4.8 Article

Mycobacterium tuberculosis mutation rate estimates from different lineages predict substantial differences in the emergence of drug-resistant tuberculosis

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NATURE GENETICS
卷 45, 期 7, 页码 784-+

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NATURE PORTFOLIO
DOI: 10.1038/ng.2656

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  1. Director's Office of the US National Institutes of Health [DP2 0D001378]
  2. National Institute of Allergy and Infectious Diseases [U19 AI076217]
  3. US National Institutes of Health Models of Infectious Disease Agent Study program [1 U54 GM088558]
  4. Howard Hughes Medical Institute Physician Scientist Early Career Award
  5. Harvard University Graduate School of Arts and Sciences
  6. Doris Duke Charitable Foundation Clinical Scientist Development Award

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A key question in tuberculosis control is why some strains of M. tuberculosis are preferentially associated with resistance to multiple drugs. We demonstrate that M. tuberculosis strains from lineage 2 (East Asian lineage and Beijing sublineage) acquire drug resistances in vitro more rapidly than M. tuberculosis strains from lineage 4 (Euro-American lineage) and that this higher rate can be attributed to a higher mutation rate. Moreover, the in vitro mutation rate correlates well with the bacterial mutation rate in humans as determined by whole-genome sequencing of clinical isolates. Finally, using a stochastic mathematical model, we demonstrate that the observed differences in mutation rate predict a substantially higher probability that patients infected with a drug-susceptible lineage 2 strain will harbor multidrug-resistant bacteria at the time of diagnosis. These data suggest that interventions to prevent the emergence of drug-resistant tuberculosis should target bacterial as well as treatment-related risk factors.

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