Department of Microbial Pathogenesis, Yale University School of Medicine, New Haven, Connecticut 06536; email:
Annu Rev Microbiol. 2016 Sep 8;70:413-33. doi: 10.1146/annurev-micro-102215-095557.
The gram-negative bacterial pathogen Legionella pneumophila creates a novel organelle inside of eukaryotic host cells that supports intracellular replication. The L. pneumophila-containing vacuole evades fusion with lysosomes and interacts intimately with the host endoplasmic reticulum (ER). Although the natural hosts for L. pneumophila are free-living protozoa that reside in freshwater environments, the mechanisms that enable this pathogen to replicate intracellularly also function when mammalian macrophages phagocytose aerosolized bacteria, and infection of humans by L. pneumophila can result in a severe pneumonia called Legionnaires' disease. A bacterial type IVB secretion system called Dot/Icm is essential for intracellular replication of L. pneumophila. The Dot/Icm apparatus delivers over 300 different bacterial proteins into host cells during infection. These bacterial proteins have biochemical activities that target evolutionarily conserved host factors that control membrane transport processes, which results in the formation of the ER-derived vacuole that supports L. pneumophila replication. This review highlights research discoveries that have defined interactions between vacuoles containing L. pneumophila and the host ER. These studies reveal how L. pneumophila creates a vacuole that supports intracellular replication by subverting host proteins that control biogenesis and fusion of early secretory vesicles that exit the ER and host proteins that regulate the shape and dynamics of the ER. In addition to recruiting ER-derived membranes for biogenesis of the vacuole in which L. pneumophila replicates, these studies have revealed that this pathogen has a remarkable ability to interfere with the host's cellular process of autophagy, which is an ancient cell autonomous defense pathway that utilizes ER-derived membranes to target intracellular pathogens for destruction. Thus, this intracellular pathogen has evolved multiple mechanisms to control membrane transport processes that center on the involvement of the host ER.
革兰氏阴性细菌病原体嗜肺军团菌在真核宿主细胞内创建了一种新的细胞器,支持细胞内复制。含有嗜肺军团菌的空泡逃避与溶酶体融合,并与宿主内质网(ER)密切相互作用。虽然嗜肺军团菌的自然宿主是生活在淡水环境中的自由生活原生动物,但使这种病原体能够在细胞内复制的机制,当哺乳动物巨噬细胞吞噬雾化细菌时也能发挥作用,人类感染嗜肺军团菌可导致一种严重的肺炎,称为军团病。一种称为 Dot/Icm 的细菌 IVB 型分泌系统对于嗜肺军团菌的细胞内复制是必不可少的。Dot/Icm 仪器在感染过程中将 300 多种不同的细菌蛋白输送到宿主细胞中。这些细菌蛋白具有生化活性,靶向控制膜运输过程的进化保守宿主因子,导致形成支持嗜肺军团菌复制的 ER 衍生空泡。这篇综述强调了定义含有嗜肺军团菌的空泡与宿主 ER 之间相互作用的研究发现。这些研究揭示了嗜肺军团菌如何通过颠覆控制从 ER 中输出的早期分泌小泡的生物发生和融合的宿主蛋白,以及调节 ER 形状和动力学的宿主蛋白,从而创建支持细胞内复制的空泡。除了招募 ER 衍生的膜来生成嗜肺军团菌复制的空泡外,这些研究还揭示了这种病原体具有显著干扰宿主细胞自噬过程的能力,自噬是一种古老的细胞自主防御途径,利用 ER 衍生的膜来靶向细胞内病原体进行破坏。因此,这种细胞内病原体已经进化出多种机制来控制以宿主 ER 为中心的膜运输过程。