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首页> 外文期刊>MBio >Identification and Characterization of a Phase-Variable Element That Regulates the Autotransporter UpaE in Uropathogenic Escherichia coli
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Identification and Characterization of a Phase-Variable Element That Regulates the Autotransporter UpaE in Uropathogenic Escherichia coli

机译:鉴定和表征调节致病性致病性大肠杆菌中自转运蛋白UpaE的相变元素

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ABSTRACT Uropathogenic Escherichia coli (UPEC) is the most common etiologic agent of uncomplicated urinary tract infection (UTI). An important mechanism of gene regulation in UPEC is phase variation that involves inversion of a promoter-containing DNA element via enzymatic activity of tyrosine recombinases, resulting in biphasic, ON or OFF expression of target genes. The UPEC reference strain CFT073 has five tyrosine site-specific recombinases that function at two previously characterized promoter inversion systems, fimS and hyxS . Three of the five recombinases are located proximally to their cognate target elements, which is typical of promoter inversion systems. The genes for the other two recombinases, IpuA and IpuB, are located distal from these sites. Here, we identified and characterized a third phase-variable invertible element in CFT073, ipuS , located proximal to ipuA and ipuB . The inversion of ipuS is catalyzed by four of the five CFT073 recombinases. Orientation of the element drives transcription of a two-gene operon containing ipuR , a predicted LuxR-type regulator, and upaE , a predicted autotransporter. We show that the predicted autotransporter UpaE is surface located and facilitates biofilm formation as well as adhesion to extracellular matrix proteins in a K-12 recombinant background. Consistent with this phenotype, the ipuS ON condition in CFT073 results in defective swimming motility, increased adherence to human kidney epithelial cells, and a positive competitive kidney colonization advantage in experimental mouse UTIs. Overall, the identification of a third phase switch in UPEC that is regulated by a shared set of recombinases describes a complex phase-variable virulence network in UPEC. IMPORTANCE Uropathogenic Escherichia coli (UPEC) is the most common cause of urinary tract infection (UTI). ON versus OFF phase switching by inversion of small DNA elements at two chromosome sites in UPEC regulates the expression of important virulence factors, including the type 1 fimbria adhesion organelle. In this report, we describe a third invertible element, ipuS , in the UPEC reference strain CFT073. The inversion of ipuS controls the phase-variable expression of upaE , an autotransporter gene that encodes a surface protein involved in adherence to extracellular matrix proteins and colonization of the kidneys in a murine model of UTI.
机译:摘要致病性大肠杆菌(UPEC)是单纯性尿路感染(UTI)的最常见病原体。 UPEC中基因调控的重要机制是相变,该相变涉及通过酪氨酸重组酶的酶促活性反转含启动子的DNA元件,从而导致靶基因双相,ON或OFF表达。 UPEC参考菌株CFT073具有五个酪氨酸位点特异性重组酶,它们在两个先前表征的启动子转化系统fimS和hyxS上起作用。五个重组酶中的三个位于其同源靶标元件的近端,这是启动子倒置系统的典型特征。其他两种重组酶IpuA和IpuB的基因位于这些位点的远端。在这里,我们确定并表征了CFT073中的第三相变可逆元素ipuS,位于ipuA和ipuB的近端。五个CFT073重组酶中的四个催化ipuS的转化。元素的方向驱动一个两基因操纵子的转录,该操纵子包含预测的LuxR型调节子ipuR和预测的自转运蛋白upaE。我们显示,预测的自转运蛋白UpaE位于表面,并有助于在K-12重组背景下生物膜形成以及对细胞外基质蛋白的粘附。与此表型一致,CFT073中的ipuS ON条件会导致游泳运动缺陷,对人肾上皮细胞的粘附增加以及在实验性小鼠UTI中具有积极的竞争性肾脏定植优势。总体而言,UPEC中由共享重组酶调控的第三相开关的识别描述了UPEC中复杂的相变毒力网络。重要说明致病性大肠杆菌(UPEC)是最常见的尿路感染(UTI)原因。通过反转UPEC中两个染色体位点上的小DNA元件来进行ON相与OFF相转换,从而调节重要毒力因子(包括1型菌毛粘附细胞器)的表达。在此报告中,我们描述了UPEC参考菌株CFT073中的第三个可逆元素ipuS。 ipuS的倒置控制了upaE的相变表达,upaE是一种自转运蛋白基因,其编码与UTI鼠模型中的细胞外基质蛋白粘附和肾脏定植有关的表面蛋白。

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