4.7 Article

Occurrence and characterization of Escherichia coli ST410 co-harbouring bla(NDM-5), bla(CMY-42) and bla(TEM-190) in a dog from the UK

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JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
卷 74, 期 5, 页码 1207-1211

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OXFORD UNIV PRESS
DOI: 10.1093/jac/dkz017

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  1. National Institute for Health Research Health Protection Research Unit (NIHR HPRU) in Healthcare Associated Infections and Antimicrobial Resistance at Oxford University
  2. Public Health England (PHE) [HPRU-2012-10041]
  3. NIHR Oxford Biomedical Research Centre
  4. PHE/University of Oxford
  5. [NE/N019989/1]

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Background/Objectives: Carbapenemase-producing Enterobacteriaceae (CPE) are a public health threat, and have been found in humans, animals and the environment. Carbapenems are not authorized for use in EU or UK companion animals, and the prevalence of carbapenem-resistant Gram-negative bacilli (CRGNB) in this population is unknown. Methods: We investigated CRGNB isolated from animal specimens received by one diagnostic laboratory from 34 UK veterinary practices (September 2015-December 2016). Any Gram-negative isolates from clinical specimens showing reduced susceptibility to fluoroquinolones and/or aminoglycosides and/or cephalosporins were investigated phenotypically and genotypically for carbapenemases. A complete genome assembly (Illumina/Nanopore) was generated for the single isolate identified to investigate the genetic context for carbapenem resistance. Results: One ST410 Escherichia coli isolate [(CARB35); 1/191, 0.5%], cultured from a wound in a springer spaniel, harboured a known carbapenem resistance gene (bla(NDM-5)). The gene was located in the chromosome on an integrated 100 kb IncF plasmid, also harbouring other drug resistance genes (mrx, sul1, ant1 and dfrA). The isolate also contained bla(CMY-42) and bla(TEM-190) on two separate plasmids (IncI1 and IncFII, respectively) that showed homology with other publicly available plasmid sequences from Italy and Myanmar. Conclusions: Even though the use of carbapenems in companion animals is restricted, the concurrent presence of bla(CMY-42) and other antimicrobial resistance genes could lead to co-selection of carbapenemase genes in this population. Further studies investigating the selection and flow of plasmids carrying important resistance genes amongst humans and companion animals are needed.

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