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Animals : an open access journal from MDPI2025; 15(20); 3045; doi: 10.3390/ani15203045

A Scoping Review of Antimicrobial Therapy in Leptospira Infections in Domestic Animals.

Abstract: Leptospirosis, caused by spp., affects multiple domestic species and can result in significant economic and public health impacts. This scoping review, conducted following the PRISMA 2020 guidelines, searched PubMed, SciELO, and Scopus for original studies that described complete therapeutic protocols (including dose, duration, and confirmed diagnosis) in dogs, cats, cattle, pigs, horses, sheep, and goats. Thirty-five studies met the criteria: 14 (40%) in cattle, 7 (20%) in swine, 2 (5.7%) in small ruminants, 7 (20%) in dogs and cats, and 5 (14.3%) in horses. In livestock, streptomycin monotherapy has predominated, demonstrating high efficacy against renal and genital carriers, but it faces regulatory restrictions in several countries. In companion animals, treatment often addressed acute cases using doxycycline and aminopenicillins, with frequent drug combinations. Horses were mainly treated with penicillin, alone or associated with other agents. Across species, protocols showed substantial heterogeneity, lack of harmonization, and limited evaluation of bacteriological cure, with most studies published before 2000. This scarcity of recent clinical trials reinforces the neglected status of animal leptospirosis. By compiling fragmented evidence, this review identifies converging practices that may serve as a preliminary consensus, highlights discrepancies and knowledge gaps, and provides an evidence-based framework to support the development of standardized, species-specific guidelines urgently needed in a One Health context.
Publication Date: 2025-10-20 PubMed ID: 41153972PubMed Central: PMC12561877DOI: 10.3390/ani15203045Google Scholar: Lookup
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  • Journal Article
  • Review

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 review summarizes existing research on antimicrobial treatments for leptospirosis across various domestic animal species, highlighting common practices, knowledge gaps, and the need for standardized treatment guidelines.

Introduction to Leptospirosis and Its Impact

  • Leptospirosis is an infectious disease caused by Leptospira bacteria affecting multiple domestic animals such as cattle, swine, horses, dogs, cats, sheep, and goats.
  • The disease has significant economic consequences due to impacts on livestock productivity and also poses a public health risk as it can be transmitted to humans (zoonotic potential).
  • Effective antimicrobial treatment in animals is critical for controlling infection and preventing transmission.

Scope and Methodology of the Review

  • Type of study: Scoping review carried out according to PRISMA 2020 guidelines.
  • Data sources: The review searched PubMed, SciELO, and Scopus databases focusing on original studies detailing complete therapeutic protocols.
  • Inclusion criteria: Studies that reported antibiotic dosage, treatment duration, and confirmed diagnosis of leptospirosis in the target domestic species.
  • Number of studies included: 35.
  • Species distribution of studies:
    • Cattle: 14 studies (40%)
    • Swine: 7 studies (20%)
    • Small ruminants (sheep/goats): 2 studies (5.7%)
    • Dogs and cats: 7 studies (20%)
    • Horses: 5 studies (14.3%)

Findings on Antimicrobial Treatments by Species

  • Livestock (Cattle, Swine, Small Ruminants):
    • Streptomycin monotherapy is the predominant antimicrobial used.
    • It shows high effectiveness, particularly in clearing renal and genital carrier states of Leptospira.
    • However, streptomycin use faces regulatory restrictions in some countries, limiting its availability or use.
  • Companion Animals (Dogs and Cats):
    • Treatment usually targets acute leptospirosis cases.
    • Doxycycline and aminopenicillins are commonly used drugs, often in combination.
    • Use of combined drug therapies is frequent but protocols vary widely.
  • Horses:
    • Treated mainly with penicillin, either alone or combined with other antimicrobials.
    • Details on specific regimens tend to be less consistent compared with other species.

Challenges and Gaps Identified

  • Marked heterogeneity and lack of consistency across treatment protocols in terms of drug choice, dosages, and durations.
  • Limited harmonization of therapeutic approaches between countries and species.
  • Scarce evaluation of bacteriological cure in the reported studies, leaving uncertainty about treatment efficacy in eliminating the organism entirely.
  • Most research articles and clinical trials are dated, with a majority published before the year 2000, indicating a lack of recent updated evidence.
  • This scarcity reinforces the neglected status of animal leptospirosis within veterinary medicine and research.

Contributions and Implications of the Review

  • This review compiles fragmented and dispersed evidence to offer a clearer picture of current antimicrobial practices for animal leptospirosis.
  • Identifies converging therapeutic practices that may serve as a foundation for developing preliminary consensus treatment guidelines.
  • Highlights key inconsistencies and areas requiring further research, particularly regarding standardized treatment protocols and bacteriological outcomes.
  • Provides an evidence-based framework to support the urgent development of species-specific antimicrobial guidelines aligned with One Health principles, emphasizing integrated human, animal, and environmental health considerations.

Cite This Article

APA
Mendes J, Aymée L, Lilenbaum W. (2025). A Scoping Review of Antimicrobial Therapy in Leptospira Infections in Domestic Animals. Animals (Basel), 15(20), 3045. https://doi.org/10.3390/ani15203045

Publication

ISSN: 2076-2615
NlmUniqueID: 101635614
Country: Switzerland
Language: English
Volume: 15
Issue: 20
PII: 3045

Researcher Affiliations

Mendes, Julia
  • Laboratory of Veterinary Bacteriology, Biomedical Institute of Fluminense Federal University, Niterói 24210-030, RJ, Brazil.
Aymée, Luiza
  • Laboratory of Veterinary Bacteriology, Biomedical Institute of Fluminense Federal University, Niterói 24210-030, RJ, Brazil.
Lilenbaum, Walter
  • Laboratory of Veterinary Bacteriology, Biomedical Institute of Fluminense Federal University, Niterói 24210-030, RJ, Brazil.

Grant Funding

  • 260003/001162/2020 / Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro

Conflict of Interest Statement

The authors declare no conflicts of interest.

References

This article includes 83 references
  1. Sykes JE, Gamage CD, Haake DA, Nally JE. Understanding leptospirosis: Application of state-of-the-art molecular typing tools with a One Health lens. Am. J. Vet. Res. 2022;83:ajvr.22.06.0104.
    doi: 10.2460/ajvr.22.06.0104pubmed: 35986911google scholar: lookup
  2. Samrot AV, Sean TC, Bhavya KS, Sahithya CS, Chan-Drasekaran S, Palanisamy R, Robinson ER, Subbiah SK, Mok PL. Leptospiral Infection, Pathogenesis and Its Diagnosis—A Review. Pathogens 2021;10:145.
    doi: 10.3390/pathogens10020145pmc: PMC7912936pubmed: 33535649google scholar: lookup
  3. Caimi K, Ruybal P. Leptospira spp.: A genus in the stage of diversity and genomic data expansion. Infect. Genet. Evol. 2020;81:104241.
    doi: 10.1016/j.meegid.2020.104241pubmed: 32061688google scholar: lookup
  4. Carvalho HGAC, Silva DM, Rodrigues GRD, Gameiro AH, Dos Santos RF, Raineri C, Lima AMC. Estimation of economic losses due to leptospirosis in dairy cattle. Prev. Vet. Med. 2024;229:106255.
  5. Abdul Rahman MS, Khor KH, Khairani-Bejo S, Lau SF, Mazlan M, Roslan MA. Risk and Predictive Factors of Leptospirosis in Dogs Diagnosed with Kidney and/or Liver Disease in Selangor, Malaysia. Animals 2021;11:3405.
    doi: 10.3390/ani11123405pmc: PMC8698145pubmed: 34944181google scholar: lookup
  6. Aymée L, Mendes J, Lilenbaum W. Bovine Genital Leptospirosis: An Update of This Important Reproductive Disease. Animals 2024;14:322.
    doi: 10.3390/ani14020322pmc: PMC10812666pubmed: 38275782google scholar: lookup
  7. Giraud-Gatineau A, Nieves C, Harrison LB, Benaroudj N, Veyrier FJ, Picardeau M. Evolutionary insights into the emergence of virulent Leptospira spirochetes. PLOS Pathog. 2024;20:e1012161.
  8. Muñoz-Zanzi C, Dreyfus A, Limothai U, Foley W, Srisawat N, Picardeau M, A Haake D. Leptospirosis—Improving Healthcare Outcomes for a Neglected Tropical Disease. Open Forum Infect. Dis. 2025;12:ofaf035.
    doi: 10.1093/ofid/ofaf035pmc: PMC11832045pubmed: 39963696google scholar: lookup
  9. Baharom M, Ahmad N, Hod R, Ja’afar MH, Arsad FS, Tangang F, Ismail R, Mohamed N, Radi MFM, Osman Y. Environmental and Occupational Factors Associated with Leptospirosis: A Systematic Review. Heliyon 2023;10:e23473.
  10. Khalil H, Santana R, de Oliveira D, Palma F, Lustosa R, Eyre MT, Carvalho-Pereira T, Reis MG, Ko AI, Diggle PJ. Poverty, sanitation, and Leptospira transmission pathways in residents from four Brazilian slums. PLOS Neglected Trop. Dis. 2021;15:e0009256.
  11. Sant’Anna da Costa R, Di Azevedo MIN, Borges ALdSB, Carvalho-Costa FA, Martins G, Lilenbaum W. Persistent High Leptospiral Shedding by Asymptomatic Dogs in Endemic Areas Triggers a Serious Public Health Concern. Animals 2021;11:937.
    doi: 10.3390/ani11040937pmc: PMC8065945pubmed: 33810226google scholar: lookup
  12. da Costa Barnabé NN, Soares RR, Barros DKS, Araújo Júnior JP, Malossi CD, Rodrigues Silva MLC, Brasil AWL, da Costa DF, Higino SSDS, Santos CSAB. The Role of Transplacental Infection in Leptospira spp. Epidemiology in Cattle in Caatinga Biome, Brazil. Microorganisms 2024;12:1044.
  13. Cilia G, Bertelloni F, Piredda I, Ponti MN, Turchi B, Cantile C, Parisi F, Pinzauti P, Armani A, Palmas B. Presence of pathogenic Leptospira spp. in the reproductive system and fetuses of wild boars (Sus scrofa) in Italy. PLOS Neglected Trop. Dis. 2020;14:e0008982.
  14. Sohm C, Willixhofer D, Fasching E, Waldner K, Deitzer N, Steiner J, Jöbstl J, Schleicher C, Schwarz M, Fuchs R. First isolation and genotyping of pathogenic Leptospira spp. from Austria. Sci. Rep. 2024;14:4467.
    doi: 10.1038/s41598-024-53775-wpmc: PMC10897423pubmed: 38409294google scholar: lookup
  15. Martins G, Lilenbaum W. Control of bovine leptospirosis: Aspects for consideration in a tropical environment. Res. Vet. Sci. 2017;112:156–160.
    doi: 10.1016/j.rvsc.2017.03.021pubmed: 28391058google scholar: lookup
  16. Sykes JE, Francey T, Schuller S, Stoddard RA, Cowgill LD, Moore GE. Updated ACVIM consensus statement on leptospirosis in dogs.. J. Vet. Intern. Med. 2023;37:1966–1982.
    doi: 10.1111/jvim.16903pmc: PMC10658540pubmed: 37861061google scholar: lookup
  17. Wunder EA, Adhikarla H, Hamond C, Owers Bonner KA, Liang L, Rodrigues CB, Bisht V, Nally JE, Alt DP, Reis MG. A live attenuated-vaccine model confers cross-protective immunity against different species of the Leptospira genus.. Elife 2021;10:e64166.
    doi: 10.7554/eLife.64166pmc: PMC7837694pubmed: 33496263google scholar: lookup
  18. Alt DP, Zuemer RL, Bolin CA. Evaluation of antibiotics for treatment of cattle infected with Leptospira borgpetersenii serovar hardjo.. J. Am. Vet. Med. Assoc. 2001;219:636–639.
    doi: 10.2460/javma.2001.219.636pubmed: 11549093google scholar: lookup
  19. Gomes LR, Correia LIV, Reis TFMD, Peres PABM, Sommerfeld S, Silva RR, Fonseca BB, Silva ACA, Lima AMC. In vitro evaluation of the antimicrobial effect of ZnO:9Ag nanoparticle and antibiotics on standard strains of Leptospira spp.. Microb. Pathog. 2025;199:107259.
    doi: 10.1016/j.micpath.2024.107259pubmed: 39736342google scholar: lookup
  20. Ishak A, Mazonakis N, Spernovasilis N, Akinosoglou K, Tsioutis C. Bactericidal versus bacteriostatic antibacterials: Clinical significance, differences and synergistic potential in clinical practice.. J. Antimicrob. Chemother. 2025;80:1–17.
    doi: 10.1093/jac/dkae380pmc: PMC11695898pubmed: 39471409google scholar: lookup
  21. Singh BR, Agri H, Karthikeyan R, Jayakumar V. Atividade antimicrobiana comparativa de amicacina e gentamicina em bactérias clinicamente importantes.. J. Pharmacol. Clin. Toxicol. 2023;11:1180.
  22. Boss J, Dance DAB, Chanthongthip A, Newton PN, Wuthiekanun V, Robinson MT. Antimicrobial Susceptibility Testing of Leptospira spp. in the Lao People’s Democratic Republic Using Disk Diffusion.. Am. J. Trop. Med. Hyg. 2019;100:1073–1078.
    doi: 10.4269/ajtmh.18-0955pmc: PMC6493943pubmed: 30887950google scholar: lookup
  23. Alt DP, Bolin CA. Preliminary evaluation of antimicrobial agents for treatment of Leptospira interrogans serovar pomona infection in hamsters and swine.. Am. J. Vet. Res. 1996;57:59–62.
    doi: 10.2460/ajvr.1996.57.01.59pubmed: 8720239google scholar: lookup
  24. Paixão G, Botelho-Fontela S, Gandra F, Reis J. Acute Leptospirosis Outbreak in Cattle: A Case Report.. Vet. Med. Sci. 2025;11:e70206.
    doi: 10.1002/vms3.70206pmc: PMC11876777pubmed: 40033970google scholar: lookup
  25. Fouché N, Graubner C, Lanz S, Schweighauser A, Francey T, Gerber V. Acute kidney injury due to Leptospira interrogans in 4 foals and use of renal replacement therapy with intermittent hemodiafiltration in 1 foal.. J. Vet. Intern. Med. 2020;34:1007–1012.
    doi: 10.1111/jvim.15713pmc: PMC7096627pubmed: 31999382google scholar: lookup
  26. Gutierrez L, Mendoza J, Rangel AB, Tapia G, Bernad MJ, Sumano H. Outpatient Clinical Trial in Dogs with Leptospirosis Treated with Enrofloxacin Hydrochloride-Dihydrate (ENRO-C). Front. Vet. Sci. 2019;6:360.
    doi: 10.3389/fvets.2019.00360pmc: PMC6803455pubmed: 31681813google scholar: lookup
  27. Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hofmann TC, Mulrow CD, Shamseer L, Tetzlaff JM, Akl EA, Brennan SE. The PRISMA 2020 statement: An updated guideline for reporting systematic reviews.. BMJ 2021;372:n71.
    doi: 10.1136/bmj.n71pmc: PMC8005924pubmed: 33782057google scholar: lookup
  28. Doherty PC. Streptomycin treatment of bovine carriers of Leptospira pomona.. N. Z. Vet. J. 1967;23:138–139.
    pubmed: 6033736
  29. Ellis WA, Montgomery J, Cassells JA. Dihydrostreptomycin treatment of bovine carriers of Leptospira interrogans serovar hardjo.. Res. Vet. Sci. 1985;39:292–295.
    doi: 10.1016/S0034-5288(18)31716-8pubmed: 2417297google scholar: lookup
  30. Gerritsen MJ, Koopmans MJ, Olyhoek T. Effect of streptomycin treatment on the shedding of and the serologic responses to Leptospira interrogans serovar hardjo subtype hardjobovis in experimentally infected cows.. Vet. Microbiol. 1993;38:129–135.
    doi: 10.1016/0378-1135(93)90080-Qpubmed: 8128596google scholar: lookup
  31. Smith CR, Corney BG, McGowan MR, McClintock CS, Ward W, Ketterer PJ. Amoxycillin as an alternative to dihydrostreptomycin sulphate for treating cattle infected with Leptospira borgpetersenii serovar hardjo.. Aust. Vet. J. 1997;75:818–821.
  32. Cortese VS, Behan S, Galvin JE, Penka DR, Ramsey D, Bryson WL, Lucas MJ. Evaluation of two antimicrobial therapies in the treatment of Leptospira borgpetersenii serovar hardjo infection in experimentally infected cattle.. Vet. Ther. 2007;8:201–208.
    pubmed: 17926305
  33. Guadelupe B, Balaro MFA, Brandão FZ, Martins GMS, Lilenbaum W. Streptomycin treatment of genital carriers of Leptospira in experimentally infected sheep on different estrous phases.. Res. Vet. Sci. 2022;152:579–581.
    doi: 10.1016/j.rvsc.2022.09.027pubmed: 36201904google scholar: lookup
  34. Doherty PC, Baynes ID. The effects of feeding oxytetracycline on leptospiruria in pigs infected with Leptospira pomona.. Aust. Vet. J. 1967;43:155–160.
  35. Ketterer PJ, Dunster PJ. Failure to eliminate Leptospira pomona from pigs by treatment with long acting oxytetracycline.. Aust. Vet. J. 1985;62:348–349.
  36. Gerritsen MJ, Koopmans MJ, Dekker TC, de Jong MC, Moerman A, Olyhoek T. Effective treatment with dihydrostreptomycin of naturally infected cows shedding Leptospira interrogans serovar hardjo subtype hardjobovis.. Am. J. Vet. Res. 1994;55:339–343.
    doi: 10.2460/ajvr.1994.55.03.339pubmed: 7514850google scholar: lookup
  37. Mughini-Gras L, Bonfanti L, Natale A, Comin A, Ferronato A, La Greca E, Patregnani T, Lucchese L, Marangon S. Application of an integrated outbreak management plan for the control of leptospirosis in dairy cattle herds.. Epidemiol. Infect. 2014;142:1172–1181.
    doi: 10.1017/S0950268813001817pmc: PMC9151234pubmed: 23920354google scholar: lookup
  38. Grippi F, Giudice E, Di Pietro S, Sciacca C, Santangelo F, Galluzzo P, Barreca S, Guercio A. Leptospira interrogans serogroup Sejroe serovar Hardjo in aborting cows: Two herd cases in Sicily (Italy). J. Vet. Res. 2020;64:73–78.
    doi: 10.2478/jvetres-2020-0021pmc: PMC7106001pubmed: 32258802google scholar: lookup
  39. Dobson KJ. Eradication of leptospirosis from two commercial piggeries in South Australia.. Aust. Vet. J. 1971;47:186–188.
  40. Hodges RT, Thomson J, Townsend KG. Leptospirosis in pigs: The efficacy of streptomycin in stopping leptospiruria.. N. Z. Vet. J. 1979;27:124–126.
    doi: 10.1080/00480169.1979.34623pubmed: 292922google scholar: lookup
  41. Edwards JD, Daines D. A leptospirosis outbreak in a piggery.. N. Z. Vet. J. 1979;27:247–248.
    doi: 10.1080/00480169.1979.34663pubmed: 294532google scholar: lookup
  42. Paz-Soldán SV, Dianderas MT, Windsor RS. Leptospira interrogans serovar canicola: A causal agent of sow abortions in Arequipa, Peru.. Trop. Anim. Health Prod. 1991;23:233–240.
    doi: 10.1007/BF02357107pubmed: 1796527google scholar: lookup
  43. Yeruham I, Bernstein M, Perl S, Irlin S, Cohen A, Yacobson B, Machnai B. Clinical and epizootiological study of a leptospirosis outbreak due to Leptospira canicola in a feedlot.. J. South Afr. Vet. Assoc. 1997;68:105–107.
    doi: 10.4102/jsava.v68i3.886pubmed: 9408897google scholar: lookup
  44. Martins G, Brandão FZ, Hamond C, Medeiros M, Lilenbaum W. Diagnosis and control of an outbreak of leptospirosis in goats with reproductive failure.. Vet. J. 2012;193:600–601.
    doi: 10.1016/j.tvjl.2012.01.016pubmed: 22365844google scholar: lookup
  45. Pimenta CLR M, da Costa DF, Silva MLC R, Pereira HD, Júnior JPA, Malossi CD, Ullmann LS, Alves CJ, de Azevedo SS. Strategies of the control of an outbreak of leptospiral infection in dairy cattle in Northeastern Brazil.. Trop. Anim. Health Prod. 2019;51:237–241.
    doi: 10.1007/s11250-018-1635-2pubmed: 29971649google scholar: lookup
  46. Bautista JM, Aranda Estrada M, Gutiérrez Olvera L, Lopez Ordaz R, Sumano López H. Treatment of bovine leptospirosis with enrofloxacin HCl 2H2O (Enro-C): A clinical trial.. Animals 2022;12:2358.
    doi: 10.3390/ani12182358pmc: PMC9495257pubmed: 36139218google scholar: lookup
  47. Aymée L, Di Azevedo MIN, Gregg W, Ezepha C, Carvalho-Costa FA, Lilenbaum W. Successful treatment with streptomycin of genital leptospirosis in naturally infected cows under field conditions.. Res. Vet. Sci. 2023;164:105020.
    doi: 10.1016/j.rvsc.2023.105020pubmed: 37738912google scholar: lookup
  48. Yoder HW, Bergman EN, Gleiser CA. Experimental canine leptospirosis. IV. Evaluation of selected antibiotics in the therapy of acute experimental Leptospira icterohemorrhagiae infections in immature dogs.. J. Infect. Dis. 1957;100:257–267.
    doi: 10.1093/infdis/100.3.257pubmed: 13439209google scholar: lookup
  49. Juvet F, Schuller S, O’Neill EJ, O’Neill PA, Nally JE. Urinary shedding of spirochaetes in a dog with acute leptospirosis despite treatment.. Vet. Rec. 2011;168:564.
    doi: 10.1136/vr.d740pubmed: 21546405google scholar: lookup
  50. Arbour J, Blais MC, Carioto L, Sylvestre D. Clinical leptospirosis in three cats (2001–2009). J. Am. Anim. Hosp. Assoc. 2012;48:256–260.
    doi: 10.5326/JAAHA-MS-5748pubmed: 22611217google scholar: lookup
  51. 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.
    doi: 10.1292/jvms.16-0361pmc: PMC6115255pubmed: 29962394google scholar: lookup
  52. Mauro T, Harkin K. Persistent leptospiruria in five dogs despite antimicrobial treatment (2000–2017). J. Am. Anim. Hosp. Assoc. 2019;55:42–47.
    doi: 10.5326/JAAHA-MS-6882pubmed: 30427719google scholar: lookup
  53. Kakita T, Yamagishi M, Oshiro S, Oyakawa C, Nagamine T, Kudeken T, Kyan H, Koizumi N. Leptospirosis with multiple organ dysfunction in a mongoose-scat-detection dog infected with Leptospira interrogans serogroup Hebdomadis, Okinawa, Japan.. J. Vet. Med. Sci. 2022;84:1324–1327.
    doi: 10.1292/jvms.22-0287pmc: PMC9586021pubmed: 36002297google scholar: lookup
  54. Divers TJ, Byars TD, Shin SJ. Renal dysfunction associated with infection of Leptospira interrogans in a horse.. J. Am. Vet. Med. Assoc. 1992;201:1391–1392.
    doi: 10.2460/javma.1992.201.09.1391pubmed: 1429185google scholar: lookup
  55. Bernard WV, Bolin C, Riddle T, Durando M, Smith BJ, Tramontin RR. Leptospiral abortion and leptospiruria in horses from the same farm.. J. Am. Vet. Med. Assoc. 1993;202:1285–1286.
    doi: 10.2460/javma.1993.202.08.1285pubmed: 8496088google scholar: lookup
  56. Frellstedt L, Slovis NM. Acute renal disease from Leptospira interrogans in three yearlings from the same farm.. Equine Vet. Educ. 2009;21:478–484.
    doi: 10.2746/095777309X467862google scholar: lookup
  57. Donahue JM, Williams NM. Emergent causes of placentitis and abortion.. Vet. Clin. North Am. Equine Pr. 2000;16:443–456.
    doi: 10.1016/S0749-0739(17)30088-3pubmed: 11219342google scholar: lookup
  58. Ellis WA. Animal leptospirosis.. Curr. Top. Microbiol. Immunol. 2015;387:99–137.
    doi: 10.1007/978-3-662-45059-8_6pubmed: 25388134google scholar: lookup
  59. Divers TJ, Chang YF, Irby NL, Smith JL, Carter CN. Leptospirosis: An important infectious disease in North American horses.. Equine Vet. J. 2019;51:287–292.
    doi: 10.1111/evj.13069pubmed: 30629756google scholar: lookup
  60. Murillo A, Goris M, Ahmed A, Cuenca R, Pastor J. Leptospirose em gatos: Revisão bibliográfica atual para orientar diagnóstico e tratamento.. J. Feline Med. Surg. 2020;22:216–228.
    doi: 10.1177/1098612X20903601pmc: PMC11132596pubmed: 32093581google scholar: lookup
  61. National Academy of Veterinary Sciences (India). Policy Paper No. 8: Leptospirosis in Animals. NAVS; New Delhi, India: 2023.
  62. Department of Animal Husbandry & Dairying (DAHD) Government of India. [(accessed on 1 September 2025)];2025 Available online: https://www.dahd.gov.in/
  63. Ministry for Primary Industries. Review of Submissions: Proposed Changes to the Import Health Standard for Bovine Germplasm. Ministry for Primary Industries; Wellington, New Zealand: 2025.
  64. Department for Environment, Food and Rural Affairs, Scottish Government, Welsh Government, Department of Agriculture and Rural Development Northern Ireland. 511EHC CON V2: Export of Bovine Semen to the Republic of South Africa. Health Certificate—Part A & B. London, UK, 2014.
  65. Di Azevedo M.I.N., Lilenbaum W. Equine genital leptospirosis: Evidence of an important silent chronic reproductive syndrome. Theriogenology 2022;192:81–88.
  66. Borges A.L.D.S.B., Aymée L., Roussouliéres I., Carvalho-Costa F.A., Di Azevedo M.I.N., Lilenbaum W. First isolation of Leptospira interrogans from follicular fluid of naturally infected cows. Vet. Microbiol. 2025;305:110522.
    doi: 10.1016/j.vetmic.2025.110522pubmed: 40262237google scholar: lookup
  67. Australian Pesticides and Veterinary Medicines Authority (APVMA). Review Findings on the Use of Dihydrostreptomycin and Streptomycin in Food-Producing Animals. APVMA; Canberra, Australia: 2021.
  68. United States Food and Drug Administration (FDA). Code of Federal Regulations—Title 21: Food and Drugs. Part 556—Tolerances for Residues of New Animal Drugs in Food. FDA; Silver Spring, MD, USA: 2021.
  69. Ministry for Primary Industries (MPI). Antimicrobial Resistance and Use in New Zealand: Surveillance and Control Policies. MPI; Wellington, New Zealand: 2020.
  70. European Medicines Agency (EMA). Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products. Off. J. Eur. Union 2019;L 4:43–167.
  71. Aktas I., Yarsan E. Pharmacokinetics of Conventional and Long-Acting Oxytetracycline Preparations in Kilis Goat. Front. Vet. Sci. 2017;4:229.
    doi: 10.3389/fvets.2017.00229pmc: PMC5743916pubmed: 29312969google scholar: lookup
  72. Zimmerman D.E., Tomas M., Miller D., Tomcsanyi L., Signorella C., Montepara C.A., Covvey J.R., Guarascio A.J.. Cephalosporins for the treatment of uncomplicated pyelonephritis: A systematic review. J. Am. Pharm. Assoc. 2023;63:1461–1471.
    doi: 10.1016/j.japh.2023.06.028pubmed: 37414282google scholar: lookup
  73. Strutzberg-Minder K., Kreienbrock L. Leptospireninfektionen beim Schwein: Epidemiologie, Diagnostik und weltweites Vorkommen. Berl. Munch. Tierarztl. Wochenschr. 2011;124:345–359.
    pubmed: 21950211
  74. Gomes Y.A., Medeiros L.S., Di Azevedo M.I.N., Loureiro A.P., Melo J.d.S.L.d., Carvalho-Costa F.A., Lilenbaum W. Identification of vaginal Leptospira in cervical-vaginal mucus of slaughtered pigs in the Amazon region. Anim. Reprod. Sci. 2022;238:106930.
  75. McCallum E.K., Constantino-Casas F., Cullen J., Warland H.J., Swales H., Linghley N., Kortum A.J., Sterritt A.J., Cogan T., Watson P.J. Infecções hepáticas leptospirais em cães sem envolvimento renal evidente. J. Vet. Intern. Med. 2019;33:141–150.
    doi: 10.1111/jvim.15340pmc: PMC6335520pubmed: 30499209google scholar: lookup
  76. Xiong CY, Yang YM, Zhou Y, He TS, Luo XW, Wang J, Mao CX. Systematic analysis of adverse effects of clinically common tetracyclines based on the FAERS database. Expert Opin. Drug Saf. 2025;24:949–957.
    doi: 10.1080/14740338.2024.2392865pubmed: 39140181google scholar: lookup
  77. Morén S, Kallberg M, Strom L. Equine uveitis: Outcome and adverse effects after one or two intravitreal low-dose gentamicin injections. Equine Vet. J. 2025;57:160–168.
    doi: 10.1111/evj.14056pmc: PMC11616955pubmed: 38329024google scholar: lookup
  78. Bertelloni F, Cilia G, Fratini F. Bacteriostatic and bactericidal effect of tigecycline on Leptospira spp.. Antibiotics 2020;9:467.
    doi: 10.3390/antibiotics9080467pmc: PMC7459466pubmed: 32751670google scholar: lookup
  79. Petakh P, Behzadi P, Oksenych V, Kamyshnyi O. Current treatment options for leptospirosis: A mini-review. Front. Microbiol. 2024;15:1403765.
    doi: 10.3389/fmicb.2024.1403765pmc: PMC11081000pubmed: 38725681google scholar: lookup
  80. Christie SAD, Hariharan S, Chakraborti S, Srinivasan N, Madanan MG. A new beginning for existing drugs: Repurposing FDA-approved drugs for the neglected re-emerging disease leptospirosis. ACS Omega 2024;9:32717–32726.
    doi: 10.1021/acsomega.4c02535pmc: PMC11292845pubmed: 39100284google scholar: lookup
  81. Benacer D, Zain SN, Ooi PT, Thong KL. Antimicrobial susceptibility of Leptospira spp. isolated from environmental, human and animal sources in Malaysia. Indian J. Med. Microbiol. 2017;35:124–128.
    doi: 10.4103/ijmm.IJMM_15_458pubmed: 28303833google scholar: lookup
  82. Pineda S, Martínez Garro JM, Salazar Flórez JE, Agudelo-Pérez S, Monroy FP, Peláez Sánchez RG. Detection of genes related to antibiotic resistance in Leptospira. Trop. Med. Infect. Dis. 2024;9:203.
    doi: 10.3390/tropicalmed9090203pmc: PMC11435864pubmed: 39330892google scholar: lookup
  83. Wuthiekanun V, Amornchai P, Langla S, White NJ, Day NPJ, Limmathurotsakul D, Peacock SJ. Antimicrobial disk susceptibility testing of Leptospira spp. using Leptospira Vanaporn Wuthiekanun (LVW) agar. Am. J. Trop. Med. Hyg. 2015;93:241–243.
    doi: 10.4269/ajtmh.15-0180pmc: PMC4530741pubmed: 26055750google scholar: lookup

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