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首页> 外文期刊>Journal of the American Veterinary Medical Association >Use of pooled protozoal cultures of preputial scraping samples obtained from bulls for the detection of Tritrichomonas foetus by means of a real-time polymerase chain reaction assay
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Use of pooled protozoal cultures of preputial scraping samples obtained from bulls for the detection of Tritrichomonas foetus by means of a real-time polymerase chain reaction assay

机译:收集的公牛刮取样本的原生动物培养物通过实时聚合酶链反应测定法检测胎儿毛滴虫

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Objective—To determine the sensitivity of a real-time PCR assay for the detection of Tritrichomonas foetus in protozoal cultures of preputial scraping samples pooled from up to 25 bulls and to determine the specificity of that assay for detection ofT foetus in cultures for individual animals.Design—Cross-sectional study.Animals—188 bulls and 150 steers.Procedures—Preputial scraping samples were collected, placed in a culture kit, and incubated at 37°C for 7 days. Cultures for individual animals were tested for T foetus by means of a real-time PCR assay. Pools of protozoal cultures were made by including fixed aliquots of samples with known positive and negative results in ratios of 1:2, 1:3, 1:5,1:10, 1:15,1:20, and 1:25. Specificities of the real-time PCR assay and culture for detection of T foetus in samples obtained from individual animals and sensitivity of real-time PCR assay for each evaluated pool ratio were determined.Results—Specificity estimates for culture and the real-time PCR assay for detection of T foetus in preputial scraping samples for individual animals were not significantly different (98.8% and 100%, respectively). Sensitivities of the real-time PCR assay for the various pooled samples with known positive and negative T foetus results were not significantly different; overall sensitivity of the assay was 94%.Conclusions and Clinical Relevance—Results indicated the evaluated real-time PCR assay had high specificity and good sensitivity for the detection of T foetus in pooled protozoal cultures of preputial scraping samples obtained from up to 25 animals.
机译:目的:确定实时PCR测定法对从多达25头公牛收集的原始刮取样品的原生动物培养物中的Tritrichomonas胎儿检测的敏感性,并确定该检测方法对个别动物培养物中T胎儿检测的特异性。设计-横断面研究。动物-188头公牛和150头公牛。程序-收集刮取的原始样品,放入培养盒中,并在37°C下孵育7天。通过实时PCR测定法测试单个动物的培养物中的T胎儿。通过包括固定等分试样的原生动物培养物池,这些试样具有已知的阳性和阴性结果,其比例为1:2、1:3、1:5、1:10、1:15、1:20和1:25。确定了从各个动物身上采集的T胎的实时PCR检测和培养的特异性,并确定了每种评估池比率的实时PCR检测的敏感性。结果-培养和实时PCR检测的特异性估计单个动物的刮取样本中T胎儿的检测没有显着差异(分别为98.8%和100%)。实时PCR检测对各种已知的阳性和阴性T胎儿结果的合并样品的敏感性没有显着差异。该方法的总体敏感性为94%。结论和临床相关性—结果表明,所评估的实时PCR方法对于从多达25只动物采集的原始刮取样本的原生动物合并培养物中的T胎儿检测具有很高的特异性和良好的敏感性。

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