Molecular Biophysics, Department for Biology, IRI Life Sciences, Humboldt-Universität zu Berlin, Invalidenstr. 42, 10115, Berlin, Germany.
Crystallography, Max Delbrück Center for Molecular Medicine, Robert-Rössle Str. 10, 13125, Berlin, Germany.
Nat Commun. 2020 Aug 28;11(1):4355. doi: 10.1038/s41467-020-18108-1.
The genome of influenza A viruses (IAV) is encoded in eight distinct viral ribonucleoproteins (vRNPs) that consist of negative sense viral RNA (vRNA) covered by the IAV nucleoprotein. Previous studies strongly support a selective packaging model by which vRNP segments are bundling to an octameric complex, which is integrated into budding virions. However, the pathway(s) generating a complete genome bundle is not known. We here use a multiplexed FISH assay to monitor all eight vRNAs in parallel in human lung epithelial cells. Analysis of 3.9 × 10 spots of colocalizing vRNAs provides quantitative insights into segment composition of vRNP complexes and, thus, implications for bundling routes. The complexes rarely contain multiple copies of a specific segment. The data suggest a selective packaging mechanism with limited flexibility by which vRNPs assemble into a complete IAV genome. We surmise that this flexibility forms an essential basis for the development of reassortant viruses with pandemic potential.
甲型流感病毒 (IAV) 的基因组编码在八个不同的病毒核糖核蛋白 (vRNP) 中,这些 vRNP 由负义病毒 RNA (vRNA) 组成,vRNA 被 IAV 核蛋白覆盖。先前的研究强烈支持一种选择包装模型,即 vRNP 片段聚集形成八聚体复合物,然后整合到出芽病毒中。然而,形成完整基因组包裹的途径尚不清楚。我们在这里使用多重 FISH 分析技术在人肺上皮细胞中同时监测所有八个 vRNA。对 3.9×10 个共定位 vRNA 斑点的分析提供了关于 vRNP 复合物片段组成的定量见解,从而对包裹途径产生了影响。复合物很少包含多个特定片段的拷贝。数据表明,vRNPs 以一种选择包装机制组装成完整的 IAV 基因组,这种机制的选择性强,灵活性有限。我们推测,这种灵活性为具有大流行潜力的重配病毒的发展提供了重要基础。