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氧化还原感受器 Rex 有助于血清型 2 的毒力和氧化应激反应。

The Redox-Sensing Regulator Rex Contributes to the Virulence and Oxidative Stress Response of Serotype 2.

机构信息

Institute of Veterinary Medicine, Jiangsu Academy of Agricultural Sciences, Nanjing, China.

Jiangsu Co-Innovation Center for the Prevention and Control of Important Animal Infectious Disease and Zoonose, Yangzhou University, Yangzhou, China.

出版信息

Front Cell Infect Microbiol. 2018 Sep 18;8:317. doi: 10.3389/fcimb.2018.00317. eCollection 2018.

Abstract

serotype 2 (SS2) is an important zoonotic pathogen responsible for septicemia and meningitis. The redox-sensing regulator Rex has been reported to play critical roles in the metabolism regulation, oxidative stress response, and virulence of various pathogens. In this study, we identified and characterized a Rex ortholog in the SS2 virulent strain SS2-1 that is involved in bacterial pathogenicity and stress environment susceptibility. Our data show that the Rex-knockout mutant strain Δrex exhibited impaired growth in medium with hydrogen peroxide or a low pH compared with the wildtype strain SS2-1 and the complementary strain CΔrex. In addition, Δrex showed a decreased level of survival in whole blood and in RAW264.7 macrophages. Further analyses revealed that Rex deficiency significantly attenuated bacterial virulence in an animal model. A comparative proteome analysis found that the expression levels of several proteins involved in virulence and oxidative stress were significantly different in Δrex compared with SS2-1. Electrophoretic mobility shift assays revealed that recombinant Rex specifically bound to the promoters of target genes in a manner that was modulated by NADH and NAD. Taken together, our data suggest that Rex plays critical roles in the virulence and oxidative stress response of SS2.

摘要

血清型 2(SS2)是一种重要的人畜共患病病原体,可导致败血症和脑膜炎。已报道,氧化还原感应调节因子 Rex 在各种病原体的代谢调节、氧化应激反应和毒力中发挥关键作用。在本研究中,我们鉴定并表征了 SS2 毒力株 SS2-1 中的 Rex 同源物,该同源物参与细菌致病性和应激环境易感性。我们的数据表明,与野生型菌株 SS2-1 和互补菌株 CΔrex 相比,Rex 敲除突变株 Δrex 在含有过氧化氢或低 pH 的培养基中的生长受到损害。此外,Δrex 在全血和 RAW264.7 巨噬细胞中的存活率降低。进一步的分析表明,Rex 缺失显著减弱了动物模型中的细菌毒力。比较蛋白质组分析发现,与 SS2-1 相比,Δrex 中与毒力和氧化应激相关的几种蛋白质的表达水平明显不同。凝胶电泳迁移率变动分析显示,重组 Rex 特异性地结合到靶基因的启动子上,这种结合方式受 NADH 和 NAD 的调节。综上所述,我们的数据表明 Rex 在 SS2 的毒力和氧化应激反应中发挥关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/866d/6154617/8e9c51f82d69/fcimb-08-00317-g0001.jpg

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