4.7 Article

Whole-genome sequencing to delineate Mycobacterium tuberculosis outbreaks: a retrospective observational study

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LANCET INFECTIOUS DISEASES
卷 13, 期 2, 页码 137-146

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ELSEVIER SCI LTD
DOI: 10.1016/S1473-3099(12)70277-3

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资金

  1. Medical Research Council
  2. Wellcome Trust
  3. National Institute for Health Research
  4. Health Protection Agency
  5. National Institute for Health Research (NIHR) Oxford Biomedical Research Centre
  6. UK Clinical Research Collaboration (UKCRC) Modernising Medical Microbiology Consortium
  7. UKCRC Translational Infection Research Initiative
  8. Medical Research Council, Biotechnology and Biological Sciences Research Council
  9. National Institute for Health Research [G0800778]
  10. Wellcome Trust at the Wellcome Trust Sanger Institute [087646/Z/08/Z, 098051]
  11. HPA for reference laboratory services
  12. MRC [G0800778, MR/J011398/1] Funding Source: UKRI
  13. Medical Research Council [MR/J011398/1, G0800778] Funding Source: researchfish
  14. National Institute for Health Research [NF-SI-0512-10047, NF-SI-0508-10279, DRF-2010-03-40] Funding Source: researchfish

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Background Tuberculosis incidence in the UK has risen in the past decade. Disease control depends on epidemiological data, which can be difficult to obtain. Whole-genome sequencing can detect microevolution within Mycobacterium tuberculosis strains. We aimed to estimate the genetic diversity of related M tuberculosis strains in the UK Midlands and to investigate how this measurement might be used to investigate community outbreaks. Methods In a retrospective observational study, we used Mumina technology to sequence M tuberculosis genomes from an archive of frozen cultures. We characterised isolates into four groups: cross-sectional, longitudinal, household, and community. We measured pairwise nucleotide differences within hosts and between hosts in household outbreaks and estimated the rate of change in DNA sequences. We used the findings to interpret network diagrams constructed from 11 community dusters derived from mycobacterial interspersed repetitive-unit variable-number tandem-repeat data. Findings We sequenced 390 separate isolates from 254 patients, induding representatives from all five major lineages of M tuberculosis. The estimated rate of change in DNA sequences was 0.5 single nucleotide polyrnorphisms (SNPs) per genome per year (95% CI 0.3-0.7) in longitudinal isolates from 30 individuals and 25 families. Divergence is rarely higher than five SNPs in 3 years. 109 (96%) of 114 paired isolates from individuals and households differed by five or fewer SNPs. More than five SNPs separated isolates from none of 69 epidemiologically linked patients, two (15%) of 13 possibly linked patients, and 13 (17%) of 75 epidemiologically unlinked patients (three-way comparison exact p<0.0001). Genetic trees and clinical and epidemiological data suggest that super-spreaders were present in two community clusters. Interpretation Whole-genome sequencing can delineate outbreaks of tuberculosis and allows inference about direction of transmission between cases. The technique could identify super-spreaders and predict the existence of undiagnosed cases, potentially leading to early treatment of infectious patients and their contacts.

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