Enisamium Inhibits SARS-CoV-2 RNA Synthesis.
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Authors
Bojkova, Denisa
Bechtel, Marco
Vial, Thomas
Boltz, David
Muzzio, Miguel
Peng, Xinjian
Sala, Federico
Cosentino, Cesare
Goy, Andrew
Guerrini, Marco
Cinatl, Jindrich
Margitich, Victor
Publication Date
2021-09-17Journal Title
Biomedicines
ISSN
2227-9059
Publisher
MDPI AG
Volume
9
Issue
9
Language
eng
Type
Article
This Version
VoR
Metadata
Show full item recordCitation
Elli, S., Bojkova, D., Bechtel, M., Vial, T., Boltz, D., Muzzio, M., Peng, X., et al. (2021). Enisamium Inhibits SARS-CoV-2 RNA Synthesis.. Biomedicines, 9 (9) https://doi.org/10.3390/biomedicines9091254
Abstract
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.
Keywords
Amizon, COVID-19, FAV00A, RNA polymerase, SARS-CoV-2, molecular dynamics simulation
Sponsorship
ZonMw (10430 01 201 0018)
Wellcome Trust (206579/Z/17/Z)
Identifiers
PMC8467925, 34572438
External DOI: https://doi.org/10.3390/biomedicines9091254
This record's URL: https://www.repository.cam.ac.uk/handle/1810/330091
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