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High-Throughput Screening of an FDA-Approved Drug Library Identifies Inhibitors against Arenaviruses and SARS-CoV-2

Authors :
Gengfu Xiao
Ke Peng
Weiwei Wan
Hao Li
Shufen Li
Leike Zhang
Sheng-Lin Zhu
Weijuan Shang
Wei Liu
Ruxue Zhang
Source :
ACS Infectious Diseases
Publication Year :
2020
Publisher :
American Chemical Society (ACS), 2020.

Abstract

Arenaviruses are a large family of enveloped negative-strand RNA viruses that include several causative agents of severe hemorrhagic fevers. Currently, there are no FDA-licensed drugs to treat arenavirus infection except for the off-labeled use of ribavirin. Here, we performed antiviral drug screening against the Old World arenavirus lymphocytic choriomeningitis virus (LCMV) using an FDA-approved drug library. Five drug candidates were identified, including mycophenolic acid, benidipine hydrochloride, clofazimine, dabrafenib, and apatinib, for having strong anti-LCMV effects. Further analysis indicated that benidipine hydrochloride inhibited LCMV membrane fusion, and an adaptive mutation on the LCMV glycoprotein D414 site was found to antagonize the anti-LCMV activity of benidipine hydrochloride. Mycophenolic acid inhibited LCMV replication by depleting GTP production. We also found mycophenolic acid, clofazimine, dabrafenib, and apatinib can inhibit the newly emerged severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Owing to their FDA-approved status, these drug candidates can potentially be used rapidly in the clinical treatment of arenavirus and SARS-CoV-2 infection.

Details

ISSN :
23738227
Volume :
7
Database :
OpenAIRE
Journal :
ACS Infectious Diseases
Accession number :
edsair.doi.dedup.....4f09233ba9abc4a1137afc932f3df443
Full Text :
https://doi.org/10.1021/acsinfecdis.0c00486