首页|表达绿色荧光蛋白的重组伪狂犬病病毒构建及在中和试验中应用

表达绿色荧光蛋白的重组伪狂犬病病毒构建及在中和试验中应用

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为了优化病毒血清中和抗体试验方法,减少传统病毒中和抗体试验的周期,本研究通过同源重组技术,构建出能够表达绿色荧光蛋白的伪狂犬gE基因缺失病毒PRV-△gE-AcGFP1.将其作为检测病毒,对gE抗体阴性血清进行病毒血清中和抗体试验,测定中和抗体效价.结果显示,利用重组病毒测定中和抗体效价的结果与传统方法无显著差异.结果表明,PRV-gE-AcGFP1可作为攻击病毒用于血清中和抗体试验,为进行方便、准确、周期短的血清中和抗体试验提供一种新的选择.
Construction of recombinant pseudorabies virus expressing green fluorescent protein and its application in neutralization test
In order to optimize the viral serum neutralizing antibody test method and reduce the cycle time of traditional viral neutralizing antibody test,a pseudorabies gE gene deletion virus PRV-△gE-AcGFP1 expressing green fluorescent protein was constructed by homologous recombination technology,and used it as a test virus for determination of neutralizing antibody potency by performing the viral serum neutralizing antibody test on gE antibody-negative sera.The results showed that there was no significant difference between the recombinant virus and the traditional method in determining the titer of neutralizing antibody.The results show that PRV-△gE-AcGFP1 could be used as test virus for serum neutralizing antibody assay,providing a new option for performing convenient,accurate and short-cycle serum neutralizing antibody tests.

pseudorabies virushomologous recombinationgreen fluorescent proteinneutraliza-tion test

任晓祥、刘立辉、肖娜、张帅、武月、赵云环、刘涛、左玉柱、范京惠

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河北农业大学动物医学院,河北保定 071001

定州市农业农村局,河北定州 073000

瑞普(保定)生物药业有限公司,河北保定 071001

伪狂犬病病毒 同源重组 绿色荧光蛋白 中和试验

河北省农业产业技术体系生猪创新团队项目河北省农业产业技术体系生猪创新团队项目

HBCT2024220201HBCT2024220401

2024

中国兽医科学
中国农业科学院兰州兽医研究所

中国兽医科学

CSTPCD北大核心
影响因子:0.524
ISSN:1673-4696
年,卷(期):2024.54(9)