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肠球菌中 ArgR 家族转录因子激活黏附菌毛和胶原结合黏附素 Ace 的表达。

Expression of Adhesive Pili and the Collagen-Binding Adhesin Ace Is Activated by ArgR Family Transcription Factors in Enterococcus faecalis.

机构信息

Department of Microbiology and Immunology, University of Minnesota, Minneapolis, Minnesota, USA.

Department of Microbiology and Immunology, University of Minnesota, Minneapolis, Minnesota, USA

出版信息

J Bacteriol. 2018 Aug 24;200(18). doi: 10.1128/JB.00269-18. Print 2018 Sep 15.

Abstract

It was shown previously that the disruption of the gene encoding a predicted ArgR family transcription factor results in a severe defect in biofilm formation , as well as a significant attenuation of virulence of strain OG1RF in multiple experimental infection models. Using transcriptome sequencing (RNA-seq), we observed -dependent changes in the expression of more than 20 genes. AhrC-repressed genes included predicted determinants of arginine catabolism and several other metabolic genes and predicted transporters, while AhrC-activated genes included determinants involved in the production of surface protein adhesins. Most notably, the structural and regulatory genes of the locus encoding adhesive pili were positively regulated, as well as the gene, encoding a collagen-binding adhesin. Using transcription reporter fusions, we determined that and a second transcription factor gene, , both function to activate the expression of , which directly activates the transcription of the pilus structural genes. Our data suggest that in the wild-type , the low levels of EbpR limit the expression of pili and that biofilm biomass is also limited by the amount of pili expressed by the bacteria. The expression of is similarly enhanced by AhrC and ArgR2, but expression is not dependent on EbpR. Our results demonstrate the existence of novel regulatory cascades controlled by a pair of ArgR family transcription factors that might function as a heteromeric protein complex. Cell surface adhesins play critical roles in the formation of biofilms, host colonization, and the pathogenesis of opportunistic infections by Here, we present new results showing that the expression of two major enterococcal surface adhesins, pili, and the collagen-binding protein Ace is positively regulated at the transcription level by two family transcription factors, AhrC and ArgR2. In the case of pili, the direct target of regulation is the gene, previously shown to activate the transcription of the pilus structural genes, while the activation of transcription appears to be directly impacted by the two ArgR proteins. These transcription factors may represent new targets for blocking enterococcal infections.

摘要

先前的研究表明,编码预测的 ArgR 家族转录因子的基因的破坏会导致生物膜形成严重缺陷,以及在多种实验感染模型中 OG1RF 菌株的毒力显著减弱。使用转录组测序(RNA-seq),我们观察到依赖于 AhrC 的超过 20 个基因的表达变化。AhrC 抑制的基因包括预测的精氨酸分解代谢决定因素和其他几种代谢基因和预测的转运蛋白,而 AhrC 激活的基因包括参与表面蛋白黏附素产生的决定因素。值得注意的是,编码黏附菌毛的结构和调节基因被正向调节,以及编码胶原结合黏附素的基因。使用转录报告基因融合,我们确定了和第二个转录因子基因都可激活结构基因的表达,从而直接激活菌毛结构基因的转录。我们的数据表明,在野生型中,EbpR 的低水平限制了菌毛的表达,生物膜生物量也受到细菌表达的菌毛数量的限制。AhrC 和 ArgR2 同样增强的表达,但不依赖于 EbpR。我们的结果表明,存在由一对 ArgR 家族转录因子控制的新型调节级联,这些因子可能作为异源二聚体蛋白复合物发挥作用。细胞表面黏附素在生物膜形成、宿主定植和机会性感染的发病机制中发挥关键作用。在这里,我们提出了新的结果,表明两种主要肠球菌表面黏附素菌毛和胶原结合蛋白 Ace 的表达在转录水平上受到两种 ArgR 家族转录因子 AhrC 和 ArgR2 的正调控。在菌毛的情况下,调节的直接靶标是基因,先前的研究表明该基因激活菌毛结构基因的转录,而基因的转录激活似乎直接受到两个 ArgR 蛋白的影响。这些转录因子可能代表阻断肠球菌感染的新靶点。

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