4.6 Article

Screening of FDA-Approved Drugs Using a MERS-CoV Clinical Isolate from South Korea Identifies Potential Therapeutic Options for COVID-19

Journal

VIRUSES-BASEL
Volume 13, Issue 4, Pages -

Publisher

MDPI
DOI: 10.3390/v13040651

Keywords

Middle East respiratory syndrome coronavirus; severe acute respiratory syndrome coronavirus disease; clinical isolate; high-content screening; FDA-approved drugs; drug repurposing; drug combinations; lung organoids; COVID-19; pandemic

Categories

Funding

  1. National Research Foundation (NRF) of Korea - Ministry of Science and ICT [2016M3A9B6918984, 2017M3A9G6068245, 2017M3A9G6068246]
  2. European Regional Development Fund, the Mobilitas Pluss Project [MOBTT39]
  3. National Research Foundation of Korea [2016M3A9B6918984] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study identified potential therapeutic options for MERS-CoV infections and suggested basis for treating COVID-19 and other coronavirus-related illnesses by screening a variety of compounds, including existing drugs and bioactives, and testing drug combinations in vitro.
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.

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