4.6 Article

RasI/R Quorum Sensing System Controls the Virulence of Ralstonia solanacearum Strain EP1

Journal

APPLIED AND ENVIRONMENTAL MICROBIOLOGY
Volume 88, Issue 15, Pages -

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/aem.00325-22

Keywords

cell-cell communication; signaling mechanism; pathogenesis; bacterial wilt

Funding

  1. Guangdong Forestry Science and Technology Innovation Project [2018KJCX009, 2020KJCX009]
  2. Key Realm R&D Program of Guangdong Province [2020B0202090001, 2018B020205003]
  3. Basic Research and Applied Basic Research Program of Guangdong Province [2020A1515110111]
  4. National Natural Science Foundation of China [31900076]
  5. Guangzhou Basic Research Program [202102020853]

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In this study, a new functional QS system (RasI/R) was identified and characterized in R. solanacearum strain EP1, which plays an important role in regulating bacterial virulence. This QS system produces and responds to the QS signal 3-OH-C12-HSL and regulates critical bacterial abilities in survival and infection. These findings provide new insight into the complicated QS regulatory networks of R. solanacearum, and offer potential targets for controlling and preventing bacterial wilt diseases.
Quorum sensing (QS) is a widely conserved bacterial regulatory mechanism that relies on production and perception of autoinducing chemical signals to coordinate diverse cooperative activities, such as virulence, exoenzyme secretion, and biofilm formation. In Ralsronia solanacearum, a phytopathogen causing severe bacterial wilt diseases in many plant species, previous studies identified the PhcBSR QS system, which plays a key role in regulation of its physiology and virulence. In this study, we found that R. solanacearum strain EP1 contains the genes encoding uncharacterized LuxI/LuxR (LuxI/R) QS homologues (RasI/RasR [designated RasI/R here)). To determine the roles of the RasI/R system in strain EP1, we constructed a specific reporter for the signals catalyzed by Rash Chromatography separation and structural analysis showed that RasI synthesized primarily N-(3-hydroxydodecanoyl)-homoserine lactone (3-OH-C12-HSL). In addition, we showed that the transcriptional expression of rasl is regulated by RasR in response to 3-OH-C12-HSL Phenotype analysis unveiled that the RasI/R system plays a critical role in modulation of cellulase production, motility, biofilm formation, oxidative stress response, and virulence of R. solanacearum EP1. We then further characterized this system by determining the RasI/R regulon using transcriptome sequencing (RNA-seq) analysis, which showed that this newly identified QS system regulates the transcriptional expression of over 154 genes associated with bacterial physiology and pathogenic properties. Taken together, the findings from this study present an essential new QS system in regulation of R. solanacearum physiology and virulence and provide new insight into the complicated regulatory mechanisms and networks in this important plant pathogen. IMPORTANCE Quorum sensing (QS) is a key regulator of virulence factors in many plant-pathogenic bacteria. Previous studies unveiled two QS systems (i.e., PhcBSR and SolI/R) in several R. solanacearum strains. The PhcBSR QS system is known for its key roles in regulation of bacterial virulence, and the LuxI/LuxR (SolI/R) QS system appears dispensable for pathogenicity in a number of R. solanacearum strains. In this study, a new functional QS system (i.e., RasI/R) was identified and characterized in R. solanacearum strain EP1 isolated from infected eggplants. Phenotype analyses showed that the RasI/R system plays an important role in regulation of a range of biological activities associated with bacterial virulence. This QS system produces and responds to the QS signal 3-OH-C12-HSL and hence regulates critical bacterial abilities in survival and infection. To date, multiple QS signaling circuits in R. solanacearum strains are still not well understood. Our findings from this study provide new insight into the complicated QS regulatory networks that govern the physiology and virulence of R. solanacearum and present a valid target and clues for the control and prevention of bacterial wilt diseases.

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