Annamalai Padmanaban, Rofail Fady, Demason Darleen A, Rao A L N
University of California, Plant Pathology, 3264 Webber Hall, Riverside, CA 92521-0122, USA.
J Virol. 2008 Feb;82(3):1484-95. doi: 10.1128/JVI.01540-07. Epub 2007 Nov 21.
Flock house virus (FHV), a bipartite RNA virus of insects and a member of the Nodaviridae family, shares viral replication features with the tripartite brome mosaic virus (BMV), an RNA virus that infects plants and is a member of the Bromoviridae family. In BMV and FHV, genome packaging is coupled to replication, a widely conserved mechanism among positive-strand RNA viruses of diverse origin. To unravel the events that modulate the mechanism of replication-coupled packaging, in this study, we have extended the transfer DNA (T-DNA)-based agroinfiltration system to express functional genome components of FHV in plant cells (Nicotiana benthamiana). Replication, intracellular membrane localization, and packaging characteristics in agroinfiltrated plant cells revealed that T-DNA plasmids of FHV were biologically active and faithfully mimicked complete replication and packaging behavior similar to that observed for insect cells. Synchronized coexpression of wild-type BMV and FHV genome components in plant cells resulted in the assembly of virions packaging the respective viral progeny RNA. To further elucidate the link between replication and packaging, coat protein (CP) open reading frames were precisely exchanged between BMV RNA 3 (B3) and FHV RNA 2 (F2), creating chimeric RNAs expressing heterologous CP genes (B3/FCP and F2/BCP). Coinfiltration of each chimera with its corresponding genome counterpart to provide viral replicase (B1+B2+B3/FCP and F1+F2/BCP) resulted in the expected progeny profiles, but virions exhibited a nonspecific packaging phenotype. Complementation with homologous replicase (with respect to CP) failed to enhance packaging specificity. Taken together, we propose that the transcription of CP mRNA from homologous replication and its translation must be synchronized to confer packaging specificity.
禽 flock house 病毒(FHV)是一种昆虫双分体 RNA 病毒,属于野田村病毒科,它与感染植物的三分体雀麦花叶病毒(BMV)具有病毒复制特征,BMV 是一种 RNA 病毒,属于雀麦病毒科。在 BMV 和 FHV 中,基因组包装与复制相偶联,这是一种在不同来源的正链 RNA 病毒中广泛保守的机制。为了揭示调节复制偶联包装机制的事件,在本研究中,我们扩展了基于转移 DNA(T-DNA)的农杆菌浸润系统,以在植物细胞(本氏烟草)中表达 FHV 的功能性基因组组分。农杆菌浸润的植物细胞中的复制、细胞内膜定位和包装特征表明,FHV 的 T-DNA 质粒具有生物活性,并忠实地模拟了与昆虫细胞中观察到的类似的完整复制和包装行为。野生型 BMV 和 FHV 基因组组分在植物细胞中的同步共表达导致了包装各自病毒子代 RNA 的病毒粒子的组装。为了进一步阐明复制与包装之间的联系,在 BMV RNA 3(B3)和 FHV RNA 2(F2)之间精确交换了衣壳蛋白(CP)开放阅读框,产生了表达异源 CP 基因的嵌合 RNA(B3/FCP 和 F2/BCP)。将每个嵌合体与其相应的基因组对应物共浸润以提供病毒复制酶(B1+B2+B3/FCP 和 F1+F2/BCP),产生了预期的子代谱,但病毒粒子表现出非特异性包装表型。用同源复制酶(相对于 CP)进行互补未能增强包装特异性。综上所述,我们提出,来自同源复制的 CP mRNA 的转录及其翻译必须同步以赋予包装特异性。