Analyze Diet
Journal of equine science2021; 32(2); 61-65; doi: 10.1294/jes.32.61

Nasal colonization and antibiotic resistance patterns of Staphylococcus species isolated from healthy horses in Tripoli, Libya.

Abstract: The present study investigated the colonization rates and antimicrobial susceptibility of Staphylococcus species isolated from the nostrils of healthy horses. A nonselective laboratory approach was applied, followed by confirmation using a Phoenix automated microbiological system. Among the 92 horses included in the study, 48.9% (45/92) carried Staphylococcus species of mostly the coagulase-negative staphylococci (CoNS) type yielding 70 Staphylococcus strains. Of these strains, 37.1% (26/70; 24 CoNS and 2 coagulase-positive staphylococci; CoPS) were identified as methicillin-resistant staphylococci (MRS) expressing significant resistance to important antimicrobial classes represented mainly by subspecies of CoNS. This is the first study reporting a high prevalence of various Staphylococcus species, particularly strains of CoNS expressing multidrug resistance patterns of public health concern, colonizing healthy horses in Libya.
Publication Date: 2021-06-18 PubMed ID: 34220273PubMed Central: PMC8240523DOI: 10.1294/jes.32.61Google 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.

This study assesses how frequent Staphylococcus bacteria is present in the nostrils of healthy horses and whether these are resistant to common antibiotics, focusing on 92 horses in Tripoli, Libya. Results showed almost half the horses carried Staphylococcus, with majority being coagulase-negative staphylococci (CoNS). Over a third of the bacteria strains were methicillin-resistant staphylococci (MRS), significantly resistant to different types of antimicrobials, with CoNS subtype being predominant. This signifies a high prevalence of drug-resistant Staphylococcus within healthy horses in Libya.

Research Methodology

  • The research was carried out by collecting and testing samples from the noses of 92 horses in Tripoli, Libya.
  • A nonselective laboratory approach, or a technique in which all types of bacteria are allowed to grow, was used to culture the samples collected from the horses.
  • The Phoenix automated microbiological system was used to confirm the presence of Staphylococcus species in the samples.

Findings

  • A total of 45 out of all 92 horses, or 48.9%, were found to be carrying some type of Staphylococcus bacteria.
  • Among these, the most common type was coagulase-negative staphylococci (CoNS), with 70 strains identified
  • Out of these 70 strains, 26 (or 37.1% of the total) were found to be methicillin-resistant staphylococci (MRS).
  • Both coagulase-negative and positive staphylococci (CoPS) showed resistance, but CoNS were more likely to be methicillin-resistant.

Significance

  • This research is important as it is the first to report such a high prevalence of Staphylococcus species, specifically drug-resistant ones, in healthy horses in Libya.
  • The presence of these multidrug-resistant staphylococci species in healthy horses raises public health concerns due to the risk of transmission to humans and other animals.
  • The high percentage of CoNS in particular, which are usually less aggressive than CoPS but are becoming increasingly drug-resistant, was noteworthy.

Cite This Article

APA
Othman AA, Hiblu MA, Abbassi MS, Abouzeed YM, Ahmed MO. (2021). Nasal colonization and antibiotic resistance patterns of Staphylococcus species isolated from healthy horses in Tripoli, Libya. J Equine Sci, 32(2), 61-65. https://doi.org/10.1294/jes.32.61

Publication

ISSN: 1340-3516
NlmUniqueID: 9503751
Country: Japan
Language: English
Volume: 32
Issue: 2
Pages: 61-65

Researcher Affiliations

Othman, Aesha A
  • Department of Microbiology and Parasitology, Faculty of Veterinary Medicine, University of Tripoli, P.O. Box 13362, Libya.
Hiblu, Murad A
  • Department of Internal Medicine, Faculty of Veterinary Medicine, University of Tripoli, P.O. Box 13662, Libya.
Abbassi, Mohamed Salah
  • University of Tunis El Manar, Institute of Veterinary Research of Tunisia, Tunis 1006, Tunisia.
Abouzeed, Yousef M
  • Department of Microbiology and Parasitology, Faculty of Veterinary Medicine, University of Tripoli, P.O. Box 13362, Libya.
Ahmed, Mohamed O
  • Department of Microbiology and Parasitology, Faculty of Veterinary Medicine, University of Tripoli, P.O. Box 13362, Libya.

References

This article includes 25 references
  1. Adams R, Smith J, Locke S, Phillips E, Erol E, Carter C, Odoi A. An epidemiologic study of antimicrobial resistance of Staphylococcus species isolated from equine samples submitted to a diagnostic laboratory.. BMC Vet. Res. 14: 42.
    pmc: PMC5800099pubmed: 29402294
  2. Ahmed M.O., Baptiste K.E.. Vancomycin-resistant enterococci: a review of antimicrobial resistance mechanisms and perspectives of human and animal health.. Microb. Drug Resist. 24: 590–606.
    pubmed: 29058560
  3. Ahmed M.O., Baptiste K.E., Daw M.A., Elramalli A.K., Abouzeed Y.M., Petersen A. Spa typing and identification of pvl genes of meticillin-resistant Staphylococcus aureus isolated from a Libyan hospital in Tripoli.. J. Glob. Antimicrob. Resist. 10: 179–181.
    pubmed: 28735052
  4. Ahmed M.O., Elramalli A.K., Baptiste K.E., Daw M.A., Zorgani A., Brouwer E., Willems R.J.L., Top J. Whole genome sequence analysis of the first vancomycin-resistant Enterococcus faecium isolates from a Libyan Hospital in Tripoli.. Microb. Drug Resist. 26: 1390–1398.
    pubmed: 32181678
  5. Asante J, Amoako D.G., Abia A.L.K., Somboro A.M., Govinden U, Bester L.A., Essack S.Y.. review of clinically and epidemiologically relevant coagulase-negative staphylococci in Africa.. Microb. Drug Resist. 26: 951–970.
    pubmed: 32043916
  6. Bannoehr J, Ben Zakour N.L., Waller A.S., Guardabassi L., Thoday K.L., van den Broek A.H., Fitzgerald J.R.. Population genetic structure of the Staphylococcus intermedius group: insights into agr diversification and the emergence of methicillin-resistant strains.. J. Bacteriol. 189: 8685–8692.
    pmc: PMC2168937pubmed: 17905991
  7. Baptiste K.E., Williams K, Willams N.J., Wattret A, Clegg P.D., Dawson S, Corkill J.E., O’Neill T., Hart C.A.. Methicillin-resistant staphylococci in companion animals.. Emerg. Infect. Dis. 11: 1942–1944.
    pmc: PMC3367626pubmed: 16485485
  8. Bietrix J, Kolenda C, Sapin A, Haenni M, Madec J.Y., Bes M, Dupieux C, Tasse J, Laurent F. Persistence and Diffusion of mecC-Positive CC130 MRSA Isolates in Dairy Farms in Meurthe-et-Moselle County (France).. Front. Microbiol. 10: 47.
    pmc: PMC6363682pubmed: 30761099
  9. Busscher J.F., van Duijkeren E., Sloet van Oldruitenborgh-Oosterbaan M.M.. The prevalence of methicillin-resistant staphylococci in healthy horses in the Netherlands.. Vet. Microbiol. 113: 131–136.
    pubmed: 16303264
  10. CLSI 2017. Clinical and Laboratory Standards Institute (CLSI); Performance Standards for Antimicrobial Susceptibility Testing, 27th ed., CLSI supplement M100.
  11. Coton E., Desmonts M.H., Leroy S., Coton M., Jamet E., Christieans S., Donnio P.Y., Lebert I., Talon R. Biodiversity of coagulase-negative Staphylococci in French cheeses, dry fermented sausages, processing environments and clinical samples.. Int. J. Food Microbiol. 137: 221–229.
    pubmed: 20061042
  12. De Martino L., Lucido M., Mallardo K., Facello B., Mallardo M., Iovane G., Pagnini U., Tufano M.A., Catalanotti P. Methicillin-resistant staphylococci isolated from healthy horses and horse personnel in Italy.. J. Vet. Diagn. Invest. 22: 77–82.
    pubmed: 20093688
  13. Elnageh H.R., Hiblu M.A., Abbassi M.S., Abouzeed Y.M., Ahmed M.O.. Prevalence and antimicrobial resistance of Staphylococcus species isolated from cats and dogs.. Open Vet. J. 10: 452–456.
    pmc: PMC7830183pubmed: 33614441
  14. Giordano N., Corallo C., Miracco C., Papakostas P., Montella A., Figura N., Nuti R. Erythema nodosum associated with Staphylococcus xylosus septicemia.. J. Microbiol. Immunol. Infect. 49: 134–137.
    pubmed: 23266237
  15. Guardabassi L., Damborg P., Stamm I., Kopp P.A., Broens E.M., Toutain P.L., ESCMID Study Group for Veterinary Microbiology. Diagnostic microbiology in veterinary dermatology: present and future.. Vet. Dermatol. 28: 146–e30.
    pubmed: 28133869
  16. 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. 50: 444–451.
    pubmed: 22752908
  17. Maddox T.W., Clegg P.D., Williams N.J., Pinchbeck G.L.. Antimicrobial resistance in bacteria from horses: epidemiology of antimicrobial resistance.. Equine Vet. J. 47: 756–765.
    pubmed: 26084443
  18. Mama O.M., Gómez P., Ruiz-Ripa L., Gómez-Sanz E., Zarazaga M., Torres C. Antimicrobial resistance, virulence, and genetic lineages of staphylococci from horses destined for human consumption: high detection of S. aureus isolates of lineage ST1640 and those carrying the lukPQ gene.. Animals (Basel) 9: 900.
    pmc: PMC6912640pubmed: 31683871
  19. Oguttu J.W., Qekwana D.N., Odoi A. An exploratory descriptive study of antimicrobial resistance patterns of staphylococcus spp. isolated from horses presented at a veterinary teaching hospital.. BMC Vet. Res. 13: 269.
    pmc: PMC5568347pubmed: 28830437
  20. Schnellmann C., Gerber V., Rossano A., Jaquier V., Panchaud Y., Doherr M.G., 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. 44: 4444–4454.
    pmc: PMC1698435pubmed: 17005735
  21. Van den Eede A., Martens A., Floré K., Denis O., Gasthuys F., Haesebrouck F., Van den Abeele A., Hermans K. MRSA carriage in the equine community: an investigation of horse-caretaker couples.. Vet. Microbiol. 163: 313–318.
    pubmed: 23434186
  22. van Duijkeren E., Ten Horn L., Wagenaar J.A., de Bruijn M., Laarhoven L., Verstappen K., de Weerd W., Meessen N., Duim B. Suspected horse-to-human transmission of MRSA ST398.. Emerg. Infect. Dis. 17: 1137–1139.
    pmc: PMC3358200pubmed: 21749795
  23. Weese S. Therapeutics in practice—treating methicillin-resistant Staphylococcus aureus.. Infection 4: 6.
  24. Xu Z., Shah H.N., Misra R., Chen J., Zhang W., Liu Y., Cutler R.R., Mkrtchyan H.V.. The prevalence, antibiotic resistance and mecA characterization of coagulase negative staphylococci recovered from non-healthcare settings in London, UK.. Antimicrob. Resist. Infect. Control 7: 73.
    pmc: PMC6000976pubmed: 29946448
  25. Yasuda R., Kawano J., Matsuo E., Masuda T., Shimizu A., Anzai T., Hashikura S. Distribution of mecA-harboring staphylococci in healthy mares.. J. Vet. Med. Sci. 64: 821–827.
    pubmed: 12399608

Citations

This article has been cited 9 times.
  1. Khalid E, Tartor YH, Ammar AM, Abdelaziz R, Mahmmod Y, Abdelkhalek A. Controlling drug-resistant bacteria in Arabian horses: bacteriophage cocktails for treating wound infections. Front Vet Sci 2025;12:1609955.
    doi: 10.3389/fvets.2025.1609955pubmed: 41169678google scholar: lookup
  2. Saraiva MMS, Rodrigues HLS, Benevides VP, de Leon CMCG, Santos SCL, Stipp DT, Givisiez PEN, Vieira RFC, Oliveira CJB. Antimicrobial Resistance Patterns of Staphylococcus aureus Cultured from the Healthy Horses' Nostrils Sampled in Distant Regions of Brazil. Antibiotics (Basel) 2025 Jul 9;14(7).
    doi: 10.3390/antibiotics14070693pubmed: 40723995google scholar: lookup
  3. Kochel-Karakulska J, Maślanko M, Woroszyło M, Szewczuk M, Grygorcewicz B, Fijałkowski K. Species diversity, virulence, and antimicrobial resistance of the nasal staphylococcal and mammaliicoccal biota of reindeer. BMC Vet Res 2025 Jun 2;21(1):394.
    doi: 10.1186/s12917-025-04680-5pubmed: 40452044google scholar: lookup
  4. Jlaytah HA, Ahmed RO, Amri SG, Aghila E, Ahmed MO. The prevalence and microbiological features of Staphylococcus species isolation from healthcare personnel in a dental clinic in Tripoli, Libya. Pan Afr Med J 2024;49:77.
  5. Qin X, Pu H, Fang X, Shang Q, Li J, Zhao Q, Wang X, Gu W. Microbial communities of Schisandra sphenanthera Rehd. et Wils. and the correlations between microbial community and the active secondary metabolites. PeerJ 2024;12:e17240.
    doi: 10.7717/peerj.17240pubmed: 38685939google scholar: lookup
  6. Sawesi OK, Elbaz AK, Mahmoud AS, Duro EM, Alteab AA, Milad KK, Bennuor EM. Hematological reference values of horses in Western Libya and their relationship to breed, age, and management. Open Vet J 2023 Dec;13(12):1696-1707.
    doi: 10.5455/OVJ.2023.v13.i12.18pubmed: 38292715google scholar: lookup
  7. Ocloo R, Nyasinga J, Munshi Z, Hamdy A, Marciniak T, Soundararajan M, Newton-Foot M, Ziebuhr W, Shittu A, Revathi G, Abouelfetouh A, Whitelaw A. Epidemiology and antimicrobial resistance of staphylococci other than Staphylococcus aureus from domestic animals and livestock in Africa: a systematic review. Front Vet Sci 2022;9:1059054.
    doi: 10.3389/fvets.2022.1059054pubmed: 36583033google scholar: lookup
  8. Khairullah AR, Sudjarwo SA, Effendi MH, Ramandinianto SC, Widodo A, Riwu KHP. A review of horses as a source of spreading livestock-associated methicillin-resistant Staphylococcus aureus to human health. Vet World 2022 Aug;15(8):1906-1915.
  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