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A novel IgY-Aptamer hybrid system for cost-effective detection of SEB and its evaluation on food and clinical samples

机译:用于经济有效地检测SEB的新型IgY-Aptamer混合系统及其对食品和临床样品的评估

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摘要

In the present study, we introduce a novel hybrid sandwich-ALISA employing chicken IgY and ssDNA aptamers for the detection of staphylococcal enterotoxin B (SEB). Cloning, expression and purification of the full length recombinant SEB was carried out. Anti-SEB IgY antibodies generated by immunizing white leg-horn chickens with purified recombinant SEB protein and were purified from the immunized egg yolk. Simultaneously, ssDNA aptamers specific to the toxin were prepared by SELEX method on microtiter well plates. The sensitivity levels of both probe molecules i.e., IgY and ssDNA aptamers were evaluated. We observed that the aptamer at 250 ngmL−1 concentration could detect the target antigen at 50 ngmL−1 and the IgY antibodies at 250 ngmL−1, could able to detect 100 ngmL−1 antigen. We further combined both the probes to prepare a hybrid sandwich aptamer linked immune sorbent assay (ALISA) wherein the IgY as capturing molecule and biotinylated aptamer as revealing probe. Limit of detection (LOD) for the developed method was determined as 50 ngmL−1. Further, developed method was evaluated with artificially SEB spiked milk and natural samples and obtained results were validated with PCR. In conclusion, developed ALISA method may provide cost-effective and robust detection of SEB from food and environmental samples.
机译:在本研究中,我们介绍了一种新颖的杂交三明治-ALISA,它采用鸡IgY和ssDNA适体来检测葡萄球菌肠毒素B(SEB)。进行了全长重组SEB的克隆,表达和纯化。抗SEB IgY抗体是通过用纯化的重组SEB蛋白免疫白腿鸡而产生的,并从免疫的蛋黄中纯化得到。同时,通过SELEX法在微量滴定孔板上制备对毒素特异的ssDNA适体。评价了两种探针分子即IgY和ssDNA适体的敏感性水平。我们观察到250 ngmL-1的适体可以检测到50 ngmL-1的靶抗原,而250 ngmL-1的IgY抗体可以检测100 ngmL-1的抗原。我们进一步结合了两种探针,以制备杂交夹心适体连接的免疫吸附测定(ALISA),其中IgY作为捕获分子,而生物素化的适体作为显示探针。所开发方法的检出限(LOD)确定为50µngmL-1。此外,用人工SEB加标牛奶和天然样品评估了开发的方法,并通过PCR验证了获得的结果。总之,开发的ALISA方法可以提供经济高效且可靠的食品和环境样品中SEB检测方法。

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