• 1

    Cox HU, Hoskins JD & Newman SS, et al. Distribution of staphylococcal species on clinically healthy cats. Am J Vet Res 1985;46:18241828.

  • 2

    Devriesse LA. Identification and characterization of staphylococci isolated from cats. Vet Microbiol 1984;9:279285.

  • 3

    Igimi S, Atobe H & Tohya Y, et al. Characterization of the most frequently encountered Staphylococcus sp. in cats. Vet Microbiol 1994;39:255260.

  • 4

    Lilenbaum W, Nunes ELC, Azeredo MAI. Prevalence and antimicrobial susceptibility of staphylococci isolated from the skin surface of clinically normal cats. Lett Appl Microbiol 1998;27:224228.

    • Search Google Scholar
    • Export Citation
  • 5

    Lilenbaum W, Esteves AL, Souza GN. Prevalence and antimicrobial susceptibility of staphylococci isolated from saliva of clinically normal cats. Lett Appl Microbiol 1999;28:448452.

    • Search Google Scholar
    • Export Citation
  • 6

    Patel A, Lloyd DH, Lamport AI. Antimicrobial resistance of feline staphylococci in south-eastern England. Vet Dermatol 1999;10:257261.

  • 7

    Espinola MB, Lilenbaum W. Prevalence of bacteria in the conjunctival sac and on the eyelid margin of clinically normal cats. J Small Anim Pract 1996;37:364366.

    • Search Google Scholar
    • Export Citation
  • 8

    Kloos WE, Bannerman TL. Update on clinical significance of coagulase-negative staphylococci. Clin Microbiol Rev 1994;7:117140.

  • 9

    Patel A, Lloyd DH & Howell SA, et al. Investigation into the potential pathogenicity of Staphylococcus felis in a cat. Vet Rec 2002;150:668669.

  • 10

    Lina G, Piemont Y & Godail-Gamot F, et al. Involvement of Panton-Valentine leudocidin-producing Staphylococcus aureus in primary skin infections and pneumonia. Clin Infect Dis 1999;29:11281132.

    • Search Google Scholar
    • Export Citation
  • 11

    Baptiste KE, Williams K & Williams NJ, et al. Methicillinresistant staphylococci in companion animals. Emerg Infect Dis 2005;11:19421944.

  • 12

    Scott GM, Thomson R & Malone-Lee J, et al. Cross-infection between animals and man: possible feline transmission of Staphylococcus aureus infection in humans? J Hosp Infect 1988;12:2934.

    • Search Google Scholar
    • Export Citation
  • 13

    Manian FA. Asymptomatic nasal carriage of mupirocinresistant, methicillin-resistant Staphylococcus aureus (MRSA) in a pet dog associated with MRSA infection in household contacts. Clin Infect Dis 2003;36:2628.

    • Search Google Scholar
    • Export Citation
  • 14

    Roberts S, O'Shea K & Morris D, et al. A real-time PCR assay to detect the Panton Valentine leukocidin toxin in staphylocci: screening Staphylococcus schleiferi subspecies coagulans strains from companion animals. Vet Microbiol 2005;107:139144.

    • Search Google Scholar
    • Export Citation
  • 15

    McDougal LA, Steward CD & Killgore GE, et al. Pulsed-field gel electrophoresis typing of oxacillin-resistant Staphylococcus aureus isolates from the United States: establishing a national database. J Clin Microbiol 2003;41:51135120.

    • Search Google Scholar
    • Export Citation
  • 16

    Oliveira DC, de Lencastre H. Multiplex PCR strategy for rapid identification of structural types and variants of the mec element in methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother 2002;46:21552161.

    • Search Google Scholar
    • Export Citation
  • 17

    Vandenesch F, Naimi T & Enright MC, et al. Communityacquired methicillin-resistant Staphylococcus aureus carrying Panton-Valentine leukocidin genes: worldwide emergence. Emerg Infect Dis 2003;9:978984.

    • Search Google Scholar
    • Export Citation
  • 18

    Werckenthin C, Cardoso M & Martel JL, et al. Antimicrobial resistance in staphylococci from animals with particular reference to bovine S. aureus, porcine S. hyicus, and canine S. intermedius. Vet Res 2001;32:341362.

    • Search Google Scholar
    • Export Citation
  • 19

    Barber M. Methicillin-resistant staphylococci. J Clin Pathol 1961;14:385393.

  • 20

    Berger-Bachi B, Rohrer S. Factors influencing methicillin resistance in staphylococci. Arch Microbiol 2002;178:165171.

  • 21

    Fey PD, Said-Salim B & Rupp ME, et al. Comparative molecular analysis of communityor hospital-acquired methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother 2003;47:196203.

    • Search Google Scholar
    • Export Citation
  • 22

    Diederen BMW, Kluytmans JAJAW. The emergence of infections with community-associated methicillin resistant Staphylococcus aureus. J Infect 2006;52:157168.

    • Search Google Scholar
    • Export Citation
  • 23

    Boag A, Loeffler A, Lloyd DH. Methicillin-resistant Staphylococcus aureus isolates from companion animals (lett). Vet Rec 2004;154:411.

  • 24

    Duquette RA, Nuttal TJ. Methicillin-resistant Staphylococcus aureus in dogs and cats: an emerging problem? J Small Anim Pract 2004;45:591597.

    • Search Google Scholar
    • Export Citation
  • 25

    Rich M, Roberts L. Methicillin-resistant Staphylococcus aureus isolates from companion animals (lett). Vet Rec 2004;154:310.

  • 26

    Tomlin J, Pead MJ & Lloyd DH, et al. Methicillin-resistant Staphylococcus aureus infections in 11 dogs. Vet Rec 1999;144:6064.

  • 27

    Weese JS. Methicillin-resistant Staphylococcus aureus: an emerging pathogen in small animals. J Am Anim Hosp Assoc 2005;41:150157.

  • 28

    Ozaki K, Yamagami T & Nomura K, et al. Abscess-forming inflammatory granulation tissue with Gram-positive cocci and prominent eosinophilic infiltration in cats: possible infection of methicillin-resistant Staphylococcus. Vet Pathol 2003;40:283287.

    • Search Google Scholar
    • Export Citation

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Clinical, microbiological, and molecular characterization of methicillin-resistant Staphylococcus aureus infections of cats

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  • 1 Department of Clinical Studies–Philadelphia, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104.
  • | 2 Department of Clinical Studies–Philadelphia, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104.
  • | 3 Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104.
  • | 4 Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104.
  • | 5 Department of Clinical Studies–Philadelphia, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104.
  • | 6 Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104.

Abstract

Objective—To compare clinical information obtained from medical records of cats with methicillin-resistant Staphylococcus aureus (MRSA) and methicillin-susceptible S aureus (MSSA) infections, evaluate antibiograms of MRSA and MSSA for multiple-drug resistance (MDR), and characterize the strain type and staphylococcal chromosome cassette (SCC)mec type of each MRSA.

Sample Population—70 S aureus isolates obtained from 46 cats.

Procedures—Clinical information obtained from medical records, including signalment, clinical signs, histologic examination of affected tissues, and outcomes, was compared between the 2 groups. Composite antibiograms of MRSA and MSSA were compared statistically. The MRSA strains were characterized by use of pulsed-field gel electrophoresis and SCCmec typing.

Results—No statistical differences in signalment or subjective differences in clinical signs or outcomes were detected between groups with MRSA or MSSA infection. Significant differences in antimicrobial resistance were detected, with MRSA having complete resistance to fluoroquinolone and macrolide antimicrobials, whereas MSSA maintained a high frequency of susceptibility. Seven pulsed-field patterns were observed in 15 MRSA strains; all but 1 were highly related. All MRSA isolates contained a type II SCCmec element.

Conclusions and Clinical Relevance—Because MDR cannot be predicted in staphylococcal infections in cats on the basis of clinical signalment, culture and susceptibility testing are recommended whenever initial empirical treatment is unsuccessful. Molecular characterization of MRSA strains suggests that there has been reverse-zoonotic transmission from humans.

Impact for Human Medicine—The SCCmec type II element is typically associated with nosocomial MRSA infections of people. Cats may serve as reservoirs for MRSA infections in humans.

Abstract

Objective—To compare clinical information obtained from medical records of cats with methicillin-resistant Staphylococcus aureus (MRSA) and methicillin-susceptible S aureus (MSSA) infections, evaluate antibiograms of MRSA and MSSA for multiple-drug resistance (MDR), and characterize the strain type and staphylococcal chromosome cassette (SCC)mec type of each MRSA.

Sample Population—70 S aureus isolates obtained from 46 cats.

Procedures—Clinical information obtained from medical records, including signalment, clinical signs, histologic examination of affected tissues, and outcomes, was compared between the 2 groups. Composite antibiograms of MRSA and MSSA were compared statistically. The MRSA strains were characterized by use of pulsed-field gel electrophoresis and SCCmec typing.

Results—No statistical differences in signalment or subjective differences in clinical signs or outcomes were detected between groups with MRSA or MSSA infection. Significant differences in antimicrobial resistance were detected, with MRSA having complete resistance to fluoroquinolone and macrolide antimicrobials, whereas MSSA maintained a high frequency of susceptibility. Seven pulsed-field patterns were observed in 15 MRSA strains; all but 1 were highly related. All MRSA isolates contained a type II SCCmec element.

Conclusions and Clinical Relevance—Because MDR cannot be predicted in staphylococcal infections in cats on the basis of clinical signalment, culture and susceptibility testing are recommended whenever initial empirical treatment is unsuccessful. Molecular characterization of MRSA strains suggests that there has been reverse-zoonotic transmission from humans.

Impact for Human Medicine—The SCCmec type II element is typically associated with nosocomial MRSA infections of people. Cats may serve as reservoirs for MRSA infections in humans.

Contributor Notes

Address correspondence to Dr. Morris.