首页> 外文OA文献 >Replication-Coupled Packaging Mechanism in Positive-Strand RNA Viruses: Synchronized Coexpression of Functional Multigenome RNA Components of an Animal and a Plant Virus in Nicotiana benthamiana Cells by Agroinfiltration▿
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Replication-Coupled Packaging Mechanism in Positive-Strand RNA Viruses: Synchronized Coexpression of Functional Multigenome RNA Components of an Animal and a Plant Virus in Nicotiana benthamiana Cells by Agroinfiltration▿

机译:正链RNA病毒中的复制耦合包装机制:通过农杆菌浸润在本氏烟草细胞中动物和植物病毒的功能性多基因组RNA组分同步共表达▿

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摘要

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.
机译:蜂房病毒(FHV)是昆虫的双分子RNA病毒,是野病毒科(Nodaviridae)的成员,它与感染植物的RNA病毒-三重溴花叶病毒(BMV)具有病毒复制功能,并且是Bromoviridae家族的成员。在BMV和FHV中,基因组包装与复制相关联,复制是多种来源的正链RNA病毒之间广泛保存的机制。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)的农业浸润系统,以在植物细胞(烟草(Nicotiana benthamiana))中表达FHV的功能基因组成分。农杆菌浸润的植物细胞中的复制,细胞内膜定位和包装特性表明FHV的T-DNA质粒具有生物学活性,忠实地模仿了完整的复制和包装行为,类似于昆虫细胞所观察到的。植物细胞中野生型BMV和FHV基因组组件的同步共表达导致包装各个病毒后代RNA的病毒体组装。为了进一步阐明复制和包装之间的联系,外壳蛋白(CP)的开放阅读框在BMV RNA 3(B3)和FHV RNA 2(F2)之间精确交换,从而产生表达异源CP基因的嵌合RNA(B3 / FCP和F2 / BCP)。每个嵌合体与其对应的基因组对应物的共渗以提供病毒复制酶(B1 + B2 + B3 / FCP和F1 + F2 / BCP)导致了预期的后代分布,但病毒体表现出非特异性包装表型。与同源复制酶(相对于CP)的互补不能增强包装特异性。两者合计,我们建议从同源复制CP mRNA的转录及其翻译必须同步以赋予包装特异性。

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