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Typing of Acinetobacter baumannii strains isolated from hospital patients by amplified ribosomal DNA restriction analysis (ARDRA).

机译:通过扩增核糖体DNA限制性酶切分析(ARDRA)对从医院患者中分离的鲍曼不动杆菌菌株进行分型。

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Eighty-one clinical Acinetobacter baumannii isolates were included in this study collected from year 2001 to 2006. The strains were originally isolated from different clinical and environmental specimens by the Microbiology Laboratory of the King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia. They were preserved in tryptic soy broth (TSB) supplemented with 20% (vol/vol) glycerol. Pure isolates were stored at -80 degrees C until used in the Research Centre, KFSH&RC. For ARDRA genomic typing, the 16S rRNA gene of each of the 81 Acinetobacter baumannii strains was amplified and restricted with the restriction enzymes Alu I, Mbo I and Msp I. Each enzyme generated 3-7 bands per strain, analyzed visually by comparing the differences in the banding patterns generated and grouped the isolates into Strain A to G, while isolates that are untypeable or undetermined were group into Strain H. ARDRA could not accurately distinguish the 81 different Acinetobacter baumannii strains using three restriction enzymes, indicating low discriminatory power for the method.
机译:2001年至2006年收集的81例临床鲍曼不动杆菌菌株被分离出。这些菌株最初是由费萨尔国王专科医院和研究中心的微生物实验室从不同的临床和环境标本中分离出来的, 沙特阿拉伯,利雅得。将它们保存在补充有20%(体积/体积)甘油的胰蛋白酶大豆肉汤(TSB)中。纯分离株在-80摄氏度下保存,直到用于KFSH&RC研究中心。为了进行ARDRA基因组分型,扩增了81个鲍曼不动杆菌菌株的16S rRNA基因,并用限制酶Alu I,Mbo I限制。 >和 Msp I 。每种酶每个菌株产生3-7条带,通过比较产生的条带模式的差异进行视觉分析,并将分离株分为A到G菌株,而无法分型或不确定的分离株归为H菌株.ARDRA无法准确区分81种不同的鲍曼不动杆菌菌株使用三种限制性酶,表明该方法的鉴别力低。

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