The Rabies Virus Interferon Antagonist P Protein Interacts with Activated STAT3 and Inhibits Gp130 Receptor Signaling

被引:59
|
作者
Lieu, Kim G. [1 ,2 ]
Brice, Aaron [1 ]
Wiltzer, Linda [1 ,2 ]
Hirst, Bevan [1 ]
Jans, David A. [2 ]
Blondel, Danielle [3 ]
Moseley, Gregory W. [1 ]
机构
[1] Monash Univ, Dept Biochem & Mol Biol, Viral Pathogenesis Lab, Clayton, Vic 3800, Australia
[2] Monash Univ, Dept Biochem & Mol Biol, Nucl Signalling Lab, Clayton, Vic 3800, Australia
[3] CNRS, Lab Virol Mol & Struct, Gif Sur Yvette, France
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
V-PROTEIN; NUCLEAR ACCUMULATION; PREVENTING STAT1; IMMUNE EVASION; DEGRADATION; TRANSDUCTION; CYTOKINE; PHOSPHOPROTEIN; LOCALIZATION; TRAFFICKING;
D O I
10.1128/JVI.00989-13
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Immune evasion by rabies virus depends on targeting of the signal transducers and activator of transcription 1 (STAT1) and STAT2 proteins by the viral interferon antagonist P protein, but targeting of other STAT proteins has not been investigated. Here, we find that P protein associates with activated STAT3 and inhibits STAT3 nuclear accumulation and Gp130-dependent signaling. This is the first report of STAT3 targeting by the interferon antagonist of a virus other than a paramyxovirus, indicating that STAT3 antagonism is important to a range of human-pathogenic viruses.
引用
收藏
页码:8261 / 8265
页数:5
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