Anti-SARS-CoV-2 activity of extracellular vesicle inhibitors: Screening, validation, and combination with remdesivir
The coronavirus disease 2019 (COVID-19) pandemic severely impacts health, economy, and society worldwide. Antiviral drugs against SARS-CoV-2 are urgently needed to cope with this global crisis. It has been found that the biogenesis and release mechanisms of viruses share a common pathway with extrac...
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th-mahidol.760382022-08-04T16:13:31Z Anti-SARS-CoV-2 activity of extracellular vesicle inhibitors: Screening, validation, and combination with remdesivir Supasek Kongsomros Ampa Suksatu Phongthon Kanjanasirirat Suwimon Manopwisedjaroen Somsak Prasongtanakij Kedchin Jearawuttanakul Suparerk Borwornpinyo Suradej Hongeng Arunee Thitithanyanont Somchai Chutipongtanate Faculty of Medicine Ramathibodi Hospital, Mahidol University Mahidol University Biochemistry, Genetics and Molecular Biology Medicine The coronavirus disease 2019 (COVID-19) pandemic severely impacts health, economy, and society worldwide. Antiviral drugs against SARS-CoV-2 are urgently needed to cope with this global crisis. It has been found that the biogenesis and release mechanisms of viruses share a common pathway with extracellular vesicles (EVs). We hypothesized that small molecule inhibitors of EV biogenesis/release could exert an anti-SARS-CoV-2 effect. Here, we screened 17 existing EV inhibitors and found that calpeptin, a cysteine proteinase inhibitor, exhibited the most potent anti-SARS-CoV-2 activity with no apparent cytotoxicity. Calpeptin demonstrated the dose-dependent inhibition against SARS-CoV-2 viral nucleoprotein expression in the infected cells with a half-maximal inhibitory concentration (IC50) of 1.44 µM in Vero-E6 and 26.92 µM in Calu-3 cells, respectively. Moreover, calpeptin inhibited the production of infectious virions with the lower IC50 of 0.6 µM in Vero E6 cells and 10.12 µM in Calu-3 cells. Interestingly, a combination of calpeptin and remdesivir, the FDA-approved antiviral drug against SARS-CoV-2 viral replication, significantly enhanced the anti-SARS-CoV-2 effects compared to monotherapy. This study discovered calpeptin as a promising candidate for anti-SARS-CoV-2 drug development. Further preclinical and clinical studies are warranted to elucidate the therapeutic efficacy of calpeptin and remdesivir combination in COVID-19. 2022-08-04T08:05:57Z 2022-08-04T08:05:57Z 2021-09-01 Article Biomedicines. Vol.9, No.9 (2021) 10.3390/biomedicines9091230 22279059 2-s2.0-85115237073 https://repository.li.mahidol.ac.th/handle/123456789/76038 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85115237073&origin=inward |
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Biochemistry, Genetics and Molecular Biology Medicine Supasek Kongsomros Ampa Suksatu Phongthon Kanjanasirirat Suwimon Manopwisedjaroen Somsak Prasongtanakij Kedchin Jearawuttanakul Suparerk Borwornpinyo Suradej Hongeng Arunee Thitithanyanont Somchai Chutipongtanate Anti-SARS-CoV-2 activity of extracellular vesicle inhibitors: Screening, validation, and combination with remdesivir |
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The coronavirus disease 2019 (COVID-19) pandemic severely impacts health, economy, and society worldwide. Antiviral drugs against SARS-CoV-2 are urgently needed to cope with this global crisis. It has been found that the biogenesis and release mechanisms of viruses share a common pathway with extracellular vesicles (EVs). We hypothesized that small molecule inhibitors of EV biogenesis/release could exert an anti-SARS-CoV-2 effect. Here, we screened 17 existing EV inhibitors and found that calpeptin, a cysteine proteinase inhibitor, exhibited the most potent anti-SARS-CoV-2 activity with no apparent cytotoxicity. Calpeptin demonstrated the dose-dependent inhibition against SARS-CoV-2 viral nucleoprotein expression in the infected cells with a half-maximal inhibitory concentration (IC50) of 1.44 µM in Vero-E6 and 26.92 µM in Calu-3 cells, respectively. Moreover, calpeptin inhibited the production of infectious virions with the lower IC50 of 0.6 µM in Vero E6 cells and 10.12 µM in Calu-3 cells. Interestingly, a combination of calpeptin and remdesivir, the FDA-approved antiviral drug against SARS-CoV-2 viral replication, significantly enhanced the anti-SARS-CoV-2 effects compared to monotherapy. This study discovered calpeptin as a promising candidate for anti-SARS-CoV-2 drug development. Further preclinical and clinical studies are warranted to elucidate the therapeutic efficacy of calpeptin and remdesivir combination in COVID-19. |
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Faculty of Medicine Ramathibodi Hospital, Mahidol University |
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Faculty of Medicine Ramathibodi Hospital, Mahidol University Supasek Kongsomros Ampa Suksatu Phongthon Kanjanasirirat Suwimon Manopwisedjaroen Somsak Prasongtanakij Kedchin Jearawuttanakul Suparerk Borwornpinyo Suradej Hongeng Arunee Thitithanyanont Somchai Chutipongtanate |
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Article |
author |
Supasek Kongsomros Ampa Suksatu Phongthon Kanjanasirirat Suwimon Manopwisedjaroen Somsak Prasongtanakij Kedchin Jearawuttanakul Suparerk Borwornpinyo Suradej Hongeng Arunee Thitithanyanont Somchai Chutipongtanate |
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Supasek Kongsomros |
title |
Anti-SARS-CoV-2 activity of extracellular vesicle inhibitors: Screening, validation, and combination with remdesivir |
title_short |
Anti-SARS-CoV-2 activity of extracellular vesicle inhibitors: Screening, validation, and combination with remdesivir |
title_full |
Anti-SARS-CoV-2 activity of extracellular vesicle inhibitors: Screening, validation, and combination with remdesivir |
title_fullStr |
Anti-SARS-CoV-2 activity of extracellular vesicle inhibitors: Screening, validation, and combination with remdesivir |
title_full_unstemmed |
Anti-SARS-CoV-2 activity of extracellular vesicle inhibitors: Screening, validation, and combination with remdesivir |
title_sort |
anti-sars-cov-2 activity of extracellular vesicle inhibitors: screening, validation, and combination with remdesivir |
publishDate |
2022 |
url |
https://repository.li.mahidol.ac.th/handle/123456789/76038 |
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1763494473219702784 |