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首页> 外文期刊>New Zealand Veterinary Journal >Use of an enzyme-linked immunosorbent assay for detecting bovine viral diarrhoea virus antibodies in individual cow milk samples.
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Use of an enzyme-linked immunosorbent assay for detecting bovine viral diarrhoea virus antibodies in individual cow milk samples.

机译:酶联免疫吸附法在检测单个牛乳样品中牛病毒性腹泻病毒抗体中的用途。

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AIMS: To calculate and verify an adjustment for the test result cut-off when testing milk samples using a bovine viral diarrhoea (BVD) antibody test so that it is a better approximation of the test on serum as the reference. Previous experience has demonstrated that different cut points may be required for results from milk and serum. METHODS: Paired milk and serum samples were collected from 90 cows from three herds in two regions of New Zealand and were tested using a commercially available bovine viral diarrhoea virus (BVD) antibody ELISA. A regression equation with second-order polynomial was developed to estimate a milk sample to positive-control optical density ratio (S/P ratio) value from a serum S/P ratio, and the milk values equivalent to the recommended serum cut points were calculated. The change in milk test result agreement with the result based on serum samples was assessed primarily using weighted Kappa statistics. RESULTS: The new cut points between negative and suspect, and suspect and positive milk samples were defined as S/P ratios of >=0.08 and >=0.13 respectively, compared to cut points for serum samples of >=0.20 and >=0.30, respectively. Using the new cut points increased the level of agreement (weighted Kappa) between serum and milk from 0.58 to 0.82. CLINICAL RELEVANCE: Milk BVD antibody testing can be used to estimate serum BVD antibody status. This is particularly useful for investigations where susceptibility to infection or the incidence of new infections is of interest. CONCLUSIONS: Using new adjusted cut points for milk, ELISA BVD antibody testing resulted in a higher level of agreement with serum samples.
机译:目的:在使用牛病毒性腹泻(BVD)抗体测试测试牛奶样品时,计算和验证测试结果截止值的调整,以便更好地近似血清作为参考。先前的经验表明,牛奶和血清的结果可能需要不同的切点。方法:从新西兰两个地区的三头牛群的90头奶牛中采集配对的牛奶和血清样本,并使用市售牛病毒性腹泻病毒(BVD)抗体ELISA进行测试。建立了具有二阶多项式的回归方程,以根据血清S / P比估算牛奶样品与阳性对照的光密度比(S / P比)值,并计算了与推荐血清切点相当的牛奶值。主要使用加权Kappa统计量评估牛奶测试结果与基于血清样本得出的结果之间的变化。结果:阴性和可疑,可疑和阳性乳样品之间的新分界点分别定义为S / P比分别> = 0.08和> = 0.13,而血清样品的分界点> = 0.20和> = 0.30,分别。使用新的切点将血清和牛奶之间的一致性(加权Kappa)水平从0.58提高到0.82。临床相关性:牛奶BVD抗体检测可用于评估血清BVD抗体状态。这对于对感染的易感性或新感染的发生率感兴趣的研究特别有用。结论:使用新调整的牛奶切点,ELISA BVD抗体检测可提高与血清样品的一致性。

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