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Development and evaluation of a MAb based competitive-ELISA using helicase domain of NS3 protein for sero-diagnosis of bovine viral diarrhea in cattle and buffaloes

机译:利用NS3解旋酶结构域基于MAb的竞争酶联免疫吸附测定法的开发和评估,用于牛和水牛的牛病毒性腹泻血清学诊断

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摘要

The aim of this study was to develop a competitive inhibition ELISA (CI-ELISA) for detection of antibodies to bovine viral diarrhea virus (BVDV) using the helicase domain of NS3 (non-structural) protein and monoclonal antibody (MAb) against it and to estimate its sensitivity and specificity using two commercial ELISA kits as independent references. The 45-kDa helicase domain of NS3 protein of BVDV was expressed in Escherichia coli and 18 MAbs were developed against it. MAb-11G8 was selected for use in CI-ELISA on the basis of maximum inhibition (90%) obtained with BVDV type 1 infected calf serum. Based on the distribution of percent inhibition of known negative sera (n = 166), a cut-off value was set at 40% inhibition. In testing 914 field serum samples of cattle (810) and buffaloes (104), the CI-ELISA showed a relative specificity of 95.75% and 97.38% and sensitivity of 96% and 94.43% with Ingenesa kit and Institut Pourquier kit, respectively. This study proved that the use of helicase domain of NS3 (45-kDa) is equally good as the whole NS3 protein (80-kDa) used in commercial kits for detection of BVDV antibodies in cattle and buffaloes.
机译:这项研究的目的是开发竞争性抑制ELISA(CI-ELISA),使用NS3(非结构性)蛋白的解旋酶结构域和针对它的单克隆抗体(MAb)检测牛病毒性腹泻病毒(BVDV)的抗体,以及使用两个市售ELISA试剂盒作为独立参考来评估其敏感性和特异性。 BVDV NS3蛋白的45 kDa解旋酶结构域在大肠杆菌中表达,并针对它开发了18个单克隆抗体。基于BVDV 1型感染小牛血清获得的最大抑制作用(90%),选择MAb-11G8用于CI-ELISA。根据已知阴性血清抑制百分比的分布(n = 166),将临界值设为40%抑制。在测试914头牛(810)和水牛(104)的野外血清样品中,CI-ELISA分别显示了Ingenesa试剂盒和Institut Pourquier试剂盒的相对特异性为95.75%和97.38%,灵敏度为96%和94.43%。这项研究证明,使用NS3的解旋酶结构域(45-kDa)与用于检测牛和水牛BVDV抗体的商业试剂盒中使用的整个NS3蛋白(80-kDa)一样好。

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