Dimech W J, Hellyar A G, Kotiw M, Marcon D, Ellis S, Carson M
Department of Microbiology, Royal Melbourne Hospital, Australia.
J Clin Microbiol. 1993 Nov;31(11):3001-6. doi: 10.1128/jcm.31.11.3001-3006.1993.
Plasmid profiles, genome restriction fragment polymorphisms, carbohydrate oxidation-fermentation reactions, methylumbelliferyl substrate hydrolysis patterns, antimicrobial susceptibilities, and results obtained with the Biolog GN biochemical substrate kit were used to type 19 common-source, but mixed-biotype, outbreak strains and one epidemiologically distinct strain of Pseudomonas pickettii. Biotyping with conventional and methylumbelliferyl substrates failed to distinguish between strains. Plasmid profile testing was found to be inconsistent and not reproducible. The Biolog GN kit allowed greater strain differentiation than restriction fragment polymorphism did (12 biotypes versus 5 biotypes); antimicrobial susceptibility testing yielded 4 biotypes, and oxidation-fermentation tests gave 3 biotypes. Oxidation-fermentation results were consistent with restriction fragment polymorphs in all but 1 of the 20 strains tested. For ease of typing, comprehensive typeability, and reproducibility, oxidation-fermentation tests should be performed initially and followed if necessary by restriction fragment polymorph analysis for the elucidation of P. pickettii infection outbreaks.
采用质粒图谱、基因组限制性片段多态性、碳水化合物氧化发酵反应、甲基伞形酮底物水解模式、抗菌药敏性以及使用Biolog GN生化底物试剂盒获得的结果,对19株共同来源但生物型混合的暴发菌株和1株在流行病学上不同的皮氏假单胞菌菌株进行分型。使用传统底物和甲基伞形酮底物进行生物分型无法区分菌株。发现质粒图谱检测不一致且不可重复。与限制性片段多态性相比,Biolog GN试剂盒能实现更大程度的菌株区分(12种生物型对5种生物型);抗菌药敏试验产生4种生物型,氧化发酵试验产生3种生物型。在20株受试菌株中,除1株外,氧化发酵结果与限制性片段多态性结果一致。为便于分型、实现全面分型能力和可重复性,应首先进行氧化发酵试验,如有必要,随后进行限制性片段多态性分析,以阐明皮氏假单胞菌感染暴发情况。