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YopE 的 ROS 抑制活性是耶尔森菌在小鼠中完全毒力所必需的。

ROS-inhibitory activity of YopE is required for full virulence of Yersinia in mice.

机构信息

Department of Molecular Biology and Microbiology, Tufts University, Boston, MA 02111, USA.

出版信息

Cell Microbiol. 2010 Jul;12(7):988-1001. doi: 10.1111/j.1462-5822.2010.01448.x. Epub 2010 Feb 9.

Abstract

YopE, a type III secreted effector of Yersinia, is a GTPase Activating Protein for Rac1 and RhoA whose catalytic activity is critical for virulence. We found that YopE also inhibited reactive oxygen species (ROS) production and inactivated Rac2. How YopE distinguishes among its targets and which specific targets are critical for Yersinia survival in different tissues are unknown. A screen identifying YopE mutants in Yersinia pseudotuberculosis that interact with different Rho GTPases showed that YopE residues at positions 102, 106, 109 and 156 discern among switch I and II regions of Rac1, Rac2 and RhoA. Two mutants, which expressed YopE alleles with different antiphagocytic, ROS-inhibitory and cell-rounding activities, YptbL109A and YptbESptP, were studied in animal infections. Inhibition of both phagocytosis and ROS production were required for splenic colonization, whereas fewer YopE activities were required for Peyer's patch colonization. This study shows that Y. pseudotuberculosis encounters multiple host defences in different tissues and uses distinct YopE activities to disable them.

摘要

耶尔森氏菌的 III 型分泌效应物 YopE 是 Rac1 和 RhoA 的 GTP 酶激活蛋白,其催化活性对毒力至关重要。我们发现 YopE 还抑制活性氧(ROS)的产生并使 Rac2 失活。YopE 如何区分其靶标,以及哪些特定靶标对耶尔森氏菌在不同组织中的存活至关重要,目前尚不清楚。一项在假结核耶尔森氏菌中筛选与不同 Rho GTPases 相互作用的 YopE 突变体的研究表明,YopE 在位置 102、106、109 和 156 的残基可区分 Rac1、Rac2 和 RhoA 的开关 I 和 II 区。两种突变体,即表达具有不同抗吞噬、抑制 ROS 产生和细胞圆化活性的 YopE 等位基因的 YptbL109A 和 YptbESptP,在动物感染中进行了研究。吞噬作用和 ROS 产生的抑制均是脾定植所必需的,而派尔集合淋巴结定植所需的 YopE 活性较少。本研究表明,假结核耶尔森氏菌在不同组织中遇到多种宿主防御机制,并利用不同的 YopE 活性来破坏它们。

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