Analyze Diet
BMC veterinary research2019; 15(1); 175; doi: 10.1186/s12917-019-1916-7

Histopathological lesions in reproductive organs, distal spinal cord and peripheral nerves of horses naturally infected with Trypanosoma equiperdum.

Abstract: Dourine, a venereal transmitted trypanosomosis caused by Trypanosoma equiperdum, has different clinical signs related to the reproductive and nervous system. Pathologic tissue changes associated with the disease are poorly described. The present study describes the histopathological lesions in naturally T. equiperdum-infected horses in the chronical stage of dourine. Results: Four chronically dourine diseased horses underwent a post-mortem examination. They were Woo test negative, but CATT/T. evansi positive, had a low packed cell volume (PCV) and exhibited obvious clinical signs of dourine. Post-mortem examination did not reveal gross lesions in the organs assumed to be responsible for the symptomatology. On histopathology, genital organs were affected, with mononuclear cell infiltration and erosions and degeneration of seminiferous tubules and perivascular lymphoplasmacytic cuffing in the uterus. In the nervous system, mononuclear cell infiltration was located in peripheral nerves, ganglia and in the spinal cord, leading to axonal degeneration. Real-time PCR using ITS primer revealed the presence of trypanosomes in these organs and conventional PCRs using maxicircle and RoTat1.2 primers further confirmed the involvement of T. equiperdum since the DNAs from the vagina, testicle, distal spinal cord, sciatic and obturator nerves found to be positive for maxicircle and negative for RoTat 1.2. Conclusions: The histopathological lesions in the spinal cord and peripheral nerves explain the incoordination of the hind legs in T. equiperdum-infected horses, whilst its presence in the genital tract exemplifies the venereal transmission.
Publication Date: 2019-05-28 PubMed ID: 31138270PubMed Central: PMC6537221DOI: 10.1186/s12917-019-1916-7Google 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.

This research article presents a study into the effects of a disease, caused by Trypanosoma equiperdum, on the reproductive organs and nervous system of horses. The study dives into the specific histopathological changes caused by the infection and reports the presence of this parasite in the spinal cord, peripheral nerves, and genital system of infected horses.

Research Context and Objectives

  • The article discusses dourine, a venereal disease in horses caused by Trypanosoma equiperdum – a parasite transmitted through mating.
  • This disease affects the horse’s nervous and reproductive systems, yet the specific tissue changes triggered by this disease are poorly understood.
  • The objective of the study was to explore the histopathological (tissue-level) lesions present in naturally infected horses during the chronic stage of the disease.

Methodology and Results

  • Four horses chronically infected with dourine were subjected to a post-mortem examination.
  • These horses were negative for Woo test, positive for CATT/T. evansi test, had a low packed cell volume (PCV), and displayed clear symptoms of dourine.
  • No gross lesions were detected in the post-mortem check of the organs associated with the disease’s symptoms.
  • However, histopathology showed that the genital organs were indeed affected, evidenced by mononuclear cell infiltration, degeneration of seminiferous tubules, and perivascular lymphoplasmacytic cuffing in the uterus.
  • Mononuclear cells were also found in peripheral nerves, ganglia, and the spinal cord, leading to axonal degeneration.
  • Real-time PCR tests using an ITS primer detected trypanosomes in these organs and conventional PCRs using maxicircle and RoTat1.2 primers further confirmed the presence of T. equiperdum as the DNAs from various organs turned out to be positive for maxicircle and negative for RoTat 1.2.

Conclusions

  • The study concluded that the histopathological lesions found in the horses’ spinal cord and peripheral nerves explain the incoordination of the hind legs in T. equiperdum-infected horses.
  • The presence of the parasite in the genital tract substantiates its venereal route of transmission.

Cite This Article

APA
Yasine A, Ashenafi H, Geldhof P, Van Brantegem L, Vercauteren G, Bekana M, Tola A, Van Soom A, Duchateau L, Goddeeris B, Govaere J. (2019). Histopathological lesions in reproductive organs, distal spinal cord and peripheral nerves of horses naturally infected with Trypanosoma equiperdum. BMC Vet Res, 15(1), 175. https://doi.org/10.1186/s12917-019-1916-7

Publication

ISSN: 1746-6148
NlmUniqueID: 101249759
Country: England
Language: English
Volume: 15
Issue: 1
Pages: 175
PII: 175

Researcher Affiliations

Yasine, Ahmed
  • Wollo University, School of Veterinary Medicine, P.O Box 1145, Dessie, Ethiopia. yasineahmed11@gmail.com.
  • Addis Ababa University, College of Veterinary Medicine, P.O Box 34, Bishoftu, Ethiopia. yasineahmed11@gmail.com.
  • Ghent University, Faculty of Veterinary Medicine, 9820, Merelbeke, Belgium. yasineahmed11@gmail.com.
Ashenafi, Hagos
  • Addis Ababa University, College of Veterinary Medicine, P.O Box 34, Bishoftu, Ethiopia.
Geldhof, Peter
  • Ghent University, Faculty of Veterinary Medicine, 9820, Merelbeke, Belgium.
Van Brantegem, Leen
  • Ghent University, Faculty of Veterinary Medicine, 9820, Merelbeke, Belgium.
Vercauteren, Griet
  • Vet-Path bvba, 9991, Adegem, Belgium.
Bekana, Merga
  • Addis Ababa University, College of Veterinary Medicine, P.O Box 34, Bishoftu, Ethiopia.
Tola, Alemu
  • Addis Ababa University, College of Veterinary Medicine, P.O Box 34, Bishoftu, Ethiopia.
Van Soom, Ann
  • Ghent University, Faculty of Veterinary Medicine, 9820, Merelbeke, Belgium.
Duchateau, Luc
  • Ghent University, Faculty of Veterinary Medicine, 9820, Merelbeke, Belgium.
Goddeeris, Bruno
  • Ghent University, Faculty of Veterinary Medicine, 9820, Merelbeke, Belgium.
  • Katholieke Universiteit Leuven, Faculty of Bioscience Engineering, 3001, Heverlee, Belgium.
Govaere, Jan
  • Ghent University, Faculty of Veterinary Medicine, 9820, Merelbeke, Belgium.

MeSH Terms

  • Animals
  • Dourine / parasitology
  • Dourine / pathology
  • Female
  • Horse Diseases / parasitology
  • Horse Diseases / pathology
  • Horses
  • Male
  • Peripheral Nervous System Diseases / parasitology
  • Peripheral Nervous System Diseases / pathology
  • Peripheral Nervous System Diseases / veterinary
  • Polymerase Chain Reaction
  • Reproductive Tract Infections / parasitology
  • Reproductive Tract Infections / pathology
  • Reproductive Tract Infections / veterinary
  • Seminiferous Tubules / parasitology
  • Seminiferous Tubules / pathology
  • Spinal Cord / parasitology
  • Spinal Cord / pathology
  • Trypanosoma / isolation & purification
  • Uterus / parasitology
  • Uterus / pathology

Grant Funding

  • VLIR (TEAM ZEIN2013PR393), / Flemish Inter-University Council-University Development Cooperation (VLIR-UOS).

Conflict of Interest Statement

The authors declare that they have no competing interests.

References

This article includes 58 references
  1. CSA . Agricultural sample survey report on livestock and livestock characteristics, volume II, Statistical bulletin 585 Addis Ababa, Ethiopia. 2017. pp. 16–20.
  2. Swann WJ. Improving the welfare of working equine animals in developing countries. Appl Anim Behav Sci 2006;100:148–151.
  3. Guyo S, Legesse S, Tonamo A. A review on welfare and management practices of working equines. Glob J Anim Sc Livers Prod Anim Breed 2015;3:203–209.
  4. Van Dijk L, Duguma BE, Hernández Gil M, Marcoppido G, Ochieng F, Schlechter P, Starkey P, Wanga C, Zanella A. Role, impact and welfare of working (traction and transport) animals. FAO Animal Production and Health Report (FAO) eng no 5. 2014.
  5. Stringer A, Lunn DP, Reid S. Science in brief: Report on the first Havemeyer workshop on infectious diseases in working equids, Addis Ababa, Ethiopia, November 2013.. Equine Vet J 2015 Jan;47(1):6-9.
    doi: 10.1111/evj.12359pubmed: 25257182google scholar: lookup
  6. Alemu T, Luckins AG, Phipps LP, Reid SW, Holmes PH. The use of enzyme linked immunosorbent assays to investigate the prevalence of Trypanosoma equiperdum in Ethiopian horses.. Vet Parasitol 1997 Aug;71(4):239-50.
    doi: 10.1016/S0304-4017(96)01139-9pubmed: 9299693google scholar: lookup
  7. Hagos A, Abebe G, Büscher P, Goddeeris BM, Claes F. Serological and parasitological survey of dourine in the Arsi-Bale highlands of Ethiopia.. Trop Anim Health Prod 2010 Apr;42(4):769-76.
    doi: 10.1007/s11250-009-9485-6pubmed: 19924557google scholar: lookup
  8. Hagos A, Degefa G, Yacob H, Fikru R, Alemu T, Feseha G, Claes F, Goddeeris BM. Seroepidemiological survey of trypanozoon infection in horses in the suspected dourine-infected Bale highlands of the Oromia region, Ethiopia.. Rev Sci Tech 2010 Dec;29(3):649-54.
    doi: 10.20506/rst.29.3.2005pubmed: 21309462google scholar: lookup
  9. Gari FR, Ashenafi H, Tola A, Goddeeris BM, Claes F. Comparative diagnosis of parasitological, serological, and molecular tests in dourine-suspected horses.. Trop Anim Health Prod 2010 Dec;42(8):1649-54.
    doi: 10.1007/s11250-010-9615-1pubmed: 20526860google scholar: lookup
  10. OIE. OIE Terrestrial Manual Version adopted by the World Assembly of Delegates of the OIE in May 2013. OIE Paris; 2013. Dourine, Chapter 2.5.3; pp. 1–6.
  11. Vulpiani MP, Carvelli A, Giansante D, Iannino F, Paganico D, Ferri N. Reemergence of dourine in Italy: clinical cases in some positive horses. J Equine Vet Sci 2013;33:468–474.
  12. Clausen PH, Gebreselassie G, Abditcho S, Mehlitz D, Staak C. Detection of trypanosome DNA in serologically positive but aparasitaemic horses suspected of dourine in Ethiopia.. Tokai J Exp Clin Med 1998 Dec;23(6):303-8.
    pubmed: 10622626
  13. Clausen PH, Chuluun S, Sodnomdarjaa R, Greiner M, Noeckler K, Staak C, Zessin KH, Schein E. A field study to estimate the prevalence of Trypanosoma equiperdum in Mongolian horses.. Vet Parasitol 2003 Jul 10;115(1):9-18.
    doi: 10.1016/S0304-4017(03)00160-2pubmed: 12860063google scholar: lookup
  14. Ahmed Y, Hagos A, Merga B, Van Soom A, Duchateau L, Goddeeris BM, Govaer J. Trypanosoma equiperdum in the horse-a neglected threat?. Vlaams Diergeneeskd Tijdschr 2018. pp. 66–75.
  15. Barrowman PR. Observations on the transmission, immunology, clinical signs and chemotherapy of dourine (Trypanosoma equiperdum infection) in horses, with special reference to cerebro-spinal fluid.. Onderstepoort J Vet Res 1976 Jun;43(2):55-66.
    pubmed: 1018890
  16. Scacchia M, Cammà C, Di Francesco G, Di Provvido A, Giunta R, Luciani M, Marino AM, Pascucci I, Caporale V. A clinical case of dourine in an outbreak in Italy.. Vet Ital 2011 Oct-Dec;47(4):473-5, 469-72.
    pubmed: 22194229
  17. Pascucci I, Di Provvido A, Cammà C, Di Francesco G, Calistri P, Tittarelli M, Ferri N, Scacchia M, Caporale V. Diagnosis of dourine in outbreaks in Italy.. Vet Parasitol 2013 Mar 31;193(1-3):30-8.
    doi: 10.1016/j.vetpar.2012.12.006pubmed: 23298562google scholar: lookup
  18. Claes F, Agbo EC, Radwanska M, Te Pas MF, Baltz T, De Waal DT, Goddeeris BM, Claassen E, Büscher P. How does Trypanosoma equiperdum fit into the Trypanozoon group? A cluster analysis by RAPD and multiplex-endonuclease genotyping approach.. Parasitology 2003 May;126(Pt 5):425-31.
    doi: 10.1017/S0031182003002968pubmed: 12793646google scholar: lookup
  19. Stephen LE. Trypanosomiasis: a veterinary perspective. New York: Pergamon Press; 1986. pp. 351–420.
  20. Ricketts S, McGladdery A, Crowhurst J, Newton R. Dourine, an emerging venereal threat to European horses. Equine Quarterly Disease Surveillance report 2011. pp. 15–18.
  21. Zablotskij VT, Georgiu C, de Waal T, Clausen PH, Claes F, Touratier L. The current challenges of dourine: difficulties in differentiating Trypanosoma equiperdum within the subgenus Trypanozoon.. Rev Sci Tech 2003 Dec;22(3):1087-96.
    doi: 10.20506/rst.22.3.1460pubmed: 15005565google scholar: lookup
  22. Hagos A, Goddeeris BM, Yilkal K, Alemu T, Fikru R, Yacob HT, Feseha G, Claes F. Efficacy of Cymelarsan and Diminasan against Trypanosoma equiperdum infections in mice and horses.. Vet Parasitol 2010 Aug 4;171(3-4):200-6.
    doi: 10.1016/j.vetpar.2010.03.041pubmed: 20417035google scholar: lookup
  23. Suganuma K, Narantsatsral S, Battur B, Yamasaki S, Otgonsuren D, Musinguzi SP, Davaasuren B, Battsetseg B, Inoue N. Isolation, cultivation and molecular characterization of a new Trypanosoma equiperdum strain in Mongolia.. Parasit Vectors 2016 Aug 31;9(1):481.
    doi: 10.1186/s13071-016-1755-3pmc: PMC5007690pubmed: 27580944google scholar: lookup
  24. Ahmed Y, Hagos A, Merga B, Alemu T, Van Soom A, Duchateau L, Goddeeris B, Govaere J. Infectiousness of equine semen in the prepatent phase of dourine. Reprod Dom Anim 2017;52(Suppl 3):66.
  25. Desquesnes M, Bosseno MF, Brenière SF. Detection of Chagas infections using Trypanosoma evansi crude antigen demonstrates high cross-reactions with Trypanosoma cruzi.. Infect Genet Evol 2007 Jul;7(4):457-62.
    doi: 10.1016/j.meegid.2007.01.007pubmed: 17337255google scholar: lookup
  26. Fikru R, Goddeeris BM, Delespaux V, Moti Y, Tadesse A, Bekana M, Claes F, De Deken R, Büscher P. Widespread occurrence of Trypanosoma vivax in bovines of tsetse- as well as non-tsetse-infested regions of Ethiopia: a reason for concern?. Vet Parasitol 2012 Dec 21;190(3-4):355-61.
    doi: 10.1016/j.vetpar.2012.07.010pubmed: 22858227google scholar: lookup
  27. Njiru ZK, Constantine CC, Guya S, Crowther J, Kiragu JM, Thompson RC, Dávila AM. The use of ITS1 rDNA PCR in detecting pathogenic African trypanosomes.. Parasitol Res 2005 Feb;95(3):186-92.
    doi: 10.1007/s00436-004-1267-5pubmed: 15619129google scholar: lookup
  28. Birhanu H, Gebrehiwot T, Goddeeris BM, Büscher P, Van Reet N. New Trypanosoma evansi Type B Isolates from Ethiopian Dromedary Camels.. PLoS Negl Trop Dis 2016 Apr;10(4):e0004556.
  29. Claes F, Verloo D, De Waal DT, Urakawa T, Majiwa P, Goddeeris BM, Buscher P. Expression of RoTat 1.2 cross-reactive variable antigen type in Trypanosoma evansi and T. equiperdum.. Ann N Y Acad Sci 2002 Oct;969:174-9.
  30. Birhanu H, Fikru R, Said M, Kidane W, Gebrehiwot T, Hagos A, Alemu T, Dawit T, Berkvens D, Goddeeris BM, Büscher P. Epidemiology of Trypanosoma evansi and Trypanosoma vivax in domestic animals from selected districts of Tigray and Afar regions, Northern Ethiopia.. Parasit Vectors 2015 Apr 9;8:212.
    pmc: PMC4403896pubmed: 25889702doi: 10.1186/s13071-015-0818-1google scholar: lookup
  31. Abebe G. Trypanosomosis in Ethiopia. Ethiop. J Biol Sci 2005;4:75–121.
  32. Dagnachew S, Bezie M, Terefe G, Abebe G, Barry JD, Goddeeris BM. Comparative clinico-haematological analysis in young Zebu cattle experimentally infected with Trypanosoma vivax isolates from tsetse infested and non-tsetse infested areas of Northwest Ethiopia.. Acta Vet Scand 2015 May 19;57(1):24.
    doi: 10.1186/s13028-015-0114-2pmc: PMC4450476pubmed: 25986858google scholar: lookup
  33. Dagnatchew Z. Trypanosomiasis in Ethiopia. International Symposia on Veterinary Epidemiology and Economics proceedings, ISVEE 3: Veterinary epidemiology and economics, proceedings of the 3rd international symposium Arlington, Virginia, USA; 1982. p. 467–73.
  34. Abebe G, Yilma J. Trypanosomosis: a threat to cattle production in Ethiopia. Rev Med Vet 1996;147:897–902.
  35. Hadush AB. Trypanosoma evansi in northern Ethiopia: epidemiology, diversity and alternative diagnostics (doctoral dissertation, KU Leuven). 2016.
  36. Mungun-Ochir B, Horiuchi N, Altanchimeg A, Koyama K, Suganuma K, Nyamdolgor U, Watanabe KI, Baatarjargal P, Mizushima D, Battur B, Yokoyama N, Battsetseg B, Inoue N, Kobayashi Y. Polyradiculoneuropathy in dourine-affected horses.. Neuromuscul Disord 2019 Jun;29(6):437-443.
    pubmed: 31101461doi: 10.1016/j.nmd.2019.03.005google scholar: lookup
  37. Seiler RJ, Omar S, Jackson AR. Meningoencephalitis in naturally occurring Trypanosoma evansi infection (surra) of horses.. Vet Pathol 1981 Jan;18(1):120-2.
    doi: 10.1177/030098588101800114pubmed: 7467062google scholar: lookup
  38. Rodrigues A, Fighera RA, Souza TM, Schild AL, Barros CS. Neuropathology of naturally occurring Trypanosoma evansi infection of horses.. Vet Pathol 2009 Mar;46(2):251-8.
    doi: 10.1354/vp.46-2-251pubmed: 19261636google scholar: lookup
  39. Losos GJ, Ikede BO. Review of pathology of diseases in domestic and laboratory animals caused by Trypanosoma congolense, T. vivax, T. brucei, T. rhodesiense and T. gambiense. Vet Pathol 1972;9(suppl 1):1–79.
  40. Kingston D, Rodgers J, Sharpe S, Berman K, Morrison L, Kenned P, Bradley B, Sutton DGM. Equine central nervous system trypanosomosis in the Gambia is caused by genetically diverse populations of Trypanosoma brucei parasites. J Equine Vet Sci 2016;39:S100–S101.
  41. Natalini CC. Spinal anesthetics and analgesics in the horse.. Vet Clin North Am Equine Pract 2010 Dec;26(3):551-64.
    pubmed: 21056299doi: 10.1016/j.cveq.2010.07.005google scholar: lookup
  42. Gizaw Y, Megersa M, Fayera T. Dourine: a neglected disease of equids.. Trop Anim Health Prod 2017 Jun;49(5):887-897.
    doi: 10.1007/s11250-017-1280-1pmc: PMC5432633pubmed: 28439783google scholar: lookup
  43. Myers RK, Mc Gavin MD. Cellular and Tissue Responses to Injury. In: McGavin MD, Zachary JF, editors. Pathologic Basis of Veterinary Disease. Fourth. St. Louis: Mosby Elsevier; 2006. pp. 3–59.
  44. Blanchard TL, Kenney RM, Timoney PJ. Venereal disease.. Vet Clin North Am Equine Pract 1992 Apr;8(1):191-203.
    doi: 10.1016/S0749-0739(17)30475-3pubmed: 1315616google scholar: lookup
  45. Jones TC, Hunt RD, King NW. Veterinary pathology. 6th ed. Baltimore: Williams and Wilkins; 1997. p. 177–96.
  46. Whitwell K. Post-mortem examination of horses. In Practice 2009;31:104–113.
    doi: 10.1136/inpract.31.3.104google scholar: lookup
  47. Slaoui M, Fiette L. Histopathology procedures: from tissue sampling to histopathological evaluation.. Methods Mol Biol 2011;691:69-82.
    pubmed: 20972747doi: 10.1007/978-1-60761-849-2_4google scholar: lookup
  48. KLUVER H, BARRERA E. A method for the combined staining of cells and fibers in the nervous system.. J Neuropathol Exp Neurol 1953 Oct;12(4):400-3.
  49. Woo PT. The haematocrit centrifuge technique for the diagnosis of African trypanosomiasis.. Acta Trop 1970;27(4):384-6.
    pubmed: 4396363
  50. Reid SA, Husein A, Copeman DB. Evaluation and improvement of parasitological tests for Trypanosoma evansi infection.. Vet Parasitol 2001 Dec 28;102(4):291-7.
    doi: 10.1016/S0304-4017(01)00539-8pubmed: 11731072google scholar: lookup
  51. Claes F, Verloo D, De Waal DT, Majiwa PA, Baltz T, Goddeeris BM, Büscher P. The expression of RoTat 1.2 variable surface glycoprotein (VSG) in Trypanosoma evansi and T. equiperdum.. Vet Parasitol 2003 Oct 20;116(3):209-16.
    doi: 10.1016/S0304-4017(02)00359-Xpubmed: 14559163google scholar: lookup
  52. Qiagen. DNeasy Blood and Tissue Handbook 07/2006. QIAGEN GmbH, QIAGEN Strasse 1, vol. 40724. Hilden; 2006.
  53. Yasine A, Daba M, Ashenafi H, Geldhof P, Van Brantegem L, Vercauteren G, Demissie T, Bekana M, Tola A, Van Soom A, Duchateau L, Goddeeris B, Govaere J. Tissue (re)distribution of Trypanosoma equiperdum in venereal infected and blood transfused horses.. Vet Parasitol 2019 Apr;268:87-97.
    doi: 10.1016/j.vetpar.2019.03.007pubmed: 30981311google scholar: lookup
  54. Brun R, Hecker H, Lun ZR. Trypanosoma evansi and T. equiperdum: distribution, biology, treatment and phylogenetic relationship (a review).. Vet Parasitol 1998 Oct;79(2):95-107.
    doi: 10.1016/S0304-4017(98)00146-0pubmed: 9806490google scholar: lookup
  55. Urakawa T, Verloo D, Moens L, Büscher P, Majiwa PA. Trypanosoma evansi: cloning and expression in Spodoptera frugiperda [correction of fugiperda] insect cells of the diagnostic antigen RoTat1.2.. Exp Parasitol 2001 Dec;99(4):181-9.
    doi: 10.1006/expr.2001.4670pubmed: 11888244google scholar: lookup
  56. Claes F, Radwanska M, Urakawa T, Majiwa PA, Goddeeris B, Büscher P. Variable Surface Glycoprotein RoTat 1.2 PCR as a specific diagnostic tool for the detection of Trypanosoma evansi infections.. Kinetoplastid Biol Dis 2004 Sep 17;3(1):3.
    doi: 10.1186/1475-9292-3-3pmc: PMC521498pubmed: 15377385google scholar: lookup
  57. Domingo GJ, Palazzo SS, Wang B, Pannicucci B, Salavati R, Stuart KD. Dyskinetoplastic Trypanosoma brucei contains functional editing complexes.. Eukaryot Cell 2003 Jun;2(3):569-77.
    doi: 10.1128/EC.2.3.569-577.2003pmc: PMC161453pubmed: 12796302google scholar: lookup
  58. Dean S, Gould MK, Dewar CE, Schnaufer AC. Single point mutations in ATP synthase compensate for mitochondrial genome loss in trypanosomes.. Proc Natl Acad Sci U S A 2013 Sep 3;110(36):14741-6.
    doi: 10.1073/pnas.1305404110pmc: PMC3767566pubmed: 23959897google scholar: lookup

Citations

This article has been cited 4 times.
  1. Abah KO, Ogwu D, Allam L, Obudu CE, Itodo JI, Sani NA. Genital lesions in cows naturally infected with trypanosomes in Abuja, Nigeria. Vet World 2021 May;14(5):1363-1370.
  2. Tanaka Y, Suganuma K, Watanabe K, Kobayashi Y. Pathology of female mice experimentally infected with an in vitro cultured strain of Trypanosoma equiperdum. J Vet Med Sci 2021 Aug 6;83(8):1212-1218.
    doi: 10.1292/jvms.21-0056pubmed: 34135196google scholar: lookup
  3. Rimayanti R, Khairullah AR, Mustofa I, Utomo B, Lestari TD, Utama S, Akintunde AO, Mulyati S, Hernawati T, Dawood AQ, Riady G, Khan IU, Rasad SD, Moses IB. Hidden menace: Understanding the devastating consequences of dourine disease in horses. Open Vet J 2025 Sep;15(9):3931-3942.
    doi: 10.5455/OVJ.2025.v15.i9.2pubmed: 41200335google scholar: lookup
  4. Hébert L, Froger D, Madeline A, Lecouturier F, Lemans C, Zientara S. European Inter-Laboratory Proficiency Test for Dourine Antibody Detection Using the Complement Fixation Test. Vet Sci 2023 Sep 26;10(10).
    doi: 10.3390/vetsci10100592pubmed: 37888544google scholar: lookup