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A Framework for Assessing the Concordance of Molecular Typing Methods and the True Strain Phylogeny of Campylobacter jejuni and C. coli Using Draft Genome Sequence Data

机译:使用基因组序列数据草稿评估空肠弯曲杆菌和大肠杆菌的分子分型方法与真菌株系统发育的一致性的框架

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摘要

Tracking of sources of sporadic cases of campylobacteriosis remains challenging, as commonly used molecular typing methods have limited ability to unambiguously link genetically related strains. Genomics has become increasingly prominent in the public health response to enteric pathogens as methods enable characterization of pathogens at an unprecedented level of resolution. However, the cost of sequencing and expertise required for bioinformatic analyses remains prohibitive, and these comprehensive analyses are limited to a few priority strains. Although several molecular typing methods are currently widely used for epidemiological analysis of campylobacters, it is not clear how accurately these methods reflect true strain relationships. To address this, we have developed a framework and associated computational tools to rapidly analyze draft genome sequence data for the assessment of molecular typing methods against a “gold standard” based on the phylogenetic analysis of highly conserved core (HCC) genes with high sequence quality. We analyzed 104 publicly available whole genome sequences (WGS) of C. jejuni and C. coli. In addition to in silico determination of multi-locus sequence typing (MLST), flaA, and porA type, as well as comparative genomic fingerprinting (CGF) type, we inferred a “reference” phylogeny based on 389 HCC genes. Molecular typing data were compared to the reference phylogeny for concordance using the adjusted Wallace coefficient (AWC) with confidence intervals. Although MLST targets the sequence variability in core genes and CGF targets insertions/deletions of accessory genes, both methods are based on multi-locus analysis and provided better estimates of true phylogeny than methods based on single loci (porA, flaA). A more comprehensive WGS dataset including additional genetically related strains, both epidemiologically linked and unlinked, will be necessary to more comprehensively assess the performance of subtyping methods for outbreak investigations and surveillance activities. Analyses of the strengths and weaknesses of widely used typing methodologies in inferring true strain relationships will provide guidance in the interpretation of this data for epidemiological purposes.
机译:追踪零星弯曲菌病病例的来源仍然具有挑战性,因为常用的分子分型方法明确连接遗传相关菌株的能力有限。基因组学在对肠道病原体的公共卫生响应中日益突出,因为方法可以以前所未有的分辨率表征病原体。但是,生物信息学分析所需的测序成本和专业知识仍然令人望而却步,并且这些全面的分析仅限于一些优先菌株。尽管目前几种分子分型方法已广泛用于弯曲杆菌的流行病学分析,但尚不清楚这些方法如何准确反映真实的菌株关系。为了解决这个问题,我们已经开发了一个框架和相关的计算工具,可以基于具有高序列质量的高度保守核心(HCC)基因的系统发育分析,快速分析基因组序列草案数据,以针对“金标准”评估分子分型方法。我们分析了空肠弯曲杆菌和大肠杆菌的104个公众可获得的全基因组序列(WGS)。除了计算机上确定多位点序列类型(MLST),flaA和porA类型以及比较基因组指纹图谱(CGF)类型外,我们还基于389 HCC基因推断出“参考”系统发育。使用调整后的华莱士系数(AWC)和置信区间,将分子分型数据与参考系统发育进行比较,以获得一致性。尽管MLST靶向核心基因的序列变异性,而CGF靶向辅助基因的插入/缺失,但这两种方法都是基于多基因座分析,并且比基于单个基因座的方法(porA,flaA)提供了更好的真实系统发育估计。为了更全面地评估暴发调查和监视活动的亚型方法的性能,需要一个更全面的WGS数据集,包括与流行病学相关和未相关的其他遗传相关菌株。分析广泛使用的分型方法在推断真实菌株之间的关系的优缺点,将为流行病学目的解释该数据提供指导。

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