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Virulence in P ectobacterium atrosepticum is regulated by a coincidence circuit involving quorum sensing and the stress alarmone, (p)pp G pp
Author(s) -
Bowden Steven D.,
Eyres Alison,
Chung Jade C. S.,
Monson Rita E.,
Thompson Arthur,
Salmond George P. C.,
Spring David R.,
Welch Martin
Publication year - 2013
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/mmi.12369
Subject(s) - quorum sensing , biology , virulence , microbiology and biotechnology , genetics , gene
Summary P ectobacterium atrosepticum ( P ca) is a Gram‐negative phytopathogen which causes disease by secreting plant cell wall degrading exoenzymes ( PCWDEs ). Previous studies have shown that PCWDE production is regulated by (i) the inter cellular quorum sensing ( QS ) signal molecule, 3‐oxo‐hexanoyl‐ l ‐homoserine lactone ( OHHL ), and (ii) the intra cellular ‘alarmone’, (p)pp G pp, which reports on nutrient limitation. Here we show that these two signals form an integrated coincidence circuit which ensures that metabolically costly PCWDE synthesis does not occur unless the population is simultaneously quorate and nutrient limited. A (p)pp G pp null Δ relA Δ spoT mutant was defective in both OHHL and PCWDE production, and nutritional supplementation of wild type cultures (which suppresses (p)pp G pp production) also suppressed OHHL and PCWDE production. There was a substantial overlap in the transcriptome of a (p)pp G pp deficient relA mutant and of a QS defective expI ( OHHL synthase) mutant, especially with regards to virulence‐associated genes. Random transposon mutagenesis revealed that disruption of rsmA was sufficient to restore PCWDE production in the (p)pp G pp null strain. We found that the ratio of RsmA protein to its RNA antagonist, rsm B , was modulated independently by (p)pp G pp and QS . While QS predominantly controlled virulence by modulating RsmA levels, (p)pp G pp exerted regulation through the modulation of the RsmA antagonist, rsm B .