Division of Cell and Molecular Biology, Imperial College London, London SW7 2AZ, UK.
Mol Microbiol. 2009 Nov;74(3):541-56. doi: 10.1111/j.1365-2958.2009.06812.x. Epub 2009 Jul 28.
Clostridium difficile is a nosocomial pathogen that can cause severe gastrointestinal infections. C. difficile encodes a family of cell wall proteins, some of which are implicated in pathogenesis. Here we have characterized CwpV, the largest member of this family. CwpV is surface expressed and post-translationally processed in a manner analogous to the major S-layer protein SlpA. Expression of cwpV is phase variable, with approximately 5% of cells in a population expressing the protein under standard laboratory growth conditions. Upstream of cwpV, inverted repeats flank a 195 bp sequence which undergoes DNA inversion. Use of a gusA transcriptional reporter demonstrated that phase variation is mediated by DNA inversion; in one orientation cwpV is expressed while in the opposite orientation the gene is silent. The inversion region contains neither the promoter nor any of the open reading frame, therefore this system differs from previously described phase variation mechanisms. The cwpV promoter is located upstream of the inversion region and we propose a model of phase variation based on intrinsic terminator formation in the OFF transcript. A C. difficile site-specific recombinase able to catalyse the inversion has been identified.
艰难梭菌是一种医院病原体,可引起严重的胃肠道感染。艰难梭菌编码一组细胞壁蛋白,其中一些与发病机制有关。在这里,我们对 CwpV 进行了表征,CwpV 是该家族中最大的成员。CwpV 表面表达,并以类似于主要 S 层蛋白 SlpA 的方式进行翻译后加工。CwpV 的表达具有阶段性变化,在标准实验室生长条件下,约有 5%的细胞表达该蛋白。在 cwpV 的上游,反向重复序列侧翼有一个 195bp 的序列,该序列发生 DNA 反转。使用 gusA 转录报告基因证明,相位变化是由 DNA 反转介导的;在一个方向上表达 cwpV,而在相反的方向上,该基因是沉默的。反转区域既不含启动子,也不含任何开放阅读框,因此该系统与先前描述的相位变化机制不同。cwpV 启动子位于反转区域的上游,我们提出了一种基于 OFF 转录物中内在终止子形成的相位变化模型。已经鉴定出能够催化反转的艰难梭菌位点特异性重组酶。