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首页> 外文期刊>Journal of Virological Methods >Accuracy, of enzyme-linked immunosorbent assays for quantification of antibodies against Aleutian mink disease virus
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Accuracy, of enzyme-linked immunosorbent assays for quantification of antibodies against Aleutian mink disease virus

机译:酶联免疫吸附法对阿留申水貂病病毒抗体定量的准确性

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There is a growing interest among mink ranchers to select their stock for tolerance to the Aleutian mink disease virus (AMDV). Enzyme-linked immunosorbent assays (ELISA) are used to identify mink which have low anti-AMDV antibody titres and are expected to tolerate the AMDV infection. The objective of this study was to calculate the accuracy of three ELISA systems which were performed on blood or serum of AMDV-inoculated American mink (Neovison vison) at five laboratories in Canada, USA, Finland, the Netherlands and Denmark. The accuracy was determined by comparing the ELISA results with antibody titres measured by the counter-immunoelectrophoresis (CIEP) using 10 two-fold serial dilutions of the plasma. Antibody titres of 880 black mink which were inoculated with a spleen homogenate from a naturally infected mink were measured between 16 and 176 weeks post-inoculation. Each ELISA result from every laboratory covered a wide range of antibody titres and the Spearman's rank correlation coefficients between CIEP and ELISA results from different laboratories varied between 0.41 and 0.83, indicating a low to moderate accuracy of ELISA systems for ranking mink by antibody titre. The recombinant VP2-based ELISA used in the Netherlands and Finland ranked the mink by antibody titres more accurately than did the AMDV-G-based ELISA platforms developed in Denmark and the USA, suggesting that the source of antigen was one of the factors affecting the accuracy of ELISA results. It was concluded that the ELISA systems, particularly those based on AMDV-G antigen, require further refinement to improve their accuracy for ranking mink by antibody titre. (C) 2016 The Authors. Published by Elsevier B.V.
机译:貂农对选择对阿留申水貂病病毒(AMDV)具有耐受性的种群的兴趣日益浓厚。酶联免疫吸附测定法(ELISA)用于鉴定抗AMDV抗体滴度低且有望耐受AMDV感染的貂皮。这项研究的目的是计算在加拿大,美国,芬兰,荷兰和丹麦的五个实验室对AMDV接种的美国水貂(Neovison vison)的血液或血清进行的三种ELISA系统的准确性。通过将ELISA结果与使用10种两倍血浆系列稀释液的反免疫电泳(CIEP)测量的抗体滴度进行比较来确定准确性。在接种后的16至176周之间,测量了880种黑貂的抗体滴度,这些抗体用来自自然感染的貂的脾匀浆接种。每个实验室的ELISA结果涵盖了广泛的抗体效价,而CIEP与不同实验室的ELISA结果之间的Spearman秩相关系数在0.41至0.83之间变化,表明ELISA系统对水貂按抗体效价进行排名的准确度较低。与丹麦和美国开发的基于AMDV-G的ELISA平台相比,荷兰和芬兰使用的基于VP2的重组ELISA通过抗体效价对水貂的排名更为准确,这表明抗原的来源是影响水痘的因素之一。 ELISA结果的准确性。结论是,ELISA系统,特别是基于AMDV-G抗原的ELISA系统,需要进一步完善以提高其通过抗体效价对水貂进行排名的准确性。 (C)2016作者。由Elsevier B.V.发布

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