Centre for Molecular Microbiology and Infection, Division of Cell and Molecular Biology, Imperial College London, London, United Kingdom.
PLoS Pathog. 2009 Dec;5(12):e1000683. doi: 10.1371/journal.ppat.1000683. Epub 2009 Dec 11.
Enteropathogenic Escherichia coli (EPEC) strains are defined as extracellular pathogens which nucleate actin rich pedestal-like membrane extensions on intestinal enterocytes to which they intimately adhere. EPEC infection is mediated by type III secretion system effectors, which modulate host cell signaling. Recently we have shown that the WxxxE effector EspT activates Rac1 and Cdc42 leading to formation of membrane ruffles and lamellipodia. Here we report that EspT-induced membrane ruffles facilitate EPEC invasion into non-phagocytic cells in a process involving Rac1 and Wave2. Internalized EPEC resides within a vacuole and Tir is localized to the vacuolar membrane, resulting in actin polymerization and formation of intracellular pedestals. To the best of our knowledge this is the first time a pathogen has been shown to induce formation of actin comets across a vacuole membrane. Moreover, our data breaks the dogma of EPEC as an extracellular pathogen and defines a new category of invasive EPEC.
肠致病性大肠杆菌(EPEC)菌株被定义为在肠上皮细胞上形成富含肌动蛋白的基底部样膜延伸的细胞外病原体,它们与肠上皮细胞紧密黏附。EPEC 感染是由 III 型分泌系统效应子介导的,这些效应子调节宿主细胞信号转导。最近我们发现,WxxxE 效应子 EspT 激活 Rac1 和 Cdc42,导致膜皱襞和片状伪足的形成。在这里,我们报告 EspT 诱导的膜皱襞促进 EPEC 侵入非吞噬细胞,这个过程涉及 Rac1 和 Wave2。内化的 EPEC 存在于液泡内,Tir 定位于液泡膜上,导致肌动蛋白聚合和细胞内基底部的形成。据我们所知,这是第一次有病原体被证明能够在液泡膜上诱导形成肌动蛋白彗星。此外,我们的数据打破了 EPEC 作为细胞外病原体的教条,并定义了一种新的侵袭性 EPEC 类别。