a Institute of Molecular Biosciences , University of Graz , Graz , Austria.
b BioTechMed-Graz , Austria.
Gut Microbes. 2019;10(2):228-234. doi: 10.1080/19490976.2018.1502538. Epub 2018 Aug 15.
Bacterial pathogens of the gastrointestinal tract alter their expression profile upon ingestion by the host and activate a variety of factors enhancing colonization and virulence. However, gene silencing during infection might be as important as gene activation to achieve full colonization fitness. Thus, we developed and successfully applied a reporter technology to identify 101 in vivo repressed (ivr) genes of the bacterial pathogen Vibrio cholerae. In depth analysis of the in vivo repressed H/Cl transporter ClcA revealed an inverse requirement along gastrointestinal colonization. ClcA could be linked to acid tolerance response required during stomach passage, but ClcA expression is detrimental during subsequent colonization of the lower intestinal tract as it exploits the proton-motive force in alkaline environments. The study summarized in this addendum demonstrates that constitutive expression of ivr genes can reduce intestinal colonization fitness of V. cholerae, highlighting the necessity to downregulate these genes in vivo.
胃肠道细菌病原体在被宿主摄入后会改变其表达谱,并激活多种增强定植和毒力的因素。然而,感染过程中的基因沉默可能与基因激活一样重要,以实现完全的定植适应性。因此,我们开发并成功应用了一种报告基因技术,以鉴定肠道病原体霍乱弧菌的 101 个体内受抑制(ivr)基因。对体内受抑制的 H/Cl 转运体 ClcA 的深入分析揭示了沿胃肠道定植的反向需求。ClcA 可能与胃酸耐受反应有关,这是在胃通过时所必需的,但在随后的下肠道定植过程中,ClcA 的表达是有害的,因为它在碱性环境中利用质子动力。本文的增刊研究表明,ivr 基因的组成型表达会降低霍乱弧菌的肠道定植适应性,这突出表明有必要在体内下调这些基因。