Baldwin Thomas J, Myklebust Karin A
Department of Veterinary Microbiology and Pathology, Washington State University, Pullman 99164, USA.
Dis Aquat Organ. 2002 Jun 3;49(3):185-90. doi: 10.3354/dao049185.
Validation of a single round PCR-based assay to confirm as Myxobolus cerebralis myxospores obtained from pepsin-trypsin digest preparations is described. The assay is a modification of a PCR assay published previously, based on the amplification of a segment of the gene encoding the 18S ribosomal subunit of M. cerebralis. The sensitivity, specificity and upper and lower detection limits were determined using known M. cerebralis and non-M. cerebralis myxospores and M. cerebralis-free fish. The sensitivity of PCR confirmation was 100% (95% confidence interval of 83.2-100%). The specificity was 100% (95% confidence interval of 87.2-100%). The upper detection limit was approximately 100,000 myxospores per reaction; the lower detection limit was approximately 50 myxospores per reaction. Given the high sensitivity and specificity of the assay, substitution of this assay for histologic confirmation of M. cerebralis infection is encouraged.
本文描述了一种基于单轮聚合酶链反应(PCR)的检测方法的验证,该方法用于确认从胃蛋白酶-胰蛋白酶消化制剂中获得的脑粘体虫粘孢子。该检测方法是对先前发表的一种PCR检测方法的改进,基于对编码脑粘体虫18S核糖体亚基的基因片段进行扩增。使用已知的脑粘体虫和非脑粘体虫粘孢子以及未感染脑粘体虫的鱼来确定该检测方法的灵敏度、特异性以及检测上限和下限。PCR确认的灵敏度为100%(95%置信区间为83.2 - 100%)。特异性为100%(95%置信区间为87.2 - 100%)。每个反应的检测上限约为100,000个粘孢子;每个反应的检测下限约为50个粘孢子。鉴于该检测方法具有高灵敏度和特异性,鼓励用此检测方法替代脑粘体虫感染的组织学确认方法。