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WDR5 通过促进衣壳核输出促进人类巨细胞病毒复制。

WDR5 Facilitates Human Cytomegalovirus Replication by Promoting Capsid Nuclear Egress.

机构信息

State Key Laboratory of Virology, CAS Center for Excellence in Brain Science and Intelligence Technology, Wuhan Institute of Virology, Wuhan, China.

University of Chinese Academy of Sciences, Beijing, China.

出版信息

J Virol. 2018 Apr 13;92(9). doi: 10.1128/JVI.00207-18. Print 2018 May 1.

Abstract

WD repeat-containing protein 5 (WDR5) is essential for assembling the VISA-associated complex to induce a type I interferon antiviral response to Sendai virus infection. However, the roles of WDR5 in DNA virus infections are not well described. Here, we report that human cytomegalovirus exploits WDR5 to facilitate capsid nuclear egress. Overexpression of WDR5 in fibroblasts slightly enhanced the infectious virus yield. However, WDR5 knockdown dramatically reduced infectious virus titers with only a small decrease in viral genome replication or gene expression. Further investigation of late steps of viral replication found that WDR5 knockdown significantly impaired formation of the viral nuclear egress complex and induced substantially fewer infoldings of the inner nuclear membrane. In addition, fewer capsids were associated with these infoldings, and there were fewer capsids in the cytoplasm. Restoration of WDR5 partially reversed these effects. These results suggest that WDR5 knockdown impairs the nuclear egress of capsids, which in turn decreases virus titers. These findings reveal an important role for a host factor whose function(s) is usurped by a viral pathogen to promote efficient replication. Thus, WDR5 represents an interesting regulatory mechanism and a potential antiviral target. Human cytomegalovirus (HCMV) has a large (∼235-kb) genome with over 170 open reading frames and exploits numerous cellular factors to facilitate its replication. HCMV infection increases protein levels of WD repeat-containing protein 5 (WDR5) during infection, overexpression of WDR5 enhances viral replication, and knockdown of WDR5 dramatically attenuates viral replication. Our results indicate that WDR5 promotes the nuclear egress of viral capsids, the depletion of WDR5 resulting in a significant decrease in production of infectious virions. This is the first report that WDR5 favors HCMV, a DNA virus, replication and highlights a novel target for antiviral therapy.

摘要

WD 重复蛋白 5(WDR5)对于组装与 VISA 相关的复合物以诱导对仙台病毒感染的 I 型干扰素抗病毒反应至关重要。然而,WDR5 在 DNA 病毒感染中的作用尚未得到很好的描述。在这里,我们报告人类巨细胞病毒利用 WDR5 促进衣壳核出芽。成纤维细胞中 WDR5 的过表达略微增强了感染性病毒的产量。然而,WDR5 的敲低极大地降低了感染性病毒滴度,而病毒基因组复制或基因表达只有很小的减少。对病毒复制的后期步骤的进一步研究发现,WDR5 的敲低显著损害了病毒核出芽复合物的形成,并导致内核膜的内折明显减少。此外,与这些内折相关的衣壳较少,细胞质中的衣壳也较少。WDR5 的恢复部分逆转了这些影响。这些结果表明,WDR5 的敲低会损害衣壳的核出芽,从而降低病毒滴度。这些发现揭示了宿主因子的重要作用,其功能被病毒病原体篡夺以促进有效的复制。因此,WDR5 代表了一种有趣的调节机制和潜在的抗病毒靶标。人巨细胞病毒(HCMV)具有一个大的(约 235-kb)基因组,有超过 170 个开放阅读框,并利用许多细胞因子来促进其复制。HCMV 感染会在感染过程中增加 WD 重复蛋白 5(WDR5)的蛋白水平,WDR5 的过表达增强病毒复制,WDR5 的敲低显著减弱病毒复制。我们的结果表明,WDR5 促进了病毒衣壳的核出芽,WDR5 的耗竭导致感染性病毒粒子的产量显著减少。这是第一个报道 WDR5 有利于 DNA 病毒 HCMV 复制的报告,并强调了抗病毒治疗的新靶标。

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