| Literature DB >> 30581112 |
Benoît-Joseph Laventie1, Matteo Sangermani1, Fabienne Estermann1, Pablo Manfredi1, Rémi Planes2, Isabelle Hug1, Tina Jaeger1, Etienne Meunier2, Petr Broz3, Urs Jenal4.
Abstract
The opportunistic human pathogen Pseudomonas aeruginosa effectively colonizes host epithelia using pili as primary adhesins. Here we uncover a surface-specific asymmetric virulence program that enhances P. aeruginosa host colonization. We show that when P. aeruginosa encounters surfaces, the concentration of the second messenger c-di-GMP increases within a few seconds. This leads to surface adherence and virulence induction by stimulating pili assembly through activation of the c-di-GMP receptor FimW. Surface-attached bacteria divide asymmetrically to generate a piliated, surface-committed progeny (striker) and a flagellated, motile offspring that leaves the surface to colonize distant sites (spreader). Cell differentiation is driven by a phosphodiesterase that asymmetrically positions to the flagellated pole, thereby maintaining c-di-GMP levels low in the motile offspring. Infection experiments demonstrate that cellular asymmetry strongly boosts infection spread and tissue damage. Thus, P. aeruginosa promotes surface colonization and infection transmission through a cooperative virulence program that we termed Touch-Seed-and-Go.Entities:
Keywords: Pseudomonas aeruginosa; asymmetric division; c-di-GMP; flagella; second messenger; surface sensing; tissue colonization; type IV pili; virulence
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Year: 2018 PMID: 30581112 DOI: 10.1016/j.chom.2018.11.008
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023