基于单克隆抗体的捕获酶联免疫吸附法检测弯曲杆菌胎儿的验证。

J Devenish, B Brooks, K Perry, D Milnes, T Burke, D McCabe, S Duff, C L Lutze-Wallace
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引用次数: 29

摘要

采用单克隆抗体(MAb)抗原捕获酶联免疫吸附法(ELISA)与常规培养法对接种于Clark’s运输富集培养基(TEM)的牛和羊田间样品进行弯曲杆菌胎儿亚种检测。这项工作是两个不同的诊断实验室之间的合作,一个在加拿大,另一个在英国。在两个实验室中,TEM样品在35℃下孵育4天,然后进行培养和ELISA检测。ELISA采用M1825单抗对C.胎儿亚种核心脂多糖(LPS)进行初步筛选。所有ELISA筛选阳性的样本,用识别血清A型和/或血清b型特异性C.胎儿亚种LPS表位的MAb M1825、M1177、M1183和M1194重新检测。加拿大的样本包括529头公牛的1060次包皮清洗,其中18次培养和ELISA均为阳性,1042次两种方法均为阴性。英国样本包括321个组织标本,主要是胃内容物和胎盘,来自190个流产的羊和牛胎儿。培养+ ELISA阴性262份,培养+ ELISA阳性52份,培养阴性+ ELISA阳性7份。70株培养阳性分离株经常规生化方法鉴定均为胎儿梭菌亚种。其中,39例经ELISA推测血清型为A型,30例推测血清型为B型,其中1例样品含有推测血清型为A型和B型的分离株。对两国联合ELISA数据进行受者操作特征分析,曲线下面积为0.997,相对于培养结果敏感性为100%,特异性为99.5%。结果表明,该方法可作为一种很好的方法,用于TEM中田间样品的筛选。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Validation of a monoclonal antibody-based capture enzyme-linked immunosorbent assay for detection of Campylobacter fetus.

A monoclonal antibody (MAb)-based antigen capture enzyme-linked immunosorbent assay (ELISA) was compared with the routine culture methodology for the detection of Campylobacter fetus subspecies from bovine and ovine field samples inoculated into Clark's transport enrichment medium (TEM). The work was a collaboration between two different diagnostic laboratories, one in Canada and the other in England. In both labs, TEM samples were incubated for 4 days at 35 degrees C and then tested by culture and ELISA. The ELISA consisted of initial screening with MAb M1825 against C. fetus subspecies core lipopolysaccharide (LPS). All samples positive on ELISA screening were then retested by ELISA with MAb M1825 and MAbs M1177, M1183, and M1194, which recognize serotype A- and/or serotype B-specific C. fetus subspecies LPS epitopes. The Canadian samples consisted of 1,060 preputial washings from 529 bulls, of which 18 were positive by both culture and ELISA and 1,042 were negative by both methods. The English samples consisted of 321 tissue specimens, mostly stomach contents and placentas, from 190 aborted ovine and bovine fetuses. A total of 262 samples were negative by culture and ELISA, 52 samples were positive by culture and ELISA, and 7 samples were culture negative but ELISA positive. The results for all 70 culture-positive isolates were confirmed by conventional biochemical methods as C. fetus subsp. fetus, with 39 presumptively identified by the ELISA as serotype A and 30 presumptively identified as serotype B and with one sample containing isolates presumptively identified as serotype A and serotype B. A receiver operating characteristic analysis of the combined ELISA data from both countries resulted in an area under the curve of 0.997, with a sensitivity of 100% and a specificity of 99.5% relative to the results of culture. The data confirm that this ELISA method can be used as an excellent test for the screening of field samples in TEM for the presence of C. fetus subspecies.

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