Yang Ji, Hart Emily, Tauschek Marija, Price G Dean, Hartland Elizabeth L, Strugnell Richard A, Robins-Browne Roy M
Department of Microbiology and Immunology, The University of Melbourne, Victoria 3010, Australia.
Mol Microbiol. 2008 Apr;68(2):314-27. doi: 10.1111/j.1365-2958.2008.06171.x. Epub 2008 Feb 19.
Regulation of virulence gene expression plays a central role in the pathogenesis of enteric bacteria as they encounter diverse environmental conditions in the gastrointestinal tract of their hosts. In this study, we investigated environmental regulation of two putative virulence determinants adcA and kfc by RegA, an AraC/XylS-like regulator, from Citrobacter rodentium, and identified bicarbonate as the environmental signal which induced transcription of adcA and kfc through RegA. Primer extension experiments showed that adcA and kfc were divergently transcribed from sigma(70) promoters. In vivo and in vitro experiments demonstrated that bicarbonate facilitated and stabilized the binding of RegA to an operator located between the two promoters. The interaction of RegA with its DNA target resulted in the formation of a nucleosome-like structure, which evidently displaced the histone-like proteins, H-NS and StpA, from the adcA and kfc promoter regions, leading to transcriptional derepression. In addition, our results indicated that RegA also behaved as a Class I activator by directly stimulating transcription initiation by RNA polymerase. This is the first report to describe the molecular mechanism by which an environmental chemical stimulates transcription of virulence-associated genes of an enteric pathogen through an AraC/XlyS-like activator.
毒力基因表达的调控在肠道细菌的致病过程中起着核心作用,因为它们在宿主胃肠道中会遇到各种不同的环境条件。在本研究中,我们调查了来自啮齿柠檬酸杆菌的一种AraC/XylS样调节因子RegA对两个假定的毒力决定因素adcA和kfc的环境调控,并确定碳酸氢盐是通过RegA诱导adcA和kfc转录的环境信号。引物延伸实验表明,adcA和kfc从σ⁷⁰启动子开始双向转录。体内和体外实验表明,碳酸氢盐促进并稳定了RegA与位于两个启动子之间的操纵子的结合。RegA与其DNA靶标的相互作用导致形成一种核小体样结构,该结构明显将类组蛋白H-NS和StpA从adcA和kfc启动子区域取代,导致转录去抑制。此外,我们的结果表明,RegA还通过直接刺激RNA聚合酶的转录起始而表现为I类激活剂。这是第一份描述环境化学物质通过AraC/XlyS样激活剂刺激肠道病原体毒力相关基因转录的分子机制的报告。