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Evaluation of the specificity of a commercial ELISA for detection of antibodies against porcine respiratory and reproductive syndrome virus in individual oral fluid of pigs collected in two different ways

机译:评估以两种不同方式采集的猪个体口腔液中针对猪呼吸道和生殖综合症病毒的抗体的商业ELISA特异性检测的评估

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Background The monitoring of infectious diseases like the porcine reproductive and respiratory syndrome (PRRS) using pen-wise oral fluid samples becomes more and more established. The collection of individual oral fluid, which would be useful in the monitoring of PRRSV negative boar studs, is rather difficult. The aim of the study was to test two methods for individual oral fluid collection from pigs and to evaluate the specificity of a commercial ELISA for detection of PRRSV antibodies in these sample matrices. For this reason, 334 serum samples from PRRSV negative pigs (group 1) and 71 serum samples from PRRSV positive pigs (group 2) were tested for PRRSV antibodies with a commercial ELISA. Individual oral fluid was collected with a cotton gauze swab from 311 pigs from group 1 and 39 pigs from group 2. Furthermore, 312 oral fluid samples from group 1 and 67 oral fluid samples from group 2 were taken with a self-drying foam swab (GenoTube). The recollected oral fluid was then analysed twice with a commercial ELISA for detection of PRRSV antibodies in oral fluid. Results All serum samples from group 1 tested negative for PRRSV antibodies. The collection of oral fluid was sufficient in all samples. Sampling with GenoTubes was less time consuming than sampling with cotton gauze swabs. False positive results were obtained in 7 (measure 1) respectively 9 (measure 2) oral fluid samples recollected from cotton gauze swabs and in 9 and 8 samples from GenoTubes. The specificity of the oral fluid ELISA was 97.4% for cotton gauze swabs and 97.3% for GenoTubes. 70 out of 71 serum samples and all oral fluid samples from group 2 tested positive for PRRSV antibodies. The sensitivity of the oral fluid ELISA was 100%. According to the kappa coefficient, the results showed an almost perfect agreement between serum and oral fluid collected in both ways (kappa?>?0.8). Conclusions Both methods used for individual oral fluid collection proved to be practical and efficient and can be used for PRRSV antibody detection. It has to be considered, however, that false positive results may occur more often than in serum samples.
机译:背景技术使用逐滴口服液样本监测诸如猪生殖和呼吸系统综合症(PRRS)等传染病的方法越来越多。收集个人口腔液非常困难,这对监测PRRSV阴性公猪螺柱很有用。这项研究的目的是测试两种从猪个人收集口腔液体的方法,并评估用于检测这些样品基质中PRRSV抗体的商业ELISA的特异性。因此,使用商业ELISA测试了PRRSV阴性猪(第1组)的334个血清样品和PRRSV阳性猪(第2组)的71个血清样品。分别用第1组的311头猪的棉纱签和第2组的39头猪的棉签收集单独的口腔液。此外,用自干泡沫拭子(第1组的312头和第2组的67头的口腔液)进行取样( GenoTube)。然后将回收的口腔液用商业ELISA分析两次,以检测口腔液中的PRRSV抗体。结果来自第1组的所有血清样品的PRRSV抗体均呈阴性。所有样品中的口腔液收集量均足够。用GenoTubes进行采样比用棉签拭子采样耗时少。从棉纱签收集的7个(措施1)和9个(措施2)口腔液样品以及从GenoTubes收集的9和8个样品中获得了假阳性结果。口服液ELISA的棉纱拭子特异性为97.4%,GenoTubes的特异性为97.3%。第2组的71份血清样品和所有口腔液体样品中有70份PRRSV抗体呈阳性。口服液ELISA的灵敏度为100%。根据卡伯系数,结果表明以两种方式收集的血清和口腔液之间几乎完全吻合(卡伯≥0.8)。结论两种用于个人口腔液收集的方法均被证明是实用且有效的,可用于PRRSV抗体检测。但是,必须考虑到,与血清样品相比,假阳性结果的发生频率可能​​更高。

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