Whole Genome Sequencing for Surveillance of Antimicrobial Resistance in .

Janine T Bossé, Yanwen Li, Jon Rogers, Roberto Fernandez Crespo, Yinghui Li, Roy R Chaudhuri, Matthew T G Holden, Duncan J Maskell, Alexander W Tucker, Brendan W Wren, Andrew N Rycroft, Paul R Langford
Author Information
  1. Janine T Bossé: Section of Paediatrics, Department of Medicine, Imperial College London London, UK.
  2. Yanwen Li: Section of Paediatrics, Department of Medicine, Imperial College London London, UK.
  3. Jon Rogers: Animal and Plant Health Agency Bury St Edmunds, UK.
  4. Roberto Fernandez Crespo: Section of Paediatrics, Department of Medicine, Imperial College London London, UK.
  5. Yinghui Li: Section of Paediatrics, Department of Medicine, Imperial College London London, UK.
  6. Roy R Chaudhuri: Department of Veterinary Medicine, University of Cambridge Cambridge, UK.
  7. Matthew T G Holden: The Wellcome Trust Sanger Institute Cambridge, UK.
  8. Duncan J Maskell: Department of Veterinary Medicine, University of Cambridge Cambridge, UK.
  9. Alexander W Tucker: Department of Veterinary Medicine, University of Cambridge Cambridge, UK.
  10. Brendan W Wren: Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine London, UK.
  11. Andrew N Rycroft: Department of Pathology and Pathogen Biology, The Royal Veterinary College Hatfield, UK.
  12. Paul R Langford: Section of Paediatrics, Department of Medicine, Imperial College London London, UK.

Abstract

The aim of this study was to evaluate the correlation between antimicrobial resistance (AMR) profiles of 96 clinical isolates of , an important porcine respiratory pathogen, and the identification of AMR genes in whole genome sequence (wgs) data. Susceptibility of the isolates to nine antimicrobial agents (ampicillin, enrofloxacin, erythromycin, florfenicol, sulfisoxazole, tetracycline, tilmicosin, trimethoprim, and tylosin) was determined by agar dilution susceptibility test. Except for the macrolides tested, elevated MICs were highly correlated to the presence of AMR genes identified in wgs data using ResFinder or BLASTn. Of the isolates tested, 57% were resistant to tetracycline [MIC ≥ 4 mg/L; 94.8% with either (B) or (H)]; 48% to sulfisoxazole (MIC ≥ 256 mg/L or DD = 6; 100% with ), 20% to ampicillin (MIC ≥ 4 mg/L; 100% with ), 17% to trimethoprim (MIC ≥ 32 mg/L; 100% with ), and 6% to enrofloxacin (MIC ≥ 0.25 mg/L; 100% with GyrAS83F). Only 33% of the isolates did not have detectable AMR genes, and were sensitive by MICs for the antimicrobial agents tested. Although 23 isolates had MIC ≥ 32 mg/L for tylosin, all isolates had MIC ≤ 16 mg/L for both erythromycin and tilmicosin, and no macrolide resistance genes or known point mutations were detected. Other than the GyrAS83F mutation, the AMR genes detected were mapped to potential plasmids. In addition to presence on plasmid(s), the (B) gene was also found chromosomally either as part of a 56 kb integrative conjugative element (ICE) in 21, or as part of a Tn insertion in 15 isolates. Our results indicate that, with the exception of macrolides, wgs data can be used to accurately predict resistance of to the tested antimicrobial agents and provides added value for routine surveillance.

Keywords

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Grants

  1. BB/G018553/1/Biotechnology and Biological Sciences Research Council
  2. BB/G019177/1/Biotechnology and Biological Sciences Research Council
  3. BB/G019274/1/Biotechnology and Biological Sciences Research Council
  4. BB/G020744/1/Biotechnology and Biological Sciences Research Council

Word Cloud

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