Department of Microbiology, Karaj Branch, Islamic Azad University, Karaj, Iran.
Razi Vaccine and Serum Research Institute (RVSRI), Agricultural Research, Education and Extension Organization (AREEO), Karaj, Iran.
Arch Razi Inst. 2024 Feb 1;79(1):201-210. doi: 10.32592/ARI.2024.79.1.201. eCollection 2024 Feb.
The most preferred method for the detection of foot-and-mouth disease (FMD) viral antigen and identification of viral serotype is the enzyme-linked immunosorbent assay (ELISA). Diagnostic tests with high sensitivity are necessary both to distinguish infected vaccinated animals and execute disease control programs for the identification of the carrier animals. The current strategies for the detection of FMD virus are mainly based on the capture antibody (sandwich) ELISA test. The usage of laying pullets as an animal bioreactor for the production of specific egg yolk antibodies (IgY) has increased in recent years due to its high yield, affinity, low price, and quick production turnover. The present study aimed to produce a concentrated and purified IgY polyclonal antibody to design a capture antibody ELISA kit against the FMD virus (FMDV) serotype A. At first, laying hens were immunized with inactivated FMDV serotype virus, and then, on days 14, 21, and 28 following vaccination, the eggs and sera were collected. Afterward, the IgY polyclonal antibodies were extracted and purified from the chicken egg yolk using a polyethylene glycol 6000-ethanol precipitation procedure. Extracts were filtered, purified by ion exchange chromatography, and dialyzed. The purified IgY concentration, estimated by Bradford assay, confirmed its presence by SDS-PAGE and Western blot and also its specific immune reaction by Ouchterlony double immunodiffusion and Dot blot tests. Moreover, for achieving the optimum concentration of antigen/antibody (sera) in sandwich ELISA, a checkerboard titration test was set up based on indirect ELISA results. Eventually, 119 previously confirmed samples (including 80 positive and 39 negative) by both real-time polymerase chain reaction (quantitative PCR, qPCR) and a commercial ELISA kit were used for evaluation of the sensitivity and accuracy of our developed Capture antibody ELISA kit. In this manner, the sensitivity and specificity of our designed kit were 100% and 98%, respectively. Accordingly, the present developed capture ELISA kit based on IgY had high sensitivity and specificity for FMD virus detection and it could be used in the future for both commercial detecting and serotyping applications.
检测口蹄疫(FMD)病毒抗原和鉴定病毒血清型最常用的方法是酶联免疫吸附试验(ELISA)。为了区分感染接种动物并执行疾病控制计划以识别带菌动物,需要高灵敏度的诊断测试。目前 FMD 病毒的检测策略主要基于捕获抗体(夹心)ELISA 测试。由于其产量高、亲和力强、价格低廉、生产周转快,近年来,将产蛋母鸡用作生产特异性卵黄抗体(IgY)的动物生物反应器的使用有所增加。本研究旨在生产浓缩和纯化的 IgY 多克隆抗体,设计针对 FMD 病毒(FMDV)血清型 A 的捕获抗体 ELISA 试剂盒。首先,用灭活的 FMDV 血清型病毒对产蛋母鸡进行免疫,然后在接种后第 14、21 和 28 天收集鸡蛋和血清。然后,使用聚乙二醇 6000-乙醇沉淀法从鸡卵黄中提取和纯化 IgY 多克隆抗体。提取物经过过滤、离子交换层析纯化并透析。Bradford assay 估计的纯化 IgY 浓度通过 SDS-PAGE 和 Western blot 证实了其存在,通过 Ouchterlony 双免疫扩散和 Dot blot 试验证实了其特异性免疫反应。此外,为了在夹心 ELISA 中达到抗原/抗体(血清)的最佳浓度,根据间接 ELISA 结果建立了棋盘滴定试验。最终,使用 119 份先前通过实时聚合酶链反应(定量 PCR,qPCR)和商业 ELISA 试剂盒确认的样本(包括 80 份阳性和 39 份阴性)来评估我们开发的捕获抗体 ELISA 试剂盒的敏感性和准确性。通过这种方式,我们设计的试剂盒的敏感性和特异性分别为 100%和 98%。因此,基于 IgY 的本研究开发的捕获 ELISA 试剂盒对口蹄疫病毒检测具有高灵敏度和特异性,可用于未来的商业检测和血清分型应用。