...
首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >The NS3 and NS4A genes as the targets of RNA interference inhibit replication of Japanese encephalitis virus in vitro and in vivo
【24h】

The NS3 and NS4A genes as the targets of RNA interference inhibit replication of Japanese encephalitis virus in vitro and in vivo

机译:作为RNA干扰靶标的NS3和NS4A基因在体外和体内抑制日本脑炎病毒的复制

获取原文
获取原文并翻译 | 示例

摘要

Japanese encephalitis virus (JEV) is a mosquito-borne flavivirus that can cause acute encephalitis with a high fatality rate. RNA interference (RNAi) is a powerful tool to silence gene expression and a potential therapy for virus infection. In this study, the antiviral ability of eight shRNA expression plasmids targeting different sites of the NS3 and NS4A genes of JEV was determined in BHK21 cells and mice. The pGP-NS3-3 and pGP-NS4A-4 suppressed 93.9% and 82.0% of JEV mRNA in cells, respectively. The virus titer in cells was reduced approximately 950-fold by pretreating with pGP-NS3-4, and 640-fold by pretreating with pGP-NS4A-4. The results of western blot and immunofluorescence analysis showed JEV E protein and viral load in cells were remarkably inhibited by shRNA expression plasmids. The viral load in brains of mice pretreated with pGP-NS3-4 or pGP-NS4A-4 were reduced approximately 2400-fold and 800-fold, respectively, and the survival rate of mice challenged with JEV were 70% and 50%, respectively. However, the antiviral ability of shRNA expression plasmids was decreased over time. This study indicates that RNAi targeting of the NS3 and NS4A genes of JEV can sufficiently inhibit the replication of JEV in vitro and in vivo, and NS3 and NS4A genes might be potential targets of molecular therapy for JEV infection. (C) 2016 Elsevier B.V. All rights reserved.
机译:日本脑炎病毒(JEV)是一种由蚊子传播的黄病毒,可导致高死亡率的急性脑炎。 RNA干扰(RNAi)是使基因表达沉默的强大工具,也是病毒感染的潜在疗法。在这项研究中,确定了BHK21细胞和小鼠中靶向JEV的NS3和NS4A基因不同位点的8个shRNA表达质粒的抗病毒能力。 pGP-NS3-3和pGP-NS4A-4分别抑制了细胞中JEV mRNA的93.9%和82.0%。用pGP-NS3-4预处理可降低细胞中的病毒滴度约950倍,用pGP-NS4A-4预处理可降低约640倍。 Western印迹和免疫荧光分析结果表明,shRNA表达质粒显着抑制了JEV E蛋白和细胞中的病毒载量。用pGP-NS3-4或pGP-NS4A-4预处理的小鼠大脑中的病毒载量分别降低了约2400倍和800倍,用JEV攻击的小鼠的存活率分别为70%和50% 。但是,shRNA表达质粒的抗病毒能力随时间而降低。这项研究表明,RNAi靶向JEV的NS3和NS4A基因可以充分抑制JEV在体内和体外的复制,并且NS3和NS4A基因可能是JEV感染的分子治疗的潜在靶标。 (C)2016 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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