共感染
病毒学
病毒复制
奥司他韦
甲型流感病毒
生物
病毒
干扰素
免疫学
微生物学
医学
2019年冠状病毒病(COVID-19)
病理
传染病(医学专业)
疾病
作者
Nagarjuna R. Cheemarla,Timothy A. Watkins,Valia T. Mihaylova,Ellen F. Foxman
标识
DOI:10.1093/infdis/jiad402
摘要
To gain insight into interactions among respiratory viruses, we modeled influenza A virus (IAV) - SARS-CoV-2 coinfections using differentiated human airway epithelial cultures. Replicating IAV induced a more robust interferon response than SARS-CoV-2 and suppressed SARS-CoV-2 replication in both sequential and simultaneous infections, whereas SARS-CoV-2 did not enhance host cell defense during influenza infection or suppress IAV replication. Oseltamivir, an antiviral targeting influenza, reduced IAV replication during coinfection but also reduced the host antiviral response and restored SARS-CoV-2 replication. These results demonstrate how perturbations in one viral infection can impact its effect on a coinfecting virus.
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