首页> 美国卫生研究院文献>Molecules >Drug Repurposing for Japanese Encephalitis Virus Infection by Systems Biology Methods
【2h】

Drug Repurposing for Japanese Encephalitis Virus Infection by Systems Biology Methods

机译:通过系统生物学方法对日本脑炎病毒感染进行药物再利用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

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.
机译:日本脑炎是由日本脑炎病毒(JEV)引起的人畜共患疾病。它主要在亚洲流行,估计每年发生69,000例。但是,尚无批准的药物可用于治疗JEV感染,现有疫苗无法控制各种类型的JEV株。药物再利用是用于发现现有药物的新适应症的新概念,最近,该概念已被用于发现新的抗病毒药物。鉴定参与JEV感染进展的宿主蛋白并将这些蛋白用作靶标是针对JEV感染进行药物改造的中心。在这项研究中,基于JEV感染的基因表达数据和全基因组关联研究(PheWAS)数据,我们使用系统生物学方法鉴定了286个参与JEV感染进展的基因。这些基因的富集分析表明,通过我们的方法鉴定的基因主要与病毒感染途径和免疫应答相关途径有关。我们发现可以靶向这些基因的硼替佐米可能对JEV感染的治疗产生影响。随后,我们使用JEV感染的小鼠模型评估了硼替佐米的抗病毒活性。结果表明,硼替佐米可以降低JEV致小鼠的致死率,减轻JEV感染小鼠的痛苦,并减少由JEV感染引起的大脑损伤。这项工作为治疗JEV感染提供了新的适应症。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号