Bowersock T L, Hooper T, Pottenger R
Department of Veterinary Pathobiology, School of Veterinary Medicine, Purdue University, W. Lafayette, IN 47907-1243.
J Vet Diagn Invest. 1992 Oct;4(4):419-22. doi: 10.1177/104063879200400409.
The use of an enzyme-linked immunosorbent assay (ELISA) as a means of detecting dermonecrotoxin-producing strains of Pasteurella multocida was investigated. The assay was evaluated as a means to identify toxigenic P. multocida isolates recovered from nasal secretions of swine with atrophic rhinitis. The sensitivity and specificity of the ELISA for detecting dermonecrotoxin-producing P. multocida strains were compared to those of mouse-inoculation and cytotoxicity assays. The ELISA was highly sensitive and more specific than animal inoculation or tissue culture assay and is thus a more effective method for screening swine herds for the presence of toxigenic strains of P. multocida. The ELISA is a rapid, effective, economical way to identify toxigenic P. multocida isolates.
研究了使用酶联免疫吸附测定法(ELISA)检测多杀性巴氏杆菌产皮肤坏死毒素菌株的方法。该测定法被评估为一种鉴定从患有萎缩性鼻炎的猪的鼻分泌物中分离出的产毒素多杀性巴氏杆菌分离株的手段。将ELISA检测产皮肤坏死毒素多杀性巴氏杆菌菌株的敏感性和特异性与小鼠接种法和细胞毒性测定法进行了比较。ELISA具有高度敏感性,且比动物接种或组织培养测定法更具特异性,因此是一种更有效的筛选猪群中多杀性巴氏杆菌产毒素菌株存在情况的方法。ELISA是一种快速、有效、经济的鉴定产毒素多杀性巴氏杆菌分离株的方法。