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一种共表达口蹄疫病毒衣壳蛋白前体P1-2A和猪细小病毒VP2蛋白的重组伪狂犬病病毒:一种三价疫苗候选物。

A recombinant pseudorabies virus co-expressing capsid proteins precursor P1-2A of FMDV and VP2 protein of porcine parvovirus: a trivalent vaccine candidate.

作者信息

Hong Qi, Qian Ping, Li Xiang-Min, Yu Xiao-Lan, Chen Huan-Chun

机构信息

Laboratory of Animal Virology, College of Veterinary Medical Sciences, Huazhong Agricultural University, Wuhan, 430070, P.R. China.

出版信息

Biotechnol Lett. 2007 Nov;29(11):1677-83. doi: 10.1007/s10529-007-9459-6. Epub 2007 Jul 13.

Abstract

Pseudorabies (PR), foot-and-mouth disease (FMD), and porcine parvovirus disease are three important infectious diseases in swine worldwide. The gene-deleted pseudorabies virus (PRV) has been used as a live-viral vector to develop multivalent genetic engineering vaccine. In this study, a recombinant PRV, which could co-express protein precursor P1-2A of FMDV and VP2 protein of PPV, was constructed using PRV TK(-)/gE(-)/LacZ(+) mutant as the vector. After homologous recombination and plaque purification, recombinant virus PRV TK(-)/gE(-)/P1-2A-VP2 was acquired and identified. Immunogenicity, safety of the recombinant PRV and its protection against PRV were confirmed in a mouse model by indirect ELISA and serum neutralization test. The results show that the recombinant PRV is a candidate vaccine strain to develop a novel trivalent vaccine against PRV, FMDV and PPV in swine.

摘要

伪狂犬病(PR)、口蹄疫(FMD)和猪细小病毒病是全球范围内猪的三种重要传染病。基因缺失伪狂犬病病毒(PRV)已被用作活病毒载体来开发多价基因工程疫苗。在本研究中,以PRV TK(-)/gE(-)/LacZ(+)突变体为载体构建了一种能共表达口蹄疫病毒蛋白前体P1-2A和猪细小病毒VP2蛋白的重组PRV。经过同源重组和蚀斑纯化,获得并鉴定了重组病毒PRV TK(-)/gE(-)/P1-2A-VP2。通过间接ELISA和血清中和试验在小鼠模型中证实了重组PRV的免疫原性、安全性及其对PRV的保护作用。结果表明,该重组PRV是开发一种新型猪用抗PRV、FMDV和PPV三价疫苗的候选疫苗株。

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