首页> 外文期刊>Zoonoses and Public Health >Estimation of the Diagnostic Accuracy of the invA-gene-based PCR Technique and a Bacteriological Culture for the Detection of Salmonella spp. in Caecal Content from Slaughtered Pigs using Bayesian Analysis
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Estimation of the Diagnostic Accuracy of the invA-gene-based PCR Technique and a Bacteriological Culture for the Detection of Salmonella spp. in Caecal Content from Slaughtered Pigs using Bayesian Analysis

机译:基于invA基因的PCR技术和细菌培养物检测沙门氏菌的诊断准确性的估计。贝叶斯分析法测定屠宰猪的盲肠含量

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The goal of this study was to estimate the accuracy of the invA-gene-based polymerase chain reaction (PCR) and a culture technique based on pre-enrichment with buffered peptone water, three selective enrichment media (selenite, tetrathionate and Rappaport-Vassiliadis broths) and four selective, solid media (Xylose-Lysine-Tergitol-4, Salmonella/Shigella, Hekton-Enteric and MacConkey), for the detection of Salmonella organisms from caecal samples from slaughter pigs. For this purpose a latent-class (Bayesian) approach was used. Two hundred and three slaughtered pigs were used after grouping them into two groups of 96 and 107 animals. Sensitivity (Se) was estimated to be 56% (95% probability interval 40, 76) for culture and 91% (81, 97) for PCR. The specificity (Sp) of the PCR was 88% (80, 95) while the Sp of the culture had been considered 100% in the statistical analysis as all culture-positive samples were confirmed by serotyping. PCR Se was not affected by the Salmonella serotypes present in the samples analysed. Accordingly, a minimum of 25.5% of the pigs was estimated to harbour Salmonella organisms in their faeces. It was concluded that bacteriology on caecal samples alone was a poor diagnostic method, and that the PCR method could be considered a cost-effective alternative to culture in Salmonella monitoring programmes. However, given the moderate Sp of this molecular technique, PCR-positive samples should be further confirmed through bacteriology.
机译:这项研究的目的是评估基于invA基因的聚合酶链反应(PCR)的准确性,以及基于缓冲蛋白ept水,三种选择性富集培养基(亚硒酸盐,四硫酸盐和Rappaport-Vassiliadis肉汤的预富集)的培养技术)和四种选择性固体培养基(木糖-赖氨酸-Tergitol-4,沙门氏菌/志贺氏菌,Hekton-Enteric和MacConkey),用于检测屠宰猪盲肠样品中的沙门氏菌。为此目的,使用了潜在类(贝叶斯)方法。将203只屠宰猪分为96和107只动物分成两组。对于培养物,灵敏度(Se)估计为56%(95%概率区间40、76),对于PCR而言,灵敏度(Se)为91%(81、97)。 PCR的特异性(Sp)为88%(80,95),而统计分析认为培养物的Sp为100%,因为所有培养阳性样品均通过血清分型确定。 PCR Se不受所分析样品中沙门氏菌血清型的影响。因此,估计至少有25.5%的猪的粪便中携带沙门氏菌。得出的结论是,仅对盲肠样品进行细菌学检查是一种较差的诊断方法,PCR方法可被视为沙门氏菌监测计划中培养的一种经济有效的替代方法。但是,鉴于该分子技术的中等Sp,应通过细菌学进一步确认PCR阳性样品。

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