Department of BioSciences, Rice University, Houston, Texas, USA.
Department of BioSciences, Rice University, Houston, Texas, USA
J Virol. 2018 Jun 29;92(14). doi: 10.1128/JVI.00745-18. Print 2018 Jul 15.
Nonenveloped gastrointestinal viruses, such as human rotavirus, can exit infected cells from the apical surface without cell lysis. The mechanism of such nonlytic exit is poorly understood. The nonenveloped Orsay virus is an RNA virus infecting the intestine cells of the nematode Dye staining results suggested that Orsay virus exits from the intestine of infected worms in a nonlytic manner. Therefore, the Orsay virus- system provides an excellent model to study viral exit. The Orsay virus genome encodes three proteins: RNA-dependent RNA polymerase, capsid protein (CP), and a nonstructural protein, δ. δ can also be expressed as a structural CP-δ fusion. We generated an ATG-to-CTG mutant virus that had a normal CP-δ fusion but could not produce free δ due to the lack of the start codon. This mutant virus showed a viral exit defect without obvious phenotypes in other steps of viral infection, suggesting that δ is involved in viral exit. Ectopically expressed free δ localized near the apical membrane of intestine cells in and colocalized with ACT-5, an intestine-specific actin that is a component of the terminal web. Orsay virus infection rearranged ACT-5 apical localization. Reduction of the ACT-5 level via RNA interference (RNAi) significantly exacerbated the viral exit defect of the δ mutant virus, suggesting that δ and ACT-5 functionally interact to promote Orsay virus exit. Together, these data support a model in which the viral δ protein interacts with the actin network at the apical side of host intestine cells to mediate the polarized, nonlytic egress of Orsay virus. An important step of the viral life cycle is how viruses exit from host cells to spread to other cells. Certain nonenveloped viruses can exit cultured cells in nonlytic ways; however, such nonlytic exit has not been demonstrated In addition, it is not clear how such nonlytic exit is achieved mechanistically Orsay virus is a nonenveloped RNA virus that infects the intestine cells of the nematode It is currently the only virus known to naturally infect Using this model, we show that the δ protein encoded by Orsay virus facilitates the nonlytic exit of the virus, possibly by interacting with host actin on the apical side of worm intestine cells.
无包膜的胃肠道病毒,如人类轮状病毒,可以从感染细胞的顶表面无细胞裂解而离开。这种非裂解性的离开机制尚未完全了解。无包膜的Orsay 病毒是一种感染线虫肠道细胞的 RNA 病毒。吉姆萨染色结果表明,Orsay 病毒以非裂解的方式从感染蠕虫的肠道中逸出。因此,Orsay 病毒系统为研究病毒逸出提供了一个极好的模型。Orsay 病毒基因组编码三种蛋白:RNA 依赖性 RNA 聚合酶、衣壳蛋白 (CP) 和一种非结构蛋白 δ。δ 也可以作为结构 CP-δ 融合蛋白表达。我们生成了一个 ATG 到 CTG 的突变病毒,该病毒有一个正常的 CP-δ 融合,但由于缺乏起始密码子,不能产生游离的 δ。该突变病毒在病毒感染的其他步骤中没有明显表型,但表现出病毒逸出缺陷,表明 δ 参与了病毒逸出。异位表达的游离 δ 定位于线虫肠道细胞的顶膜附近,并与 ACT-5 共定位,ACT-5 是肠特异性肌动蛋白,是终末网的组成部分。Orsay 病毒感染使 ACT-5 在上皮的定位发生重排。通过 RNA 干扰 (RNAi) 降低 ACT-5 水平显著加剧了 δ 突变病毒的病毒逸出缺陷,表明 δ 和 ACT-5 以功能相互作用促进 Orsay 病毒的出芽。综上所述,这些数据支持一种模型,即病毒 δ 蛋白与宿主肠细胞顶侧的肌动蛋白网络相互作用,从而介导 Orsay 病毒的极化、非裂解性出芽。病毒生命周期的一个重要步骤是病毒如何从宿主细胞中逸出并传播到其他细胞。某些无包膜病毒可以以非裂解的方式从培养的细胞中逸出;然而,这种非裂解性的逸出尚未被证明。此外,其机制尚不清楚。Orsay 病毒是一种感染线虫肠道细胞的无包膜 RNA 病毒。它是目前已知的唯一一种自然感染秀丽隐杆线虫的病毒。使用这个模型,我们表明 Orsay 病毒编码的 δ 蛋白通过与线虫肠道细胞顶侧的宿主肌动蛋白相互作用,促进病毒的非裂解性逸出。