GacA reduces virulence and increases competitiveness in planta in the tumorigenic olive pathogen Pseudomonas savastanoi pv. savastanoi

dc.centroFacultad de Cienciases_ES
dc.contributor.authorLavado-Benito, Carla
dc.contributor.authorMurillo, Jesús
dc.contributor.authorMartínez Gil, Marta
dc.contributor.authorRamos-Rodríguez, Cayo Juan
dc.contributor.authorRodríguez-Moreno, Luis Gabriel
dc.date.accessioned2025-06-17T08:52:55Z
dc.date.available2025-06-17T08:52:55Z
dc.date.issued2024-02-05
dc.departamentoBiología Celular, Genética y Fisiologíaes_ES
dc.descriptionThe author(s) declare financial support was received for the research, authorship, and/or publication of this article. This research was supported by project grants PID2020-115177RB-C21 and PID2020-115177RB-C22 financed by the Spanish Ministry of Science and Innovation (MCIN)/Agencia Estatal de Investigacioń (AEI)/10.13039/501100011033/ and by the European Regional Development Fund (ERDF) “A way to make Europe”. CL-B was supported by the FPI2018-084276 predoctoral grant. Open access was partially funded by grant QUAL21 012 IHSM, Consejería de Universidad, Investigación e Innovación, Junta de Andalucıa.es_ES
dc.description.abstractGacS/GacA is a widely distributed two-component system playing an essential role as a key global regulator, although its characterization in phytopathogenic bacteria has been deeply biased, being intensively studied in pathogens of herbaceous plants but barely investigated in pathogens of woody hosts. P. savastanoi pv. savastanoi (Psv) is characterized by inducing tumours in the stem and branches of olive trees. In this work, the model strain Psv NCPPB 3335 and a mutant derivative with a complete deletion of gene gacA were subjected to RNA-Seq analyses in a minimum medium and a medium mimicking in planta conditions, accompanied by RT-qPCR analyses of selected genes and phenotypic assays. These experiments indicated that GacA participates in the regulation of at least 2152 genes in strain NCPPB 3335, representing 37.9 % of the annotated CDSs. GacA also controls the expression of diverse rsm genes, and modulates diverse phenotypes, including motility and resistance to oxidative stresses. As occurs with other P. syringae pathovars of herbaceous plants, GacA regulates the expression of the type III secretion system and cognate effectors. In addition, GacA also regulates the expression of WHOP genes, specifically encoded in P. syringe strains isolated from woody hosts, and genes for the biosynthesis of phytohormones. A gacA mutant of NCPPB 3335 showed increased virulence, producing large immature tumours with high bacterial populations, but showed a significantly reduced competitiveness in planta. Our results further extend the role of the global regulator GacA in the virulence and fitness of a P. syringae pathogen of woody hostses_ES
dc.identifier.citationFront. Plant Sci. 15:1347982es_ES
dc.identifier.doi10.3389/fpls.2024.1347982
dc.identifier.urihttps://hdl.handle.net/10630/39007
dc.language.isoenges_ES
dc.publisherFrontiers Mediaes_ES
dc.relation.projectIDPID2020-115177RB-C21es_ES
dc.relation.projectIDPID2020-115177RB-C22es_ES
dc.relation.projectIDFPI2018-084276es_ES
dc.relation.projectIDQUAL21 012 IHes_ES
dc.rightsAttribution 4.0 Internacional*
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectPseudomonas syringae - Genéticaes_ES
dc.subjectBacterias fitopatógenases_ES
dc.subjectBacterias gram negativases_ES
dc.subject.otherPseudomonas savastanoies_ES
dc.subject.otherPseudomonas syringaees_ES
dc.subject.otherGacS/GacA two component systemes_ES
dc.subject.otherRNA-seq analysises_ES
dc.subject.otherwoody hostes_ES
dc.titleGacA reduces virulence and increases competitiveness in planta in the tumorigenic olive pathogen Pseudomonas savastanoi pv. savastanoies_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublication00be32a4-e0df-4f77-b832-835236a7d1d0
relation.isAuthorOfPublicationd56a3a3f-db4e-425f-9ac5-cd4b41cecc03
relation.isAuthorOfPublication.latestForDiscovery00be32a4-e0df-4f77-b832-835236a7d1d0

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