| Literature DB >> 16477032 |
Sebastien Gagneux1, Kathryn DeRiemer, Tran Van, Midori Kato-Maeda, Bouke C de Jong, Sujatha Narayanan, Mark Nicol, Stefan Niemann, Kristin Kremer, M Cristina Gutierrez, Markus Hilty, Philip C Hopewell, Peter M Small.
Abstract
Mycobacterium tuberculosis remains a major cause of morbidity and mortality worldwide. Studies have reported human pathogens to have geographically structured population genetics, some of which have been linked to ancient human migrations. However, no study has addressed the potential evolutionary consequences of such longstanding human-pathogen associations. Here, we demonstrate that the global population structure of M. tuberculosis is defined by six phylogeographical lineages, each associated with specific, sympatric human populations. In an urban cosmopolitan environment, mycobacterial lineages were much more likely to spread in sympatric than in allopatric patient populations. Tuberculosis cases that did occur in allopatric hosts disproportionately involved high-risk individuals with impaired host resistance. These observations suggest that mycobacterial lineages are adapted to particular human populations. If confirmed, our findings have important implications for tuberculosis control and vaccine development.Entities:
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Year: 2006 PMID: 16477032 PMCID: PMC1413851 DOI: 10.1073/pnas.0511240103
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205