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VraH是金黄色葡萄球菌VraDEH系统的第三个组成部分,参与对加里道霉素和达托霉素的耐药性及致病性。

VraH Is the Third Component of the Staphylococcus aureus VraDEH System Involved in Gallidermin and Daptomycin Resistance and Pathogenicity.

作者信息

Popella Peter, Krauss Sophia, Ebner Patrick, Nega Mulugeta, Deibert Julia, Götz Friedrich

机构信息

Microbial Genetics, Interfaculty Institute of Microbiology and Infection Medicine, University of Tübingen, Tübingen, Germany.

Microbial Genetics, Interfaculty Institute of Microbiology and Infection Medicine, University of Tübingen, Tübingen, Germany

出版信息

Antimicrob Agents Chemother. 2016 Mar 25;60(4):2391-401. doi: 10.1128/AAC.02865-15. Print 2016 Apr.

Abstract

In bacteria, extracellular signals are transduced into the cell predominantly by two-component systems (TCSs) comprising a regulatory unit triggered by a specific signal. Some of the TCSs control executing units such as ABC transporters involved in antibiotic resistance. For instance, inStaphylococcus aureus, activation of BraSR leads to the upregulation ofvraDEexpression that encodes an ABC transporter playing a role in bacitracin and nisin resistance. In this study, we show that the small staphylococcal transmembrane protein VraH forms, together with VraDE, a three-component system. Although the expression ofvraHin the absence ofvraDEwas sufficient to mediate low-level resistance, only this VraDEH entity conferred high-level resistance against daptomycin and gallidermin. In most staphylococcal genomes,vraHis located immediately downstream ofvraDE, forming an operon, whereas in some species it is localized differently. In an invertebrate infection model, VraDEH significantly enhancedS. aureuspathogenicity. In analogy to the TCS connectors, VraH can be regarded as an ABC connector that modulates the activity of ABC transporters involved in antibiotic resistance.

摘要

在细菌中,细胞外信号主要通过双组分系统(TCSs)转导至细胞内,该系统由一个由特定信号触发的调节单元组成。一些双组分系统控制执行单元,如参与抗生素抗性的ABC转运蛋白。例如,在金黄色葡萄球菌中,BraSR的激活导致vraDE表达上调,vraDE编码一种在杆菌肽和乳链菌肽抗性中起作用的ABC转运蛋白。在本研究中,我们表明小的葡萄球菌跨膜蛋白VraH与VraDE一起形成了一个三组分系统。虽然在没有vraDE的情况下vraH的表达足以介导低水平抗性,但只有这种VraDEH实体赋予了对达托霉素和加里德明的高水平抗性。在大多数葡萄球菌基因组中,vraH位于vraDE的紧邻下游,形成一个操纵子,而在一些物种中它的定位不同。在无脊椎动物感染模型中,VraDEH显著增强了金黄色葡萄球菌的致病性。类似于双组分系统连接蛋白,VraH可被视为一种ABC连接蛋白,它调节参与抗生素抗性的ABC转运蛋白的活性。

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