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A double antibody sandwich enzyme-linked immunosorbent assay for detection of soft-shelled turtle iridovirus antigens

机译:双抗体夹心酶联免疫吸附法检测甲鱼虹膜病毒抗原

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摘要

A double antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) for detection of the soft-shelled turtle iridovirus (STIV) was developed using a specific monoclonal antibody (mAb) against STIV and anti-STIV rabbit serum. Using DAS-ELISA, the detection limit of STIV was found to be 10  PFU/ml. The positive rate of 15 STIV samples was 100%, while the positive rate of 100 other aquatic virus samples was 0%. These data show that DAS-ELISA is highly specific and sensitive for the detection of STIV. In clinical tests, 128 samples isolated from pond-reared turtles were subjected to DAS-ELISA and PCR. The overall agreement between the results obtained by DAS-ELISA and PCR was 98.4%. The results indicate that the DAS-ELISA method could be used for diagnosing diseases caused by STIV.
机译:使用针对STIV和抗STIV兔血清的特异性单克隆抗体(mAb),开发了用于检测甲鱼虹膜病毒(STIV)的双抗体夹心酶联免疫吸附测定(DAS-ELISA)。使用DAS-ELISA,STIV的检出限为10 PFU / ml。 15个STIV样品的阳性率为100%,而其他100个水生病毒样品的阳性率为0%。这些数据表明DAS-ELISA对STIV的检测具有高度特异性和敏感性。在临床测试中,对从池塘饲养的乌龟中分离出的128个样品进行了DAS-ELISA和PCR。通过DAS-ELISA和PCR获得的结果之间的总体一致性为98.4%。结果表明,DAS-ELISA方法可用于STIV引起的疾病的诊断。

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