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BAG3 a Host Cochaperone Facilitates Varicella-Zoster Virus Replication

机译:BAG3宿主伴侣蛋白促进水痘-带状疱疹病毒复制

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摘要

Varicella-zoster virus (VZV) establishes a lifelong latent infection in the dorsal root ganglia of the host. During latency, a subset of virus-encoded regulatory proteins is detected; however, they are excluded from the nucleus. ORF29p, a single-stranded DNA binding protein, is one of these latency-associated proteins. We searched for cell proteins that interact with ORF29p and identified BAG3. BAG3, Hsp70/Hsc70, and Hsp90 colocalize with ORF29p in nuclear transcription/replication factories during lytic replication of VZV. Pharmacological intercession of Hsp90 activity with ansamycin antibiotics or depletion of BAG3 by small interfering RNA results in inhibition of virus replication. Replication in BAG3-depleted cell lines is restored by complementation with exogenous BAG3. Alteration of host chaperone activity provides a novel means of regulating virus replication.
机译:水痘带状疱疹病毒(VZV)在宿主的背根神经节中建立终生潜伏感染。在潜伏期中,会检测到一部分病毒编码的调节蛋白。但是,它们被排除在原子核之外。 ORF29p是一种单链DNA结合蛋白,是与潜伏期相关的蛋白之一。我们搜索了与ORF29p相互作用的细胞蛋白并鉴定了BAG3。在VZV的裂解复制过程中,BAG3,Hsp70 / Hsc70和Hsp90与ORF29p在核转录/复制工厂中共定位。 Hsp90活性与安沙霉素抗生素的药理学代调或BAG3的小干扰RNA耗竭导致病毒复制受到抑制。通过与外源BAG3互补,可以恢复BAG3缺失的细胞系中的复制。宿主伴侣活性的改变提供了调节病毒复制的新手段。

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