State Key Laboratory for Animal Disease Control and Prevention, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, China.
Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai, China.
Appl Microbiol Biotechnol. 2024 Apr 8;108(1):290. doi: 10.1007/s00253-024-13127-0.
For the development of a competitive ELISA (cELISA) to detect serum antibodies against the Mycoplasma mycoides subsp. Mycoides (Mmm) (strain PG1), the causative agent of contagious bovine pleuropneumonia (CBPP), all the proteins of this pathogen were analyzed. Then, a specific extracellular region of a transmembrane protein with the potential for diagnosis was identified. After that, a monoclonal antibody (Mab) named 3A8 was obtained using this extracellular region as an immunogen. Finally, a cELISA was established with the extracellular domain of this transmembrane protein as the coating antigen, Mab 3A8 as the competitive antibody, and HRP-labeled goat anti-mouse IgG as the enzyme-labeled antibody. This established method was used to detect the antibody dynamic regularity of goats which are artificially immunized Mmm and was also compared with a commercial ELISA kit. Further, the sera of 1011 different cattle from border provinces of China were monitored using a candidate Mab 3A8 cELISA. The detection results of known background sera used in this study indicate that a candidate diagnostic marker was successfully identified by analyzing all the coding proteins of Mmm in this research, and the cELISA established based on the Mab 3A8 against this protein can detect CBPP-positive serum with specificity and has no cross-reaction with other related epidemic disease-positive sera. In addition, we tested the sera collected from the border areas of China using the established ELISA, and no positive sample was detected. The research protocol of the CBPP cELISA established in this study is different from the traditional method, which can greatly reduce the investment of manpower and capital and save development time. We believe that this study's protocol could serve as a reference for the development of detection methods for mycoplasma and other complex pathogens. KEY POINTS: • A Mmm-specific diagnostic marker was obtained based on protein characteristics. • A cELISA was established for CBPP serum antibody detection. • The serological investigation was conducted for CBPP in the border areas of China.
为了开发一种用于检测引起传染性牛胸膜肺炎(CBPP)的牛支原体亚种(Mmm)(PG1 株)血清抗体的竞争 ELISA(cELISA),分析了该病原体的所有蛋白质。然后,鉴定出一种具有诊断潜力的跨膜蛋白的特定细胞外区域。此后,使用该细胞外区域作为免疫原获得了一种称为 3A8 的单克隆抗体(Mab)。最后,使用该跨膜蛋白的细胞外结构域作为包被抗原,Mab 3A8 作为竞争抗体,HRP 标记的山羊抗小鼠 IgG 作为酶标抗体,建立了 cELISA。该方法用于检测人工免疫 Mmm 的山羊的抗体动态规律,并与商业 ELISA 试剂盒进行了比较。此外,使用候选 Mab 3A8 cELISA 监测了来自中国边境省份的 1011 份不同牛的血清。本研究中使用的已知背景血清的检测结果表明,通过分析本研究中 Mmm 的所有编码蛋白,成功鉴定出候选诊断标志物,基于该蛋白的 Mab 3A8 建立的 cELISA 可以特异性检测 CBPP 阳性血清,与其他相关传染病阳性血清无交叉反应。此外,我们使用建立的 ELISA 检测了来自中国边境地区的血清,未检测到阳性样本。本研究中建立的 CBPP cELISA 的研究方案与传统方法不同,可以大大减少人力和资本的投入,节省开发时间。我们相信,本研究的方案可以为支原体和其他复杂病原体的检测方法的开发提供参考。 要点: • 根据蛋白质特性获得了 Mmm 特异性诊断标志物。 • 建立了用于 CBPP 血清抗体检测的 cELISA。 • 对中国边境地区的 CBPP 进行了血清学调查。