Hornak Katherine E, Lanchy Jean-Marc, Lodmell J Stephen
Division of Biological Sciences, University of Montana, Missoula, MT 59812, USA.
Center for Biomolecular Structure and Dynamics, University of Montana, Missoula, MT 59812, USA.
Viruses. 2016 Jul 15;8(7):194. doi: 10.3390/v8070194.
The Bunyaviridae represents the largest family of segmented RNA viruses, which infect a staggering diversity of plants, animals, and insects. Within the family Bunyaviridae, the Phlebovirus genus includes several important human and animal pathogens, including Rift Valley fever virus (RVFV), severe fever with thrombocytopenia syndrome virus (SFTSV), Uukuniemi virus (UUKV), and the sandfly fever viruses. The phleboviruses have small tripartite RNA genomes that encode a repertoire of 5-7 proteins. These few proteins accomplish the daunting task of recognizing and specifically packaging a tri-segment complement of viral genomic RNA in the midst of an abundance of host components. The critical nucleation events that eventually lead to virion production begin early on in the host cytoplasm as the first strands of nascent viral RNA (vRNA) are synthesized. The interaction between the vRNA and the viral nucleocapsid (N) protein effectively protects and masks the RNA from the host, and also forms the ribonucleoprotein (RNP) architecture that mediates downstream interactions and drives virion formation. Although the mechanism by which all three genomic counterparts are selectively co-packaged is not completely understood, we are beginning to understand the hierarchy of interactions that begins with N-RNA packaging and culminates in RNP packaging into new virus particles. In this review we focus on recent progress that highlights the molecular basis of RNA genome packaging in the phleboviruses.
布尼亚病毒科是最大的分节段RNA病毒家族,可感染种类惊人的植物、动物和昆虫。在布尼亚病毒科中,白蛉病毒属包括几种重要的人类和动物病原体,如裂谷热病毒(RVFV)、严重发热伴血小板减少综合征病毒(SFTSV)、乌昆耶米病毒(UUKV)以及白蛉热病毒。白蛉病毒具有小型的三分体RNA基因组,可编码5至7种蛋白质。这几种蛋白质要在大量宿主成分存在的情况下,完成识别并特异性包装病毒基因组RNA三分体互补序列这一艰巨任务。随着新生病毒RNA(vRNA)的第一条链合成,最终导致病毒粒子产生的关键成核事件在宿主细胞质中很早就开始了。vRNA与病毒核衣壳(N)蛋白之间的相互作用有效地保护并屏蔽RNA免受宿主影响,还形成了介导下游相互作用并驱动病毒粒子形成的核糖核蛋白(RNP)结构。尽管目前尚不完全清楚所有三个基因组对应物如何被选择性地共同包装,但我们开始了解从N-RNA包装开始、以RNP包装进新病毒颗粒告终的相互作用层次结构。在本综述中,我们重点关注突出白蛉病毒RNA基因组包装分子基础的最新进展。