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Molecular Genotyping of Staphylococcus aureus Strains: Comparison of Repetitive Element Sequence-Based PCR with Various Typing Methods and Isolation of a Novel Epidemicity Marker

机译:金黄色葡萄球菌菌株的分子基因分型:基于重复元素序列的PCR与各种分型方法的比较和新型流行病标记的分离

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摘要

Repetitive sequence-based (Rep)-PCR genotyping as described here is based on the presence of homologues of Mycoplasma pneumoniae repeat-like elements in Staphylococcus. In this study we comparatively evaluated the usefulness of rep-PCR typing with two sets of well-defined collections of Staphylococcus aureus strains. Rep-PCR analysis of the first collection of S. aureus strains (n = 59) and one Staphylococcus intermedius strain showed 14 different rep-PCR patterns, with each pattern harboring 6 to 15 DNA fragments. The discriminatory power of rep-PCR typing compared well to those of arbitrarily primed PCR (average of 20 types) and pulsed-field gel electrophoresis (11 types). S. aureus strain collection I comprised four outbreak-related groups of isolates. The isolates in only one group were found to have identical rep-PCR profiles. However, in an analysis of isolates from three additional independent local outbreaks (n for outbreaks 1 and 2 = 5, n for outbreak 3 = 12), identical rep-PCR types were found among strains isolated during each outbreak. Therefore, we conclude that rep-PCR genotyping may be an easy and fast method for monitoring of the epidemiology of nosocomial Staphylococcus infections. Rep-PCR analysis of strain collection II, which consisted of epidemic and nonepidemic methicillin-resistant S. aureus (MRSA) strains, revealed that a cluster of similar rep-PCR profiles was found among MRSA isolates which were more frequently isolated and which were most often associated with outbreaks.
机译:本文所述的基于重复序列的(Rep)-PCR基因分型是基于葡萄球菌中肺炎支原体重复样元件的同源物的存在。在这项研究中,我们通过两组金黄色葡萄球菌菌株的明确定义集合,比较评估了rep-PCR分型的有效性。对第一批金黄色葡萄球菌菌株(n = 59)和一个中间葡萄球菌菌株的Rep-PCR分析显示了14种不同的rep-PCR模式,每种模式包含6至15个DNA片段。与任意引物PCR(平均20种类型)和脉冲场凝胶电泳(11种类型)相比,rep-PCR类型的辨别能力很好。金黄色葡萄球菌菌株集合I包括四个与爆发相关的分离株组。发现仅一组中的分离物具有相同的rep-PCR谱。但是,在对另外三个独立的局部暴发的分离株进行分析(暴发1和2 = 5,暴发3 = 12,n)中,在每次暴发期间分离出的菌株中发现了相同的rep-PCR类型。因此,我们得出结论,rep-PCR基因分型可能是监测医院内葡萄球菌感染流行病学的简便快捷方法。由流行性和非流行性耐甲氧西林金黄色葡萄球菌(MRSA)菌株组成的菌株收集II的Rep-PCR分析表明,在MRSA分离株中发现了相似的rep-PCR谱图簇,这些分离株更常见且分离度最高通常与爆发有关。

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