Lanyon Sasha R, Reichel Michael P
School of Animal and Veterinary Sciences, Roseworthy Campus, University of Adelaide, Roseworthy, South Australia, Australia
School of Animal and Veterinary Sciences, Roseworthy Campus, University of Adelaide, Roseworthy, South Australia, Australia.
J Vet Diagn Invest. 2016 May;28(3):345-9. doi: 10.1177/1040638716633496. Epub 2016 Mar 26.
Antigen enzyme-linked immunosorbent assay (ELISA) is used for the detection of Bovine viral diarrhea virus persistently infected (BVDV PI) cattle; however, colostrum-derived antibodies may interfere with antigen detection in serum from young PI calves. Our study aimed to assess serum pretreatment methods for reducing such interference. Dilution of PI serum with serum containing specific antibody showed that antibody levels equivalent to those observed in colostrum-fed calves were able to eliminate all antigen signals in a serum sample. Serum was treated with ethylenediamine tetra-acetic acid at pH 4.5, 5.5, 6.5, and 7.5, then boiled, centrifuged, and the supernatant-recovered. BVDV antibody was undetectable by ELISA in supernatants from treated samples, and the antigen ELISA signal was improved. Maximum antigen signal recovery of >90% was achieved at pH 5 ± 0.5. When this optimal treatment method was applied to field samples from 3 PI calves (which were negative in the antigen-capture ELISA without treatment), the antigen signal improved and gave a positive result in each case. Pretreatment may provide an improvement in the detection of young PI calves.
抗原酶联免疫吸附测定(ELISA)用于检测持续感染牛病毒性腹泻病毒(BVDV PI)的牛;然而,初乳来源的抗体可能会干扰幼龄PI犊牛血清中的抗原检测。我们的研究旨在评估减少此类干扰的血清预处理方法。用含有特异性抗体的血清稀释PI血清表明,与初乳喂养犊牛中观察到的抗体水平相当的抗体能够消除血清样本中的所有抗原信号。血清在pH 4.5、5.5、6.5和7.5下用乙二胺四乙酸处理,然后煮沸、离心,并回收上清液。ELISA在处理后样本的上清液中未检测到BVDV抗体,且抗原ELISA信号得到改善。在pH 5±0.5时实现了>90%的最大抗原信号回收率。当将这种最佳处理方法应用于3头PI犊牛的现场样本(未经处理的抗原捕获ELISA检测为阴性)时,抗原信号得到改善,且每种情况下均给出阳性结果。预处理可能会改善幼龄PI犊牛的检测。