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Enisamium Inhibits SARS-CoV-2 RNA Synthesis
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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8467925/ https://www.ncbi.nlm.nih.gov/pubmed/34572438 http://dx.doi.org/10.3390/biomedicines9091254 |
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author | Elli, Stefano Bojkova, Denisa Bechtel, Marco Vial, Thomas Boltz, David Muzzio, Miguel Peng, Xinjian Sala, Federico Cosentino, Cesare Goy, Andrew Guerrini, Marco Müller, Lutz Cinatl, Jindrich Margitich, Victor te Velthuis, Aartjan J. W. |
author_facet | Elli, Stefano Bojkova, Denisa Bechtel, Marco Vial, Thomas Boltz, David Muzzio, Miguel Peng, Xinjian Sala, Federico Cosentino, Cesare Goy, Andrew Guerrini, Marco Müller, Lutz Cinatl, Jindrich Margitich, Victor te Velthuis, Aartjan J. W. |
author_sort | Elli, Stefano |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8467925 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84679252021-09-27 Enisamium Inhibits SARS-CoV-2 RNA Synthesis Elli, Stefano Bojkova, Denisa Bechtel, Marco Vial, Thomas Boltz, David Muzzio, Miguel Peng, Xinjian Sala, Federico Cosentino, Cesare Goy, Andrew Guerrini, Marco Müller, Lutz Cinatl, Jindrich Margitich, Victor te Velthuis, Aartjan J. W. Biomedicines Article 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. MDPI 2021-09-17 /pmc/articles/PMC8467925/ /pubmed/34572438 http://dx.doi.org/10.3390/biomedicines9091254 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Elli, Stefano Bojkova, Denisa Bechtel, Marco Vial, Thomas Boltz, David Muzzio, Miguel Peng, Xinjian Sala, Federico Cosentino, Cesare Goy, Andrew Guerrini, Marco Müller, Lutz Cinatl, Jindrich Margitich, Victor te Velthuis, Aartjan J. W. Enisamium Inhibits SARS-CoV-2 RNA Synthesis |
title | Enisamium Inhibits SARS-CoV-2 RNA Synthesis |
title_full | Enisamium Inhibits SARS-CoV-2 RNA Synthesis |
title_fullStr | Enisamium Inhibits SARS-CoV-2 RNA Synthesis |
title_full_unstemmed | Enisamium Inhibits SARS-CoV-2 RNA Synthesis |
title_short | Enisamium Inhibits SARS-CoV-2 RNA Synthesis |
title_sort | enisamium inhibits sars-cov-2 rna synthesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8467925/ https://www.ncbi.nlm.nih.gov/pubmed/34572438 http://dx.doi.org/10.3390/biomedicines9091254 |
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