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首页> 外文期刊>Journal of Clinical Microbiology >Improved Multiple-Locus Variable-Number Tandem-Repeat Assay for Staphylococcus aureus Genotyping, Providing a Highly Informative Technique Together with Strong Phylogenetic Value
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Improved Multiple-Locus Variable-Number Tandem-Repeat Assay for Staphylococcus aureus Genotyping, Providing a Highly Informative Technique Together with Strong Phylogenetic Value

机译:改进的金黄色葡萄球菌基因分型的多位点可变数串联重复测定,提供了具有高度系统信息和高度系统发育价值的技术

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We describe an improved multiple-locus variable-number tandem-repeat (VNTR) analysis (MLVA) scheme for genotyping Staphylococcus aureus. We compare its performance to those of multilocus sequence typing (MLST) and spa typing in a survey of 309 strains. This collection includes 87 epidemic methicillin-resistant S. aureus (MRSA) strains of the Harmony collection, 75 clinical strains representing the major MLST clonal complexes (CCs) (50 methicillin-sensitive S. aureus [MSSA] and 25 MRSA), 135 nasal carriage strains (133 MSSA and 2 MRSA), and 13 published S. aureus genome sequences. The results show excellent concordance between the techniques' results and demonstrate that the discriminatory power of MLVA is higher than those of both MLST and spa typing. Two hundred forty-two genotypes are discriminated with 14 VNTR loci (diversity index, 0.9965; 95% confidence interval, 0.9947 to 0.9984). Using a cutoff value of 45%, 21 clusters are observed, corresponding to the CCs previously defined by MLST. The variability of the different tandem repeats allows epidemiological studies, as well as follow-up of the evolution of CCs and the identification of potential ancestors. The 14 loci can conveniently be analyzed in two steps, based upon a first-line simplified assay comprising a subset of 10 loci (panel 1) and a second subset of 4 loci (panel 2) that provides higher resolution when needed. In conclusion, the MLVA scheme proposed here, in combination with available on-line genotyping databases (including http://mlva.u-psud.fr/), multiplexing, and automatic sizing, can provide a basis for almost-real-time large-scale population monitoring of S. aureus.
机译:我们描述了一种改进的 m 多变- l ocus v 可变- n umbr andem- r epeat(VNTR) a 分析(MLVA)方案对金黄色葡萄球菌进行基因分型。我们将其性能与 m ulti l 轨迹 s 序列 t yping(MLST)和 spa 输入对309个菌株的调查。该集合包括87种耐甲氧西林流行的 S。 Harmony收集的金黄色葡萄球菌(MRSA)菌株,代表主要MLST克隆复合物(CC)的75种临床菌株(50种对甲氧西林敏感的金黄色葡萄球菌 [MSSA]和25种MRSA),135鼻运输菌株(133 MSSA和2 MRSA),以及13种已发表的 S。金黄色葡萄球菌的基因组序列。结果表明该技术的结果之间具有极好的一致性,并表明MLVA的识别能力高于MLST和 spa 类型。用14个VNTR基因座区分了242个基因型(多样性指数,0.9965; 95%置信区间,0.9947至0.9984)。使用45%的临界值,观察到21个簇,对应于以前由MLST定义的CC。不同串联重复序列的变异性使得可以进行流行病学研究,以及对CC演变和潜在祖先的追踪。基于包括10个基因座的子集(面板1)和包含4个基因座的第二子集(面板2)的一线简化测定,可以在两个步骤中方便地分析14个基因座,后者在需要时提供更高的分辨率。总之,此处提出的MLVA方案与可用的在线基因分型数据库(包括http://mlva.u-psud.fr/),多路复用和自动调整大小相结合,可以为几乎实时提供基础对 S的大规模人口监测。金黄色

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