Seropositivity for Pathogenic Leptospira in Dogs, Cats, and Horses at a Teaching Veterinary Hospital in Southern Chile.
Abstract: At a veterinary hospital in southern Chile, we conducted an epidemiological study involving domestic dogs, cats, and horses to determine the seropositivity for pathogenic spp., identify the infecting serogroups, measure antibody titers, and characterize seropositive animals by sex and age. None of the sampled animals showed clinical signs of leptospirosis. The microscopic agglutination test, using a panel of eight serogroups, was used for diagnosis. The seropositivity was 36.5% (95% confidence interval [CI] = 24.5-48.4) in dogs, 12.9% (95% CI = 2.6-23.1) in cats, and 45.2% (95% CI = 30.1-60.2) in horses. Serological reactions were detected for the Tarassovi and Canicola serogroups in dogs, Sejroe, Canicola, Icterohaemorrhagiae, and Grippotyphosa in horses, and Tarassovi in cats. The most frequent antibody titers were 1:200 and 1:400 in dogs, 1:400 in cats, and 1:800 in horses. The distribution of seropositivity varied by sex and age across different animal species. The seropositivity for pathogenic in dogs, cats, and horses attending a veterinary hospital underscores the role of domestic animals as sentinels for zoonotic diseases. This finding has implications for epidemiological surveillance systems in increasing awareness of seropositivity and establishing specific prevention measures to mitigate the risk of leptospirosis transmission.
Publication Date: 2025-09-03 PubMed ID: 41003563PubMed Central: PMC12474481DOI: 10.3390/tropicalmed10090253Google 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.
Overview
- This study investigated the presence of antibodies against pathogenic Leptospira bacteria in dogs, cats, and horses at a veterinary hospital in southern Chile, assessing infection rates, specific bacterial types, and correlations with animal characteristics without clinical symptoms.
Study Objective and Context
- The research aimed to determine the seropositivity rates (presence of antibodies indicating exposure) for pathogenic Leptospira species in domestic animals — dogs, cats, and horses.
- It focused on identifying infecting serogroups (distinct groups of Leptospira identified by specific antigens), measuring antibody levels (titers), and analyzing the data in relation to animal sex and age.
- All animals sampled were asymptomatic for leptospirosis, meaning none showed clinical signs of the disease.
Methodology
- Samples from dogs, cats, and horses were collected at a teaching veterinary hospital in southern Chile.
- Diagnosis was conducted using the microscopic agglutination test (MAT), a standard serological test for leptospirosis.
- The MAT panel included eight different Leptospira serogroups, enabling identification of the specific serogroups causing antibody production.
Key Findings on Seropositivity Rates
- Dogs had a seropositivity rate of 36.5% with a 95% confidence interval (CI) ranging from 24.5% to 48.4%, indicating a moderate to high exposure level.
- Cats showed a lower seropositivity rate of 12.9% (95% CI = 2.6-23.1%), suggesting less frequent exposure or infection.
- Horses exhibited the highest seropositivity at 45.2% (95% CI = 30.1-60.2%), highlighting a notable prevalence in this species.
Identified Infecting Serogroups
- In dogs, antibodies were detected against the Tarassovi and Canicola serogroups.
- Horses had antibodies reactive to multiple serogroups: Sejroe, Canicola, Icterohaemorrhagiae, and Grippotyphosa.
- Cats primarily showed seropositivity for the Tarassovi serogroup.
Antibody Titers Distribution
- Dog antibody levels typically ranged at dilutions of 1:200 and 1:400, indicative of exposure but not necessarily recent infection.
- Cats had antibody titers mostly at 1:400, suggesting a moderate immune response.
- Horses displayed higher titers at 1:800, which may imply stronger or more recent exposure.
Demographic Variations in Seropositivity
- The study found variations in seropositivity based on sex and age across the three species, although specific patterns were not detailed in the abstract.
- This suggests that certain age groups or sexes might be more at risk or have different exposure patterns to Leptospira.
Significance and Implications
- The presence of antibodies against pathogenic Leptospira in apparently healthy domestic animals highlights their role as sentinels—indicators of the risk of leptospirosis in the environment.
- These findings underscore the need for enhanced epidemiological surveillance to monitor and control zoonotic diseases effectively.
- Improved awareness and the development of specific prevention strategies for leptospirosis transmission are crucial, especially in regions where domestic animals and humans interact closely.
Cite This Article
APA
Azócar-Aedo L, Meniconi G, Pino-Olguín C, Gallardo M.
(2025).
Seropositivity for Pathogenic Leptospira in Dogs, Cats, and Horses at a Teaching Veterinary Hospital in Southern Chile.
Trop Med Infect Dis, 10(9), 253.
https://doi.org/10.3390/tropicalmed10090253 Publication
Researcher Affiliations
- Facultad de Medicina Veterinaria, Escuela de Medicina Veterinaria, Universidad San Sebastián, Sede de la Patagonia, Puerto Montt 5480000, Chile.
- Facultad de Medicina Veterinaria, Escuela de Medicina Veterinaria, Universidad San Sebastián, Sede de la Patagonia, Puerto Montt 5480000, Chile.
- Facultad de Medicina Veterinaria, Escuela de Medicina Veterinaria, Universidad San Sebastián, Sede de la Patagonia, Puerto Montt 5480000, Chile.
- Facultad de Medicina y Ciencias de la Salud, Escuela de Medicina Veterinaria, Universidad Mayor, Campus Huechuraba, Santiago 8580000, Chile.
Conflict of Interest Statement
The authors declare no conflicts of interest.
References
This article includes 82 references
- Romero-Vivaz CM, Falconar AK. Leptospira spp. y leptospirosis humana.. Salud Uninorte 2016;32:123–143.
- Garba B, Bahaman A, Bejo S, Zakaria Z, Mutalib A, Bande A. Major epidemiological factors associated with leptospirosis in Malaysia.. Acta Trop 2018;178:242–247.
- Bouscaren N, de Coignac CB, Lastère S, Musso S, Teissier Y, Formont Y. Leptospirosis in French Polynesia: 11 years of surveillance data, 2007–2017.. New Microbes New Infect 2019;29:100518.
- Urbanskas E, Karveliene B, Radzijevskaja J. Leptospirosis: Classification, epidemiology, and methods of detection. A review.. Biologija 2022;68:129–136.
- Coburn J, Picardeau M, Woods C, Veldman T, Haake D. Pathogenesis insights from an ancient and ubiquitous spirochete.. PLoS Pathog 2021;17:e1009836.
- Schneider M, Jancloes M, Buss D, Aldighieri S, Bertherat E, Najera P, Galan D, Durski K, Espinal M. Leptospirosis: A silent epidemic disease.. Int. J. Environ. Res. Public Health 2013;10:7229–7234.
- Levett P. Leptospirosis.. Clin. Microbiol. Rev 2001;14:296–326.
- Wang W, Gao Y, Ji J, Huang Z, Xiong B, Xiang S. Trends and advances in Leptospira, a bibliometric analysis.. Front. Microbiol 2025;15:1514738.
- Mathieu P. Virulence of the zoonotic agent of leptospirosis: Still terra incognita?. Nat. Rev. Microbiol 2017;15:297–307.
- Haake DA, Levett P. Leptospira and Leptospirosis.. .
- Azócar-Aedo L, Smits H, Monti G. Leptospirosis in dogs and cats: Epidemiology, clinical disease, zoonotic implications, and prevention.. Arch. Med. Vet 2014;46:337–348.
- Goarant C. Leptospirosis: Risk factors and management challenges in developing countries.. Res. Rep. Trop. Med 2016;7:49–62.
- Barragan V, Olivas S, Keim P, Pearson T. Critical knowledge gaps in our understanding of environmental cycling and transmission of Leptospira spp.. Appl. Environ. Microbiol 2017;83:e01190-17.
- Sykes JE, Francey T, Schuller S, Stoddard R, Cowgill L, Moore G. 2023 Updated ACVIM consensus statement on leptospirosis in dogs.. J. Vet. Intern. Med 2023;37:1966–1982.
- Rodríguez A, Ferro B, Varona M, Santafé M. Exposure to Leptospira in stray dogs in the city of Cali.. Biomédica 2004;24:291–295.
- Lima M, Mittestainer J, de Rocha J, De Carvalho R, Verotti B, Pellicciari P, Victoria C, Langoni H. Principal zoonoses in small animals: A brief review.. Vet. Zootec. 2017;24:84–106.
- Bolin C. Diagnosis of leptospirosis: A reemerging disease of companion animals.. Semin. Vet. Med. Surg. Small Anim. 1996;11:166–171.
- Murillo M, Goris M, Ahmed A, Cuenca R, Pastor J. Leptospirosis in cats. Current literature review to guide diagnosis and management.. J. Feline Med. Surg. 2020;22:216–228.
- Ricardo T, Azócar-Aedo L, Signorini M, Previtali A. Leptospiral infection in domestic cats: Systematic review with meta-analysis.. Prev. Vet. Med. 2023;212:105851.
- Ellis W. Animal leptospirosis.. Curr. Top. Microbiol. Immunol. 2015;387:99–137.
- Malalana F, Blundell R, Pinchbeck G, Mcgowan C. The role of Leptospira spp. in horses affected with recurrent uveitis in the UK.. Equine Vet. J. 2017;49:706–709.
- Divers T, Chang Y, Irby N, Smith J, Carter C. Leptospirosis: An important infectious disease in North American horses.. Equine Vet. J. 2019;51:287–292.
- Uribe M, Azócar-Aedo L, Gallardo M. Serosurveillance of pathogenic Leptospira in ruminants from a veterinary teaching hospital.. Austral J. Vet. Sci. 2025;57:e5709.
- Tuemmers C, Tüders C, Rojas C, Serri M, Espinoza R, Castillo C. Prevalence of leptospirosis in vague dogs captured in Temuco city, 2011.. Rev. Chil. Infect. 2013;30:252–257.
- Azócar-Aedo L, Monti G. Seroprevalence of pathogenic Leptospira spp. in domestic dogs from southern Chile and risk factors associated with different environments.. Prev. Vet. Med. 2023;206:105707.
- Dorsch R, Ojeda J, Salgado M, Monti G, Collado B, Tomckowiack C, Tejeda C, Müller A, Eberhard T, Klaasen H. Cats shedding pathogenic Leptospira spp.—An underestimated zoonotic risk?. PLoS ONE 2020;22:e0239991.
- Azócar-Aedo L, Monti G, Jara R. Leptospira spp. in domestic cats from different environments: Prevalence of antibodies and risk factors associated with the seropositivity.. Animals 2014;4:612–626.
- Tuemmers C, Quezada G, Morales R, Serri M. Seroprevalence of Leptospira spp. in draft horses from indigenous communities in the Araucanía Region, Chile.. Rev. Chil. Infectol. 2021;38:580–582.
- Moreno T, Ramírez R, Azócar-Aedo L. Seroprevalence of pathogenic Leptospira, infecting serogroups and antibody titers detected in horses from Los Lagos region, southern Chile.. Chil. J. Agric. Anim. Sci. 2024;40:341–352.
- Zamora J, Riedemann S, Tadich N. A serological survey of leptospirosis in sheep in Chile.. Rev. Latinoam. Microbiol. 1999;41:73–76.
- Zamora J, Kruze J, Riedemann S. Leptospirosis de los animales domésticos en el Sur de Chile. Estudio Serológico.. Zoon Public. Health. 1975;22:544–555.
- Díaz E, Arroyo G, Sáenz C, Mena L, Barragán V. Leptospirosis in horses: Sentinels for a neglected zoonosis? A systematic review.. Vet. World. 2023;16:2110–2119.
- Ricardo T, Azócar-Aedo L, Monti G, Previtali A. Seroprevalence of pathogenic Leptospira serogroups in asymptomatic domestic dogs and cats: Systematic review and meta-analysis.. Front. Vet. Sci. 2024;11:1301959.
- . Código Sanitario Para Los Animales Terrestres.. 2023.
- Rabinowitz P, Scotch M, Conti L. Human and animal sentinels for shared health risks.. Vet. Ital. 2009;45:23–24.
- Hernández R, Fernández C, Baptista L. Metodología de la Investigación.. 2011.
- Faine S, Adler B, Bolin C, Perolat P. Leptospira and Leptospirosis.. 1999.
- WHO-ILS. Human Leptospirosis: Guidance for Diagnosis, Surveillance and Control.. 2003.
- Miotto B.A, Tozzi B, De Souza M, Alves A, Zanolli L, Heinemann M, Moreno M, Lilenbaum W, Hagiwara M. Diagnosis of acute canine leptospirosis using multiple laboratory tests and characterization of isolated strains.. BMC Vet. Res. 2018;14:222.
- Tapia A. Frecuencia de Presentación de Sueros Reaccionantes a Leptospira interrogans y Leptospira borgpetersenii en una Población de Equinos de tiro Urbano de la Región Metropolitana de Chile.. 2014.
- Bolwell C, Adams B, Collins-Emerson J, Scarfe K, Nisa S, Gordon E, Rogers C, Benschop J. Longitudinal testing of Leptospira antibodies in horses located near a leptospirosis outbreak in alpacas.. Vet. Sci. 2022;9:426.
- Romanowski T, Días R, Heinemann M, Carvalho S, Silva T, Martins A, Caetano G, Ferreira J, Santos J, Borsanelli A. Seroprevalence of equine leptospirosis in the state of Goiás, Brazil.. Vet. Sci. 2023;10:590.
- Silva R, Riedemann S. Frequency of canine leptospirosis in dogs attending veterinary practices determined through Microscopic Agglutination Test and comparison with isolation and immunofluorescence techniques.. Arch. Med. Vet. 2007;39:269–274.
- Beaglehole R, Bonita R, Kjellstrõm T. Basic Epidemiology.. 2003.
- Santiago M, Hervada H, Naveira G, Silva C, Fariñas H, Vásquez E, Bacallao J, Mujica O. El programa EPIDAT: Usos y perspectivas.. Rev. Panam. Salud Publica. 2010;27:80–82.
- Noordhuizen J, Frankena K, Van der Hoofd C, Graat E. Application of Quantitative Methods in Veterinary Epidemiology.. 1997.
- Vogt A, Rodan I, Brown M, Brown S, Buffington C, Forman M, Neilson J, Sparkes A. AAFP-AAHA: Feline life stage guidelines.. J. Feline Med. Surg. 2010;12:43–54.
- Harvey N. How Old Is My Dog? Identification of rational age groupings in pet dogs based upon normative age-linked processes.. Front. Vet. Sci. 2010;8:643085.
- Ricardo T, Bazán L, Beltramini L, Prieto Y, Montiel A, Margenet L, Schmeling F, Chiani J, Signorini M, Previtali M. Seroprevalence of Leptospira antibodies in dogs and cats from Santa Fe, a city in East-Central Argentina endemic for leptospirosis.. Prev. Vet. Med. 2014;229:106239.
- Cruz J, Sánchez A, Vera L. Characterization and prevalence of oral diseases in creole horses, Department of Caldas, Colombia.. Rev. Med. Vet. 2012;23:39–50.
- Hazra A, Gogtay N. Biostatistics series module 4: Comparing groups- categorical variables.. Indian. J. Dermatol. 2016;61:385–392.
- Schmidt P. Companion animals as sentinels for public health.. Vet. Clin. Small Anim. 2009;39:241–250.
- Lelu M, Muñoz-Zanzi C, Higgins B, Galloway R. Seroepidemiology of leptospirosis in dogs from rural and slum communities of Los Ríos Region, Chile.. BMC Vet. Res. 2015;11:31.
- Guzmán D, Diaz E, Sáenz C, Álvarez H, Cueva R, Zapata-Ríos G, Prado-Vivar B, Falconí M, Pearson T, Barragan V. Domestic dogs in indigenous Amazonian communities: Key players in Leptospira cycling and transmission?. PLOS Neg. Trop. Dis. 2024;18:e0011671.
- McCreight K, Barbosa L, Odoi A, Reed P, Rajeev S. Leptospira seroprevalence in dogs, cats, and horses in Tennessee, USA.. J. Vet. Diagn. Investig. 2024;37:119–125.
- Sohn-Hausner N, Kmetiuk L, da Silva E, Langoni H, Biondo A. One Health approach to leptospirosis: Dogs as environmental sentinels for identification and monitoring of human risk areas in Southern Brazil.. Trop. Med. Infect. Dis. 2023;8:435.
- Toro A. Determinación a Través del Test de ELISA de Anticuerpos Contra Leptospira en Felinos Pacientes del Hospital Clínico Veterinario de la Universidad de Concepción en Chillán.. 2002.
- Azócar-Aedo L. Global prevalence and epidemiology of leptospirosis in domestic cats, a systematic review and meta-analysis.. Vet. Mex. OA. 2022;9:e1129.
- Miotto B, Camelo Q, Miranda A, Mendes de Oliveira A, Barreto M, Hagiwara M, Bergmann S. Current knowledge on leptospirosis in cats: A systematic review with metanalysis on direct detection, serological response, and clinical data.. Res. Vet. Sci. 2024;167:105292.
- Bay-Schmith N. Prevalencia de Leptospirosis Equina en Caballos Jugadores de Polo de la Octava Región de Chile.. 2004.
- Troncoso I, Toro I, Guzmán A, Fuentealba J, Fischer K. Serological evaluation of Leptospira interrogans in horses from an equestrian center in Linares province, Chile.. CES Med. Vet. Zootec. 2013;8:101–107.
- Tadich T, Tapia C, González D. Seroprevalence of Leptospira spp. in working horses located in the central region of Chile.. J. Equine Vet. Sci. 2016;38:14–18.
- Orlando S, Páez K, Sánchez E, De la Cruz C, Calderón J, Arcos F, Torres-Lasso P, Calvopiña M, Garcia-Bereguiain M. Racehorses from a breeding farm in Tropical Ecuador have a high seroprevalence of anti-Leptospira spp. antibodies: A paradigm for leptospirosis management from a One Health perspective.. Front. Trop. Dis. 2023;4:1061038.
- Simbizi B, Saulez M, Potts A, Lötter C, Gummow B. A study of leptospirosis in South African horses and associated risk factors.. Prev. Vet. Med. 2016;134:6–15.
- Baharom M, Ahmad N, Hod R, Ha’afar M, Arsad F, Tangang F, Ismail R, Mohamed N, Radi M, Osma Y. Environmental and occupational factors associated with leptospirosis: A systematic review.. Heliyon 2024;10:e23473.
- Nurfitri F, Sukesi T, Mulasari S. Risk factor analysis of leptospirosis incidence in endemic areas.. Adv. Healthc. Res. 2025;3:297–313.
- Talukder H, Muñoz-Zanzi C, Salgado M, Berg S, Yang A. Identifying the drivers related to animal reservoirs, environment, and socio-demography of human leptospirosis in different community types of Southern Chile: An application of machine learning algorithm in One Health perspective.. Pathogens 2024;13:687.
- Rabinowitz P, Scotch M, Conti L. Animals as sentinels: Using comparative medicine to move beyond the laboratory.. ILAR J. 2010;51:262–267.
- Scotch M, Odofin L, Rabinowitz P. Linkages between animal and human health sentinel data.. BMC Vet. Res. 2009;5:15.
- Cilia G, Bertelloni F, Angelini M, Cerri D, Fratini F. Leptospira survey in wild boar (Sus. scrofa) hunted in Tuscany, central Italy.. Pathogens 2020;9:377.
- Cilia G, Bertelloni F, Fratini F. Leptospira infections in domestic and wild animals.. Pathogens 2020;9:573.
- Balcázar L, Azócar-Aedo L, Barrera V, Meniconi G, Muñoz V, Valencia-Soto C. Detection of antibodies for pathogenic Leptospira in wild mammals and birds from southern Chile—First record of seropositivity in a guiña (Leopardus guigna). Animals 2024;14:601.
- Luna A, Moles C, Gavaldón R, Nava V, Salazar G. La leptospirosis canina y su problemática en México.. Rev. Salud Anim. 2008;30:1–11.
- Ojeda J, Salgado M, Encina C, Santamaria C, Monti G. Evidence of interspecies transmission of pathogenic Leptospira between livestock and a domestic cat dwelling in a dairy cattle farm.. J. Vet. Med. Sci. 2018;80:1305–1308.
- Wegmann E. Leptospirosis en caballos.. Arch. Med. Vet. 1983;15:59–64.
- . Report of the First Meeting of the Leptospirosis Burden Epidemiology Reference Group.. .
- Greene C, Sykes J, Brown C, Hartmann K. Leptospirosis.. Enfermedades Infecciosas del Perro y el Gato 2008.
- Riedemann S, Zamora J, Cabezas X. Detección de aglutininas antileptospira en sueros de roedores silvestres del área rural de Valdivia, Chile.. Av. Cienc. Vet. 1994;9:1.
- Luna J, Salgado M, Tejeda C, Moroni M, Monti G. Assessment of risk factors in synanthropic and wild rodents infected by pathogenic Leptospira spp. captured in Southern Chile.. Animals 2020;10:2133.
- Correa J, Bucarey S, Cattan P, Landaeta-Aqueveque L, Ramírez-Estrada J. Renal carriage of Leptospira species in rodents from Mediterranean Chile: The Norway rat (Rattus norvegicus) as a relevant host in agricultural lands.. Acta Trop. 2017;176:105–108.
- . Decreto 7. Aprueba el Reglamento Sobre Notificación de Enfermedades Transmisibles de Declaración Obligatoria y su Vigilancia.. 2020.
- . Informe Epidemiológico Anual Leptospirosis, Chile.. 2021.
Citations
This article has been cited 0 times.Use Nutrition Calculator
Check if your horse's diet meets their nutrition requirements with our easy-to-use tool Check your horse's diet with our easy-to-use tool
Talk to a Nutritionist
Discuss your horse's feeding plan with our experts over a free phone consultation Discuss your horse's diet over a phone consultation
Submit Diet Evaluation
Get a customized feeding plan for your horse formulated by our equine nutritionists Get a custom feeding plan formulated by our nutritionists