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Methicillin-resistant staphylococci isolated from healthy horses and horse personnel in Italy.

Abstract: Methicillin-resistant staphylococci (MRS) were isolated from nasal swabs of 56 of 159 (35.2%; 95% confidence interval [CI]: 27.9-43.2%) healthy horses. Two nasal swabs were collected from each horse; 43 of 159 (27%; 95% CI: 20.5-34.8%) of the cohort were colonized by MRS strains in 1 nostril, while in the remaining 13 of 159 (8.2%; 95% CI: 4.6-13.9%), different or identical MRS strains were isolated in both nostrils. Of the 29 humans in close contact with the horses tested, 4 (13.8%; 95% CI: 4.5-32.6%) were found to be carriers of MRS. All isolates were coagulase negative with the exception of 2 coagulase-positive MRS strains, Staphylococcus aureus and Staphylococcus pseudintermedius, both isolated from horses. To assay the methicillin resistance, a susceptibility test to oxacillin with standardized disk diffusion method, a PBP-2a latex agglutination test, and a methicillin resistance gene (mecA) polymerase chain reaction assay were performed. Pulsed-field gel electrophoresis patterns of isolates from horses and humans in close contact with the horses revealed similarity. The results suggest evidence of transmission between animals, from animals to humans, and vice versa.
Publication Date: 2010-01-23 PubMed ID: 20093688DOI: 10.1177/104063871002200114Google Scholar: Lookup
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  • Journal Article

Summary

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This study focuses on the occurrence of methicillin-resistant staphylococci (MRS) in healthy horses and individuals closely interacting with them in Italy. The findings indicate that both horses and humans were carriers of MRS, suggesting possible animal-to-human and human-to-animal transmission.

Methodology

  • The researchers sampled 159 healthy horses using nasal swabs. They collected two swabs from each horse, one from each nostril.
  • The team also tested 29 humans that had close contact with the horses.
  • To determine the presence of MRS, they performed several tests including: a susceptibility test to oxacillin using a standardized disk diffusion method, a PBP-2a latex agglutination test, and a methicillin resistance gene (mecA) polymerase chain reaction assay.
  • The scientists used pulsed-field gel electrophoresis to compare the genetic patterns of the isolates derived from horses and humans.

Findings

  • The study found that 35.2% of the sampled horses had MRS in their nostrils. Single nostril colonization was identified in 27% horses, and both nostrils were affected in 8.2% horses.
  • Among humans in close contact with horses, 13.8% were discovered to be carriers of MRS.
  • All MRS isolates from both horses and humans were coagulase negative, with two exceptions of coagulase-positive strains (Staphylococcus aureus and Staphylococcus pseudintermedius) isolated from horses.

Implications

  • The researchers concluded that the presence of MRS in both horses and humans may suggest possible transmission between animals and humans, and vice versa.
  • This study raises concerns about the potential for MRS spreading within equine facilities and between horses and individuals in close contact with them. This indicates a need for proper preventive measures to avoid the spread of this antibiotic-resistant bacteria.

Cite This Article

APA
De Martino L, Lucido M, Mallardo K, Facello B, Mallardo M, Iovane G, Pagnini U, Tufano MA, Catalanotti P. (2010). Methicillin-resistant staphylococci isolated from healthy horses and horse personnel in Italy. J Vet Diagn Invest, 22(1), 77-82. https://doi.org/10.1177/104063871002200114

Publication

ISSN: 1040-6387
NlmUniqueID: 9011490
Country: United States
Language: English
Volume: 22
Issue: 1
Pages: 77-82

Researcher Affiliations

De Martino, Luisa
  • Dipartimento di Medicina Sperimentale, Sezione di Microbiologia e Microbiologia Clinica, Seconda Università di Napoli, Via Costantipoli, 16-80138 Napoli, Italy.
Lucido, Maria
    Mallardo, Karina
      Facello, Bruna
        Mallardo, Michelina
          Iovane, Giuseppe
            Pagnini, Ugo
              Tufano, Maria Antonietta
                Catalanotti, Piergiorgio

                  MeSH Terms

                  • Animals
                  • Carrier State
                  • Female
                  • Horse Diseases / epidemiology
                  • Horse Diseases / microbiology
                  • Horses
                  • Humans
                  • Italy / epidemiology
                  • Male
                  • Methicillin Resistance
                  • Methicillin-Resistant Staphylococcus aureus / isolation & purification
                  • Nose / microbiology
                  • Staphylococcal Infections / microbiology
                  • Staphylococcal Infections / transmission

                  Citations

                  This article has been cited 23 times.
                  1. Zehr JD, Sun Q, Ceres K, Merrill A, Tyson GH, Ceric O, Guag J, Pauley S, McQueary HC, Sams K, Reboul G, Mitchell PK, Anderson R, Franklin-Guild R, Guarino C, Cronk BD, Burbick CR, Wolking R, Peak L, Zhang Y, McDowall R, Krishnamurthy A, Slavic D, Sekhon PK, Needle D, Gibson R, Cazer C, Rodriguez J, Harris B, Stanhope MJ, Goodman LB. Population and pan-genomic analyses of Staphylococcus pseudintermedius identify geographic distinctions in accessory gene content and novel loci associated with AMR. Appl Environ Microbiol 2025 May 21;91(5):e0001025.
                    doi: 10.1128/aem.00010-25pubmed: 40272117google scholar: lookup
                  2. Al-Taii NA, Al-Gburi NM, Khalil NK. Detection of biofilm formation and antibiotics resistance of Staphylococcus spp. isolated from humans' and birds' oral cavities. Open Vet J 2024 Sep;14(9):2215-2223.
                    doi: 10.5455/OVJ.2024.v14.i9.9pubmed: 39553752google scholar: lookup
                  3. Suepaul S, Stegger M, Boyen F, Georges K, Butaye P. The Diversity and Zoonotic Potential of Staphylococcus pseudintermedius in Humans and Pet Dogs in Trinidad and Tobago. Antibiotics (Basel) 2023 Jul 31;12(8).
                    doi: 10.3390/antibiotics12081266pubmed: 37627686google scholar: lookup
                  4. Fernández-Fernández R, Lozano C, Reuben RC, Ruiz-Ripa L, Zarazaga M, Torres C. Comprehensive Approaches for the Search and Characterization of Staphylococcins. Microorganisms 2023 May 18;11(5).
                  5. Marshall K, Marsella R. Evolution of the Prevalence of Antibiotic Resistance to Staphylococcus spp. Isolated from Horses in Florida over a 10-Year Period. Vet Sci 2023 Jan 18;10(2).
                    doi: 10.3390/vetsci10020071pubmed: 36851375google scholar: lookup
                  6. Silva V, Correia E, Pereira JE, González-Machado C, Capita R, Alonso-Calleja C, Igrejas G, Poeta P. Exploring the Biofilm Formation Capacity in S. pseudintermedius and Coagulase-Negative Staphylococci Species. Pathogens 2022 Jun 16;11(6).
                    doi: 10.3390/pathogens11060689pubmed: 35745543google scholar: lookup
                  7. Silva V, Caniça M, Manageiro V, Verbisck N, Tejedor-Junco MT, González-Martin M, Corbera JA, Poeta P, Igrejas G. Staphylococcus aureus and Methicillin-Resistant Coagulase-Negative Staphylococci in Nostrils and Buccal Mucosa of Healthy Camels Used for Recreational Purposes. Animals (Basel) 2022 May 13;12(10).
                    doi: 10.3390/ani12101255pubmed: 35625101google scholar: lookup
                  8. Godijk NG, Bootsma MCJ, Bonten MJM. Transmission routes of antibiotic resistant bacteria: a systematic review. BMC Infect Dis 2022 May 20;22(1):482.
                    doi: 10.1186/s12879-022-07360-zpubmed: 35596134google scholar: lookup
                  9. Silva V, Alfarela C, Caniça M, Manageiro V, Nóvoa M, Leiva B, Kress M, Capelo JL, Poeta P, Igrejas G. A One Health Approach Molecular Analysis of Staphylococcus aureus Reveals Distinct Lineages in Isolates from Miranda Donkeys (Equus asinus) and Their Handlers. Antibiotics (Basel) 2022 Mar 10;11(3).
                    doi: 10.3390/antibiotics11030374pubmed: 35326837google scholar: lookup
                  10. Carroll KC, Burnham CD, Westblade LF. From canines to humans: Clinical importance of Staphylococcus pseudintermedius. PLoS Pathog 2021 Dec;17(12):e1009961.
                    doi: 10.1371/journal.ppat.1009961pubmed: 34855921google scholar: lookup
                  11. Othman AA, Hiblu MA, Abbassi MS, Abouzeed YM, Ahmed MO. Nasal colonization and antibiotic resistance patterns of Staphylococcus species isolated from healthy horses in Tripoli, Libya. J Equine Sci 2021 Jun;32(2):61-65.
                    doi: 10.1294/jes.32.61pubmed: 34220273google scholar: lookup
                  12. Grzyb J, Pawlak K. Staphylococci and fecal bacteria as bioaerosol components in animal housing facilities in the Zoological Garden in Chorzów. Environ Sci Pollut Res Int 2021 Oct;28(40):56615-56627.
                    doi: 10.1007/s11356-021-14594-ypubmed: 34061267google scholar: lookup
                  13. Ruiz-Ripa L, Gómez P, Alonso CA, Camacho MC, Ramiro Y, de la Puente J, Fernández-Fernández R, Quevedo MÁ, Blanco JM, Báguena G, Zarazaga M, Höfle U, Torres C. Frequency and Characterization of Antimicrobial Resistance and Virulence Genes of Coagulase-Negative Staphylococci from Wild Birds in Spain. Detection of tst-Carrying S. sciuri Isolates. Microorganisms 2020 Aug 29;8(9).
                    doi: 10.3390/microorganisms8091317pubmed: 32872433google scholar: lookup
                  14. Schwarz S, Feßler AT, Loncaric I, Wu C, Kadlec K, Wang Y, Shen J. Antimicrobial Resistance among Staphylococci of Animal Origin. Microbiol Spectr 2018 Jul;6(4).
                  15. Zhou Z, Zhang M, Li H, Yang H, Li X, Song X, Wang Z. Prevalence and molecular characterization of Staphylococcus aureus isolated from goats in Chongqing, China. BMC Vet Res 2017 Nov 25;13(1):352.
                    doi: 10.1186/s12917-017-1272-4pubmed: 29178873google scholar: lookup
                  16. Ruzauskas M, Couto N, Kerziene S, Siugzdiniene R, Klimiene I, Virgailis M, Pomba C. Prevalence, species distribution and antimicrobial resistance patterns of methicillin-resistant staphylococci in Lithuanian pet animals. Acta Vet Scand 2015 Jun 2;57(1):27.
                    doi: 10.1186/s13028-015-0117-zpubmed: 26032539google scholar: lookup
                  17. Börjesson S, Gómez-Sanz E, Ekström K, Torres C, Grönlund U. Staphylococcus pseudintermedius can be misdiagnosed as Staphylococcus aureus in humans with dog bite wounds. Eur J Clin Microbiol Infect Dis 2015 Apr;34(4):839-44.
                    doi: 10.1007/s10096-014-2300-ypubmed: 25532507google scholar: lookup
                  18. van Balen J, Mowery J, Piraino-Sandoval M, Nava-Hoet RC, Kohn C, Hoet AE. Molecular epidemiology of environmental MRSA at an equine teaching hospital: introduction, circulation and maintenance. Vet Res 2014 Mar 19;45(1):31.
                    doi: 10.1186/1297-9716-45-31pubmed: 24641543google scholar: lookup
                  19. Schmidt VM, Williams NJ, Pinchbeck G, Corless CE, Shaw S, McEwan N, Dawson S, Nuttall T. Antimicrobial resistance and characterisation of staphylococci isolated from healthy Labrador retrievers in the United Kingdom. BMC Vet Res 2014 Jan 14;10:17.
                    doi: 10.1186/1746-6148-10-17pubmed: 24423104google scholar: lookup
                  20. Mallardo K, Nizza S, Fiorito F, Pagnini U, De Martino L. A comparative evaluation of methicillin-resistant staphylococci isolated from harness racing-horses, breeding mares and riding-horses in Italy. Asian Pac J Trop Biomed 2013 Mar;3(3):169-73.
                    doi: 10.1016/S2221-1691(13)60044-1pubmed: 23620832google scholar: lookup
                  21. Karakulska J, Fijałkowski K, Nawrotek P, Pobucewicz A, Poszumski F, Czernomysy-Furowicz D. Identification and methicillin resistance of coagulase-negative staphylococci isolated from nasal cavity of healthy horses. J Microbiol 2012 Jun;50(3):444-51.
                    doi: 10.1007/s12275-012-1550-6pubmed: 22752908google scholar: lookup
                  22. Schwendener S, Perreten V. New MLSB resistance gene erm(43) in Staphylococcus lentus. Antimicrob Agents Chemother 2012 Sep;56(9):4746-52.
                    doi: 10.1128/AAC.00627-12pubmed: 22733067google scholar: lookup
                  23. Huber H, Ziegler D, Pflüger V, Vogel G, Zweifel C, Stephan R. Prevalence and characteristics of methicillin-resistant coagulase-negative staphylococci from livestock, chicken carcasses, bulk tank milk, minced meat, and contact persons. BMC Vet Res 2011 Jan 27;7:6.
                    doi: 10.1186/1746-6148-7-6pubmed: 21272304google scholar: lookup