Pathogens. Feasibility of Known RNA Polymerase Inhibitors as Anti-SARS-CoV-2 Drugs

[tetano]

Pathogens. 2020 Apr 26;9(5). pii: E320. doi: 10.3390/pathogens9050320.
Feasibility of Known RNA Polymerase Inhibitors as Anti-SARS-CoV-2 Drugs.


Neogi U^1,2, Hill KJ^2,3, Ambikan AT¹, Heng X⁴, Quinn TP⁴, Byrareddy SN⁵, S?nnerborg A^2,3,6, Sarafianos SG⁷, Singh K^1,2,3,8.

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Abstract

Coronaviruses (CoVs) are positive-stranded RNA viruses that infect humans and animals. Infection by CoVs such as HCoV-229E, -NL63, -OC43 and -HKU1 leads to the common cold, short lasting rhinitis, cough, sore throat and fever. However, CoVs such as Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV), Middle East Respiratory Syndrome Coronavirus (MERS-CoV), and the newest SARS-CoV-2 (the causative agent of COVID-19) lead to severe and deadly diseases with mortality rates ranging between ~1 to 35% depending on factors such as age and pre-existing conditions. Despite continuous global health threats to humans, there are no approved vaccines or drugs targeting human CoVs, and the recent outbreak of COVID-19 emphasizes an urgent need for therapeutic interventions. Using computational and bioinformatics tools, here we present the feasibility of reported broad-spectrum RNA polymerase inhibitors as anti- SARS-CoV-2 drugs targeting its main RNA polymerase, suggesting that investigational and approved nucleoside RNA polymerase inhibitors have potential as anti-SARS-CoV-2 drugs. However, we note that it is also possible for SARS-CoV-2 to evolve and acquire drug resistance mutations against these nucleoside inhibitors.



KEYWORDS:

COVID-19; MERS-CoV; RNA polymerase; SARS-CoV; SARS-CoV-2; coronavirus; nsp12


PMID:32357471DOI:10.3390/pathogens9050320