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Drug Repurposing for Japanese Encephalitis Virus Infection by Systems Biology Methods

Japanese encephalitis is a zoonotic disease caused by the Japanese encephalitis virus (JEV). It is mainly epidemic in Asia with an estimated 69,000 cases occurring per year. However, no approved agents are available for the treatment of JEV infection, and existing vaccines cannot control various typ...

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Autores principales: Lv, Bo-Min, Tong, Xin-Yu, Quan, Yuan, Liu, Meng-Yuan, Zhang, Qing-Ye, Song, Yun-Feng, Zhang, Hong-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320907/
https://www.ncbi.nlm.nih.gov/pubmed/30567313
http://dx.doi.org/10.3390/molecules23123346
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author Lv, Bo-Min
Tong, Xin-Yu
Quan, Yuan
Liu, Meng-Yuan
Zhang, Qing-Ye
Song, Yun-Feng
Zhang, Hong-Yu
author_facet Lv, Bo-Min
Tong, Xin-Yu
Quan, Yuan
Liu, Meng-Yuan
Zhang, Qing-Ye
Song, Yun-Feng
Zhang, Hong-Yu
author_sort Lv, Bo-Min
collection PubMed
description Japanese encephalitis is a zoonotic disease caused by the Japanese encephalitis virus (JEV). It is mainly epidemic in Asia with an estimated 69,000 cases occurring per year. However, no approved agents are available for the treatment of JEV infection, and existing vaccines cannot control various types of JEV strains. Drug repurposing is a new concept for finding new indication of existing drugs, and, recently, the concept has been used to discover new antiviral agents. Identifying host proteins involved in the progress of JEV infection and using these proteins as targets are the center of drug repurposing for JEV infection. In this study, based on the gene expression data of JEV infection and the phenome-wide association study (PheWAS) data, we identified 286 genes that participate in the progress of JEV infection using systems biology methods. The enrichment analysis of these genes suggested that the genes identified by our methods were predominantly related to viral infection pathways and immune response-related pathways. We found that bortezomib, which can target these genes, may have an effect on the treatment of JEV infection. Subsequently, we evaluated the antiviral activity of bortezomib using a JEV-infected mouse model. The results showed that bortezomib can lower JEV-induced lethality in mice, alleviate suffering in JEV-infected mice and reduce the damage in brains caused by JEV infection. This work provides an agent with new indication to treat JEV infection.
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spelling pubmed-63209072019-01-14 Drug Repurposing for Japanese Encephalitis Virus Infection by Systems Biology Methods Lv, Bo-Min Tong, Xin-Yu Quan, Yuan Liu, Meng-Yuan Zhang, Qing-Ye Song, Yun-Feng Zhang, Hong-Yu Molecules Article Japanese encephalitis is a zoonotic disease caused by the Japanese encephalitis virus (JEV). It is mainly epidemic in Asia with an estimated 69,000 cases occurring per year. However, no approved agents are available for the treatment of JEV infection, and existing vaccines cannot control various types of JEV strains. Drug repurposing is a new concept for finding new indication of existing drugs, and, recently, the concept has been used to discover new antiviral agents. Identifying host proteins involved in the progress of JEV infection and using these proteins as targets are the center of drug repurposing for JEV infection. In this study, based on the gene expression data of JEV infection and the phenome-wide association study (PheWAS) data, we identified 286 genes that participate in the progress of JEV infection using systems biology methods. The enrichment analysis of these genes suggested that the genes identified by our methods were predominantly related to viral infection pathways and immune response-related pathways. We found that bortezomib, which can target these genes, may have an effect on the treatment of JEV infection. Subsequently, we evaluated the antiviral activity of bortezomib using a JEV-infected mouse model. The results showed that bortezomib can lower JEV-induced lethality in mice, alleviate suffering in JEV-infected mice and reduce the damage in brains caused by JEV infection. This work provides an agent with new indication to treat JEV infection. MDPI 2018-12-18 /pmc/articles/PMC6320907/ /pubmed/30567313 http://dx.doi.org/10.3390/molecules23123346 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lv, Bo-Min
Tong, Xin-Yu
Quan, Yuan
Liu, Meng-Yuan
Zhang, Qing-Ye
Song, Yun-Feng
Zhang, Hong-Yu
Drug Repurposing for Japanese Encephalitis Virus Infection by Systems Biology Methods
title Drug Repurposing for Japanese Encephalitis Virus Infection by Systems Biology Methods
title_full Drug Repurposing for Japanese Encephalitis Virus Infection by Systems Biology Methods
title_fullStr Drug Repurposing for Japanese Encephalitis Virus Infection by Systems Biology Methods
title_full_unstemmed Drug Repurposing for Japanese Encephalitis Virus Infection by Systems Biology Methods
title_short Drug Repurposing for Japanese Encephalitis Virus Infection by Systems Biology Methods
title_sort drug repurposing for japanese encephalitis virus infection by systems biology methods
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320907/
https://www.ncbi.nlm.nih.gov/pubmed/30567313
http://dx.doi.org/10.3390/molecules23123346
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