- -

Virus variants with differences in the P1 protein coexist in a Plum pox virus population and display particular host-dependent pathogenicity features

RiuNet: Repositorio Institucional de la Universidad Politécnica de Valencia

Compartir/Enviar a

Citas

Estadísticas

  • Estadisticas de Uso

Virus variants with differences in the P1 protein coexist in a Plum pox virus population and display particular host-dependent pathogenicity features

Mostrar el registro sencillo del ítem

Ficheros en el ítem

dc.contributor.author Maliogka, Varvara I. es_ES
dc.contributor.author Salvador, Beatriz es_ES
dc.contributor.author CARBONELL, ALBERTO es_ES
dc.contributor.author Saenz, Pilar es_ES
dc.contributor.author San Leon, David es_ES
dc.contributor.author Oliveros, Juan Carlos es_ES
dc.contributor.author Delgadillo, Ma Otilia es_ES
dc.contributor.author García, Juan Antonio es_ES
dc.contributor.author Simon-Mateo, Carmen es_ES
dc.date.accessioned 2021-02-12T04:31:20Z
dc.date.available 2021-02-12T04:31:20Z
dc.date.issued 2012-10 es_ES
dc.identifier.issn 1464-6722 es_ES
dc.identifier.uri http://hdl.handle.net/10251/161162
dc.description.abstract [EN] Subisolates segregated from an M-type Plum pox virus (PPV) isolate, PPV-PS, differ widely in pathogenicity despite their high degree of sequence similarity. A single amino acid substitution, K109E, in the helper component proteinase (HCPro) protein of PPV caused a significant enhancement of symptom severity in herbaceous hosts, and notably modified virus infectivity in peach seedlings. The presence of this substitution in certain subisolates that induced mild symptoms in herbaceous hosts and did not infect peach seedlings suggested the existence of uncharacterized attenuating factors in these subisolates. In this study, we show that two amino acid changes in the P1 protein are specifically associated with the mild pathogenicity exhibited by some PS subisolates. Site-directed mutagenesis studies demonstrated that both substitutions, W29R and V139E, but especially W29R, resulted in lower levels of virus accumulation and symptom severity in a woody host, Prunus persica. Furthermore, when W29R and V139E mutations were expressed concomitantly, PPV infectivity was completely abolished in this host. In contrast, the V139E substitution, but not W29R, was found to be responsible for symptom attenuation in herbaceous hosts. Deep sequencing analysis demonstrated that the W29R and V139E heterogeneities already existed in the original PPV-PS isolate before its segregation in different subisolates by local lesion cloning. These results highlight the potential complexity of potyviral populations and the relevance of the P1 protein of potyviruses in pathogenesis and viral adaptation to the host. es_ES
dc.description.sponsorship We wish to thank Elvira Dominguez for technical assistance. This work was supported by grants BIO2010-18541 from the Spanish Ministerio de Educacion y Ciencia (MEC), SAL/0185/2006 from Comunidad de Madrid and KBBE-204429 from the European Union. B. S. was a recipient of a Formacion de Personal Investigador fellowship from MEC. es_ES
dc.language Inglés es_ES
dc.publisher Blackwell Publishing es_ES
dc.relation.ispartof Molecular Plant Pathology es_ES
dc.rights Reserva de todos los derechos es_ES
dc.subject Ppv es_ES
dc.subject P1 es_ES
dc.subject Plum pox virus es_ES
dc.title Virus variants with differences in the P1 protein coexist in a Plum pox virus population and display particular host-dependent pathogenicity features es_ES
dc.type Artículo es_ES
dc.identifier.doi 10.1111/j.1364-3703.2012.00796.x es_ES
dc.relation.projectID info:eu-repo/grantAgreement/MICINN//BIO2010-18541/ES/FACTORES DE LA INTERACCION PLANTA-VIRUS RELEVANTES PARA EL CONTROL DEL VIRUS DE LA SHARKA Y PARA SU USO COMO HERRAMIENTA BIOTECNOLOGICA/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/EC/FP7/204429/EU/Sharka Containment/
dc.relation.projectID info:eu-repo/grantAgreement/CAM//SAL%2F0185%2F2006/ es_ES
dc.rights.accessRights Abierto es_ES
dc.contributor.affiliation Universitat Politècnica de València. Instituto Universitario Mixto de Biología Molecular y Celular de Plantas - Institut Universitari Mixt de Biologia Molecular i Cel·lular de Plantes es_ES
dc.description.bibliographicCitation Maliogka, VI.; Salvador, B.; Carbonell, A.; Saenz, P.; San Leon, D.; Oliveros, JC.; Delgadillo, MO.... (2012). Virus variants with differences in the P1 protein coexist in a Plum pox virus population and display particular host-dependent pathogenicity features. Molecular Plant Pathology. 13(8):877-886. https://doi.org/10.1111/j.1364-3703.2012.00796.x es_ES
dc.description.accrualMethod S es_ES
dc.relation.publisherversion https://doi.org/10.1111/j.1364-3703.2012.00796.x es_ES
dc.description.upvformatpinicio 877 es_ES
dc.description.upvformatpfin 886 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion es_ES
dc.description.volume 13 es_ES
dc.description.issue 8 es_ES
dc.identifier.pmid 22458641 es_ES
dc.identifier.pmcid PMC6638729 es_ES
dc.relation.pasarela S\377812 es_ES
dc.contributor.funder Comunidad de Madrid es_ES
dc.contributor.funder European Commission es_ES
dc.contributor.funder Ministerio de Ciencia e Innovación es_ES
dc.description.references Adams, M. J., Antoniw, J. F., & Fauquet, C. M. (2004). Molecular criteria for genus and species discrimination within the family Potyviridae. Archives of Virology, 150(3), 459-479. doi:10.1007/s00705-004-0440-6 es_ES
dc.description.references Ayme, V., Petit-Pierre, J., Souche, S., Palloix, A., & Moury, B. (2007). Molecular dissection of the potato virus Y VPg virulence factor reveals complex adaptations to the pvr2 resistance allelic series in pepper. Journal of General Virology, 88(5), 1594-1601. doi:10.1099/vir.0.82702-0 es_ES
dc.description.references Biebricher, C. K., & Eigen, M. (s. f.). What Is a Quasispecies? Quasispecies: Concept and Implications for Virology, 1-31. doi:10.1007/3-540-26397-7_1 es_ES
dc.description.references Brantley, J. D., & Hunt, A. G. (1993). The N-terminal protein of the polyprotein encoded by the potyvirus tobacco vein mottling virus is an RNA-binding protein. Journal of General Virology, 74(6), 1157-1162. doi:10.1099/0022-1317-74-6-1157 es_ES
dc.description.references Charron, C., Nicolaï, M., Gallois, J.-L., Robaglia, C., Moury, B., Palloix, A., & Caranta, C. (2008). Natural variation and functional analyses provide evidence for co-evolution between plant eIF4E and potyviral VPg. The Plant Journal, 54(1), 56-68. doi:10.1111/j.1365-313x.2008.03407.x es_ES
dc.description.references Chiang, C.-H., Lee, C.-Y., Wang, C.-H., Jan, F.-J., Lin, S.-S., Chen, T.-C., … Yeh, S.-D. (2007). Genetic analysis of an attenuated Papaya ringspot virus strain applied for cross-protection. European Journal of Plant Pathology, 118(4), 333-348. doi:10.1007/s10658-007-9130-z es_ES
dc.description.references Chung, B. Y.-W., Miller, W. A., Atkins, J. F., & Firth, A. E. (2008). An overlapping essential gene in the Potyviridae. Proceedings of the National Academy of Sciences, 105(15), 5897-5902. doi:10.1073/pnas.0800468105 es_ES
dc.description.references Domingo, E., & Holland, J. J. (1997). RNA VIRUS MUTATIONS AND FITNESS FOR SURVIVAL. Annual Review of Microbiology, 51(1), 151-178. doi:10.1146/annurev.micro.51.1.151 es_ES
dc.description.references EIGEN, M. (1996). On the nature of virus quasispecies. Trends in Microbiology, 4(6), 216-218. doi:10.1016/0966-842x(96)20011-3 es_ES
dc.description.references Hajimorad, M. R., Wen, R.-H., Eggenberger, A. L., Hill, J. H., & Maroof, M. A. S. (2011). Experimental Adaptation of an RNA Virus Mimics Natural Evolution. Journal of Virology, 85(6), 2557-2564. doi:10.1128/jvi.01935-10 es_ES
dc.description.references Holmes, E. C., & Moya, A. (2002). Is the Quasispecies Concept Relevant to RNA Viruses? Journal of Virology, 76(1), 460-462. doi:10.1128/jvi.76.1.460-462.2002 es_ES
dc.description.references Jenkins, G. M., Worobey, M., Woelk, C. H., & Holmes, E. C. (2001). Evidence for the Non-quasispecies Evolution of RNA Viruses. Molecular Biology and Evolution, 18(6), 987-994. doi:10.1093/oxfordjournals.molbev.a003900 es_ES
dc.description.references Jridi, C., Martin, J.-F., Marie-Jeanne, V., Labonne, G., & Blanc, S. (2006). Distinct Viral Populations Differentiate and Evolve Independently in a Single Perennial Host Plant. Journal of Virology, 80(5), 2349-2357. doi:10.1128/jvi.80.5.2349-2357.2006 es_ES
dc.description.references Li, H., & Durbin, R. (2010). Fast and accurate long-read alignment with Burrows–Wheeler transform. Bioinformatics, 26(5), 589-595. doi:10.1093/bioinformatics/btp698 es_ES
dc.description.references López-Moya, J. J., & Garcı́a, J. A. (2000). Construction of a stable and highly infectious intron-containing cDNA clone of plum pox potyvirus and its use to infect plants by particle bombardment. Virus Research, 68(2), 99-107. doi:10.1016/s0168-1702(00)00161-1 es_ES
dc.description.references Moxon, S., Schwach, F., Dalmay, T., MacLean, D., Studholme, D. J., & Moulton, V. (2008). A toolkit for analysing large-scale plant small RNA datasets. Bioinformatics, 24(19), 2252-2253. doi:10.1093/bioinformatics/btn428 es_ES
dc.description.references Nakahara, K. S., Shimada, R., Choi, S.-H., Yamamoto, H., Shao, J., & Uyeda, I. (2010). Involvement of the P1 Cistron in Overcoming eIF4E-Mediated Recessive Resistance Against Clover yellow vein virus in Pea. Molecular Plant-Microbe Interactions®, 23(11), 1460-1469. doi:10.1094/mpmi-11-09-0277 es_ES
dc.description.references Ohshima, K., Akaishi, S., Kajiyama, H., Koga, R., & Gibbs, A. J. (2009). Evolutionary trajectory of turnip mosaic virus populations adapting to a new host. Journal of General Virology, 91(3), 788-801. doi:10.1099/vir.0.016055-0 es_ES
dc.description.references Pruss, G., Ge, X., Shi, X. M., Carrington, J. C., & Bowman Vance, V. (1997). Plant viral synergism: the potyviral genome encodes a broad-range pathogenicity enhancer that transactivates replication of heterologous viruses. The Plant Cell, 9(6), 859-868. doi:10.1105/tpc.9.6.859 es_ES
dc.description.references Rajamäki, M.-L., Kelloniemi, J., Alminaite, A., Kekarainen, T., Rabenstein, F., & Valkonen, J. P. T. (2005). A novel insertion site inside the potyvirus P1 cistron allows expression of heterologous proteins and suggests some P1 functions. Virology, 342(1), 88-101. doi:10.1016/j.virol.2005.07.019 es_ES
dc.description.references Rohožková, J., & Navrátil, M. (2011). P1 peptidase – a mysterious protein of family Potyviridae. Journal of Biosciences, 36(1), 189-200. doi:10.1007/s12038-011-9020-6 es_ES
dc.description.references Sáenz, P., Riechmann, J. L., Dallot, S., Quiot, L., Garcı́a, J. A., Cervera, M. T., & Quiot, J.-B. (2000). Identification of a pathogenicity determinant of Plum pox virus in the sequence encoding the C-terminal region of protein P3+6K1. Journal of General Virology, 81(3), 557-566. doi:10.1099/0022-1317-81-3-557 es_ES
dc.description.references Sáenz, P., Quiot, L., Quiot, J.-B., Candresse, T., & García, J. A. (2001). Pathogenicity Determinants in the Complex Virus Population of a Plum pox virus Isolate. Molecular Plant-Microbe Interactions®, 14(3), 278-287. doi:10.1094/mpmi.2001.14.3.278 es_ES
dc.description.references Salvador, B., García, J. A., & Simón-Mateo, C. (2006). Causal agent of sharka disease: Plum pox virus genome and function of gene products. EPPO Bulletin, 36(2), 229-238. doi:10.1111/j.1365-2338.2006.00979.x es_ES
dc.description.references Salvador, B., Delgadillo, M. O., Sáenz, P., García, J. A., & Simón-Mateo, C. (2008). Identification of Plum pox virus Pathogenicity Determinants in Herbaceous and Woody Hosts. Molecular Plant-Microbe Interactions®, 21(1), 20-29. doi:10.1094/mpmi-21-1-0020 es_ES
dc.description.references SALVADOR, B., SAÉNZ, P., YANGÜEZ, E., QUIOT, J. B., QUIOT, L., DELGADILLO, M. O., … SIMÓN-MATEO, C. (2008). Host-specific effect of P1 exchange between two potyviruses. Molecular Plant Pathology, 9(2), 147-155. doi:10.1111/j.1364-3703.2007.00450.x es_ES
dc.description.references Soumounou, Y., & Laliberte, J.-F. (1994). Nucleic acid-binding properties of the P1 protein of turnip mosaic potyvirus produced in Escherichia coli. Journal of General Virology, 75(10), 2567-2573. doi:10.1099/0022-1317-75-10-2567 es_ES
dc.description.references Suehiro, N., Natsuaki, T., Watanabe, T., & Okuda, S. (2004). An important determinant of the ability of Turnip mosaic virus to infect Brassica spp. and/or Raphanus sativus is in its P3 protein. Journal of General Virology, 85(7), 2087-2098. doi:10.1099/vir.0.79825-0 es_ES
dc.description.references Valli, A., Martín-Hernández, A. M., López-Moya, J. J., & García, J. A. (2006). RNA Silencing Suppression by a Second Copy of the P1 Serine Protease ofCucumber Vein Yellowing Ipomovirus, a Member of the FamilyPotyviridaeThat Lacks the Cysteine Protease HCPro. Journal of Virology, 80(20), 10055-10063. doi:10.1128/jvi.00985-06 es_ES
dc.description.references Valli, A., López-Moya, J. J., & García, J. A. (2007). Recombination and gene duplication in the evolutionary diversification of P1 proteins in the family Potyviridae. Journal of General Virology, 88(3), 1016-1028. doi:10.1099/vir.0.82402-0 es_ES
dc.description.references Vancanneyt, G., Schmidt, R., O’Connor-Sanchez, A., Willmitzer, L., & Rocha-Sosa, M. (1990). Construction of an intron-containing marker gene: Splicing of the intron in transgenic plants and its use in monitoring early events in Agrobacterium-mediated plant transformation. Molecular and General Genetics MGG, 220(2), 245-250. doi:10.1007/bf00260489 es_ES
dc.description.references Verchot, J., & Carrington, J. C. (1995). Debilitation of plant potyvirus infectivity by P1 proteinase-inactivating mutations and restoration by second-site modifications. Journal of Virology, 69(3), 1582-1590. doi:10.1128/jvi.69.3.1582-1590.1995 es_ES
dc.description.references Verchot, J., & Carrington, J. C. (1995). Evidence that the potyvirus P1 proteinase functions in trans as an accessory factor for genome amplification. Journal of Virology, 69(6), 3668-3674. doi:10.1128/jvi.69.6.3668-3674.1995 es_ES
dc.description.references Verchot, J., Koonin, E. V., & Carrington, J. C. (1991). The 35-kDa protein from the N-terminus of the potyviral polyprotein functions as a third virus-encoded proteinase. Virology, 185(2), 527-535. doi:10.1016/0042-6822(91)90522-d es_ES


Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem