CIRI - Centre International de Recherche en Infectiologie, Univ. Lyon, Université Claude Bernard Lyon 1, Lyon, France.
Laboratory P4-Jean Mérieux, Lyon, France.
Emerg Microbes Infect. 2024 Dec;13(1):2348508. doi: 10.1080/22221751.2024.2348508. Epub 2024 Jun 6.
The Crimean-Congo hemorrhagic fever virus (CCHFV) is a tick-borne bunyavirus that causes high mortality in humans. This enveloped virus harbors two surface glycoproteins (GP), Gn and Gc, that are released by processing of a glycoprotein precursor complex whose maturation takes place in the ER and is completed through the secretion pathway. Here, we characterized the trafficking network exploited by CCHFV GPs during viral assembly, envelopment, and/or egress. We identified membrane trafficking motifs in the cytoplasmic domains (CD) of CCHFV GPs and addressed how they impact these late stages of the viral life cycle using infection and biochemical assays, and confocal microscopy in virus-producing cells. We found that several of the identified CD motifs modulate GP transport through the retrograde trafficking network, impacting envelopment and secretion of infectious particles. Finally, we identified PACS-2 as a crucial host factor contributing to CCHFV GPs trafficking required for assembly and release of viral particles.
克里米亚-刚果出血热病毒(CCHFV)是一种蜱传布尼亚病毒,可导致人类死亡率很高。这种包膜病毒携带两种表面糖蛋白(GP),Gn 和 Gc,它们通过糖蛋白前体复合物的加工释放,该复合物的成熟发生在内质网中,并通过分泌途径完成。在这里,我们描述了 CCHFV GPs 在病毒组装、包膜和/或出芽过程中利用的运输网络。我们在 CCHFV GPs 的细胞质结构域(CD)中鉴定了膜运输基序,并使用感染和生化测定以及病毒产生细胞中的共聚焦显微镜来研究它们如何影响病毒生命周期的这些晚期阶段。我们发现,鉴定出的几个 CD 基序可调节 GP 通过逆行运输网络的运输,从而影响感染性颗粒的包膜和分泌。最后,我们确定 PACS-2 是一个关键的宿主因子,有助于 CCHFV GPs 的运输,这对于病毒颗粒的组装和释放是必需的。