Legionella pneumophila Dot/Icm translocated substrates: a sum of parts

被引:111
作者
Ensminger, Alexander W. [2 ]
Isberg, Ralph R. [1 ,2 ]
机构
[1] Tufts Univ, Sch Med, Howard Hughes Med Inst, Boston, MA 02111 USA
[2] Tufts Univ, Sch Med, Dept Mol Biol & Microbiol, Boston, MA 02111 USA
基金
美国国家卫生研究院;
关键词
SECRETION SYSTEM; PHAGOSOME TRAFFICKING; PROTEIN; RAB1; IDENTIFICATION; MACROPHAGES; RECRUITMENT; APOPTOSIS; VACUOLES; MEMBERS;
D O I
10.1016/j.mib.2008.12.004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Legionella pneumophila is an intracellular pathogen of freshwater amoeba and of alveolar macrophages in human hosts. After phagocytosis, L. pneumophila establishes a unique intracellular vacuolar niche that avoids entry into the lysosomal network. Critical for L. pneumophila intracellular growth is the Dot/Icm type IVB translocation system. Although over 80 substrates of the Dot/Icm apparatus have been identified, individual substrates are often genetically redundant, complicating their analysis. Deletion of critical Dot/Icm translocation system components causes a variety of defects during intracellular growth. Many of these effects on the host cell likely result from the actions of one or more Dot/Icm translocated substrates. Loss of single substrates never generates the profound effects observed in strains lacking translocation system components.
引用
收藏
页码:67 / 73
页数:7
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