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逆转录病毒载体介导的 RNA 干扰抑制猪瘟病毒复制的体外研究。

In vitro inhibition of CSFV replication by retroviral vector-mediated RNA interference.

机构信息

College of Animal Science and Veterinary Medicine, Jilin University, 5333 XiAn Da Road, Changchun 130062, China.

出版信息

J Virol Methods. 2010 Nov;169(2):316-21. doi: 10.1016/j.jviromet.2010.07.036. Epub 2010 Aug 4.

Abstract

Classical swine fever (CSF) is a highly contagious viral disease of pigs which causes major economic losses worldwide. No specific drug is currently available for the effective treatment of CSFV infection. RNA interference (RNAi) technology depends on effective delivery systems, for which several effective vectors have recently been developed. Three retroviral plasmids containing siRNA genes targeting different regions of N(pro) and NS4A have been constructed, and 3 replication-incompetent retroviral vectors have been produced in the human embryo kidney cell line GP2-293 by retroviral plasmid transfection. PK-15 cells were then infected with these replication-incompetent retroviral vectors and screened for siRNA stably expressing PK-15 cell clones. Growth of CSFV in such siRNA stably expressing cell clones resulted in a 186-fold reduction in viral genome copies and, at 72 h post-infection, only a small % of cells showed infection by indirect immunofluorescence microscopy, and effective inhibition of virus replication persisted for up to 120 h. Retroviral vector-mediated RNAi can therefore be used to study the specific function of viral genes associated with CSFV replication and may have potential therapeutic application.

摘要

经典猪瘟(CSF)是一种高度传染性的猪病毒病,在全球范围内造成重大经济损失。目前尚无针对 CSFV 感染的特效药物。RNA 干扰(RNAi)技术依赖于有效的递送系统,最近已经开发出几种有效的载体。构建了三个含有靶向 N(pro)和 NS4A 不同区域的 siRNA 基因的逆转录病毒质粒,并通过逆转录质粒转染在人胚肾细胞系 GP2-293 中产生了 3 种复制缺陷型逆转录病毒载体。然后用这些复制缺陷型逆转录病毒载体感染 PK-15 细胞,并筛选稳定表达 siRNA 的 PK-15 细胞克隆。在这些稳定表达 siRNA 的细胞克隆中,CSFV 的生长导致病毒基因组拷贝数减少 186 倍,在感染后 72 小时,只有小比例的细胞通过间接免疫荧光显微镜显示感染,病毒复制的有效抑制持续长达 120 小时。因此,逆转录病毒载体介导的 RNAi 可用于研究与 CSFV 复制相关的病毒基因的特定功能,并可能具有潜在的治疗应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c26/7112837/8be89fff1dcc/gr1.jpg

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