首页> 外文期刊>Clinical and diagnostic laboratory immunology >Evaluation of two recombinant Maedi-visna virus proteins for use in an enzyme-linked immunosorbent assay for the detection of serum antibodies to ovine lentiviruses.
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Evaluation of two recombinant Maedi-visna virus proteins for use in an enzyme-linked immunosorbent assay for the detection of serum antibodies to ovine lentiviruses.

机译:评价用于酶联免疫吸附测定的两种重组Maedi-visna病毒蛋白,以检测针对绵羊慢病毒的血清抗体。

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Defined segments of the gag polyprotein and transmembrane envelope glycoprotein from Maedi-visna virus were expressed as glutathione S-transferase fusion proteins in Escherichia coli and evaluated singly and in combination for use in an enzyme-linked immunosorbent assay (ELISA). Two hundred sixty field serum specimens from 15 sheep flocks were tested in parallel with recombinant and whole-virus antigens, and the relative sensitivities and specificities of the recombinant antigens were calculated. When the recombinant gag and transmembrane proteins were used in combination, a sensitivity of 97.4% and a specificity of 99.4% relative to whole-virus antigen were observed, indicating the utility of these proteins in diagnostic testing.
机译:来自Maedi-visna病毒的gag多蛋白和跨膜包膜糖蛋白的定义片段在大肠杆菌中表达为谷胱甘肽S-转移酶融合蛋白,并单独或组合评估用于酶联免疫吸附测定(ELISA)。从重组羊和全病毒抗原中平行检测了来自15个羊群的260个野外血清标本,并计算了重组抗原的相对敏感性和特异性。当重组gag蛋白和跨膜蛋白结合使用时,相对于全病毒抗原的敏感性为97.4%,特异性为99.4%,表明这些蛋白在诊断测试中的实用性。

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