Contrasting regulation of the ecp common pilus operon in Citrobacter rodentium: essential roles of a distal element and IHF even in the absence of H-NS

IF 3.4 3区 生物学 Q3 MICROBIOLOGY
María I. Isidro-Coxca, Verónica I. Martínez-Santos, Andrés Escalera-Maurer, José L. Puente
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引用次数: 0

Abstract

The Escherichia coli common pilus (ECP) is a chaperone–usher pilus widely distributed in E. coli and other enterobacteria, where it mediates adhesion, biofilm formation, and colonization. Citrobacter rodentium, a surrogate model for the human attaching-and-effacing pathogens enteropathogenic and enterohemorrhagic E. coli, contains a conserved ecp operon (Cr-ecp) whose regulation has substantially diverged from E. coli. Cr-ecp expression is induced under static DMEM growth at temperatures below 37 °C, driven by a σ⁷⁰-dependent promoter embedded in a regulatory region of approximately 410 bp. We identified an essential distal regulatory element (DRE) between positions − 378 and − 359 relative to the transcription start site, with a 10-bp core required for promoter activity. In contrast to the EcpR-dependent model in E. coli, the ecpR ortholog is dispensable under the conditions tested. The nucleoid-associated proteins IHF and H-NS bind the regulatory region; IHF is strictly required for activation even when H-NS is absent. These findings define a regulatory architecture distinct from E. coli ecp.

啮齿类柠檬酸杆菌中ecp共同菌毛操纵子的调控对比:即使在没有H-NS的情况下,远端元素和IHF的重要作用。
大肠杆菌共同菌毛(Escherichia coli common pilus, ECP)是一种广泛分布于大肠杆菌和其他肠杆菌中的伴侣-引导菌毛,在大肠杆菌中介导粘附、生物膜形成和定植。啮齿类柠檬酸杆菌(Citrobacter rodentium)是人类肠致病性和肠出血性大肠杆菌附着和清除病原体的替代模型,它含有一个保守的ecp操纵子(Cr-ecp),其调控与大肠杆菌有很大的差异。Cr-ecp在低于37°C的温度下在静态DMEM生长下被诱导表达,由嵌入约410 bp调控区域的σ⁷⁰依赖启动子驱动。我们在转录起始位点的- 378和- 359位点之间发现了一个重要的远端调控元件(DRE),其核心长度为10bp,是启动子活性所必需的。与大肠杆菌中依赖ecpR的模型相反,在测试条件下,ecpR同源物是可有可无的。核相关蛋白IHF和H-NS结合调控区;即使在H-NS缺失的情况下,IHF也是激活所必需的。这些发现定义了一种不同于大肠杆菌的调控结构。
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来源期刊
Archives of Microbiology
Archives of Microbiology 生物-微生物学
CiteScore
4.90
自引率
3.60%
发文量
601
审稿时长
3 months
期刊介绍: Research papers must make a significant and original contribution to microbiology and be of interest to a broad readership. The results of any experimental approach that meets these objectives are welcome, particularly biochemical, molecular genetic, physiological, and/or physical investigations into microbial cells and their interactions with their environments, including their eukaryotic hosts. Mini-reviews in areas of special topical interest and papers on medical microbiology, ecology and systematics, including description of novel taxa, are also published. Theoretical papers and those that report on the analysis or ''mining'' of data are acceptable in principle if new information, interpretations, or hypotheses emerge.
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