Deletion of two-component regulatory systems increases the virulence of Mycobacterium tuberculosis
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Parish, T
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Univ London London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1E 7HT, EnglandUniv London London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1E 7HT, England
Parish, T
[1
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Smith, DA
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Univ London London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1E 7HT, EnglandUniv London London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1E 7HT, England
Smith, DA
[1
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Kendall, S
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Univ London London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1E 7HT, EnglandUniv London London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1E 7HT, England
Kendall, S
[1
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Casali, N
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Univ London London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1E 7HT, EnglandUniv London London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1E 7HT, England
Casali, N
[1
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Bancroft, GJ
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Univ London London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1E 7HT, EnglandUniv London London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1E 7HT, England
Bancroft, GJ
[1
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Stoker, NG
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Univ London London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1E 7HT, EnglandUniv London London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1E 7HT, England
Stoker, NG
[1
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[1] Univ London London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1E 7HT, England
Two-component regulatory signal transduction systems are widely distributed among bacteria and enable the organisms to make coordinated changes in gene expression in response to a variety of environmental stimuli. The genome sequence of Mycobacterium tuberculosis contains 11 complete two-component systems, four isolated homologous regulators, and three isolated homologous sensors. We have constructed defined mutations in six of these genes and measured virulence in a SCID mouse model. Mice infected with four of the mutants (deletions of devR, tcrXY, trcS, and kdpDE) died more rapidly than those infected with wild-type bacteria. The other two mutants (narL and Rv3220c) showed no change compared to the wild-type H37Rv strain. The most hypervirulent mutant (devRDelta) also grew more rapidly in the acute stage of infection in immunocompetent mice and in gamma interferon-activated macrophages. These results define a novel class of genes in this pathogen whose presence slows down its multiplication in vivo or increases its susceptibility to host killing mechanisms. Thus, M. tuberculosis actively maintains a balance between its own survival and that of the host.