Abt. Mikrobiologie, Universität Osnabrück, Osnabrück, Germany.
Infect Immun. 2014 Jun;82(6):2657-67. doi: 10.1128/IAI.00023-14. Epub 2014 Apr 7.
The invasion of polarized epithelial cells by Salmonella enterica requires the cooperative activity of the Salmonella pathogenicity island 1 (SPI1)-encoded type III secretion system (T3SS) and the SPI4-encoded adhesin SiiE. The invasion of polarized cells is more efficient than that of nonpolarized cells, and we observed the formation of clusters of bacteria on infected cells. Here we demonstrate that the invasion of polarized cells is a highly cooperative activity. Using a novel live-cell imaging approach, we visualized the cooperative entry of multiple bacteria into ruffles induced on the apical surfaces of polarized cells. The induction of membrane ruffles by activity of Salmonella enables otherwise noninvasive mutant strains to enter polarized host cells. Bacterial motility and chemotaxis were of lower importance for cooperativity in polarized-cell invasion. We propose that cooperative invasion is a key factor for the very efficient entry into polarized cells and a factor contributing to epithelial damage and intestinal inflammation.
沙门氏菌属入侵极化上皮细胞需要沙门氏菌致病性岛 1(SPI1)编码的 III 型分泌系统(T3SS)和 SPI4 编码的黏附因子 SiiE 的协同作用。极化细胞的入侵比非极化细胞更有效率,我们观察到感染细胞上细菌簇的形成。在这里,我们证明了极化细胞的入侵是一种高度协同的活动。使用一种新的活细胞成像方法,我们可视化了多个细菌进入极化细胞顶表面诱导的皱襞中的协同进入。沙门氏菌活性引起的细胞膜皱襞使原本不能入侵的突变株能够进入极化宿主细胞。细菌的运动性和趋化性对极化细胞入侵的协同性的重要性较低。我们提出,协同入侵是非常有效地进入极化细胞的关键因素,也是导致上皮损伤和肠道炎症的因素之一。