Ellis J A, Hassard L, Morley P S
Department of Veterinary Microbiology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Canada.
J Vet Diagn Invest. 1995 Apr;7(2):183-9. doi: 10.1177/104063879500700203.
A microneutralization enzyme-linked immunosorbent assay (ELISA) was developed to detect specific antibodies to bovine respiratory syncytial viruses (BRSVs) in cattle sera using a monoclonal antibody to the fusion protein of the virus. Serum from 20 naturally exposed, 24 experimentally infected, and 15 immunized cattle were evaluated using 3 different BRSV isolates. Antibody titers determined with the microneutralization ELISA were compared with those derived from a classical virus neutralization assay, an indirect ELISA, and a fusion inhibition assay. These studies demonstrated a high degree of correlation (usually 0.90) among the assays. Furthermore, the results showed that immunization of cattle with one isolate (subgroup) of BRSV induced antibody responses that cross-reacted with at least 2 disparate isolates. These results document the utility of the microneutralization ELISA in assessing functionally important antibody responses to BRSVs in cattle.
利用针对该病毒融合蛋白的单克隆抗体,开发了一种微中和酶联免疫吸附测定(ELISA),用于检测牛血清中针对牛呼吸道合胞病毒(BRSV)的特异性抗体。使用3种不同的BRSV分离株对20头自然感染、24头实验感染和15头免疫牛的血清进行了评估。将微中和ELISA测定的抗体滴度与经典病毒中和试验、间接ELISA和融合抑制试验得出的抗体滴度进行了比较。这些研究表明各测定方法之间具有高度相关性(通常为0.90)。此外,结果显示用一种BRSV分离株(亚组)免疫牛会诱导产生与至少2种不同分离株发生交叉反应的抗体反应。这些结果证明了微中和ELISA在评估牛对BRSV的功能重要抗体反应方面的实用性。