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一种用于检测牛1型疱疹病毒(BHV - 1)抗体的定量酶联免疫吸附测定法。

A quantitative enzyme-linked immunosorbent assay for bovine herpesvirus type 1 (BHV-1) antibody.

作者信息

Lyaku J R, Nettleton P F, Scott G R

机构信息

Moredun Research Institute, Edinburgh, U.K.

出版信息

Biologicals. 1990 Jul;18(3):199-205. doi: 10.1016/1045-1056(90)90007-m.

Abstract

A quantitative enzyme-linked immunosorbent assay (ELISA) was developed to detect and measure antibody to bovine herpesvirus type 1 (BHV-1) in cattle sera. The optical density produced from a single dilution of test serum was compared with a standard curve and the results were read and printed out from a computer interfaced to a multichannel ELISA reader. The printed results were expressed in ELISA units. The ELISA results obtained on 370 cattle sera were compared with those of the serum neutralisation test (SNT). An agreement of 90.5% was obtained when reciprocal SNT titres equal to or greater than 4 and IgG ELISA units equal to or greater than 50 were taken as indicative of a specific reaction. Of the 370 sera, 35 gave discrepant results of which 21 were SNT positive/IgG ELISA negative and 14 were SNT negative/IgG ELISA positive. When the SNT positive sera negative in the IgG ELISA were tested in an IgM ELISA, 19 were found to be positive. Thus, when the IgG and IgM ELISA results were combined the overall agreement between the ELISA and SNT increased to 95.7%. The IgG ELISA had a sensitivity of 82.4% and specificity of 94.4% relative to the SNT, whereas the combined IgG and IgM ELISA results gave a sensitivity and specificity of 98.3% and 94.4% respectively. There was a good positive correlation between the two tests (r = 0.86).

摘要

已开发出一种定量酶联免疫吸附测定法(ELISA),用于检测和测量牛血清中针对牛疱疹病毒1型(BHV-1)的抗体。将测试血清单次稀释产生的光密度与标准曲线进行比较,结果通过与多通道ELISA读数器相连的计算机读取并打印出来。打印结果以ELISA单位表示。将在370份牛血清上获得的ELISA结果与血清中和试验(SNT)的结果进行比较。当将SNT滴度倒数等于或大于4且IgG ELISA单位等于或大于50视为特异性反应时,一致性为90.5%。在这370份血清中,有35份结果不一致,其中21份为SNT阳性/I gG ELISA阴性,14份为SNT阴性/I gG ELISA阳性。当在IgM ELISA中检测IgG ELISA呈阴性的SNT阳性血清时,发现19份为阳性。因此,当将IgG和IgM ELISA结果结合起来时,ELISA与SNT之间的总体一致性提高到95.7%。相对于SNT,IgG ELISA的敏感性为82.4%,特异性为94.4%,而IgG和IgM ELISA结果相结合时,敏感性和特异性分别为98.3%和94.4%。两种检测方法之间存在良好的正相关性(r = 0.86)。

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