Hartstein A I, Morthland V H, Rourke J W, Sykes R, Rashad A L
Department of Hospital Infection Control, University Hospitals, Portland, Oregon.
Diagn Microbiol Infect Dis. 1993 Jan;16(1):35-41. doi: 10.1016/0732-8893(93)90128-t.
We compared plasmid DNA analysis, biotyping by Vitek, and disk diffusion antimicrobic susceptibility as subtyping tests of Klebsiella pneumoniae and Klebsiella oxytoca. The 92 tested isolates were from alternate, culture-positive patients over 6 months. No outbreak or cluster of infections was recognized during this interval. Plasmid DNA was detected in 85% of the isolates. Each isolate except one had a reproducible absence of plasmid DNA or a reproducible plasmid DNA profile on repetitive testing. Restriction endonuclease enzyme analysis of plasmid DNA was necessary to distinguish differences among some isolates that had only large plasmids. Isolates with only large plasmids represented 18% of the collection. Of the 78 isolates with plasmid DNA, all but two were considered different from one another by plasmid DNA analysis. Biotyping and antimicrobic susceptibility testing were not highly reproducible. In addition, biotyping did not demonstrate a sufficient variety of patterns among the isolates for subtyping purposes. We conclude that plasmid DNA analysis is very useful as a subtyping test for isolates of K. pneumoniae and K. oxytoca. Neither biotyping nor antimicrobial susceptibility as performed in our laboratory had sufficient discriminatory power and reproducibility for subtyping these organisms.
我们比较了质粒DNA分析、Vitek系统的生物分型以及纸片扩散法药敏试验,以此作为肺炎克雷伯菌和产酸克雷伯菌的分型检测方法。92株受试菌株来自6个月以上交替出现的培养阳性患者。在此期间未发现感染暴发或聚集性感染。85%的菌株检测到质粒DNA。除1株外,每株菌株在重复检测时均呈现可重复的质粒DNA缺失或质粒DNA图谱。对于一些仅含有大质粒的菌株,需要进行质粒DNA的限制性内切酶分析来区分差异。仅含有大质粒的菌株占所收集菌株的18%。在78株含有质粒DNA的菌株中,除2株外,其余通过质粒DNA分析均被认为彼此不同。生物分型和药敏试验的重复性不高。此外,生物分型在菌株中未显示出足够多样的模式用于分型目的。我们得出结论,质粒DNA分析作为肺炎克雷伯菌和产酸克雷伯菌菌株的分型检测方法非常有用。在我们实验室进行的生物分型和药敏试验对于这些微生物的分型均没有足够的鉴别力和重复性。