Sir William Dunn School of Pathology, University of Oxford, Oxford, UK.
Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.
Nat Microbiol. 2019 Nov;4(11):1781-1789. doi: 10.1038/s41564-019-0513-7. Epub 2019 Jul 22.
Influenza A viruses (IAVs) constitute a major threat to human health. The IAV genome consists of eight single-stranded viral RNA segments contained in separate viral ribonucleoprotein (vRNP) complexes that are packaged together into a single virus particle. The structure of viral RNA is believed to play a role in assembling the different vRNPs into budding virions and in directing reassortment between IAVs. Reassortment between established human IAVs and IAVs harboured in the animal reservoir can lead to the emergence of pandemic influenza strains to which there is little pre-existing immunity in the human population. While previous studies have revealed the overall organization of the proteins within vRNPs, characterization of viral RNA structure using conventional structural methods is hampered by limited resolution and an inability to resolve dynamic components. Here, we employ multiple high-throughput sequencing approaches to generate a global high-resolution structure of the IAV genome. We show that different IAV genome segments acquire distinct RNA conformations and form both intra- and intersegment RNA interactions inside influenza virions. We use our detailed map of IAV genome structure to provide direct evidence for how intersegment RNA interactions drive vRNP cosegregation during reassortment between different IAV strains. The work presented here is a roadmap both for the development of improved vaccine strains and for the creation of a framework to 'risk assess' reassortment potential to better predict the emergence of new pandemic influenza strains.
甲型流感病毒(IAV)对人类健康构成重大威胁。IAV 基因组由八个单链病毒 RNA 片段组成,这些片段包含在单独的病毒核糖核蛋白(vRNP)复合物中,并包装在单个病毒粒子中。病毒 RNA 的结构被认为在将不同的 vRNPs 组装成芽生病毒粒子以及在指导 IAV 之间重配方面发挥作用。已建立的人源 IAV 与动物库中携带的 IAV 之间的重配可导致大流行性流感株的出现,而人类对此种病毒株几乎没有预先存在的免疫力。虽然先前的研究已经揭示了 vRNPs 中蛋白质的总体组织,但使用常规结构方法对病毒 RNA 结构进行特征描述受到分辨率有限和无法解析动态成分的阻碍。在这里,我们采用多种高通量测序方法来生成 IAV 基因组的全局高分辨率结构。我们表明,不同的 IAV 基因组片段获得不同的 RNA 构象,并在流感病毒粒子内形成内部和片段间的 RNA 相互作用。我们使用我们对 IAV 基因组结构的详细图谱来提供直接证据,证明片段间 RNA 相互作用如何在不同 IAV 株之间的重配过程中驱动 vRNP 共分离。这里介绍的工作为开发改进的疫苗株以及创建“风险评估”重配潜力的框架提供了路线图,以更好地预测新的大流行性流感株的出现。