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用于检测牛新孢子虫特异性抗体的新型酶联免疫吸附测定法。

Novel ELISA for detection of Neospora-specific antibodies in cattle.

作者信息

Williams D J, McGarry J, Guy F, Barber J, Trees A J

机构信息

Division of Parasite and Vector Biology, Liverpool School of Tropical Medicine/Faculty of Veterinary Science, University of Liverpool.

出版信息

Vet Rec. 1997 Mar 29;140(13):328-31. doi: 10.1136/vr.140.13.328.

Abstract

An enzyme-linked immunosorbent assay (ELISA) to detect antibodies to Neospora species in cattle was developed. Whole formalin-fixed Neospora caninum (NC-Liverpool) tachyzoites were used as antigen and a monoclonal antibody to bovine immunoglobulin light chain and an anti-mouse horseradish peroxidase conjugate were used to reveal bound antibody. A panel of 46 sera, negative by the immunofluorescent antibody test (IFAT), were used in the ELISA at a serum dilution of 1:500 to calculate the negative cut-off value of OD405 = 0.77. There was a 95 per cent agreement between the results of the ELISA and the IFAT with 104 serum samples. The specificity and sensitivity of the ELISA were 96 per cent and 95 per cent, respectively, when compared with the IFAT. No significant cross-reaction was observed with the sera from cattle infected experimentally with Toxoplasma gondii, Cryptosporidium parvum, Babesia divergens, Sarcocystis cruzi, Eimeria alabamensis or E bovis. A significantly modified version of the test is now commercially available.

摘要

开发了一种用于检测牛新孢子虫属抗体的酶联免疫吸附测定(ELISA)。用全福尔马林固定的犬新孢子虫(NC-利物浦株)速殖子作为抗原,使用抗牛免疫球蛋白轻链单克隆抗体和抗小鼠辣根过氧化物酶结合物来显示结合的抗体。一组46份经免疫荧光抗体试验(IFAT)检测为阴性的血清,以1:500的血清稀释度用于ELISA,以计算OD405 = 0.77的阴性临界值。ELISA结果与104份血清样本的IFAT结果之间有95%的一致性。与IFAT相比,ELISA的特异性和敏感性分别为96%和95%。在用刚地弓形虫、微小隐孢子虫、分歧巴贝斯虫、克鲁斯肉孢子虫、阿拉巴马艾美耳球虫或牛艾美耳球虫进行实验性感染的牛血清中未观察到明显的交叉反应。现在有一种经过显著改进的该检测方法已在市场上销售。

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