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PCR amplification of rRNA intergenic spacer regions as a method for epidemiologic typing of Clostridium difficile.

机译:PCR扩增rRNA基因间隔区作为一种艰难梭菌流行病学分型方法。

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摘要

From January to March 1993, a suspected outbreak of antibiotic-associated diarrhea occurred on a pediatric oncology ward of the Clinical Center Hospital at the National Institutes of Health. Isolates of Clostridium difficile obtained from six patients implicated in this outbreak were typed by both PCR amplification of rRNA intergenic spacer regions (PCR ribotyping) and restriction endonuclease analysis of genomic DNA. Comparable results were obtained with both methods; five of the six patients were infected with the same strain of C. difficile. Subsequent analysis of 102 C. difficile isolates obtained from symptomatic patients throughout the Clinical Center revealed the existence of 41 distinct and reproducible PCR ribotypes. These data suggest that PCR ribotyping provides a discriminatory, reproducible, and simple alternative to conventional molecular approaches for typing strains of C. difficile.
机译:从1993年1月至3月,在美国国立卫生研究院临床中心医院的儿科肿瘤病房,怀疑发生了与抗生素有关的腹泻。通过涉及rRNA基因间间隔区的PCR扩增(PCR核糖分型)和基因组DNA的限制性核酸内切酶分析,对从6例与此次暴发有关的患者中获得的艰难梭菌分离株进行分型。两种方法均获得了可比的结果。六名患者中有五名感染了相同的艰难梭菌菌株。随后在整个临床中心对有症状患​​者进行的102株艰难梭菌分离株的分析显示,存在41种不同且可重复的PCR核糖型。这些数据表明,PCR核糖分型法为区分艰难梭菌菌株提供了一种与常规分子方法不同的,可重复的,简单的替代方法。

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