Patent Application
20210292787
This application is based on, and claims benefit of and priority to, Chinese Patent Application No. CN202010196617.0 filed on Mar. 19, 2020, the contents of which are hereby incorporated by reference in their entirety for all purposes.
The present application contains a Sequence Listing which has been submitted in ASCII format via EFS-Web and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Mar. 19, 2020, is named SEQUENCE_LISTING_GWP202004365.txt and is 12 kB in size.
The present invention relates to the technical field of genetic engineering, and in particular, to a pseudotyped insect baculovirus gene transfer system and a pseudotyped baculovirus for shrimps, and a construction method and use thereof. That is, the present invention relates to a pseudotyped insect baculovirus gene transfer system exhibiting tropism for shrimps and a pseudotyped insect baculovirus exhibiting tropism for shrimps, and a construction method thereof, and use thereof in adult shrimp tissues and in vitro cultured shrimp cells.
Bac-to-Bac insect baculovirus expression system (Invitrogen) is a well-developed gene transfer technology for insect cells. The system consists of a transfer plasmid, a helper plasmid, a baculovirus plasmid (Bacmid) and a competent bacterial cell (DH10Bac). Based on the transposition of E. coli transposase Tn7, the purpose to quickly recombine a foreign gene into the Bacmid in E. coli and amplify the recombinant baculovirus is successfully achieved by this system. The transfer plasmid (pFASTBac1) is characterized in that the strong insect promoter PPH (promoter of polyhedrin gene) and the multiple cloning site thereafter are flanked by the left and right Tn7 transposase recognition sites, Tn7L and Tn7R, respectively. The baculovirus plasmid (Bacmid) is characterized in that a prokaryotic low-copy plasmid replicon (mini-F), a kanamycin resistance gene, and a LacZ gene with the transposase recognition site attTn7 inserted therein (non-frameshift insertion) are inserted. The helper plasmid is a transposase expression plasmid. The host cell of DH10Bac is an E. coli competent cell stably transformed with the helper plasmid and the baculovirus plasmid.
The technical process of the insect baculovirus expression system is as follows: a foreign gene such as GUS (β-D-glucuronidase) is cloned to the multiple cloning site (MCS) of the transfer plasmid pFastBac1, and the recombinant plasmid pFastBac-GUS is purified; then the recombinant plasmid obtained is transformed into a E. coli competent cell of DH10Bac, and under the action of transposase expressed by the helper plasmid, the GUS gene along with its promoter PPH is transposed to the attTn7 site in Bacmid; Bacmid-GUS recombinant plasmid is extracted and purified; Bacmid-GUS recombinant plasmid is transfected into an insect packaging cell of sf9, and a Bacmid-GUS recombinant virus is packaged and purified; and the packaged virus is used to infect a target cell to achieve the transfer and expression of the foreign gene in the target cell.
However, studies have shown that the insect baculovirus expression system cannot effectively infect a shrimp cell, indicating that the system has an extremely low tropism for a shrimp cell, and cannot be used for studies on the gene transfer in shrimp tissues and cells.
At present, owing to a lack of an efficient gene transfer and expression technology for adult shrimps and in vitro cultured shrimp cells, the development of researches on genetically modified shrimps and shrimp gene editing is significantly hampered.
The present invention is intended to provide a pseudotyped insect baculovirus gene transfer system and a pseudotyped baculovirus for shrimps, and a construction method and use thereof. The pseudotyped insect baculovirus gene transfer system for shrimps disclosed in the present invention can achieve stable and efficient transfer and expression of a foreign gene in shrimp tissues and in vitro cultured shrimp cells.
The present invention provides a pseudotyped insect baculovirus gene transfer system for shrimps, including a Bac-to-Bac insect baculovirus expression system, an expression plasmid carrying a shrimp virus-source envelope protein gene and an insect packaging cell.
Preferably, the expression plasmid carrying shrimp virus-source envelope protein gene includes the expression plasmid carrying shrimp white spot syndrome virus (WSSV) envelope protein gene.
Preferably, the envelope protein gene in the shrimp virus envelope protein gene expression plasmid has a nucleotide sequence as shown in SEQ ID NO. 1.
Preferably, a framework vector for constructing the shrimp virus envelope protein gene expression plasmid includes pcDNA3.1.
The present invention also provides a construction method of a pseudotyped insect baculovirus for shrimps based on the gene transfer system according to the above technical solution, including the following steps:
1) constructing, with a Bac-to-Bac insect baculovirus expression system, an insect baculovirus recombinant plasmid carrying a foreign gene; and
2) co-transfecting the insect baculovirus recombinant plasmid obtained in step 1) and the expression plasmid carrying the shrimp virus envelope protein gene into an insect packaging cell to obtain a pseudotyped insect baculovirus for shrimps.
The present invention also provides a pseudotyped insect baculovirus for shrimps constructed by the construction method based on the above technical solution.
The present invention also provides the use of the gene transfer system based on the above technical solution or the pseudotyped insect baculovirus for shrimps based on the above technical solution in the expression of a foreign gene in a shrimp cell.
Preferably, the shrimp cell includes an in-vitro-cultivated shrimp cell, and the in-vitro-cultivated shrimp cell includes a primarily cultured shrimp peripheral hemolymph cells.
The present invention also provides the use of the gene transfer system based on the above technical solution or the pseudotyped insect baculovirus for shrimps based on the above technical solution in the expression of a foreign gene in an adult shrimp tissue.
Preferably, the adult shrimp tissue includes gill, heart and intestine tissues of an adult shrimp.
The invention provides a pseudotyped insect baculovirus gene transfer system for shrimps. The gene transfer system disclosed in the present invention is a system obtained from an improvement based on the existing Bac-to-Bac insect baculovirus expression system. A shrimp virus envelope protein is introduced into a baculovirus envelope by co-transfecting an expression plasmid carrying shrimp virus envelope protein gene and an insect baculovirus recombinant plasmid carrying a foreign gene, obtained by a Bac-to-Bac insect baculovirus expression system, into an insect packaging cell. With significantly-improved packaging efficiency and tropism for a shrimp cell, the obtained pseudotyped baculovirus can be successfully used for studies on gene transfer in adult shrimps and shrimp cells, and the shortcomings of the prior art are overcome.
The system of the present invention has the following advantages: (1) Compared with the existing Bac-to-Bac insect baculovirus expression system on the market that cannot infect shrimps (such as, adult shrimp tissues and in-vitro-cultivated shrimp cells), the system of the present invention has a significantly-higher infection and expression ability in adult shrimp tissues, exhibiting 100% infection and expression instead. (2) The envelope protein gene in the system of the present invention exists independently of the baculovirus plasmid (Bacmid), and only intends to increase the packaging efficiency for baculovirus and the infection and expression efficiency, and the plasmid DNA thereof will not enter a shrimp cell, thereby improving the biological safety of the system. (3) In the system of the present invention, the problem that the gene transfer is difficult to achieve for adult shrimps and shrimp cells (in-vitro-cultivated shrimp cells), and any foreign gene can be efficiently transferred to and expressed in a shrimp cell.
The present invention provides a pseudotyped insect baculovirus gene transfer system for shrimps, including a Bac-to-Bac insect baculovirus expression system, a shrimp virus envelope protein gene expression plasmid and an insect packaging cell. Specifically, the pseudotyped insect baculovirus gene transfer system for shrimps disclosed in the present invention is obtained from the successful modification based on an insect baculovirus expression system by preparing a pseudotyped insect baculovirus. In this system, the tropism for adult shrimp tissues and in-vitro-cultivated shrimp cells and the infection and expression efficiency are significantly improved. In a specific embodiment of the present invention, a virus, with an envelope that includes both the envelope protein derived from an insect baculovirus and the envelope protein VP28 derived from a shrimp virus, is prepared. In the present invention, the Bac-to-Bac insect baculovirus expression system includes a transfer plasmid (pFASTBac1), a helper plasmid, a baculovirus plasmid (Bacmid), and a competent cell (DH10Bac). The baculovirus plasmid (Bacmid) carries a prokaryotic low-copy plasmid replicon (mini-F), a kanamycin resistance gene, and a LacZ gene with the transposase recognition site attTn7 inserted therein (non-frameshift insertion). A foreign gene can be recombined to the transposase recognition site of attTn7 to form an insect baculovirus recombinant plasmid carrying the foreign gene.
In the present invention, the expression plasmid carrying shrimp virus envelope protein gene includes the expression plasmid carrying WSSV envelope protein gene. In the present invention, the WSSV envelope protein preferably includes VP28, VP19 and the like. In a specific embodiment of the present invention, the WSSV envelope protein is preferably VP28, and more preferably modified VP28 driven by a cytomegalovirus (CMV) promoter (hereafter, VP28 mentioned in the present invention refers to modified shrimp virus envelope protein VP28). In the present invention, the envelope protein gene in the shrimp virus envelope protein gene expression plasmid has a nucleotide sequence as shown in SEQ ID NO. 1. The corresponding amino acid sequence is shown as SEQ ID NO. 2. The plasmid including the nucleotide sequence shown as SEQ ID NO. 1 of the present invention can efficiently express the VP28 protein of a shrimp virus in insect cells sf9. In the present invention, a framework vector for constructing the shrimp virus envelope protein gene expression plasmid includes pcDNA3.1. When the envelope protein is VP28, the corresponding plasmid is an eukaryotic expression vector pcDNA-VP28. In the present invention, by co-transfecting the pcDNA-VP28 plasmid with an insect baculovirus (Bacmid) recombinant plasmid into packaging cells, the packaging efficiency for an insect baculovirus can be significantly improved, and the introduction of the shrimp virus envelope protein into the envelope of the packaged virus greatly increases the tropism for a shrimp cell.
The present invention also provides a construction method of a pseudotyped insect baculovirus for shrimps based on the gene transfer system according to the above technical solution, including the following steps:
1) constructing, with a Bac-to-Bac insect baculovirus expression system, an insect baculovirus recombinant plasmid carrying a foreign gene; and
2) co-transfecting the insect baculovirus recombinant plasmid obtained in step 1) and the expression plasmid carrying shrimp virus envelope protein gene into an insect packaging cell to obtain a pseudotyped insect baculovirus for shrimps.
In the present invention, an insect baculovirus recombinant plasmid carrying a foreign gene is constructed using a Bac-to-Bac insect baculovirus expression system. In the present invention, no special restriction is imposed on the construction method, and a Bac-to-Bac insect baculovirus expression system well known to those skilled in the art may be adopted.
In the present invention, after an insect baculovirus recombinant plasmid is obtained, the insect baculovirus recombinant plasmid is co-transfected with the expression plasmid carrying shrimp virus envelope protein gene into an insect packaging cell to obtain a pseudotyped insect baculovirus for shrimps. Conditions for the co-transfection are not particularly defined in the present invention. In a specific embodiment, the Bacmid-GUS recombinant virus plasmid and pcDNA3.1-VP28 of the present invention are co-transfected at a ratio preferably of 3:1. After co-transfection, preferably, the steps of collecting the cell culture supernatant, purifying and concentrating are also included in the present invention. The pseudotyped insect baculovirus for shrimps constructed by the construction method of the present invention can efficiently infect adult shrimps and shrimp cells.
Specifically, in the present invention, an insect baculovirus recombinant plasmid carrying a foreign gene is co-transfected with the expression plasmid pcDNA-VP28 into an insect cell sf9; 4 days later, the cell culture supernatant is collected and centrifuged to obtain a first passage (P1) virus supernatant; the first passage virus is used to infect a cell sf9; 4 days later, the cell culture supernatant is collected again and centrifuged to obtain a second passage (P2) virus supernatant; and the second passage virus supernatant is ultra-centrifuged, purified and concentrated to obtain a pseudotyped insect baculovirus exhibiting tropism for a shrimp cell. The envelope of a virion obtained in the present invention includes not only the envelope protein derived from an insect baculovirus, but also the envelope protein VP28 derived from a shrimp virus. The introduction of the shrimp virus envelope protein VP28 in the present invention can greatly improve the packaging efficiency and the tropism for a shrimp cell of the pseudotyped insect baculovirus. In a more specific embodiment of the present invention, the pseudotyped baculovirus Bacmid-GUS/VP28 is prepared preferably as follows: with the transfection reagent Cellfectin II (Invitrogen), the Bacmid-GUS recombinant virus plasmid and the pcDNA-VP28 plasmid are co-transfected into an insect cell sf9 at a ratio of 3:1, and a virus is packaged; 4 days later, a cell culture supernatant is collected and centrifuged to obtain a P1 virus; the P1 virus is used to infect a cell sf9 for amplification; 4 days later, the cell culture supernatant is collected and filtered by a 0.45 μm filter membrane; the filtrate is ultra-centrifuged to isolate and purify the P2 virus; and the obtained virus is dispensed and stored in a refrigerator at −80° C.
The present invention also provides a pseudotyped insect baculovirus for shrimps constructed by the construction method based on the above technical solution. The infection and expression of the virus of the present invention in adult shrimp tissues are tissue-specific, and the infection and expression efficiency in gill, heart and intestine tissues of a shrimp can be as high as 100%, but no expression of a foreign gene can be detected in Oka organs and muscle tissues. The infection and expression of the virus of the present invention in shrimp cells (in-vitro-cultivated cells) are also cell-specific, and the virus can successfully infect an in-vitro-cultivated shrimp peripheral hemolymph cells, but cannot infect an in-vitro-cultivated shrimp embryonic cell.
The present invention also provides the use of the gene transfer system based on the above technical solution or the pseudotyped insect baculovirus for shrimps based on the above technical solution in the expression of a foreign gene in a shrimp cell.
In the present invention, the shrimp cell includes an in-vitro-cultivated shrimp cell, and the in-vitro-cultivated shrimp cell includes a primary shrimp peripheral hemolymph cells.
In the present invention, the adult shrimp tissue includes gill, heart and intestine tissues of an adult shrimp.
In a specific embodiment of the present invention, with GUS reporter gene (β-D-glucuronidase) as a foreign gene, a Bac-to-Bac insect baculovirus expression system (Cat. No. 10359-016) of Invitrogen is improved as follows: GUS reporter gene is cloned to the multiple cloning site of a transfer plasmid of pFastBac1, and the recombinant plasmid pFastBac-GUS is purified; the recombinant plasmid pFastBac-GUS is transformed into an E. coli competent cell DH10Bac, and GUS is transposed to the attTn7 site in Bacmid to obtain a recombinant virus plasmid Bacmid-GUS; the recombinant virus plasmid Bacmid-GUS is extracted and purified; the obtained Bacmid-GUS recombinant virus plasmid DNA and the pcDNA-VP28 plasmid are co-transfected into a packaging cell sf9, and a pseudotyped baculovirus Bacmid-GUS/VP28 is obtained by packaging; the pseudotyped baculovirus Bacmid-GUS/VP28 is purified and concentrated, and the virus titer is determined; and the packaged virus is used to infect an adult shrimp tissue or in-vitro-cultivated shrimp cell to achieve the transfer and expression of the foreign gene in the target tissue or cell. In the present invention, the nucleotide sequence of the GUS reporter gene is shown as SEQ ID NO. 3, and the amino acid sequence of a protein corresponding to the GUS reporter gene is shown as SEQ ID NO. 4.
The transfer plasmid pFastBac1, E. coli competent cell DH10Bac and packaging cell sf9 involved in the present invention are all derived from the Bac-to-Bac insect baculovirus expression system (Cat. No. 10359-016).
The transfer plasmid pFASTBac1 includes a strong insect promoter PPH (polyhedrin gene promoter), a multiple cloning site, and the flanking Tn7 transposase recognition sites of Tn7R and Tn7L.
The host cell DH10Bac is an E. coli competent cell stably transformed with a helper plasmid and a baculovirus plasmid (Bacmid).
The baculovirus plasmid (Bacmid) includes a prokaryotic low-copy plasmid replicon (mini-F), a kanamycin resistance gene (Kann), and a LacZ gene with the transposase recognition site attTn7 inserted therein (non-frameshift insertion). The helper plasmid is a transposase expression plasmid.
In the present invention, the titer of the packaged virus is determined as follows: a concentrated virus solution is used to infect sf9 cells; X-Gluc (Solarbio Science & Technology Co., Ltd.) staining is performed, and Sf9 cells stained into blue is counted; and titer is calculated for the concentrated virus solution.
In the present invention, an adult shrimp tissue is infected with the virus as follows: a concentrated virus solution is injected into an adult shrimp muscle tissue; and 4 days later, different shrimp tissues are taken for X-Gluc staining to observe the expression of the GUS reporter gene.
In the present invention, an in-vitro-cultivated shrimp cell is infected with the virus as follows: the original medium for the in-vitro-cultivated shrimp cell is replaced with an antibiotic- and serum-free medium; a concentrated virus solution is added to the culture supernatant at a certain amount; and 4 days later, X-Gluc staining is performed to observe the expression of the GUS reporter gene.
The pseudotyped insect baculovirus gene transfer system and virus for shrimps, and the construction method and use thereof disclosed in the invention are further described in detail below with reference to specific examples. The technical solutions of the present invention include, but are not limited to, the following examples.
Cloning and Modification of the Open Reading Frame Nucleic Acid Sequence of Shrimp WSSV Virus Envelope Protein Gene (VP28), and Construction of Eukaryotic Expression Vector pcDNA3.1-VP28 for the Gene.
Genomic DNA of a WSSV-infected shrimp was extracted using a DNA extraction kit of Transgen Biotech Co., LTD (Easypure Marine Animal Genomic DNA kit, Cat. No. EE151-01), and the specific operations were carried out according to the kit instructions. The nucleic acid sequence of the open reading frame of shrimp virus VP28 gene was improved by PCR amplification primers, that is, VP28 gene-specific primers along with BamHI and EcoRI restriction sites were designed: a forward mutation primer sequence: 5′-CGCGGATCCATTGCCACCATGGATCTTTCTTTCAC-3′ (SEQ ID NO. 5); and a reverse mutation primer sequence: 5′-CCGGAATTCGTTACTCGGTCTCAGTGCC-3′ (SEQ ID NO. 6). The target fragment was obtained by PCR amplification. The PCR reaction system and procedure were as follows: the 50 μl reaction system consisted of 5.0 μl 10×PCR buffer (including Mg2+), 4.0 μl 2.5 mmol/L dNTPs, 2.5 μL 10 μmol/L upstream and downstream primers, 0.5 μL 5 IU/μL Taq DNA polymerase, 2 μL genomic DNA, and 33.5 μL ddH2O; and the PCR reaction procedure included: pre-denaturation at 95° C. for 10 min; 30 repetitions of the following cycle: denaturation at 95° C. for 45 s, annealing at 60° C. for 45 s, and extension at 72° C. for 50 s; and final extension at 72° C. for 10 min. The PCR product was assayed by 1% agarose gel electrophoresis, and sent to a sequencing company for sequencing. (
A plasmid pcDNA3.1-V5/HisA (Invitrogen) was digested with BamHI and EcoRI endonucleases, and a VP28 sequence (SEQ ID NO: 1) carrying the same cohesive termini (BamHI/EcoRI) was inserted therein to obtain pcDNA-VP28 (
The Cloning of a Foreign Gene into a Donor Plasmid pFastBac1.
The construction of pFastBac1-GUS recombinant plasmid was adopted as an example (
GUS gene-specific primers including BamHI and EcoRI restriction sites were designed: a forward primer sequence: 5′-CGCGGATCCATGGTCCGTCCTGTAGAAAC-3′ (SEQ ID NO. 7); and a reverse primer sequence: 5′-CCGGAATTCTCATTGTTTGCCTCCCTGCT-3′ (SEQ ID NO. 8). The target fragment was obtained by PCR amplification. The PCR reaction system and procedure were as follows: the 50 μL reaction system consisted of 25 μL 2× Hieff PCR Master Mix (including Mg2+), 2.5 μL 10 μmol/L upstream and downstream primers, 2 μL genomic DNA, and 18 μL ddH2O; and the PCR reaction procedure included: pre-denaturation at 95° C. for 5 min; 30 repetitions of the following cycle: denaturation at 95° C. for 45 s, annealing at 55° C. for 45 s, and extension at 72° C. for 90 s; and final extension at 72° C. for 10 min. The PCR product was assayed by 1% agarose gel electrophoresis, and sent to a sequencing company for sequencing.
A plasmid pFastBac1 (Invitrogen) was digested with BamHI and EcoRI endonucleases, and a GUS sequence carrying the same cohesive termini (BamHI/EcoRI) was inserted therein to obtain pFastBac1-GUS.
Recombination of a Foreign Gene into a Virus Plasmid Bacmid.
The construction of Bacmid-GUS was adopted as an example (
A pFastBac1-GUS plasmid was transformed into DH10Bac competent cells. The transformed product was plated, and blue-white screening and bacterial PCR detection were performed to obtain a recombinant Bacmid including GUS gene: Bacmid-GUS.
Preparation, Concentration and Purification of a Recombinant Baculovirus.
Bacmid-GUS was adopted as an example.
Bacmid-GUS recombinant baculovirus plasmid DNA was transfected into Sf9 insect cells using Cellfectin II transfection reagent. The optimization result of the optimal conditions for transfection of Bacmid-GUS plasmid in sf9 cells is shown in
X-gluc staining was performed to detect the protein expression of the GUS gene. The specific method was as follows: the medium in a culture well was discarded; the monolayer cells were washed with PBS, and added with a cell fixative including 2% formaldehyde and 0.05% glutaraldehyde for 5 min of fixation at room temperature; the fixative was discarded, and the cells were washed twice with PBS and added with 20 mg/mL X-Gluc for staining; the cells were incubated at 28° C. for 12 h; and the staining results were recorded by a light microscope.
Preparation, Concentration and Purification of a Pseudotyped Insect Baculovirus.
Bacmid-GUS/VP28 was adopted as an example.
A pseudotyped baculovirus Bacmid-GUS/VP28 was obtained from successful packaging by co-transfecting the plasmid Bacmid-GUS and pcDNA-VP28 into insect cells Sf9. As shown in
P1 virus was collected to infect sf9 cells once again, the insect baculovirus was amplified, and then P2 virus was isolated and purified (E to H in
Titer Determination for an Insect Baculovirus.
The virus titer was determined by the expression of the GUS reporter gene. The infection of baculovirus Bacmid-GUS or Bacmid-GUS/VP28 in Sf9 cells was taken as an example.
The baculovirus Bacmid-GUS or Bacmid-GUS/VP28 solution was serially diluted to 10−1-10−7 times with serum- and penicillin/streptomycin-free SIM insect cell culture medium, and then 100 μL of the virus dilution was added to each well of the 96-well cell culture plate; and on day 4 after the infection, X-gluc staining was performed to detect the expression of the GUS reporter gene, and the virus titer was calculated. Calculation formula: virus titer TU/mL (transduction units per mL)=positive cells %×total cells×dilution factor/virus solution volume (mL).
As shown in
As shown in
Infection of an Insect Baculovirus in an In-Vitro-Cultivated Shrimp Cell
The infection of Baculovirus of Bamcid-GUS and Bacmid-GUS/VP28 in primarily cultured shrimp peripheral hemolymph cells and embryonic cells was adopted as an example.
The primarily cultured shrimp peripheral hemolymph cells were infected with the virus as follows: the primarily cultured shrimp peripheral hemolymph cells were inoculated to a 48-well cell culture plate; after hemolymph cells grew adherently for 5 h, the original medium was discarded, and 100 μL of concentrated virus solution (diluted with 1.5×L-15 medium) was added to each well; after the virus was incubated for 4 h, the medium was replaced with the normal 1.5×L-15 complete medium; and on day 5 after virus infection, X-Gluc staining was performed to detect the expression of the GUS reporter gene. As shown in
Above results also show that an unmodified insect baculovirus Bac-to-Bac gene transfer and expression system exhibits an extremely low tropism for a shrimp cell, and cannot directly be used for studies on the gene transfer in shrimp cells. The introduction of VP28 envelope protein of the shrimp virus can significantly improve the tropism of the pseudotyped baculovirus Bacmid-GUS/VP28 for shrimp peripheral hemolymph cells, thereby facilitating the infection and expression of the pseudotyped baculovirus in shrimp peripheral hemolymph cells.
The primary shrimp embryonic cells were infected with the virus as follows: shrimp embryonic cells were inoculated to a 48-well cell culture plate; after embryonic cells grew adherently for 2 days, the original medium was discarded, and 100 μL of concentrated virus solution (diluted with 1.5×L-15 medium) was added to each well; after the virus was incubated for 4 h, the medium was replaced with the normal 1.5×L-15 complete medium; and on day 5 after virus infection, X-Gluc staining was performed to detect the expression of the GUS reporter gene. As shown in
X-Gluc staining is performed on shrimp cells in the same manner as that for Sf9 insect cells.
Infection of an Insect Baculovirus in an Adult Shrimp Tissue
Bacmid-GUS and Bacmid-GUS/VP28 were adopted as examples.
The infection of above two baculoviruses in adult shrimps was conducted by intramuscular injection. The specific method was as follows: with a microsyringe, a baculovirus was injected at a site about 1 mm to the right of the middle abdominal line between the first pair of natatorial legs of a shrimp; after injection, the injection site was gently pressed, and then the shrimp was placed in sea water; on day 5 after virus injection, gill, Oka organ, heart, muscle and intestine tissues were taken from the shrimp and placed in 1.5 mL centrifuge tubes separately; tissue-specific GUS staining solution was added to each tube, and the resulting mixture was incubated in a 28° C. incubator for 12 h in the dark; then each tissue was washed with PBS to remove the staining solution; and images were acquired for each tissue by a stereomicroscope and the staining results were recorded.
As shown in
However, as shown in
As shown in
GUS staining was performed on adult shrimp tissues as follows: a GUS tissue staining solution was prepared in the dark just before use, with 1 mL of tissue staining solution including 830 μL of nuclease-free sterile water, 100 μL of 1 M sodium phosphate solution, 20 μL of 0.5 M EDTA-2Na, 10 μL of 10% TritonX-100, 20 μL of 50 mM potassium ferricyanide solution and 20 μL of 0.1 M X-Gluc solution (50 mg/mL); the GUS tissue staining solution was added to a centrifuge tube including a tissue, with the tissue being immersed; the centrifuge tube was incubated overnight in a 28° C. incubator; the centrifuge tube was taken out from the incubator, and the staining solution was carefully discarded; the tissue was picked up by a tweezer and placed in a small dish filled with PBS; and the tissue was observed under a stereomicroscope, and results were recorded by photographing.
In conclusion, the pseudotyped baculovirus gene transfer system constructed by the present invention can achieve an infection and expression efficiency up to 100% in adult shrimp tissues, significantly superior to the unmodified baculovirus gene transfer and expression system.
Moreover, the construction method of the present invention is also applicable to other envelope proteins of the WSSV, such as VP19, and envelope proteins of other shrimp viruses. The introduction of a different shrimp virus envelope protein into an insect baculovirus will result in a prepared pseudotyped baculovirus with a different tissue- and cell-specificity.
The above descriptions are merely preferred implementations of the present invention. It should be noted that a person of ordinary skill in the art may further make several improvements and modifications without departing from the principle of the present invention, but such improvements and modifications should be deemed as falling within the protection scope of the present invention.
| Number | Date | Country | Kind |
|---|---|---|---|
| CN202010196617.0 | Mar 2020 | CN | national |
