4.8 Article

Emergence and spread of a human-transmissible multidrug-resistant nontuberculous mycobacterium

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SCIENCE
卷 354, 期 6313, 页码 751-757

出版社

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.aaf8156

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资金

  1. Wellcome Trust [098051, 107032AIA]
  2. Medical Research Council
  3. UK Cystic Fibrosis Trust
  4. Papworth Hospital
  5. National Institute for Health Research (NIHR) Cambridge Biomedical Research Centre
  6. NIHR Specialist Respiratory Biomedical Research Unit, Imperial College London
  7. UK Clinical Research Collaboration Translational Infection Research Initiative
  8. CF Foundation Therapeutics grant
  9. Australian National Health and Medical Research Council
  10. National Services Division
  11. NHS Scotland
  12. European Nucleotide Archive [ERP001039]
  13. National Research Ethics Service (NRES) [12/EE/0158]
  14. National Information Governance Board (NIGB) [ECC 3-03 (f)/2012]
  15. Scottish centers from NHS Scotland Multiple Board Caldicott Guardian Approval (NHS Tayside AR/SW)
  16. Wellcome Trust [107032/Z/15/Z] Funding Source: Wellcome Trust
  17. Cystic Fibrosis Trust [PJ561, SRC002] Funding Source: researchfish
  18. Medical Research Council [974668, G1001712] Funding Source: researchfish
  19. National Institute for Health Research [CL-2006-13-003] Funding Source: researchfish
  20. Wellcome Trust [107032/Z/15/Z] Funding Source: researchfish
  21. MRC [G1001712] Funding Source: UKRI

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Lung infections with Mycobacterium abscessus, a species of multidrug-resistant nontuberculous mycobacteria, are emerging as an important global threat to individuals with cystic fibrosis (CF), in whom M. abscessus accelerates inflammatory lung damage, leading to increased morbidity and mortality. Previously, M. abscessus was thought to be independently acquired by susceptible individuals from the environment. However, using whole-genome analysis of a global collection of clinical isolates, we show that the majority of M. abscessus infections are acquired through transmission, potentially via fomites and aerosols, of recently emerged dominant circulating clones that have spread globally. We demonstrate that these clones are associated with worse clinical outcomes, show increased virulence in cell-based and mouse infection models, and thus represent an urgent international infection challenge.

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