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dc.contributor.authorLópez Sánchez-Ortiz, Anselmo
dc.contributor.authorvan Kan, Jan A.L.
dc.contributor.authorBeenen, Henriek G.
dc.contributor.authorDolcet-Sanjuan, Ramon
dc.contributor.authorTeixidó, Neus
dc.contributor.authorTorres, Rosario
dc.contributor.authorVILANOVA, LAURA
dc.contributor.otherProducció Vegetalca
dc.date.accessioned2024-09-20T09:40:53Z
dc.date.available2024-09-20T09:40:53Z
dc.date.issued2024-08-16
dc.identifier.citationAnselmo López, Jan A. L. van Kan, Henriek G Beenen, Ramon Dolcet-Sanjuan, Neus Teixidó, Rosario Torres, and Laura Vilanova. 2024. “Evaluation of Cell Death-Inducing Activity of Monilinia Spp. Effectors in Several Plants Using a Modified TRV Expression System.” Frontiers in Plant Science 15 (August). https://doi.org/10.3389/fpls.2024.1428613. ‌ca
dc.identifier.issn1664-462Xca
dc.identifier.urihttp://hdl.handle.net/20.500.12327/3281
dc.description.abstractIntroduction: Brown rot is the most important fungal disease affecting stone fruit and it is mainly caused by Monilinia fructicola, M. laxa and M. fructigena. Monilinia spp. are necrotrophic plant pathogens with the ability to induce plant cell death by the secretion of different phytotoxic molecules, including proteins or metabolites that are collectively referred to as necrotrophic effectors (NEs). Methods: We exploited the genomes of M. fructicola, M. laxa and M. fructigena to identify their common group of secreted effector proteins and tested the ability of a selected set of effectors to induce cell death in Nicotiana benthamiana, Solanum lycopersicum and Prunus spp. leaves. Results: Fourteen candidate effector genes of M. fructicola, which displayed high expression during infection, were transiently expressed in plants by agroinfiltration using a modified Tobacco Rattle Virus (TRV)-based expression system. Some, but not all, effectors triggered leaf discoloration or cell death in N. benthamiana and S. lycopersicum, which are non-hosts for Monilinia and in Prunus spp., which are the natural hosts. The effector MFRU_030g00190 induced cell death in almost all Prunus genotypes tested, but not in the Solanaceous plants, while MFRU_014g02060, which is an ortholog to BcNep1, caused necrosis in all plant species tested. Conclusion: This method provides opportunities for screening Prunus germplasm with Monilinia effector proteins, to serve as a tool for identifying genetic loci that confer susceptibility to brown rot disease.ca
dc.description.sponsorshipThe author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by national project PID2020-115702RB-C22/AEI/10.13039/501100011033 from the Spanish Government (MINECO) and by funding received from the CERCA Programme SGR-01477/Generalitat de Catalunya. LV received funding from the postdoctoral fellowships programme Beatriu de Pinós, funded by the Secretary of Universities and Research (Government of Catalonia) and by the Horizon 2020 programme of the European Union (MSCA grant 801370) and AL is recipient of a IRTA Sponsored Fellowship 2022.ca
dc.format.extent10ca
dc.language.isoengca
dc.publisherFrontiers Mediaca
dc.relation.ispartofFrontiers in Plant Scienceca
dc.rightsAttribution 4.0 Internationalca
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleEvaluation of cell death-inducing activity of Monilinia spp. effectors in several plants using a modified TRV expression systemca
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.relation.projectIDMCIN/ Programa Estatal de Generación de Conocimiento y Fortalecimiento Científico y Tecnológico del Sistema de I+D+i y Programa Estatal de I+D+i orientada a los retos de la Sociedad/ PID2020-115702RB-C22/ES/Bases moleculares de la podredumbre parda causada por Monilinia spp. en los distintos estados fenológicos de Prunus persica/PEACH&BROWNca
dc.relation.projectIDEC/H2020/801370/EU/Beatriu de Pinos-3 Postdoctoral Programme/BP3ca
dc.subject.udc632ca
dc.identifier.doihttps://doi.org/10.3389/fpls.2024.1428613ca
dc.contributor.groupFructiculturaca
dc.contributor.groupPostcollitaca


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