Carlsson H E, Hurvell B, Lindberg A A
Acta Pathol Microbiol Scand C. 1976 Jun;84(3):168-76. doi: 10.1111/j.1699-0463.1976.tb00016.x.
An enzyme linked immunosorbent assay (ELISA) using phenolwater extracted lipopolysaccarides as antigen was used for detection and quantitation of antibodies against Brucella and Yersinia bacteria in rabbit antisera. ELISA was found to be from ten to hundred-fold more sensitive than the commonly used tube agglutination assay (Widal). In addition, both direct and inhibition assays using ELISA revealed antigenic differences between Brucella abortus and Yersinia enterocolitica O-group V, previously undetected in tube agglutination and complement fixation studies. These data raise the possibility of a sensitive and specific assay for detection of anti-Brucella antibodies in human sera.
采用以酚水提取的脂多糖为抗原的酶联免疫吸附测定(ELISA)法,检测和定量兔抗血清中针对布鲁氏菌和耶尔森氏菌的抗体。结果发现ELISA法的灵敏度比常用的试管凝集试验(肥达氏试验)高10至100倍。此外,使用ELISA法的直接检测和抑制检测均显示,流产布鲁氏菌和小肠结肠炎耶尔森氏菌O群V之间存在抗原差异,这在之前的试管凝集试验和补体结合试验研究中未被发现。这些数据增加了一种用于检测人血清中抗布鲁氏菌抗体的灵敏且特异检测方法的可能性。