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首页> 外文期刊>Journal of Clinical Microbiology >Comparative evaluation of an enzyme-linked immunosorbent assay (ELISA) to detect antibodies directed against glycoprotein I of pseudorabies virus and a conventional ELISA and neutralization tests.
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Comparative evaluation of an enzyme-linked immunosorbent assay (ELISA) to detect antibodies directed against glycoprotein I of pseudorabies virus and a conventional ELISA and neutralization tests.

机译:酶联免疫吸附测定(ELISA)的比较评估,以检测针对伪狂犬病病毒糖蛋白I的抗体,以及常规ELISA和中和测试。

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To determine whether a newly developed enzyme-linked immunosorbent assay (ELISA), which detects antibodies directed against glycoprotein I (gI) of pseudorabies virus, is suitable for serodiagnosis, it was compared with a conventional ELISA and two neutralization tests. The gI ELISA was 99.2% as sensitive and 100% as specific as the conventional ELISA. Antibody titers measured by the gI ELISA were lower than those measured by the conventional ELISA, comparable to those measured by the 24-h neutralization test, and higher than those measured by the 1-h neutralization test. After experimental infections in pigs, antibodies were first detected by the gI ELISA on postinoculation day (PID) 14, by both neutralization tests on PID 7, and by the ELISA on PID 10. All four tests showed the same rate of decline of maternal antibodies in pigs born to sows that had been vaccinated with inactivated vaccine. Thus, not only is the gI ELISA unique in being able to differentiate infected pigs from those vaccinated with gI-negative vaccines, but it is also as useful as a conventional ELISA and as neutralization tests for serodiagnosis.
机译:为了确定新开发的酶联免疫吸附测定(ELISA)是否适合血清学诊断,该酶联免疫吸附测定(ELISA)可检测针对伪狂犬病病毒糖蛋白I(gI)的抗体,将其与常规ELISA和两次中和测试进行比较。 gI ELISA的灵敏度是常规ELISA的99.2%,特异性是100%。通过gI ELISA测得的抗体滴度低于常规ELISA测得的抗体滴度,与通过24小时中和试验测得的抗体滴度相当,并且高于通过1小时中和试验测得的抗体滴度。在猪进行实验性感染后,首先在接种后第14天通过gI ELISA,通过PID 7进行中和测试以及通过PID 10进行ELISA检测抗体。所有四个测试均显示母体抗体的下降速率相同接种灭活疫苗的母猪出生的猪中。因此,gI ELISA不仅在区分感染的猪和接种gI阴性疫苗的猪方面具有独特性,而且还可用作常规ELISA和中和血清学诊断试剂。

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