCCTTGCTTA
|
|
CGTCCAACAAAGAATGAGCATAGCCCCAAATCGGGTGTCACAAGCCCGGCCTAGTGTGCA
|
|
GTTACGGTACCCCAATGGAAAAGCCAACGAAAATTTCGTTTTTGACGAAAACGGGTCAGA
|
|
CGTGGAGGCATAA
|
|
>M. sexta-Peptidoglycan recognition protein 2 (MsPGRP2); GQ293365.1
|
(SEQ ID NO: 111)
|
TAATCATTAGAAAAATGGCGAGCTTCGCTTTAATAGTTATCCTTAGCGTAATTGGCTTTA
|
|
TATCGGCCTATCCTAGTCCTGAAGGTTACAGTTCTGCCTTCAACTTTCCATTCGTAACCA
|
|
AGGAGCAGTGGGGCGGCAGGGAGGCACGCACGTCGACGCCACTCAACCACCCAGTGCAGT
|
|
TCGTGGTGATCCACCACAGTTACATTCCCGGCGTGTGCCTCAGCCGGGACGAGTGCGCGC
|
|
GCAGCATGCGCTCCATGCAGAACTTCCACATGAACAGTAACGGGTGGAGTGATATTGGAT
|
|
ACAACTTCGCTGTCGGCGGTGAAGGGTCGGTGTACGAGGGCCGCGGCTGGGACGCGGTCG
|
|
GCGCACACGCAGCTGGCTATAACAGTAACAGTATCGGCATCGTGCTCATCGGCGATTTTG
|
|
TTTCAAACCTCCCGCCGGCGGTGCAAATGCAAACCACACAAGAATTGATCGCAGCGGGCG
|
|
TGCGACTCGGTTACATCAGGCCCAACTACATGCTCATCGGGCATCGTCAGGTCTCCGCCA
|
|
CTGAGTGCCCAGGAACCAGACTCTTCAACGAAATCACCAACTGGAACAACTTCGTGAGG
|
|
>M. sexta-Beta-1, 3-glucan-recognition protein 2 (MsßGRP2); AY135522.1
|
(SEQ ID NO: 112)
|
GAGCGTCTGTTTGTTCGCAACCATTGCGGGCTGCTTGGGCCAGCGAGGGGGTCCATACAA
|
|
GGTGCCTGATGCGAAACTCGAAGCTATCTACCCCAAAGGCTTGAGAGTCTCTGTGCCAGA
|
|
TGATGGCTACTCCCTATTTGCCTTCCACGGCAAGCTCAATGAGGAGATGGAAGGTTTAGA
|
|
GGCTGGCCATTGGTCCAGAGACATCACCAAAGCGAAGCAGGGCAGATGGATATTCAGAGA
|
|
TAGGAATGCTGAGCTGAAGCTTGGAGACAAAATTTACTTCTGGACTTACGTTATTAAGGA
|
|
TGGATTGGGATACAGGCAGGACAATGGAGAATGGACTGTTACAGAATTCGTCAATGAGAA
|
|
CGGTACAGTGGTGGACACTAGTACAGCGCCGCCACCAGTAGCACCCGCCGTTTCAGAGGA
|
|
AGATCAATCGCCAGGTCCTCAGTGGAGACCTTGCGAAAGATCCCTGACTGAGTCCTTGGC
|
|
CCGCGAACGCGTTTGCAAAGGCAGCCTTGTCTTTAGCGAGGACTTTGATGGTTCCAGTTT
|
|
GGCCGACTTGGGCAATTGGACCGCTGAAGTCAGATTCCCTGGCGAACCGGACTACCCGTA
|
|
CAACTTGTACACTACGGACGGCACTGTGGGATTCGAAAGTGGGTCTCTGGTGGTGAGACC
|
|
CGTCATGACCGAGTCCAAATACCACGAGGGCATCATATACGACCGCCTCGACCTTGAGAG
|
|
ATGTACAGGACAGCTGGGTACGCTGGAATGCAGGCGAGAGAGCAGCGGCGGTCAGATTGT
|
|
ACCACCTGTGATGACAGCTAAACTGGCCACTCGACGCAGCTTCGCGTTCAAGTTCGGCAG
|
|
GATCGATATAAAGGCGAAGATGCCGCGCGGGGACTGGTTGATACCAGAACTCAACCTCGA
|
|
ACCTTTAGATAACATATACGGCAACCAGCGATACGCTTCGGGTCTCATGCGGGTCGCGTT
|
|
CGTGAGAGGAAACGATGTATACGCCAAGAAGCTCTACGGAGGTCCGATAATGTCCGACGC
|
|
GGACCCGTTCAGGTCCATGCTGTTGAAGGACAAGCAAGGGTTGGCCAACTGGAATAATGA
|
|
TTACCACGTCTACTCGCTGCTGTGGAAGCCTAACGGTTTAGAGCTGATGGTGGACGGTGA
|
|
AGTGTACGGCACCATCGACGCTGGCGATGGCTTCTACCAGATTGCGAAGAACAACCTCGT
|
|
GAGCCACGCCTCGCAGTGGCTCAAGGGCACCGTCATGGCGCCGTTTGATGAAAAGTTCTT
|
|
CATCACTCTGGGTCTTCGCGTGGCGGGTATCCACGACTTCACGGACGGTCCGGGCAAACC
|
|
TTGGGAGAACAAGGG
|
|
>M. sexta-Relish family protein 2A (MsREL2A); HM363513.1
|
(SEQ ID NO: 113)
|
ATGTCCTCTTGTCCAAGCGACTATGATCCCAGTGAATCGTCCAAATCTCCACAAAGTATT
|
|
TGGGAGTCAGGAGGATACAGTTCTCCGTCGCAACAAGTTCCTCAATTGACTTCTAACTTA
|
|
ACAGAATTGTCTGTTGATCACAGCTATAGATACAATGGAAATGGACCATATCTACAGATC
|
|
ACAGAGCAACCACAGAAATACTTTCGGTTCCGTTATGTTAGCGAGATGGTGGGAACACAT
|
|
GGATGTTTGCTTGGCAAATCTTATACAACAAACAAAGTTAAAACTCATCCGACAGTTGAA
|
|
CTCGTGAATTACACCGGTCGAGCCCTGATAAAGTGCCAACTATCGCAAAACAAGAGCGAA
|
|
GACGAACACCCGCACAAACTGCTCGATGAACAAGACAGAGACATGAGCCACCACGTTCCC
|
|
GAGCACGGCAGTTATAGAGTGGTATTTGCTGGTATGGGTATAATTCATGCTGCCAAAAAG
|
|
GAAGTTGCGGGGTGGCTCTATAGAAAATATATACAGCAGAACAAGAATGAAAAGTTTAAT
|
|
AAGAAAGAGCTCGAAGCGCATTGTGAGAGGATGTCCAAAGAGATCGATTTAAATATAGTT
|
|
AGACTGAAGTTTAGCGCTCACGATATTGACACTGGCATTGAAATTTGCCGGCCAGTGTTC
|
|
TCTGAACCCATTTATAATTTGAAGTGTGCGTCTACGAATGATTTGAAAATATGCCGCATA
|
|
AGCCGTTGTTACGGTAGACCGAGAGGCGGCGAAGATATCTTCATATTTGTCGAAAAGGTC
|
|
AACAAGAAAAACATCCAAGTTCGGTTCTTTAGACTGGAAAACGGGGAGCGCACCTGGTCA
|
|
GCGATGGCGAACTTTCTGCTAAGCGATGTTCACCACCAATACGCTATCGCTTTTAGAACG
|
|
CCACCGTACGTCAATCACCAAATTTCTGAAGACGTGCAAGTTTTTATAGAACTCGTACGC
|
|
CCTTCAGACGGTAGGACGAGCGCTCCCATGGAGTTCACATACAAGGCTGAGCAAATCTAT
|
|
AAACAGAACAAGAAACGTAAAACTACTTCGTCGTACTCGTCGCTCGACAGCTCCTCAGGT
|
|
TCGGCCGGTTCAATTAAAAGCATCAGCGAACTGCCCGCGCCCGTTGTTTTTGCTGAAAAC
|
|
GTAAGTTTTTTCTATGACACATTACTCATTCTTCAACCCATGACGAATCTATAA
|
|
>M. sexta-Spatzle (MsSPZ1A); GQ249944.1
|
(SEQ ID NO: 114)
|
ACGAACAACCTGACAGACGGATAGCGGGACGGTCAGCACAATACGAACATTTAAGAACAA
|
|
ACGAGAGGTCTCTCCCGGTCTACAGCGAGACCCAGAGGATACAAGCAGAAGAGAGAAGAA
|
|
GACACAGTTCGAGACTAGAAGAACCGAGACAACGTGCTGAGAATGGTTCATATAAGATAT
|
|
TGAATAACCCTCCGAAACCCTGTATTACTAATAGGAGAAGTCAAATTGATTCGTCGAATG
|
|
ATAGGGTAGTGTTCCCCGGTCCGACTTCAGAAAGGTCGTACGTACCCGAAGTGCCAGAGG
|
|
AATGCAAGAAAATCGGCATATGCGACAGTATACCGAATTACCCAGAAGAACACGTAGCTA
|
|
ATATTATATCTCGACTTGGAGACAAAGGAAAAGTATTACAAATAGACGAACTGGACGTAT
|
|
CAGACACTCCAGATATCGCCCAGAGGTTGGGTCCGCAGGAGGACAACATGGAACTATGTA
|
|
GCTTTAGAGAAAAGATTTTTTACCCCAAGGCAGCGCCAGACAAAGATGGAAATTGGTTCT
|
|
TCGTTGTGAATTCAAAAGAAAACCCAGTACAGGGTTATAAAGTTGAAATTTGCGACCGTC
|
|
AGCAATTACCATGCGCGGAGTTCGCGAGCTTCCAACAGGGATATGAAGCGAGGTGCATCC
|
|
AGAAATACGTTCGCCGGACCATGTTGGCGTTGGATCCCAAGGGTCAGATGACCGACATGC
|
|
CCCTTAAAGTGCCCAGCTGTTGCTCATGCGTGGCCAAATTGAC
|
|
>M. sexta-Toll receptor (MsTOLL); EF442782.1
|
(SEQ ID NO: 115)
|
ATGCAGGCTCGGCGGTGGTGCGCGGCACTGCTATTAATGCAGATGCTGAGCTGGCTCGGA
|
|
GTCAGTGGACACTTACCGCGTCCCGAGTGCGCGCCAGCCGCAGATTGCCAACTTATACGA
|
|
GACAACATAATCGATGGATATGCACAATTCTACTTCAACGTATCAGGACATGAAGTGAAA
|
|
TTTGAACATTACATCGGAAACGACTTCGATGTCGAATTGTCATGCAATTACATCGCCATG
|
|
GACAACGCAATGCTGCCGCGGTTCTCAACGACCTTTTCAGTCAACGTAATAGTGGTTAAA
|
|
GAATGTGCTTTGCCAAGAAGTGGGTCAATCGATGCCGCTGTCGCTGCACTTAATATCAAC
|
|
GTTTTGACGGAGCTGACTCTGGACAAATTCCTAGAGCCGGCGGTGATCACGCGCGCACAT
|
|
CTTACCAGTTTACAACGACTAGAGAGGCTGGAGCTACACGGTAACTCAAACACAAGCCTC
|
|
GCCCCCGGCGCACTGGCCGCGCTCTCCGCCGCGTCCGCACTGAAATGTCTTGTATTGCAT
|
|
GCAGTACGCGTGCCCGCCGCTGACCTGGCGCGCTTGCCGTCGTCACTGCAAGAACTAGCG
|
|
TTGTTGGATGTGGGCGCTGCGAGTATGCATTTAGATTCATCGGTTAATTTGACGTCACTC
|
|
TTCGTAATCGATACACATTATCCTGTCGTCGTGAATGTGAGCAACGCCGTTGCGCTCAGA
|
|
GACTTGCACATAAATACCCCAAGTACTGTGTTGACCGAAGACGTGCTCCCGTCGTCACTC
|
|
AACTCACTTGAACTAGAGGGGTGGAACGAAACGCATCCGGTGCCTAAGACACGTTGTGTA
|
|
CTACTTAAGGAACTTAATGTAATCGGCACCGACAATGATGCCTATCCGGTGACTCT
|
|
>M. sexta-Valine Rich Midgut Protein (MsVMP1); NCBI accession number not assigned
|
as yet
|
(SEQ ID NO: 116)
|
ACGGACCTTCCGTTGGACCNGCCATCATCGGCGCTGGAGACATCGCTGTCGGCCCTGCTA
|
|
TCGTCGACTTCCCTTTCCCCGACGGCGGTGCCGTGTCTGCCCCCGTTGAGCCTTCCCCCA
|
|
TCGCCATCGGACCCGCTATCGTCGGTGAATCCCCTATCTCCGTCGGACCTGCCATCGTTG
|
|
AGGCCGGAGACATCGCTGTTGGACCCGCTATCATCGACTTCCCCCTTCCCGACGGTGGCG
|
|
CCGTGTCCGCCCCCGTTGAGGTTTCTCCCGTCGACTCCGTCGTCGTCGGCCCTGCCGCCG
|
|
GCTCTCAGAGCTCTCCCCTCGTCCAGATCATCATCAACGTTAAGGCCCCCGCTGGTGCCG
|
|
GCCCCGTTGTCGATGCCGTCGCTGACAAGCCCATGGACATCATTGATGTTATGCCCGTCG
|
|
TCGACCCTGCTGATTTCGTGGACCTCACCCCCGTTGTAGAGCCTGTAGAAGTCGTCGACA
|
|
TTGTCGATGTCATGCCCGTGGTTGACCCCATCAACATCATCGATGTTATGCCTGTTGTTA
|
|
AGCCCGTAAACCCCCTTGCCCGTTCTT
|
|
>M. sexta-Chitin synthase 2 (MSCHS2); AY821560.1
|
(SEQ ID NO: 117)
|
ATGGCCGCAACTACACCAGGTTTTAAGAAGTTAGCAGACGATTCTGAGGATTCAGATACA
|
|
GAATACACCCCGCTGTATGATGACGGTGATGAAATAGATCAAAGAACTGCACAAGAAACA
|
|
AAAGGATGGAATCTATTTCGAGAGATTCCGGTGAAAAAGGAGAGTGGATCTATGGCCACA
|
|
AAAAATTGGATAGAAACAAGCGTAAAAATCATAAAAGTGCTTGCCTACATATTGGTTTTT
|
|
TGTGCTGTACTGGGTTCCGCAGTCATAGCTAAAGGAACTCTTCTATTTATTACGTCACAA
|
|
CTGAAGAAAGACAGACAAATTACTCACTGCAATAGACGACTTGCTTTAGACCAACAGTTC
|
|
ATAACGGTACACAGTTTAGAAGAAAGAATAACATGGCTATGGGCAGCACTTATTGTATTC
|
|
GGTGTGCCGGAGTTAGGGGTGTTTTTGAGATCCGTCAGGATATGCTTCTTCAAAACTGCC
|
|
AAGAAACCAACCAAAACACAGTTTATTATTGCTTTCATAACAGAGACACTACAAGCAATA
|
|
GGAATAGCAGCACTTGTATTAATAATTCTACCAGAATTAGACGCTGTGAAAGGAGCCATG
|
|
TTGATGAACGCCACGTGCGCTATCCCTGCATTGCTAAACATTTTCACGAGAGACCGAATG
|
|
GATTCTAAGTTTTCTATAAAATTGATATTGGATGTATTGGCGATATCGGCACAAGCCACG
|
|
GCGTTTGTTGTTTGGCCTCTTATGGAAAGAACGCCAGTTCTATGGACCATACCAGTTGCA
|
|
TGTGTGTTAGTGTCTCTAGGCTTCTGGGAGAATTTTGTTGACACCTACAATAAAAGTTAT
|
|
GTTTTTACGGTGCTGCAGGAACTACGCGACAACCTCAAGAGGACTCGGTACTACACTCAG
|
|
CGGGTGCTATCTGTTTGGAAGATTATAGTGTTTATGGCATGCATTTTAATATCGCTGCAT
|
|
ATGCAAAATGACAATCCGTTTACCTTTTTCACTCACGCCAGCAAAGCCTTTGGAGAGAGA
|
|
CAGTATGTCGTTAACGAGGTTCTAATAGTAGTCCGAGATGACGAAACCATAGGCTATGAC
|
|
GTCACCGGAGGTATATTCGAATTGGACGCGATATGGACCTCAGCATTGTGGGTCGCATTA
|
|
ATTCAAGTGGGAGCAGCCTACTTCTGTTTCGGAAGTGGCAAGTTTGCTTGCAAAATTCTT
|
|
ATACAAAATTTTAGTTTCACTTTAGCATTGACTCTCGTCGGGCCCGTGGCAATCAACCTC
|
|
CTTATTGCTTTCTGCGGAATGAGAAATGCAGACCCTTGCGCTTTCCATAGAACTATACCT
|
|
GACAATTTGTTTTACGAGATACCACCTGTG
|
|
>M. sexta-Beta-fructofuranosidase 1 (MsSuc1); GQ293363.1
|
(SEQ ID NO: 118)
|
TTGCTGTGCGTTTTCCTTGGTAGTGTATCGTCATGTTGCGTTAATGGGCGGTACTACCCG
|
|
AGGTACCATTTGTCGCCACCGCATGGCTGGATGAACGACCCCAACGGATTCTGCTACTTC
|
|
AAAGGTGAATACCATATGTTTTACCAGTACAATCCCATGTCAAGTTTGGAGGCTGGCATA
|
|
GCTCATTGGGGTCATGCGAAAAGTAAAGATTTGTGCCATTGGAAACACTTAGACCCGCCA
|
|
TCTATCCTGATCAGTGGTACGATCAAACGGGAGTATTTTCTGGAAGTGCGCTAGTAGAGA
|
|
ATGACGTCATGTACCTTTATTATACTGGAAATGTAAATCTTACTGATGAAATGCCATTTG
|
|
AGGGACAATTCCAAGCTCTTGGTATCAGTACTGACGGTGTCCACGTAGAAAAGTATAAAG
|
|
ACAATCCAATAATGTACACGCCAAACCATCAACCTCACATCCGAGACCCAAAAGTTTGGG
|
|
AACACGACGGCTCTTATTATATGGTCTTAGGAAACGCATATGATGATTATACAAAGGGCC
|
|
AAATAGTTATGTACGAATCATCAGACAAGATCAACTGGCAAGAAGTAACTATACTATATA
|
|
AATCAAATGGATCTTTCGGTTACATGTGGGAGTGTCCAGATTTATTCGAAATAGACGGCA
|
|
AGTTTGTACTTCTGTTCTCTCCTCAAGGCGTGAAGTCTGTGGGCGATATGTACCAGAATC
|
|
TGTATCAAGCAGGATACATCGTCGGAGAATTCGATTACGATACTCATTCATTCACAATAC
|
|
TAACCGAATTCAGAGAATTGGATCACGGTCATGATTTTTACGCTACACAAACAATGAAAG
|
|
ATCCTAGTGGAAGAAGAATAGTCGTTGCTTGGGCAAGT
|
|
>M. sexta-Beta-1 tubulin (MsßTub); AF030547
|
(SEQ ID NO: 119)
|
ATGAGGGAAATCGTGCACATCCAGGCTGGCCAATGCGGCAACCAGATCGGAGCTAAGTTC
|
|
TGGGAGATCATCTCTGACGAGCATGGCATCGACCCCACCGGCGCTTACCATGGCGACTCG
|
|
GACCTGCAGCTGGAGCGCATCAACGTGTACTACAATGAGGCCTCCGGCGGCAAGTACGTG
|
|
CCGCGCGCCATCCTCGTGGACCTCGAGCCCGGCACCATGGACTCTGTCCGCTCCGGACCT
|
|
TTCGGACAGATCTTCCGCCCGGACAACTTCGTCTTCGGACAGTCCGGCGCCGGTAACAAC
|
|
TGGGCCAAGGGACACTACACAGAGGGCGCCGAGCTTGTCGACTCGGTCTTAGACGTCGTA
|
|
CGTAAGGAAGCAGAATCATGCGACTGCCTCCAGGGATTCCAACTCACACACTCGCTCGGC
|
|
GGCGGTACCGGTTCCGGAATGGGCACCCTCCTTATCTCCAAAATCAGGGAAGAATACCCC
|
|
GACAGAATTATGAACACATATTCAGTTGTACCATCACCCAAAGTGTCTGATACAGTAGTA
|
|
GAACCTTACAATGCAACACTGTCAGTCCACCAACTCGTAGAAAACACCGACGAAACCTAC
|
|
TGTATCGACAATGAGGCTCTCTATGACATCTGCTTCCGCACGCTCAAACTTTCCACACCC
|
|
ACATATGGCGACCTTAACCACCTGGTGTCGCTCACAATGTCCGGCGTGACCACCTGCCTC
|
|
AGGTTCCCCGGTCAGCTGAATGCGGATCTCCGCAAGCTGGCGGTGAACATGGTGCCCTTC
|
|
CCGCGTCTGCACTTCTTCATGCCGGGCTTCGCTCCGCTCACGTCGCGCGGCAGCCAGCAG
|
|
TACCGCGCCCTCACCGTGCCCGAACTCACCCAGCAGATGTTCGACGCTAAGAACATGATG
|
|
GCGGCGTGCGACCCGCGTCACGGCCGCTACCTCACCGTCGCCGCCATCTTCCGTGGTCGC
|
|
ATGTCCATGAAGGAGGTCGACGAGCAGATGCTCAACATCCAGAACAAGAACTCGTCGTAC
|
|
TTCGTTGAATGGATCCCCAACAACGTGAAGACCGCCGTGTGCGACATCCCGCCCCGTGGT
|
|
CTCAAGATGTCGGCCACTTTCATCGGCAACTCCACCGCTATCCAGGAGCTGTTCAAGCGC
|
|
ATCTCTGAACAGTTCACCGCTATGTTCAGGCGCAAGGCTTTCTTGCATTGGTACACCGGC
|
|
GAGGGCATGGACGAGATGGAGTTCACCGAGGCCGAGAGCAACATGAACGACCTGGTGTCC
|
|
GAGTACCAACAGTACCAGGAGGCCACCGCCGACGAGGACGCCGAGTTCGACGAGGAGCAA
|
|
GAGCAGGAGATCG
|
|
>P. xylostella-Peptidoglycan recognition protein 2 (PxPGRP2); ACB32179.1
|
(SEQ ID NO: 120)
|
CCCGATACAGTTGGAGTACCTGCCCCGGCCCCTGGGGCTGGTGGTGGTCCAGCACACCGC
|
|
CACCCCCGCGTGTGACACTGACGCCGCGTGTGTGGAGCTGGTGCAGAACATACAGACCAA
|
|
TCATATGGATGTGCTGAAGTTTTGGGATATTGGACCGAACTTCCTGATTGGTGGGAACGG
|
|
CAAGGTGTACGAGGGCCCTGGTTGGCTGCACGTCGGCGCCCACACTTACGGCTACAACAG
|
|
GAAGTCTATCGGGATCTCTTTCATTAGGAATTTTAATGCTAAGACCCCAACAAAAGCAGC
|
|
GTTGAATGCGGCTGAAGCATTGCTGAAGTGTGGAGTGAGAGAAGGACACCTGTCTCACTC
|
|
ATACGCAGTGGTCGGCCATAGACAACTGATCGCAACAGAGAGCCCAGGCAGGAAACTGTA
|
|
CCAAATCATCAGGCGCTGG
|
|
>P. xylostella-Immune Deficiency Protein (PxIMD); Px003008
|
(SEQ ID NO: 121)
|
TCCCGAAGCCACCTAGAGAACCGGTAGAGACTACAGAGACATCACAAAATAATACCGAAA
|
|
ATCAACCTTACAATGTCGAAGAAGAGGAAATACCCGAACCAGAAAAGCCTAAGAAAGAAA
|
|
AAAAGAATCCCAAGCCTACCAAAAAAACTTTCTTTAATCGTGACAAAACTAACAAACACG
|
|
ACGATACCCGCAAACATACAAAATCCGGAAAGGACCAGACATCAATTAATACTCAAGGTA
|
|
ACTTGAAAATTATACTTCCTGTAACTTAAACGGCCCGTTGACCCCAGTTTACCTTTCGCC
|
|
TTTCTTGATATATTTTTGTAATCCAGCCTTACTTTGGTAATACATACTTGCCCCACTTGT
|
|
ATTTAGTTAATGGTGGCACTAGCTAGATAGTAATGTTAAATGATGATAAGCAGTAGTGAT
|
|
TCATCATTCAAATGTATCATTGTCCTTTAATGTTAAGCGCAAATAGATTTTCATTGTTCT
|
|
CCCATGTGCTTCATGTTTTATGTATTTATAGGTAGGTACTTAATGTTTTATAAATATTTT
|
|
TTTGTTAATTGGGAATCCCCAGTCCCCATTGTCTGGACCAGTTTATATATAATTGAACTA
|
|
ACAAGAGTGTGCTTTAAATACTATTCTCTGCAATTATGATAATTAAACAACATGAATTTC
|
|
TCTTCACTTCCCTTCTCTTATTTAAATAATATTGTAGGAAACTGTAATAACTAATACAAG
|
|
ATTATAAATTTCATTCTAGCAACTGGTGATGTAATCCATGTGGTAAATTCCAAAGATGTG
|
|
CAGGTCGGCCATCAGTATGTGTACAACATGGGAACTCCCGGAGCTAACTCACAGAAGAAT
|
|
AACCCATTTGATGATGAAGAAACAGTAGAAAAGACAAATCTAATAACTCTGGTCATGGAA
|
|
GCAAAAATTATGGTAATAACACATTTTTAACTAGGCATAAGGTCATAATTTAGCCAGAAT
|
|
CATCAGCTTGT
|
|
>P. xylostella-Cactus (PxCac); Px016665
|
(SEQ ID NO: 122)
|
CAATGCTGCGGAGGGTCTATGCGGGTGGACACCTCTACACGTAGCGGCGGCGCGAGGCGA
|
|
CGTCGACACGGCTCGCTACTTGCTCGAGAAGTGCGCTGGCGTCGATCCCTCTGCCCTGGA
|
|
CTACGCCGGTCGTACGGCCAGGAAACTGGCGTTGAAGAATAAAGCGGCCGCCCTGTTTGA
|
|
CGGCAGTGAGGGCAGCGAGGAGGAGGATAGTGACAGTGAGGATGAGATGCTTCTGGAAAG
|
|
CGACCAGAGTCTGTTCGACCGGATCCGTGACGGTATGAACGCCATCAACGTCGCCTGA
|
|
>P. xylostella-Dorsal (PxDor); Px000110
|
(SEQ ID NO: 123)
|
TAACCTGTGCCAGCAACCAATGGCTCCTATGGCGCAGCAGCTGATGGACCCGTCCCCCAG
|
|
CGACCCACCCTCCATCACGGGGCTGCTGATGGATCGCCCGGACCAGCCCTACTCCGGGGA
|
|
GCTGTCTGGACTCTCCGCCCTGCTGGCTGAGGCAGCCCCCGCAGAGATGCTCAGCGATAG
|
|
CCTCAACAGACTGTCTACGGGGGACTTGTTGAGACAAGTTGATATGTGA
|
|
>P. xylostella-Beta 1-3 glucan recognition protein 2 (PxßGRP2); Q8MU95.1
|
(SEQ ID NO: 124)
|
GAAGGATTGAAGTGAGCGCCAGAATGCCGCGCGGTGATTGGTTGATTCCAGATATTCTGC
|
|
TGGAGCCGAAAGAAAACCTTTACGGAGTACGCAATTACGCGTCAGGTCTACTCAGCATAG
|
|
CCTCAGTCAGAGGAAACACTGCTTACTCGAAGACCCTCAAAGGAGGCCCCATACTGTGTG
|
|
ACAAGGAACCGCAGAGAAGTGCCAAGTTGAGCGAAAAAGTTGGATATGACCATTGGAATA
|
|
AAGCCTTCCATAACTACACCATGATTTGGGCACCAAGTGGCATCACCATGCTGGTGGACG
|
|
GCGAGCAGTACGGGGACATCCGTCCCGGCGACGGCTTCAGCCAGGACCCGGCGGTGAGCA
|
|
GCGTGGTGGCCGCGCCGCAGTGGCTGAAGGGCACCAGCATGGCGCCCTTTGATGTTATGT
|
|
TCTACATATCCCTTGGTCTCCGCGTGGGCGGAGTGAACGACTTCCCCGACACTCCTGAGA
|
|
AGCCGTGGAAGAACAAGGCCACTAAAGCCATGCTGAATTTCTGGAACGCCCGGGAACAGT
|
|
GGCAGAGCAGCTGGTTTGAGGACACCACTGCACTCCTCATAGACTATGTCAGGGTTTATG
|
|
CGCTGTGA
|
|
>P. xylostella-Chitin synthase 1 (PxCHS1); KX420688.1
|
(SEQ ID NO: 125)
|
CGTATCTCGCACGACCTGAAAGAGCTGCGAAACTCATCCGTCTTTTCCTTCTTTATGATC
|
|
AATGCCCTCTTTGTTCTCATCGTATTCTTGCTGCAACTGAACAAGGACAACCTCCACATA
|
|
AAGTGGCCCTTCGGAGTCAAAACTAACATTACGTATGATGAGGTGACGCAAGAGGTGCTG
|
|
ATCTCCAAGGATACCTGCAACTAGAGCCTATTGGTCTGGTGTTCGTGTTCTTTTTCGCAT
|
|
TGATTTTAGTCATCCAGTTCACTGCCATGTTGTTCCATCGATTCGGAACTTTGTCGCATA
|
|
TATTATCGTCTACGGAACTGAACTGGTTCTGCAATAAGAAGGCGGAAGACTTATCTCAAG
|
|
ACGCACTGCTAGATAAGAATGCGATAGCAATAGTGAAGGATCTCCAGAAACTAAACGGGC
|
|
TCGATGACGGGTATGACAATGACTCGGGGTCGGGCCCGCACAATGTGGGAAGGAGAAAGA
|
|
CGATACACAACCTGGAGAAAGCGAGACAGAAGAAGAGGAACATAGGAACGCTCGACGTCG
|
|
CTTTCAAGAAGCGATTCTTCAACATGAACGCTAATGAAGGACCAGGAACACCAGTTCTGA
|
|
ACCGCAAGATGACGTTGCGAAGAGAGACGTTGAAGGCGTTGGAAACGAGGAGGAATTCTG
|
|
TGATGGCCGAACGAAGGAAGTCGCAAATGCAAACACTTGGAGCTAACAACGAATATGGAG
|
|
TCACTGGAATCTTAAACAACAACCCAGCGGTGATGCCGCGCCACCGGCCGTCGACAGCCA
|
|
ACATTTCGGTCAAGGACGTCTTCGCGGAACCCAACGGGGGACAAGTGAACCGAGGGTACG
|
|
AGACCACGCACGGCGACGAGGGAGACGGCAACTCCATCAGACTGCAGCCGAGAACCAACC
|
|
AGGTCTCCTTCCAGGGGAGATACCAATAA
|
|
>P. xylostella-Beta tubulin (PxBTUB); KX420688.1
|
(SEQ ID NO: 126)
|
GAAGGAGGTCGACGAGCAAATGTTGAACATCCAGAACAAGAACAGCAGCTACTTCGTCGA
|
|
ATGGATCCCGAACAACGTCAAAACGGCCGTGTGCGACATACCGCCTCGTGGACTGAAGAT
|
|
GTCTGCCACCTTTATCGGGAACACGACAGCAATCCAAGAGCTCTTCAAGAGGATTTCTGA
|
|
GCAGTTCACTGCTATGTTCAGGAGGGAAGCGTTCCTCCACTGGTATACTGGTGAAGGCAT
|
|
GGACGAGATGGAGTTCACAGAGGCGGAGAGCAACATGAACGACCTGGTCTCCGAGTACCA
|
|
GCAGTACCAGGACGCCACGGCTGAAGACGAGGGAGAATTCGACGAGGATATTGAAGACGA
|
|
GTGA
|
|
>S. frugiperda-Peptidoglycan recognition protein 1 (SfPGRP1); rep_c7951
|
(SEQ ID NO: 127)
|
CCTGATTGGTGGAAACGGGAGAGTTTATGAAGGAGCCGGCTGGCATCACGTTGGGGCCCA
|
|
TACTTTGGGATACAATGCAAGATCTGTGGGGATCTCCTTCATTGGCGATTTTAGAACAAA
|
|
ATTACCAACACCCGAAGCACTGAAAGCCTTCAACAGTCTCCTGGAATGTGGAGTCACGAA
|
|
CAATTATCTGTCAAAGGACTATCACCTGGTGGCCCATAGTCAGCTCTCTATGACTGACAG
|
|
TCCYGGAGACATGYTGAGGAAGCAGGTGGAATCGTGGCCTCMTTGGCTGGATAATGCCAA
|
|
AGACATACTTAAGTAGAARAAGACTAAACGCCGTACTTTGAGCCATTTAATGGTTACTTA
|
|
ACCCAGTCCTTAGCAATTTGATACAAGGCCAATGTCTCTAAGGGCGGCAGTAAAGGTCAA
|
|
AACACATTTAATGAGTGTGTTTAAGATTTTGCTAGTGAAAATTGTTTTGAAGTACGTATT
|
|
TGATGTAAGTGATGATATCAGTACCCTTAGTATGAGTTTGCTTTACGTTCCACGAGATGG
|
|
AAACGAGAGCGCGTTCGGCGCTCTGATTGGTTCGTTCATTCATGCCGGCC
|
|
>S. frugiperda-Attacin (SfAtta); rep_c9395
|
(SEQ ID NO: 128)
|
GCCAGACATCTACCACAGGACCACTCAACGTACGACCAAGTACAACTCCTCGGGTTCGAC
|
|
GAAGATGGACGACCAGTGTTTGAGCACGAAGACTTACTCCCAGAACTAGAGGAGTCCTAC
|
|
CAGCCAGAGCACCTGGCGAGGACTCGCAGACAGGCGCAGGGCAGCGTCACCCTCAACTCC
|
|
GACGGCGGCATAGGCCTGGGCGCTAAGATCCCGCTCGCACACAACGACAAGAATGTGGTG
|
|
AGCGCCATCGGCTCCATGGACTTCAACAACAAGTTGCAGCCTGCTTCCAAGGGCTTCGGT
|
|
CTGGCTCTGGACAACGTCAACGGGCACGGACTGACGGTGATGAAGGAAAGTATCCCCGGG
|
|
TTCGGGGACAGGCTGTCGGGCGCTGGCAAGCTGAACGTGTTCCACAACGACAACCACAAC
|
|
GTGGCCGTGACCGGCTCTCTCGCCAGGAACATGCCCAGCATCCCGAACGTGCCCAACTTC
|
|
AACACGTACGGCGGGGGCGTCGACTACATGTACAAGAACAAGGTGGGAGCGTCTCTGGGC
|
|
ATGGCCAGTACTCCGTTCTTGGACCGCAAGGACTACTCCGCGATGGGCAACCTGAACCTG
|
|
TTCCGCAGCCCGACCACTACCGTGGACTTCAGCGGCGGCTTTAAGAAGTTCGAATCTCCC
|
|
TTCATGAGCAGCGGCTGGAAGCCTAACTTCGGCCTTACTTTCGGCAGATCTTTCTAGATA
|
|
TATTTTGTAATCTAAATTTAACTTTAACTTTGTTGTATAATATTTTGTCGAATTAAGATC
|
|
AGTATTGTTCATACTAATATTATATTATCAGTGTTTCTTATAAATTAA
|
|
>S. frugiperda-Hemolymph proteinase 10 (SfHP10); c12881
|
(SEQ ID NO: 129)
|
CAAGGCTCGTACCTTGCAGTTGAACCGACAATCTATTCCTAAAGCCTTTTTAAGGTCAGG
|
|
AAAAATAGTTCCTACATCTAAATGCAGTAGAATTTGCGAAACGAATTTAAATAAAAATGG
|
|
CGTCGATTGTGTTTGTGATTTTGTGTGTTACCGTCGCTGCGGTGAAAAGCGCGATTTTAA
|
|
ACCCGTGGAGTAAAGTTGAGGCCAACAAATGTGGTGTAGAAGCCAGTACTAACTTGGTCC
|
|
ATCACAATCCATGGTTGGTCTACATCGAGTATTGGCGTGGAAACTCAGATACTGAGATCC
|
|
GATGCGCCGGTACTTTAATCGACAGCAAACATGTCGTCACAGCTGCCCACTGCGTTAGGA
|
|
CTCTGAAGTTTAGTCATTTGATCGCCCGTCTTGGCGAATACGACGTAAATTCTAAGGAGG
|
|
ACTGCGTTCAGGGCGTGTGTGCCGATCCCATCGTCAGAATCAAGGTGGCTGAGATCATCG
|
|
TGCATCCTAACTACAGCAACCGGGAACA
|
|
>S. frugiperda-Trypsin like serine protease (SfTSP); rep_c48453
|
(SEQ ID NO: 130)
|
AGCAACAAAATGCGTGTCCTCGCTTGCTTGGCCCTTCTCTTAGCTGTGGTAGCAGCCGTC
|
|
CCCTCCAATCCCCAGAGGATTGTGGGTGGTTCGGTCACCACCATTGACCGGTACCCCACC
|
|
ATTGCATCCCTGCTGTACTCGTGGAACTTGAGTTCCTACTGGCAGGCGTGCGGTGGTTCC
|
|
ATCTTGAACAACCGTGCCATCCTTACTGCTGCCCACTGCACAGTTGGTGACGCCGCCAAC
|
|
AGATGGAGAATCCGTCTTGGCTCCACCTGGGCCAACAGCGGTGGTGTCGTTCACAACGTC
|
|
AACACTAACATCGTCCACCCCTCATACAACTCTGCAACTTTGAACAACGACATCGCTATC
|
|
CTCCGCTCCGCCACCACCTTCTCCTTCAACAACAATGTTCAGGCTGCCTCCATTGCTGGT
|
|
GCCAACTACTTGCCCGGTGACAACACCGCCGCCTGGGCCGCTGGATGGGGAACTACCTCC
|
|
GCTGGTGGCTCTAGCTCTGAGCAGCTCCATCACGTTGAGCTGCGCATCATCAACCAGGCT
|
|
ACTTGCAAAAACAATTACGCTACCCGCGGTATCACCATCACCTACAACATGTTGTGCTCT
|
|
GGCTGGCCCACCGGTGGTCGCGACCAGTGCCAGGGTGACTCTGGTGGTCCTCTCTACCAC
|
|
AACGGCATCGTTGTTGGTGTCTGCTCTTTCGGTATTGGCTGTGCTCAG
|
|
>S. frugiperda-C Type Lectin 6 (SfCTL6); Joint2_ rep_c448
|
(SEQ ID NO: 131)
|
AACAGTTTTCTATTGGCAGTCAAAGACTTCAGTCGAAAAATAATCCTCATCAGAGTCGTG
|
|
AAGCAAGGTGCCCAAAATATAATGTAACCTAGATACCTATTAATAAATTATTTGTCAACC
|
|
AAAACGTTACGTTCAAAGTCCTTAAAATCAAAATATCTTATGATTAGTTTTGATTTAAAA
|
|
ATAGAGGTTCGAAATCGCCAACCCAAATAGGTTTAGTTTACGATTCAGGAAAAATCCTAA
|
|
CGTAGGGAAACATTATTTTACAAGACTTTTGGCTTAAAAACTTTGAGAACCAATGTCAAA
|
|
TTTGATAATAACTAATGAGGTATAAAAGCTTGATCCTATTAGGACTTATTTTCATAACAC
|
|
CATCGAGTTTGTATTTAATRRAGACGTGKGTTAACTAACAACATGAAGACCGGTGTAAAA
|
|
TATTCTGTTMTTTGGATATTCTCTCTATTYTGCTATATAGAGGCAACATTTCGTTGTGAC
|
|
TACACGTACAGCAAGGAAGCGAAGGGCTGGTTCAAACATGTGGTGATACCAGCTACTTGG
|
|
GCTGACGCACGWCTGCACTGCACGTTGGAAGGTGCAACGCTGGCTTCTCCACTCAACCAG
|
|
GCTATMAGTAATGAGATGCAGTCCMTCCTGGCRAACCTCTCGGCGCTGCAATCAGAAGTC
|
|
TTCACTGGAATTCACRCGACTKTTTCACGRMRCAACTTATATCATACYATYGAAGGTATA
|
|
CCTCTTAGTAAAATTCCATTAGATTGGGCAACAAATGAGCCAAATGGTGGGAGAGATGAA
|
|
AACTGTATCACGTTTAACTCCGATGGCCAAGCGGCAGACAGATCCTGTAARGAGACTCGA
|
|
CCTTACATCTGCTACCGACACACWACTAAAGTGACTGTGKCCAATGAATGTGGGACTGTA
|
|
GATCCTGAATACAATTTGGATAAAAGAACGGGCKCYTGCTATAAGTTCCACACRGTACCT
|
|
CGCACGTTCGAGCGTGCCAACTTCGCGTGTTCTGCTGAAGGTG
|
|
>S. frugiperda-Cecropin (SfCec); rep_c42380
|
(SEQ ID NO: 132)
|
TTCGTGTCGTATCACTAGAGTTCGAAATACAAAATAATAATACATTTATTATTTTGCCAT
|
|
AATTAATAATAAAGTTATTTTATTTCATAATAATAATGAATTTCACAAAGATATTTTGTT
|
|
TGTTTTTGTCTTGCTTTGTTTTGATGGCGACCGTGTCAGGAGCTCCTGAACCGAGGTGGA
|
|
AATTCTTCAAGAAAGTGGAGAAGTTGGGCCAAAACATCCGCKATGGTATCATAAAGGCAG
|
|
GACCCGCAGTGGCCGTGGTGGGATCAGCRGCAGCCATWGGAAAGTGAKCCCTACGACCTG
|
|
AGACATGAAGACTAATATCCAYTAAAATAASAATATTGAGGCKTATAATATTAATTTATT
|
|
RTRTTTGTAAATTAAATTATTTGTAAGATAA
|
|
>S. frugiperda-Beta 1, 3 glucanase recognition protein (SfßGRP2); EF641300
|
(SEQ ID NO: 133)
|
GCAACAATCGCACCAACTCTTTCGTGCGCAGTGGAAGTTTGTTCATCCGTCCCTCTCTAA
|
|
CATCAGACGAGTTCGGAGAAGCTTTCCTCTCATCTGGACACTGGAACGTCGAGGGTGGTG
|
|
CTCCTGCTGATAGATGCACAAATCCACAATGGTGGGGTTGCGAGAGAACAGGCACGCCGA
|
|
CCAACATTTTGAACCCAATCAAGAGTGCTCGTGTCCGTACCGTCAATTCCTTCAGCTTCC
|
|
GTTACGGACGCCTCGAAGTCCGCGCTAAAATGCCCGCCGGAGATTGGATTTGGCCAGCTA
|
|
TCTGGTTGATGCCTGCGTACAACACTTACGGTACTTGGCCCGCATCAGGAGAGATTGACT
|
|
TAGTTGAGTCCCGAGGCAACCGTAACATGTTCCACAATGGTGTCCATATCGGTACACAGG
|
|
AAGCAGGCTCGACCTTGCACTACGGACCTTACCCAGCGATGAACGGTTGGGAGCGCGCCC
|
|
ATTGGGTCAGAAGGAACCCT
|
|
>S. frugiperda-joint2_rep_c16438 (Sfrc16438); Un-annotated
|
(SEQ ID NO: 134)
|
TCGTTCTCCTCGTCGCTTTCTTGGGGACCTCATGGTTTACGGGAGATGTTTCTGCGAGTC
|
|
CGCGGCCGCAAGAGCCGCGTGTGGATCAAAATCCGAATCAGGTGTCACCTTATGGAGGGT
|
|
CCGGGTACCACGCACCTCCGCAGTACCAACCGCAGTACCAACCACAGCCGTACTACCCAC
|
|
AGCCGCAGTACTACCCACAGCCGTACTACCCACCTCCTCAGTATTACCCACCGCAGCCAC
|
|
AAACACCTGAGAATGCTCCACTCATAAACACATGGAATGGTTTCCACGACTGGGCTCAGA
|
|
ATATCGTTCAAAGTGCTTTGGGGCAGAAATTCCCGAAAGGTAGACAGTAACTTTTTAATT
|
|
GTCAATTGAAGATAAGGCCCATTTCACCAACTGCTGTTTAATTTTAAGGAGCTCCTAAAC
|
|
TAACATAGGTGACACTTAGCGATATTCTGGATTTTTTGTGAACGTATAAATAATATCCAA
|
|
ATGTAAAAGATAAGAGGCCAAGAA
|
|
>S. frugiperda-Chitin synthase B (SfChsB); AY52599)
|
(SEQ ID NO: 135)
|
GAATTTAGGAGCAGCGTGCGGGCGCATCCATCCTGTGGGCTCAGGCTTCATGGCATGGTA
|
|
TCAAATGTTCGAGTACGCTATTGGTCATTGGCTGCAAAAGGCGACTGAACACATGATTGG
|
|
CTGTGTACTCTGTAGCCCTGGATGCTTCTCCCTCTTCAGAGGAAAGGCTTTGATGGACGA
|
|
CAACGTTATGAAGAAATATACCTTAACTTCCCACGAGGCACGACACTATGTGCAATACGA
|
|
TCAAGGCGAGGACCGTTGGTGCACGCTACTGCTGCAGCGCGGGTACCGCGTGGAGTACAG
|
|
CGCGGTGTCGGACGCGTACACGCACTGCCCCGAGCACTTCGACGAGTTCTTCAACCAGCG
|
|
CCGCCGCTGGGTGCCCTCCACGCTCGCCAACATCTTCGACCTGCTCGGCAGCGCCAAGCT
|
|
CACCGTCAAGTCCAACGACAACATCTCCACCCTCTATATAGTCTATCAGTTCATGTTGAT
|
|
AGTGGGTACGGTGTTGGGTCCCGGCACGATCTTCCTGATGATGGGGGGAGCCATGAACGC
|
|
CATCATTCAGATCAGCAACGCGTACGCGATGATGTTGAACCTCGTACCACTCGTCATCTT
|
|
CCTTATAGTCTGTATGACTTGTCAGTCAAAGACGCAGCTCTTCCTCGCTAACCTCATAAC
|
|
ATGCGCATACGCAATGGTGATGATGATCGTGATAGTGGGGATAGTTCTGCAGATAGTGGA
|
|
GGATGGATGGCTGGCTCCGTCCAGTATGTTCACAGCTTTAATATTCGGTACATTCTTCGT
|
|
CACCGCGGCACTACACCCGCAAGAGATCAAATGTTTGTTGTTCATAGCAGTGTACTATGT
|
|
AACCATCCCTAGTATGTACATGTTGTTGATCATATACTCCATCTGTAATCTCAACAACGT
|
|
ATCCTGGGGTACCAGGGAGACACCGCAGAAGAAAACTGCTAAGGAAATG
|
|
>T. castaneum-Peptidoglycan recognition protein 2 (TcPGRP2); XM_965754.3
|
(SEQ ID NO: 136)
|
ATGAGTGGCAGTGACCCTTTAACAAATACCCAACAATCCGATCAAGATTATTACCATCCA
|
|
CTCTGTTATTCAATTCAAGTGGACGACGAAAATGAACAATCAGCTCTCCTGCCCGCATTT
|
|
CATCAAAGGAAAAGTTTGCGAGTTCAGGATAAAATCTTTATTGTATTTTTATTTTCAATT
|
|
CTAATTACCGGACTAGCCATTGGCCTCTATCTCCTTGCAACTGAGGGACACGAATGGAAA
|
|
GCTGCAGGAGTCTATAATATTACAGTTCGGGAACAGTGGCAAGCTCACGTCCCTTCATCA
|
|
ACAATGCCAAAGTTGGAACTTCCCGTAAGAAGAGTTTTATTTCTTCCTGCAAATACCACT
|
|
AGCTGCGGCAGCAAATCCCACTGTGCCAAAGTCCTCCAGGAACTACAATTACAGCATATG
|
|
CTGCAGTGGAAAGAACCTGACATCTCCTACAATTTCATAATGACTGCAGATGGCAGAATT
|
|
TTCGAGGGGAGAGGATGGGACTTTGAAACTTCTGTTCAAAATTGTACGGTTAATGATACT
|
|
GTGACAGTTGCTTTTTTGGACGAATTAGATGCGAAAGCACCGACGTTTAGACAAGCTGAA
|
|
GCGGCAAAAATGTTCCTGGAAGT
|
|
>T. castaneum-Beta 1-3 glucan binding protein (TcßGRP2); XM_966587.4
|
(SEQ ID NO: 137)
|
ACATTACAACGTTCCGCGACCCTCAATCCAAGCATTCAGGCCCCGTGGCTTCAAAGTGAG
|
|
CATCCCTCATACTGAAGGCATCCAATTATTCGCCTTTCATGGAAATATTAATAAACCCCT
|
|
GCACGGTCTCGAGGCCGGACAATTTTCCCAAGACGTCCTCCAAAGGGAGGGAGACGAGTG
|
|
GGTGTTCCAAGACTCCAGTGCCAAATTAAACGTGGGAGATAAAATCTATTATTGGCTCTT
|
|
TATCATTAAAGAAGACCTGGGCTACAGATACGATCACGGCGAGTACGAAGTGAAAGTTTT
|
|
AGCCACCCGTGACTTCGATTCTCCTCAAACAACCTCTGTGACGCCGAATCTTGCCCCCAA
|
|
TCTCGGCATTTGCGAAAAGGTGATGGTAAATCTCACGCGGAAGCTGCTCGATTTGCAGCA
|
|
AGAAATTGAGTCCCTTAGGGAGACGAACGATATTTTGGAGGATATGGTTCAGAAGCACAC
|
|
TGATACGGCGACTACTCTCACTTTGGACGGCTTGATGATAAAGGATGACGACGAACTTGT
|
|
TTCGGTGATTCAAGCAATTATTAAAGATAAACTTGGACTAAAAAGCAGGATTCAAAATGT
|
|
GACGAGGCAGGAGAATGGAATGGTCAAGTTTCAAGTGGCGAGTTTGAGAGAAAAGTTGGA
|
|
GGTTGTCAAAGCGGCCAAAAGAAAACTCAAGTCGTCGAGCTTTACGATCACGTATTAA
|
|
>T. castaneum-midgut protein (TcMDGP); XM_971351
|
(SEQ ID NO: 138)
|
CCGTTGAAGAGGATGCCCAGTGAAGAAATCAGTATCAGTGATCTGCCTAGCGAAATGAAA
|
|
GAAGTTTTACTAGAAATTAGCCCGAACTTTGATGAAAATCTGAAACGGGCTTTCAGGAAC
|
|
GAAGGAGTGAGGCTGCAGAGAGTGCAGAACAATGGACGATTTATTCATCAGCTGGACGAC
|
|
GTTCTCTTATCCATAGACGATACCAAAATCGAGTTACGCAACCTGAAATTCCCCTGGATC
|
|
CCCGACTTCCGCATCGTGGACTTGTCCAGCGACCTGCCCATGTCATGCCTCGACCTAAAC
|
|
CTAAACCTGGGCAATTTGCGAATTGAGGGCGAGTACGAAGCCAACAACACCACACTCAGG
|
|
CGATGGCTCCCGGTATCTCACATTGGTCGAATCGTGATCGGTTTTAACAACGTCCGAGCG
|
|
AACGGAAAAGTCGGACTCGTGCTCGAGCAGGATTCTTTCGTTCCGCAGAATTATGATATT
|
|
AGATATGAGCCGACGGATGTTGTTATTAGGGTTAGCTATCACGTGGATGGCGAGAATGAG
|
|
GTGCAAAATGAGATTAGCAATTCAGATATTGAGGCCACGCTAGGCAAGACCGTGTGGGTG
|
|
CAGTTGACTGAGATATTGTCCAACCTGTTGCATAGGCAATTGGGCGAGGTTGTAGTGGAG
|
|
T
|
|
>T. castaneum-Chitin synthase 2 (TcCHS2); EFA 10719.1
|
(SEQ ID NO: 139)
|
ATGGCGGCGCGTCATCGCTTTGCCACAGGGAGCCCTGAGGAAACAGAGCCCCTGTATTCG
|
|
TCGACGCAAATGCCCGAAAAAGTCCGGGAAAAATGGAACGTCTTCGACGACCCCCCAAGA
|
|
GAGCCCACTTCGGTTCCGAAGTCAAAAGAACCTACATCGAGTGGGGGGTGAAGTTTTTGA
|
|
AAGTTGTGACAATCATAACTGTGTTTTTTGTGGTCCTTGGTGCTGCAGTGGTTTCGAAAG
|
|
GGACAACCTTGTTCATGACGTCACAAATAAAAAAGAATGTGACAAGGGCTTATTGCAACA
|
|
AAAAGATAGACCGCAACCTCCAATTCGTCGTCTCCCTCCCCGAAGTGGAGCGCGTGCAAT
|
|
GGATCTGGCTCCTCATTTTCGCTTACTTGATCCCCGAAGTGGGTACCTGGATCCGCGCCG
|
|
TCCGCAAATGCCTCTACAAGCTCTGGAAAATGCCCTCCCTCTCCGAATTCCTCTCCCTCT
|
|
TCGGCACGGAAACGTGCCCCGCCATCGGAAGCGCAATTTTGATATTCGTCGTCCTCCCCG
|
|
AGCTGGACGTCGTCAAAGGGGCGATGCTCACAAACGCGGTTTGTTTCGTGCCCGGAGTTG
|
|
TGGCAATGTTCTCGCGCAAACCGTGCTCCATAAACGAGAACCTGAAAATGGGGCTGGACA
|
|
TCGCCAGCATAACTGCACAGGCGTCAAGCTTCGTGGTGTGGCCCTTGGTTGAAAATAACC
|
|
CGACCTTGTACCTAATCCCCGTTTCCGTGATTTTGATTTCGGTGGGT
|
The breadth and scope of the present disclosure should not be limited by any of the above-described exemplary embodiments, but should be defined only in accordance with the following claims and their equivalents.
REFERENCES
- 1. http World Wide Web internet site “fao.org/3/a-av013e.pdf”.
- 2. Polaszek A. (1998). African Cereal Stem Borers: Economic Importance, Taxonomy Natural Enemies and Control. Wallingford, UK: CABI. 530 pp.
- 3. http World Wide Web internet site “cnbc.com/2015/05/08/insects-feast-on-plants-endangering-crops-and-costing-billions.html”.
- 4. Khan Z R. et al. (2014). Achieving food security for one million sub-Saharan African poor through push-pull innovation by 2020. Philosophical Transactions of the Royal Society B: Biological Sciences, 369 (1639), 20120284.
- 5. Tabashnik B E. et al. (2013). Insect resistance to Bt crops: lessons from the first billion acres. Nat. Biotech. 31, 510-521.
- 6. Campagne et al. (2013). Dominant inheritance of field-evolved resistance to Bt corn in Busseola fusca. PLoS ONE 8(7):e69675.
- 7. http World Wide Web internet site “dtnpf.com/agriculture/web/ag/news/article/2016/08/10/rootworm-resistance-pyramided-bt”.
- 8. Terenius O. et al. (2011). RNA interference in Lepidoptera: An overview of successful and unsuccessful studies and implications for experimental design. Journal of Insect Physiology 57, 231-245.
- 9. Gayatri Priya N. et al. (2012). Host Plant Induced Variation in Gut Bacteria of Helicoverpa armigera. PLoS ONE. 7(1):e30768.
- 10. Peñuelas J and Terradas J (2014). The foliar microbiome. Trends Plant Sci. Volume 19, Issue 5, 278-280.
- 11. Casanova-Torres and Goodrich-Blair (2013). Immune Signaling and Antimicrobial Peptide Expression in Lepidoptera. Insects. 4, 320-338.
- 12. Tang X. et al. (2012). Complexity and Variability of Gut Commensal Microbiota in Polyphagous Lepidopteran Larvae. PLoS ONE. 7(7):e36978.
- 13. Ryu J, et al. (2008). Innate immune homeostasis by the homeobox gene caudal and commensal-gut mutualism in Drosophila. Science. 319, 777-82.
- 14. Shrestha S. et al. (2009). An inhibitor of NF-kB encoded in Cotesia plutella bracovirus inhibits expression of antimicrobial peptides and enhances pathogenicity of Bacillus thuringiensis. Journal of Asia-Pacific Entomology. 12, 277-283.
- 15. Buchon N. et al. (2013). Gut homeostasis in a microbial world: insights from Drosophila melanogaster. Nat. Rev. Microbiol. 11, 615-626.
- 16. Karlin S and Altschul S F (1990). Method for assessing the statistical significance of molecular sequence features by using general scoring schemes. Proc. Natl. Acad. Sci. USA. 87, 2264-2268.
- 17. Watson J M. et al. (2005) RNA silencing platforms in plants. FEBS Letters. 579, 5982-8987.
- 18. Zhong X. et al. (2012). A Toll-Spatzle Pathway in the Tobacco Hornworm, Manduca sexta. 42(7), 514-524.
- 19. Zhang X. et al. (2015). Phylogenetic analysis and expression profiling of the pattern recognition receptors: Insights into molecular recognition of invading pathogens in Manduca sexta. Insect Biochem. Mol. Biol. 62, 38-50.
- 20. Cao X. et al. (2015). The immune signaling pathways of Manduca sexta. Insect Biochem. Mol. Biol. 62, 64-74.
- 21. Wang et al. (2006). Interaction of β-1,3-Glucan with Its Recognition Protein Activates Hemolymph Proteinase 14, an Initiation Enzyme of the Prophenoloxidase Activation System in Manduca sexta. J. Biol. Chem. 281(14), 9271-9278.
- 22. Ward N and Moreno-Hagelsieb G (2014). Quickly Finding Orthologs as Reciprocal Best Hits with BLAT, LAST, and UBLAST: How Much Do We Miss? PLoS ONE 9(7), e101850.
- 23. Timmons L. et al. (2001). Ingestion of bacterially expressed ds RNAs can produce specific and potent genetic interference in Caenorhabditis elegans. Gene 263, 103-112.
- 24. Kanost M R. et al. (2016). Multifaceted Biological Insights From a Draft Genome Sequence of the Tobacco Hornworm Moth, Manduca Sexta. Insect Biochem. Mol. Biol. 76, 118-147.
- 25. Odman-Naresh J. et al. (2013). A lepidopteran-specific gene family encoding valine-rich midgut proteins. PLoS ONE 8:e82015.
- 26. Engel P and Moran N A (2013). The gut microbiota of insects—diversity in structure and function. FEMS microbiology reviews. 37(5), 699-735.
- 27. Siepel A. et al. (2005), Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes Genome Res. 15,1034-1050.
- 28. Pauchet Y. et al. (2010). Pyrosequencing the Manduca sexta larval midgut transcriptome: messages for digestion, detoxification and defence. Insect Mol Biol. 19, 61-75.
- 29. Kim S H and Lee W J (2014). Role of DUOX in gut inflammation: lessons from Drosophila model of gut-microbiota interactions. Front. Cell. Infect. Microbiol. 3, 116.
- 30. Lee W J and Hase K (2014). Gut microbiota-generated metabolites in animal health and disease. Nat. Chem. Biol. 10, 416-424.
- 31. Brummett et al. (2017). The immune properties of Manduca sexta transferrin. Insect Biochem Mol Biol. 81, 1-9.
- 32. Xia Xu et al. (2012). Manduca sexta Gloverin Binds Microbial Components and is Active against Bacteria and Fungi. Dev Comp Immunol. 38(2), 275-284.
- 33. Gunaratna R T and Jiang 1-1 (2013). A comprehensive analysis of the Manduca sexta immunotranscriptome. Dev. Comp. Immunol. 39, 388-398,
- 34. Broderick N A. et al. (2009). Contributions of gut bacteria to Bacillus thuringiensis-induced mortality vary across a range of Lepidoptera. BMC Biol. 7:11.
- 35. Gregory R. Richards (2008). Xenorhabdus nematophila lrhA is necessary for motility, lipase activity, toxin expression, and virulence in Manduca sexta insects. Journal of Bacteriology. 190, 4870-4879.
- 36. Timmons and Fire (1998). A. Specific interference by ingested dsRNA. Nature. 395, 854.
- 37. Kamath R S. et al. (2000). Effectiveness of specific RNA-mediated interference through ingested double-stranded RNA in Caenorhabditis elegans. Genome Biol. 2, 1-10.
- 38. Cao et al. (2018). A systematic study of RNAi effects and dsRNA stability in Tribolium castaneum and Acyrthosiphon pisum, following injection and ingestion of analogous dsRNAs. Int. J. Mol. Sci. 19, 1079.
- 39. Rajkunar A P3 et al. (2015). Experimental validation of methods for differential gene expression analysis and sample pooling in RNA-seq. BMWC Genomics. 16(1), 548.
- 40. Zhang et al. (2015). Full crop protection from an insect pest by expression of long double-stranded RNAs in plastids. Science. 347, 991.
- 41. Kim S R, Yao R, Han Q, Christensen B M and Li J (2005). Identification and molecular characterization of a prophenoloxidase involved in Aedes aegypti chorion melanization. Insect molecular biology. 2005; 14(2):185-194.
- 42. Packey C D and Sartor R B (2009). Commensal Bacteria, Traditional and Opportunistic Pathogens, Dysbiosis and Bacterial Killing in Inflammatory Bowel Diseases. Current opinion in infectious diseases. 2009; 22(3):292-301.
- 43. Arakane et al. (2005). The Tribolium chitin synthase genes TcCHS1 and TcCHS2 are specialized for synthesis of epidermal cuticle and midgut peritrophic matrix. Insect Molecular Biology 14(5), 453-463.
- 44. Morris et al. (2009). Tribolium castaneum larval gut transcriptome and proteome: A resource for the study of the coleopteran gut J. Proteome Res. 8(8):3889-98.