病毒学
体外
RNA聚合酶
核糖核酸
病毒
冠状病毒
生物
聚合酶
2019年冠状病毒病(COVID-19)
疾病
传染病(医学专业)
基因
医学
生物化学
病理
作者
Stefano Elli,Denisa Bojková,Marco Bechtel,Thomas Vial,David A. Boltz,Miguel Muzzio,Xinjian Peng,F. Sala,Cesare Cosentino,Andrew Goy,Marco Guerrini,Lutz Müller,Jindřich Činátl,Victor Margitich,Aartjan J. W. te Velthuis
出处
期刊:Biomedicines
[MDPI AG]
日期:2021-09-17
卷期号:9 (9): 1254-1254
被引量:5
标识
DOI:10.3390/biomedicines9091254
摘要
Pandemic SARS-CoV-2 causes a mild to severe respiratory disease called coronavirus disease 2019 (COVID-19). While control of the SARS-CoV-2 spread partly depends on vaccine-induced or naturally acquired protective herd immunity, antiviral strategies are still needed to manage COVID-19. Enisamium is an inhibitor of influenza A and B viruses in cell culture and clinically approved in countries of the Commonwealth of Independent States. In vitro, enisamium acts through metabolite VR17-04 and inhibits the activity of the influenza A virus RNA polymerase. Here we show that enisamium can inhibit coronavirus infections in NHBE and Caco-2 cells, and the activity of the SARS-CoV-2 RNA polymerase in vitro. Docking and molecular dynamics simulations provide insight into the mechanism of action and indicate that enisamium metabolite VR17-04 prevents GTP and UTP incorporation. Overall, these results suggest that enisamium is an inhibitor of SARS-CoV-2 RNA synthesis in vitro.
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