共 53 条
Legionella pneumophila Dot/Icm translocated substrates: a sum of parts
被引:111
作者:

Ensminger, Alexander W.
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机构:
Tufts Univ, Sch Med, Dept Mol Biol & Microbiol, Boston, MA 02111 USA Tufts Univ, Sch Med, Howard Hughes Med Inst, Boston, MA 02111 USA

Isberg, Ralph R.
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h-index: 0
机构:
Tufts Univ, Sch Med, Howard Hughes Med Inst, Boston, MA 02111 USA
Tufts Univ, Sch Med, Dept Mol Biol & Microbiol, Boston, MA 02111 USA Tufts Univ, Sch Med, Howard Hughes Med Inst, Boston, MA 02111 USA
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.
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页码:67 / 73
页数:7
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机构: Columbia Univ Coll Phys & Surg, Columbia Genome Ctr, New York, NY 10032 USA

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