...
首页> 外文期刊>Journal of Virological Methods >Effective inhibition of replication of infectious bursal disease virus by miRNAs delivered by vectors and targeting the VP2 gene.
【24h】

Effective inhibition of replication of infectious bursal disease virus by miRNAs delivered by vectors and targeting the VP2 gene.

机译:通过载体递送并靶向VP2基因的miRNA有效抑制传染性法氏囊病病毒的复制。

获取原文
获取原文并翻译 | 示例
           

摘要

RNA interference (RNAi) is a potent mechanism against a variety of viral infections. Infectious bursal disease virus (IBDV) causes an important disease economically in chickens, which is difficult to control. As part of the development of viral vector-mediated RNAi strategy against the disease, five anti-VP2 small interference RNAs were selected for construction of microRNA (miRNA) expression vectors tailored for avian cells. Transfection of DF-1 cells with the five vectors resulted in significant inhibition of VP2-EGFP reporter gene expression. More effective miVP2A and miVP2E were selected for further study using single or double miRNA expression vectors. After demonstration of specific miRNA expression, the gene silencing effects were determined in the vector-transfected and IBDV-infected cells. Reverse transcriptase PCR and virus titration showed inhibition rates from 76 to 82% on VP2 expression and significant decreases in virus titer by individual and co-expressed miVP2A and miVP2E. The inhibitory effects lasted for at least 120 h after infection with IBDV. These data suggest that the miRNAs targeting the VP2 can inhibit efficiently replication of IBDV.
机译:RNA干扰(RNAi)是对抗多种病毒感染的有效机制。传染性法氏囊病病毒(IBDV)在经济上会引起鸡的重要疾病,难以控制。作为针对这种疾病的病毒载体介导的RNAi策略发展的一部分,选择了五个抗VP2小干扰RNA来构建适合禽类细胞的microRNA(miRNA)表达载体。用这五个载体转染DF-1细胞会明显抑制VP2-EGFP报告基因的表达。使用单或双miRNA表达载体选择更有效的miVP2A和miVP2E进行进一步研究。在证明了特定的miRNA表达后,确定了载体转染和IBDV感染细胞的基因沉默效果。逆转录酶PCR和病毒滴定显示,对VP2表达的抑制率从76%降至82%,并且单独和共表达的miVP2A和miVP2E的病毒滴度显着降低。 IBDV感染后抑制作用持续至少120小时。这些数据表明靶向VP2的miRNA可以有效抑制IBDV的复制。

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