Thomassin Jenny-Lee, Leclerc Jean-Mathieu, Giannakopoulou Natalia, Zhu Lei, Salmon Kristiana, Portt Andrea, Daigle France, Le Moual Hervé, Gruenheid Samantha
Department of Microbiology and Immunology, McGill University, Montreal, QC, Canada.
Département de Microbiologie, Infectiologie et Immunologie, Université de Montréal, Montréal, QC, Canada.
Infect Immun. 2017 Jan 26;85(2). doi: 10.1128/IAI.00654-16. Print 2017 Feb.
Citrobacter rodentium is a murine pathogen used to model intestinal infections caused by the human diarrheal pathogens enterohemorrhagic and enteropathogenic Escherichia coli During infection, bacteria use two-component systems (TCSs) to detect changing environmental cues within the host, allowing for rapid adaptation by altering the expression of specific genes. In this study, 26 TCSs were identified in C. rodentium, and quantitative PCR (qPCR) analysis showed that they are all expressed during murine infection. These TCSs were individually deleted, and the in vitro and in vivo effects were analyzed to determine the functional consequences. In vitro analyses only revealed minor differences, and surprisingly, type III secretion (T3S) was only affected in the ΔarcA strain. Murine infections identified 7 mutants with either attenuated or increased virulence. In agreement with the in vitro T3S assay, the ΔarcA strain was attenuated and defective in colonization and cell adherence. The ΔrcsB strain was among the most highly attenuated strains. The decrease in virulence of this strain may be associated with changes to the cell surface, as Congo red binding was altered, and qPCR revealed that expression of the wcaA gene, which has been implicated in colanic acid production in other bacteria, was drastically downregulated. The ΔuvrY strain exhibited increased virulence compared to the wild type, which was associated with a significant increase in bacterial burden within the mesenteric lymph nodes. The systematic analysis of virulence-associated TCSs and investigation of their functions during infection may open new avenues for drug development.
鼠柠檬酸杆菌是一种鼠类病原体,用于模拟由人类腹泻病原体肠出血性大肠杆菌和肠致病性大肠杆菌引起的肠道感染。在感染过程中,细菌利用双组分系统(TCSs)来检测宿主体内不断变化的环境线索,通过改变特定基因的表达实现快速适应。在本研究中,在鼠柠檬酸杆菌中鉴定出26个双组分系统,定量PCR(qPCR)分析表明它们在鼠类感染期间均有表达。这些双组分系统被逐个删除,并分析其体外和体内效应以确定功能后果。体外分析仅显示出微小差异,令人惊讶的是,III型分泌(T3S)仅在ΔarcA菌株中受到影响。鼠类感染鉴定出7个毒力减弱或增强的突变体。与体外T3S检测结果一致,ΔarcA菌株毒力减弱,在定殖和细胞黏附方面存在缺陷。ΔrcsB菌株是毒力减弱程度最高的菌株之一。该菌株毒力的降低可能与细胞表面的变化有关,因为刚果红结合发生了改变,qPCR显示wcaA基因(在其他细菌中与结肠酸产生有关)的表达大幅下调。与野生型相比,ΔuvrY菌株表现出毒力增强,这与肠系膜淋巴结内细菌载量的显著增加有关。对与毒力相关的双组分系统进行系统分析并研究其在感染过程中的功能,可能为药物开发开辟新途径。