Bhinder Ganive, Sham Ho Pan, Chan Justin M, Morampudi Vijay, Jacobson Kevan, Vallance Bruce A
Division of Gastroenterology, BC Children's Hospital, Canada.
J Vis Exp. 2013 Feb 19(72):e50222. doi: 10.3791/50222.
This protocol outlines the steps required to produce a robust model of infectious disease and colitis, as well as the methods used to characterize Citrobacter rodentium infection in mice. C. rodentium is a gram negative, murine specific bacterial pathogen that is closely related to the clinically important human pathogens enteropathogenic E. coli and enterohemorrhagic E. coli. Upon infection with C. rodentium, immunocompetent mice suffer from modest and transient weight loss and diarrhea. Histologically, intestinal crypt elongation, immune cell infiltration, and goblet cell depletion are observed. Clearance of infection is achieved after 3 to 4 weeks. Measurement of intestinal epithelial barrier integrity, bacterial load, and histological damage at different time points after infection, allow the characterization of mouse strains susceptible to infection. The virulence mechanisms by which bacterial pathogens colonize the intestinal tract of their hosts, as well as specific host responses that defend against such infections are poorly understood. Therefore the C. rodentium model of enteric bacterial infection serves as a valuable tool to aid in our understanding of these processes. Enteric bacteria have also been linked to Inflammatory Bowel Diseases (IBDs). It has been hypothesized that the maladaptive chronic inflammatory responses seen in IBD patients develop in genetically susceptible individuals following abnormal exposure of the intestinal mucosal immune system to enteric bacteria. Therefore, the study of models of infectious colitis offers significant potential for defining potentially pathogenic host responses to enteric bacteria. C. rodentium induced colitis is one such rare model that allows for the analysis of host responses to enteric bacteria, furthering our understanding of potential mechanisms of IBD pathogenesis; essential in the development of novel preventative and therapeutic treatments.
本方案概述了构建传染病和结肠炎稳健模型所需的步骤,以及用于表征小鼠柠檬酸杆菌感染的方法。柠檬酸杆菌是一种革兰氏阴性、鼠类特异性细菌病原体,与临床上重要的人类病原体肠致病性大肠杆菌和肠出血性大肠杆菌密切相关。感染柠檬酸杆菌后,免疫功能正常的小鼠会出现适度且短暂的体重减轻和腹泻。组织学上,可观察到肠道隐窝延长、免疫细胞浸润和杯状细胞减少。感染在3至4周后清除。在感染后的不同时间点测量肠道上皮屏障完整性、细菌载量和组织学损伤,有助于表征易感染的小鼠品系。细菌病原体在其宿主肠道中定殖的毒力机制,以及抵御此类感染的特定宿主反应,目前尚不清楚。因此,柠檬酸杆菌肠道细菌感染模型是帮助我们理解这些过程的宝贵工具。肠道细菌也与炎症性肠病(IBD)有关。据推测,IBD患者中出现的适应性不良慢性炎症反应,是在遗传易感个体中,肠道黏膜免疫系统异常暴露于肠道细菌后发生的。因此,对感染性结肠炎模型的研究为确定宿主对肠道细菌的潜在致病反应提供了巨大潜力。柠檬酸杆菌诱导的结肠炎就是这样一种罕见的模型,它可以分析宿主对肠道细菌的反应,加深我们对IBD发病机制潜在机制的理解;这对开发新的预防和治疗方法至关重要。