Division of Virology, Department of Pathology, University of Cambridge, Addenbrooke's Hospital, Hills Road, Cambridge, CB2 0QQ, UK.
Lewis Thomas Laboratory, Department of Molecular Biology, Princeton University, Washington Road, Princeton, 08544 NJ, USA.
Cell Mol Life Sci. 2021 Dec;78(23):7237-7256. doi: 10.1007/s00018-021-03957-w. Epub 2021 Oct 22.
Influenza A viruses cause a mild-to-severe respiratory disease that affects millions of people each year. One of the many determinants of disease outcome is the innate immune response to the viral infection. While antiviral responses are essential for viral clearance, excessive innate immune activation promotes lung damage and disease. The influenza A virus RNA polymerase is one of viral proteins that affect innate immune activation during infection, but the mechanisms behind this activity are not well understood. In this review, we discuss how the viral RNA polymerase can both activate and suppress innate immune responses by either producing immunostimulatory RNA species or directly targeting the components of the innate immune signalling pathway, respectively. Furthermore, we provide a comprehensive overview of the polymerase residues, and their mutations, associated with changes in innate immune activation, and discuss their putative effects on polymerase function based on recent advances in our understanding of the influenza A virus RNA polymerase structure.
甲型流感病毒可引起轻度至重度呼吸道疾病,每年影响数百万人。疾病结局的众多决定因素之一是对病毒感染的固有免疫反应。虽然抗病毒反应对于清除病毒至关重要,但过度的固有免疫激活会促进肺部损伤和疾病。甲型流感病毒 RNA 聚合酶是影响感染期间固有免疫激活的众多病毒蛋白之一,但该活性背后的机制尚不清楚。在这篇综述中,我们讨论了病毒 RNA 聚合酶如何通过产生免疫刺激性 RNA 种类或直接靶向固有免疫信号通路的成分,分别激活和抑制固有免疫反应。此外,我们还全面概述了与固有免疫激活变化相关的聚合酶残基及其突变,并根据我们对甲型流感病毒 RNA 聚合酶结构的最新理解,讨论了它们对聚合酶功能的潜在影响。