Instituto de Medicina Preventiva Veterinaria, Universidad Austral de Chile, Valdivia, Chile.
Instituto de Medicina Preventiva Veterinaria, Universidad Austral de Chile, Valdivia, Chile.
Prev Vet Med. 2020 Sep;182:105076. doi: 10.1016/j.prevetmed.2020.105076. Epub 2020 Jun 23.
The objective of this study was to estimate the performance of the peptide magnetic separation PCR test (PMS-PCR) for the diagnosis of Mycobacterium avium subsp. paratuberculosis (MAP) in sub-clinically infected dairy cattle. Twenty-one herds were randomly selected from a source population of 131 commercial dairy herds with a known history of MAP infection, located in the De Los Rios and De Los Lagos regions, in southern Chile. In the selected herds, all milking cows with ≥2 parities and without any clinical signs were sampled, collecting feces and blood-serum samples. The PMS-PCR test was used to analyze the fecal samples, while serum samples were analyzed using a commercial ELISA kit. A Bayesian latent class model was used to estimate the sensitivity (Se) and specificity (Sp) of the diagnostic tests. A total of 1381 animals were sampled in the 21 selected dairy herds, with an average sample size of 65 animals per herd (range 10-721). The PMS-PCR test had a greater Se than the ELISA test, with a median of 85.5 % (posterior probability interval (PPI) 95 %: 79.3-91.0%), while the ELISA test presented a median of 21.7 % (95 % PPI: 18.3-25.4%). On the other hand, the ELISA test had a better Sp than the PMS-PCR test, with a median of 97.7 % (95 % PPI: 96.6-98.5%), whereas PMS-PCR presented a median of 90.8 % (95 % PPI: 88.3-93.9%). Model results showed that PMS-PCR has a better Se than all available tests for MAP diagnosis in subclinical animals. However, this test should be used with care in herds with high infection rates, where a high MAP environmental load is expected, potentially increasing the frequency of false positive cases due to the pass-through phenomenon.
本研究旨在评估肽磁分离 PCR 检测(PMS-PCR)在亚临床感染奶牛中诊断禽分枝杆菌副结核亚种(MAP)的性能。从智利南部德洛斯里奥斯和德洛斯 Lagos 地区已知存在 MAP 感染史的 131 个商业奶牛场的源人群中随机选择了 21 个牛群。在选定的牛群中,采集了所有产奶量≥2 胎且无任何临床症状的奶牛的粪便和血清样本。使用 PMS-PCR 检测分析粪便样本,使用商业 ELISA 试剂盒分析血清样本。采用贝叶斯潜在类别模型估计诊断试验的敏感性(Se)和特异性(Sp)。在 21 个选定的奶牛场中,共对 1381 头动物进行了采样,每个牛群的平均采样量为 65 头(范围为 10-721 头)。PMS-PCR 检测的 Se 高于 ELISA 检测,中位数为 85.5%(95%后验概率区间(PPI):79.3-91.0%),而 ELISA 检测的中位数为 21.7%(95% PPI:18.3-25.4%)。另一方面,ELISA 检测的 Sp 优于 PMS-PCR 检测,中位数为 97.7%(95% PPI:96.6-98.5%),而 PMS-PCR 检测的中位数为 90.8%(95% PPI:88.3-93.9%)。模型结果表明,PMS-PCR 在亚临床动物中诊断 MAP 的所有现有检测方法中具有更好的 Se。然而,在预期 MAP 环境负荷较高的高感染率牛群中,应谨慎使用该检测方法,因为由于穿透现象,可能会增加假阳性病例的频率。