Correa Nidia E, Peng Fen, Klose Karl E
Department of Biology, University of Texas San Antonio, 6900 N. Loop 1604 W., San Antonio, Texas 78249, USA.
J Bacteriol. 2005 Sep;187(18):6324-32. doi: 10.1128/JB.187.18.6324-6332.2005.
Vibrio cholerae, the causative agent of the human diarrheal disease cholera, is a motile bacterium with a single polar flagellum, and motility has been inferred to be an important aspect of virulence. The V. cholerae flagellar hierarchy is organized into four classes of genes. The expression of each class of genes within a flagellar hierarchy is generally tightly regulated in other bacteria by both positive and negative regulatory elements. To further elucidate flagellar biogenesis in V. cholerae, we characterized the roles of the three putative regulatory genes, flhF, flhG, and VC2061. V. cholerae flhF and flhG mutants appeared nonmotile in a soft agar assay. Electron microscopy revealed that the flhF mutant lacked a polar flagellum, while interestingly, the flhG mutant possessed multiple (8 to 10) polar flagella per cell. The transcriptional activity of class III and class IV gene promoters in the flhF mutant was decreased, suggesting that FlhF acts as a positive regulator of class III gene transcription. The transcription of all four classes of flagellar promoters was increased in the flhG mutant, suggesting that FlhG acts as a negative regulator of class I gene transcription. Additionally, the ability to colonize the infant mouse intestine was reduced for the flhG mutant (approximately 10-fold), indicating that the negative regulation of class I flagellar genes enhances virulence. The V. cholerae VC2061 mutant was motile and produced a polar flagellum indistinguishable from that of the wild type, and the transcriptional activities of the four classes of flagellar promoters were similar to that of the wild type. Our results indicate that FlhG and FlhF regulate class I and class III flagellar transcription, respectively, while VC2061 plays no detectable role in V. cholerae flagellar biogenesis.
霍乱弧菌是人类腹泻病霍乱的病原体,是一种具有单根极鞭毛的运动性细菌,运动性被认为是毒力的一个重要方面。霍乱弧菌的鞭毛层级由四类基因组成。在其他细菌中,鞭毛层级内每类基因的表达通常受到正调控元件和负调控元件的严格调控。为了进一步阐明霍乱弧菌的鞭毛生物合成,我们对三个假定的调控基因flhF、flhG和VC2061的作用进行了表征。在软琼脂试验中,霍乱弧菌flhF和flhG突变体似乎不具有运动性。电子显微镜显示,flhF突变体缺乏极鞭毛,而有趣的是,flhG突变体每个细胞拥有多个(8至10根)极鞭毛。flhF突变体中III类和IV类基因启动子的转录活性降低,表明FlhF作为III类基因转录的正调控因子发挥作用。flhG突变体中所有四类鞭毛启动子的转录均增加,表明FlhG作为I类基因转录的负调控因子发挥作用。此外,flhG突变体在定殖幼鼠肠道方面的能力降低(约10倍),表明I类鞭毛基因的负调控增强了毒力。霍乱弧菌VC2061突变体具有运动性,并产生了与野生型无法区分的极鞭毛,四类鞭毛启动子的转录活性与野生型相似。我们的结果表明,FlhG和FlhF分别调节I类和III类鞭毛转录,而VC2061在霍乱弧菌鞭毛生物合成中未发挥可检测到的作用。