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Equine veterinary journal1983; 15(4); 317-320; doi: 10.1111/j.2042-3306.1983.tb01809.x

Leptospiral infection in horses in Northern Ireland: serological and microbiological findings.

Abstract: Thirteen strains of pathogenic leptospires were isolated from 12 of 91 horses; seven strains belonged to the Australis serogroup (serotype bratislava) with three, two and one strains belonging to the Icterohaemorrhagiae, Hebdomadis (serotype hardjo) and Autumnalis serogroups respectively. Using leptospires isolated from horses and others representing the known parasitic Leptospira serogroups, a sample of 650 mares' sera was tested for agglutinating antibodies. Antibodies were found in 89.1 per cent of sera. The predominant reaction was to serotype bratislava, strain S/1334/79, isolated in this study, antibodies to which were detected in 81.8 per cent of sera. It is suggested that serotype bratislava may be adapted to, and maintained by, the horse population in Northern Ireland.
Publication Date: 1983-10-01 PubMed ID: 6641678DOI: 10.1111/j.2042-3306.1983.tb01809.xGoogle Scholar: Lookup
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  • Journal Article

Summary

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The study reports on the prevalence of a bacterial infection called Leptospira among horses in Northern Ireland, emphasizing the dominant presence of a particular strain—serotype bratislava. They discovered this by testing a large sample of mare’s blood for antibodies to the bacteria.

Study Design and Findings

  • Experts extracted thirteen strains of the Leptospira bacteria from 12 out of 91 horses tested, indicating that more than one strain can exist in a single animal.
  • The bulk of these strains—seven out of thirteen—fell into the Australis serogroup, specifically the serotype bratislava. The others belonged to the Icterohaemorrhagiae, Hebdomadis (serotype hardjo), and Autumnalis serogroups.
  • The researchers then tested a broad sample of 650 mare’s blood serum (a component of blood) for agglutinating antibodies. These antibodies indicate the presence of certain bacteria in the body and vary depending on the specific strain of Leptospira.
  • A whopping 89.1% of these serum samples contained antibodies, suggesting an alarmingly high prevalence of Leptospirosis in the horse population. Interestingly, the majority of these horses—81.8%—exhibited antibodies to the bratislava strain identified in the prior testing phase.

Implications and Conclusions

  • The scientists posited that this dominant reaction to serotype bratislava may indicate that this particular strain of Leptospira is well-adapted to horses, with the potential for the horse population to act as a reservoir for it.
  • This deduction aligns with the idea of host-adapted strains of bacteria, which have evolved to survive and proliferate in specific host species. Such strains might be less pathogenic (disease-causing) within their host species but become threatening when transmitted to others.
  • Thus, the control of Leptospirosis among the horse population of Northern Ireland may require specific measures aimed at reducing the prevalence of this preferred serotype.

Cite This Article

APA
Ellis WA, O'Brien JJ, Cassells JA, Montgomery J. (1983). Leptospiral infection in horses in Northern Ireland: serological and microbiological findings. Equine Vet J, 15(4), 317-320. https://doi.org/10.1111/j.2042-3306.1983.tb01809.x

Publication

ISSN: 0425-1644
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 15
Issue: 4
Pages: 317-320

Researcher Affiliations

Ellis, W A
    O'Brien, J J
      Cassells, J A
        Montgomery, J

          MeSH Terms

          • Animals
          • Antibodies, Bacterial / analysis
          • Antigens, Bacterial / immunology
          • Female
          • Horse Diseases / immunology
          • Horse Diseases / microbiology
          • Horses
          • Kidney / microbiology
          • Leptospira / classification
          • Leptospira / immunology
          • Leptospira / isolation & purification
          • Leptospirosis / immunology
          • Leptospirosis / microbiology
          • Leptospirosis / veterinary
          • Northern Ireland
          • Serotyping

          Citations

          This article has been cited 18 times.
          1. Kirmse L, Thieme K, Doherr MG, Eule JC. Evaluation of Laboratory Techniques for the Diagnosis of Leptospira-Associated Equine Recurrent Uveitis (ERU) With Focus on the Goldmann-Witmer Coefficient. Vet Ophthalmol 2026 Jan;29(1):e70132.
            doi: 10.1111/vop.70132pubmed: 41518147google scholar: lookup
          2. Żmudzki J, Ostrowska M, Arent Z, Frant M, Kochanowski M, Nowak A, Zębek S, Kalinowski D, Podgórska K. Seroprevalence of equine leptospirosis in Poland (2019-2023). Equine Vet J 2026 Mar;58(2):523-532.
            doi: 10.1111/evj.70069pubmed: 40760779google scholar: lookup
          3. Chinchilla D, Sánchez I, Montero D, Picardeau M, Gutiérrez R. In-house isolation protocol from human serum samples demonstrates the circulating of a broad diversity of Leptospira serogroups in Costa Rica. Sci Rep 2025 Mar 20;15(1):9614.
            doi: 10.1038/s41598-025-93301-0pubmed: 40113886google scholar: lookup
          4. Hamond C, Adam EN, Stone NE, LeCount K, Anderson T, Putz EJ, Camp P, Hicks J, Stuber T, van der Linden H, Bayles DO, Sahl JW, Schlater LK, Wagner DM, Nally JE. Identification of equine mares as reservoir hosts for pathogenic species of Leptospira. Front Vet Sci 2024;11:1346713.
            doi: 10.3389/fvets.2024.1346713pubmed: 38784659google scholar: lookup
          5. Grippi F, Blanda V, Galluzzo P, Bongiorno M, Sciacca C, Arcuri F, D'Agostino R, Giacchino I, Gucciardi F, D'Incau M, Bertasio C, Torina A, Guercio A. A Canine Leptospirosis Clinical Case Due to Leptospira interrogans (Serogroup Icterohaemorrhagiae) in a Dog Kennel in Castelvetrano (Western Sicily, South Italy). Vet Sci 2023 Aug 6;10(8).
            doi: 10.3390/vetsci10080508pubmed: 37624294google scholar: lookup
          6. Wollanke B, Gerhards H, Ackermann K. Infectious Uveitis in Horses and New Insights in Its Leptospiral Biofilm-Related Pathogenesis. Microorganisms 2022 Feb 7;10(2).
          7. Aliberti A, Blanda V, Di Marco Lo Presti V, Macaluso G, Galluzzo P, Bertasio C, Sciacca C, Arcuri F, D'Agostino R, Ippolito D, Pruiti Ciarello F, Torina A, Grippi F. Leptospira interrogans Serogroup Pomona in a Dairy Cattle Farm in a Multi-Host Zootechnical System. Vet Sci 2022 Feb 16;9(2).
            doi: 10.3390/vetsci9020083pubmed: 35202336google scholar: lookup
          8. Putz EJ, Nally JE. Investigating the Immunological and Biological Equilibrium of Reservoir Hosts and Pathogenic Leptospira: Balancing the Solution to an Acute Problem?. Front Microbiol 2020;11:2005.
            doi: 10.3389/fmicb.2020.02005pubmed: 32922382google scholar: lookup
          9. Siqueira CC, Fraga DBM, Chagas-Junior AD, Athanazio DA, Silva MMN, Cerqueira RB, da C McBride FW, Pinna MH, Ayres MCC. Seroprevalence and risk factors associated with equineleptospirosis in the metropolitan region of Salvador and Recôncavo Baiano region, Bahia state (NE Brazil). Trop Anim Health Prod 2020 Jan;52(1):31-39.
            doi: 10.1007/s11250-019-01956-5pubmed: 31289965google scholar: lookup
          10. Nally JE, Arent Z, Bayles DO, Hornsby RL, Gilmore C, Regan S, McDevitt AD, Yearsley J, Fanning S, McMahon BJ. Emerging Infectious Disease Implications of Invasive Mammalian Species: The Greater White-Toothed Shrew (Crocidura russula) Is Associated With a Novel Serovar of Pathogenic Leptospira in Ireland. PLoS Negl Trop Dis 2016 Dec;10(12):e0005174.
            doi: 10.1371/journal.pntd.0005174pubmed: 27935961google scholar: lookup
          11. Hamond C, Pinna A, Martins G, Lilenbaum W. The role of leptospirosis in reproductive disorders in horses. Trop Anim Health Prod 2014 Jan;46(1):1-10.
            doi: 10.1007/s11250-013-0459-3pubmed: 23990441google scholar: lookup
          12. Arent ZJ, Andrews S, Adamama-Moraitou K, Gilmore C, Pardali D, Ellis WA. Emergence of novel Leptospira serovars: a need for adjusting vaccination policies for dogs?. Epidemiol Infect 2013 Jun;141(6):1148-53.
            doi: 10.1017/S0950268812002087pubmed: 22998981google scholar: lookup
          13. Båverud V, Gunnarsson A, Engvall EO, Franzén P, Egenvall A. Leptospira seroprevalence and associations between seropositivity, clinical disease and host factors in horses. Acta Vet Scand 2009 Mar 30;51(1):15.
            doi: 10.1186/1751-0147-51-15pubmed: 19331656google scholar: lookup
          14. Prescott JF. Leptospirosis in farm animals: the hidden disease. Can Vet J 1986 Nov;27(11):424.
            pubmed: 17422711
          15. Lees VW, Gale SP. Titers to Leptospira species in horses in Alberta. Can Vet J 1994 Oct;35(10):636-40.
            pubmed: 7994706
          16. Webster JP, Ellis WA, Macdonald DW. Prevalence of Leptospira spp. in wild brown rats (Rattus norvegicus) on UK farms. Epidemiol Infect 1995 Feb;114(1):195-201.
            doi: 10.1017/s0950268800052043pubmed: 7867738google scholar: lookup
          17. Kitson-Piggot AW, Prescott JF. Leptospirosis in horses in Ontario. Can J Vet Res 1987 Oct;51(4):448-51.
            pubmed: 3330964
          18. Ellis WA, Montgomery JM, Thiermann AB. Restriction endonuclease analysis as a taxonomic tool in the study of pig isolates belonging to the Australis serogroup of Leptospira interrogans. J Clin Microbiol 1991 May;29(5):957-61.
            doi: 10.1128/jcm.29.5.957-961.1991pubmed: 1647408google scholar: lookup