Kühbacher Andreas, Gouin Edith, Mercer Jason, Emmenlauer Mario, Dehio Christoph, Cossart Pascale, Pizarro-Cerdá Javier
Unité des Interactions Bactéries Cellules, Pasteur Institute.
J Vis Exp. 2013 Sep 19(79):e51043. doi: 10.3791/51043.
Bacterial intracellular pathogens can be conceived as molecular tools to dissect cellular signaling cascades due to their capacity to exquisitely manipulate and subvert cell functions which are required for the infection of host target tissues. Among these bacterial pathogens, Listeria monocytogenes is a Gram positive microorganism that has been used as a paradigm for intracellular parasitism in the characterization of cellular immune responses, and which has played instrumental roles in the discovery of molecular pathways controlling cytoskeletal and membrane trafficking dynamics. In this article, we describe a robust microscopical assay for the detection of late cellular infection stages of L. monocytogenes based on the fluorescent labeling of InlC, a secreted bacterial protein which accumulates in the cytoplasm of infected cells; this assay can be coupled to automated high-throughput small interfering RNA screens in order to characterize cellular signaling pathways involved in the up- or down-regulation of infection.
细菌细胞内病原体可被视为剖析细胞信号级联反应的分子工具,因为它们能够精确操纵和颠覆宿主靶组织感染所需的细胞功能。在这些细菌病原体中,单核细胞增生李斯特菌是一种革兰氏阳性微生物,在细胞免疫反应的表征中被用作细胞内寄生的范例,并且在发现控制细胞骨架和膜运输动力学的分子途径中发挥了重要作用。在本文中,我们描述了一种基于对InlC进行荧光标记的强大显微镜检测方法,用于检测单核细胞增生李斯特菌的晚期细胞感染阶段,InlC是一种分泌型细菌蛋白,会在受感染细胞的细胞质中积累;该检测方法可与自动化高通量小干扰RNA筛选相结合,以表征参与感染上调或下调的细胞信号通路。