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Screening of FDA-Approved Drugs Using a MERS-CoV Clinical Isolate from South Korea Identifies Potential Therapeutic Options for COVID-19
Therapeutic options for coronaviruses remain limited. To address this unmet medical need, we screened 5406 compounds, including United States Food and Drug Administration (FDA)-approved drugs and bioactives, for activity against a South Korean Middle East respiratory syndrome coronavirus (MERS-CoV)...
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/PMC8069929/ https://www.ncbi.nlm.nih.gov/pubmed/33918958 http://dx.doi.org/10.3390/v13040651 |
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author | Ko, Meehyun Chang, So Young Byun, Soo Young Ianevski, Aleksandr Choi, Inhee Pham Hung d’Alexandry d’Orengiani, Anne-Laure Ravlo, Erlend Wang, Wei Bjørås, Magnar Kainov, Denis E. Shum, David Min, Ji-Young Windisch, Marc P. |
author_facet | Ko, Meehyun Chang, So Young Byun, Soo Young Ianevski, Aleksandr Choi, Inhee Pham Hung d’Alexandry d’Orengiani, Anne-Laure Ravlo, Erlend Wang, Wei Bjørås, Magnar Kainov, Denis E. Shum, David Min, Ji-Young Windisch, Marc P. |
author_sort | Ko, Meehyun |
collection | PubMed |
description | Therapeutic options for coronaviruses remain limited. To address this unmet medical need, we screened 5406 compounds, including United States Food and Drug Administration (FDA)-approved drugs and bioactives, for activity against a South Korean Middle East respiratory syndrome coronavirus (MERS-CoV) clinical isolate. Among 221 identified hits, 54 had therapeutic indexes (TI) greater than 6, representing effective drugs. The time-of-addition studies with selected drugs demonstrated eight and four FDA-approved drugs which acted on the early and late stages of the viral life cycle, respectively. Confirmed hits included several cardiotonic agents (TI > 100), atovaquone, an anti-malarial (TI > 34), and ciclesonide, an inhalable corticosteroid (TI > 6). Furthermore, utilizing the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), we tested combinations of remdesivir with selected drugs in Vero-E6 and Calu-3 cells, in lung organoids, and identified ciclesonide, nelfinavir, and camostat to be at least additive in vitro. Our results identify potential therapeutic options for MERS-CoV infections, and provide a basis to treat coronavirus disease 2019 (COVID-19) and other coronavirus-related illnesses. |
format | Online Article Text |
id | pubmed-8069929 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80699292021-04-26 Screening of FDA-Approved Drugs Using a MERS-CoV Clinical Isolate from South Korea Identifies Potential Therapeutic Options for COVID-19 Ko, Meehyun Chang, So Young Byun, Soo Young Ianevski, Aleksandr Choi, Inhee Pham Hung d’Alexandry d’Orengiani, Anne-Laure Ravlo, Erlend Wang, Wei Bjørås, Magnar Kainov, Denis E. Shum, David Min, Ji-Young Windisch, Marc P. Viruses Article Therapeutic options for coronaviruses remain limited. To address this unmet medical need, we screened 5406 compounds, including United States Food and Drug Administration (FDA)-approved drugs and bioactives, for activity against a South Korean Middle East respiratory syndrome coronavirus (MERS-CoV) clinical isolate. Among 221 identified hits, 54 had therapeutic indexes (TI) greater than 6, representing effective drugs. The time-of-addition studies with selected drugs demonstrated eight and four FDA-approved drugs which acted on the early and late stages of the viral life cycle, respectively. Confirmed hits included several cardiotonic agents (TI > 100), atovaquone, an anti-malarial (TI > 34), and ciclesonide, an inhalable corticosteroid (TI > 6). Furthermore, utilizing the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), we tested combinations of remdesivir with selected drugs in Vero-E6 and Calu-3 cells, in lung organoids, and identified ciclesonide, nelfinavir, and camostat to be at least additive in vitro. Our results identify potential therapeutic options for MERS-CoV infections, and provide a basis to treat coronavirus disease 2019 (COVID-19) and other coronavirus-related illnesses. MDPI 2021-04-09 /pmc/articles/PMC8069929/ /pubmed/33918958 http://dx.doi.org/10.3390/v13040651 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 Ko, Meehyun Chang, So Young Byun, Soo Young Ianevski, Aleksandr Choi, Inhee Pham Hung d’Alexandry d’Orengiani, Anne-Laure Ravlo, Erlend Wang, Wei Bjørås, Magnar Kainov, Denis E. Shum, David Min, Ji-Young Windisch, Marc P. Screening of FDA-Approved Drugs Using a MERS-CoV Clinical Isolate from South Korea Identifies Potential Therapeutic Options for COVID-19 |
title | Screening of FDA-Approved Drugs Using a MERS-CoV Clinical Isolate from South Korea Identifies Potential Therapeutic Options for COVID-19 |
title_full | Screening of FDA-Approved Drugs Using a MERS-CoV Clinical Isolate from South Korea Identifies Potential Therapeutic Options for COVID-19 |
title_fullStr | Screening of FDA-Approved Drugs Using a MERS-CoV Clinical Isolate from South Korea Identifies Potential Therapeutic Options for COVID-19 |
title_full_unstemmed | Screening of FDA-Approved Drugs Using a MERS-CoV Clinical Isolate from South Korea Identifies Potential Therapeutic Options for COVID-19 |
title_short | Screening of FDA-Approved Drugs Using a MERS-CoV Clinical Isolate from South Korea Identifies Potential Therapeutic Options for COVID-19 |
title_sort | screening of fda-approved drugs using a mers-cov clinical isolate from south korea identifies potential therapeutic options for covid-19 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8069929/ https://www.ncbi.nlm.nih.gov/pubmed/33918958 http://dx.doi.org/10.3390/v13040651 |
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