首页> 美国卫生研究院文献>Journal of Clinical Microbiology >In vivo stability and discriminatory power of methicillin-resistant Staphylococcus aureus typing by restriction endonuclease analysis of plasmid DNA compared with those of other molecular methods.
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In vivo stability and discriminatory power of methicillin-resistant Staphylococcus aureus typing by restriction endonuclease analysis of plasmid DNA compared with those of other molecular methods.

机译:与其他分子方法相比通过质粒DNA的限制性内切酶分析耐甲氧西林金黄色葡萄球菌分型的体内稳定性和判别能力。

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摘要

We evaluated test discriminatory power and DNA type alterations among methicillin-resistant Staphylococcus aureus strains by testing 199 sequential isolates from 39 patients collected over 30 to 228 days. Isolates were typed by one or three different methods (restriction endonuclease analysis of plasmid DNA [REAP] with or without pulsed-field gel electrophoresis of genomic DNA [PFGE] and immunoblotting [IB]). REAP was highly discriminatory compared with PFGE and IB. However, the initial isolates from 4 of the 39 patients lacked detectable plasmid DNA and could not be typed by REAP. Typing of individual patient isolates showed that a different REAP type was identified only once every 138 days. Among 25 comparisons, seven sequential isolate pairs demonstrating REAP differences were also different by PFGE and IB. This likely represented the presence of more than one strain. Eighteen other pairs with REAP differences were identical or related to one another by PFGE and IB typing, and 17 of these differences were likely caused by a single genetic alteration within the same strain or clone. The rate of PFGE differences explicable by single genetic alterations among sequential isolates identical by REAP was similar to the overall rate for REAP differences in the whole collection. We conclude that REAP and PFGE typing differences explicable by single genetic alterations are relatively infrequent but not rare. These isolates should be examined by alternative typing systems to further support or refute clonality.
机译:我们通过测试从30到228天收集的39例患者的199个连续分离株,评估了耐甲氧西林金黄色葡萄球菌菌株之间的鉴别能力和DNA类型改变。通过一种或三种不同的方法(对质粒DNA进行限制性核酸内切酶分析[REAP],使用或不使用基因组DNA的脉冲场凝胶电泳[PFGE]和免疫印迹[IB])对分离物进行分型。与PFGE和IB相比,REAP具有很高的歧视性。但是,这39例患者中有4例的最初分离株缺乏可检测的质粒DNA,无法通过REAP进行分型。个别患者分离株的分型显示,每138天仅发现一次不同的REAP类型。在25个比较中,证实REAP差异的七个顺序隔离株对也因PFGE和IB而不同。这可能表示存在多个菌株。通过PFGE和IB分型,其他18个具有REAP差异的对相同或彼此相关,其中17个差异可能是由同一菌株或克隆中的单个遗传改变引起的。通过REAP相同的顺序分离株之间的单个遗传改变可以解释的PFGE差异的比率与整个集合中REAP差异的总体比率相似。我们得出的结论是,单基因改变可解释的REAP和PFGE类型差异相对少见,但并不罕见。这些分离株应通过替代分型系统进行检查,以进一步支持或驳斥克隆性。

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