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Genomic insights into the rapid emergence and evolution of MDR in Staphylococcus pseudintermedius.
McCarthy, Alex J; Harrison, Ewan M; Stanczak-Mrozek, Kinga; Leggett, Bernadette; Waller, Andrew; Holmes, Mark A; Lloyd, David H; Lindsay, Jodi A; Loeffler, Anette.
Affiliation
  • McCarthy AJ; Institute of Infection and Immunity, St George's, University of London, London, UK.
  • Harrison EM; Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.
  • Stanczak-Mrozek K; Institute of Infection and Immunity, St George's, University of London, London, UK.
  • Leggett B; Pathobiology Unit, University Veterinary Hospital, School of Veterinary Medicine, University College Dublin, Dublin, Ireland.
  • Waller A; Centre of Preventive Medicine, Animal Health Trust, Newmarket, UK.
  • Holmes MA; Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.
  • Lloyd DH; Veterinary Clinical Sciences and Services, Royal Veterinary College, Hawkshead Campus, University of London, London, UK.
  • Lindsay JA; Institute of Infection and Immunity, St George's, University of London, London, UK.
  • Loeffler A; Veterinary Clinical Sciences and Services, Royal Veterinary College, Hawkshead Campus, University of London, London, UK aloeffler@rvc.ac.uk.
J Antimicrob Chemother ; 70(4): 997-1007, 2015 Apr.
Article in En | MEDLINE | ID: mdl-25527273
OBJECTIVES: MDR methicillin-resistant Staphylococcus pseudintermedius (MRSP) strains have emerged rapidly as major canine pathogens and present serious treatment issues and concerns to public health due to their, albeit low, zoonotic potential. A further understanding of the genetics of resistance arising from a broadly susceptible background of S. pseudintermedius is needed. METHODS: We sequenced the genomes of 12 S. pseudintermedius isolates of varied STs and resistance phenotypes. RESULTS: Nine distinct clonal lineages had acquired either staphylococcal cassette chromosome (SCC) mec elements and/or Tn5405-like elements carrying up to five resistance genes [aphA3, sat, aadE, erm(B), dfrG] to generate MRSP, MDR methicillin-susceptible S. pseudintermedius and MDR MRSP populations. The most successful and clinically problematic MDR MRSP clones, ST68 SCCmecV(T) and ST71 SCCmecII-III, have further accumulated mutations in gyrA and grlA conferring resistance to fluoroquinolones. The carriage of additional mobile genetic elements (MGEs) was highly variable, suggesting that horizontal gene transfer is frequent in S. pseudintermedius populations. CONCLUSIONS: Importantly, the data suggest that MDR MRSP evolved rapidly by the acquisition of a very limited number of MGEs and mutations, and that the use of many classes of antimicrobials may co-select for the spread and emergence of MDR and XDR strains. Antimicrobial stewardship will need to be comprehensive, encompassing human medicine and veterinary disciplines to successfully preserve antimicrobial efficacy.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Staphylococcus / Drug Resistance, Multiple, Bacterial / Biological Evolution / Anti-Bacterial Agents Limits: Animals / Humans Language: En Journal: J Antimicrob Chemother Year: 2015 Document type: Article Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Staphylococcus / Drug Resistance, Multiple, Bacterial / Biological Evolution / Anti-Bacterial Agents Limits: Animals / Humans Language: En Journal: J Antimicrob Chemother Year: 2015 Document type: Article Country of publication: Reino Unido