Devenish J, Brooks B, Perry K, Milnes D, Burke T, McCabe D, Duff S, Lutze-Wallace C L
Canadian Food Inspection Agency, Ottawa Laboratory Fallowfield, 3851 Fallowfield Rd., P.O. Box 11300 Stn. H, Ottawa, Ontario K2H 8P9, Canada.
Clin Diagn Lab Immunol. 2005 Nov;12(11):1261-8. doi: 10.1128/CDLI.12.11.1261-1268.2005.
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.
将基于单克隆抗体(MAb)的抗原捕获酶联免疫吸附测定(ELISA)与常规培养方法进行比较,以检测接种到克拉克转运增菌培养基(TEM)中的牛和羊野外样本中的胎儿弯曲杆菌亚种。这项工作是加拿大和英国的两个不同诊断实验室之间的合作。在两个实验室中,TEM样本均在35℃下孵育4天,然后通过培养和ELISA进行检测。ELISA包括先用针对胎儿弯曲杆菌亚种核心脂多糖(LPS)的单克隆抗体M1825进行初步筛选。然后,对ELISA筛选呈阳性的所有样本,用单克隆抗体M1825以及识别胎儿弯曲杆菌亚种血清型A和/或血清型B特异性LPS表位的单克隆抗体M1177、M1183和M1194进行ELISA复测。加拿大的样本包括来自529头公牛的1060份包皮冲洗液,其中18份培养和ELISA均呈阳性,1042份两种方法均呈阴性。英国的样本包括来自190例流产的羊和牛胎儿的321份组织标本,主要是胃内容物和胎盘。共有262份样本培养和ELISA均呈阴性,52份样本培养和ELISA均呈阳性,7份样本培养阴性但ELISA阳性。所有70株培养阳性分离株的结果均通过常规生化方法确认为胎儿弯曲杆菌亚种胎儿亚种,其中39株ELISA初步鉴定为血清型A,30株初步鉴定为血清型B,1份样本包含初步鉴定为血清型A和血清型B的分离株。对来自两个国家的ELISA综合数据进行的受试者工作特征分析得出曲线下面积为0.997,相对于培养结果,灵敏度为100%,特异性为99.5%。数据证实,这种ELISA方法可作为一种出色的检测方法,用于筛选TEM中的野外样本是否存在胎儿弯曲杆菌亚种。