Critical role of multidrug efflux pump in the pathogenicity of Listeria monocytogenes
| Project/Area Number |
24659196
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| Research Category |
Grant-in-Aid for Challenging Exploratory Research
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| Allocation Type | Multi-year Fund |
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| Research Field |
Bacteriology (including Mycology)
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| Research Institution | Kyoto University |
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Principal Investigator |
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| Project Period (FY) |
2012
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| Project Status |
Completed (Fiscal Year 2012)
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| Budget Amount *help |
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2012: ¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
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| Keywords | 細菌 / リステリア / マクロファージ / インターフェロン |
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| Research Abstract |
Among various strains of Listeria monocytogenes, LO28 strain is highly capable of inducing IFNmechanism of the IFN-β-inducing ability of LO28 was investigated. It was found that LO28 secretes a large amount of cyclic-di AMP that probably triggers IFNactivation of STING-dependent signal pathway. The secretion of cyclic di-AMP was dependent on MdrT, a multidrug resistant transporter, and L028 exhibited a very high level of mdrT expression due to functional impairment of TetR, a negative regulator of mdrT. Furthermore, an infection experiment revealed that the strong expression of mdrT decreases the pathogenicity of L. monocytogenes whereas type I IFN receptor knockout mice were resistant to L. monocytogenes infection compared to wild type mice. Result suggested that cyclic di-AMP may promote resistance independently of IFNcontribute to secrete some other factors that are implicated in the control of L. monocytogenes replication in vivo.
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Report
(2 results)
Research Products
(25 results)
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[Journal Article] Del Carmen Sasiain M. Two genetically-related multidrug-resistant Mycobacterium tuberculosis strains induce divergent outcomes of infection in two human macrophage models2013
Author(s)
Yokobori N, Lopez B, Geffner L, Sabio Y Garcia C, Schierloh P, Barrera L, de la Barrera S, Sakai S, Kawamura I, Mitsuyama M, Ritacco V
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Journal Title
Infect Genet Evol.
Volume: 16
Pages: 151-156
DOI
Related Report
Peer Reviewed
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