Analyze Diet
Epidemiology and infection2012; 141(1); 33-35; doi: 10.1017/S0950268812000416

The role of horses in the transmission of leptospirosis in an urban tropical area.

Abstract: The objective of this study was to demonstrate the presence of leptospires in equine urine, as evidence for a potential role of horses in transmission of this organism. Thoroughbred horses (aged 2-5 years, n = 276) from Rio de Janeiro, Brazil, were studied. After a severe storm, the premises of the animals remained flooded for 72 h. Blood samples for serology were collected on days 20 and 35 (day of storm = day 0). On day 20, 132 (47·8%) horses were seroreactive (titre ≥200) and, of these, 23 (31·0%) had increased antibody titres on day 35. Furthermore, 34 urine samples (for PCR and culture) were collected from seroreactive horses on day 35. Copenhageni was the most frequent serovar (88·8% of reactive titres). Although none of the urine samples were culture positive, 12 (35·2%) were PCR positive. This is apparently the first report of evidence of leptospires in urban horses. Furthermore, we suggest that these animals can play a role in the transmission of leptospirosis in urban areas.
Publication Date: 2012-03-15 PubMed ID: 22417781PubMed Central: PMC9152048DOI: 10.1017/S0950268812000416Google 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
  • Research Support
  • Non-U.S. Gov't

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 discusses a study aimed at finding evidence of leptospires in horse urine to ascertain the role of these animals in the transmission of leptospirosis in urban tropical areas.

Objective of the Study

  • The main objective of the study was to provide evidence for the presence of Leptospira organisms in horse urine. The researchers aimed to establish if horses play a role in the transmission of leptospirosis, a bacterial disease that affects humans and animals. This study forms the basis for understanding the potential risk associated with horses in the spread of the disease in urban tropical areas.

Location and Subjects

  • The study was conducted in Rio De Janeiro, Brazil, with thoroughbred horses aged between 2 to 5 years. A total of 276 horses were chosen for the study. The choice of location and subjects was strategic to the study, as horses in this environment experienced specific conditions that facilitated the study.

Methods

  • The horse’s premises flooded for 72 hours after a severe storm. Following this, blood samples were acquired for serology assessment on the 20th and 35th day, with the stormy day set at day zero.
  • From a total of 132 seroreactive horses (titres ≥200) identified on the 20th day, 23 showed an increase in antibody titres on day 35. These seroreactive horses were the ones from which the researchers drew urine samples for PCR and culture tests.

Findings

  • The serovar Copenhageni was found to be the most common among the reactive titres, accounting for 88.8% of cases.
  • A total of 34 urine samples were collected from these horses. Despite none of these showing a positive culture, 12 (35.2%) were PCR positive — a clear indicator of the presence of Leptospira in the urine.

Conclusion

  • The study concluded that there is evidence of the presence of leptospires in urban horses. The researchers propose that this observation indicates horses could potentially play a role in the transmission of leptospirosis in urban areas.
  • This study is reportedly the first of its kind to provide such insights. Although, it is important to gather more evidence to firm up this suggestion.

Cite This Article

APA
Hamond C, Martins G, Lawson-Ferreira R, Medeiros MA, Lilenbaum W. (2012). The role of horses in the transmission of leptospirosis in an urban tropical area. Epidemiol Infect, 141(1), 33-35. https://doi.org/10.1017/S0950268812000416

Publication

ISSN: 1469-4409
NlmUniqueID: 8703737
Country: England
Language: English
Volume: 141
Issue: 1
Pages: 33-35

Researcher Affiliations

Hamond, C
  • Laboratory of Veterinary Bacteriology, Department of Microbiology and Parasitology, Universidade Federal Fluminense, Rio de Janeiro, Brazil.
Martins, G
    Lawson-Ferreira, R
      Medeiros, M A
        Lilenbaum, W

          MeSH Terms

          • Animals
          • Antibodies, Bacterial / blood
          • Brazil
          • Horse Diseases / microbiology
          • Horses
          • Humans
          • Leptospirosis / microbiology
          • Leptospirosis / veterinary
          • Polymerase Chain Reaction
          • Tropical Climate
          • Urban Population
          • Urine / microbiology

          Conflict of Interest Statement

          None.

          References

          This article includes 10 references
          1. Robertson C. Spatial epidemiology of suspected clinical leptospirosis in Sri Lanka. Epidemiology and Infection 2011; 7: 1–13.
            pubmed: 21676347
          2. de Faria MT. Carriage of Leptospira interrogans among domestic rats from an urban setting highly endemic for leptospirosis in Brazil. Acta Tropica 2008; 108: 1–5.
            pmc: PMC2596941pubmed: 18721789
          3. Desvars A. Animal leptospirosis in small tropical areas. Epidemiology and Infection 2011; 139: 167–188.
            pubmed: 20875197
          4. Adler B, de la Peña Moctezuma A. Leptospira and leptospirosis. Veterinary Microbiology 2010; 140: 287–296.
            pubmed: 19345023
          5. Gamage CD. Prevalence and carrier status of leptospirosis in smallholder dairy cattle and peridomestic rodents in Kandy, Sri Lanka. Vector Borne and Zoonotic Disease 2011; 11: 1041–1047.
            pubmed: 21284522
          6. Hashimoto VY. Occurrence of antibodies against Leptospira spp. in horses of the urban area of Londrina, Paraná, Brazil. Revista do Instituto de Medicina Tropical de São Paulo 2007; 49: 327–330.
            pubmed: 18026641
          7. Jung BY. Seroprevalence of Leptospira spp. in clinically healthy racing horses in Korea. Journal of Veterinary Medical Science 2010; 72: 197–201.
            pubmed: 19942812
          8. Pinna MH. Outbreak of equine leptospirosis by S. Bratislava. Online Journal of Veterinary Research 2007; 11: 1–4.
          9. Houwers DJ. Agglutinating antibodies against pathogenic Leptospira in healthy dogs and horses indicate common exposure and regular occurrence of subclinical infections. Veterinary Microbiology 2011; 148: 449–451.
            pubmed: 20863632
          10. Stoddard RA. Detection of pathogenic Leptospira spp. through TaqMan polymerase chain reaction targeting the LipL32 gene. Diagnostic Microbiology and Infectious Disease 2009; 64: 247–255.
            pubmed: 19395218

          Citations

          This article has been cited 13 times.
          1. Imandar M, Javadi A, Abdollahpour G, Mahale PRS, Qanbari A, Mirzaalimohammadi M, Taherkhani E, Olfatifar M, Nikkhahi F, Eslahi AV, Badri M. Detection of Antibodies Against Leptospira interrogans Serovars Among Stabled Horses in Qazvin Province of Iran as a One-Health Concern. Vet Med Sci 2025 Sep;11(5):e70520.
            doi: 10.1002/vms3.70520pubmed: 40719640google scholar: lookup
          2. Díaz EA, Arroyo G, Sáenz C, Mena L, Barragán V. Leptospirosis in horses: Sentinels for a neglected zoonosis? A systematic review. Vet World 2023 Oct;16(10):2110-2119.
          3. Romanowski TNA, Dias RA, Heinemann MB, Carvalho SF, Silva TA, Martins ADS, Caetano GDDC, Ferreira Júnior Á, Santos JPD, Borsanelli AC. Seroprevalence of Equine Leptospirosis in the State of Goiás, Brazil. Vet Sci 2023 Sep 25;10(10).
            doi: 10.3390/vetsci10100590pubmed: 37888542google scholar: lookup
          4. Browne ES, Pereira M, Barreto A, Zeppelini CG, de Oliveira D, Costa F. Prevalence of human leptospirosis in the Americas: a systematic review and meta-analysis. Rev Panam Salud Publica 2023;47:e126.
            doi: 10.26633/RPSP.2023.126pubmed: 37609525google scholar: lookup
          5. Azócar-Aedo L. Basic Aspects and Epidemiological Studies on Leptospirosis Carried Out in Animals in Chile: A Bibliographic Review. Trop Med Infect Dis 2023 Feb 1;8(2).
            doi: 10.3390/tropicalmed8020097pubmed: 36828513google 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. Geiger T, Gerhards H, Wollanke B. Detection of Anti-LipL32 Antibodies in Serum Samples from Horses with Chronic Intraocular Infection with Leptospira spp. Pathogens 2021 Oct 14;10(10).
            doi: 10.3390/pathogens10101325pubmed: 34684272google scholar: lookup
          8. Wasiński B, Paschalis-Trela K, Trela J, Czopowicz M, Kita J, Żychska M, Cywińska A, Markowska-Daniel I, Carter C, Witkowski L. Serological Survey of Leptospira Infection in Arabian Horses in Poland. Pathogens 2021 Jun 1;10(6).
            doi: 10.3390/pathogens10060688pubmed: 34206112google scholar: lookup
          9. Bolwell CF, Rogers CW, Benschop J, Collins-Emerson JM, Adams B, Scarfe KR, Gee EK. Seroprevalence of Leptospira in Racehorses and Broodmares in New Zealand. Animals (Basel) 2020 Oct 23;10(11).
            doi: 10.3390/ani10111952pubmed: 33114082google scholar: lookup
          10. Akter R, Legione A, Sansom FM, El-Hage CM, Hartley CA, Gilkerson JR, Devlin JM. Detection of Coxiella burnetii and equine herpesvirus 1, but not Leptospira spp. or Toxoplasma gondii, in cases of equine abortion in Australia - a 25 year retrospective study. PLoS One 2020;15(5):e0233100.
            doi: 10.1371/journal.pone.0233100pubmed: 32453753google scholar: lookup
          11. Trimble AC, Blevins CA, Beard LA, Deforno AR, Davis EG. Seroprevalence, frequency of leptospiuria, and associated risk factors in horses in Kansas, Missouri, and Nebraska from 2016-2017. PLoS One 2018;13(10):e0206639.
            doi: 10.1371/journal.pone.0206639pubmed: 30372498google scholar: lookup
          12. Martins G, Lilenbaum W. The panorama of animal leptospirosis in Rio de Janeiro, Brazil, regarding the seroepidemiology of the infection in tropical regions. BMC Vet Res 2013 Dec 1;9:237.
            doi: 10.1186/1746-6148-9-237pubmed: 24289165google scholar: lookup
          13. 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