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首页> 外文期刊>Veterinary Microbiology >Feasibility of pooled-sample testing for the detection of porcine reproductive and respiratory syndrome virus antibodies on serum samples by ELISA.
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Feasibility of pooled-sample testing for the detection of porcine reproductive and respiratory syndrome virus antibodies on serum samples by ELISA.

机译:ELISA法检测血清样本中猪繁殖与呼吸综合征病毒抗体的混合样本测试的可行性。

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摘要

Surveillance of porcine reproductive and respiratory syndrome (PRRS) in negative sow farms is usually performed by testing for the presence of antibodies against PRRS virus in serum with a commercial ELISA test. The objective of this study was to evaluate the feasibility of pooling serum samples for detection of PRRS virus antibodies by ELISA. The effect of pool size on the sensitivity and specificity of the ELISA test was evaluated by testing true positive samples and false positive samples, respectively, diluted in negative sera. The effect of three different cut-off values for the interpretation of the diagnostic test (0.4, 0.3 and 0.2) was evaluated as well. Furthermore, the obtained sensitivity and specificity estimates were used to calculate the herd sensitivity and herd specificity of surveillance protocols in different scenarios. The results showed that pooling serum samples to detect PRRSV antibodies resulted in a decrease in sensitivity and an increase in specificity, compared to testing individual samples, while the reduction of the s/p cut-off value recommended by the manufacturer (0.4) had the opposite effect. We describe an approach that can increase the herd sensitivity of a surveillance protocol for breeding herds, while maintaining high herd specificity and low testing costs. This can be achieved by sampling a larger number of animals and running the samples in pools. Therefore, the conventional monitoring protocols based on ELISA on individual samples can be improved by using pooled-sample testing.
机译:阴性母猪场中的猪繁殖与呼吸综合症(PRRS)的监测通常通过商业ELISA试验检测血清中是否存在针对PRRS病毒的抗体来进行。这项研究的目的是评估合并血清样品以通过ELISA检测PRRS病毒抗体的可行性。通过分别测试在阴性血清中稀释的真阳性样品和假阳性样品,评估库大小对ELISA测试的敏感性和特异性的影响。还评估了三个不同的临界值对诊断测试的解释的影响(0.4、0.3和0.2)。此外,将获得的敏感性和特异性估计值用于计算不同方案中监测方案的种群敏感性和种群特异性。结果表明,与检测单个样品相比,合并血清样品检测PRRSV抗体会导致灵敏度降低和特异性提高,而制造商建议降低s / p临界值(0.4)可以降低检测范围。相反的效果。我们描述了一种方法,该方法可以提高监视协议的繁殖群的敏感性,同时保持较高的群特异性和较低的测试成本。这可以通过对大量动物进行采样并在池中运行样本来实现。因此,可以通过使用合并样品测试来改进基于ELISA的常规监测方案。

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