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Inhibition of RIG-I-Mediated Signaling by Kaposis Sarcoma-Associated Herpesvirus-Encoded Deubiquitinase ORF64

机译:卡波西氏肉瘤相关疱疹病毒编码去泛素酶ORF64对RIG-I介导信号的抑制作用。

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摘要

Virus infection triggers interferon (IFN)-mediated innate immune defenses in part through viral nucleic acid interactions. However, the immune recognition mechanisms by which the host identifies incoming DNA viruses are still elusive. Here, we show that increased levels of Kaposi's sarcoma-associated herpesvirus (KSHV) persistency are observed in retinoic acid-inducible gene I (RIG-I)-deficient cells and that KSHV ORF64, a tegument protein with deubiqutinase (DUB) activity, suppresses RIG-I-mediated IFN signaling by reducing the ubiquitination of RIG-I, crucial for its activation. This study suggests that RIG-I plays a potential role in sensing KSHV infection and that KSHV ORF64 DUB counteracts RIG-I signaling.
机译:病毒感染部分地通过病毒核酸相互作用触发干扰素(IFN)介导的先天免疫防御。但是,宿主识别传入的DNA病毒的免疫识别机制仍然难以捉摸。在这里,我们显示在视黄酸诱导型基因I(RIG-I)缺乏的细胞中观察到了卡波西氏肉瘤相关疱疹病毒(KSHV)持久性水平的升高,并且具有去泛素酶(DUB)活性的外皮蛋白KSHV ORF64抑制了RIG-I介导的IFN信号传导可通过减少RIG-I的泛素化来实现,这对于激活它至关重要。这项研究表明,RIG-I在感测KSHV感染中起潜在作用,而KSHV ORF64 DUB抵消了RIG-I信号传导。

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