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基于高分辨率熔解曲线分析的牛源凝固酶阴性葡萄球菌种属鉴定。

High-resolution melt analysis for species identification of coagulase-negative staphylococci derived from bovine milk.

机构信息

Department of Production Animal Health, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, Canada.

出版信息

Diagn Microbiol Infect Dis. 2013 Mar;75(3):227-34. doi: 10.1016/j.diagmicrobio.2012.11.008. Epub 2012 Dec 27.

Abstract

Coagulase-negative staphylococci (CNS) are the most frequently isolated pathogens isolated from bovine milk. In this study, we report a rapid assay for species identification of CNS using high-resolution melt analysis (HRMA) of 16S rDNA sequences. Real-time polymerase chain reaction amplification of 16S rRNA gene fragment, spanning the variable region V1 and V2, was performed with a resulting amplicon of 215 bp. A library of distinct melt curves of reference strains of 13 common CNS species was created using HRMA. Sequencing of 16S rRNA and rpoB genes, and, when needed, tuf gene, of 100 CNS isolates obtained from Canadian Bovine Mastitis Research Network was done to determine their species identity, allowing for subsequent evaluation of the performance of HRMA for field isolates of bovine CNS. A combination of HRMA and sequencing revealed that Staphylococcus chromogenes, S. xylosus, S. simulans, and S. sciuri had multiple genotypes, complicating their resolution by HRMA. As the 3 genotypes of S. chromogenes had distinct melt curves, the 3 distinct genotypes were employed as reference strains in a blinded trial of 156 CNS isolates to identify S. chromogenes. HRMA correctly identified all S. chromogenes isolates which were later confirmed by sequencing. Staphylococcus chromogenes (68%) was most frequently found among the CNS isolates, followed by S. haemolyticus (10%) and S. xylosus (6%). The present study revealed that HRMA of 16S rRNA gene (V1-V2) could be used as a rapid, efficient, low-cost, and minimally cumbersome technique for S. chromogenes identification, the most common CNS derived from bovine milk.

摘要

凝固酶阴性葡萄球菌(CNS)是从牛奶中分离出来的最常见的病原体。在本研究中,我们报告了一种使用 16S rDNA 序列高分辨率熔解分析(HRMA)快速鉴定 CNS 种属的方法。采用实时聚合酶链反应扩增 16S rRNA 基因片段,跨越可变区 V1 和 V2,得到 215bp 的扩增子。使用 HRMA 构建了 13 种常见 CNS 种属参考菌株的独特熔解曲线文库。对从加拿大牛乳腺炎研究网络获得的 100 株 CNS 分离株的 16S rRNA 和 rpoB 基因进行测序,必要时还对 tuf 基因进行测序,以确定其种属身份,从而随后评估 HRMA 对牛 CNS 田间分离株的性能。HRMA 结合测序结果表明,金黄色葡萄球菌、木糖葡萄球菌、模拟葡萄球菌和松鼠葡萄球菌有多种基因型,这使得它们的 HRMA 分辨率变得复杂。由于 S. chromogenes 的 3 种基因型具有不同的熔解曲线,因此将这 3 种不同的基因型作为参考菌株,用于 156 株 CNS 分离株的盲法试验,以鉴定 S. chromogenes。HRMA 正确鉴定了所有后来通过测序确认的 S. chromogenes 分离株。在 CNS 分离株中,最常见的是 S. chromogenes(68%),其次是 S. haemolyticus(10%)和 S. xylosus(6%)。本研究表明,16S rRNA 基因(V1-V2)的 HRMA 可作为一种快速、高效、低成本且操作简单的技术,用于鉴定 S. chromogenes,这是从牛奶中分离出来的最常见的 CNS。

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