Prigent-Combaret C, Brombacher E, Vidal O, Ambert A, Lejeune P, Landini P, Dorel C
Unité de Microbiologie et Génétique, CNRS UMR 5122, Institut National des Sciences Appliquées de Lyon, 69621 Villeurbanne Cedex, France.
J Bacteriol. 2001 Dec;183(24):7213-23. doi: 10.1128/JB.183.24.7213-7223.2001.
The Escherichia coli OmpR/EnvZ two-component regulatory system, which senses environmental osmolarity, also regulates biofilm formation. Up mutations in the ompR gene, such as the ompR234 mutation, stimulate laboratory strains of E. coli to grow as a biofilm community rather than in a planktonic state. In this report, we show that the OmpR234 protein promotes biofilm formation by binding the csgD promoter region and stimulating its transcription. The csgD gene encodes the transcription regulator CsgD, which in turn activates transcription of the csgBA operon encoding curli, extracellular structures involved in bacterial adhesion. Consistent with the role of the ompR gene as part of an osmolarity-sensing regulatory system, we also show that the formation of biofilm by E. coli is inhibited by increasing osmolarity in the growth medium. The ompR234 mutation counteracts adhesion inhibition by high medium osmolarity; we provide evidence that the ompR234 mutation promotes biofilm formation by strongly increasing the initial adhesion of bacteria to an abiotic surface. This increase in initial adhesion is stationary phase dependent, but it is negatively regulated by the stationary-phase-specific sigma factor RpoS. We propose that this negative regulation takes place via rpoS-dependent transcription of the transcription regulator cpxR; cpxR-mediated repression of csgB and csgD promoters is also triggered by osmolarity and by curli overproduction, in a feedback regulation loop.
大肠杆菌的OmpR/EnvZ双组分调节系统可感知环境渗透压,也能调控生物膜的形成。ompR基因的上位突变,如ompR234突变,可刺激大肠杆菌实验室菌株以生物膜群落形式生长,而非浮游状态生长。在本报告中,我们表明OmpR234蛋白通过结合csgD启动子区域并刺激其转录来促进生物膜形成。csgD基因编码转录调节因子CsgD,CsgD进而激活编码卷曲菌毛(参与细菌黏附的细胞外结构)的csgBA操纵子的转录。与ompR基因作为渗透压感应调节系统一部分的作用一致,我们还表明,生长培养基中渗透压的增加会抑制大肠杆菌生物膜的形成。ompR234突变可抵消高培养基渗透压对黏附的抑制作用;我们提供的证据表明,ompR234突变通过大幅增加细菌对非生物表面的初始黏附来促进生物膜形成。这种初始黏附的增加依赖于稳定期,但受到稳定期特异性σ因子RpoS的负调控。我们提出,这种负调控是通过转录调节因子cpxR的rpoS依赖性转录发生的;在一个反馈调节回路中,渗透压和卷曲菌毛的过量产生也会触发cpxR介导的对csgB和csgD启动子的抑制。