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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Main Authors: Supasek Kongsomros, Ampa Suksatu, Phongthon Kanjanasirirat, Suwimon Manopwisedjaroen, Somsak Prasongtanakij, Kedchin Jearawuttanakul, Suparerk Borwornpinyo, Suradej Hongeng, Arunee Thitithanyanont, Somchai Chutipongtanate
Other Authors: Faculty of Medicine Ramathibodi Hospital, Mahidol University
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Published: 2022
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/76038
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spelling 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
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Biochemistry, Genetics and Molecular Biology
Medicine
spellingShingle 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
description 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.
author2 Faculty of Medicine Ramathibodi Hospital, Mahidol University
author_facet 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
format Article
author Supasek Kongsomros
Ampa Suksatu
Phongthon Kanjanasirirat
Suwimon Manopwisedjaroen
Somsak Prasongtanakij
Kedchin Jearawuttanakul
Suparerk Borwornpinyo
Suradej Hongeng
Arunee Thitithanyanont
Somchai Chutipongtanate
author_sort 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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