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.
MeSH Terms
Adaptation, Physiological
Disease Transmission, Infectious
Genetic Variation
Genomics
Geography
Humans
Molecular Epidemiology
Mycobacterium tuberculosis/genetics,pathogenicity,physiology
San Francisco/epidemiology
Tuberculosis/epidemiology,microbiology,transmission
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
Gagneux Sebastien
Institute for Systems Biology, Seattle, WA 98103, USA. sgagneux@systemsbiology.org
DeRiemer Kathryn
Van Tran
Kato-Maeda Midori
de Jong Bouke C
Narayanan Sujatha
Nicol Mark
Niemann Stefan
Kremer Kristin
Gutierrez M Cristina
Hilty Markus
Hopewell Philip C
Small Peter M
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