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与液体和固体培养基以及酶联免疫吸附测定法相比,实时聚合酶链反应用于检测副结核分枝杆菌亚种。

Real-time PCR, compared to liquid and solid culture media and ELISA, for the detection of Mycobacterium avium ssp. paratuberculosis.

作者信息

Alinovi Catherine A, Ward Michael P, Lin Tsang Long, Moore George E, Wu Ching Ching

机构信息

Department of Comparative Pathobiology, Purdue University, W Lafayette, IN 47907-2027, USA.

出版信息

Vet Microbiol. 2009 Apr 14;136(1-2):177-9. doi: 10.1016/j.vetmic.2008.10.012. Epub 2008 Nov 1.

Abstract

A goal of Johne's disease control programs is to accurately detect Mycobacterium avium ssp. paratuberculosis (MAP) infected cattle as quickly as possible to reduce disease transmission. A newly introduced real-time PCR provides results rapidly, but its accuracy in the field has not been evaluated. Fecal and serum samples collected from dairy cows in northern Indiana were used to estimate the sensitivity and specificity of a newly licensed real-time PCR test for direct fecal detection of Mycobacterium avium ssp. paratuberculosis (MAP). Results of the real-time PCR were evaluated in parallel with solid and liquid media culture systems and a serum ELISA for detection of MAP antibodies to determine the accuracy of the real-time PCR and the tests' potential usefulness in the field. A total of 143 samples were tested by all four methods. Using prior published estimates for sensitivity and specificity of each of the tests and Bayesian methodology, the sensitivity and specificity of the real-time PCR test was estimated to be 0.60 and 0.97, respectively. The accuracy of real-time PCR (0.90) was comparable to both solid (0.91) and liquid (0.93) culture. Because real-time PCR accuracy is comparable to standard culture methods, it is a useful new test. In addition, test results are obtained as rapidly as an ELISA, but are more accurate than the ELISA (0.82). This makes real-time PCR an attractive test and should shorten the quarantine period required for new purchases of unknown MAP-status animals into herds participating in an MAP control program.

摘要

约内氏病防控计划的一个目标是尽快准确检测出感染副结核分枝杆菌(MAP)的牛,以减少疾病传播。一种新引入的实时荧光定量聚合酶链反应(PCR)能快速得出结果,但其在实际应用中的准确性尚未得到评估。从印第安纳州北部的奶牛采集粪便和血清样本,用于评估一种新获得许可的实时荧光定量PCR检测方法直接检测粪便中副结核分枝杆菌(MAP)的敏感性和特异性。将实时荧光定量PCR的结果与固体和液体培养基培养系统以及检测MAP抗体的血清酶联免疫吸附测定(ELISA)进行平行评估,以确定实时荧光定量PCR的准确性及其在实际应用中的潜在效用。所有四种方法共检测了143份样本。利用先前公布的每种检测方法的敏感性和特异性估计值以及贝叶斯方法,估计实时荧光定量PCR检测的敏感性和特异性分别为0.60和0.97。实时荧光定量PCR的准确性(0.90)与固体培养(0.91)和液体培养(0.93)相当。由于实时荧光定量PCR的准确性与标准培养方法相当,它是一种有用的新检测方法。此外,获得检测结果的速度与ELISA一样快,但比ELISA更准确(0.82)。这使得实时荧光定量PCR成为一种有吸引力的检测方法,并且应该会缩短将未知MAP感染状况的新购入动物引入参与MAP控制计划的牛群所需的隔离期。

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