An enzyme-linked immunosorbent assay to detect antibodies against glycoprotein gE of bovine herpesvirus 1 allows differentiation between infected and vaccinated cattle

被引:84
作者
VanOirschot, JT
Kaashoek, MJ
MarisVeldhuis, MA
Weerdmeester, K
Rijsewijk, FAM
机构
[1] Intervet International, 5830 AA, Boxmeer
[2] Department of Mammalian Virology, Inst. Anim. Sci. and Hlth. (ID-DLO), 8200 AB Lelystad
关键词
bovine herpesvirus 1; differentiation; gE enzyme-linked immunosorbent assay; infection; vaccination;
D O I
10.1016/S0166-0934(97)00073-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A blocking enzyme-linked immunosorbent assay (ELISA) was developed for detecting antibodies against glycoprotein gE (gE) of bovine herpesvirus 1 (BHV1). The assay is based on the use of two monoclonal antibodies directed against different antigenic domains on gE. Sera from uninfected cattle and cattle that had been repeatedly vaccinated with gE-negative marker vaccines scored negative, whereas sera from cattle naturally or experimentally infected with BHV1 field strains scored positive in the gE-ELISA. Antibodies against gE appeared in the serum around 11 days after infection. Cattle that were first vaccinated and then challenged, thus having less virus replication, also became gE-seropositive. The sensitivity and specificity of the gE-ELISA is high, and therefore the gE-ELISA is suitable for differentiating between infected cattle and vaccinated cattle with a gE-negative vaccine. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:23 / 34
页数:12
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