Document Detail


Inhibition of interferon regulatory factor 3 activation by paramyxovirus V protein.
MedLine Citation:
PMID:  22532687     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The V protein of Sendai virus (SeV) suppresses innate immunity, resulting in enhancement of viral growth in mouse lungs and viral pathogenicity. The innate immunity restricted by the V protein is induced through activation of interferon regulatory factor 3 (IRF3). The V protein has been shown to interact with melanoma differentiation-associated gene 5 (MDA5) and to inhibit beta interferon production. In the present study, we infected MDA5-knockout mice with V-deficient SeV and found that MDA5 was largely unrelated to the innate immunity that the V protein suppresses in vivo. We therefore investigated the target of the SeV V protein. We previously reported interaction of the V protein with IRF3. Here we extended the observation and showed that the V protein appeared to inhibit translocation of IRF3 into the nucleus. We also found that the V protein inhibited IRF3 activation when induced by a constitutive active form of IRF3. The V proteins of measles virus and Newcastle disease virus inhibited IRF3 transcriptional activation, as did the V protein of SeV, while the V proteins of mumps virus and Nipah virus did not, and inhibition by these proteins correlated with interaction of each V protein with IRF3. These results indicate that IRF3 is important as an alternative target of paramyxovirus V proteins.
Authors:
Takashi Irie; Katsuhiro Kiyotani; Tomoki Igarashi; Asuka Yoshida; Takemasa Sakaguchi
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2012-04-24
Journal Detail:
Title:  Journal of virology     Volume:  86     ISSN:  1098-5514     ISO Abbreviation:  J. Virol.     Publication Date:  2012 Jul 
Date Detail:
Created Date:  2012-06-08     Completed Date:  2012-08-15     Revised Date:  2013-05-20    
Medline Journal Info:
Nlm Unique ID:  0113724     Medline TA:  J Virol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  7136-45     Citation Subset:  IM    
Affiliation:
Department of Virology, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.
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MeSH Terms
Descriptor/Qualifier:
Animals
DEAD-box RNA Helicases / deficiency,  immunology
Immune Evasion*
Interferon Regulatory Factor-3 / antagonists & inhibitors*,  immunology
Mice
Mice, Inbred C57BL
Mice, Knockout
Phosphoproteins / immunology,  metabolism
Sendai virus / immunology,  pathogenicity*
Viral Proteins / genetics,  immunology,  metabolism*
Viral Structural Proteins / immunology,  metabolism
Virulence Factors / deficiency,  immunology,  metabolism*
Chemical
Reg. No./Substance:
0/36 kDa V protein, Newcastle disease virus; 0/Interferon Regulatory Factor-3; 0/Irf3 protein, mouse; 0/Phosphoproteins; 0/V protein, Nipah virus; 0/V protein, Paramyxovirus; 0/V protein, Sendai virus; 0/V protein, measles virus; 0/Viral Proteins; 0/Viral Structural Proteins; 0/Virulence Factors; EC 3.6.1.-/DEAD-box RNA Helicases; EC 3.6.1.-/Ifih1 protein, mouse
Comments/Corrections

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