Tunér K, Baron E J, Summanen P, Finegold S M
Huddinge University Hospital, Karolinska Institute, Stockholm, Sweden.
J Clin Microbiol. 1992 Dec;30(12):3225-9. doi: 10.1128/jcm.30.12.3225-3229.1992.
Identification of fusobacteria from clinical specimens currently requires analysis of metabolic end products by gas-liquid chromatography in addition to certain biochemical and enzymatic tests because of the relative biochemical inactivity of these bacteria. Even the finding of pointed, thin gram-negative cells on Gram-stained slides can no longer be relied on for identification of Fusobacterium nucleatum, since at least four other species of fusobacteria have been seen to exhibit similar morphology. We examined 46 clinical isolates and six American Type Culture Collection type strains of fusobacteria by conventional methods and by the Microbial ID Systems MIDI software package for analyzing cellular fatty acid patterns measured by capillary column gas-liquid chromatography. Distinctive patterns of major fatty acids could be used to reliably identify most clinical isolates to the species level. The MIDI system identified 89% of the isolates correctly and provides an alternative to conventional methods.
由于这些细菌相对缺乏生化活性,目前从临床标本中鉴定梭杆菌除了进行某些生化和酶学检测外,还需要通过气液色谱法分析代谢终产物。即使在革兰氏染色玻片上发现尖细的革兰氏阴性菌,也不能再依靠其来鉴定具核梭杆菌,因为至少已发现其他四种梭杆菌也呈现出类似的形态。我们通过传统方法以及用于分析毛细管柱气液色谱法测定的细胞脂肪酸模式的微生物鉴定系统MIDI软件包,对46株临床分离株和6株美国典型培养物保藏中心的梭杆菌标准菌株进行了检测。主要脂肪酸的独特模式可用于将大多数临床分离株可靠地鉴定到种水平。MIDI系统正确鉴定了89%的分离株,为传统方法提供了一种替代方法。