Tankaew Pallop, Srisawat Wanwisa, Singhla Tawatchai, Tragoolpua Khajornsak, Kataoka Yasushi, Sawada Takuo, Sthitmatee Nattawooti
Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai 50100, Thailand.
Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50200, Thailand.
J Microbiol Methods. 2018 Feb;145:20-27. doi: 10.1016/j.mimet.2017.12.005. Epub 2017 Dec 12.
The ELISA is recognized as an efficient diagnostic tool for antibody detection, but there is no standard ELISA assay for detection of antibodies against hemorrhagic septicemia (HS) in cattle. The present study reports on an indirect ELISA assay for antibody detection of HS in dairy cows, and evaluates the sensitivity (Se) and specificity (Sp) of the method using a Bayesian approach. An indirect ELISA was developed with two types of heat extract antigens, Pasteurella multocida strains P-1256 and M-1404, as coating antigens. A checkerboard titration was employed using dairy cow sera immunized with P. multocida bacterin and colostrum-deprived calf sera. The concentrations of heat extract antigen (160μg/mL), sample serum (1:100) and goat anti-bovine immunoglobulin G labeled with horseradish peroxidase (1:2000) were optimal for the assay. The cut-off values were 0.147 and 0.128 for P-1256 and M-1404 coating antigens, and there were no differences in the results of tests with positive and negative sera (p<0.05). The characteristics of three diagnostic tests were evaluated using a one-population Bayesian model, assuming conditional dependence between two types of coating antigen-based ELISAs and indirect hemagglutination assay (IHA). A total of 415 sera samples from dairy cows without HS vaccination and no history of disease were tested. The Se and Sp of the P-1256 and M-1404 ELISAs were higher than those of the IHA. The Se and Sp of the P-1256 ELISA were 90.3% and 90.1%, while the Se and Sp of the M-1404 ELISA were 92.1% and 71.9%. The median values of Se and Sp from the IHA were 36.0% and 58.2%.
酶联免疫吸附测定(ELISA)被认为是一种用于抗体检测的有效诊断工具,但目前尚无用于检测牛出血性败血症(HS)抗体的标准ELISA检测方法。本研究报道了一种用于检测奶牛HS抗体的间接ELISA检测方法,并使用贝叶斯方法评估了该方法的敏感性(Se)和特异性(Sp)。以两种热提取抗原,即多杀性巴氏杆菌菌株P-1256和M-1404作为包被抗原,开发了一种间接ELISA。使用用多杀性巴氏杆菌菌苗免疫的奶牛血清和初乳缺乏的犊牛血清进行棋盘滴定。热提取抗原浓度(160μg/mL)、样品血清(1:100)和辣根过氧化物酶标记的山羊抗牛免疫球蛋白G(1:2000)的浓度对该检测最为适宜。P-1256和M-14,04包被抗原的临界值分别为0.147和0.128,阳性和阴性血清检测结果无差异(p<0.05)。使用单总体贝叶斯模型评估三种诊断检测的特性,假设基于两种包被抗原的ELISA和间接血凝试验(IHA)之间存在条件依赖性。对415份未接种HS疫苗且无疾病史的奶牛血清样本进行了检测。P-1256和M-1404 ELISA的Se和Sp高于IHA。P-1256 ELISA的Se和Sp分别为90.3%和90.1%,而M-1404 ELISA的Se和Sp分别为92.1%和71.9%。IHA的Se和Sp中位数分别为36.0%和58.2%。