Stenbaek E I, Schirmer A L
National Veterinary Laboratory, Copenhagen, Denmark.
Vet Microbiol. 1994 Apr;39(3-4):231-44. doi: 10.1016/0378-1135(94)90160-0.
An inhibition Enzyme Immuno Assay (EIA) for detection of antibodies against A. pleuropneumoniae serotype 2 (App-2) in pig sera, based on the inhibition of the binding of an App-2 specific monoclonal antibody was established. The monoclonal antibody (mAb 102-G02) was found to be directed against an epitope on the O-chain of App-2 LPS. Some App-2 isolates did not react with the mAb 102-G02. These isolates are referred to as App-2X. In the inhibition EIA highly purified App-2 LPS ws used to coat microtiter plates. Serial dilutions of pig sera were added to the plates prior to the mAb 102-G02. The degree of binding of App-2 antibodies from pig sera was determined as the percentage inhibition of the mAb 102-G02. Pig sera from specific pathogen free (SPF) herds, from experimentally infected animals, and from conventionel herds were tested. A serum dilution of 1/200 was found to be optimal, when using 50% inhibition as the discriminating inhibition percentage. Serum from App-2X infected herds showed a lower reactivity as compared to serum from App-2 infected herds. No crossreactivity was observed with serum from pigs infected with other App serotypes. The sensitivity and specificity were 100% and 98.9%, respectively.
建立了一种抑制酶免疫分析(EIA)方法,用于检测猪血清中抗胸膜肺炎放线杆菌2型(App-2)的抗体,该方法基于抑制App-2特异性单克隆抗体的结合。发现单克隆抗体(mAb 102-G02)针对App-2脂多糖O链上的一个表位。一些App-2分离株不与mAb 102-G02反应。这些分离株被称为App-2X。在抑制EIA中,使用高度纯化的App-2脂多糖包被微量滴定板。在加入mAb 102-G02之前,将猪血清的系列稀释液加入板中。猪血清中App-2抗体的结合程度以mAb 102-G02的抑制百分比来确定。对来自无特定病原体(SPF)猪群、实验感染动物和常规猪群的猪血清进行了检测。当以50%抑制作为区分抑制百分比时,发现1/200的血清稀释度是最佳的。与App-2感染猪群的血清相比,App-2X感染猪群的血清反应性较低。未观察到与感染其他App血清型的猪的血清有交叉反应。敏感性和特异性分别为100%和98.9%。