Transcriptomes of Ralstonia solanacearum during root colonization of Solanum commersonii

Autor: Puigvert, Marina, Guarischi-Sousa, Rodrigo, Zuluaga, Paola, Coll, Núria S., Macho, Alberto P., Setubal, João C., Valls, Marc
Přispěvatelé: Ministerio de Economía y Competitividad (España), Generalitat de Catalunya, European Commission, Chinese Academy of Sciences, Universidad de Barcelona, Sao Paulo Research Foundation, Universitat de Barcelona
Jazyk: angličtina
Rok vydání: 2017
Předmět:
Zdroj: Recercat. Dipósit de la Recerca de Catalunya
instname
Dipòsit Digital de la UB
Universidad de Barcelona
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
ResearcherID
Digital.CSIC. Repositorio Institucional del CSIC
Popis: Bacterial wilt of potatoes—also called brown rot—is a devastating disease caused by the vascular pathogen Ralstonia solanacearum that leads to significant yield loss. As in other plant-pathogen interactions, the first contacts established between the bacterium and the plant largely condition the disease outcome. Here, we studied the transcriptome of R. solanacearum UY031 early after infection in two accessions of the wild potato Solanum commersonii showing contrasting resistance to bacterial wilt. Total RNAs obtained from asymptomatic infected roots were deep sequenced and for 4,609 out of the 4,778 annotated genes in strain UY031 were recovered. Only 2 genes were differentially-expressed between the resistant and the susceptible plant accessions, suggesting that the bacterial component plays a minor role in the establishment of disease. On the contrary, 422 genes were differentially expressed (DE) in planta compared to growth on a synthetic rich medium. Only 73 of these genes had been previously identified as DE in a transcriptome of R. solanacearum extracted from infected tomato xylem vessels. Virulence determinants such as the Type Three Secretion System (T3SS) and its effector proteins, motility structures, and reactive oxygen species (ROS) detoxifying enzymes were induced during infection of S. commersonii. On the contrary, metabolic activities were mostly repressed during early root colonization, with the notable exception of nitrogen metabolism, sulfate reduction and phosphate uptake. Several of the R. solanacearum genes identified as significantly up-regulated during infection had not been previously described as virulence factors. This is the first report describing the R. solanacearum transcriptome directly obtained from infected tissue and also the first to analyze bacterial gene expression in the roots, where plant infection takes place. We also demonstrate that the bacterial transcriptome in planta can be studied when pathogen numbers are low by sequencing transcripts from infected tissue avoiding prokaryotic RNA enrichment.
This work was funded by projects AGL2013-46898-R, AGL2016-78002-R, and RyC 2014-16158 from the Spanish Ministry of Economy and Competitiveness. We also acknowledge financial support from the “Severo Ochoa Program for Centres of Excellence in R&D” 2016-2019 (SEV-2015-0533) and the CERCA Program of the Catalan Government (Generalitat de Catalunya) and from COST Action SUSTAIN (FA1208) from the European Union. APM is funded by the Chinese Academy of Sciences and the Chinese 1000 Talents Program. MP holds an APIF doctoral fellowship from Universitat de Barcelona and received a travel fellowship allowed by Fundació Montcelimar and Universitat de Barcelona to carry out a short stay in JCS's lab. RGS holds a doctoral fellowship; grant 2012/15197-1, São Paulo Research Foundation (FAPESP) and JCS has a CNPq research fellowship.
Databáze: OpenAIRE
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