TY - JOUR KW - Genes, Bacterial KW - Genome, Bacterial KW - Geography KW - Humans KW - leprosy KW - Mycobacterium leprae KW - Phylogeny KW - Polymorphism, Single Nucleotide KW - Recombination, Genetic AU - Monot M AU - Honore N AU - Garnier T AU - Zidane N AU - Sherafi D AU - Paniz-Mondolfi A AU - Matsuoka M AU - Taylor MG AU - Donoghue H AU - Bouwman A AU - Mays S AU - Watson CL AU - Lockwood DN AU - Khamesipour A AU - Khamispour A AU - Dowlati Y AU - Jianping S AU - Rea T AU - Vera-Cabrera L AU - Stefani M AU - Banu S AU - Macdonald M AU - Sapkota BR AU - Spencer JS AU - Thomas J AU - Harshman K AU - Singh P AU - Busso P AU - Gattiker A AU - Rougemont J AU - Brennan PJ AU - Cole S AB -
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 (6x coverage), and Illumina resequencing technology was used to obtain the sequences of strains Thai53 (38x coverage) and NHDP63 (46x 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.
BT - Nature genetics C1 - http://www.ncbi.nlm.nih.gov/pubmed/19881526?dopt=Abstract DA - 2009 Dec DO - 10.1038/ng.477 IS - 12 J2 - Nat. Genet. LA - eng N2 -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 (6x coverage), and Illumina resequencing technology was used to obtain the sequences of strains Thai53 (38x coverage) and NHDP63 (46x 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.
PY - 2009 SP - 1282 EP - 9 T2 - Nature genetics TI - Comparative genomic and phylogeographic analysis of Mycobacterium leprae. UR - https://www.nature.com/articles/ng.477.pdf VL - 41 SN - 1546-1718 ER -