scholarly journals Drug Repurposing for Japanese Encephalitis Virus Infection by Systems Biology Methods

Molecules ◽  
2018 ◽  
Vol 23 (12) ◽  
pp. 3346 ◽  
Author(s):  
Bo-Min Lv ◽  
Xin-Yu Tong ◽  
Yuan Quan ◽  
Meng-Yuan Liu ◽  
Qing-Ye Zhang ◽  
...  

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.

Author(s):  
Bo-Min Lv ◽  
Xin-Yu Tong ◽  
Yuan Quan ◽  
Meng-Yuan Liu ◽  
Qing-Ye Zhang ◽  
...  

Japanese encephalitis is a zoonotic disease caused by 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 resist various types of JEV strains. Drug repurposing is a new concept for finding new indication of existing drugs, and recently, it 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 participating in the progress of JEV infection using the 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 potential effect on the treatment of JEV infection. Subsequently, we evaluated the antiviral activity of bortezomib using the JEV-infected mice 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 a new method for the development of antiviral agents.


2019 ◽  
Vol 64 (3) ◽  
Author(s):  
Jiao Guo ◽  
Xiaoying Jia ◽  
Yang Liu ◽  
Shaobo Wang ◽  
Junyuan Cao ◽  
...  

ABSTRACT The mosquito-borne Japanese encephalitis virus (JEV) causes serious illness worldwide that is associated with high morbidity and mortality. Currently, there are no effective drugs approved for the treatment of JEV infection. Drug-repurposing screening is an alternative approach to discover potential antiviral agents. In this study, high-content screening (HCS) of a natural extracts library was performed, and two hit FDA-approved Na+/K+-ATPase inhibitors, ouabain and digoxin, were identified as having robust efficiency against JEV infection with the selectivity indexes over 1,000. The results indicated that ouabain and digoxin blocked the JEV infection at the replication stage by targeting the Na+/K+-ATPase. Furthermore, it was proven that ouabain significantly reduced the morbidity and mortality caused by JEV in a BALB/c mouse model. This work demonstrated that Na+/K+-ATPase could serve as the target of treatment of JEV infection, and ouabain has the potential to be developed as an effective anti-JEV drug.


Neuroreport ◽  
2000 ◽  
Vol 11 (9) ◽  
pp. 1933-1937 ◽  
Author(s):  
Chun-Jung Chen ◽  
Su-Lan Liao ◽  
Ming-Der Kuo ◽  
Yu-Ming Wang

2018 ◽  
Vol 14 (7) ◽  
pp. e1007166 ◽  
Author(s):  
Hsin-Ping Chiu ◽  
Han Chiu ◽  
Chao-Fu Yang ◽  
Yi-Ling Lee ◽  
Feng-Lan Chiu ◽  
...  

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