Isaac Dervla T, Isberg Ralph
Department of Microbiology & Molecular Biology, Tufts University School of Medicine, 150 Harrison Avenue, Boston, MA 02111, USA.
Future Microbiol. 2014;9(3):343-59. doi: 10.2217/fmb.13.162.
Macrophages are the front line of immune defense against invading microbes. Microbes, however, have evolved numerous and diverse mechanisms to thwart these host immune defenses and thrive intracellularly. Legionella pneumophila, a Gram-negative pathogen of amoebal and mammalian phagocytes, is one such microbe. In humans, it causes a potentially fatal pneumonia referred to as Legionnaires' disease. Armed with the Icm/Dot type IV secretion system, which is required for virulence, and approximately 300 translocated proteins, Legionella is able to enter host cells, direct the biogenesis of its own vacuolar compartment, and establish a replicative niche, where it grows to high levels before lysing the host cell. Efforts to understand the pathogenesis of this bacterium have focused on characterizing the molecular activities of its many effectors. In this article, we highlight recent strides that have been made in understanding how Legionella effectors mediate host-pathogen interactions.
巨噬细胞是抵御入侵微生物的免疫防御第一线。然而,微生物已经进化出许多不同的机制来挫败这些宿主免疫防御并在细胞内茁壮成长。嗜肺军团菌是一种感染变形虫和哺乳动物吞噬细胞的革兰氏阴性病原体,就是这样一种微生物。在人类中,它会引发一种可能致命的肺炎,称为军团病。嗜肺军团菌拥有毒力所需的Icm/Dot IV型分泌系统以及大约300种转运蛋白,能够进入宿主细胞,指导自身液泡区室的生物发生,并建立一个复制龛,在宿主细胞裂解之前在其中大量繁殖。了解这种细菌发病机制的努力集中在表征其许多效应器的分子活性上。在本文中,我们重点介绍了在理解嗜肺军团菌效应器如何介导宿主-病原体相互作用方面取得的最新进展。