Under stressful conditions in nature, Escherichia coli forms biofilms for long-term survival. Curli fimbriae are an essential architecture for cell-cell contacts within biofilms. Structural components and assembly factors of curli are encoded by two operons, csgBA and csgDEFG. The csgD gene product controls transcription of both operons. Reflecting the response of csgD expression to external stresses, a number of transcription factors participate in the regulation of the csgD promoter. Analysis of the csgD mRNA obtained from E. coli mutants in different transcription factors indicated that CpxR and H-NS act as repressors while OmpR, RstA and IHF act as activators. An acid-stress response regulator, RstA, activates csgD only under acidic conditions. These five factors bind within a narrow region of about 200 bp upstream of the csgD promoter. After pair-wise promoter-binding assays, the increase in csgD transcription in the stationary phase was suggested to be due, at least in part, to the increase in IHF level cancelling the silencing effect of H-NS. In addition, we propose a novel regulation model of this complex csgD promoter through cooperation between the two positive factors (OmpR-IHF and RstA-IHF) and also between the two negative factors (CpxR-H-NS).
INTRODUCTIONBacteria can switch from a single-cell planktonic growth mode to a multicellular community (biofilm) mode. During such a growth transition state, cell morphology, physiology and metabolism are markedly altered (PrigentCombaret et al., 2001;Schembri et al., 2003;Beloin et al., 2004;Ren et al., 2004). In single-cell growth mode, cell motility using flagella is critical for adaptation to environments. The master regulator FlhCD complex plays a key role in controlling transcription of a set of genes for flagella formation (Claret & Huges, 2000). When Escherichia coli cells switch their life mode from single planktonic cell growth to multicellular community (biofilm) mode, the genetic system for flagella formation is turned off and the genes involved in cell-cell adhesion are activated. The biofilm matrix is a complex architecture of cell aggregates that are attached on the surface of inorganic solid materials in nature or on eukaryotic tissues in host animals. After a comprehensive analysis of a set of E. coli mutants, each lacking one of 3985 non-essential genes, a total of 110 genes were indicated to be involved in biofilm formation (Niba et al., 2007).During biofilm development, curli fimbriae, the major biofilm component, play a key role in both initial adhesion to solid surfaces and subsequent cell-cell interactions (Vidal et al., 1998;Chapman et al., 2002;Prigent-Combaret et al., 2000). Curli fimbriae also mediate bacterial adhesion to host cells and invasion, and activation of both the proinflammatory response and the immune system (Bian et al., 2000;Zogaj et al., 2001). Accordingly, curli participate in virulence phenotypes (Hammar et al., 1995; Vidal et al., 1998;Bian et al., 2000; Gophna et al., 2001;Cookson et al., 2002). A set of polysacch...