评估特异性鸡 IgY 抗体的价值,开发口蹄疫诊断捕获抗体 ELISA 试剂盒。

Q3 Veterinary Archives of Razi Institute Pub Date : 2024-02-01 DOI:10.32592/ARI.2024.79.1.201
Z Ivani, M M Ranjbar, B Hemati, N Harzandi, S M Azimi
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引用次数: 0

摘要

检测口蹄疫(FMD)病毒抗原和鉴定病毒血清型的首选方法是酶联免疫吸附试验(ELISA)。高灵敏度的诊断检测对于区分受感染的疫苗接种动物和执行疾病控制计划以识别带菌动物都是必要的。目前检测口蹄疫病毒的策略主要基于捕获抗体(夹心)酶联免疫吸附试验。由于蛋鸡卵黄抗体(IgY)产量高、亲和力强、价格低廉、生产周转快,近年来越来越多地使用蛋鸡作为生产特异性蛋黄抗体(IgY)的动物生物反应器。本研究旨在生产浓缩纯化的 IgY 多克隆抗体,以设计针对口蹄疫病毒(FMDV)血清型 A 的捕获抗体 ELISA 试剂盒。首先用灭活的口蹄疫病毒血清型病毒对蛋鸡进行免疫接种,然后在接种后第 14、21 和 28 天收集鸡蛋和血清。然后用聚乙二醇 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、离子交换色谱纯化和透析。用布拉德福德测定法估算纯化的 IgY 浓度,用 SDS-PAGE 和 Western 印迹法确认其存在,还用 Ouchterlony 双免疫扩散和 Dot 印迹试验确认其特异性免疫反应。此外,为了使夹心酶联免疫吸附试验中的抗原/抗体(血清)达到最佳浓度,还根据间接酶联免疫吸附试验的结果建立了棋盘滴定试验。最终,119 份先前通过实时聚合酶链式反应(定量 PCR,qPCR)和商业 ELISA 试剂盒确认的样本(包括 80 份阳性样本和 39 份阴性样本)被用于评估我们开发的捕获抗体 ELISA 试剂盒的灵敏度和准确性。结果表明,我们设计的试剂盒的灵敏度和特异性分别为 100%和 98%。因此,目前开发的基于 IgY 的捕获抗体 ELISA 试剂盒在口蹄疫病毒检测方面具有很高的灵敏度和特异性,将来可用于商业检测和血清分型应用。
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Evaluation of specific chicken IgY antibody value developing diagnostic capture antibody ELISA kit against Foot and Mouth disease.

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.

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来源期刊
Archives of Razi Institute
Archives of Razi Institute Veterinary-Veterinary (all)
CiteScore
1.50
自引率
0.00%
发文量
108
审稿时长
12 weeks
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