Zhang Yang, Wu Yan, He Jiawei, Lai Jiacui, Ding Honglei
Laboratory of Veterinary Mycoplasmology, College of Veterinary Medicine, Southwest University, Chongqing, China.
Front Vet Sci. 2024 Oct 29;11:1472979. doi: 10.3389/fvets.2024.1472979. eCollection 2024.
Accurate detection is a prerequisite for effective prevention and control of infection. ELISA is the most popular method for the clinical detection of because of its convenience, low cost, and high detection rate. However, the cross-reactivity of commercially available ELISA kits with other avian pathogen-positive sera needs to be addressed. The aim of this study was to establish an ELISA method with high specificity for the detection of anti- antibodies in chicken serum to evaluate the infection status on poultry farms. The recombinant MS087 (rMS087) protein was expressed in BL21 (DE3) and purified by Ni affinity chromatography. An antibody against rMS087 was generated by immunizing BALB/c mice. Bioinformatic analysis revealed that MS087 was conserved among strains. Western blotting and indirect immunofluorescence results indicated that MS087 was not only localized in the cytoplasm and on the membrane but also secreted by the organism. For the established ELISA method based on rMS087, the optimal antigen concentration, blocking buffer, blocking duration, serum dilution, serum incubation duration, secondary antibody dilution, secondary antibody incubation duration and colorimetric reaction duration were 2 μg/mL, 1% BSA, 3 h, 1:500, 1.5 h, 1:20,000, 2 h and 5 min, respectively. Validation of the rMS087-based ELISA revealed a cut-off value of 0.5. The coefficients of variation of both the intra-batch and inter-batch methods were less than 9%. The assay was able to differentiate positive serum against from antisera against nine other avian pathogens and was able to recognize -positive sera at a dilution of 1:1,000. Compared with the commercial ELISA method, the rMS087-based ELISA has the potential to recognize more positive sera against . Collectively, the rMS087-based ELISA is a reproducible, specific, and sensitive serological method for detecting antibodies against in chicken serum and has robust potential for large-scale serological epidemiology of infection on poultry farms.
准确检测是有效预防和控制感染的前提条件。酶联免疫吸附测定(ELISA)因其便捷、成本低且检测率高,是临床检测中最常用的方法。然而,市售ELISA试剂盒与其他禽病原体阳性血清的交叉反应性问题需要解决。本研究的目的是建立一种具有高特异性的ELISA方法,用于检测鸡血清中的抗[病原体名称]抗体,以评估家禽养殖场的[病原体名称]感染状况。重组MS087(rMS087)蛋白在大肠杆菌BL21(DE3)中表达,并通过镍亲和层析法进行纯化。通过免疫BALB/c小鼠产生了抗rMS087的抗体。生物信息学分析表明,MS087在[病原体名称]菌株中具有保守性。蛋白质免疫印迹法和间接免疫荧光结果表明,MS087不仅定位于细胞质和细胞膜上,而且由该生物体分泌。对于基于rMS087建立的ELISA方法,最佳抗原浓度、封闭缓冲液、封闭时间、血清稀释度、血清孵育时间、二抗稀释度、二抗孵育时间和比色反应时间分别为2μg/mL、1%牛血清白蛋白(BSA)、3小时、1:500、1.5小时、1:20000、2小时和5分钟。基于rMS087的ELISA验证显示临界值为0.5。批内和批间方法的变异系数均小于9%。该检测方法能够区分针对[病原体名称]的阳性血清与针对其他九种禽病原体的抗血清,并且能够识别稀释度为1:1000的[病原体名称]阳性血清。与商业ELISA方法相比,基于rMS087的ELISA有潜力识别更多针对[病原体名称]的阳性血清。总体而言,基于rMS087的ELISA是一种可重复、特异且灵敏的血清学方法,用于检测鸡血清中针对[病原体名称]的抗体,在禽养殖场[病原体名称]感染的大规模血清学流行病学研究中具有强大的潜力。