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用于检测牛血清中抗副结核分枝杆菌抗体的五种酶联免疫吸附测定(ELISA)试剂盒的评估。

Evaluation of five ELISA test kits for the measurement of antibodies against Mycobacterium avium subspecies paratuberculosis in bovine serum.

作者信息

Köhler Heike, Burkert Beate, Pavlik Ivo, Diller Roland, Geue Lutz, Conraths Franz J, Martin Gerald

机构信息

Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Molecular Pathogenesis, Jena, Germany.

出版信息

Berl Munch Tierarztl Wochenschr. 2008 May-Jun;121(5-6):203-10.

Abstract

Five commercially available ELISA tests for the detection of antibodies against Mycobacterium avium subsp. paratuberculosis in bovine serum were evaluated at the individual animal level using sera from 286 paratuberculosis-free and 110 paratuberculosis-infected dairy cattle. Sensitivity (Se) and specificity (Sp) of the tests were estimated after determination of the cut-off dtheta by TG-ROC analysis or using the cut-off values recommended by the manufacturers, respectively. When the dtheta cut-off values were applied, the five ELISA tests showed sub-optimal Se and Sp. Adopting the cut-offs recommended by the manufacturers, the Sp of four of the five ELISA increased, two tests reaching Sp > or = 99.0%. Test sensitivity clearly depended on the disease state of the animals examined. Se was significantly higher in clinically diseased than in latently infected dairy cattle. Calculation of the positive and negative predictive values indicated that, depending on the test, a considerable proportion of false positive and false negative results have to be expected. Therefore, the suitability of antibody detection for the diagnosis of paratuberculosis in individual animals is questioned.

摘要

使用来自286头无副结核病和110头感染副结核病的奶牛血清,在个体动物水平上对5种市售用于检测牛血清中抗副结核分枝杆菌亚种抗体的ELISA检测方法进行了评估。分别通过TG-ROC分析确定临界值dtheta或使用制造商推荐的临界值后,估计了检测方法的敏感性(Se)和特异性(Sp)。应用dtheta临界值时,5种ELISA检测方法的Se和Sp均未达到最佳。采用制造商推荐的临界值时,5种ELISA检测方法中有4种的Sp提高,其中2种检测方法的Sp≥99.0%。检测敏感性明显取决于所检测动物的疾病状态。临床患病奶牛的Se显著高于潜伏感染奶牛。阳性和阴性预测值的计算表明,根据检测方法的不同,预计会出现相当比例的假阳性和假阴性结果。因此,抗体检测用于个体动物副结核病诊断的适用性受到质疑。

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