ArticleProceedings of the National Academy of Sciences of the United States of America2011
Dispersal of Mycobacterium tuberculosis via the Canadian fur trade.
Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.
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Who cites it
25 citing papers in PubMed, 66 citations in OpenAlex.
- Cross-continental transmission and host adaptation ofiMetaOmics · 2025Article
- South Asian origin and global transmission history ofmSystems · 2025Article
- The Many Hosts of Mycobacteria 9 (MHM9): A conference report.Tuberculosis (Edinburgh, Scotland) · 2023Article
- Distribution and origins ofMicrobial genomics · 2023Article
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- Connection between two historical tuberculosis outbreak sites in Japan, Honshu, by a newEpidemiology and infection · 2022Article
- A systemic approach to assess the potential and risks of wildlife culling for infectious disease control.Communications biology · 2020Review
- Extensive global movement of multidrug-resistantThorax · 2019Article
- Lineage specific histories of Mycobacterium tuberculosis dispersal in Africa and Eurasia.Molecular ecology · 2019Article
- Genomic analysis of the emergence of drug-resistant strains of Mycobacterium tuberculosis in the Middle East.Scientific reports · 2019Article
- Dispersal ofFrontiers in microbiology · 2019Article
- China's tuberculosis epidemic stems from historical expansion of four strains of Mycobacterium tuberculosis.Nature ecology & evolution · 2018Article
- Global expansion ofScience advances · 2018Article
- Epidemiological and genomic determinants of tuberculosis outbreaks in First Nations communities in Canada.BMC medicine · 2018Article
- Molecular Epidemiology of Tuberculosis in British Columbia, Canada: A 10-Year Retrospective Study.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2018Article
- Application of whole genome sequence analysis to the study of Mycobacterium tuberculosis in Nunavut, Canada.PloS one · 2017Article
- Co-evolution of Mycobacterium tuberculosis and Homo sapiens.Immunological reviews · 2015Review
- Article
- Diversity of Mycobacterium tuberculosis across Evolutionary Scales.PLoS pathogens · 2015Article
- Comparative genomics of mycobacteria: some answers, yet more new questions.Cold Spring Harbor perspectives in medicine · 2014Review
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Authors and funding
13 authors at 6 institutions in 2 countries.
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Abstract
Patterns of gene flow can have marked effects on the evolution of populations. To better understand the migration dynamics of Mycobacterium tuberculosis, we studied genetic data from European M. tuberculosis lineages currently circulating in Aboriginal and French Canadian communities. A single M. tuberculosis lineage, characterized by the DS6(Quebec) genomic deletion, is at highest frequency among Aboriginal populations in Ontario, Saskatchewan, and Alberta; this bacterial lineage is also dominant among tuberculosis (TB) cases in French Canadians resident in Quebec. Substantial contact between these human populations is limited to a specific historical era (1710-1870), during which individuals from these populations met to barter furs. Statistical analyses of extant M. tuberculosis minisatellite data are consistent with Quebec as a source population for M. tuberculosis gene flow into Aboriginal populations during the fur trade era. Historical and genetic analyses suggest that tiny M. tuberculosis populations persisted for ∼100 y among indigenous populations and subsequently expanded in the late 19th century after environmental changes favoring the pathogen. Our study suggests that spread of TB can occur by two asynchronous processes: (i) dispersal of M. tuberculosis by minimal numbers of human migrants, during which small pathogen populations are sustained by ongoing migration and slow disease dynamics, and (ii) expansion of the M. tuberculosis population facilitated by shifts in host ecology. If generalizable, these migration dynamics can help explain the low DNA sequence diversity observed among isolates of M. tuberculosis and the difficulties in global elimination of tuberculosis, as small, widely dispersed pathogen populations are difficult both to detect and to eradicate.
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