开发 A 种轮状病毒的微基因组检测方法

Viruses Pub Date : 2024-08-31 DOI:10.3390/v16091396
Ola Diebold, Shu Zhou, Colin Peter Sharp, Blanka Tesla, Hou Wei Chook, Paul Digard, Eleanor R. Gaunt
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引用次数: 0

摘要

RNA 病毒聚合酶具有成功复制和转录基因组所需的多种功能。对病毒 RNA 依赖性 RNA 聚合酶(RdRps)进行分子研究的一个重要工具是 "小基因组 "或 "小复制子 "试验,在这种试验中,病毒 RdRps 在没有完全感染病毒的情况下在细胞中重组。通常,表达病毒聚合酶蛋白和其他辅助因子的质粒与表达编码荧光或发光报告基因的 RNA 的质粒共同转染,RNA 的两侧是病毒的非翻译区,其中含有病毒 RdRp 识别所需的顺式作用元件。这样就重建了病毒转录/复制机制,并能通过报告蛋白信号的相关性来测量病毒 RdRp 的活性。在此,我们报告了利用萤火虫荧光素酶报告基因开发的基于质粒的 "第一代 "甲型轮状病毒迷你基因组检测方法。
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Towards the Development of a Minigenome Assay for Species A Rotaviruses
RNA virus polymerases carry out multiple functions necessary for successful genome replication and transcription. A key tool for molecular studies of viral RNA-dependent RNA polymerases (RdRps) is a ‘minigenome’ or ‘minireplicon’ assay, in which viral RdRps are reconstituted in cells in the absence of full virus infection. Typically, plasmids expressing the viral polymerase protein(s) and other co-factors are co-transfected, along with a plasmid expressing an RNA encoding a fluorescent or luminescent reporter gene flanked by viral untranslated regions containing cis-acting elements required for viral RdRp recognition. This reconstitutes the viral transcription/replication machinery and allows the viral RdRp activity to be measured as a correlate of the reporter protein signal. Here, we report on the development of a ‘first-generation’ plasmid-based minigenome assay for species A rotavirus using a firefly luciferase reporter gene.
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