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Ribavirin shows antiviral activity against SARS-CoV-2 and downregulates the activity of TMPRSS2 and the expression of ACE2 in vitro.

Authors :
Unal MA
Bitirim CV
Summak GY
Bereketoglu S
Cevher Zeytin I
Besbinar O
Gurcan C
Aydos D
Goksoy E
Kocakaya E
Eran Z
Murat M
Demir N
Aksoy Ozer ZB
Somers J
Demir E
Nazir H
Ozkan SA
Ozkul A
Azap A
Yilmazer A
Akcali KC
Source :
Canadian journal of physiology and pharmacology [Can J Physiol Pharmacol] 2021 May; Vol. 99 (5), pp. 449-460. Date of Electronic Publication: 2021 Mar 09.
Publication Year :
2021

Abstract

Ribavirin is a guanosine analog with broad-spectrum antiviral activity against RNA viruses. Based on this, we aimed to show the anti-SARS-CoV-2 activity of this drug molecule via in vitro, in silico, and molecular techniques. Ribavirin showed antiviral activity in Vero E6 cells following SARS-CoV-2 infection, whereas the drug itself did not show any toxic effect over the concentration range tested. In silico analysis suggested that ribavirin has a broad-spectrum impact on SARS-CoV-2, acting at different viral proteins. According to the detailed molecular techniques, ribavirin was shown to decrease the expression of TMPRSS2 at both mRNA and protein levels 48 h after treatment. The suppressive effect of ribavirin in ACE2 protein expression was shown to be dependent on cell types. Finally, proteolytic activity assays showed that ribavirin also showed an inhibitory effect on the TMPRSS2 enzyme. Based on these results, we hypothesized that ribavirin may inhibit the expression of TMPRSS2 by modulating the formation of inhibitory G-quadruplex structures at the TMPRSS2 promoter. As a conclusion, ribavirin is a potential antiviral drug for the treatment against SARS-CoV-2, and it interferes with the effects of TMPRSS2 and ACE2 expression.

Details

Language :
English
ISSN :
1205-7541
Volume :
99
Issue :
5
Database :
MEDLINE
Journal :
Canadian journal of physiology and pharmacology
Publication Type :
Academic Journal
Accession number :
33689451
Full Text :
https://doi.org/10.1139/cjpp-2020-0734