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首页|期刊导航|中国兽医科学|牛分枝杆菌融合蛋白ESAT-6/CFP-10/Rv3872抗体间接ELISA检测方法的建立与应用

牛分枝杆菌融合蛋白ESAT-6/CFP-10/Rv3872抗体间接ELISA检测方法的建立与应用

王文浩 储岳峰 葛家振 宋国栋 刘一健 宋银娟 郑福英 李仁阁 陈胜利 李劼

中国兽医科学2026,Vol.56Issue(8):1067-1076,10.
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中国兽医科学2026,Vol.56Issue(8):1067-1076,10.DOI:10.16656/j.issn.1673-4696.2026.0109

牛分枝杆菌融合蛋白ESAT-6/CFP-10/Rv3872抗体间接ELISA检测方法的建立与应用

Establishment and application of an indirect ELISA for detecting antibodies against Mycobacterium bovis based on the fusion protein ESAT-6/CFP-10/Rv3872

王文浩 1储岳峰 1葛家振 2宋国栋 2刘一健 2宋银娟 2郑福英 2李仁阁 2陈胜利 2李劼3

作者信息

  • 1. 石河子大学动物科技学院,新疆石河子 832000||中国农业科学院兰州兽医研究所兰州大学动物医学与生物安全学院动物疫病防控全国重点实验室,甘肃兰州 730000
  • 2. 中国农业科学院兰州兽医研究所兰州大学动物医学与生物安全学院动物疫病防控全国重点实验室,甘肃兰州 730000
  • 3. 石河子大学动物科技学院,新疆石河子 832000
  • 折叠

摘要

Abstract

To develop an indirect enzyme-linked immunosorbent assay(iELISA)for detecting anti-bodies against Mycobacterium bovis(Mb),the Mb genes ESAT6,CFP10,and Rv3872 were selected and connected via a flexible(GGGS)4 linker.The fused sequence was cloned into the pET-28a(+)vector and expressed as a recombinant protein ESAT-6/CFP-10/Rv3872(E-C-R).This recombinant protein was employed as the coating antigen for the establishment and performance evaluation of the iELISA.Optimization experi-ments identified the following conditions as optimal:antigen coating concentration of 100 ng/mL,blocking with 10 g/L betaine solution at 4℃ for 12 h,serum dilution at 1∶100 and incubation at 37℃for 1 h,HRP-conjugated sheep anti-bovine IgG at 1∶10 000 dilution with incubation at 37℃ for 60 min,and substrate color development for 15 min.Under these conditions,the cut-off value(D450nm)was deter-mined to be 0.39.Comparative validation demonstrated that the developed iELISA exhibited higher sen-sitivity than a commercial indirect ELISA kit,and no cross-reactivity with sera positive for Salmonel-la,Mycobacterium avium subsp.paratuberculosis,Mycoplasma bovis,Brucella,or Escherichia coli.Both intra-and inter-assay coefficients of variation were below 10%.The developed iELISA demonstrated good sensitivity,specificity,and reproducibility.Moreover,the antigen-coated plates and reagents maintained stability for over 12 months under storage at 2 to 8℃.When applied to 100 clinical serum samples,the overall agreement rates with the tuberculin skin test,a commercial antibody strip,and a commercial iELISA kit were 87%(87/100),86%(86/100),and 93%(93/100),respectively.In conclusion,this study successfully established a highly sensitive,specific,reproducible,and stable iELISA for detecting Mb antibodies,providing a novel tool for the serological diagnosis of bovine tuberculosis.

关键词

牛分枝杆菌/融合蛋白/抗体/间接ELISA

Key words

Mycobacterium bovis/tandem protein/antibody/indirect ELISA

分类

农业科技

引用本文复制引用

王文浩,储岳峰,葛家振,宋国栋,刘一健,宋银娟,郑福英,李仁阁,陈胜利,李劼..牛分枝杆菌融合蛋白ESAT-6/CFP-10/Rv3872抗体间接ELISA检测方法的建立与应用[J].中国兽医科学,2026,56(8):1067-1076,10.

基金项目

甘肃省联合科研基金重大项目(25JRRA1085) (25JRRA1085)

中国农业科学院创新工程计划项目(CAAS-ZDRW-202410) (CAAS-ZDRW-202410)

甘肃省科技重大专项计划项目(23ZDNA007) (23ZDNA007)

中国兽医科学

1673-4696

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