首页> 美国卫生研究院文献>Canadian Journal of Comparative Medicine >Comparison of bacterial culture polymerase chain reaction and a mix-enzyme-linked immunosorbent assay for the detection of Salmonella status in grow-to-finish pigs in western Canada with a Bayesian approach
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Comparison of bacterial culture polymerase chain reaction and a mix-enzyme-linked immunosorbent assay for the detection of Salmonella status in grow-to-finish pigs in western Canada with a Bayesian approach

机译:贝叶斯方法比较细菌培养聚合酶链反应和混合酶联免疫吸附法检测加拿大西部成年猪的沙门氏菌状况

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摘要

Among grow-to-finish pigs from 10 herds in Alberta and Saskatchewan, 23 (16%) of 144 fecal samples were culture-positive and 40 (28%) of 144 pigs were seropositive for Salmonella. With a Bayesian model specifying dependence between the 2 tests, the sensitivity (Se) of culture and real-time polymerase chain reaction (RT-PCR) was 79% to 86%, depending on the cut-off value for the enzyme-linked immunosorbent assay (ELISA). Culture specificity (Sp) was assumed to be 100%; RT-PCR Sp was found to be 94%. The ELISA Se was 76% and 51% at optical density cut-off values ≥ 20% and ≥ 40%, respectively; the Sp was 94% at each cut-off value. The model showed some sensitivity to ELISA prior information, the ELISA Se being approximately 8% lower when informative prior information was specified in the model. When there was no adjustment for dependence between culture and RT-PCR, the posterior estimates for both culture and RT-PCR Se were 11% higher than with the conditional-dependence model and had considerably narrower probability intervals, which suggests that correlation between culture and PCR is important and should be adjusted for in future studies.
机译:在来自艾伯塔省和萨斯喀彻温省的10个畜群的成年猪中,144份粪便样品中有23株(16%)的沙门氏菌呈阳性,而144头猪中有40株(28%)的沙门氏菌血清呈阳性。使用贝叶斯模型指定两次测试之间的依赖性,根据酶联免疫吸附剂的临界值,培养和实时聚合酶链反应(RT-PCR)的敏感性(Se)为79%至86%分析(ELISA)。假定文化特异性(Sp)为100%;发现RT-PCR Sp为94%。在光密度截止值≥20%和≥40%时,ELISA Se分别为76%和51%;每个截止值的Sp均为94%。该模型显示出对ELISA先验信息的敏感性,当在模型中指定了先验信息时,ELISA Se大约降低8%。当不对培养物和RT-PCR之间的依赖性进行调整时,对于培养物和RT-PCR Se的后验估计均比条件依赖模型高11%,并且概率区间显着缩小,这表明培养物与RT-PCR之间的相关性较窄。 PCR很重要,应在以后的研究中进行调整。

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