4.8 Article

The global distribution and spread of the mobilized colistin resistance gene mcr-1

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NATURE COMMUNICATIONS
卷 9, 期 -, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s41467-018-03205-z

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资金

  1. Newton Trust UK-China NSFC initiative [MR/P007597/1, 81661138006]
  2. BBSRC GCRF scheme
  3. EPSRC [EP/F500351/1]
  4. Wellcome Trust on a Genomic Medicine and Statistics DPhil grant
  5. European Union: European regional development fund (ERDF)
  6. Conseil Regional de La Reunion
  7. Centre de Cooperation internationale en Recherche agronomique pour le Developpement (CIRAD)
  8. National Natural Science Foundation of China [81625014]
  9. Dorothy Hodgkin Fellowship - Royal Society [DH140195]
  10. Sir Henry Dale Fellowship - Wellcome Trust [109385/Z/15/Z]
  11. Sir Henry Dale Fellowship - Royal Society [109385/Z/15/Z]
  12. Wellcome Trust [102541/A/13/Z]
  13. Royal Society [102541/A/13/Z]
  14. Sir Henry Dale Fellowship
  15. MRC [MR/P007597/1] Funding Source: UKRI
  16. Medical Research Council [MR/P007597/1] Funding Source: researchfish

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Colistin represents one of the few available drugs for treating infections caused by carbapenem-resistant Enterobacteriaceae. As such, the recent plasmid-mediated spread of the colistin resistance gene mcr-1 poses a significant public health threat, requiring global monitoring and surveillance. Here, we characterize the global distribution of mcr-1 using a data set of 457 mcr-1-positive sequenced isolates. We find mcr-1 in various plasmid types but identify an immediate background common to all mcr-1 sequences. Our analyses establish that all mcr-1 elements in circulation descend from the same initial mobilization of mcr-1 by an ISApl1 transposon in the mid 2000s (2002-2008; 95% highest posterior density), followed by a marked demographic expansion, which led to its current global distribution. Our results provide the first systematic phylogenetic analysis of the origin and spread of mcr-1, and emphasize the importance of understanding the movement of antibiotic resistance genes across multiple levels of genomic organization.

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