Bérubé A, Trudel M, Payment P
Centre de Recherche en Virologie, Institut Armand-Frappier, Laval, Quebec, Canada.
Appl Environ Microbiol. 1989 Jun;55(6):1640-1. doi: 10.1128/aem.55.6.1640-1641.1989.
Legionella pneumophila was detected and identified by an immunoblot assay using a monoclonal antibody specific to serogroups 1 to 8. Samples containing L. pneumophila were plated on buffered charcoal yeast extract agar supplemented with glycine, vancomycin, and polymyxin B. After incubation at 35 degrees C for 3 days, colonies were transferred to nitrocellulose membranes by blotting. Simultaneous detection and identification of L. pneumophila were done by treating the membrane with the monoclonal antibody and a peroxidase conjugate to mouse immunoglobulins. A diffuse cross-reaction was observed with Pseudomonas fluorescens colonies, but this was a low-level reaction that could easily be differentiated from the strong specific reactions to L. pneumophila.
嗜肺军团菌通过使用针对血清群1至8的单克隆抗体的免疫印迹试验进行检测和鉴定。将含有嗜肺军团菌的样本接种在补充有甘氨酸、万古霉素和多粘菌素B的缓冲活性炭酵母提取物琼脂上。在35℃孵育3天后,通过印迹法将菌落转移到硝酸纤维素膜上。通过用单克隆抗体和与小鼠免疫球蛋白结合的过氧化物酶处理该膜,同时进行嗜肺军团菌的检测和鉴定。观察到荧光假单胞菌菌落有弥漫性交叉反应,但这是一种低水平反应,很容易与对嗜肺军团菌的强特异性反应区分开来。