首页> 外文期刊>Journal of Clinical Microbiology >Core Genome Multilocus Sequence Typing and Single Nucleotide Polymorphism Analysis in the Epidemiology of Brucella melitensis Infections
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Core Genome Multilocus Sequence Typing and Single Nucleotide Polymorphism Analysis in the Epidemiology of Brucella melitensis Infections

机译:流行病学布鲁氏菌感染的流行病学中核心基因组多基因座序列分型和单核苷酸多态性分析

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The use of whole-genome sequencing (WGS) using next-generation sequencing (NGS) technology has become a widely accepted method for microbiology laboratories in the application of molecular typing for outbreak tracing and genomic epidemiology. Several studies demonstrated the usefulness of WGS data analysis through single-nucleotide polymorphism (SNP) calling from a reference sequence analysis for Brucella melitensis , whereas gene-by-gene comparison through core-genome multilocus sequence typing (cgMLST) has not been explored so far. ABSTRACT The use of whole-genome sequencing (WGS) using next-generation sequencing (NGS) technology has become a widely accepted method for microbiology laboratories in the application of molecular typing for outbreak tracing and genomic epidemiology. Several studies demonstrated the usefulness of WGS data analysis through single-nucleotide polymorphism (SNP) calling from a reference sequence analysis for Brucella melitensis , whereas gene-by-gene comparison through core-genome multilocus sequence typing (cgMLST) has not been explored so far. The current study developed an allele-based cgMLST method and compared its performance to that of the genome-wide SNP approach and the traditional multilocus variable-number tandem repeat analysis (MLVA) on a defined sample collection. The data set was comprised of 37 epidemiologically linked animal cases of brucellosis as well as 71 isolates with unknown epidemiological status, composed of human and animal samples collected in Italy. The cgMLST scheme generated in this study contained 2,704 targets of the B. melitensis 16M reference genome. We established the potential criteria necessary for inclusion of an isolate into a brucellosis outbreak cluster to be ≤6 loci in the cgMLST and ≤7 in WGS SNP analysis. Higher phylogenetic distance resolution was achieved with cgMLST and SNP analysis than with MLVA, particularly for strains belonging to the same lineage, thereby allowing diverse and unrelated genotypes to be identified with greater confidence. The application of a cgMLST scheme to the characterization of B. melitensis strains provided insights into the epidemiology of this pathogen, and it is a candidate to be a benchmark tool for outbreak investigations in human and animal brucellosis.
机译:使用下一代测序(NGS)技术的全基因组测序(WGS)已成为微生物实验室在分子分型用于暴发追踪和基因组流行病学应用中的一种广泛接受的方法。多项研究表明,通过对布鲁氏菌的参考序列分析调用单核苷酸多态性(SNP)进行WGS数据分析是有用的,而迄今为止,尚未探索通过核心基因组多基因座序列类型(cgMLST)进行基因对基因的比较。 。摘要使用下一代测序(NGS)技术的全基因组测序(WGS)已成为微生物实验室在分子类型用于暴发追踪和基因组流行病学应用中的一种广泛接受的方法。多项研究表明,通过对布鲁氏菌的参考序列分析调用单核苷酸多态性(SNP)进行WGS数据分析是有用的,而迄今为止,尚未探索通过核心基因组多基因座序列类型(cgMLST)进行基因对基因的比较。 。当前的研究开发了一种基于等位基因的cgMLST方法,并将其性能与全基因组SNP方法和传统的多基因座可变数串联重复分析(MLVA)的性能进行了比较。该数据集包括37例与流行病学相关的布鲁氏菌病动物病例以及71例流行病学状况未知的分离株,其中包括在意大利收集的人类和动物样本。在这项研究中生成的cgMLST方案包含2704个B. melitensis 16M参考基因组靶标。我们建立了将分离株纳入布鲁氏菌病爆发群所需的潜在标准,其在cgMLST中的位点≤6,在WGS SNP分析中的位点≤7。与MLVA相比,通过cgMLST和SNP分析可获得更高的系统发生距离分辨率,尤其是对于属于同一谱系的菌株,从而可以更可靠地鉴定出各种无关的基因型。将cgMLST方案应用于melitensis菌株的鉴定为这种病原体的流行病学提供了见识,并且它有望成为人类和动物布鲁氏菌病暴发调查的基准工具。

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