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High Genotypic Diversity Among Methicillin-resistant Staphylococcus Pseudintermedius Isolated from Canine Infections in Denmark

Overview
Journal BMC Vet Res
Publisher Biomed Central
Date 2016 Jul 1
PMID 27357502
Citations 15
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Abstract

Background: Methicillin-resistant Staphylococcus pseudintermedius (MRSP) has emerged globally in companion animals in the last decade. In Europe, the multidrug-resistant sequence type (ST)71 is widespread, but recently other clones have appeared. The objective of this study was to examine genotypic diversity and antimicrobial resistance of clinical MRSP isolates obtained from dogs, including dogs sampled on multiple occasions, in Denmark over a six-year period. For that purpose a total of 46 clinical MRSP isolates obtained from 36 dogs between 2009 and 2014 were subjected to antimicrobial susceptibility testing, multilocus-sequence typing (MLST) and SCCmec typing.

Results: Twenty-three sequence types were identified with ST71, mostly associated with SCCmec II-III, as the most common occurring in 13 dogs. Among the remaining 33 isolates, 19 belonged to clonal complex (CC)258 comprising ST258-SCCmec IV and its single- and double-locus variants. These were susceptible to 4-7 of the 22 antibiotics tested, whereas CC71 isolates were susceptible to only 2-5 antibiotics. Clone-specific differences were especially pronounced for fluoroquinolones and aminoglycosides with most CC71 isolates being resistant and almost all CC258 isolates being susceptible. Sixteen of the 19 CC258 isolates had oxacillin MICs of 0.5 g/L, whereas MICs for CC71 isolates were consistently above 4 g/L. Four of five dogs representing multiple isolates had distinct STs on different sampling events.

Conclusions: The overall genotypic diversity of MRSP is high in Denmark indicating multiple acquisitions of SCCmec into distinct clones, and mutational evolution, which appears to be particularly rapid for certain ancestral clones such as ST258. ST71-SCCmec II-III is the most common MRSP lineage and is typically multidrug-resistant. CC258-SCCmec IV isolates, which emerged in Denmark since 2012, display susceptibility to a wider range of antimicrobials. The isolation of distinct STs in individual dogs over time suggests repeated exposure or short-term genetic evolution of MRSP clones within patients.

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References
1.
Kondo Y, Ito T, Ma X, Watanabe S, Kreiswirth B, Etienne J . Combination of multiplex PCRs for staphylococcal cassette chromosome mec type assignment: rapid identification system for mec, ccr, and major differences in junkyard regions. Antimicrob Agents Chemother. 2006; 51(1):264-74. PMC: 1797693. DOI: 10.1128/AAC.00165-06. View

2.
Lee S, Ender M, Adhikari R, Smith J, Berger-Bachi B, Cook G . Fitness cost of staphylococcal cassette chromosome mec in methicillin-resistant Staphylococcus aureus by way of continuous culture. Antimicrob Agents Chemother. 2007; 51(4):1497-9. PMC: 1855501. DOI: 10.1128/AAC.01239-06. View

3.
Sasaki T, Tsubakishita S, Tanaka Y, Sakusabe A, Ohtsuka M, Hirotaki S . Multiplex-PCR method for species identification of coagulase-positive staphylococci. J Clin Microbiol. 2010; 48(3):765-9. PMC: 2832457. DOI: 10.1128/JCM.01232-09. View

4.
Perreten V, Kadlec K, Schwarz S, Gronlund Andersson U, Finn M, Greko C . Clonal spread of methicillin-resistant Staphylococcus pseudintermedius in Europe and North America: an international multicentre study. J Antimicrob Chemother. 2010; 65(6):1145-54. DOI: 10.1093/jac/dkq078. View

5.
Kadlec K, van Duijkeren E, Wagenaar J, Schwarz S . Molecular basis of rifampicin resistance in methicillin-resistant Staphylococcus pseudintermedius isolates from dogs. J Antimicrob Chemother. 2011; 66(6):1236-42. DOI: 10.1093/jac/dkr118. View