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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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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. |
format | Online Article Text |
id | pubmed-3927656 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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