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短发夹 RNA 靶向猪肾细胞系中核衣壳基因抑制猪传染性脑脊髓炎病毒复制。

Inhibition of porcine hemagglutinating encephalomyelitis virus replication by short hairpin RNAs targeting of the nucleocapsid gene in a porcine kidney cell line.

机构信息

College of Animal Science and Veterinary Medicine, Jilin University, Changchun 130062, China.

出版信息

J Virol Methods. 2012 Feb;179(2):414-8. doi: 10.1016/j.jviromet.2011.11.007. Epub 2011 Nov 26.

Abstract

Porcine hemagglutinating encephalomyelitis virus (PHEV), which causes porcine encephalomyelitis and is widespread among swine worldwide. RNA interference (RNAi) pathways have emerged as important regulators of virus-host cell interactions. In this study, two siRNA expression plasmids (shN1 and shN2) were generated to target two different coding regions of the nucleocapsid protein (N) of PHEV. The shRNAs were transiently transfected into a porcine kidney cell line, PK-15, to determine whether these constructs inhibited PHEV production. Our results revealed that both shRNAs were highly capable of inhibiting viral RNA genome replication, especially shN2. Next, stable transfection of shN2 was used to produce two siRNA stably expressing PK-15 cell clones (shN2-1 and shN2-2), and these two lines were infected with PHEV. The analysis of cytopathic effects (CPE) demonstrated that shN2-1 and shN2-2 were capable of protecting cells against PHEV infection with high specificity and efficiency. Furthermore, effective inhibition of viral replication persisted for up to 120 h by a TCID(50) assay. These results indicated that RNAi targeting of the N gene could facilitate studies of the specific function of viral genes associated with PHEV replication and may have potential therapeutic applications.

摘要

猪传染性脑脊髓炎病毒(PHEV)可引起猪脑脊髓炎,在世界范围内广泛存在于猪群中。RNA 干扰(RNAi)途径已成为病毒-宿主细胞相互作用的重要调节因子。在本研究中,我们构建了两个靶向 PHEV 核衣壳蛋白(N)的不同编码区的 siRNA 表达质粒(shN1 和 shN2)。将这些 shRNA 瞬时转染到猪肾细胞系 PK-15 中,以确定这些构建体是否抑制了 PHEV 的产生。我们的结果表明,这两种 shRNA 都能够高效抑制病毒 RNA 基因组的复制,尤其是 shN2。接下来,我们使用稳定转染的方法稳定表达 shN2,产生了两个能够稳定表达 siRNA 的 PK-15 细胞克隆(shN2-1 和 shN2-2),并用 PHEV 感染这些细胞。细胞病变效应(CPE)分析表明,shN2-1 和 shN2-2 能够高效且特异地保护细胞免受 PHEV 感染。此外,通过 TCID(50) 测定,在长达 120 h 的时间内持续有效地抑制了病毒的复制。这些结果表明,针对 N 基因的 RNAi 可促进与 PHEV 复制相关的病毒基因的特定功能研究,并可能具有潜在的治疗应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbd5/7112858/2573891a1555/gr1.jpg

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