Animal Health Service, Thuringian Animal Diseases Fund, Victor-Goerttler-Straße 4, 07745 Jena, Germany.
Animal Health Service, Thuringian Animal Diseases Fund, Victor-Goerttler-Straße 4, 07745 Jena, Germany.
J Dairy Sci. 2023 Dec;106(12):9228-9243. doi: 10.3168/jds.2022-21902. Epub 2023 Aug 23.
The early detection of major mastitis pathogens is crucial for the udder health management of dairy herds. Testing of pooled milk samples, either individual test-day cow samples (TDCS) or aseptically collected pre-milk quarter samples (PMQS) may provide an easy to use and cost-effective group level screening tool. Therefore, the aim of this study was (1) to evaluate the sensitivity (Se) and specificity (Sp) of 2 commercial multiplex real-time PCR test kits applied to pooled milk samples using a Bayesian latent class analysis and (2) to estimate the probability of detection in relation to the pool size and the number of cows positively tested by bacteriological culture (BC) within a pool. Pools of 10, 20 and 50 cows were assembled from 1,912 test-day samples and 7,336 PMQS collected from a total of 2,045 cows from 2 commercial dairy farms. Two commercial quantitative real-time PCR kits were applied to detect Staphylococcus aureus, Streptococcus agalactiae, and Streptococcus dysgalactiae in the pooled samples, and a BC was applied to PMQS yielding a cumulative pool result. A pool was considered BC-positive if it contained at least one BC-positive PMQS. Pathogens were more frequently detected in the PMQS pools than in the TDCS pools. Pools of 10 cows showed the highest probability of detection irrespective of sample type or type of PCR kit compared with larger pool sizes. Estimation with a Bayesian latent class analysis resulted in a median Se in PMQS pools of 10 cows for Staph. aureus of 63.3% for PCR kit I, 78.1% for PCR kit II, and 95.5% for BC; the Sp values were 97.0%, 97.6%, and 89.1%, respectively. The estimated median Se for Strep. species for PCR kits ranged between 77.5 and 85.6% and for BC between 73.7% and 79.2%; the median Sp values ranged between 93.6 and 99.2% for PCR kits, and between 96.9% and 97.4% for BC. In addition, the probability of detection increased with an increasing number of BC-positive cows per pool. To achieve a probability of detection of 90%, the estimated number of positive cows in PMQS pools of 10 cows for kit I was 4.1 for Staph. aureus, 1.5 for Strep. agalactiae, and 1.3 for Strep. dysgalactiae; for the equivalent TDCS pools and pathogens, 6.9, 1.9, and 2.0 positive cows were required, respectively. For Kit II and PMQS pools, the number of positive cows required was 2.8 for Staph. aureus, 1.4 for Strep. agalactiae, and 1.2 for Strep. dysgalactiae; for the equivalent TDCS pools and pathogens, 5.3, 1.8, and 2.0 positive cows were required, respectively. In conclusion, the type of samples used for pooling, the pool size and the number of infected cows per pool determine the probability of detecting an infection with major mastitis pathogens within a pool by PCR testing.
早期检测主要乳腺炎病原体对于奶牛乳房健康管理至关重要。对混合奶样进行检测,无论是个体奶牛测试日样本(TDCS)还是无菌采集的前乳区样本(PMQS),都可能提供一种易于使用且具有成本效益的群体水平筛查工具。因此,本研究的目的是:(1)使用贝叶斯潜在类别分析评估 2 种商业多重实时 PCR 检测试剂盒应用于混合奶样的灵敏度(Se)和特异性(Sp);(2)估计与池大小和池中经细菌培养(BC)阳性的奶牛数量有关的检测概率。从 2 个商业奶牛场的 2045 头奶牛中,共收集了 1912 个测试日样本和 7336 个 PMQS,用于组装 10、20 和 50 头奶牛的混合池。应用 2 种商业定量实时 PCR 试剂盒检测混合样本中的金黄色葡萄球菌、无乳链球菌和停乳链球菌,并应用 BC 检测 PMQS,得到累积的混合池结果。如果混合池包含至少一个 BC 阳性 PMQS,则认为混合池为 BC 阳性。与 TDCS 池相比,PMQS 池更频繁地检测到病原体。与较大的池大小相比,无论样本类型或 PCR 试剂盒类型如何,10 头奶牛的池均显示出最高的检测概率。使用贝叶斯潜在类别分析进行估计,结果表明,对于金黄色葡萄球菌,PCR 试剂盒 I 的 PMQS 池的中位 Se 为 63.3%,PCR 试剂盒 II 的中位 Se 为 78.1%,BC 的中位 Se 为 95.5%;相应的 Sp 值分别为 97.0%、97.6%和 89.1%。用于 Strep. 物种的估计中位 Se 范围在 PCR 试剂盒之间为 77.5%至 85.6%,BC 之间为 73.7%至 79.2%;PCR 试剂盒的中位 Sp 值范围为 93.6%至 99.2%,BC 的中位 Sp 值范围为 96.9%至 97.4%。此外,随着池中 BC 阳性奶牛数量的增加,检测概率也随之增加。要达到 90%的检测概率,对于 PCR 试剂盒 I 的 10 头奶牛 PMQS 池,金黄色葡萄球菌需要 4.1 头阳性奶牛,无乳链球菌需要 1.5 头阳性奶牛,停乳链球菌需要 1.3 头阳性奶牛;对于等效的 TDCS 池和病原体,分别需要 6.9、1.9 和 2.0 头阳性奶牛。对于试剂盒 II 和 PMQS 池,金黄色葡萄球菌需要 2.8 头阳性奶牛,无乳链球菌需要 1.4 头阳性奶牛,停乳链球菌需要 1.2 头阳性奶牛;对于等效的 TDCS 池和病原体,分别需要 5.3、1.8 和 2.0 头阳性奶牛。总之,用于混合的样本类型、池大小以及每个池中的感染奶牛数量决定了通过 PCR 检测在池内检测到主要乳腺炎病原体感染的概率。