病毒学
大流行
生物
体外
甲型流感病毒
病毒
病毒复制
聚合酶
人流感
复制(统计)
疾病
解热药
正粘病毒科
微生物学
大流行性流感
免疫学
聚合酶链反应
H5N1亚型流感病毒
病毒性疾病
流感大流行
抗病毒治疗
高致病性
H5N1基因结构
作者
Matthew L. Turnbull,Yingxue Wang,Simon Clare,Gauthier Lieber,Stephanie L. Williams,Marko Noerenberg,Akira J T Alexander,Sara Clohisey Hendry,Douglas G Stewart,Joseph Hughes,Simon Swingler,Spyros Lytras,Emma L Davies,Katherine Harcourt,Katherine Smollett,Rute M. Pinto,Hui-Min Lee,Eleanor R. Gaunt,Colin Loney,Johanna S. Jung
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2025-11-27
卷期号:390 (6776)
标识
DOI:10.1126/science.adq4691
摘要
Host body temperature can define a virus’s replicative profile—influenza A viruses (IAVs) adapted to 40° to 42°C in birds are less temperature sensitive in vitro compared with human isolates adapted to 33° to 37°C. In this work, we show that avian-origin PB1 polymerase subunits enable IAV replication at elevated temperatures, including avian-origin PB1s from the 1918, 1957, and 1968 pandemic viruses. Using a model system to ensure biosafety, we show that a small increase in body temperature protects against severe disease in mice and that this protection is overcome by a febrile temperature–resistant PB1. These findings indicate that although elevated temperature itself can be a potent antiviral defense, it may not be effective against all influenza strains. These data inform both the clinical use of antipyretics and IAV surveillance efforts.
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