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金黄色葡萄球菌中由MgrA同源物SarZ介导的一种新的氧化感应与调控途径。

A new oxidative sensing and regulation pathway mediated by the MgrA homologue SarZ in Staphylococcus aureus.

作者信息

Chen Peng R, Nishida Satoshi, Poor Catherine B, Cheng Alice, Bae Taeok, Kuechenmeister Lisa, Dunman Paul M, Missiakas Dominique, He Chuan

机构信息

Department of Chemistry, 929 East 57th Street, The University of Chicago, Chicago, IL, USA.

出版信息

Mol Microbiol. 2009 Jan;71(1):198-211. doi: 10.1111/j.1365-2958.2008.06518.x. Epub 2008 Nov 5.

Abstract

Oxidative stress serves as an important host/environmental signal that triggers a wide range of responses from the human pathogen Staphylococcus aureus. Among these, a thiol-based oxidation sensing pathway through a global regulator MgrA controls the virulence and antibiotic resistance of the bacterium. Herein, we report a new thiol-based oxidation sensing and regulation system that is mediated through a parallel global regulator SarZ. SarZ is a functional homologue of MgrA and is shown to affect the expression of approximately 87 genes in S. aureus. It uses a key Cys residue, Cys-13, to sense oxidative stress and to co-ordinate the expression of genes involved in metabolic switching, antibiotic resistance, peroxide stress defence, virulence, and cell wall properties. The discovery of this SarZ-mediated regulation, mostly independent from the MgrA-based regulation, fills a missing gap of oxidation sensing and response in S. aureus.

摘要

氧化应激是一种重要的宿主/环境信号,可触发人类病原体金黄色葡萄球菌的多种反应。其中,一种通过全局调节因子MgrA的基于硫醇的氧化感应途径控制着该细菌的毒力和抗生素耐药性。在此,我们报告了一种新的基于硫醇的氧化感应和调节系统,该系统由平行的全局调节因子SarZ介导。SarZ是MgrA的功能同源物,已证明它会影响金黄色葡萄球菌中约87个基因的表达。它利用关键的半胱氨酸残基Cys-13来感知氧化应激,并协调参与代谢转换、抗生素耐药性、过氧化物应激防御、毒力和细胞壁特性的基因表达。这一主要独立于基于MgrA的调节的SarZ介导调节的发现,填补了金黄色葡萄球菌氧化感应和反应方面的一个缺失空白。

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本文引用的文献

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