Klapproth J-M A, Meyer F
Division of Digestive Diseases, Department of Internal Medicine, Emory University School of Medicine, Atlanta, GA 30322, USA.
Dtsch Med Wochenschr. 2009 Feb;134(9):417-20. doi: 10.1055/s-0029-1208066. Epub 2009 Feb 17.
Gastrointestinal infections are a significant cause of diarrhea and a worldwide problem with annually one billion illnesses and 3 to 4 million deaths. Gram negative bacteria like Enteropathogenic E. coli (EPEC) in developing countries and Enterohemorrhagic E. coli (EHEC) in the developed world are responsible for the majority of acute diarrheal episodes, especially among children less than three years of age. Pathogenic E. coli are supplied with an arsenal of effector proteins to modify and neutralize specific cellular functions of the host organism.
Based on personal and extensively published results we provide a selected overview of Gram negative virulence functions with a focus on lymphostatin.
Lymphostatin is an effector protein encoded by lifA/efa-1 (lymphocyte inhibitory factor A/ EHEC factor for adherence). lifA/efa-1 and homologous genes have been identified in EPEC, EHEC, and mouse pathogen Citrobacter rodentium, as well as various Chlamydia strains. Multiple groups have shown that in various EHEC strains lifA/efa-1 is part of a larger pathogenicity island responsible for increased virulence. Statistically, DNA Microarray analysis associated lifA/efa-1 as the single most imortant gene with diarrhea caused by EPEC. Interestingly, lifA/efa-1 encodes for two critical enzymatic activities that have been identified in other pathogenic bacteria: glucosyltransferase- in Clostridium- and protease activity in Yersinia strains. In vitro studies identified lymphostatin as an effector protein with an immunosuppressive effect on peripheral blood and gastrointestinal mucosa T lymphocytes. Further, lymphostatin regulates the barrier function of epithelial monolayer cultures: activation of small GTPase RhoA and inhibition of Cdc42 lead to disassembly of adherens junctions and tight junctions, respectively. Besides an effect on immune and epithelial barrier function, lymphostatin also functions as an adhesion factor for EPEC and EHEC, is essential for colonization of mouse and calf intestine, and regulates bacterial effector proteins.
Lymphostatin is a common toxin in Gram negative bacteria with multiple functions: cell adhesion, immunosuppression, disruption of epithelial barrier function, and intestinal colonization.
胃肠道感染是腹泻的一个重要原因,是一个全球性问题,每年有10亿人次患病,300万至400万人死亡。发展中国家的肠道致病性大肠杆菌(EPEC)和发达国家的肠出血性大肠杆菌(EHEC)等革兰氏阴性菌是大多数急性腹泻发作的病因,尤其是在3岁以下儿童中。致病性大肠杆菌配备了一系列效应蛋白,以改变和中和宿主生物体的特定细胞功能。
基于个人及广泛发表的研究结果,我们重点围绕淋巴抑素,对革兰氏阴性菌的毒力功能进行了概述。
淋巴抑素是一种由lifA/efa-1(淋巴细胞抑制因子A/黏附性EHEC因子)编码的效应蛋白。在EPEC、EHEC、小鼠病原体鼠柠檬酸杆菌以及各种衣原体菌株中已鉴定出lifA/efa-1及其同源基因。多个研究小组表明,在各种EHEC菌株中,lifA/efa-1是一个更大的致病岛的一部分,该致病岛导致毒力增加。从统计学角度来看,DNA微阵列分析将lifA/efa-1确定为与EPEC引起的腹泻最相关的单一重要基因。有趣的是,lifA/efa-1编码两种在其他致病细菌中已鉴定出的关键酶活性:梭菌中的葡糖基转移酶活性和耶尔森菌属菌株中的蛋白酶活性。体外研究确定淋巴抑素是一种对外周血和胃肠道黏膜T淋巴细胞具有免疫抑制作用的效应蛋白。此外,淋巴抑素调节上皮单层培养物的屏障功能:小GTP酶RhoA的激活和Cdc42的抑制分别导致黏附连接和紧密连接的解体。除了对免疫和上皮屏障功能有影响外,淋巴抑素还是EPEC和EHEC的黏附因子,对小鼠和小牛肠道的定植至关重要,并调节细菌效应蛋白。
淋巴抑素是革兰氏阴性菌中的一种常见毒素,具有多种功能:细胞黏附、免疫抑制、破坏上皮屏障功能和肠道定植。