Vidy Aurore, Chelbi-Alix Mounira, Blondel Danielle
Unité Mixte de Virologie Moléculaire et Structurale UMR 2472, CNRS, 91198 Gif sur Yvette Cedex, France.
J Virol. 2005 Nov;79(22):14411-20. doi: 10.1128/JVI.79.22.14411-14420.2005.
Rabies virus P protein is a cofactor of RNA polymerase. We investigated other potential roles of P (CVS strain) by searching for cellular partners using two-hybrid screening. We isolated a cDNA encoding the signal transducer and activator of transcription 1 (STAT1) that is a critical component of interferon type I (IFN-alpha/beta) and type II (IFN-gamma) signaling. We confirmed this interaction by glutathione S-transferase-pull-down assay. Deletion mutant analysis indicated that the carboxy-terminal part of P interacted with a region containing the DNA-binding domain and the coiled-coil domain of STAT1. The expression of P protein inhibits IFN-alpha- and IFN-gamma-induced transcriptional responses, thus impairing the IFN-induced antiviral state. Mechanistic studies indicate that P protein does not induce STAT1 degradation and does not interfere with STAT1 phosphorylation but prevents IFN-induced STAT1 nuclear accumulation. These results indicate that rabies P protein overcomes the antiviral response of the infected cells.
狂犬病病毒P蛋白是RNA聚合酶的辅助因子。我们通过双杂交筛选寻找细胞伴侣,研究了P(CVS毒株)的其他潜在作用。我们分离出了一个编码信号转导和转录激活因子1(STAT1)的cDNA,它是I型干扰素(IFN-α/β)和II型干扰素(IFN-γ)信号传导的关键组成部分。我们通过谷胱甘肽S-转移酶下拉实验证实了这种相互作用。缺失突变分析表明,P的羧基末端部分与包含STAT1的DNA结合结构域和卷曲螺旋结构域的区域相互作用。P蛋白的表达抑制IFN-α和IFN-γ诱导的转录反应,从而损害IFN诱导的抗病毒状态。机制研究表明,P蛋白不会诱导STAT1降解,也不会干扰STAT1磷酸化,但会阻止IFN诱导的STAT1核内积累。这些结果表明,狂犬病P蛋白克服了被感染细胞的抗病毒反应。