Patent Grant
10920241
This application is a U.S. National Phase Application under 35 U.S.C. § 371 of International Patent Application No. PCT/NL2016/050684, filed Oct. 4, 2016 and claims the priority of EP 15188418.6, filed Oct. 5, 2015, all of which are incorporated by reference in their entireties. The International Application was published on Apr. 13, 2017 as International Publication No. WO 2017/061859 A1.
A sequence listing created on Apr. 3, 2018 as the ASCII text file “Seq1st_10114_006653_US0” having a file size of 261.9 bytes, is incorporated herein by reference in its entirety.
The present disclosure provides new attenuated Pepino mosaic viruses useful in the control of plant disease. Compositions for biological control of plant disease are also provided as well as methods for the induction of cross-protection and increased resistance against Pepino mosaic virus in plants.
The present invention concerns the field of biological control in agriculture and horticulture, in particular, the control of plant pathogens.
Tomato is susceptible to various viral diseases, and one of the causal agents, Pepino mosaic virus (PepMV), has recently become a major limiting factor with regard to tomato production. PepMV belongs to the Potexvirus genus of the Alphaflexiviridae family PepMV has rapidly spread throughout commercial tomato cropping and is currently found throughout Europe and North-America (Jorda et al., 2001; Cotillon et al., 2002; Verhoeven et al., 2003; Ling et al., 2008). The RNA genome of PepMV encompasses approximately 6.4 kb and contains five open reading frames that encode a RNA-dependent polymerase (RdRp), a triple gene block (TGB), a coat protein (CP), and two short untranslated sequences flanking the coding regions (Aguilar et al., 2002; Cotillon et al., 2002). Isolates of PepMV group into four separate strains (genotypes) based on sequence similarity, namely the Peruvian (LP)-strain to which the original PepMV isolate belongs, the European (EU)-strain that was found in Europe in 1999 (Van der Vlugt et al., 2000), the CH2-strain that was discovered in infected tomato seeds in Chile, and the US1-strain that was discovered in diseased tomato plants in the USA (Ling, 2007). Symptom severity varies between different isolates of PepMV (Van der Vlugt et al., 2000) and differences in severity do not necessarily coincide with differences in genotype (Hanssen et al., 2008).
PepMV induces a wide range of symptoms on tomato (Van der Vlugt et al., 2000; Jorda et al., 2001), such as mosaic, leaf distortion, nettle-like heads, single yellow spots, interveinal chlorosis and fruit discoloration. Tomato plants display symptoms shortly after infection with PepMV and, in general, subsequently recover (Van der Vlugt & Stijger, 2008). Symptoms may, however, return later during the growing season. Expression of symptoms may also depend on environmental conditions, such as temperature and light intensity (Jorda et al., 2001; Van der Vlugt & Stijger, 2008). PepMV is sometimes suggested to cause yield losses in tomato, but the highest economic losses are attributed to symptoms that affect the commercial value of tomato fruits, such as flaming, marbling, blotchy ripening and fruit size reduction (Soler et al., 2000; Spence et al., 2006).
PepMV is transmitted efficiently by contaminated hands, clothing or tools (Van der Vlugt & Stijger, 2008). Direct contact between healthy and infected plants during routine crop handling also suffices to spread PepMV infection. The incidence of PepMV on tomato is very high in some tomato cultivation areas, where the virus may affect up to 90% of the greenhouses (Soler-Aleixandre et al., 2005). To stay free of virus is challenging under such circumstances.
There exists a need in the art to protect plants from PepMV infection and to prevent or reduce plant diseases associated with PepMV infection.
In one aspect, the disclosure provides an attenuated Pepino mosaic virus comprising a nucleic acid molecule comprising a nucleic acid sequence, wherein the nucleotide at the position corresponding to 2605 of SEQ ID NO:1 is G, the nucleotide at the position corresponding to 3156 of SEQ ID NO:1 is T, and/or the nucleotide at the position corresponding to 3422 SEQ ID NO: 1 is G. Preferably, the nucleic acid sequence is at least 80% identical to SEQ ID NO: 1.
In one aspect, the disclosure provides an attenuated Pepino mosaic virus comprising a nucleic acid molecule comprising a nucleic acid sequence encoding arginine at the position according to 868 of SEQ ID NO:2 and/or encodes phenylalanine at the position according to 1052 of SEQ ID NO:2. Preferably, the nucleic acid sequence is at least 80% identical to SEQ ID NO: 1, SEQ ID NO: 3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, or SEQ ID NO: 7. More preferably, the nucleic acid sequence is at least 80% identical to SEQ ID NO: 1.
In one aspect, the disclosure provides an isolated nucleic acid molecule comprising a nucleic acid sequence having at least 95% identity to a nucleic acid sequence selected from SEQ ID NO:1, SEQ ID NO: 3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, or SEQ ID NO: 7, wherein the nucleic acid sequence encodes arginine at the position according to 868 of SEQ ID NO:2 and/or encodes phenylalanine at the position according to 1052 of SEQ ID NO:2. In preferred embodiments, the isolated nucleic acid molecule encodes an amino acid sequence having at least 95% identity to any one of the amino acid sequences depicted in
In one aspect, the disclosure provides an RNA-dependent RNA polymerase wherein the polymerase has an arginine at the position according to 868 of SEQ ID NO:2, a phenylalanine at the position according to 1052 of SEQ ID NO:2, a phenylalanine at the position corresponding to 956 of SEQ ID NO:2, and/or an asparagine at the position corresponding to 1325 of SEQ ID NO:2. Preferably said polymerase has an arginine at the position according to 868 of SEQ ID NO:2 and a phenylalanine at the position according to 1052 of SEQ ID NO:2. Preferably said polymerase has a phenylalanine at the position corresponding to 956 of SEQ ID NO:2 and an asparagine at the position corresponding to 1325 of SEQ ID NO:2. Preferably said polymerase has an arginine at the position according to 868 of SEQ ID NO:2 and a phenylalanine at the position corresponding to 956 of SEQ ID NO:2. In some embodiments the RNA-dependent RNA polymerases has at least 50%, at least 70%, at least 80%, or at least 90% identity to any one of the amino acid sequences depicted in
In one aspect, the disclosure provides an attenuated Pepino mosaic virus comprising a nucleic acid molecule comprising a nucleic acid sequence, wherein the nucleotide at the position corresponding to 2675 of SEQ ID NO:8 is G, the nucleotide at the position corresponding to 3226 of SEQ ID NO:8 is T, and/or the nucleotide at the position corresponding to 3492 SEQ ID NO: 8 is G. Preferably, the nucleic acid sequence is at least 80% identical to SEQ ID NO: 8.
In one aspect, the disclosure provides an attenuated Pepino mosaic virus comprising a nucleic acid molecule comprising a nucleic acid sequence encoding arginine at the position according to 886 of SEQ ID NO:9 and/or encodes phenylalanine at the position according to 1070 of SEQ ID NO:9. Preferably, the nucleic acid sequence is at least 80% identical to SEQ ID NO: 1, SEQ ID NO: 3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, or SEQ ID NO: 7. More preferably, the nucleic acid sequence has at least 95%, at least 99%, or 100% identity to. SEQ ID NO: 8.
In one aspect, the disclosure provides an RNA-dependent RNA polymerase having at least 50%, at least 70%, at least 80%, least 90%, at least 99% or at least 100% identity to SEQ ID NO:9, wherein the polymerase has an arginine at the position according to 886 of SEQ ID NO:9 and/or a phenylalanine at the position according to 1070 of SEQ ID NO:9. Preferably said polymerase has an arginine at the position according to 886 of SEQ ID NO: 9 and a phenylalanine at the position according to 1070 of SEQ ID NO:9. Preferably said polymerase has a phenylalanine at the position corresponding to 974 of SEQ ID NO:2 and an asparagine at the position corresponding to 1343 of SEQ ID NO:2. Preferably said polymerase has an arginine at the position according to 886 of SEQ ID NO:2 and a phenylalanine at the position corresponding to 974 of SEQ ID NO:2. The invention also provides a nucleic acid molecule encoding a polymerase as indicated in this paragraph.
In one aspect the disclosure provides a vector, preferably an expression vector, comprising a nucleic acid molecule as disclosed herein. In one aspect the disclosure provides an isolated polypeptide encoded by a nucleic acid molecule disclosed herein. In one aspect the disclosure provides an antibody specific for the polypeptide encoded by a nucleic acid molecule as disclosed herein.
In one aspect the disclosure provides a composition for biological control of plant disease comprising an attenuated Pepino mosaic virus as disclosed herein, a nucleic acid molecule as disclosed herein or a vector as disclosed herein; and an agriculturally acceptable carrier.
In one aspect the disclosure provides a method for identifying a pepino mosaic virus (PepMV)-resistant plant, comprising
a) exposing a plant or plant part to an attenuated Pepino mosaic virus as disclosed herein, a nucleic acid molecule as disclosed herein, a vector as disclosed herein, or the compositions as disclosed herein;
b) exposing the plant or plant part to an infective dosage of PepMV, and
c) identifying said plant as PepMV-resistant plant when, after said exposure,
disease-symptoms in said plant or plant part are reduced or delayed and/or PepMV accumulation in said plant or plant parts is reduced or delayed in comparison to a control PepMV infected plant.
In one aspect the disclosure provides a method for the detection of a pepino mosaic virus (PepMV) comprising providing a sample suspected of containing PepMV and detecting a PepMV virus as disclosed herein, a nucleic acid molecule as disclosed herein or a vector as disclosed herein. The method is useful among others to determine whether an application of the attenuated virus to a plant has been successful. The method is also useful to determine the extent of infection of a particular patch of crop. Particularly with a PepMV as disclosed herein. The sample is typically prepared from a plant or a part thereof that is susceptible to PepMV infection and/or replication. A sample is suspected of containing PepMV when there is reason to believe that the PepMV is present in the sample. A sample is also suspected of containing PepMV when the sample is from plant of which it needs to be verified that it does or does not contain a PepMV of the invention. Such a sample can be for instance from a plant in a greenhouse in the situation when in a nearby greenhouse a PepMV infection has been reported. It can also be from a plant with one or more symptoms that point towards a PepMV infection and one wants to confirm this. The invention also provides method for the detection of PepMV as described herein wherein the term “sample suspected of containing PepMV” is replaced by the term “sample of a plant susceptible to PepMV infection”.
In one aspect the disclosure provides a method for producing a pepino mosaic virus (PepMV)-resistant plant, comprising
In one aspect the disclosure provides a PepMV-resistant plant comprising an attenuated Pepino mosaic virus as disclosed herein or a nucleic acid molecule as disclosed herein.
In one aspect the disclosure provides a method for controlling infection or disease in a plant comprising applying an effective amount of an attenuated Pepino mosaic virus as disclosed herein, a nucleic acid molecule as disclosed herein, a vector as disclosed herein, or the compositions as disclosed herein to said plant.
In one aspect the disclosure provides an attenuated Pepino mosaic virus as disclosed herein, a nucleic acid molecule as disclosed herein, a vector as disclosed herein, or the compositions as disclosed herein for use in controlling infection or disease in a plant. In particular, the use is for inducing resistance to PepMV.
The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawings will be provided by the Office upon request and payment of the necessary fee.
Cross-protection is the phenomenon of protecting crops against virulent isolates of viruses by pre-treatment with closely related attenuated isolates of the virus. In the 1970s, it was first applied successfully against infection of tomato with Tobacco mosaic virus in several countries (Burgyán & Gáborjányi, 1984). Attenuated isolates may be selected among naturally occurring or be developed by the introduction of mutations into such isolates, for example using random mutagenesis. A strategy in which attenuated isolates are applied to plants relies on the identification of an isolate that has as little impact on total yield and fruit quality as possible, and effectively protects against more virulent isolates at the same time.
While not wishing to be bound by theory, cross-protection may be due to RNA silencing activity induced by the protective isolate (Ratcliff et al., 1999; Valkonen et al., 2002). The role of post-transciptional gene silencing (PTGS) in cross-protection was demonstrated by the observation that two viral constructs derived from different viruses, but sharing a common sequence, could suppress each other when co-inoculated in plants (Ratcliff et al., 1999). PTGS is an antiviral defense mechanism in plants, which targets double stranded RNA (dsRNA) for degradation in a sequence-specific manner. In cross-protection, it is thought that the mild strain ‘primes’ the defense system of the plant so that it operates against subsequent infection by severe strains.
In the study of Schenk et al. (2010), attenuated isolates of PepMV were tested (EU-Att1 and PE-Att1). The attenuated isolates effectively reduced the effects of isolates of PepMV with aggressive symptoms (namely, EU-Ch11 and EU-Nec1). Total virus accumulation, symptom severity and yield losses were significantly reduced in cross-protected plants compared to the single infections by the aggressive isolates. The yields of the cross-protected plants were on a similar level as those of uninfected plants. Although plants cross-protected by the attenuated isolates reduced symptoms, infection by the attenuated isolates alone also produced symptoms (Table 2 of Schenk et al.) The attenuated isolates caused symptoms shortly after inoculation, a pattern which has also been observed in other trials (Spence et al., 2006). Overall, the symptom severity correlated to virus accumulation, but accumulation alone did not explain all differences in symptom severity. In turn, symptom severity was negatively correlated to yield. The two symptoms that had the largest effect on yield i.e. leaf deformation and leaf necrosis, affected the leaf area of the plants, which would explain the observed yield losses. One aspect of the present invention is the provision of an attenuated virus that cross-protects plants from further PepMV infection while causing minimal symptoms from exposure to the attenuated virus alone.
Accordingly, one aspect of the disclosure provides Pepino mosaic viruses, in particular attenuated viruses. As is known to a skilled person, an attenuated virus is a virus that has been modified from a wild-type pathogenic virus. An attenuated virus has reduced pathogenicity as compared to the wild-type virus. In addition, an attenuated virus disclosed herein can be used to cross-protect plants against infection from virulent PepMV isolates.
The disclosure identifies several nucleotide positions in PepMV which play a role in the symptoms induced by PepMV infection. Specifically, the disclosure provides PepMV viruses and nucleic acid molecules, wherein the nucleic acid sequence encodes arginine at the position corresponding to 868 of SEQ ID NO:2 (corresponding to position 886 of SEQ ID NO:9) and/or encodes phenylalanine at the position corresponding to 1052 of SEQ ID NO:2 (corresponding to position 1070 of SEQ ID NO:9).
The disclosure provides that the nucleotides at positions 2605 and 3156 of SEQ ID NO: 1 (corresponding to positions 2675 and 3226 of SEQ ID NO: 8), and consequently the amino acids encoded (in part) by these nucleotides, play a role in the pathogenic symptoms. Specifically, an amino acid change from lysine to arginine at position 868 of SEQ ID NO:2 (corresponding to position 886 of SEQ ID NO:9) and an amino acid change from leucine to phenylalanine at position 1052 of SEQ ID NO: 2 (corresponding to position 1070 of SEQ ID NO:9) results in a PepMV attenuated virus. In the pathogenic viruses depicted in
The disclosure also provides that additional nucleotides—and the amino acids which they encode—also play a role in pathogenic symptoms. Accordingly, in some embodiments the viruses and nucleic acid molecules disclosed herein contain one or more of the following: a C at the nucleotide position corresponding to 191 of SEQ ID NO: 1 (position 261 of SEQ ID NO: 8); a C at the nucleotide position corresponding to 2354 of SEQ ID NO: (position 2424 of SEQ ID NO: 8); a T at the nucleotide position corresponding to 2768 of SEQ ID NO: 1(position 2838 of SEQ ID NO: 8); a T at position corresponding to 2868 of SEQ ID NO:1 (position 2938 of SEQ ID NO: 8); a G at the nucleotide position corresponding to 3422 of SEQ ID NO: 1 (position 3492 of SEQ ID NO: 8); and/or have an A at the nucleotide position corresponding to 3975 of SEQ ID NO: 1 (position 4045 of SEQ ID NO: 8). In some embodiments the viruses or nucleic acid molecules disclosed herein contain at least two, at least three, at least four, at least five, or all 6 of the nucleotides listed above. These six nucleotides are unique to both the VCA attenuated virus and the VC1 attenuated virus as compared to the virulent CH2 strains depicted in
See
The VCA virus was found to have nucleotide substitutions resulting in amino acid changes in the RNA-dependent RNA polymerase gene of the virus. SEQ ID NO:2 depicts the partial amino acid sequence of the RNA-dependent RNA polymerase from VCA. SEQ ID NO:9 depicts the complete amino acid sequence of the RNA-dependent RNA polymerase from VCA
VCA (SEQ ID NO:1/SEQ ID NO:8) is an exemplary attenuated virus of the CH2 strain. The disclosure also provides attenuated viruses from other PepMV strains. Four amino acids in SEQ ID NO:2 were found to be unique when compared to wild-type EU, LP, CH2, and US1 isolates. Arginine at position 868 of SEQ ID NO:2 (886 of SEQ ID NO:9) corresponds to position 887 in the alignment shown in
In some embodiments, the virus is an attenuated virus of a EU strain. Exemplary wild-type EU viral sequences are depicted in SEQ ID Nos:3-5. In some embodiments, the virus is an attenuated virus of a US1 strain. An exemplary wild-type US1 viral sequence is depicted in SEQ ID NO:6. In some embodiments, the virus is an attenuated virus of an LP strain. An exemplary wild-type LP viral sequence is depicted in SEQ ID NO:7.
PepMV viruses have, on the average, around 80% nucleic acid sequence identity. Accordingly, in preferred embodiments the PepMV viruses have a nucleic acid sequence at least 80% identical to SEQ ID NO:1, wherein the nucleic acid sequence encodes arginine at the position corresponding to 868 of SEQ ID NO:2 and/or encodes phenylalanine at the position corresponding to 1052 of SEQ ID NO:2 (or rather, encodes arginine at position 887 of
The disclosure also provides an isolated nucleic acid molecule comprising a nucleic acid sequence at least 80%, at least 90%, preferably at least 95%, more preferably at least 98%, and most preferably at least 99% identical to SEQ ID NO:1, SEQ ID NO:8, SEQ ID NO: 3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, or SEQ ID NO: 7, wherein the nucleic acid sequence encodes arginine at the position corresponding to 868 of SEQ ID NO:2 and/or encodes phenylalanine at the position corresponding to 1052 of SEQ ID NO:2 (or rather, encodes arginine at position 887 of
In some embodiments, the nucleotide at the position corresponding to 2605 of SEQ ID NO:1 (2675 of SEQ ID NO:8) is G; the nucleotide at the position corresponding to 3156 of SEQ ID NO: 1 (3226 of SEQ ID NO:8) is T and/or the nucleotide at the position corresponding to 3422 SEQ ID NO: 1 (3492 of SEQ ID NO:8) is G. In preferred embodiments, the nucleotide at the position corresponding to 2605 of SEQ ID NO:1 (2675 of SEQ ID NO:8) is G and/or the nucleotide at the position corresponding to 3156 of SEQ ID NO: 1 (3226 of SEQ ID NO:8) is T. In preferred embodiments, the nucleic acid molecules comprise one or more of the following: a C at the nucleotide position corresponding to 191 of SEQ ID NO: 1 (position 261 of SEQ ID NO: 8); a C at the nucleotide position corresponding to 2354 of SEQ ID NO: 1 (position 2424 of SEQ ID NO: 8); a T at the nucleotide position corresponding to 2768 of SEQ ID NO: 1 (position 2838 of SEQ ID NO: 8); a T at position corresponding to 2868 of SEQ ID NO:1 (position 2938 of SEQ ID NO: 8); and/or have an A at the nucleotide position corresponding to 3975 of SEQ ID NO: 1 (position 4045 of SEQ ID NO: 8). Such nucleic acid molecules are useful, for example, for producing the viruses disclosed herein.
As used herein, the term “isolated” refers to a protein, peptide or nucleic acid molecule which is substantially separated from other (sub)cellular components. The term includes a nucleic acid molecule or protein which has been removed from its naturally occurring environment, as well as recombinant or cloned DNA isolates and chemically synthesized analogues or analogues biologically synthesized by heterologous systems.
A further aspect of the disclosure provides vectors and expression vectors comprising the nucleic acid molecules and viruses disclosed herein. Expression vectors useful in the present disclosure include vaccinia virus, retroviruses, and baculovirus. The expression vector may comprise the nucleic acid sequences disclosed herein or a fragment thereof that is under control of or operatively linked to a regulatory element, such as a promoter. The segment of DNA referred to as the promoter is responsible for the regulation of the transcription of DNA into mRNA. The expression vector may comprise one or more promoters suitable for the expression of the gene in, e.g., plant cells, fungal cells, bacterial cells, yeast cells, insect cells or other eukaryotic cells.
The viruses and nucleic acid molecules disclosed herein can be made by any method known to one of skill in the art. Methods of generating full length cDNA clones of the RNA genome of PepMV have been described, see, e.g., Hasiow-Jaroszewsk et al. Arch Virol (2009) 154:853-856. In addition, the cloning of both EU and CH2 PepMV clones has also been described in Duff-Farrier et al., Molecular Plant Pathology (2015) 16:308-315. Duff-Farrier et al. describes the construction of cDNA from PepMV EU and CH2 isolates and well as the introduction of chimeric sequences into the cDNA. Infectious RNA was synthesized in vitro, which was used to infect plants. Similar methods can be used to generate the viruses and nucleic acid molecules with sequences described herein.
The viruses and nucleic acid molecules discloses herein are useful for producing plants with increased resistance to PepMV, in particular to disease causing strains of PepMV such as the Peruvian (LP) strain, the European (EU) strain, the CH2 strain, first identified in Chile, and the US1 strain, identified in the United States. Accordingly, the disclosure provides attenuated viruses and nucleic acid molecules for controlling PepMV infection and/or PepMV disease in a plant. As used herein, controlling PepMV infection includes the reduction, prevention, or delay of PepMV accumulation in a plant. As used herein, controlling PepMV disease includes the reduction, prevention, or delay of PepMV symptoms.
The nucleic acid molecules disclosed herein, the polypetides encoded by said nucleic acid molecules, as well as antibodies recognizing said polypeptides are all useful for, e.g., detecting infection by the attenuated virus and thereby detecting plants with increased resistance to PepMV.
The viruses and nucleic acid molecules disclosed herein may be provided in compositions comprising an agriculturally acceptable carrier. Such compositions can be used for the biological control of plant disease. Preferably, the composition comprises and anti-oxidant, a phosphate buffer and/or a sulphite (sulphite can help prevent rotting). Preferably, the compositions have a pH range of 6-8.5, more preferably a pH of 7.7±0.5. Preferably the compositions comprise one or more of the following: mono-basic potassium phosphate, di-basic sodium phosphate dodecahydrate, and/or sodium sulphite. More preferably, the compositions comprises 0.4-1.6 g of mono-basic potassium phosphate per liter, more preferably around 0.8 g/L; 15-60 g of di-basic sodium phosphate dodecahydrate per liter, more preferably around 30 g/L; and 1-4 g sodium sulphite per liter, more preferably around 2 g/L.
The viruses may be propagated in a suitable plant host. The tissue from infected plants is ground and the homogenate (the sap) can be used to prepare the compositions disclosed herein. Alternatively, the nucleic acid molecules disclosed herein may be cloned into a vector for replication in another host.
The host range of PepMV is mainly restricted to plant species of the Solanaceae family Tomato (Solanum lycopersicum) is one of the most economically important natural host of PepMV. Pepino plant (S. muricatum) is a host in Peru and China (Jones et al., 1980; Soler et al., 2002; Zhang et al., 2003). In surveys in Peru, PepMV has been found to be naturally present in wild Solanum species (S. chilense, S. chmielewskii, S. parviflorum and S. peruvianum).
Infections, symptomless or with mild symptoms have also been observed in weed species which are member of families of Amaranthaceae, Asteraceae, Boraginaceae, Brassicaceae, Chenopodiaceae, Compositae, Convolvulaceae, Malvaceae, Plantaginaceae, Polygonaceae and Solanaceae. (Córdoba et al., 2004; Jordá et al., 2001; Kazinczi et al., 2005, Papayiannis et al., 2012; Salomone & Roggero 2002; Soler et al., 2002; Stobbs et al., 2009). Most of these infections were found in the vicinity of tomato greenhouses. PepMV has also been detected in a few potato cultivars (e.g., Solanum tuberosum cv. ‘Yungay’).
Several species have been found to be experimentally-susceptible to infection by PepMV following artificial inoculation, including eggplant (Solanum melongena) which was found to be infected by PepMV by mechanical inoculation (Salomone & Roggero, 2002; Verhoeven et al., 2003). Some cultivars of potato (S. tuberosum) can also be experimentally infected by PepMV (Jones et al., 1980). PepMV can infect Datura metel, D. stramonium, Nicotiana debneyi, N. benthamiana systemically (Jones et al., 1980; Verhoeven et al., 2003). Some PepMV isolates can infect N. glutinosa and N. tabacum (LP and some EU isolates; Verhoeven et al., 2003).
Preferably, the term “plant” refers to any plant which is capable of being infected with PepMV. In some embodiments, the plant belongs to the Solanaceae family, in particular the genus Solanum or Lycopersicon. As is known to the skilled person, the nomenclature for tomato plants has recently changed. For example, Solanum juglandifolium is now referred to as Lycopersicon juglandifolium. A preferred plant is a tomato plant.
As used herein, the term “plant part” includes, for example, single cells and tissues from pollen, ovules, leaves, embryos, roots, root tips, anthers, flowers, fruits, stems shoots, and seeds; as well as pollen, ovules, leaves, embryos, roots, root tips, anthers, flowers, fruits, stems, shoots, scions, rootstocks, seeds, protoplasts, calli, and the like.
PepMV induces a wide range of symptoms on tomato, such as yellow mosaic, leaf distortion, leaf blistering or bubbling, nettle-like heads, single yellow spots, inter-veinal chlorosis, severe leaf mosaics, leaf or stem necrosis and
Expression of symptoms may depend on environmental conditions, such as temperature and light intensity. Low environmental temperatures and low light intensity result in more severe damage (Jorda et al., 2001; Van der Vlugt & Stijger, 2008). PepMV is sometimes suggested to cause yield losses in tomato, but the highest economic losses are attributed to symptoms that affect the commercial value of tomato fruits, such as flaming, marbling, blotchy ripening and fruit size reduction (Soler et al., 2000; Spence et al., 2006; Hanssen & Thomma, 2010). In addition, the so-called ‘tomato collapse’, a sudden and progressive wilt of tomato which can lead to plant death is probably caused by PepMV accumulation in the vascular system (Soler-Aleixandre et al., 2005). Striking differences in the severity of symptomatology have been reported (Verhoeven et al., 2003; Hanssen et al., 2008) and not all isolates cause typical PepMV symptoms such as marbled and flamed fruits (Hanssen et al., 2009).
Symptoms in plants can be characterized either qualitatively or quantitatively.
The viruses disclosed herein are also useful for inducing resistance in “tolerant plants”, i.e., plants which may become infected with the virus and further its spread but remain symptomless or will have mild symptoms.
Several methods have been developed to detect PepMV. A robust method to detect PepMV in plants is DAS-ELISA (Van der Vlugt et al., 2002). Commercially available polyclonal antibodies can be purchased at Prime Diagnostics (Wageningen, The Netherlands). Different PCR-assays have been described to detect PepMV: a general potexvirus detection method (Van der Vlugt & Berendsen, 2002), a real-time immunocapture RT-PCR (Mansilla et al., 2003; Matínez-Culebras et al., 2002; Ling, 2005; Ling et al., 2007) and sensitive real-time PCR assays (Alfaro-Fernández et al., 2009; Johnson & Walcott, 2012; Gutiérrez-Aguirre et al., 2009). Simultaneous detection of multiple plant viruses including PepMV can be performed by using micro-arrays (Boonham et al., 2007) and deep sequencing (Li et al., 2012). Preferably, the accumulation of PepMV in a plant is determined using a quantitative detection method (e.g. an ELISA method or a quantitative reverse transcriptase-polymerase chain reaction [RT-PCR]).
A further aspect of the disclosure provides isolated polypeptides expressed by the viruses. In some embodiments the polypeptide is a RNA-dependent polymerase (RdRp) or a coat protein (CP). Preferably, the polypeptide is RdRp.
A further aspect of the disclosure provides antibodies specific for the polypeptides disclosed herein, preferably RdRp. In preferred embodiments, the antibody recognizes an antigen specific to VCA, but does not recognize the CH2, the US-1, the EU, or the LP strains. Preferably the antigen comprises the arginine at the position corresponding to 868 of SEQ ID NO:2 and/or the phenylalanine at the position corresponding to 1052 of SEQ ID NO:2 (or rather, the arginine at the position corresponding to 886 of SEQ ID NO:9 and/or the phenylalanine at the position corresponding to 1070 of SEQ ID NO:9).
A further aspect of the disclosure provides a method for producing said antibodies comprising immunizing a host (such as a mouse) with the attenuated virus, or a protein or peptide fragment thereof; harvesting from blood (including serum) or splenocytes of said host antibodies against said virus, protein or peptide fragment. In a preferred embodiment, the method further comprises selecting one antibody-producing splenocyte, fusing said splenocyte to an immortalized hybridoma cell line and allowing said hybridoma fusion to produce monoclonal antibodies. Preferably, the antigen is in part encoded by a nucleic acid sequence wherein the nucleotide at the position corresponding to 2605 of SEQ ID NO:1 (2675 of SEQ ID NO:8) is G; the nucleotide at the position corresponding to 3156 of SEQ ID NO: 1 (3226 of SEQ ID NO:8) is T and/or the nucleotide at the position corresponding to 3422 SEQ ID NO: 1 (3492 of SEQ ID NO:8) is G. More preferably, the antigen is in part encoded by a nucleic acid sequence wherein the nucleotide at the position corresponding to 2605 of SEQ ID NO:1 (2675 of SEQ ID NO:8) is G and/or the nucleotide at the position corresponding to 3156 of SEQ ID NO: 1 (3226 of SEQ ID NO:8) is T.
A further aspect of the disclosure provides a method for detecting the presence of the attenuated virus in a plant sample comprising reacting said sample with an antibody according to the disclosure. Suitable methods for performing immunoassays are well-known to a skilled person and include, e.g., radio-immunoassay (RIA), immunogold labeling, immunosorbent electron microscopy (ISEM), enzyme-linked immunosorbent assay (ELISA), Western blotting and immunoblotting.
A further aspect of the disclosure provides a method for identifying a pepino mosaic virus (PepMV)-resistant plant, comprising
It is clear to a skilled person that step a) includes an incubation period of sufficient duration to allow establishment of the attenuated virus. Preferably, such incubation period is at least one week, more preferably at least 5 weeks. In some embodiments, the presence of virus in the plant can be confirmed by one of the methods disclosed herein. It is also clear to a skilled person that step b) includes an incubation period of sufficient duration to allow establishment of the PepMV virus and detectable symptoms in control plants. Preferably, such incubation period is at least one week, more preferably at least 5 weeks.
As used herein, “resistant” refers to a reduction in multiplication of PepMV, a reduction of movement/spread of the virus to other cells, and/or a reduction or delay in the development of disease symptoms after infection with PepMV. Resistance can be determined by comparing a PepMV infected plant with a plant exposed to VCA and PepMV. Preferably, the PepMV referred to above is a CH2, US-1, EU, or LP strains, however, it also includes other disease causing PepMV strains.
Preferably, the accumulation of PepMV in a plant is determined using a quantitative detection method (e.g. an ELISA method or PCR, such as a quantitative reverse transcriptase-polymerase chain reaction [RT-PCR]).
As used herein, an “infective dosage” refers to the dosage of viral particles or viral nucleic acid molecule capable of infecting a plant. As is clear to as skilled person, the dosage may vary between plant species.
Methods of exposing a plant or a plant part to virus are well-known in the art and include dusting, coating, injecting, rubbing, rolling, dipping, spraying, or brushing. Exemplary methods include mechanical innoculation (e.g., rubbing plants or plant parts with infected plant material) and spraying plants with a solution containing virus particles or viral nucleic acid (see Example 1). The attenuated virus may be isolated from infected plants or other sources by any method known to one of the art.
As is known to a skilled person, cross protection may not lead to resistance in 100% of plants of the same species. Typically, cross protection protects more that 50% of the plants, preferably more than 80% of the plants.
A further aspect of the disclosure provides a method for producing a pepino mosaic virus (PepMV)-resistant plant using the attenuated viruses or nucleic acid molecules disclosed herein for cross-protection. Also provided are methods for controlling or preventing plant disease, in particular PepMV causing disease. Also provided are methods for controlling or preventing infection by PepMV. The methods comprise exposing a plant or plant part to an infective dosage of the attenuated virus, the nucleic acid molecules disclosed herein, or the compositions disclosed herein. In some embodiments, the methods further comprise detecting the attenuated virus in said plants or plant parts, such as by a method disclosed herein.
The disclosure also provides for PepMV-resistant plants comprising the attenuated virus or the nucleic acid sequences disclosed herein. Such plants may have been infected by the attenuated virus or are the progeny of a plant infected by the virus. The plants may also have been transformed by the nucleic acid molecules disclosed herein or a vector comprising the nucleic acid molecule. Progeny of said plants are also encompassed by the invention. Such plants are obtainable by the methods described herein.
PepMV is an RNA virus. As such it is preferred that the nucleic acid molecule that is comprised in the virion is RNA. Sequences indicated herein contain a T and as such refer to DNA. Wherein herein reference is made to a virus comprising a nucleic acid molecule with a certain nucleic acid sequence and reference is made to a DNA sequence in the context of a virus, it is of course clear to the person skilled in the art that the corresponding RNA sequence is intended. In other words that the reference is to the SEQ ID wherein the T is replaced by a U. Vectors and other compositions that do not refer to a virus or virus particle can have the referenced DNA, an RNA with the same sequence or a combination thereof.
As used herein, “to comprise” and its conjugations is used in its non-limiting sense to mean that items following the word are included, but items not specifically mentioned are not excluded. In addition the verb “to consist” may be replaced by “to consist essentially of” meaning that a compound or adjunct compound as defined herein may comprise additional component(s) than the ones specifically identified, said additional component(s) not altering the unique characteristic of the invention.
The articles “a” and “an” are used herein to refer to one or to more than one (i.e., to at least one) of the grammatical object of the article. By way of example, “an element” means one element or more than one element.
The word “approximately” or “about” when used in association with a numerical value (approximately 10, about 10) preferably means that the value may be the given value of 10 more or less 1% of the value.
Fakhro A, Von Bargen S, Bandte M and Büttner C (2010) Pepino mosaic virus, a first report of a virus infecting tomato in Syria. Phytopathologia Mediterranea 49: 99-101.
Hanssen I M, Paeleman A, Vandewoestijne E, Van Bergen L, Bragard C, Lievens B, Vanachter A C R C and Thomma B P H J (2009) Pepino mosaic virus isolates and differential symptomatology in tomato. Plant Pathology 58: 450-460.
Hasiów-Jaroszewska B and Borodynko N (2012) Characterization of the necrosis determinant of the European genotype of pepino mosaic virus by site-specific mutagenesis of an infectious cDNA clone. Archives of Virology 157: 337-341.
The invention is further explained in the following examples. These examples do not limit the scope of the invention, but merely serve to clarify the invention.
VC1 is a mild isolate of the CH2 strain of pepino mosaic virus (PepMV). During wintertime, VC1 infection can produce unwanted symptoms in inoculated plants, namely, nettle-heads and growth retardation. New variants of the CH2 strain were produced in order to identify viruses that would offer cross-protection but with reduced unwanted symptoms. In this trial, the new mild isolate VCA is compared with VC1 for symptoms and their cross-protection effectivity. The RNA-dependent RNA-polymerase (RdRp) of VCA was sequenced and was found to comprise a mixture of closely related viruses having the sequence of SEQ ID NO:1. Additional sequencing was performed to determine the complete coding sequence of the RdRp which is depicted in SEQ ID NO:8. The overlapping sequences of SEQ ID NO:1 and 8 are identical with the exception of position 6290 of SEQ ID NO:8. A“C” is present at this position in SEQ ID NO:8 instead of a “T” in the SEQ ID NO:1. This may reflect a mutation, but does not lead to an amino acid change.
A sequence alignment of VCA with known PepMV viruses is depicted in
Set-Up:
Tomato plants of the cultivar Merlice (on rootstock) were used. Each row of 12 plants was a different treatment. The plants were grown in two greenhouse compartments. The set temperatures were 20° C. at daytime and 18° C. at nighttime. The trial lasted 3 months. Inoculations were carried out by the rubbing protocol (see below).
Plants were innoculated first with mild isolates (VC1 or VCA) and tested with ELISA to determine infection. The results of the ELISA are shown below.
Approximately six weeks (39 days) after the first inoculation the plants were innoculated with the virulent isolate (CHD).
Results
Infection with the mild isolates VCA and VC1 resulted in very mild symptoms, namely, light bubbling on the young leaves and minor nettle-heads (
Conclusions
VC1 infection can produce unwanted symptoms in inoculated plants, namely, nettle-heads and growth retardation. In this trial, the new mild isolate VCA is compared with VC1 for the induction of symptoms in treated plants.
Tomato plants of the cultivar Komeett were used. Inoculations were carried out by the rubbing protocol (see below). Plants were innoculated with mild isolates (VC1 or VCA) and tested two weeks later with ELISA to determine infection. It was found on average 95% of the virus inoculated plants had been infected. The virus-free plants remained free until the end of the test. Treatment with either VCA or VC1 resulted in the development of light symptoms, such as leaf misformation. However, plants treated with VCA (
Material and Methods:
Rubbing Protocol:
Knead frozen or fresh infected plant material. Take 7.5-10 ml of extracted plant sap or 7.5-10 ml virus suspension of virus product.
Put the 7.5-10 ml in a plastic tray
Dilute virus suspension 10-times with PBS
Add 1-2% (w/v) carborundum
Mix suspension well.
Put disposable gloves on your hands.
Stir with your fingers and thumb in the suspension.
Inoculate two leaves on each plant in upper half on a leaflet by rubbing 5-times leaflet between thumb and index finger. Leaves should be damaged a little bit. (light discolouration, without holes).
Dip for each plant your finger and inoculate the plant
After inoculation, collect all residual material and put this in a garbage bin or waste container. The residual material should be disinfected by 100-200 ppm hypochlorite and after that it can be processed as regular waste.
Test after 14 (±2) days the percentage of infected plants. This can be determined by the method ELISA.
High pressure spraying protocol:
Usage of spraying liquid: 0.5 L/m.
Measure the needed amount of cold tap water and put this in the tank of the spraying cart.
Prepare virus solution
Add carborundum 800 gram/100 L to spraying liquid.
Mix carborundum well in spray cart, by hand, cover your fore-arm in a disposable overboot, circulate to contents of the tank
Pressure on nozzles in spraying arm: 12-15 bar
Spraying width: 1.20 m, 6 nozzles
Spraying height: 10-15 cm above the plants.
Check the nozzles for blockages and evenness of spray.
After inoculation, collect all residual material and put this in a garbage bin or waste container. The residual material should be disinfected by 100-200 ppm hypochlorite and after that it can be processed as regular waste.
Test after 14 (±2) days the percentage of infected plants. This can be determined by the ELISA method.
ELISA for Measuring PepMV in Sample
Reagents for performing DAS-ELISA were obtained from PRIME Diagnostics, Wageningen, The Netherlands. The ELISAs were carried out according to the manufacturer's instructions.
| Number | Date | Country | Kind |
|---|---|---|---|
| 15188418 | Oct 2015 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/NL2016/050684 | 10/4/2016 | WO | 00 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2017/061859 | 4/13/2017 | WO | A |
| Entry |
|---|
| Schenk et al, Europ J Plant Pathol 127: 249-261, 2010 (Year: 2010). |
| International Search Report and Written Opinion in corresponding PCT Application No. PCT/NL2016/050684, dated Oct. 3, 2017. |
| Beata Hasiw-Jaroszewska et al:, Single 1.2.4-13 mutation converts mild pathotype of the Pepino mosaic virus into necrotic one, Virus Research. Amsterdam. NL., vol. 159. No. 1., Apr. 22, 2011 (Apr. 22, 2011). pp. 57-61. |
| I. M. Hanssen et al: “Pepino mosaic virus isolates and differential symptomatology in tomato”, Plant Pathology. vol. 58, No. 3, Feb. 18, 2009 (Feb. 19, 2009). pp. 450-460. |
| Godwill Mih Chewachong: “Engineering Plant Virus “Vaccines” Using Pepino Mosaic Virus as a Model”, Ph. D. thesis, 2013. pp. i-xviii, 1-102. |
| Martijn F Schenk et al: “The use of attenuated isolates of Pepino mosaic virus for cross-protection”, European Journal of Plant Pathology Kluwer Academic Publishers. DO, vol. 127m No. 2, Mar. 1, 2010 (Mar. 1, 2010), pp. 249-261. |
| Godwi LL M. Chewachong et al: “Generation of an Attenuated. Cross-Protective Pepino mosaic virus Variant Through Alignment-Guided Mutagenesis of the Viral Capsid Protein”, Phytopathology, vol. 105, No. 1, Jan. 2015 (Jan. 2015), pp. 126-134. |
| Beata Hasiow-Jaroszewska et al:, “Ratio of mutated versus wild-type coat protein sequences in Pepino mosaic virus determines the nature and severity of yellowing symptoms on tomato plants”, Molecular Plant Pathology, vol. 14, No. 9, Jul. 15, 2013 (Jul. 15, 2013), pp. 923-933. |
| Beata Hasiow-Jaroszewska et al:, “A method for detection and discrimination of Pepino mosaic virus isolates using high resolution melting analysis of the triple gene block 3”, Journal of Virological Methods, vol. 193, No. 1, May 13, 2013 (May 13, 2013), pp. 1-5. |
| Inge M. Hanssen et al, “Pepino mosaic virus : a successful pathogen that rapidly evolved from emerging to endemic in tomato crops”, Molecular Plant Pathology, vol. 11, No. 2, Nov. 12, 2009 (Nov. 12, 2009). pp. 179-189. |
| Number | Date | Country | |
|---|---|---|---|
| 20190048323 A1 | Feb 2019 | US |
