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嗜肺军团菌吞噬体的细胞内命运是如何确定的?

How is the intracellular fate of the Legionella pneumophila phagosome determined?

作者信息

Segal G, Shuman H A

机构信息

Dept of Microbiology, College of Physicians & Surgeons, Columbia University, New York, NY 10032, USA.

出版信息

Trends Microbiol. 1998 Jul;6(7):253-5. doi: 10.1016/s0966-842x(98)01308-0.

DOI:10.1016/s0966-842x(98)01308-0
PMID:9717210
Abstract

The following pair of articles, the first by Gil Segal and Howard Shuman, and the second by James Kirby and Ralph Isberg (Trends Microbiol. 6, 256-258), explore the genetics and function of the icm/dot genes of Legionella pneumophila. This gene family is implicated in several aspects of virulence and appears to constitute components of a conjugal transfer system that has been adopted to prevent phagosome-lysosome fusion in the host cell and to mediate host cytotoxicity by pore formation. Whether these functions are natural consequences or operate in parallel remains to be discovered.

摘要

以下两篇文章,第一篇由吉尔·西格尔和霍华德·舒曼撰写,第二篇由詹姆斯·柯比和拉尔夫·伊斯伯格撰写(《微生物学趋势》6卷,256 - 258页),探讨了嗜肺军团菌icm/dot基因的遗传学和功能。这个基因家族与毒力的多个方面有关,似乎构成了一个接合转移系统的组成部分,该系统已被用于防止宿主细胞中的吞噬体 - 溶酶体融合,并通过形成孔道介导宿主细胞毒性。这些功能是自然结果还是并行发挥作用仍有待发现。

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1
How is the intracellular fate of the Legionella pneumophila phagosome determined?嗜肺军团菌吞噬体的细胞内命运是如何确定的?
Trends Microbiol. 1998 Jul;6(7):253-5. doi: 10.1016/s0966-842x(98)01308-0.
2
Pore-forming activity is not sufficient for Legionella pneumophila phagosome trafficking and intracellular growth.成孔活性对于嗜肺军团菌吞噬体运输和细胞内生长并不充分。
Mol Microbiol. 1999 Jun;32(5):990-1001. doi: 10.1046/j.1365-2958.1999.01410.x.
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Characterization of Legionella pneumophila pmiA, a gene essential for infectivity of protozoa and macrophages.嗜肺军团菌pmiA基因的特性研究,该基因是原生动物和巨噬细胞感染所必需的基因。
Infect Immun. 2005 Oct;73(10):6272-82. doi: 10.1128/IAI.73.10.6272-6282.2005.
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Intracellular multiplication and human macrophage killing by Legionella pneumophila are inhibited by conjugal components of IncQ plasmid RSF1010.嗜肺军团菌的细胞内增殖及对人类巨噬细胞的杀伤作用受到IncQ质粒RSF1010接合成分的抑制。
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[Intracellular survival and replication of legionella pneumophila within host cells].[嗜肺军团菌在宿主细胞内的存活与复制]
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Multiple substrates of the Legionella pneumophila Dot/Icm system identified by interbacterial protein transfer.通过细菌间蛋白质转移鉴定出的嗜肺军团菌Dot/Icm系统的多种底物
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The Legionella Kinase LegK2 Targets the ARP2/3 Complex To Inhibit Actin Nucleation on Phagosomes and Allow Bacterial Evasion of the Late Endocytic Pathway.嗜肺军团菌激酶LegK2靶向ARP2/3复合物,以抑制吞噬体上的肌动蛋白成核,并使细菌逃避晚期内吞途径。
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Rapid escape of the dot/icm mutants of Legionella pneumophila into the cytosol of mammalian and protozoan cells.嗜肺军团菌的dot/icm突变体快速逃逸至哺乳动物细胞和原生动物细胞的胞质溶胶中。
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Evidence that Dot-dependent and -independent factors isolate the Legionella pneumophila phagosome from the endocytic network in mouse macrophages.有证据表明,依赖Dot和不依赖Dot的因子将嗜肺军团菌吞噬体与小鼠巨噬细胞的内吞网络隔离开来。
Cell Microbiol. 2001 Feb;3(2):99-114. doi: 10.1046/j.1462-5822.2001.00093.x.
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Environmental mimics and the Lvh type IVA secretion system contribute to virulence-related phenotypes of Legionella pneumophila.环境模拟物和嗜肺军团菌的IVA型分泌系统有助于其毒力相关表型。
Infect Immun. 2007 Feb;75(2):723-35. doi: 10.1128/IAI.00956-06. Epub 2006 Nov 13.

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Structural Insight into How Bacteria Prevent Interference between Multiple Divergent Type IV Secretion Systems.细菌如何防止多种不同的IV型分泌系统之间相互干扰的结构洞察。
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Front Microbiol. 2011 May 6;2:98. doi: 10.3389/fmicb.2011.00098. eCollection 2011.
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