Abstract

Biofilm dispersal is a genetically programmed response enabling bacterial cells to exit the biofilm in response to particular physiological or environmental conditions. In Pseudomonas putida biofilms, nutrient starvation triggers c-di-GMP hydrolysis by phosphodiesterase BifA, releasing inhibition of protease LapG by the c-di-GMP effector protein LapD, and resulting in proteolysis of the adhesin LapA and the subsequent release of biofilm cells. Here we demonstrate that the stringent response, a ubiquitous bacterial stress response, is accountable for relaying the nutrient stress signal to the biofilm dispersal machinery. Mutants lacking elements of the stringent response – (p)ppGpp sythetases [RelA and SpoT] and/or DksA – were defective in biofilm dispersal. Ectopic (p)ppGpp synthesis restored biofilm dispersal in a ∆relA ∆spoT mutant. In vivo gene expression analysis showed that (p)ppGpp positively regulates transcription of bifA, and negatively regulates transcription of lapA and the lapBC, and lapE operons, encoding a LapA-specific secretion system. Further in vivo and in vitro characterization revealed that the PbifA promoter is dependent on the flagellar σ factor FliA, and positively regulated by ppGpp and DksA. Our results indicate that the stringent response stimulates biofilm dispersal under nutrient limitation by coordinately promoting LapA proteolysis and preventing de novo LapA synthesis and secretion.

Highlights

  • Alternation between a free-swimming planktonic lifestyle and the formation of structured highly cooperative polymer-encased sessile communities, known as biofilms, is a staple of bacterial life in the environment[1]

  • We recently showed that the phosphodiesterase (PDE) BifA is responsible for the drop in c-di-GMP levels that signals biofilm dispersal in P. putida[24]

  • In P. putida and other γ and β proteobacteria, (p)ppGpp is synthesized by two proteins: RelA, whose activity is induced under amino acid starvation, and SpoT, which responds to other forms of nutritional stress, such as carbon, iron, oxygen or fatty acid limitation, and bears (p)ppGpp hydrolase activity[30]

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Summary

Introduction

Alternation between a free-swimming planktonic lifestyle and the formation of structured highly cooperative polymer-encased sessile communities, known as biofilms, is a staple of bacterial life in the environment[1]. Extended incubation of the ∆dksA ppGpp[0] mutant dilution set to 26 hours resulted in a similar increase in biofilm accumulation, while dispersal was still not observed (Supplementary Fig. S1). A ∆relA mutant (PP1437) showed a phenotype indistinguishable from that of the wild-type (Fig. 1d), suggesting that the (p)ppGpp synthesis activity of SpoT is sufficient to support a normal biofilm growth cycle under our experimental conditions.

Results
Conclusion

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