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通过针对基质蛋白基因的 RNA 干扰抑制鸡胚成纤维细胞中的新城疫病毒复制。

Inhibition of Newcastle disease virus replication by RNA interference targeting the matrix protein gene in chicken embryo fibroblasts.

机构信息

Department of Veterinary Preventive Medicine, College of Animal Science and Veterinary Medicine, Jilin University, Xi'an Road 5333, Changchun, Jilin 130062, China.

出版信息

J Virol Methods. 2010 Jul;167(1):107-11. doi: 10.1016/j.jviromet.2010.02.014. Epub 2010 Feb 18.

Abstract

Newcastle disease (ND) is an infectious viral disease of birds caused by the Newcastle disease virus (NDV), also known as avian paramyxovirus type 1 (AMPV-1), which leads to severe economic losses in the poultry industry worldwide. In this study, the application of RNA interference (RNAi) for inhibiting the replication of NDV in cell culture by targeting the viral matrix protein gene (M) is described. Two M-specific shRNA-expressing plasmid constructs, named pS(M641) and pS(M827), were evaluated for antiviral activity against the NDV strain NA-1 by cytopathic effects (CPE), virus titration and real-time RT-PCR. After 36h of infection, both pS(M641) and pS(M827) reduced virus titers by 79.4- and 31.6-fold, respectively, and they down-regulated mRNA expression levels of the matrix protein gene M by 94.6% and 84.8%, respectively, in chicken embryo fibroblast (CEF) cells, while only pS(M641) significantly decreased CPE, compared to the control group. These results indicated that the M gene 641 and 827 sites represent potential antiviral therapy targets, and RNAi targeting of the M gene could not only represent an effective treatment in Newcastle disease but also aid as a method for studying the replication of NDV.

摘要

新城疫(ND)是一种由新城疫病毒(NDV)引起的鸟类传染病,也称为禽副黏病毒 1 型(AMPV-1),它会导致全球家禽业遭受严重的经济损失。在本研究中,描述了通过针对病毒基质蛋白基因(M)应用 RNA 干扰(RNAi)来抑制细胞培养中 NDV 复制的方法。评估了两种针对 M 基因的特异性 shRNA 表达质粒构建体,命名为 pS(M641)和 pS(M827),用于抑制 NDV 株 NA-1 的抗病毒活性,通过细胞病变效应(CPE)、病毒滴定和实时 RT-PCR 进行评估。感染后 36 小时,pS(M641)和 pS(M827)分别将病毒滴度降低了 79.4-和 31.6 倍,并且它们分别将基质蛋白基因 M 的 mRNA 表达水平下调了 94.6%和 84.8%,在鸡胚成纤维细胞(CEF)中,与对照组相比,只有 pS(M641)显著降低了 CPE。这些结果表明,M 基因 641 和 827 位点代表潜在的抗病毒治疗靶标,并且针对 M 基因的 RNAi 不仅可以作为新城疫的有效治疗方法,还可以作为研究 NDV 复制的方法。

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