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Journal of clinical microbiology2025; 64(3); e0052525; doi: 10.1128/jcm.00525-25

Revisiting genital leptospirosis in large animals: impacts on reproductive health, diagnostic challenges, and future directions.

Abstract: Leptospirosis, caused by spp. infection, is a globally significant zoonotic disease that affects a wide range of animals. Although renal colonization is well-documented, genital infection by leptospires remained less explored for decades, despite its impact on reproduction. Evidence suggests that genital infection occurs as a primary condition rather than secondary to renal colonization, particularly in cattle suffering from bovine genital leptospirosis (BGL), linked to chronic infections by strains of the Sejroe serogroup. In horses, a similar condition is suggested to be associated with strains of serogroup Australis. Molecular studies confirmed the presence of DNA in uterine, follicular, and vaginal samples, strengthening the hypothesis of an independent genital physiopathology. Despite significant advances in molecular diagnostics, the detection of genital carriers remains challenging, requiring refined methodologies beyond standard serology. This review critically examines the historical detection of spp. in genital samples of cattle, small ruminants, swine, and equines, emphasizing its relevance to reproductive health. Moreover, we highlight the limitations of current diagnostic approaches, advocating for increased use of genital samples in leptospirosis research of large animals and shedding light on future directions regarding genital leptospirosis in livestock research. Enhanced understanding and diagnosis of genital leptospirosis will contribute to better livestock reproductive management and disease prevention.
Publication Date: 2025-12-04 PubMed ID: 41342544PubMed Central: PMC12977509DOI: 10.1128/jcm.00525-25Google Scholar: Lookup
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  • Journal Article
  • Review

Summary

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Overview

  • This research article reviews the impact of genital leptospirosis infections in large animals, focusing on its role in reproductive health problems, difficulties in diagnosis, and potential future research directions.

Background on Leptospirosis

  • Leptospirosis is a zoonotic disease caused by infection with Leptospira spp.
  • It affects many animal species globally, and is known especially for kidney (renal) colonization by the bacteria.
  • Genital infections by Leptospira have been much less studied compared to renal infections, despite their importance in animal reproduction.

Genital Infection and Its Significance

  • Emerging evidence suggests genital leptospiral infections can occur as a primary infection and not just secondary to kidney colonization.
  • In cattle, bovine genital leptospirosis (BGL) is associated mainly with chronic infections from strains of the Sejroe serogroup.
  • Similar genital infections have been suggested in horses, linked to strains from the Australis serogroup.
  • Molecular biology studies have detected Leptospira DNA in reproductive tract tissues, such as uterine, follicular, and vaginal samples, confirming genital colonization and supporting the idea of genital-specific disease processes.

Diagnostic Challenges

  • Standard serological tests, which detect antibodies against Leptospira, are often inadequate for identifying genital carriers.
  • There is a need for improved and more sensitive diagnostic methods that specifically focus on genital samples to reliably detect infection.
  • Current molecular diagnostic advances offer potential but still face challenges related to sample collection, bacterial load, and intermittent shedding.

Implications for Reproductive Health in Livestock

  • Genital leptospirosis can cause reproductive failures in large animals, impacting productivity and economic outcomes in livestock farming.
  • Recognition of genital infection as a separate and important disease entity underscores the need for targeted management and treatment strategies.
  • Improved diagnostics will facilitate early detection, enabling better reproductive health management and disease control.

Future Directions in Research and Livestock Management

  • The review advocates for increased scientific focus on obtaining and testing genital samples in leptospirosis research for cattle, small ruminants, swine, and equines.
  • Better understanding of the pathology and epidemiology of genital leptospirosis can inform vaccine development and biosecurity measures.
  • Integrating modern molecular methods with traditional epidemiological approaches could enhance detection and surveillance of genital leptospirosis.
  • Ultimately, these advances will support improved animal welfare, reproductive efficiency, and reduced zoonotic risks associated with Leptospira infections.

Cite This Article

APA
Borges ALdSB, Aymée L, Lilenbaum W, Di Azevedo MIN. (2025). Revisiting genital leptospirosis in large animals: impacts on reproductive health, diagnostic challenges, and future directions. J Clin Microbiol, 64(3), e0052525. https://doi.org/10.1128/jcm.00525-25

Publication

ISSN: 1098-660X
NlmUniqueID: 7505564
Country: United States
Language: English
Volume: 64
Issue: 3
Pages: e0052525
PII: e00525-25

Researcher Affiliations

Borges, Ana Luiza Dos Santos Baptista
  • Laboratory of Veterinary Bacteriology, Biomedical Institute, Federal Fluminense University, Niterói, Rio de Janeiro, Brazil.
Aymée, Luiza
  • Laboratory of Veterinary Bacteriology, Biomedical Institute, Federal Fluminense University, Niterói, Rio de Janeiro, Brazil.
Lilenbaum, Walter
  • Laboratory of Veterinary Bacteriology, Biomedical Institute, Federal Fluminense University, Niterói, Rio de Janeiro, Brazil.
Di Azevedo, Maria Isabel Nogueira
  • Laboratory of Investigation in Medical Microbiology, Institute of Microbiology, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.

MeSH Terms

  • Animals
  • Leptospirosis / veterinary
  • Leptospirosis / diagnosis
  • Leptospirosis / microbiology
  • Leptospira / isolation & purification
  • Leptospira / genetics
  • Leptospira / classification
  • Cattle
  • Reproductive Health
  • Horses
  • Female
  • Swine
  • Livestock / microbiology
  • Reproductive Tract Infections / veterinary
  • Reproductive Tract Infections / diagnosis
  • Reproductive Tract Infections / microbiology
  • Cattle Diseases / diagnosis
  • Cattle Diseases / microbiology
  • Genital Diseases, Female / veterinary
  • Genital Diseases, Female / diagnosis
  • Genital Diseases, Female / microbiology
  • Zoonoses / microbiology

Conflict of Interest Statement

The authors declare no conflict of interest.

References

This article includes 111 references
  1. Karpagam KB, Ganesh B. Leptospirosis: a neglected tropical zoonotic infection of public health importance—an updated review. Eur J Clin Microbiol Infect Dis 39:835–846.
    doi: 10.1007/s10096-019-03797-4pubmed: 31898795google scholar: lookup
  2. Sykes JE, Reagan KL, Nally JE, Galloway RL, Haake DA. Role of diagnostics in epidemiology, management, surveillance, and control of leptospirosis. Pathogens 11:395.
    doi: 10.3390/pathogens11040395pmc: PMC9032781pubmed: 35456070google scholar: lookup
  3. Caimi K, Ruybal P. Leptospira spp., a genus in the stage of diversity and genomic data expansion. Infect Genet Evol 81:104241.
    doi: 10.1016/j.meegid.2020.104241pubmed: 32061688google scholar: lookup
  4. Klosowski ML, Bohn AA. Microscopic detection of Leptospira bacterial organisms in urine sediment from a young dog with leptospirosis and a review of the pathobiology and diagnosis of canine leptospirosis. Vet Clin Pathol 52:112–118.
    doi: 10.1111/vcp.13129pubmed: 35619239google scholar: lookup
  5. 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 10:145.
    doi: 10.3390/pathogens10020145pmc: PMC7912936pubmed: 33535649google scholar: lookup
  6. Hsu S-H, Yang C-W. Insight into the structure, functions, and dynamics of the Leptospira outer membrane proteins with the pathogenicity. Membranes (Basel) 12:300.
    doi: 10.3390/membranes12030300pmc: PMC8951592pubmed: 35323775google scholar: lookup
  7. Mejía L, Prado B, Cárdenas P, Trueba G, González-Candelas F. The impact of genetic recombination on pathogenic Leptospira. Infect Genet Evol 102:105313.
    doi: 10.1016/j.meegid.2022.105313pubmed: 35688386google scholar: lookup
  8. Hagedoorn NN, Maze MJ, Carugati M, Cash-Goldwasser S, Allan KJ, Chen K, Cossic B, Demeter E, Gallagher S, German R, Galloway RL, Habuš J, Rubach MP, Shiokawa K, Sulikhan N, Crump JA. Global distribution of Leptospira serovar isolations and detections from animal host species: a systematic review and online database. Trop Med Int Health 29:161–172.
    doi: 10.1111/tmi.13965pmc: PMC11076152pubmed: 38351504google scholar: lookup
  9. Vincent AT, Schiettekatte O, Goarant C, Neela VK, Bernet E, Thibeaux R, Ismail N, Mohd Khalid MKN, Amran F, Masuzawa T, Nakao R, Amara Korba A, Bourhy P, Veyrier FJ, Picardeau M. Revisiting the taxonomy and evolution of pathogenicity of the genus Leptospira through the prism of genomics. PLoS Negl Trop Dis 13:e0007270.
  10. Matiz-González JM, Ballesteros-Ballesteros JA, Hernández M, Mejorano-Fonseca JA, Cuervo C, Faccini-Martínez ÁA, Hidalgo M, Pérez-Torres J, Silva-Ramos CR. Genetic diversity of P1/pathogenic Leptospira species hosted by bats worldwide. Zoonoses Public Health 71:457–468.
    doi: 10.1111/zph.13126pubmed: 38509439google scholar: lookup
  11. Sohm C, Steiner J, Jöbstl J, Wittek T, Firth C, Steinparzer R, Desvars-Larrive A. A systematic review on leptospirosis in cattle: a European perspective. One Health 17:100608.
  12. Divers TJ, Chang Y ‐F., Irby NL, Smith JL, Carter CN. Leptospirosis: an important infectious disease in North American horses. Equine Vet J 51:287–292.
    doi: 10.1111/evj.13069pubmed: 30629756google scholar: lookup
  13. Gomes de Araújo H, Limeira CH, Viviane Ferreira de Aquino V, Longo Ribeiro Vilela V, José Alves C, Silvano dos Santos Higino S, Santos C de SAB, Azevedo SS de. Global seropositivity of swine leptospirosis: systematic review and meta-analysis. TropicalMed 8:158.
    doi: 10.3390/tropicalmed8030158pmc: PMC10059827pubmed: 36977159google scholar: lookup
  14. Balamurugan V, Alamuri A, Kumar KV, Varghese B, Govindaraj G, Hemadri D, Roy P. Prevalence of anti-leptospiral antibodies and frequency distribution of Leptospira serovars in small ruminants in enzootic South Peninsular India. Vet World 14:2023–2030.
  15. Grégoire F, Bakinahe R, Petitjean T, Boarbi S, Delooz L, Fretin D, Saulmont M, Mori M. Laboratory diagnosis of bovine abortions caused by non-maintenance pathogenic Leptospira spp.: necropsy, serology and molecular study out of a Belgian experience. Pathogens 9:413.
    doi: 10.3390/pathogens9060413pmc: PMC7350382pubmed: 32466444google scholar: lookup
  16. Sohm C, Willixhofer D, Fasching E, Waldner K, Deitzer N, Steiner J, Jöbstl J, Schleicher C, Schwarz M, Fuchs R, Bourhy P, Käsbohrer A, Wittek T, Firth C, Steinparzer R, Desvars-Larrive A. First isolation and genotyping of pathogenic Leptospira spp. from Austria. Sci Rep 14:4467.
    doi: 10.1038/s41598-024-53775-wpmc: PMC10897423pubmed: 38409294google scholar: lookup
  17. 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 11:2005.
    doi: 10.3389/fmicb.2020.02005pmc: PMC7456838pubmed: 32922382google scholar: lookup
  18. Cilia G, Bertelloni F, Fratini F. Leptospira infections in domestic and wild animals. Pathogens 9:573.
    doi: 10.3390/pathogens9070573pmc: PMC7400056pubmed: 32679834google scholar: lookup
  19. Loureiro AP, Lilenbaum W. Genital bovine leptospirosis: a new look for an old disease. Theriogenology 141:41–47.
  20. Di Azevedo MIN, Lilenbaum W. Equine genital leptospirosis: evidence of an important silent chronic reproductive syndrome. Theriogenology 192:81–88.
  21. Gomes YA, Medeiros LS, Di Azevedo MIN, Loureiro AP, Loria de Melo J dos S, Carvalho-Costa FA, Lilenbaum W. Identification of vaginal Leptospira in cervical-vaginal mucus of slaughtered pigs in the Amazon region. Anim Reprod Sci 238:106930.
  22. Aymée L, Mendes J, Lilenbaum W. Bovine genital leptospirosis: an update of this important reproductive disease. Animals (Basel) 14:322.
    doi: 10.3390/ani14020322pmc: PMC10812666pubmed: 38275782google scholar: lookup
  23. Borges AL dos SB, Aymée L, Carvalho-Costa FA, Lilenbaum W, Di Azevedo MIN. Molecular epidemiology of Leptospira spp. serogroup Sejroe associated with chronic bovine leptospirosis. Vet Microbiol 298:110238.
    doi: 10.1016/j.vetmic.2024.110238pubmed: 39216324google scholar: lookup
  24. Di Azevedo MIN, Kremer F, Ezepha C, Greco JPG, da Silva ICV, Bourhy P, Lilenbaum W. Comparative genomics of Leptospira santarosai reveals genomic adaptations in bovine genital strains. Front Microbiol 15:1517151.
    doi: 10.3389/fmicb.2024.1517151pmc: PMC11747425pubmed: 39839101google scholar: lookup
  25. 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 229:106255.
  26. Orjuela AG, Parra-Arango JL, Sarmiento-Rubiano LA. Bovine leptospirosis: effects on reproduction and an approach to research in Colombia. Trop Anim Health Prod 54:251.
    doi: 10.1007/s11250-022-03235-2pmc: PMC9360731pubmed: 35943610google scholar: lookup
  27. Ellis WA, Thiermann AB. Isolation of leptospires from the genital tracts of Iowa cows. Am J Vet Res 47:1694–1696.
    pubmed: 3752677
  28. Aymée L, Reis L, Soares AC, de Souza GN, Lilenbaum W. Detecting Leptospira spp. infection in cows by PCR: what is the best sample to test?. Theriogenology 231:154–159.
  29. Gonçalves DD, Pastre GB, Rey LMR, Fazoli KGZ, Silva LL da, Ferreira LR de P, Fritzen JTT, Chideroli RT, Durel L, Decuadro-Hansen G, Lourenço ELB, Piau Junior R, Barbosa LN, Pereira U de P, Santos IC dos. Leptospira spp. in naturally infected dairy cow from a Brazilian border region. Vector Borne Zoonotic Dis 21:864–869.
    doi: 10.1089/vbz.2021.0040pubmed: 34546095google scholar: lookup
  30. da Costa Barnabé NN, Soares RR, Barros DKS, Araújo Júnior JP, Malossi CD, Rodrigues Silva MLC, Brasil AW de L, da Costa DF, Higino SS dos S, Santos C de SAB, de Azevedo SS, Alves CJ. The role of transplacental infection in Leptospira spp. epidemiology in cattle in Caatinga Biome, Brazil. Microorganisms 12:1044.
  31. Pereira PV dos S, Di Azevedo MIN, Arashiro EKN, Watanabe YF, Correia LFL, Lilenbaum W, Souza-Fabjan JMG. The presence of Leptospira spp. in the follicular fluid of naturally infected cows affects the overall efficiency of the in vitro embryo production technique.. Anim Reprod Sci 266:107492.
  32. Pedrosa J, Ezepha C, Aymée L, Lilenbaum W. Cellular inflammatory response in the bovine uterus by Leptospira infection may be related to embryo death and subfertility.. Microb Pathog 185:106449.
    doi: 10.1016/j.micpath.2023.106449pubmed: 37972741google scholar: lookup
  33. Bielanski A, Surujballi O, Golsteyn Thomas E, Tanaka E. Sanitary status of oocytes and embryos collected from heifers experimentally exposed to Leptospira borgpetersenii serovar hardjobovis.. Anim Reprod Sci 54:65–73.
    doi: 10.1016/s0378-4320(98)00145-6pubmed: 9877053google scholar: lookup
  34. Loureiro AP, Pestana C, Medeiros MA, Lilenbaum W. High frequency of leptospiral vaginal carriers among slaughtered cows.. Anim Reprod Sci 178:50–54.
  35. Di Azevedo MIN, Pires BC, Libonati H, Pinto PS, Cardoso Barbosa LF, Carvalho-Costa FA, Lilenbaum W. Extra-renal bovine leptospirosis: molecular characterization of the Leptospira interrogans Sejroe serogroup on the uterus of non-pregnant cows.. Vet Microbiol 250:108869.
    doi: 10.1016/j.vetmic.2020.108869pubmed: 33010572google scholar: lookup
  36. Di Azevedo MIN, Pires BC, Barbosa LFC, Carvalho‐Costa FA, Lilenbaum W. Characterization of leptospiral DNA in the follicular fluid of non‐pregnant cows.. Vet Rec 188:e143.
    doi: 10.1002/vetr.143pubmed: 33960475google scholar: lookup
  37. dos Santos Pereira PV, Di Azevedo MIN, dos Santos Baptista Borges AL, Loureiro AP, Martins G, Carvalho-Costa FA, Souza-Fabjan JMG, Lilenbaum W. Bovine genital leptospirosis: evidence of ovarian infection by Leptospira interrogans.. Vet Microbiol 271:109489.
    doi: 10.1016/j.vetmic.2022.109489pubmed: 35738096google scholar: lookup
  38. Aymée L, Gregg WRR, Loureiro AP, Di Azevedo MIN, Pedrosa J de S, Melo J dos SL de, Carvalho-Costa FA, de Souza GN, Lilenbaum W. Bovine genital leptospirosis and reproductive disorders of live subfertile cows under field conditions.. Vet Microbiol 261:109213.
    doi: 10.1016/j.vetmic.2021.109213pubmed: 34481272google scholar: lookup
  39. Aymée L, Di Azevedo MIN, Borges AL dos SB, Carvalho-Costa FA, Lilenbaum W. Leptospira spp. strains associated with bovine genital leptospirosis (BGL).. Microb Pathog 173:105841.
    doi: 10.1016/j.micpath.2022.105841pubmed: 36309182google scholar: lookup
  40. Aymée L, Nogueira Di Azevedo MI, de Souza Pedrosa J, Loria de Melo J dos S, Carvalho-Costa FA, Lilenbaum W. The role of Leptospira santarosai serovar Guaricura as agent of bovine genital leptospirosis.. Vet Microbiol 268:109413.
    doi: 10.1016/j.vetmic.2022.109413pubmed: 35390628google scholar: lookup
  41. Barnabé NN da C, Soares RR, Barros DKS, Nogueira DB, Costa FTR da, Araújo Júnior JP, Malossi CD, Ullmann LS, Costa DF da, Silva MLCR, Higino SS dos S, Santos C de SAB, Azevedo SS de, Alves CJ. Bovine leptospirosis in Caatinga Biome, Brazil: new insights into diagnosis and epidemiology.. TropicalMed 8:177.
    doi: 10.3390/tropicalmed8030177pmc: PMC10053506pubmed: 36977178google scholar: lookup
  42. Loureiro AP, Martins G, Pinto P, Narduche L, Teixeira RC, Lilenbaum W. Usage of a selective media (EMJH-STAFF) in primary culturing of pathogenic leptospires from bovine clinical samples.. Lett Appl Microbiol 61:603–606.
    doi: 10.1111/lam.12501pubmed: 26408270google scholar: lookup
  43. Director A, Penna B, Hamond C, Loureiro AP, Martins G, Medeiros MA, Lilenbaum W. Isolation of Leptospira interrogans Hardjoprajitno from vaginal fluid of a clinically healthy ewe suggests potential for venereal transmission.. J Med Microbiol 63:1234–1236.
    doi: 10.1099/jmm.0.065466-0pubmed: 24934563google scholar: lookup
  44. Loureiro AP, Hamond C, Pinto P, Bremont S, Bourhy P, Lilenbaum W. Molecular analysis of leptospires from serogroup Sejroe obtained from asymptomatic cattle in Rio de Janeiro — Brazil reveals genetic proximity to serovar Guaricura.. Res Vet Sci 105:249–253.
    doi: 10.1016/j.rvsc.2016.02.012pubmed: 27033941google scholar: lookup
  45. da Silva JD, Viana MP, Lima Pereira Calado LG, César Lima AM, Fernandes Alves FS, Pinheiro RR, da Costa DF, Pinheiro da Silva GC, de Azevedo SS, Alves CJ. Cross-sectional survey for sheep leptospirosis in the northeast region of Brazil.. Prev Vet Med 197:105525.
  46. Gaytán-Camarillo F, Rico-Chávez O, Palomares-Resendiz EG, Gutiérrez-Hernández JL, Díaz-Aparicio E, Herrera-López E. Spatial autocorrelation and co-occurrence of six serovarieties of Leptospira in goat herds of the State of Guanajuato, Mexico. Braz J Microbiol 52:953–960.
    doi: 10.1007/s42770-021-00429-ypmc: PMC8105431pubmed: 33483895google scholar: lookup
  47. Guzman-Barragan BL, Martínez-Rodríguez LC, Tobón-Torreglosa JC, Tafur-Gómez GA. Seroprevalence and risk factors for Leptospira spp. in small ruminants of semi-arid zone in northeastern Colombia. Trop Anim Health Prod 54.
    doi: 10.1007/s11250-021-03019-0pubmed: 34893919google scholar: lookup
  48. Santos JC de A, de Vasconcelos IFF, Nogueira DB, Junior JPA, Malossi CD, Ullmann LS, Santos C de SAB, Alves CJ, Silva MLCR, de Azevedo SS. New insights on Leptospira sp. infection in ewes maintained in field semiarid conditions. Acta Trop 234:106610.
  49. Hamond C, Martins G, Bremont S, Medeiros MA, Bourhy P, Lilenbaum W. Predominance of Leptospira interrogans serovar Bratislava DNA in vaginal fluid of mares suggests sexual transmission of leptospirosis. Anim Reprod Sci 151:275–279.
  50. Hamond C, Pestana CP, Rocha-de-Souza CM, Cunha LER, Brandão FZ, Medeiros MA, Lilenbaum W. Presence of leptospires on genital tract of mares with reproductive problems. Vet Microbiol 179:264–269.
    doi: 10.1016/j.vetmic.2015.06.014pubmed: 26211968google scholar: lookup
  51. Aymée L, Dantas FTDR, Ezepha C, Motta D, Carvalho-Costa FA, Di Azevedo MIN, Lilenbaum W. Placental abnormalities associated with Leptospira interrogans infection in naturally infected mares. J Equine Vet Sci 138:105099.
    doi: 10.1016/j.jevs.2024.105099pubmed: 38763365google scholar: lookup
  52. Alayil AL, Horwood PF, Gummow B, Picard JA, Joone CJ. Leptospiral infection in domestic mares in North Queensland. Aust Veterinary J 103:63–65.
    doi: 10.1111/avj.13395pubmed: 39611368google scholar: lookup
  53. Strutzberg-Minder K, Tschentscher A, Beyerbach M, Homuth M, Kreienbrock L. Passive surveillance of Leptospira infection in swine in Germany. Porc Health Manag 4:10.
    doi: 10.1186/s40813-018-0086-5pmc: PMC5872537pubmed: 29610674google scholar: lookup
  54. Ellis WA, Thiermann AB. Isolation of Leptospira interrogans serovar bratislava from sows in Iowa. Am J Vet Res 47:1458–1460.
    pubmed: 3740615
  55. Ellis WA, McParland PJ, Bryson DG, Thiermann AB, Montgomery J. Isolation of leptospires from the genital tract and kidneys of aborted sows. Veterinary Record 118:294–295.
    doi: 10.1136/vr.118.11.294pubmed: 3705357google scholar: lookup
  56. Bolin CA, Cassells JA. Isolation of Leptospira interrogans serovars bratislava and hardjo from swine at slaughter. J Vet Diagn Invest 4:87–89.
    doi: 10.1177/104063879200400121pubmed: 1554777google scholar: lookup
  57. Miraglia F, Moreno AM, Gomes CR, Paixão R, Liuson E, Morais ZM, Maiorka P, Seixas FK, Dellagostin OA, Vasconcellos SA. Isolation and characterization of Leptospira interrogans from pigs slaughtered in São Paulo State, Brazil. Braz J Microbiol 39:501–507.
  58. Ramos ACF, Souza GN, Lilenbaum W. Influence of leptospirosis on reproductive performance of sows in Brazil. Theriogenology 66:1021–1025.
  59. Terayama Y, Maeda M, Hata Y, Kawasaki Y, Koizumi N. A probable cluster of premature birth and stillbirth caused by Leptospira interrogans serogroup Hebdomadis in an integrated swine farm in Nagasaki Prefecture, Japan. J Vet Med Sci 86:1040–1044.
    doi: 10.1292/jvms.24-0215pmc: PMC11442401pubmed: 39111848google scholar: lookup
  60. Diaz EA, Luna L, Burgos-Mayorga A, Donoso G, Guzman DA, Baquero MI, Pearson T, Barragan VA. First detection of Leptospira santarosai in the reproductive track of a boar: a potential threat to swine production and public health. PLoS One 17:e0274362.
  61. Chinchilla D, Nieves C, Gutiérrez R, Sordoillet V, Veyrier FJ, Picardeau M. Phylogenomics of Leptospira santarosai, a prevalent pathogenic species in the Americas.. PLoS Negl Trop Dis 17:e0011733.
  62. Deka RP, Magnusson U, Grace D, Lindahl J. Bovine brucellosis: prevalence, risk factors, economic cost and control options with particular reference to India- a review.. Infect Ecol Epidemiol 8:1556548.
  63. Bradley EA, Lockaby G. Leptospirosis and the environment: a review and future directions.. Pathogens 12:1167.
    doi: 10.3390/pathogens12091167pmc: PMC10538202pubmed: 37764975google scholar: lookup
  64. Martins G, Lilenbaum W. Control of bovine leptospirosis: aspects for consideration in a tropical environment.. Res Vet Sci 112:156–160.
    doi: 10.1016/j.rvsc.2017.03.021pubmed: 28391058google scholar: lookup
  65. Alt DP, Zuerner RL, Bolin CA. Evaluation of antibiotics for treatment of cattle infected with Leptospira borgpetersenii serovar hardjo.. J Am Vet Med Assoc 219:636–639.
    doi: 10.2460/javma.2001.219.636pubmed: 11549093google scholar: lookup
  66. Regassa AG, Obsu LL. The role of asymptomatic cattle for leptospirosis dynamics in a herd with imperfect vaccination.. Sci Rep 14:23775.
    doi: 10.1038/s41598-024-72613-7pmc: PMC11467461pubmed: 39390012google scholar: lookup
  67. de Oliveira NR, Santos FDS, dos Santos VAC, Maia MAC, Oliveira TL, Dellagostin OA. Challenges and strategies for developing recombinant vaccines against leptospirosis: role of expression platforms and adjuvants in achieving protective efficacy.. Pathogens 12:787.
    doi: 10.3390/pathogens12060787pmc: PMC10305058pubmed: 37375478google scholar: lookup
  68. WOAH. Manual of diagnostic tests and vaccines for terrestrial animals.. 12th ed. World Organization for Animal Health, Paris.
  69. Asoh T, Miyahara S, Villanueva S, Kanemaru T, Takigawa T, Mori H, Gloriani NG, Yoshida S-I, Saito M. Protective role of stratum corneum in percutaneous Leptospira infection in a hamster model.. Microb Pathog 182:106243.
    doi: 10.1016/j.micpath.2023.106243pubmed: 37422175google scholar: lookup
  70. Nakamura S. Motility of the zoonotic spirochete Leptospira: insight into association with pathogenicity.. Int J Mol Sci 23:1859.
    doi: 10.3390/ijms23031859pmc: PMC8837006pubmed: 35163781google scholar: lookup
  71. Surdel MC, Coburn J. Leptospiral adhesins: from identification to future perspectives.. Front Microbiol 15:1458655.
    doi: 10.3389/fmicb.2024.1458655pmc: PMC11350617pubmed: 39206373google scholar: lookup
  72. Monti G, Montes V, Tortosa P, Tejeda C, Salgado M. Urine shedding patterns of pathogenic Leptospira spp. in dairy cows.. Vet Res 54:64.
    doi: 10.1186/s13567-023-01190-wpmc: PMC10391894pubmed: 37525220google scholar: lookup
  73. Dhaliwal GS, Murray RD, Dobson H, Montgomery J, Ellis WA. Presence of antigen and antibodies in serum and genital discharges of cows from dairy herds naturally infected with Leptospira interrogans serovar hardjo.. Res Vet Sci 60:163–167.
    doi: 10.1016/S0034-5288(96)90012-0pubmed: 8685539google scholar: lookup
  74. Hamond C, LeCount K, Putz EJ, Bayles DO, Camp P, Goris MGA, van der Linden H, Stone NE, Schlater LK, Sahl JW, Wagner DM, Nally JE. Bovine leptospirosis due to persistent renal carriage of Leptospira borgpetersenii serovar Tarassovi.. Front Vet Sci 9:848664.
    doi: 10.3389/fvets.2022.848664pmc: PMC9019706pubmed: 35464389google scholar: lookup
  75. Guedes IB, Souza GO de, Rocha K de S, Cavalini MB, Damasceno Neto MS, Castro JF de P, Souza Filho AF de, Negrão MP, Cortez A, Moraes CCG de, Heinemann MB. Leptospira strains isolated from cattle in the Amazon region, Brazil, evidence of a variety of species and serogroups with a high frequency of the Sejroe serogroup.. Comp Immunol Microbiol Infect Dis 74:101579.
    doi: 10.1016/j.cimid.2020.101579pubmed: 33246243google scholar: lookup
  76. Macchi MV, Suanes A, Salaberry X, Dearmas BE, Rivas E, Piaggio J, Gil AD. Leptospirosis as a cause of infertility in Uruguayan beef cattle. Prev Vet Med 228:106227.
  77. Ellis WA, Songer JG, Montgomery J, Cassells JA. Prevalence of Leptospira interrogans serovar hardjo in the genital and urinary tracts of non-pregnant cattle. Vet Rec 118:11–13.
    doi: 10.1136/vr.118.1.11pubmed: 3511601google scholar: lookup
  78. Bolin CA, Cassells JA, Zuerner RL, Trueba G. Effect of vaccination with a monovalent Leptospira interrogans serovar hardjo type hardjo-bovis vaccine on type hardjo-bovis infection of cattle. Am J Vet Res 52:1639–1643.
    doi: 10.2460/ajvr.1991.52.10.1639pubmed: 1767985google scholar: lookup
  79. Dhaliwaly GS, Murray RD, Dobson H, Montgomery J, Ellis WA, Baker JR. Presence of antigen and antibodies in serum and genital discharges of heifers after experimental intrauterine inoculation with Leptospira interrogans serovar hardjo. Res Vet Sci 60:157–162.
    doi: 10.1016/S0034-5288(96)90011-9pubmed: 8685538google scholar: lookup
  80. Cabral Pires B, Berzin Grapiglia J, Moreira L, Jaeger LH, Carvalho-Costa FA, Lilenbaum W. Occurrence of uterine carriers for Leptospira interrogans on slaughtered cows. Microb Pathog 114:163–165.
    doi: 10.1016/j.micpath.2017.11.056pubmed: 29197523google scholar: lookup
  81. Borges AL dos SB, Aymée L, Roussouliéres I, Carvalho-Costa FA, Di Azevedo MIN, Lilenbaum W. First isolation of Leptospira interrogans from follicular fluid of naturally infected cows. Vet Microbiol 305:110522.
    doi: 10.1016/j.vetmic.2025.110522pubmed: 40262237google scholar: lookup
  82. Pedrosa J, Ezepha C, Carvalho‐Costa FA, Di Azevedo MIN, Lilenbaum W. A neglected part of bovine genital leptospirosis: bulls. Reprod Domestic Animals 59:e14747.
    doi: 10.1111/rda.14747pubmed: 39582142google scholar: lookup
  83. Barnabé NNC, Soares RR, Nogueira DB, Araújo Júnior JP, Malossi CD, Costa DF, Silva M, Higino SSS, Azevedo SS, Alves CJ. Leptospirose genital bovina: achados em touros mantidos em condições do bioma Caatinga. Pesqui Veterinária Bras 43:e07376.
  84. Chávez-Sánchez JF, Galaviz-Silva L, Molina-Garza ZJ, Zapata-Benavides P, Cedillo-Rosales S, Elizondo-Luévano JH, Kačániová M, Ávalos-Ramírez R. Risk factors associated with the seroprevalence of leptospirosis in small ruminants from a semi-arid region of Mexico. Pathogens 14:344.
    doi: 10.3390/pathogens14040344pmc: PMC12030318pubmed: 40338267google scholar: lookup
  85. Lilenbaum W, Varges R, Brandão FZ, Cortez A, de Souza SO, Brandão PE, Richtzenhain LJ, Vasconcellos SA. Detection of Leptospira spp. in semen and vaginal fluids of goats and sheep by polymerase chain reaction. Theriogenology 69:837–842.
  86. Soares RR, Barnabé NN da C, Nogueira DB, da Silva LSC, Júnior JPA, Malossi CD, Ullmann LS, da Costa DF, Silva MLCR, dos Santos Higino SS, de Azevedo SS, Alves CJ. Serological, molecular and bacteriological approaches for detecting Leptospira sp. carrier rams maintained in semiarid conditions. Acta Trop 213:105759.
  87. Guadelupe B, Balaro MFA, Brandão FZ, Martins GM de S, Lilenbaum W. Streptomycin treatment of genital carriers of Leptospira in experimentally infected sheep on different estrous phases. Res Vet Sci 152:579–581.
    doi: 10.1016/j.rvsc.2022.09.027pubmed: 36201904google scholar: lookup
  88. 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 164:105020.
    doi: 10.1016/j.rvsc.2023.105020pubmed: 37738912google scholar: lookup
  89. Martins G, Guadelupe B, Aymée L, Balaro MFA, Pinto PH, Di Azevedo MIN, Brandão FZ, Lilenbaum W. The efficacy of vaccination in the prevention of renal and genital leptospirosis in experimentally infected sheep. TropicalMed 7:321.
    doi: 10.3390/tropicalmed7100321pmc: PMC9607635pubmed: 36288062google scholar: lookup
  90. Loria J, Reis L, Roussouliéres I, Pinto PHN, Balaro MFA, Lilenbaum W. Genital route in experimental infection, a promising approach to study genital leptospirosis in ruminants. Vet J 305:106127.
    doi: 10.1016/j.tvjl.2024.106127pubmed: 38710383google scholar: lookup
  91. Cilia G, Bertelloni F, Piredda I, Ponti MN, Turchi B, Cantile C, Parisi F, Pinzauti P, Armani A, Palmas B, Noworol M, Cerri D, Fratini F. 2020. Presence of pathogenic Leptospira spp. in the reproductive system and fetuses of wild boars (Sus scrofa) in Italy. PLoS Negl Trop Dis 14:e0008982. doi: 10.1371/journal.pntd.0008982
  92. Fernandes JJ, Araújo Júnior JP, Malossi CD, Ullmann LS, da Costa DF, Silva MLCR, Alves CJ, de Azevedo SS, Higino SS dos S. 2020. High frequency of seropositive and carriers of Leptospira spp. in pigs in the semiarid region of northeastern Brazil. Trop Anim Health Prod 52:2055–2061. doi: 10.1007/s11250-020-02203-y
    doi: 10.1007/s11250-020-02203-ypubmed: 32026195google scholar: lookup
  93. Wilson-Welder JH, Alt DP, Nally JE, Olsen SC. 2021. Bovine immune response to vaccination and infection with Leptospira borgpetersenii serovar hardjo. mSphere 6:e00988-20. doi: 10.1128/mSphere.00988-20
    doi: 10.1128/mSphere.00988-20pmc: PMC8546708pubmed: 33762318google scholar: lookup
  94. Picardeau M. 2020. Leptospira and leptospirosis. Methods Mol Biol 2134:271–275. doi: 10.1007/978-1-0716-0459-5_24
    doi: 10.1007/978-1-0716-0459-5_24pubmed: 32632877google scholar: lookup
  95. Mazzotta E, Ceglie L, Giurisato I, Bellinati L, Lucchese L, Marchione S, Natale A. 2021. Persistence of Leptospira borgpetersenii serovar hardjo in refrigerated raw milk: a transmission risk of leptospirosis to humans. Pathogens 10:291. doi: 10.3390/pathogens10030291
    doi: 10.3390/pathogens10030291pmc: PMC7998812pubmed: 33802583google scholar: lookup
  96. Goarant C, Girault D, Thibeaux R, Soupé-Gilbert M-E. 2020. Isolation and culture of Leptospira from clinical and environmental samples. Methods Mol Biol 2134:1–9. doi: 10.1007/978-1-0716-0459-5_1
    doi: 10.1007/978-1-0716-0459-5_1pubmed: 32632854google scholar: lookup
  97. Adler B, de la Peña Moctezuma A. 2010. Leptospira and leptospirosis. Vet Microbiol 140:287–296. doi: 10.1016/j.vetmic.2009.03.012
    doi: 10.1016/j.vetmic.2009.03.012pubmed: 19345023google scholar: lookup
  98. Pinto PS, Loureiro AP, Penna B, Lilenbaum W. 2015. Usage of Leptospira spp. local strains as antigens increases the sensitivity of the serodiagnosis of bovine leptospirosis. Acta Trop 149:163–167. doi: 10.1016/j.actatropica.2015.05.008
  99. Aymée L, Dos Santos Baptista Borges AL, de Souza GN, Lilenbaum W. 2024. Is microscopic agglutination test a reliable method for diagnosing the bovine genital leptospirosis syndrome? Vet Res Commun 48:4185–4189. doi: 10.1007/s11259-024-10560-4
    doi: 10.1007/s11259-024-10560-4pubmed: 39340735google scholar: lookup
  100. Soo ZMP, Khan NA, Siddiqui R. 2020. Leptospirosis: increasing importance in developing countries. Acta Trop 201:105183. doi: 10.1016/j.actatropica.2019.105183
  101. Di Azevedo MIN, Lilenbaum W. 2021. An overview on the molecular diagnosis of animal leptospirosis. Lett Appl Microbiol 72:496–508. doi: 10.1111/lam.13442
    doi: 10.1111/lam.13442pubmed: 33332656google scholar: lookup
  102. Kakita T, Kuba Y, Kyan H, Okano S, Morita M, Koizumi N. 2021. Molecular and serological epidemiology of Leptospira infection in cats in Okinawa Island, Japan. Sci Rep 11:10365. doi: 10.1038/s41598-021-89872-3
    doi: 10.1038/s41598-021-89872-3pmc: PMC8121857pubmed: 33990653google scholar: lookup
  103. Radyuk EV, Breneva NV, Budaeva SE, Makenov MT, Stukolova OА, Bulanenko VP, Le LAT, Dao MN, Nguyen CV, Bui Thi NT, Luong MT, Nguyen TN, Balakhonov SV, Karan LS. 2024. Leptospira infection in bats in Vietnam. Acta Trop 257:107298. doi: 10.1016/j.actatropica.2024.107298
  104. Haake DA, Levett PN. 2015. Leptospirosis in humans. Curr Top Microbiol Immunol 387:65–97. doi: 10.1007/978-3-662-45059-8_5
    doi: 10.1007/978-3-662-45059-8_5pmc: PMC4442676pubmed: 25388133google scholar: lookup
  105. Nally JE, Hornsby RL, Alt DP, Bayles D, Wilson-Welder JH, Palmquist DE, Bauer NE. 2018. Isolation and characterization of pathogenic leptospires associated with cattle. Vet Microbiol 218:25–30. doi: 10.1016/j.vetmic.2018.03.023
    doi: 10.1016/j.vetmic.2018.03.023pubmed: 29685217google scholar: lookup
  106. Philip N, Garba B, Neela VK. 2018. Long-term preservation of Leptospira spp.: challenges and prospects. Appl Microbiol Biotechnol 102:5427–5435. doi: 10.1007/s00253-018-9047-9
    doi: 10.1007/s00253-018-9047-9pubmed: 29736823google scholar: lookup
  107. Marquez A, Djelouadji Z, Lattard V, Kodjo A. 2017. Overview of laboratory methods to diagnose leptospirosis and to identify and to type leptospires. Int Microbiol 20:184–193. doi: 10.2436/20.1501.01.302
    doi: 10.2436/20.1501.01.302pubmed: 29529330google scholar: lookup
  108. Pinhata JMW, Blanco RM, Romero EC. 2018. Evaluation of inhibitors for development of a selective medium for isolation of Leptospira spp. from clinical samples. Lett Appl Microbiol 66:558–564. doi: 10.1111/lam.12887
    doi: 10.1111/lam.12887pubmed: 29575146google scholar: lookup
  109. Steinparzer R, Mair T, Unterweger C, Steinrigl A, Schmoll F. 2021. Influence of selective agents (EMJH-STAFF), sample filtration and pH on Leptospira interrogans serovar icterohaemorrhagiae cultivation and isolation from swine urine. Vet Sci 8:90. doi: 10.3390/vetsci8060090
    doi: 10.3390/vetsci8060090pmc: PMC8226611pubmed: 34070655google scholar: lookup
  110. Guedes IB, de Souza Rocha K, Negrão MP, de Souza GO, de Paula Castro JF, Cavalini MB, de Souza Filho AF, Neto MSD, Aizawa J, de Moraes CCG, Heinemann MB. 2020. Leptospira transport medium (LTM): a practical tool for leptospires isolation. J Microbiol Methods 175:105995. doi: 10.1016/j.mimet.2020.105995
    doi: 10.1016/j.mimet.2020.105995pubmed: 32593629google scholar: lookup
  111. Mendes J, Aymée L, Lilenbaum W. 2025. A scoping review of antimicrobial therapy in Leptospira infections in domestic animals. Animals (Basel) 15:3045. doi: 10.3390/ani15203045
    doi: 10.3390/ani15203045pmc: PMC12561877pubmed: 41153972google scholar: lookup

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    doi: 10.1007/s12602-026-10949-4pubmed: 41801646google scholar: lookup