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Quantitative Estimation of the Stability of Methicillin-Resistant Staphylococcus aureus Strain-Typing Systems by Use of Kaplan-Meier Survival Analysis

机译:利用Kaplan-Meier生存分析定量评估耐甲氧西林金黄色葡萄球菌菌株分型系统的稳定性

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摘要

Knowledge concerning stability is important in the development and assessment of microbial molecular typing systems and is critical for the interpretation of their results. Typing system stability is usually measured as the fraction of isolates that change type after several in vivo passages, but this does not necessarily reflect in vivo stability. The aim of this study was to utilize survival analysis to provide an informative quantitative measure of in vivo stability and to compare the stabilities of various techniques employed in typing methicillin-resistant Staphylococcus aureus (MRSA). We identified 100 MRSA pairs (isolated from the same patient ≥1 month apart) and typed them using multilocus sequence typing (MLST), phage-derived open reading frame (PDORF) typing, toxin gene profiling (TGP), staphylococcal cassette chromosome mec (SCCmec) subtyping, pulsed-field gel electrophoresis (PFGE), and spa sequence typing. Discordant isolate pairs, belonging to different MLST clonal complexes, were excluded, leaving 81 pairs for analysis. The stabilities of these methods were examined using Kaplan-Meier survival analysis, and discriminatory power was measured by Simpson's index of diversity. The probability percentages that the type remained unchanged at 6 months for spa sequence typing, TGP, multilocus variable number of tandem repeats analysis (MLVA), SCCmec subtyping, PDORF typing, and PFGE were 95, 95, 88, 82, 71, and 58, respectively, while the Simpson's indices of diversity were 0.48, 0.47, 0.70, 0.72, 0.89, and 0.88, respectively. Survival analysis using sequential clinical isolates adds an important quantitative dimension to the measurement of stability of a microbial typing system. Of the methods compared here, PDORF typing provides high discriminatory power, comparable with that of PFGE, and a level of stability suitable for MRSA surveillance and outbreak investigations.
机译:有关稳定性的知识在微生物分子分型系统的开发和评估中很重要,对解释其结果也至关重要。分型系统的稳定性通常以几次体内传代后改变类型的分离物的分数来衡量,但这不一定反映出体内稳定性。这项研究的目的是利用生存分析为体内稳定性提供一种有用的定量方法,并比较用于鉴定耐甲氧西林金黄色葡萄球菌(MRSA)的各种技术的稳定性。我们鉴定了100对MRSA(分离自相距≥1个月的同一患者),并使用多基因座序列分型(MLST),噬菌体开放阅读框(PDORF)分型,毒素基因谱(TGP),葡萄球菌盒式染色体mec( SCCmec)分型,脉冲场凝胶电泳(PFGE)和spa序列分型。属于不同MLST克隆复合体的不一致分离株对被排除在外,剩下81对用于分析。使用Kaplan-Meier生存分析检查了这些方法的稳定性,并通过辛普森多样性指数测量了判别力。 Spa序列分型,TGP,多位点串联重复序列分析(MLVA),SCCmec分型,PDORF分型和PFGE在6个月时类型保持不变的概率百分比分别为95、95、88、82、71和58辛普森多样性指数分别为0.48、0.47、0.70、0.72、0.89和0.88。使用顺序临床分离株进行的生存分析为微生物分型系统的稳定性测量增加了重要的定量维度。在这里比较的方法中,PDORF分型提供了与PFGE相当的高辨别力,并且具有适合MRSA监测和暴发调查的稳定性。

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