首页> 外文期刊>Journal of bacteriology >Global Phylogeny of Mycobacterium tuberculosis Based on Single Nucleotide Polymorphism (SNP) Analysis: Insights into Tuberculosis Evolution, Phylogenetic Accuracy of Other DNA Fingerprinting Systems, and Recommendations for a Minimal Standard SNP Set
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Global Phylogeny of Mycobacterium tuberculosis Based on Single Nucleotide Polymorphism (SNP) Analysis: Insights into Tuberculosis Evolution, Phylogenetic Accuracy of Other DNA Fingerprinting Systems, and Recommendations for a Minimal Standard SNP Set

机译:基于单核苷酸多态性(SNP)分析的结核分枝杆菌的全球系统发育:对结核病进化,其他DNA指纹系统的系统发育准确性的了解以及对最小标准SNP集的建议

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We analyzed a global collection of Mycobacterium tuberculosis strains using 212 single nucleotide polymorphism (SNP) markers. SNP nucleotide diversity was high (average across all SNPs, 0.19), and 96% of the SNP locus pairs were in complete linkage disequilibrium. Cluster analyses identified six deeply branching, phylogenetically distinct SNP cluster groups (SCGs) and five subgroups. The SCGs were strongly associated with the geographical origin of the M. tuberculosis samples and the birthplace of the human hosts. The most ancestral cluster (SCG-1) predominated in patients from the Indian subcontinent, while SCG-1 and another ancestral cluster (SCG-2) predominated in patients from East Asia, suggesting that M. tuberculosis first arose in the Indian subcontinent and spread worldwide through East Asia. Restricted SCG diversity and the prevalence of less ancestral SCGs in indigenous populations in Uganda and Mexico suggested a more recent introduction of M. tuberculosis into these regions. The East African Indian and Beijing spoligotypes were concordant with SCG-1 and SCG-2, respectively; X and Central Asian spoligotypes were also associated with one SCG or subgroup combination. Other clades had less consistent associations with SCGs. Mycobacterial interspersed repetitive unit (MIRU) analysis provided less robust phylogenetic information, and only 6 of the 12 MIRU microsatellite loci were highly differentiated between SCGs as measured by GST. Finally, an algorithm was devised to identify two minimal sets of either 45 or 6 SNPs that could be used in future investigations to enable global collaborations for studies on evolution, strain differentiation, and biological differences of M. tuberculosis.
机译:我们使用212个单核苷酸多态性(SNP)标记分析了全球结核分枝杆菌菌株。 SNP核苷酸多样性很高(所有SNP的平均值为0.19),并且96%的SNP位点对处于完全连锁不平衡状态。聚类分析确定了六个深分支,系统发育上不同的SNP聚类组(SCG)和五个亚组。 SCG与 M的地理起源密切相关。结核样本和人类宿主的出生地。来自印度次大陆的患者中祖先群最多(SCG-1),而来自东亚的患者中则以SCG-1和另一个祖先群(SCG-2)为主。结核病首先出现在印度次大陆,并通过东亚传播到全世界。 SCG多样性受到限制以及祖先SCG在乌干达和墨西哥的土著居民中普遍存在,这表明最近又引入了 M。结核病进入这些区域。东非印度人和北京的血腥型分别与SCG-1和SCG-2一致。 X和中亚的血吸虫型也与一种SCG或亚组组合相关。其他进化枝与SCG的联系不太一致。通过 G ST 测量,分枝杆菌散布的重复单位(MIRU)分析提供的系统发育信息较差,并且12个MIRU微卫星基因座中只有6个在SCG之间高度分化。最后,设计了一种算法来识别45个或6个SNP的两个最小集合,这些最小集合可用于将来的研究中,以实现全球合作以研究 M的进化,菌株分化和生物学差异。结核病

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