Swildens Bas, Wisselink Henk J, Engel Bas, Smith Hilde E, Nielen Mirjam, Verheijden Jos H M, Stegeman J Arjan
Faculty of Veterinary Medicine, Department of Farm Animal Herd Health and Reproduction, P.O. Box 80151, Yalelaan 7, 3584 CL Utrecht 3058 TD, The Netherlands.
Vet Microbiol. 2005 Aug 30;109(3-4):223-8. doi: 10.1016/j.vetmic.2005.04.024.
In this study, the sensitivity (Se) and specificity (Sp) of a PCR for the detection of EF-positive Streptococcus suis serotype 2 strains in tonsillar swabs of live sows were assessed. We sampled 471 sows originating from four farrow-to-finish farms by tonsillar swabbing and collected their tonsils after slaughter. On these specimens, a PCR, a bacterial examination (BE) or both were performed for the detection of EF-positive S. suis serotype 2 strains. Swab-PCR, Tonsil-PCR and Tonsil-BE were regarded as three integral tests. A Bayesian approach was used to calculate the Se and Sp of the tests. Se and Sp for Swab-PCR were 0.63 (95% credibility interval <0.52, 0.74>) and 0.96 (<0.92, 0.99>), respectively. Values for Se and Sp of Tonsil-PCR amounted to 0.88 (<0.75, 0.96>) and 0.94 (<0.87, 0.99>), respectively. For Tonsil-BE, Se was 0.65 (<0.51, 0.76>) and Sp was 0.97 (<0.91, 0.99>). Repetition of the swabbing procedure after 10 min resulted in a higher Se 0.85 (<0.67, 0.96>) than the Se of the first-Swab-PCR. Repetition of the PCR on the same sample did not result in any significant changes in the outcome of the analysis.
在本研究中,评估了一种用于检测活母猪扁桃体拭子中EF阳性猪链球菌2型菌株的PCR的敏感性(Se)和特异性(Sp)。我们通过扁桃体拭子对来自四个从仔猪到育肥猪养殖场的471头母猪进行了采样,并在屠宰后收集了它们的扁桃体。对这些样本进行了PCR、细菌检查(BE)或两者都进行,以检测EF阳性猪链球菌2型菌株。拭子-PCR、扁桃体-PCR和扁桃体-BE被视为三个完整的检测。采用贝叶斯方法计算检测的Se和Sp。拭子-PCR的Se和Sp分别为0.63(95%可信区间<0.52, 0.74>)和0.96(<0.92, 0.99>)。扁桃体-PCR的Se和Sp值分别为0.88(<0.75, 0.96>)和0.94(<0.87, 0.99>)。对于扁桃体-BE,Se为0.65(<0.51, 0.76>),Sp为0.97(<0.91, 0.99>)。10分钟后重复拭子采样程序,其Se为0.85(<0.67, 0.96>),高于首次拭子-PCR的Se。对同一样本重复PCR并未导致分析结果有任何显著变化。