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Nitazoxanide inhibits the replication of Japanese encephalitis virus in cultured cells and in a mouse model

BACKGROUND: Japanese encephalitis virus (JEV) has a significant impact on public health. An estimated three billion people in 'at-risk’ regions remain unvaccinated and the number of unvaccinated individuals in certain Asian countries is increasing. Consequently, there is an urgent need for the...

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Autores principales: Shi, Zixue, Wei, Jianchao, Deng, Xufang, Li, Shuqing, Qiu, Yafeng, Shao, Donghua, Li, Beibei, Zhang, Keyu, Xue, Feiqun, Wang, Xiaodu, Ma, Zhiyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927656/
https://www.ncbi.nlm.nih.gov/pubmed/24456815
http://dx.doi.org/10.1186/1743-422X-11-10
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author Shi, Zixue
Wei, Jianchao
Deng, Xufang
Li, Shuqing
Qiu, Yafeng
Shao, Donghua
Li, Beibei
Zhang, Keyu
Xue, Feiqun
Wang, Xiaodu
Ma, Zhiyong
author_facet Shi, Zixue
Wei, Jianchao
Deng, Xufang
Li, Shuqing
Qiu, Yafeng
Shao, Donghua
Li, Beibei
Zhang, Keyu
Xue, Feiqun
Wang, Xiaodu
Ma, Zhiyong
author_sort Shi, Zixue
collection PubMed
description BACKGROUND: Japanese encephalitis virus (JEV) has a significant impact on public health. An estimated three billion people in 'at-risk’ regions remain unvaccinated and the number of unvaccinated individuals in certain Asian countries is increasing. Consequently, there is an urgent need for the development of novel therapeutic agents against Japanese encephalitis. Nitazoxanide (NTZ) is a thiazolide anti-infective licensed for the treatment of parasitic gastroenteritis. Recently, NTZ has been demonstrated to have antiviral properties. In this study, the anti-JEV activity of NTZ was evaluated in cultured cells and in a mouse model. METHODS: JEV-infected cells were treated with NTZ at different concentrations. The replication of JEV in the mock- and NTZ-treated cells was examined by virus titration. NTZ was administered at different time points of JEV infection to determine the stage at which NTZ affected JEV replication. Mice were infected with a lethal dose of JEV and intragastrically administered with NTZ from 1 day post-infection. The protective effect of NTZ on the JEV-infected mice was evaluated. FINDINGS: NTZ significantly inhibited the replication of JEV in cultured cells in a dose dependent manner with 50% effective concentration value of 0.12 ± 0.04 μg/ml, a non-toxic concentration in cultured cells (50% cytotoxic concentration = 18.59 ± 0.31 μg/ml). The chemotherapeutic index calculated was 154.92. The viral yields of the NTZ-treated cells were significantly reduced at 12, 24, 36 and 48 h post-infection compared with the mock-treated cells. NTZ was found to exert its anti-JEV effect at the early-mid stage of viral infection. The anti-JEV effect of NTZ was also demonstrated in vivo, where 90% of mice that were treated by daily intragastric administration of 100 mg/kg/day of NTZ were protected from a lethal challenge dose of JEV. CONCLUSIONS: Both in vitro and in vivo data indicated that NTZ has anti-JEV activity, suggesting the potential application of NTZ in the treatment of Japanese encephalitis.
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spelling pubmed-39276562014-02-19 Nitazoxanide inhibits the replication of Japanese encephalitis virus in cultured cells and in a mouse model Shi, Zixue Wei, Jianchao Deng, Xufang Li, Shuqing Qiu, Yafeng Shao, Donghua Li, Beibei Zhang, Keyu Xue, Feiqun Wang, Xiaodu Ma, Zhiyong Virol J Research BACKGROUND: Japanese encephalitis virus (JEV) has a significant impact on public health. An estimated three billion people in 'at-risk’ regions remain unvaccinated and the number of unvaccinated individuals in certain Asian countries is increasing. Consequently, there is an urgent need for the development of novel therapeutic agents against Japanese encephalitis. Nitazoxanide (NTZ) is a thiazolide anti-infective licensed for the treatment of parasitic gastroenteritis. Recently, NTZ has been demonstrated to have antiviral properties. In this study, the anti-JEV activity of NTZ was evaluated in cultured cells and in a mouse model. METHODS: JEV-infected cells were treated with NTZ at different concentrations. The replication of JEV in the mock- and NTZ-treated cells was examined by virus titration. NTZ was administered at different time points of JEV infection to determine the stage at which NTZ affected JEV replication. Mice were infected with a lethal dose of JEV and intragastrically administered with NTZ from 1 day post-infection. The protective effect of NTZ on the JEV-infected mice was evaluated. FINDINGS: NTZ significantly inhibited the replication of JEV in cultured cells in a dose dependent manner with 50% effective concentration value of 0.12 ± 0.04 μg/ml, a non-toxic concentration in cultured cells (50% cytotoxic concentration = 18.59 ± 0.31 μg/ml). The chemotherapeutic index calculated was 154.92. The viral yields of the NTZ-treated cells were significantly reduced at 12, 24, 36 and 48 h post-infection compared with the mock-treated cells. NTZ was found to exert its anti-JEV effect at the early-mid stage of viral infection. The anti-JEV effect of NTZ was also demonstrated in vivo, where 90% of mice that were treated by daily intragastric administration of 100 mg/kg/day of NTZ were protected from a lethal challenge dose of JEV. CONCLUSIONS: Both in vitro and in vivo data indicated that NTZ has anti-JEV activity, suggesting the potential application of NTZ in the treatment of Japanese encephalitis. BioMed Central 2014-01-23 /pmc/articles/PMC3927656/ /pubmed/24456815 http://dx.doi.org/10.1186/1743-422X-11-10 Text en Copyright © 2014 Shi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Shi, Zixue
Wei, Jianchao
Deng, Xufang
Li, Shuqing
Qiu, Yafeng
Shao, Donghua
Li, Beibei
Zhang, Keyu
Xue, Feiqun
Wang, Xiaodu
Ma, Zhiyong
Nitazoxanide inhibits the replication of Japanese encephalitis virus in cultured cells and in a mouse model
title Nitazoxanide inhibits the replication of Japanese encephalitis virus in cultured cells and in a mouse model
title_full Nitazoxanide inhibits the replication of Japanese encephalitis virus in cultured cells and in a mouse model
title_fullStr Nitazoxanide inhibits the replication of Japanese encephalitis virus in cultured cells and in a mouse model
title_full_unstemmed Nitazoxanide inhibits the replication of Japanese encephalitis virus in cultured cells and in a mouse model
title_short Nitazoxanide inhibits the replication of Japanese encephalitis virus in cultured cells and in a mouse model
title_sort nitazoxanide inhibits the replication of japanese encephalitis virus in cultured cells and in a mouse model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927656/
https://www.ncbi.nlm.nih.gov/pubmed/24456815
http://dx.doi.org/10.1186/1743-422X-11-10
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