Seroprevalence, frequency of leptospiuria, and associated risk factors in horses in Kansas, Missouri, and Nebraska from 2016-2017.
Abstract: Leptospirosis is a worldwide veterinary and public health concern, and well recognized infectious disease of horses. Seroprevalence rates vary with geography, but many studies have confirmed a high exposure rate. The correlation between seropositivity and shedding status has not been made in horses, however. The aims of this study were to use semi-nested PCR on urine from apparently healthy horses to determine period prevalence of leptospiral shedding and to correlate these findings with MAT results to establish associations with client based survey data regarding horse management and environment. Serum and free-catch urine were collected from 204 healthy horses between May 2016-December 2017. Serum was used to determine GGT, creatinine concentrations, and six serovar MAT. Urine samples were submitted for PCR testing of leptospiral 23S rRNA. Client consent and survey data were collected for all subjects. Potential risk factors included drinking water source, exposure to livestock and dogs, geographical location, season, and precipitation. Two horses were positive on urine PCR for leptospirosis (shedding prevalence 1%), yet only one had a high reciprocal MAT titer of ≥ 800. Both horses were negative on urine PCR one month later without treatment. Approximately 77% of horses (157/204) were seroreactive (MAT reciprocal titer ≥ 100) with titers to serogroup Australis detected more frequently than others (47.5%; (97/204)). Apparently healthy horses infrequently shed Leptospira spp. in urine, yet seroreactivity in clinically normal horses is high (77%), confirming high exposure rates to Leptospira spp. in the Central Midwest.
Publication Date: 2018-10-29 PubMed ID: 30372498PubMed Central: PMC6205653DOI: 10.1371/journal.pone.0206639Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
- Clinical Study
- Diagnostic Technique
- Disease Prevalence
- Disease Transmission
- Epidemiology
- Equine Health
- Geographical Differences
- Horses
- Infectious Disease
- Leptospira
- Microscopic Agglutination Test
- Polymerase Chain Reaction
- Public Health
- Risk Factors
- Serodiagnosis
- Seroprevalence
- Urine Analysis
- Veterinary Medicine
- Veterinary Research
- Zoonotic Diseases
Summary
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This research study focused on assessing the prevalence of leptospirosis shedding and its association with seropositivity in horses situated in Kansas, Missouri, and Nebraska. The study also sought to link these findings with factors such as horse management and environment.
Study Design and Scope
- To carry out the study, serum and urine samples were gathered from 204 healthy horses over one and a half years (May 2016 to December 2017).
- The organization conducted semi-nested PCR on the urine samples to ascertain the prevalence of leptospiral (a bacteria causing Leptospirosis) shedding.
- This was then cross-referenced with findings from an indirect immunofluorescent antibody test (MAT).
- Participants also filled in a survey on horse management and the environment in which the horses were kept. Factors considered here included the drinking water source, exposure to livestock and dogs, geographical location, the season, and rainfall.
Findings
- Out of all the test subjects, only two horses were found to be shedding leptospira, pointing to a shedding prevalence of 1%.
- However, only one of the two horses showed a high level of reciprocal MAT titer of ≥ 800. Additionally, both horses were found to be negative for Leptospirosis one month later without any treatment.
- When it came to seroreactivity, about 77% of the horses (157 out of 204) were seroreactive, pointing to high exposure rates to Leptospirosis. Here, the Australis serogroup was noted more frequently than other variations of the bacteria.
Conclusion
- The research concluded that the shedding of Leptospira spp. in urine among healthy horses is relatively infrequent.
- However, there is a high seroreactivity (77%) to Leptospira spp. amongst clinically normal horses, which aligns with the high exposure rates in the Central Midwest region where the study was conducted.
Per the results, the research provides a wealth of insights about the state of Leptospirosis among horses in the Central Midwest and advances understanding about the disease’s prevalence and prompt management.
Cite This Article
APA
Trimble AC, Blevins CA, Beard LA, Deforno AR, Davis EG.
(2018).
Seroprevalence, frequency of leptospiuria, and associated risk factors in horses in Kansas, Missouri, and Nebraska from 2016-2017.
PLoS One, 13(10), e0206639.
https://doi.org/10.1371/journal.pone.0206639 Publication
Researcher Affiliations
- Department of Clinical Sciences, College of Veterinary Medicine, Kansas State University, Manhattan, Kansas, United States of America.
- Department of Clinical Sciences, College of Veterinary Medicine, Kansas State University, Manhattan, Kansas, United States of America.
- Department of Clinical Sciences, College of Veterinary Medicine, Kansas State University, Manhattan, Kansas, United States of America.
- Department of Clinical Sciences, College of Veterinary Medicine, Kansas State University, Manhattan, Kansas, United States of America.
- Department of Clinical Sciences, College of Veterinary Medicine, Kansas State University, Manhattan, Kansas, United States of America.
MeSH Terms
- Animals
- Female
- Horse Diseases / epidemiology
- Horse Diseases / etiology
- Horse Diseases / microbiology
- Horse Diseases / urine
- Horses / microbiology
- Horses / urine
- Kansas / epidemiology
- Leptospira / genetics
- Leptospirosis / etiology
- Leptospirosis / microbiology
- Leptospirosis / urine
- Leptospirosis / veterinary
- Male
- Missouri / epidemiology
- Nebraska / epidemiology
- Polymerase Chain Reaction / veterinary
- RNA, Ribosomal, 23S / genetics
- Risk Factors
- Seroepidemiologic Studies
Conflict of Interest Statement
Funds for this work were provided generously by Zoetis Inc (EGD), the Department of Clinical Sciences at the Kansas State University Veterinary Health Center (ACT), and by the Dr. John G. and Mildred L. Gish Research Fund for Large Animal Research at Kansas State University (ACT). No competing interests exist between the commercial funding source (Zoetis Inc.) and the submitting authors relating to employment, consultancy, patents, products in development, or marketed products. Non-financial competing interests: Ram Raghavan was a previous mentor involved with this project and a member of the editorial board of a PLOS journals. This does not alter our adherence to PLOS ONE policies on sharing data and materials.
References
This article includes 30 references
- Divers TJ, Chang YF. Leptospirosis. In: Robinson NE, Sprayberry KA, eds. Current Therapy in Equine Medicine 2009; Vol 6 6th ed St. Louis, MO: Saunders Elsevier:145–147.
- Divers TJ, Chang YF. Equine leptospirosis: diagnosis, treatment and prevention. 24th Annual ACVIM Forum, Louisville, Kentucky, USA, 31 May-3 June, 2006.
- Delph KM, Sharpe E, Beard LA, Rankin AJ. Haemolytic anaemia and bilateral uveitis associated with leptospirosis in a 6‐year‐old Quarter Horse gelding. Equine Veterinary Education 2018. March;30(3):132–6.
- Erol E, Jackson CB, Steinman M, Meares K, Donahoe J, Kelly N. A diagnostic evaluation of real‐time PCR, fluorescent antibody and microscopic agglutination tests in cases of equine leptospiral abortion. Equine veterinary journal 2015. March 1;47(2):171–4.
- Frellstedt L. Equine recurrent uveitis: A clinical manifestation of leptospirosis. Equine Veterinary Education 2009. October 1;21(10):546–52.
- Gerding JC, Gilger BC. Prognosis and impact of equine recurrent uveitis. Equine veterinary journal 2016. May 1;48(3):290–8.
- Niedermaier G, Wollanke B, Hoffmann R, Rem S, Gerhards H. Detection of leptospira in the vitreous body of horses without ocular diseases and of horses with equine recurrent uveitis (ERU) using transmission-electron microscopy. DTW. Deutsche Tierarztliche Wochenschrift 2006. November;113(11):418–22.
- Rohrbach BW, Ward DA, Hendrix DV, Cawrse‐Foss M, Moyers TD. Effect of vaccination against leptospirosis on the frequency, days to recurrence and progression of disease in horses with equine recurrent uveitis. Veterinary ophthalmology 2005. May 1;8(3):171–9.
- Verma A, Stevenson B, Adler B. Leptospirosis in horses. Veterinary microbiology 2013. November 29;167(1–2):61–6.
- Zoetis LLC. 2015; Data on file, Study Report No. B850R-US-12-011; Study Report No. B951R-US-13-04; Study Report No. B951R-US-13-046; Study Report No. B951R-US-15-092. https://www.zoetisus.com/products/horses/lepto-eq-innovator/index.aspx
- Ye C, Yan W, McDonough PL, McDonough SP, Mohamed H, Divers TJ. Serodiagnosis of equine leptospirosis by enzyme-linked immunosorbent assay using four recombinant protein markers. Clinical and Vaccine Immunology 2014. April 1;21(4):478–83.
- Hamond C, Martins G, Lilenbaum W. Subclinical leptospirosis may impair athletic performance in racing horses. Tropical animal health and production 2012. December 1;44(8):1927–30.
- Scarcelli E, Piatti RM, Fedullo JD, Simon F, Cardoso MV, Castro V. Leptospira spp detection by Polymerase Chain Reaction (PCR) in clinical samples of captive black-capped capuchin monkey (Cebus apella). Brazilian Journal of Microbiology 2003. June;34(2):143–6.
- Hamond C, Martins G, Loureiro AP, Pestana C, Lawson-Ferreira R, Medeiros MA. Urinary PCR as an increasingly useful tool for an accurate diagnosis of leptospirosis in livestock. Veterinary research communications 2014. March 1;38(1):81–5.
- Fang F, Collins‐Emerson JM, Cullum A, Heuer C, Wilson PR, Benschop J. Shedding and seroprevalence of pathogenic Leptospira spp. in sheep and cattle at a New Zealand abattoir. Zoonoses and public health 2015. June 1;62(4):258–68.
- Delaude A, Rodriguez-Campos S, Dreyfus A, Counotte MJ, Francey T, Schweighauser A. Canine leptospirosis in Switzerland—A prospective cross-sectional study examining seroprevalence, risk factors and urinary shedding of pathogenic leptospires. Preventive veterinary medicine 2017. June 1;141:48–60.
- Båverud V, Gunnarsson A, Engvall EO, Franzén P, Egenvall A. Leptospira seroprevalence and associations between seropositivity, clinical disease and host factors in horses. Acta Veterinaria Scandinavica 2009. December;51(1):15.
- Harkin KR, Hays MP. Variable-number tandem-repeat analysis of leptospiral DNA isolated from canine urine samples molecularly confirmed to contain pathogenic leptospires. Journal of the American Veterinary Medical Association 2016. August 15;249(4):399–405.
- Woo TH, Patel BK, Smythe LD, Symonds ML, Norris MA, Dohnt MF. Identification of pathogenic Leptospira genospecies by continuous monitoring of fluorogenic hybridization probes during rapid-cycle PCR. Journal of clinical microbiology 1997. December 1;35(12):3140–6.
- Harkin KR, Roshto YM, Sullivan JT. Clinical application of a polymerase chain reaction assay for diagnosis of leptospirosis in dogs. Journal of the American Veterinary Medical Association 2003. May 1;222(9):1224–9.
- Harkin KR, Roshto YM, Sullivan JT, Purvis TJ, Chengappa MM. Comparison of polymerase chain reaction assay, bacteriologic culture, and serologic testing in assessment of prevalence of urinary shedding of leptospires in dogs. Journal of the American Veterinary Medical Association 2003. May 1;222(9):1230–3.
- Rojas P, Monahan AM, Schuller S, Miller IS, Markey BK, Nally JE. Detection and quantification of leptospires in urine of dogs: a maintenance host for the zoonotic disease leptospirosis. European journal of clinical microbiology & infectious diseases 2010. October 1;29(10):1305–9.
- Llewellyn JR, Krupka-Dyachenko I, Rettinger AL, Dyachenko V, Stamm I, Kopp PA. Urinary shedding of leptospires and presence of Leptospira antibodies in healthy dogs from Upper Bavaria. Berliner und Munchener tierarztliche Wochenschrift 2016;129(5–6):251–7.
- OIE. Manual of diagnostic tests and vaccines for terrestrial animals. 2012; 6ath edn. World Organisation for Animal Health, Paris. Online Access: http://www.oie.int/manual-of-diagnostic-tests-and-vaccines-for-terrestrial-animals/.
- Levett PN. Leptospirosis. Clin Microbiol Rev 2001; 14(2):296–326.
- Blatti S, Overesch G, Gerber V, Frey J, Hüssy D. Seroprevalence of Leptospira spp. in clinically healthy horses in Switzerland. Schweizer Archiv fur Tierheilkunde 2011. October 1;153(10):449.
- Hamond C, Martins G, Lawson-Ferreira R, Medeiros MA, Lilenbaum W. The role of horses in the transmission of leptospirosis in an urban tropical area. Epidemiology & Infection 2013. January;141(1):33–5.
- Wangdi C, Picard J, Tan R, Condon F, Dowling B, Gummow B. Equine leptospirosis in tropical Northern Queensland. Australian veterinary journal 2013. May 1;91(5):190–7.
- Barwick RS, Mohammed HO, McDonough PL, White ME. Epidemiologic features of equine Leptospira interrogans of human significance. Preventive veterinary medicine 1998. August 7;36(2):153–65.
- Fink JM, Moore GE, Landau R, Vemulapalli R. Evaluation of three 5′ exonuclease–based real-time polymerase chain reaction assays for detection of pathogenic Leptospira species in canine urine. Journal of Veterinary Diagnostic Investigation 2015. March;27(2):159–66.
Citations
This article has been cited 7 times.- Ramsay L, Eberhardt C, Schoster A. Acute leptospirosis in horses: A retrospective study of 11 cases (2015-2023). J Vet Intern Med 2024 Sep-Oct;38(5):2729-2738.
- 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.
- Quintero-Vélez JC, Rodas JD, Rojas CA, Ko AI, Wunder EA. Leptospira Infection in Rural Areas of Urabá Region, Colombia: A Prospective Study. Am J Trop Med Hyg 2022 Dec 14;107(6):1267-1277.
- Bolwell C, Gee E, 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 Aug 12;9(8).
- 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).
- Fagre AC, Mayo CE, Pabilonia KL, Landolt GA. Seroprevalence of Leptospira spp. in Colorado equids and association with clinical disease. J Vet Diagn Invest 2020 Sep;32(5):718-721.
- Vera E, Taddei S, Cavirani S, Schiavi J, Angelone M, Cabassi CS, Schiano E, Quintavalla F. Leptospira Seroprevalence in Bardigiano Horses in Northern Italy. Animals (Basel) 2019 Dec 20;10(1).
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