State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing 100071, PR China.
J Gen Virol. 2010 May;91(Pt 5):1218-23. doi: 10.1099/vir.0.013854-0. Epub 2009 Dec 16.
RNA elements within the flavivirus genome may play essential regulatory roles during virus replication. Here, recombinant West Nile virus (WNV) NS5 protein was used in combination with WNV subgenomic RNA templates to establish in vitro RNA-dependent RNA polymerase and RNA-binding assays. These assays identified mutations in the stem-loop A (SLA) region of the 5' untranslated region (5'UTR) altering NS5 RNA synthesis and RNA-binding capability. These mutations were then introduced into the full-length WNV genome by reverse genetics. Further analysis of the mutant viruses showed that deletion of nt 46-60, which disrupted the stem and side loop of SLA, greatly compromised virus replication, whereas mutations that destroyed the top loop of SLA required for RNA synthesis in vitro did not significantly alter virus replication. These results suggest that SLA present in the 5'UTR of WNV is essential for RNA synthesis in vitro and for virus replication.
病毒基因组中的 RNA 元件可能在病毒复制过程中发挥重要的调节作用。在这里,我们使用重组西尼罗河病毒(WNV)NS5 蛋白与 WNV 亚基因组 RNA 模板结合,建立了体外 RNA 依赖性 RNA 聚合酶和 RNA 结合测定法。这些测定法鉴定了改变 NS5 RNA 合成和 RNA 结合能力的 5' 非翻译区(5'UTR)茎环 A(SLA)区域中的突变。然后,通过反向遗传学将这些突变引入全长 WNV 基因组中。对突变病毒的进一步分析表明,破坏 SLA 茎和侧环的 nt 46-60 缺失极大地削弱了病毒复制,而体外 RNA 合成所需的破坏 SLA 顶部环的突变则没有显著改变病毒复制。这些结果表明,WNV 5'UTR 中的 SLA 对于体外 RNA 合成和病毒复制是必需的。