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首页|期刊导航|河南农业科学|猪伪狂犬病病毒gE蛋白单克隆抗体的制备与鉴定

猪伪狂犬病病毒gE蛋白单克隆抗体的制备与鉴定

王瑞宁 王勋 李鸽 李青梅 李存法 杨苏珍 郭军庆

河南农业科学2024,Vol.53Issue(12):167-173,7.
河南农业科学2024,Vol.53Issue(12):167-173,7.DOI:10.15933/j.cnki.1004-3268.2024.12.017

猪伪狂犬病病毒gE蛋白单克隆抗体的制备与鉴定

Preparation and Identification of Monoclonal Antibody against gE Protein of Porcine Pseudorabies Virus

王瑞宁 1王勋 2李鸽 3李青梅 4李存法 5杨苏珍 4郭军庆4

作者信息

  • 1. 河南牧业经济学院 动物医药学院,河南 郑州 450046||河南省农业科学院 动物疫病防控研究所,河南 郑州 450002
  • 2. 洛阳职业技术学院 食品与药品学院,河南 洛阳 471023||河南省动物疫病与公共卫生工程研究中心,河南 洛阳 471023
  • 3. 西北农林科技大学 动物医学院,陕西 杨凌 712100
  • 4. 河南省农业科学院 动物疫病防控研究所,河南 郑州 450002
  • 5. 河南牧业经济学院 动物医药学院,河南 郑州 450046
  • 折叠

摘要

Abstract

In order to develop an immunodiagnostic reagent for porcine pseudorabies virus(PRV),BALB/c mice were immunized with the recombinant gE protein expressed in HEK293F cells.The spleen cells of immunized mice and SP2/0 myeloma cells were fused to generate hybridoma cells.Indirect ELISA and immunoperoxidase monolayer assay(IPMA)were used to screen positive hybridoma cells so as to prepare and identify monoclonal antibodies against the gE protein of PRV.The outcomes demonstrated that two hybridoma cell strains,named 2B5 and 8F7,respectively,which steadily secreted monoclonal antibody against the gE protein were developed.The ELISA titers of ascites were all 1∶1 000 000.IgG1 was the heavy chain and Kappa was the light chain,according to the monoclonal antibody isotype assay.The specificity assay revealed that the two monoclonal antibodies only reacted with PRV and not with other viruses.SDS-PAGE results showed that the purified monoclonal antibodies had high-purity specific bands at about 50 ku and 25 ku.The two monoclonal antibody strains could react specifically with 293T cells transfected with gE plasmid according to indirect immunofluorescence assay(IFA)detection.Western blot showed that the specific protein band appearing in the culture supernatant of two hybridoma cells was about 120 ku,indicating that the two monoclonal antibodies could specifically recognize PRV.To summarize,this study successfully prepared two strains of monoclonal antibodies against gE protein,exhibiting excellent specificity and high titer,which provided crucial biological materials required for the subsequent development of diagnostic kits.

关键词

猪伪狂犬病病毒/gE蛋白/单克隆抗体/间接免疫荧光试验

Key words

Porcine pseudorabies virus/gE protein/Monoclonal antibody/Indirect immunofluorescence assay

分类

农业科技

引用本文复制引用

王瑞宁,王勋,李鸽,李青梅,李存法,杨苏珍,郭军庆..猪伪狂犬病病毒gE蛋白单克隆抗体的制备与鉴定[J].河南农业科学,2024,53(12):167-173,7.

基金项目

河南省重大科技专项(221100110600-03) (221100110600-03)

河南省科技攻关项目(232102520012 ()

242102111031) ()

河南省农业科学院科技创新团队项目(2023TD03) (2023TD03)

河南农业科学

OA北大核心CSTPCD

1004-3268

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