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Pig BVDV-2 non-structural protein (N-pro) links to cellular antiviral response in vitro

机译:猪BVDV-2非结构蛋白(N-Pro)在体外链接到细胞抗病毒反应

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摘要

In this study, we constructed for the first time a full-length cDNA clone of pig-original bovine viral diarrhea virus 2 (BVDV-2) strain SH-28, modified the cDNA clone (pASH28) for mutant pASH Delta N-pro and derived virus strain vASH Delta N-pro by deleting the genomic region encoding the N-pro polypeptide, and examined significance of protein N-pro for antiviral responses in vitro. Data showed that N-pro-deletion mutant virus vASH Delta N-pro led to significant overexpression of oligo adenylate synthetase (OAS), myxovirus-resistant protein 1 (Mx1), and ubiquitin-like protein 15 (ISG15). Data also revealed that overexpression of N-pro, but not NS2 and NS3 proteins, resulted in significant down-regulation of OAS, Mx1, and ISG15 production (p <= 0.05) in bovine cells as well as porcine cells transfected with N-pro recombinant eukaryotic expression plasmids. N-pro (but not NS2 and NS3) was also found to inhibit poly(IC) from inducing production of type I interferon (IFN-I). These results indicated that protein N-pro may play multiple roles in regulating antiviral response in host cells interfered by pig BVDV-2 strain, and provided useful information to understand better the mechanism of BVDV-2 persistent infection in pigs.
机译:在这项研究中,我们为第一次构建了猪原牛病毒腹泻病毒2(BVDV-2)菌株SH-28的全长cDNA克隆,修饰了突变体纸δn-Pro的cDNA克隆(Pash28)和通过删除编码N-Pro多肽的基因组区域来衍生的病毒菌株VASH DERTA N-PRO,并检查蛋白质N-PRO在体外抗病毒反应的重要性。数据显示N-Pro-Deletion突变体病毒Vash Delta N-Pro导致寡核酸吲哚合成酶(OAS),骨髓病毒抗性蛋白1(MX1)和泛素样蛋白15(ISG15)的显着过表达。数据还表明,N-Pro的过表达,但不是NS2和NS3蛋白,导致牛细胞中的OAS,MX1和ISG15产生(P <= 0.05)的显着下调,以及用N-转染的猪细胞Pro重组真核表达质粒。还发现N-Pro(但不是NS2和NS3)抑制聚(IC)诱导I型干扰素(IFN-1)的产生。这些结果表明,蛋白质N-Pro可以在猪BVDV-2菌株干扰的宿主细胞中调节抗病毒反应中发挥多种作用,并提供了有用的信息,以了解猪中BVDV-2持续感染的机制。

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