共 45 条
Mycobacterium marinum Erp is a virulence determinant required for cell wall integrity and intracellular survival
被引:68
作者:

Cosma, Christine L.
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机构:
Univ Washington, Dept Microbiol, Seattle, WA 98195 USA Univ Washington, Dept Microbiol, Seattle, WA 98195 USA

Klein, Kathryn
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h-index: 0
机构: Univ Washington, Dept Microbiol, Seattle, WA 98195 USA

Kim, Rosa
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h-index: 0
机构: Univ Washington, Dept Microbiol, Seattle, WA 98195 USA

Beery, Dana
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h-index: 0
机构: Univ Washington, Dept Microbiol, Seattle, WA 98195 USA

Ramakrishnan, Lalita
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h-index: 0
机构: Univ Washington, Dept Microbiol, Seattle, WA 98195 USA
机构:
[1] Univ Washington, Dept Microbiol, Seattle, WA 98195 USA
[2] Univ Washington, Dept Immunol, Seattle, WA 98195 USA
[3] Univ Washington, Dept Med, Seattle, WA 98195 USA
关键词:
D O I:
10.1128/IAI.02061-05
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
The Mycobacterium tuberculosis exported repetitive protein (Erp) is a virulence determinant required for growth in cultured macrophages and in vivo. To better understand the role of Erp in Mycobacterium pathogenesis, we generated a mutation in the erp homologue of Mycobacterium marinum, a close genetic relative of M. tuberculosis. erp-deficient M. marinum was growth attenuated in cultured macrophage monolayers and during chronic granulomatous infection of leopard frogs, suggesting that Erp function is similarly required for the virulence of both M. tuberculosis and M. marinum. To pinpoint the step in infection at which Erp is required, we utilized a zebrafish embryo infection model that allows M. marinum infections to be visualized in real-time, comparing the erp-deficient strain to a Delta RD1 mutant whose stage of attenuation was previously characterized in zebrafish embryos. A detailed microscopic examination of infected embryos revealed that bacteria lacking Erp were compromised very early in infection, failing to grow and/or survive upon phagocytosis by host macrophages. In contrast, Delta RD1 mutant bacteria grow normally in macrophages but fail to induce host macrophage aggregation and subsequent cell-to-cell spread. Consistent with these in vivo findings, erp-deficient but not RD1-deficient bacteria exhibited permeability defects in vitro, which may be responsible for their specific failure to survive in host macrophages.
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页码:3125 / 3133
页数:9
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