Analyze Diet
Veterinary microbiology2005; 109(3-4); 285-296; doi: 10.1016/j.vetmic.2005.06.003

Methicillin-resistant Staphylococcus aureus (MRSA) isolated from animals and veterinary personnel in Ireland.

Abstract: Reports of methicillin-resistant Staphylococcus aureus (MRSA) in animals have become more frequent in recent years. This paper documents the recovery of MRSA from animals with respiratory, urinary tract or wound infection and from animals subjected to surgical procedures following treatment in one veterinary hospital and 16 private veterinary clinics in different geographical locations throughout Ireland. MRSA was recovered from 25 animals comprising 14 dogs, eight horses, one cat, one rabbit and a seal, and also from 10 attendant veterinary personnel. Clinical susceptibility testing suggested that the 35 isolates fell into two different groups. One group of isolates (Group 1) was resistant to one or more of the following classes of antimicrobials: macrolides, lincosamines, tetracyclines and/or fluoroquinolones. The second group (Group 2) was resistant to macrolides, aminoglycosides, tetracyclines and trimethoprim/sulphamethoxazole and variably resistant to fluoroquinolones, lincosamines and rifampicin. One isolate in Group 2 was susceptible to trimethoprim. Epidemiological typing by antibiogram-resistogram (AR) typing, biotyping and by chromosomal DNA restriction fragment length polymorphism analysis using SmaI digestion followed by pulsed field gel electrophoresis (PFGE), confirmed these two major clusters. PFGE analysis showed that most isolates from non-equine animals were indistinguishable from each other and from the isolates from personnel caring for these animals. MRSA was isolated from eight horses which attended six different veterinary practices before referral to an equine veterinary hospital. Isolates from the eight horses and from their attendant personnel had PFGE patterns that were indistinguishable and were unlike the patterns obtained from the other isolates. Comparison of PFGE patterns of isolates from veterinary sources with patterns from MRSA recovered in human hospitals showed that the most frequently occurring pattern of MRSA from non-equine animals was indistinguishable from the predominant pattern obtained from the most prevalent MRSA strain in the human population in Ireland. However, the patterns of the isolates from horses were unlike any patterns previously reported in Irish studies of human isolates. This study shows that transmission of two strains of MRSA is occurring in veterinary practices in Ireland and that one strain may have arisen from human hospitals. The source of the second strain remains to be determined.
Publication Date: 2005-07-20 PubMed ID: 16026939DOI: 10.1016/j.vetmic.2005.06.003Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research article explores the occurrence and spread of Methicillin-resistant Staphylococcus aureus (MRSA), a type of bacteria resistant to certain antibiotics, in animals and veterinary personnel in Ireland.

Study Background and Execution

  • The study involved a collection of MRSA samples from animals with infections (respiratory, urinary tract, wound) and those that had undergone surgical procedures. Sampling locations were spread across a veterinary hospital and 16 private veterinary clinics throughout Ireland.
  • Besides animals, MRSA samples were also collected from 10 attending veterinary personnel for a more holistic assessment of MRSA transmission.
  • The animals affected by MRSA included 14 dogs, eight horses, a cat, a rabbit, and a seal.

Clinical Susceptibility and Typing

  • The research identified two groups (Group 1 and Group 2) of MRSA based on their resistance to different classes of antimicrobials. Group 1 showed resistance to one or more of the macrolides, lincosamines, tetracyclines, and/or fluoroquinolones while Group 2 showed resistance to macrolides, aminoglycosides, tetracyclines, trimethoprim/sulphamethoxazole, and variable resistance to fluoroquinolones, lincosamines, and rifampicin.
  • These groups were confirmed through epidemiological typing methods like antibiogram-resistogram (AR) typing, biotyping, and chromosomal DNA restriction fragment length polymorphism analysis.

Results and Analysis

  • The Pulsed Field Gel Electrophoresis (PFGE) analysis, which separates large molecules of DNA, revealed that most MRSA isolates from non-equine animals (animals other than horses) were very much alike each other and also those of the personnel taking care of these animals.
  • Eight horses and their attending personnel showed a unique MRSA pattern that differed from other non-equine samples, suggesting that different strains of MRSA were identified in the equine group.
  • Despite the differences, the most common MRSA pattern among non-equine animals was identical to the most frequent MRSA pattern found in humans in Ireland. The MRSA strain from horses, meanwhile, displayed a pattern not previously documented in humans in Ireland.

Conclusions

  • The paper underscores that two strains of MRSA are being spread in veterinary practices in Ireland, with one potentially originating from human hospitals. The source of the second strain found among the horses still needs to be identified.

Cite This Article

APA
O'Mahony R, Abbott Y, Leonard FC, Markey BK, Quinn PJ, Pollock PJ, Fanning S, Rossney AS. (2005). Methicillin-resistant Staphylococcus aureus (MRSA) isolated from animals and veterinary personnel in Ireland. Vet Microbiol, 109(3-4), 285-296. https://doi.org/10.1016/j.vetmic.2005.06.003

Publication

ISSN: 0378-1135
NlmUniqueID: 7705469
Country: Netherlands
Language: English
Volume: 109
Issue: 3-4
Pages: 285-296

Researcher Affiliations

O'Mahony, R
  • Faculty of Veterinary Medicine, University College Dublin, Belfield, Dublin 4, Ireland.
Abbott, Y
    Leonard, F C
      Markey, B K
        Quinn, P J
          Pollock, P J
            Fanning, S
              Rossney, A S

                MeSH Terms

                • Animal Technicians
                • Animals
                • Anti-Bacterial Agents / pharmacology
                • Anti-Bacterial Agents / therapeutic use
                • Cat Diseases / drug therapy
                • Cat Diseases / epidemiology
                • Cat Diseases / microbiology
                • Cats
                • DNA, Bacterial / chemistry
                • DNA, Bacterial / genetics
                • Dog Diseases / drug therapy
                • Dog Diseases / epidemiology
                • Dog Diseases / microbiology
                • Dogs
                • Electrophoresis, Gel, Pulsed-Field / veterinary
                • Humans
                • Ireland / epidemiology
                • Methicillin Resistance / genetics
                • Microbial Sensitivity Tests / veterinary
                • Occupational Diseases / microbiology
                • Occupational Exposure
                • Staphylococcal Infections / drug therapy
                • Staphylococcal Infections / microbiology
                • Staphylococcal Infections / veterinary
                • Staphylococcus aureus / genetics
                • Staphylococcus aureus / isolation & purification
                • Veterinarians

                Citations

                This article has been cited 44 times.
                1. Allano M, Arsenault J, Archambault M, Fairbrother JH, Sauvé F. Prevalence and Risk Factors of Staphylococcus aureus Nasal Colonization in Horses Admitted to a Veterinary Teaching Hospital. J Vet Intern Med 2025 May-Jun;39(3):e70027.
                  doi: 10.1111/jvim.70027pubmed: 40135807google scholar: lookup
                2. Kabir A, Lamichhane B, Habib T, Adams A, El-Sheikh Ali H, Slovis NM, Troedsson MHT, Helmy YA. Antimicrobial Resistance in Equines: A Growing Threat to Horse Health and Beyond-A Comprehensive Review. Antibiotics (Basel) 2024 Jul 29;13(8).
                  doi: 10.3390/antibiotics13080713pubmed: 39200013google scholar: lookup
                3. Khairullah AR, Sudjarwo SA, Effendi MH, Ramandinianto SC, Gelolodo MA, Widodo A, Riwu KHP, Kurniawati DA. Pet animals as reservoirs for spreading methicillin-resistant Staphylococcus aureus to human health. J Adv Vet Anim Res 2023 Mar;10(1):1-13.
                  doi: 10.5455/javar.2023.j641pubmed: 37155545google scholar: lookup
                4. Shoaib M, Aqib AI, Muzammil I, Majeed N, Bhutta ZA, Kulyar MF, Fatima M, Zaheer CF, Muneer A, Murtaza M, Kashif M, Shafqat F, Pu W. MRSA compendium of epidemiology, transmission, pathophysiology, treatment, and prevention within one health framework. Front Microbiol 2022;13:1067284.
                  doi: 10.3389/fmicb.2022.1067284pubmed: 36704547google scholar: lookup
                5. Devnath P, Karah N, Graham JP, Rose ES, Asaduzzaman M. Evidence of Antimicrobial Resistance in Bats and Its Planetary Health Impact for Surveillance of Zoonotic Spillover Events: A Scoping Review. Int J Environ Res Public Health 2022 Dec 23;20(1).
                  doi: 10.3390/ijerph20010243pubmed: 36612565google scholar: lookup
                6. Sauvé F. Staphylococcal cutaneous infection in horses: From the early 2000s to the present. Can Vet J 2021 Sep;62(9):1001-1006.
                  pubmed: 34475588
                7. Dalton KR, Rock C, Carroll KC, Davis MF. One Health in hospitals: how understanding the dynamics of people, animals, and the hospital built-environment can be used to better inform interventions for antimicrobial-resistant gram-positive infections. Antimicrob Resist Infect Control 2020 Jun 1;9(1):78.
                  doi: 10.1186/s13756-020-00737-2pubmed: 32487220google scholar: lookup
                8. Thapaliya D, Hellwig EJ, Kadariya J, Grenier D, Jefferson AJ, Dalman M, Kennedy K, DiPerna M, Orihill A, Taha M, Smith TC. Prevalence and Characterization of Staphylococcus aureus and Methicillin-Resistant Staphylococcus aureus on Public Recreational Beaches in Northeast Ohio. Geohealth 2017 Dec;1(10):320-332.
                  doi: 10.1002/2017GH000106pubmed: 32158979google scholar: lookup
                9. Aklilu E, Hui Ying C. First mecC and mecA Positive Livestock-Associated Methicillin Resistant Staphylococcus aureus (mecC MRSA/LA-MRSA) from Dairy Cattle in Malaysia. Microorganisms 2020 Jan 21;8(2).
                  doi: 10.3390/microorganisms8020147pubmed: 31973159google scholar: lookup
                10. Older CE, Diesel AB, Lawhon SD, Queiroz CRR, Henker LC, Rodrigues Hoffmann A. The feline cutaneous and oral microbiota are influenced by breed and environment. PLoS One 2019;14(7):e0220463.
                  doi: 10.1371/journal.pone.0220463pubmed: 31361788google scholar: lookup
                11. Cuny C, Abdelbary MMH, Köck R, Layer F, Scheidemann W, Werner G, Witte W. Methicillin-resistant Staphylococcus aureus from infections in horses in Germany are frequent colonizers of veterinarians but rare among MRSA from infections in humans. One Health 2016 Dec;2:11-17.
                  doi: 10.1016/j.onehlt.2015.11.004pubmed: 28616471google scholar: lookup
                12. Older CE, Diesel A, Patterson AP, Meason-Smith C, Johnson TJ, Mansell J, Suchodolski JS, Rodrigues Hoffmann A. The feline skin microbiota: The bacteria inhabiting the skin of healthy and allergic cats. PLoS One 2017;12(6):e0178555.
                  doi: 10.1371/journal.pone.0178555pubmed: 28575016google scholar: lookup
                13. Guérin F, Fines-Guyon M, Meignen P, Delente G, Fondrinier C, Bourdon N, Cattoir V, Léon A. Nationwide molecular epidemiology of methicillin-resistant Staphylococcus aureus responsible for horse infections in France. BMC Microbiol 2017 May 3;17(1):104.
                  doi: 10.1186/s12866-016-0924-zpubmed: 28468636google scholar: lookup
                14. McManus BA, Coleman DC, Deasy EC, Brennan GI, O' Connell B, Monecke S, Ehricht R, Leggett B, Leonard N, Shore AC. Comparative Genotypes, Staphylococcal Cassette Chromosome mec (SCCmec) Genes and Antimicrobial Resistance amongst Staphylococcus epidermidis and Staphylococcus haemolyticus Isolates from Infections in Humans and Companion Animals. PLoS One 2015;10(9):e0138079.
                  doi: 10.1371/journal.pone.0138079pubmed: 26379051google scholar: lookup
                15. Steinman A, Masarwa S, Tirosh-Levy S, Gleser D, Kelmer G, Adler A, Carmeli Y, Schwaber MJ. Methicillin-Resistant Staphylococcus aureus spa Type t002 Outbreak in Horses and Staff at a Veterinary Teaching Hospital after Its Presumed Introduction by a Veterinarian. J Clin Microbiol 2015 Sep;53(9):2827-31.
                  doi: 10.1128/JCM.00090-15pubmed: 26085620google scholar: lookup
                16. Weese JS, Giguère S, Guardabassi L, Morley PS, Papich M, Ricciuto DR, Sykes JE. ACVIM consensus statement on therapeutic antimicrobial use in animals and antimicrobial resistance. J Vet Intern Med 2015 Mar-Apr;29(2):487-98.
                  doi: 10.1111/jvim.12562pubmed: 25783842google scholar: lookup
                17. Abdelbary MM, Wittenberg A, Cuny C, Layer F, Kurt K, Wieler LH, Walther B, Skov R, Larsen J, Hasman H, Fitzgerald JR, Smith TC, Wagenaar JA, Pantosti A, Hallin M, Struelens MJ, Edwards G, Böse R, Nübel U, Witte W. Phylogenetic analysis of Staphylococcus aureus CC398 reveals a sub-lineage epidemiologically associated with infections in horses. PLoS One 2014;9(2):e88083.
                  doi: 10.1371/journal.pone.0088083pubmed: 24505386google scholar: lookup
                18. Schemann K, Firestone SM, Taylor MR, Toribio JA, Ward MP, Dhand NK. Perceptions of vulnerability to a future outbreak: a study of horse managers affected by the first Australian equine influenza outbreak. BMC Vet Res 2013 Jul 31;9:152.
                  doi: 10.1186/1746-6148-9-152pubmed: 23902718google scholar: lookup
                19. Hower S, Phillips MC, Brodsky M, Dameron A, Tamargo MA, Salazar NC, Jackson CR, Barrett JB, Davidson M, Davis J, Mukherjee S, Ewing RY, Gidley ML, Sinigalliano CD, Johns L, Johnson FE 3rd, Adebanjo O, Plano LR. Clonally related methicillin-resistant Staphylococcus aureus isolated from short-finned pilot whales (Globicephala macrorhynchus), human volunteers, and a bayfront cetacean rehabilitation facility. Microb Ecol 2013 May;65(4):1024-38.
                  doi: 10.1007/s00248-013-0178-3pubmed: 23508733google scholar: lookup
                20. van Balen J, Kelley C, Nava-Hoet RC, Bateman S, Hillier A, Dyce J, Wittum TE, Hoet AE. Presence, distribution, and molecular epidemiology of methicillin-resistant Staphylococcus aureus in a small animal teaching hospital: a year-long active surveillance targeting dogs and their environment. Vector Borne Zoonotic Dis 2013 May;13(5):299-311.
                  doi: 10.1089/vbz.2012.1142pubmed: 23473216google scholar: lookup
                21. Barton M, Hawkes M, Moore D, Conly J, Nicolle L, Allen U, Boyd N, Embree J, Van Horne L, Le Saux N, Richardson S, Moore A, Tran D, Waters V, Vearncombe M, Katz K, Weese JS, Embil J, Ofner-Agostini M, Ford-Jones EL. Guidelines for the prevention and management of community-associated methicillin-resistant Staphylococcus aureus: A perspective for Canadian health care practitioners. Can J Infect Dis Med Microbiol 2006 Sep;17 Suppl C(Suppl C):4C-24C.
                  pubmed: 23365589
                22. Cinquepalmi V, Monno R, Fumarola L, Ventrella G, Calia C, Greco MF, Vito Dd, Soleo L. Environmental contamination by dog’s faeces: a public health problem?. Int J Environ Res Public Health 2012 Dec 24;10(1):72-84.
                  doi: 10.3390/ijerph10010072pubmed: 23263659google scholar: lookup
                23. Moodley A, Espinosa-Gongora C, Nielsen SS, McCarthy AJ, Lindsay JA, Guardabassi L. Comparative host specificity of human- and pig- associated Staphylococcus aureus clonal lineages. PLoS One 2012;7(11):e49344.
                  doi: 10.1371/journal.pone.0049344pubmed: 23166643google scholar: lookup
                24. Aklilu E, Zakaria Z, Hassan L, Hui Cheng C. Molecular relatedness of methicillin-resistant S. aureus isolates from staff, environment and pets at University Veterinary Hospital in Malaysia. PLoS One 2012;7(8):e43329.
                  doi: 10.1371/journal.pone.0043329pubmed: 22937034google scholar: lookup
                25. Waltzek TB, Cortés-Hinojosa G, Wellehan JF Jr, Gray GC. Marine mammal zoonoses: a review of disease manifestations. Zoonoses Public Health 2012 Dec;59(8):521-35.
                26. Hoet AE, Johnson A, Nava-Hoet RC, Bateman S, Hillier A, Dyce J, Gebreyes WA, Wittum TE. Environmental methicillin-resistant Staphylococcus aureus in a veterinary teaching hospital during a nonoutbreak period. Vector Borne Zoonotic Dis 2011 Jun;11(6):609-15.
                  doi: 10.1089/vbz.2010.0181pubmed: 21417926google scholar: lookup
                27. David MZ, Daum RS. Community-associated methicillin-resistant Staphylococcus aureus: epidemiology and clinical consequences of an emerging epidemic. Clin Microbiol Rev 2010 Jul;23(3):616-87.
                  doi: 10.1128/CMR.00081-09pubmed: 20610826google scholar: lookup
                28. Ishihara K, Shimokubo N, Sakagami A, Ueno H, Muramatsu Y, Kadosawa T, Yanagisawa C, Hanaki H, Nakajima C, Suzuki Y, Tamura Y. Occurrence and molecular characteristics of methicillin-resistant Staphylococcus aureus and methicillin-resistant Staphylococcus pseudintermedius in an academic veterinary hospital. Appl Environ Microbiol 2010 Aug;76(15):5165-74.
                  doi: 10.1128/AEM.02780-09pubmed: 20543040google scholar: lookup
                29. Soares Magalhães RJ, Loeffler A, Lindsay J, Rich M, Roberts L, Smith H, Lloyd DH, Pfeiffer DU. Risk factors for methicillin-resistant Staphylococcus aureus (MRSA) infection in dogs and cats: a case-control study. Vet Res 2010 Sep-Oct;41(5):55.
                  doi: 10.1051/vetres/2010028pubmed: 20423695google scholar: lookup
                30. Shore AC, Rossney AS, Kinnevey PM, Brennan OM, Creamer E, Sherlock O, Dolan A, Cunney R, Sullivan DJ, Goering RV, Humphreys H, Coleman DC. Enhanced discrimination of highly clonal ST22-methicillin-resistant Staphylococcus aureus IV isolates achieved by combining spa, dru, and pulsed-field gel electrophoresis typing data. J Clin Microbiol 2010 May;48(5):1839-52.
                  doi: 10.1128/JCM.02155-09pubmed: 20335411google scholar: lookup
                31. Tokateloff N, Manning ST, Weese JS, Campbell J, Rothenburger J, Stephen C, Bastura V, Gow SP, Reid-Smith R. Prevalence of methicillin-resistant Staphylococcus aureus colonization in horses in Saskatchewan, Alberta, and British Columbia. Can Vet J 2009 Nov;50(11):1177-80.
                  pubmed: 20119542
                32. Faires MC, Traverse M, Tater KC, Pearl DL, Weese JS. Methicillin-resistant and -susceptible Staphylococcus aureus infections in dogs. Emerg Infect Dis 2010 Jan;16(1):69-75.
                  doi: 10.3201/eid1601.081758pubmed: 20031045google scholar: lookup
                33. Faires MC, Gehring E, Mergl J, Weese JS. Methicillin-resistant Staphylococcus aureus in marine mammals. Emerg Infect Dis 2009 Dec;15(12):2071-2.
                  doi: 10.3201/eid1512.090220pubmed: 19961710google scholar: lookup
                34. Hanselman BA, Kruth SA, Rousseau J, Weese JS. Coagulase positive staphylococcal colonization of humans and their household pets. Can Vet J 2009 Sep;50(9):954-8.
                  pubmed: 19949556
                35. Walther B, Monecke S, Ruscher C, Friedrich AW, Ehricht R, Slickers P, Soba A, Wleklinski CG, Wieler LH, Lübke-Becker A. Comparative molecular analysis substantiates zoonotic potential of equine methicillin-resistant Staphylococcus aureus. J Clin Microbiol 2009 Mar;47(3):704-10.
                  doi: 10.1128/JCM.01626-08pubmed: 19109463google scholar: lookup
                36. Stein RA. Methicillin-resistant Staphylococcus aureus--the new zoonosis. Int J Infect Dis 2009 May;13(3):299-301.
                  doi: 10.1016/j.ijid.2008.09.008pubmed: 19042144google scholar: lookup
                37. Kolappaswamy K, Shipley ST, Tatarov II, DeTolla LJ. Methicillin-resistant Staphylococcus non-aureus infection in an irradiated rhesus macaque (Macaca mulatta). J Am Assoc Lab Anim Sci 2008 May;47(3):64-7.
                  pubmed: 18459716
                38. Weese JS, Lefebvre SL. Risk factors for methicillin-resistant Staphylococcus aureus colonization in horses admitted to a veterinary teaching hospital. Can Vet J 2007 Sep;48(9):921-6.
                  pubmed: 17966332
                39. Boost MV, O'Donoghue MM, James A. Prevalence of Staphylococcus aureus carriage among dogs and their owners. Epidemiol Infect 2008 Jul;136(7):953-64.
                  doi: 10.1017/S0950268807009326pubmed: 17678561google scholar: lookup
                40. Rossney AS, Shore AC, Morgan PM, Fitzgibbon MM, O'Connell B, Coleman DC. The emergence and importation of diverse genotypes of methicillin-resistant Staphylococcus aureus (MRSA) harboring the Panton-Valentine leukocidin gene (pvl) reveal that pvl is a poor marker for community-acquired MRSA strains in Ireland. J Clin Microbiol 2007 Aug;45(8):2554-63.
                  doi: 10.1128/JCM.00245-07pubmed: 17581935google scholar: lookup
                41. Hanselman BA, Kruth SA, Rousseau J, Low DE, Willey BM, McGeer A, Weese JS. Methicillin-resistant Staphylococcus aureus colonization in veterinary personnel. Emerg Infect Dis 2006 Dec;12(12):1933-8.
                  doi: 10.3201/eid1212.060231pubmed: 17326947google scholar: lookup
                42. Sasaki T, Kikuchi K, Tanaka Y, Takahashi N, Kamata S, Hiramatsu K. Methicillin-resistant Staphylococcus pseudintermedius in a veterinary teaching hospital. J Clin Microbiol 2007 Apr;45(4):1118-25.
                  doi: 10.1128/JCM.02193-06pubmed: 17267624google scholar: lookup
                43. Schnellmann C, Gerber V, Rossano A, Jaquier V, Panchaud Y, Doherr MG, Thomann A, Straub R, Perreten V. Presence of new mecA and mph(C) variants conferring antibiotic resistance in Staphylococcus spp. isolated from the skin of horses before and after clinic admission. J Clin Microbiol 2006 Dec;44(12):4444-54.
                  doi: 10.1128/JCM.00868-06pubmed: 17005735google scholar: lookup
                44. Bemis DA, Jones RD, Hiatt LE, Ofori ED, Rohrbach BW, Frank LA, Kania SA. Comparison of tests to detect oxacillin resistance in Staphylococcus intermedius, Staphylococcus schleiferi, and Staphylococcus aureus isolates from canine hosts. J Clin Microbiol 2006 Sep;44(9):3374-6.
                  doi: 10.1128/JCM.01336-06pubmed: 16954277google scholar: lookup