Abstract |
Severe acute respiratory syndrome (SARS) coronavirus is highly pathogenic in humans and evades innate immunity at multiple levels. It has evolved various strategies to counteract the production and action of type I interferons, which mobilize the front-line defense against viral infection. In this study we demonstrate that SARS coronavirus M protein inhibits gene transcription of type I interferons. M protein potently antagonizes the activation of interferon-stimulated response element-dependent transcription by double-stranded RNA, RIG-I, MDA5, TBK1, IKKepsilon, and virus-induced signaling adaptor (VISA) but has no influence on the transcriptional activity of this element when IRF3 or IRF7 is overexpressed. M protein physically associates with RIG-I, TBK1, IKKepsilon, and TRAF3 and likely sequesters some of them in membrane-associated cytoplasmic compartments. Consequently, the expression of M protein prevents the formation of TRAF3.TANK.TBK1/ IKKepsilon complex and thereby inhibits TBK1/ IKKepsilon-dependent activation of IRF3/IRF7 transcription factors. Taken together, our findings reveal a new mechanism by which SARS coronavirus circumvents the production of type I interferons.
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Authors | Kam-Leung Siu, Kin-Hang Kok, Ming-Him James Ng, Vincent K M Poon, Kwok-Yung Yuen, Bo-Jian Zheng, Dong-Yan Jin |
Journal | The Journal of biological chemistry
(J Biol Chem)
Vol. 284
Issue 24
Pg. 16202-16209
(Jun 12 2009)
ISSN: 0021-9258 [Print] United States |
PMID | 19380580
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Adaptor Proteins, Signal Transducing
- Coronavirus M Proteins
- IRF3 protein, human
- Interferon Regulatory Factor-3
- Interferon Type I
- M protein, SARS-CoV
- TANK protein, human
- TNF Receptor-Associated Factor 3
- TRAF3 protein, human
- Viral Matrix Proteins
- Protein Serine-Threonine Kinases
- TBK1 protein, human
- I-kappa B Kinase
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Topics |
- Adaptor Proteins, Signal Transducing
(metabolism)
- Coronavirus M Proteins
- Gene Expression Regulation
(immunology)
- HeLa Cells
- Humans
- I-kappa B Kinase
(metabolism)
- Interferon Regulatory Factor-3
(metabolism)
- Interferon Type I
(genetics, immunology)
- Kidney
(cytology)
- Phosphorylation
- Protein Serine-Threonine Kinases
(metabolism)
- Severe acute respiratory syndrome-related coronavirus
(immunology)
- Severe Acute Respiratory Syndrome
(immunology, virology)
- Signal Transduction
(immunology)
- TNF Receptor-Associated Factor 3
(metabolism)
- Viral Matrix Proteins
(immunology, metabolism)
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