Identification of broad anti-coronavirus chemical agents for repurposing against SARS-CoV-2 and variants of concern.
Drug synergy in vitro
Human coronavirus drug screen at single cell resolution in arrayed format
Human explant nasal and bronchial epithelial cells
Mycophenolic acid
Posaconazole
Post-entry coronavirus inhibition
Repurposing methylene blue
SARS-CoV-2 variants of concern
Journal
Current research in virological science
ISSN: 2666-478X
Titre abrégé: Curr Res Virol Sci
Pays: Netherlands
ID NLM: 101774440
Informations de publication
Date de publication:
2022
2022
Historique:
received:
13
12
2021
revised:
04
01
2022
accepted:
04
01
2022
pubmed:
25
1
2022
medline:
25
1
2022
entrez:
24
1
2022
Statut:
ppublish
Résumé
Endemic human coronaviruses (hCoVs) 229E and OC43 cause respiratory disease with recurrent infections, while severe acute respiratory syndrome (SARS)-CoV-2 spreads across the world with impact on health and societies. Here, we report an image-based multicycle infection procedure with α-coronavirus hCoV-229E-eGFP in an arrayed chemical library screen of 5440 clinical and preclinical compounds. Toxicity counter selection and challenge with the β-coronaviruses OC43 and SARS-CoV-2 in tissue culture and human airway epithelial explant cultures (HAEEC) identified four FDA-approved compounds with oral availability. Methylene blue (MB, used for the treatment of methemoglobinemia), Mycophenolic acid (MPA, used in organ transplantation) and the anti-fungal agent Posaconazole (POS) had the broadest anti-CoV spectrum. They inhibited the shedding of SARS-CoV-2 and variants-of-concern (alpha, beta, gamma, delta) from HAEEC in either pre- or post exposure regimens at clinically relevant concentrations. Co-treatment of cultured cells with MB and the FDA-approved SARS-CoV-2 RNA-polymerase inhibitor Remdesivir reduced the effective anti-viral concentrations of MB by 2-fold, and Remdesivir by 4 to 10-fold, indicated by BLISS independence synergy modelling. Neither MB, nor MPA, nor POS affected the cell delivery of SARS-CoV-2 or OC43 (+)sense RNA, but blocked subsequent viral RNA accumulation in cells. Unlike Remdesivir, MB, MPA or POS did not reduce the release of viral RNA in post exposure regimen, thus indicating infection inhibition at a post-replicating step as well. In summary, the data emphasize the power of unbiased, full cycle compound screens to identify and repurpose broadly acting drugs against coronaviruses.
Identifiants
pubmed: 35072124
doi: 10.1016/j.crviro.2022.100019
pii: S2666-478X(22)00001-0
pmc: PMC8760634
doi:
Types de publication
Journal Article
Langues
eng
Pagination
100019Informations de copyright
© 2022 The Authors.
Déclaration de conflit d'intérêts
The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: UFG has been a consultant and stock owner in 3V-Biosciences (now Sagimet Biosciences), a consultant to F. Hoffmann-La Roche Ltd and to Union Therapeutics A/S. The authors filed a patent application on the use of MPA for the treatment of COVID-19 (EP20213904, European Patent Office, University of Zurich).
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