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一种用于检测伪狂犬病病毒糖蛋白I抗体的酶联免疫吸附测定法:一种区分感染猪和接种疫苗猪的血清学方法。

Development of an ELISA for detection of antibodies to glycoprotein I of Aujeszky's disease virus: a method for the serological differentiation between infected and vaccinated pigs.

作者信息

van Oirschot J T, Houwers D J, Rziha H J, Moonen P J

机构信息

Central Veterinary Institute, Lelystad, The Netherlands.

出版信息

J Virol Methods. 1988 Dec;22(2-3):191-206. doi: 10.1016/0166-0934(88)90102-4.

Abstract

A blocking ELISA was developed to distinguish between Aujeszky's disease virus (ADV)-infected and vaccinated pigs, on the basis of presence or absence of serum antibodies to glycoprotein I (gI) of ADV. The gI-ELISA detects antibodies that block the reaction of monoclonal antibodies to one or two epitopes on gI of ADV. The ADV-gI antibody response appeared between one and two weeks post-infection and persisted at a high level for at least seven months. Five of the nine ADV-vaccine strains examined were found to be "gI-negative". Pigs vaccinated with a gI-negative vaccine did not develop an ADV-gI antibody response until they were challenge-exposed to a virulent strain of ADV. The gI-ELISA is highly specific, sensitive and suitable for large-scale sero-epidemiological studies to identify infected pigs in populations vaccinated with gI-negative vaccines. The gI-ELISA provides, therefore, a basis for ADV-eradication programmes, which introduces a novel concept in the control of animal virus diseases.

摘要

基于是否存在针对伪狂犬病病毒(ADV)糖蛋白I(gI)的血清抗体,开发了一种阻断ELISA法,用于区分感染ADV的猪和接种疫苗的猪。gI-ELISA检测可阻断单克隆抗体与ADV gI上一个或两个表位反应的抗体。ADV-gI抗体反应在感染后1至2周出现,并在高水平持续至少7个月。在所检测的9种ADV疫苗株中,有5种被发现是“gI阴性”。接种gI阴性疫苗的猪在受到强毒ADV毒株攻击之前,不会产生ADV-gI抗体反应。gI-ELISA具有高度特异性、敏感性,适用于大规模血清流行病学研究,以识别接种gI阴性疫苗群体中的感染猪。因此,gI-ELISA为ADV根除计划提供了基础,这在动物病毒病控制方面引入了一个新概念。

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