4.8 Article

Comparative genomic and phylogeographic analysis of Mycobacterium leprae

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NATURE GENETICS
卷 41, 期 12, 页码 1282-U39

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NATURE PORTFOLIO
DOI: 10.1038/ng.477

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  1. Fondation Raoul Follereau
  2. Genopole programme
  3. US National Institutes of Health
  4. National Institute of Allergy and Infectious Diseases [RO1-AI47197-01A1, NO1-AI25469]

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Reductive evolution and massive pseudogene formation have shaped the 3.31-Mb genome of Mycobacterium leprae, an unculturable obligate pathogen that causes leprosy in humans. The complete genome sequence of M. leprae strain Br4923 from Brazil was obtained by conventional methods (6 x coverage), and Illumina resequencing technology was used to obtain the sequences of strains Thai53 (38 x coverage) and NHDP63 (46 x coverage) from Thailand and the United States, respectively. Whole-genome comparisons with the previously sequenced TN strain from India revealed that the four strains share 99.995% sequence identity and differ only in 215 polymorphic sites, mainly SNPs, and by 5 pseudogenes. Sixteen interrelated SNP subtypes were defined by genotyping both extant and extinct strains of M. leprae from around the world. The 16 SNP subtypes showed a strong geographical association that reflects the migration patterns of early humans and trade routes, with the Silk Road linking Europe to China having contributed to the spread of leprosy.

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