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通过聚合酶链反应(PCR)检测活母猪扁桃体拭子中细胞外因子阳性的2型猪链球菌菌株。

Detection of extracellular factor-positive Streptococcus suis serotype 2 strains in tonsillar swabs of live sows by PCR.

作者信息

Swildens Bas, Wisselink Henk J, Engel Bas, Smith Hilde E, Nielen Mirjam, Verheijden Jos H M, Stegeman J Arjan

机构信息

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.

出版信息

Vet Microbiol. 2005 Aug 30;109(3-4):223-8. doi: 10.1016/j.vetmic.2005.04.024.

Abstract

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.

摘要

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。

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