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MERS-CoV papain-like protease has deISGylating and deubiquitinating activities

机译:MERS-CoV木瓜蛋白酶样蛋白酶具有去ISG化和去泛素化的活性

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摘要

Coronaviruses encode papain-like proteases (PLpro) that are often multifunctional enzymes with protease activity to process the viral replicase polyprotein and deubiquitinating (DUB)/deISGylating activity, which is hypothesized to modify the innate immune response to infection. Here, we investigate the predicted DUB activity of the PLpro domain of the recently described Middle East Respiratory Syndrome Coronavirus (MERS-CoV). We found that expression of MERS-CoV PLpro reduces the levels of ubiquitinated and ISGylated host cell proteins; consistent with multifunctional PLpro activity. Further, we compared the ability of MERS-CoV PLpro and Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV) PLpro to block innate immune signaling of proinflammatory cytokines. We show that expression of SARS-CoV and MERS-CoV PLpros blocks upregulation of cytokines CCL5, IFN-β and CXCL10 in stimulated cells. Overall these results indicate that the PLpro domains of MERS-CoV and SARS-CoV have the potential to modify the innate immune response to viral infection and contribute to viral pathogenesis.
机译:冠状病毒编码的木瓜蛋白酶样蛋白酶(PLpro)通常是具有蛋白酶活性的多功能酶,具有加工病毒复制酶多蛋白和去泛素化(DUB)/ deISGylating活性的作用,假定该酶可以修饰对感染的先天免疫应答。在这里,我们调查了最近描述的中东呼吸系统综合症冠状病毒(MERS-CoV)的PLpro域的预测DUB活性。我们发现,MERS-CoV PLpro的表达降低了泛素化和ISGylated宿主细胞蛋白的水平;与多功能PLpro活动一致。此外,我们比较了MERS-CoV PLpro和严重急性呼吸系统综合症冠状病毒(SARS-CoV)PLpro阻断促炎细胞因子的先天免疫信号传导的能力。我们表明SARS冠状病毒和MERS冠状病毒PLpros的表达阻止刺激细胞中细胞因子CCL5,IFN-β和CXCL10的上调。总体而言,这些结果表明,MERS-CoV和SARS-CoV的PLpro结构域具有修饰对病毒感染的先天免疫应答并促进病毒发病机理的潜力。

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