Intracellular passage within macrophages affects the trafficking of virulent tubercle bacilli upon reinfection of other macrophages in a serum-dependent manner

K.A. McDonough , M.A. Florczyk , Y. Kress
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引用次数: 21

Abstract

Setting: The interaction of tubercle bacilli with macrophages is central to understanding of tuberculosis disease.

Objective: The objective was to determine whether prior passage within macrophages affects the behavior of Mycobacterium tuberculosis (Mtb) upon re-entry into other macrophages.

Design: Transmission electron microscopy was used to monitor fusion of bacterial phagosomes with late endosomal/lysosomal compartments using thoria as a fluid phase marker. Two-dimensional polyacrylamide gel electrophoresis was used to study bacterial protein expression within macrophages.

Results: H37Rv and BCG expressed novel proteins within macrophages. H37Rv also underwent less fusion after intracellular (IC) (24.2±7.7%) than extracellular (XC) (67.4±5.5%) passage when the bacteria entered new macrophages in small clusters. These effects were inhibited by serum, and were not observed with H37Ra or BCG bacteria (78.9±1.6% fused for all conditions). In addition, vacuoles which contained single bacilli were less likely to acquire markers (26.9±2.6%) than those that contained multiple bacilli (77.3±2.8%).

Conclusion: These results indicate that phagolysosomal fusion patterns can be modulated by a variety of factors and that virulent Mtb bacteria may express proteins within macrophages that alter their interaction with these host cells.

巨噬细胞内的细胞传代以血清依赖的方式影响毒性结核杆菌在其他巨噬细胞再感染时的运输
背景:结核杆菌与巨噬细胞的相互作用是了解结核病的核心。目的:目的是确定先前在巨噬细胞内传代是否影响结核分枝杆菌(Mtb)再次进入其他巨噬细胞时的行为。设计:采用透射电子显微镜监测细菌吞噬体与晚期内体/溶酶体隔室的融合,使用钍作为液相标记物。采用二维聚丙烯酰胺凝胶电泳技术研究巨噬细胞内细菌蛋白的表达。结果:H37Rv和BCG在巨噬细胞内表达新蛋白。H37Rv细胞内传代(IC)(24.2±7.7%)比细胞外传代(XC)(67.4±5.5%)更少融合,当细菌以小簇形式进入新的巨噬细胞时。血清可抑制上述效应,而H37Ra和卡介苗细菌均未观察到这些效应(在所有条件下融合率为78.9±1.6%)。此外,含有单个杆菌的液泡获得标记物的可能性(26.9±2.6%)低于含有多个杆菌的液泡(77.3±2.8%)。结论:这些结果表明吞噬溶酶体融合模式可以被多种因素调节,并且毒力强的结核分枝杆菌可能在巨噬细胞内表达改变其与宿主细胞相互作用的蛋白质。
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