Inhibition of tick-borne encephalitis virus in cell cultures by ribavirin

Tick-borne encephalitis virus (TBEV) belonging to arboviruses is a major member of zoonotic pathogens. TBEV infection causes severe human encephalitis without specific antiviral drugs. Due to its use of antiviral drug against a wide range of viruses, we investigated antiviral effect of ribavirin aga...

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Main Authors: Wan-Da Tang, Hai-Lin Tang, Hao-Ran Peng, Rui-Wen Ren, Ping Zhao, Lan-Juan Zhao
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-06-01
Series:Frontiers in Microbiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fmicb.2023.1182798/full
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author Wan-Da Tang
Hai-Lin Tang
Hao-Ran Peng
Rui-Wen Ren
Ping Zhao
Lan-Juan Zhao
author_facet Wan-Da Tang
Hai-Lin Tang
Hao-Ran Peng
Rui-Wen Ren
Ping Zhao
Lan-Juan Zhao
author_sort Wan-Da Tang
collection DOAJ
description Tick-borne encephalitis virus (TBEV) belonging to arboviruses is a major member of zoonotic pathogens. TBEV infection causes severe human encephalitis without specific antiviral drugs. Due to its use of antiviral drug against a wide range of viruses, we investigated antiviral effect of ribavirin against TBEV in susceptible human cell lines A549 and SH-SY5Y. Ribavirin displayed minor cytotoxicity on multiple cell lines. Ribavirin obviously impaired TBEV replication and protected the infected cells from cytopathic effect. Importantly, ribavirin markedly inhibited TBEV propagation, as evidenced by impairment of TBEV production and viral RNA replication. Treatment with ribavirin (co-treatment and post-treatment) led to a dose-dependent reduction in TBEV titers as well as the viral RNA levels. Antiviral protein myxovirus resistance A mRNA expression was significantly up-regulated and signal transducer and activator of transcription 3 was activated in TBEV-infected A549 cells upon the ribavirin treatment. Induction of inflammatory cytokine tumor necrosis factor alpha by TBEV was decreased in A549 cells with the treatment of ribavirin, whereas interleukin 1 beta release appeared to be unaffected. These results suggest that ribavirin might represent a promising safe and effective antiviral drug against TBEV.
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spelling doaj.art-6629d5d6cedb424ca3c92b0efa65b3b22023-06-12T04:21:47ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2023-06-011410.3389/fmicb.2023.11827981182798Inhibition of tick-borne encephalitis virus in cell cultures by ribavirinWan-Da Tang0Hai-Lin Tang1Hao-Ran Peng2Rui-Wen Ren3Ping Zhao4Lan-Juan Zhao5Department of Microbiology, Faculty of Naval Medicine, Naval Medical University, Shanghai, ChinaDepartment of Microbiology, Faculty of Naval Medicine, Naval Medical University, Shanghai, ChinaDepartment of Microbiology, Faculty of Naval Medicine, Naval Medical University, Shanghai, ChinaCenter for Disease Control and Prevention of Southern Theater Command, Guangzhou, ChinaDepartment of Microbiology, Faculty of Naval Medicine, Naval Medical University, Shanghai, ChinaDepartment of Microbiology, Faculty of Naval Medicine, Naval Medical University, Shanghai, ChinaTick-borne encephalitis virus (TBEV) belonging to arboviruses is a major member of zoonotic pathogens. TBEV infection causes severe human encephalitis without specific antiviral drugs. Due to its use of antiviral drug against a wide range of viruses, we investigated antiviral effect of ribavirin against TBEV in susceptible human cell lines A549 and SH-SY5Y. Ribavirin displayed minor cytotoxicity on multiple cell lines. Ribavirin obviously impaired TBEV replication and protected the infected cells from cytopathic effect. Importantly, ribavirin markedly inhibited TBEV propagation, as evidenced by impairment of TBEV production and viral RNA replication. Treatment with ribavirin (co-treatment and post-treatment) led to a dose-dependent reduction in TBEV titers as well as the viral RNA levels. Antiviral protein myxovirus resistance A mRNA expression was significantly up-regulated and signal transducer and activator of transcription 3 was activated in TBEV-infected A549 cells upon the ribavirin treatment. Induction of inflammatory cytokine tumor necrosis factor alpha by TBEV was decreased in A549 cells with the treatment of ribavirin, whereas interleukin 1 beta release appeared to be unaffected. These results suggest that ribavirin might represent a promising safe and effective antiviral drug against TBEV.https://www.frontiersin.org/articles/10.3389/fmicb.2023.1182798/fulltick-borne encephalitis virusribavirinmyxovirus resistance Asignal transducer and activator of transcription 3tumor necrosis factor alpha
spellingShingle Wan-Da Tang
Hai-Lin Tang
Hao-Ran Peng
Rui-Wen Ren
Ping Zhao
Lan-Juan Zhao
Inhibition of tick-borne encephalitis virus in cell cultures by ribavirin
Frontiers in Microbiology
tick-borne encephalitis virus
ribavirin
myxovirus resistance A
signal transducer and activator of transcription 3
tumor necrosis factor alpha
title Inhibition of tick-borne encephalitis virus in cell cultures by ribavirin
title_full Inhibition of tick-borne encephalitis virus in cell cultures by ribavirin
title_fullStr Inhibition of tick-borne encephalitis virus in cell cultures by ribavirin
title_full_unstemmed Inhibition of tick-borne encephalitis virus in cell cultures by ribavirin
title_short Inhibition of tick-borne encephalitis virus in cell cultures by ribavirin
title_sort inhibition of tick borne encephalitis virus in cell cultures by ribavirin
topic tick-borne encephalitis virus
ribavirin
myxovirus resistance A
signal transducer and activator of transcription 3
tumor necrosis factor alpha
url https://www.frontiersin.org/articles/10.3389/fmicb.2023.1182798/full
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AT ruiwenren inhibitionoftickborneencephalitisvirusincellculturesbyribavirin
AT pingzhao inhibitionoftickborneencephalitisvirusincellculturesbyribavirin
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