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首页|期刊导航|动物医学进展|基于LppA蛋白的丝状支原体山羊亚种抗体间接ELISA检测方法的建立与应用

基于LppA蛋白的丝状支原体山羊亚种抗体间接ELISA检测方法的建立与应用

马勇杰 刘建行 张淑霞 张琪 许信刚

动物医学进展2026,Vol.47Issue(8):44-49,6.
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动物医学进展2026,Vol.47Issue(8):44-49,6.

基于LppA蛋白的丝状支原体山羊亚种抗体间接ELISA检测方法的建立与应用

Development and Application of an Indirect ELISA Based on the LppA Protein for Detecting Antibodies against Mycoplasma mycoides subsp.Capri

马勇杰 1刘建行 1张淑霞 1张琪 1许信刚1

作者信息

  • 1. 西北农林科技大学动物医学院,陕西杨凌 712100
  • 折叠

摘要

Abstract

An indirect enzyme-linked immunosorbent assay(ELISA)based on recombinant LppA was de-veloped for the detection of antibodies against Mycoplasma mycoides subsp.capri(Mme).The LppA gene was cloned and expressed in Escherichia coli,and the recombinant protein was used as the coating an-tigen.The recombinant LppA protein had an apparent molecular mass of approximately 49 ku and was spe-cifically recognized by Mmc-positive goat serum in Western blot analysis.The optimal antigen coating con-centration was 4 μg/mL,and the optimal dilutions of the serum and HRP-conjugated rabbit anti-goat IgG were 1:100 and 1:2 500,respectively.The cutoff OD450 value was determined to be 0.378.Both the intra-assay and inter-assay coefficients of variation were below 10%.No cross-reactivity was observed with sera positive for Chlamydia abortus,Coxiella burnetii,or caprine astrovirus.Mmc-positive serum remained positive at a dilution of 1:1 024.Among 288 clinical goat serum samples tested using the developed assay,126 were positive,corresponding to a seropositivity rate of 43.75%.The indirect ELISA developed in this study for detecting antibodies against Mmc provides a useful technical tool for epidemiological investiga-tions of Mmc.

关键词

丝状支原体山羊亚种/LppA蛋白/原核表达/酶联免疫吸附试验

Key words

Mycoplasma mycoides subsp.capri/LppA protein/Prokaryotic expression/Enzyme-linked im-munosorbent assay

分类

农业科技

引用本文复制引用

马勇杰,刘建行,张淑霞,张琪,许信刚..基于LppA蛋白的丝状支原体山羊亚种抗体间接ELISA检测方法的建立与应用[J].动物医学进展,2026,47(8):44-49,6.

基金项目

国家重点研发计划(2021YFD1600704) (2021YFD1600704)

省级农业专项资金项目(XNDY2210) (XNDY2210)

动物医学进展

1007-5038

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