Full Virulence of <i>Pseudomonas aeruginosa</i> Requires OprF

Laurène Fito-Boncompte(Université de Bretagne Sud), Annelise Chapalain(Institut National de la Recherche Scientifique), Emeline Bouffartigues(Université de Rouen Normandie), Hichem Chaker(Centre National de la Recherche Scientifique), Olivier Lesouhaitier(Université de Rouen Normandie), Gwendoline Gicquel(Université de Rouen Normandie), Alexis Bazire(Université de Bretagne Sud), Amar Madi(Université de Rouen Normandie), Nathalie Connil(Université de Rouen Normandie), Wilfried Véron(Université de Rouen Normandie), Laure Taupin(Université de Bretagne Sud), Bertrand Toussaint(Centre National de la Recherche Scientifique), Pierre Cornélis(Vrije Universiteit Brussel), Qing Wei(Vrije Universiteit Brussel), Koki Shioya(Université de Bretagne Sud), Éric Déziel(Institut National de la Recherche Scientifique), Marc Feuilloley(Université de Rouen Normandie), Nicole Orange(Université de Rouen Normandie), Alain Dufour(Université de Bretagne Sud), Sylvie Chevalier(Université de Rouen Normandie)
Infection and Immunity
December 29, 2010
Cited by 159

Abstract

OprF is a general outer membrane porin of Pseudomonas aeruginosa, a well-known human opportunistic pathogen associated with severe hospital-acquired sepsis and chronic lung infections of cystic fibrosis patients. A multiphenotypic approach, based on the comparative study of a wild-type strain of P. aeruginosa, its isogenic oprF mutant, and an oprF-complemented strain, showed that OprF is required for P. aeruginosa virulence. The absence of OprF results in impaired adhesion to animal cells, secretion of ExoT and ExoS toxins through the type III secretion system (T3SS), and production of the quorum-sensing-dependent virulence factors pyocyanin, elastase, lectin PA-1L, and exotoxin A. Accordingly, in the oprF mutant, production of the signal molecules N-(3-oxododecanoyl)-l-homoserine lactone and N-butanoyl-l-homoserine lactone was found to be reduced and delayed, respectively. Pseudomonas quinolone signal (PQS) production was decreased, while its precursor, 4-hydroxy-2-heptylquinoline (HHQ), accumulated in the cells. Taken together, these results show the involvement of OprF in P. aeruginosa virulence, at least partly through modulation of the quorum-sensing network. This is the first study showing a link between OprF, PQS synthesis, T3SS, and virulence factor production, providing novel insights into virulence expression.


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