Bouffartigues Emeline, Moscoso Joana A, Duchesne Rachel, Rosay Thibaut, Fito-Boncompte Laurène, Gicquel Gwendoline, Maillot Olivier, Bénard Magalie, Bazire Alexis, Brenner-Weiss Gerald, Lesouhaitier Olivier, Lerouge Patrice, Dufour Alain, Orange Nicole, Feuilloley Marc G J, Overhage Joerg, Filloux Alain, Chevalier Sylvie
EA 4312-Laboratory of Microbiology Signals and Microenvironment, University of Rouen - Normandy University Evreux, France.
MRC Centre for Molecular Bacteriology and Infection, Department of Life Sciences, Imperial College London London, UK.
Front Microbiol. 2015 Jun 23;6:630. doi: 10.3389/fmicb.2015.00630. eCollection 2015.
OprF is the major outer membrane porin in bacteria belonging to the Pseudomonas genus. In previous studies, we have shown that OprF is required for full virulence expression of the opportunistic pathogen Pseudomonas aeruginosa. Here, we describe molecular insights on the nature of this relationship and report that the absence of OprF leads to increased biofilm formation and production of the Pel exopolysaccharide. Accordingly, the level of c-di-GMP, a key second messenger in biofilm control, is elevated in an oprF mutant. By decreasing c-di-GMP levels in this mutant, both biofilm formation and pel gene expression phenotypes were restored to wild-type levels. We further investigated the impact on two small RNAs, which are associated with the biofilm lifestyle, and found that expression of rsmZ but not of rsmY was increased in the oprF mutant and this occurs in a c-di-GMP-dependent manner. Finally, the extracytoplasmic function (ECF) sigma factors AlgU and SigX displayed higher activity levels in the oprF mutant. Two genes of the SigX regulon involved in c-di-GMP metabolism, PA1181 and adcA (PA4843), were up-regulated in the oprF mutant, partly explaining the increased c-di-GMP level. We hypothesized that the absence of OprF leads to a cell envelope stress that activates SigX and results in a c-di-GMP elevated level due to higher expression of adcA and PA1181. The c-di-GMP level can in turn stimulate Pel synthesis via increased rsmZ sRNA levels and pel mRNA, thus affecting Pel-dependent phenotypes such as cell aggregation and biofilm formation. This work highlights the connection between OprF and c-di-GMP regulatory networks, likely via SigX (ECF), on the regulation of biofilm phenotypes.
OprF是假单胞菌属细菌中的主要外膜孔蛋白。在先前的研究中,我们已经表明OprF是机会性病原体铜绿假单胞菌充分表达毒力所必需的。在此,我们描述了对这种关系本质的分子见解,并报告OprF的缺失导致生物膜形成增加和Pel胞外多糖的产生。相应地,生物膜控制中的关键第二信使c-di-GMP在oprF突变体中水平升高。通过降低该突变体中的c-di-GMP水平,生物膜形成和pel基因表达表型均恢复到野生型水平。我们进一步研究了对与生物膜生活方式相关的两种小RNA的影响,发现rsmZ而非rsmY的表达在oprF突变体中增加,并且这是以c-di-GMP依赖性方式发生的。最后,胞外功能(ECF)σ因子AlgU和SigX在oprF突变体中表现出更高的活性水平。SigX调控子中参与c-di-GMP代谢的两个基因PA1181和adcA(PA4843)在oprF突变体中上调,部分解释了c-di-GMP水平的升高。我们推测OprF的缺失导致细胞包膜应激,激活SigX并由于adcA和PA1181的更高表达而导致c-di-GMP水平升高。c-di-GMP水平进而可以通过增加rsmZ sRNA水平和pel mRNA来刺激Pel合成,从而影响诸如细胞聚集和生物膜形成等依赖Pel的表型。这项工作突出了OprF与c-di-GMP调控网络之间的联系,可能通过SigX(ECF)对生物膜表型进行调控。