Seroprevalence of Borrelia burgdorferi sensu lato and Anaplasma phagocytophilum Infections in German Horses.
Abstract: There are limited data on Lyme borreliosis (LB), a tick-borne disease caused by the Borrelia burgdorferi sensu lato complex, in horses. Seropositivity is not necessarily associated with clinical disease. Data on seropositivity against Borrelia burgdorferi and Anaplasma phagocytophilum in German horses are sparse. Therefore, serum samples from horses (n = 123) suspected of having Lyme borreliosis and clinically healthy horses (n = 113) from the same stables were tested for specific antibodies against Borrelia burgdorferi sensu lato and Anaplasma phagocytophilum. The samples were screened for antibodies against Borrelia burgdorferi (ELISA and an IgG line immunoblot assay). Furthermore, the samples were examined for antibodies against B. burgdorferi and Anaplasma phagocytophilum with a validated rapid in-house test (SNAP® 4Dx Plus® ELISA). The clinical signs of suspect horses included lameness (n = 36), poor performance (n = 19), and apathy (n = 12). Twenty-three percent (n = 26) of suspect horses and 17% (n = 18) of clinically healthy horses were seropositive for having a Borrelia burgdorferi sensu lato infection (p = 0.371), showing that the detection of specific antibodies against B. burgdorferi alone is not sufficient for a diagnosis of equine LB. Anaplasma phagocytophilum seropositivity and seropositivity against both pathogens was 20%/6% in suspect horses and 16%/2% in the clinically healthy population, showing only minor differences (p = 0.108). Unspecific testing for antibodies against B. burgdorferi without clinical suspicion of Lyme borreliosis is not recommended since the clinical relevance of seropositivity against Borrelia burgdorferi sensu lato remains to be elucidated.
Publication Date: 2023-06-14 PubMed ID: 37370494PubMed Central: PMC10295046DOI: 10.3390/ani13121984Google 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 study assesses the prevalence of Lyme borreliosis (LB) and Anaplasma phagocytophilum infections in German horses indicating that the presence of antibodies specific to these infections doesn’t guarantee a diagnosis of LB. The research reveals a minor difference in seropositivity between suspected and clinically healthy horses, advising against nonspecific tests for LB antibodies without clinical suspicion.
Overview of Methodology and Findings
- The study used blood samples from 123 horses suspected of having Lyme borreliosis (LB) and 113 from those clinically healthy but living in the same stables.
- These samples were subjected to two tests: an enzyme-linked immunoassay (ELISA) and an immunoglobulin G (IgG) line immunoblot assay. These are standard diagnostic tests used to identify specific antibodies against Borrelia burgdorferi sensu lato—the bacteria complex that causes LB—and Anaplasma phagocytophilum—another tick-borne bacteria that can infect horses.
- In addition to these, a validated rapid in-house test (SNAP 4Dx Plus ELISA) was also used. This test is particularly useful for identifying antibodies against both mentioned pathogens.
- Among the horses suspected of having LB, the most common symptoms were lameness, poor performance, and apathy.
- Interestingly, the research found that 23% of the suspect horses and 17% of the clinically healthy horses tested positive for Borrelia burgdorferi sensu lato infection. This presented a conclusion that the presence of specific antibodies alone is not sufficient to diagnose LB in horses.
- A similar insignificant difference was observed when testing for Anaplasma phagocytophilum, with the seropositivity in suspect horses being 20% and in healthy horses being 16%.
Implications of the Findings
- The study suggests that testing for antibodies against Borrelia burgdorferi sensu lato without clear clinical suspicion of LB is not recommended. This is due to the detected seropositivity even in clinically healthy horses.
- This implies that the clinical significance or consequences of seropositivity against this pathogen in horses is not definitively understood and remains to be clarified.
- The minor difference in seropositivity rates between suspect and healthy horses is another crucial point that needs further investigation. This result could either point to a high exposure rate in all horses or reflect the unspecific clinical presentation and failure to correctly identify affected horses.
Cite This Article
APA
Gehlen H, Inerle K, Bartel A, Stöckle SD, Ulrich S, Briese B, Straubinger RK.
(2023).
Seroprevalence of Borrelia burgdorferi sensu lato and Anaplasma phagocytophilum Infections in German Horses.
Animals (Basel), 13(12).
https://doi.org/10.3390/ani13121984 Publication
Researcher Affiliations
- Equine Clinic: Surgery and Radiology, Freie Universitaet Berlin, 14163 Berlin, Germany.
- Equine Clinic: Surgery and Radiology, Freie Universitaet Berlin, 14163 Berlin, Germany.
- Institute for Veterinary Epidemiology and Biostatistics, Freie Universitaet Berlin, 14163 Berlin, Germany.
- Equine Clinic: Surgery and Radiology, Freie Universitaet Berlin, 14163 Berlin, Germany.
- Chair of Bacteriology and Mycology, Department of Veterinary Sciences, Faculty of Veterinary Medicine, Institute for Infectious Diseases and Zoonosis, Ludwig-Maximilians-Universität, 85764 Oberschleißheim, Germany.
- Equine Clinic: Surgery and Radiology, Freie Universitaet Berlin, 14163 Berlin, Germany.
- Chair of Bacteriology and Mycology, Department of Veterinary Sciences, Faculty of Veterinary Medicine, Institute for Infectious Diseases and Zoonosis, Ludwig-Maximilians-Universität, 85764 Oberschleißheim, Germany.
Conflict of Interest Statement
The authors declare no conflict of interest.
References
This article includes 103 references
- Burgess E.C, Gillette D, Pickett J.P. Arthritis and panuveitis as manifestations of Borrelia burgdorferi infection in a Wisconsin pony. J. Am. Vet. Med. Assoc. 1986;189:1340–1342.
- Burgess E.C, Mattison M. Encephalitis associated with Borrelia burgdorferi infection in a horse. J. Am. Vet. Med. Assoc. 1987;191:1457–1458.
- Hahn C.N, Mayhew I.G, Whitwell K.E, Smith K.C, Carey D, Carter S.D, Read R.A. A possible case of Lyme borreliosis in a horse in the UK. Equine Vet. J. 1996;28:84–88.
- Karlsson M, Hovind-Hougen K, Svenungsson B, Stiernstedt G. Cultivation and characterization of spirochetes from cerebrospinal fluid of patients with Lyme borreliosis. J. Clin. Microbiol. 1990;28:473–479.
- Divers T.J, Gardner R.B, Madigan J.E, Witonsky S.G, Bertone J.J, Swinebroad E.L, Schutzer S.E, Johnson A.L. Borrelia burgdorferi Infection and Lyme Disease in North American Horses: A Consensus Statement. J. Vet. Intern. Med. 2018;32:617–632.
- Burgess B. Lyme Disease in horses. Can. Vet. J. 1988;29:393–394.
- Magnarelli L.A, Anderson J.F, Shaw E, Post J.E, Palka F.C. Borreliosis in equids in northeastern United States. Am. J. Vet. Res. 1988;49:359–362.
- Magnarelli L.A, Anderson J.F. Class-specific and polyvalent enzyme-linked immunosorbent assays for detection of antibodies to Borrelia burgdorferi in equids. J. Am. Vet. Med. Assoc. 1989;195:1365–1368.
- Browning A, Carter S.D, Barnes A, May C, Bennett D. Lameness associated with Borrelia burgdorferi infection in the horse. Vet. Rec. 1993;132:610–611.
- Liebisch G, Assmann G, Liebisch A. Infektion mit Borrelia burgdorferi sl als Krankheitsursache der Lyme-Borreliose bei Pferden in Deutschland. Prakt. Tierarzt. 1999;80:498–516.
- Manion T.B, Bushmich S.L, Khan M.I, Dinger J, Werner H, Mittel L, Laurendeau M, Reilly M. Suspected clinical Lyme disease in horses: Serological and antigen testing differences between clinically ill and clinically normal horses from an endemic region. J. Equine Vet. Sci. 2001;21:229–234.
- Durrani A.Z, Goyal S.M, Kamal N. Retrospective study on seroprevalence of Borrelia burgdorferi antibodies in horses in Minnesota. J. Equine Vet. Sci. 2011;31:427–429.
- Laus F, Veronesi F, Passamonti F, Paggi E, Cerquetella M, Hyatt D, Tesei B, Fioretti D.P. Prevalence of tick borne pathogens in horses from Italy. J. Vet. Med. Sci. 2013;75:715–720.
- Funk R, Pleasant R, Witonsky S, Reeder D, Werre S, Hodgson D. Seroprevalence of Borrelia burgdorferi in horses presented for Coggins testing in Southwest Virginia and change in positive test results approximately 1 year later. J. Vet. Intern. Med. 2016;30:1300–1304.
- Maloney E, Lindenmayer J. Seroprevalence and Clinical Signs of Lyme Disease in Cape Cod Horses. Equine Pract. 1992.
- Lindenmayer J, Weber M, Onderdonk A. Borrelia burgdorferi infection in horses. J. Am. Vet. Med. Assoc. 1989;194:1384.
- Marcus L, Patterson M, Gilfillan R, Urband P. Antibodies to Borrelia burgdorferi in New England horses: Serologic survey. Am. J. Vet. Res. 1985;46:2570–2571.
- Cohen D, Bosler E.M, Bernard W, Meirs D, Eisner R, Schulze T.L. Epidemiologic studies of Lyme disease in horses and their public health significance. Ann. N. Y. Acad. Sci. 1988;539:244–257.
- Bernard W, Cohen D, Bosler E, Zamos D. Serologic survey for Borrelia burgdorferi antibody in horses referred to a mid-Atlantic veterinary teaching hospital. J. Am. Vet. Med. Assoc. 1990;196:1255–1258.
- Cohen N, Heck F, Heim B, Flad D, Bosler E, Cohen D. Seroprevalence of antibodies to Borrelia burgdorferi in a population of horses in central Texas. J. Am. Vet. Med. Assoc. 1992;201:1030–1034.
- Käsbohrer A, Schönberg A. Serologische Untersuchungen zum Vorkommen von Borrelia burgdorferi bei Haustieren in Berlin (West). Berl. Munch. Tierarztl. Wochenschr. 1990;103:374–378.
- Tasai M, Takashima I, Kariwa H, Hashimoto N, Kondo T, Sugiura T, Kamada M. Serological survey of Lyme borreliosis in horses in Japan by immunofluorescent antibody test and fluorescent enzyme-linked immunosorbent assay. Bull. Equine Res. Inst. 1993;1993:37–42.
- Gerhards H, Wollanke B. Antibody titers against Borrelia in horses in serum and in eyes and occurrence of equine recurrent uveitis. Berl. Munch. Tierarztl. Wochenschr. 1996;109:273–278.
- Carter S, May C, Barnes A, Bennett D. Borrelia burgdorferi infection in UK horses. Equine Vet. J. 1994;26:187–190.
- Magnarelli L.A, IJdo J.W, Van Andel A.E, Wu C, Padula S.J, Fikrig E. Serologic confirmation of Ehrlichia equi and Borrelia burgdorferi infections in horses from the northeastern United States. J. Am. Vet. Med. Assoc. 2000;217:1045–1050.
- Štefančíková A, Štepánová G, Pet’ko B, Nadzamová D, Szestáková E, Škardová I, Leinstein R. Prevalence of antibodies to Borrelia burgdorferi in horses of East Slovakia. Vet. Med. 2000;45:227–231.
- Stefancikova A, Adaszek Ł, Pet’ko B, Winiarczyk S, Dudinak V. Serological evidence of Borrelia burgdorferi sensu lato in horses and cattle from Poland and diagnostic problems of Lyme borreliosis. Ann. Agric. Environ. Med. AAEM. 2008;15:37–43.
- Egenvall A, Franzén P, Gunnarsson A, Engvall E.O, Vågsholm I, Wikström U.-B, Artursson K. Cross-sectional study of the seroprevalence to Borrelia burgdorferi sensu lato and granulocytic Ehrlichia spp. and demographic, clinical and tick-exposure factors in Swedish horses. Prev. Vet. Med. 2001;49:191–208.
- Salinas-Mélendez J, de la Garza S.G, Riojas-Valdés V, González A.W, Avalos-Ramírez R. Antibody detection against Borrelia burgdorferi in horses located in the suburban areas of Monterrey, Nuevo León. Rev. Latinoam. Microbiol. 2001;43:161–164.
- Müller I, Khanakah G, Kundi M, Stanek G. Horses and Borrelia: Immunoblot patterns with five Borrelia burgdorferi sensu lato strains and sera from horses of various stud farms in Austria and from the Spanish Riding School in Vienna. Int. J. Med. Microbiol. 2002;291:80–87.
- Schoenert S, Grabner A, Heidrich J, Schoenberg A, Noeckler K, Bahn P, Luge E, Brem S, Mueller W. Lyme disease in the horse? Comparative studies of direct and indirect testing for Borrelia burgdorferi. Prakt. Tierarzt. 2002;83:1064–1068.
- Bhide M, Yilmaz Z, Golcu E, Torun S, Mikula I. Seroprevalence of anti-Borrelia burgdorferi antibodies in dogs and horses in Turkey. Ann. Agric. Environ. Med. 2008;15:85–90.
- Hansen M.G, Christoffersen M, Thuesen L.R, Petersen M.R, Bojesen A.M. Seroprevalence of Borrelia burgdorferi sensu lato and Anaplasma phagocytophilum in Danish horses. Acta Vet. Scand. 2010;52:1–6.
- Kiss T, Cadar D, Krupaci A.F, Bordeanu A, Brudaşcă G.F, Mihalca A.D, Mircean V, Gliga L, Dumitrache M.O, Spînu M. Serological reactivity to Borrelia burgdorferi sensu lato in dogs and horses from distinct areas in Romania. Vector-Borne Zoonotic Dis. 2011;11:1259–1262.
- Ebani V.V, Bertelloni F, Pinzauti P, Cerri D. Seroprevalence of Leptospira spp. and Borrelia burgdorferi sensu lato in Italian horses. Ann. Agric. Environ. Med. 2012;19:237–240.
- Veronesi F, Laus F, Passamonti F, Tesei B, Fioretti D.P, Genchi C. Occurrence of Borrelia lusitaniae infection in horses. Vet. Microbiol. 2012;160:535–538.
- Lee S.-H, Yun S.-H, Choi E, Park Y.-S, Lee S.-E, Cho G.-J, Kwon O.-D, Kwak D. Serological detection of Borrelia burgdorferi among horses in Korea. Korean J. Parasitol. 2016;54:97.
- Meersschaert C, Cerri S, Pitel P.-H, De Waele V, Hendrickx G, Amory H. Seroprevalence of Borrelia burgdorferi in horses in the southern part of Belgium: A “one health” driven study; Proceedings of the AESA Congress; Liege, Belgium. 7–9 September 2016.
- Craft J.E, Grodzicki R.L, Steere A.C. Antibody response in Lyme disease: Evaluation of diagnostic tests. J. Infect. Dis. 1984;149:789–795.
- Christen H.J, Hanefeld F, Eiffert H, Thomssen R. Epidemiology and clinical manifestations of Lyme borreliosis in childhood: A prospective multicentre study with special regard to neuroborreliosis. Acta Paediatr. 1993;82:1–76.
- Frey A.B, Rao T.D. Single exposure of mice to Borrelia burgdorferi elicits immunoglobulin G antibodies characteristic of secondary immune response without production of interleukin-4 by immune T cells. Infect. Immun. 1995;63:2596–2603.
- Dattwyler R.J, Volkman D.J, Luft B.J. Immunologic Aspects of Lyme Borreliosis. Rev. Infect. Dis. 1989;11:S1494–S1498.
- Hubálek Z, Halouzka J. Distribution of Borrelia burgdorferi sensu lato genomic groups in Europe, a review. Eur. J. Epidemiol. 1997;13:951–957.
- Anderson J.F. Epizootiology of Borrelia in Ixodes tick vectors and reservoir hosts. Rev. Infect. Dis. 1989;11((Suppl. S6)):S1451–S1459.
- Lane R.S, Piesman J, Burgdorfer W. Lyme borreliosis: Relation of its causative agent to its vectors and hosts in North America and Europe. Annu. Rev. Entomol. 1991;36:587–609.
- Narankhajid M, Yeruult C, Gurbadam A, Battsetseg J, Aberle S.W, Bayartogtokh B, Joachim A, Duscher G.G. Some aspects on tick species in Mongolia and their potential role in the transmission of equine piroplasms, Anaplasma phagocytophilum and Borrelia burgdorferi L. Parasitol. Res. 2018;117:3557–3566.
- Fingerle V, Eiffert H, Gessner A, Göbel U, Hofmann H, Hunfeld K, Krause A, Pfister H, Reischl U, Sing A. MiQ 12 Lyme-Borreliose. Qualitätsstandards in der Mikrobiologisch-Infektiologischen Diagnostik. Urban und Fischer/Elsevier; Munich, Germany: 2017.
- Priest H.L, Irby N.L, Schlafer D.H, Divers T.J, Wagner B, Glaser A.L, Chang Y.F, Smith M.C. Diagnosis of Borrelia-associated uveitis in two horses. Vet. Ophthalmol. 2012;15:398–405.
- Rosa P.A, Schwan T.G. A specific and sensitive assay for the Lyme disease spirochete Borrelia burgdorferi using the polymerase chain reaction. J. Infect. Dis. 1989;160:1018–1029.
- Krupka I. Infektionen Mit Borrelia burgdorferi sensu lato und Deren Serologischer Nachweis Mittels Spezifischer C6-Peptide bei Hunden Sowie im Murinen Infektionsmodell. Ph.D. Dissertation. Universität Leipzig; Leipzig, Germany: 2010.
- Johnson B.J. Lyme Disease: An Evidence-Based Approach. CABI; Wallingford, UK: 2011.
- Dattwyler R.J, Volkman D.J, Luft B.J, Halperin J.J, Thomas J, Golightly M.G. Seronegative Lyme disease. Dissociation of specific T- and B-lymphocyte responses to Borrelia burgdorferi. N. Engl. J. Med. 1988;319:1441–1446.
- Gribble D.H. Equine ehrlichiosis. J. Am. Vet. Med. Assoc. 1969;155:462–469.
- Von Loewenich F, Stumpf G, Baumgarten B, Röllinghoff M, Dumler J, Bogdan C. A case of equine granulocytic ehrlichiosis provides molecular evidence for the presence of pathogenic Anaplasma phagocytophilum (HGE agent) in Germany. Eur. J. Clin. Microbiol. Infect. Dis. 2003;22:303–305.
- Levi O, Waner T, Baneth G, Keysary A, Bruchim Y, Silverman J, Harrus S. Seroprevalence of Anaplasma phagocytophilum among healthy dogs and horses in Israel. J. Vet. Med. Ser. B. 2006;53:78–80.
- Salvagni C.A, Dagnone A.S, Gomes T.S, Mota J.S, Andrade G.M, Baldani C.D, Machado R.Z. Serologic evidence of equine granulocytic anaplasmosis in horses from central West Brazil. Rev. Bras. De Parasitol. Veterinária. 2010;19:135–140.
- Madigan J, Hietala S, Chalmers S, DeRock E. Seroepidemiologic survey of antibodies to Ehrlichia equi in horses of northern California. J. Am. Vet. Med. Assoc. 1990;196:1962–1964.
- Leblond A, Pradier S, Pitel P, Fortier G, Boireau P, Chadoeuf J, Sabatier P. An epidemiological survey of equine anaplasmosis (Anaplasma phagocytophilum) in southern France. Rev. Sci. Et Tech. Int. Off. Epizoot. 2005;24:899–908.
- Maurizi L, Marié J.-L, Courtin C, Gorsane S, Chal D, Davoust B. Seroprevalence survey of equine anaplasmosis in France and in sub-Saharan Africa. Clin. Microbiol. Infect. 2009;15:68–69.
- Passamonti F, Fabrizia V, Katia C, Stefano C, Giacomo C, Luisa M.M, Daniela P.F, Andrea V.S, Mauro C. Anaplasma phagocytophilum in horses and ticks: A preliminary survey of Central Italy. Comp. Immunol. Microbiol. Infect. Dis. 2010;33:73–83.
- Butler C, Nijhof A, Jongejan F, Van der Kolk J. Anaplasma phagocytophilum infection in horses in the Netherlands. Vet. Rec. 2008;162:216–217.
- Amusategui I, Sainz A, Tesouro M.A. Serological evaluation of Anaplasma phagocytophilum infection in livestock in northwestern Spain. Ann. N. Y. Acad. Sci. 2006;1078:487–490.
- Praskova I, Bezdekova B, Zeman P, Jahn P. Seroprevalence of Anaplasma phagocytophilum in horses in the Czech Republic. Ticks Tick-Borne Dis. 2011;2:111–115.
- Munderloh U.G, Madigan J.E, Dumler J.S, Goodman J.L, Hayes S.F, Barlough J.E, Nelson C.M, Kurtti T.J. Isolation of the equine granulocytic ehrlichiosis agent, Ehrlichia equi, in tick cell culture. J. Clin. Microbiol. 1996;34:664–670.
- Goodman J.L, Nelson C, Vitale B, Madigan J.E, Dumler J.S, Kurtti T.J, Munderloh U.G. Direct cultivation of the causative agent of human granulocytic ehrlichiosis. N. Engl. J. Med. 1996;334:209–215.
- Pusterla N, Huder J.B, Feige K, Lutz H. Identification of a granulocytic Ehrlichia strain isolated from a horse in Switzerland and comparison with other rickettsiae of the Ehrlichia phagocytophila genogroup. J. Clin. Microbiol. 1998;36:2035–2037.
- Sells D.M, Hildebrandt P.K, Lewis G.E, Nyindo M.B, Ristic M. Ultrastructural observations on Ehrlichia equi organisms in equine granulocytes. Infect. Immun. 1976;13:273–280.
- Barlough J.E, Madigan J.E, DeRock E, Bigornia L. Nested polymerase chain reaction for detection of Ehrlichia equi genomic DNA in horses and ticks (Ixodes pacificus). Vet. Parasitol. 1996;63:319–329.
- Pusterla N, Huder J.B, Leutenegger C.M, Braun U, Madigan J.E, Lutz H. Quantitative real-time PCR for detection of members of the Ehrlichia phagocytophila genogroup in host animals and Ixodes ricinus ticks. J. Clin. Microbiol. 1999;37:1329–1331.
- Drazenovich N, Foley J, Brown R.N. Use of real-time quantitative PCR targeting the msp2 protein gene to identify cryptic Anaplasma phagocytophilum infections in wildlife and domestic animals. Vector Borne Zoonotic Dis. 2006;6:83–90.
- Franzén P, Aspan A, Egenvall A, Gunnarsson A, Aberg L, Pringle J. Acute clinical, hematologic, serologic, and polymerase chain reaction findings in horses experimentally infected with a European strain of Anaplasma phagocytophilum. J. Vet. Intern. Med. 2005;19:232–239.
- Pusterla N, Madigan J.E. Anaplasma phagocytophilum infection. In: Sellon D.C., Long M.T., editors. Equine Infectious Diseases. Saunders; St. Louis, MI, USA: 2014. pp. 344–347.
- Songer J.G, Post K.W. The family Anaplasmataceae. In: Songer J.G., Post K.W., editors. Veterinary Microbiology: Bacterial and Fungal Agents of Animal Disease. Saunders; St. Louis, MI, USA: 2005. pp. 325–326.
- Madigan J.E, Gribble D. Equine ehrlichiosis in northern California: 49 cases (1968–1981). J. Am. Vet. Med. Assoc. 1987;190:445–448.
- Tsachev I, Pantchev N, Marutsov P, Petrov V, Gundasheva D, Baymakova M. Serological Evidence of Borrelia burgdorferi, Anaplasma phagocytophilum and Ehrlichia spp. Infections in Horses from Southeastern Bulgaria. Vector Borne Zoonotic Dis. 2018;18:588–594.
- Tsachev I, Baymakova M, Pantchev N. Seroprevalence of Anaplasma phagocytophilum, Ehrlichia spp. and Borrelia burgdorferi infections in horses: First report from Northern Bulgaria—Short communication. Acta Vet. Hung. 2019;67:197–203.
- Cerri S, Meersschaert C, Houben R, Pitel P.-H, De Waele V, Hendrickx G, Amory H. Diagnostic Value of Serologic Tests and Seroprevalence of Borreliosis in Horses Living in Southern Belgium; Proceedings of the 9th ECEIM Congress; Helsinki, Finland. 3–5 November 2016.
- Doby J, Chevrier S, Couatarmanac’h A. Spirochétose à tiques par Borrelia burgdorferi chez le cheval en Bretagne. Résultats d’une enquête sérologique portant sur 400 chevaux. Bull. Soc. Fr. Parasitol. 1987;5:285–295.
- Fritz C.I. Retrospektive Betrachtung Serologischer Ergebnisse Verschiedener Borrelien-Antikörper-Nachweisverfahren unter dem Aspekt einer Möglichen Kategorisierung Klinischer Befunde bei Equiden. LMU; Munich, Germany: 2018.
- Palm K. Nachweis Spezifischer Antikörper gegen Borrelia Burgdorferi in Equinen Serumproben aus dem Bayerischen Haupt-und Landgestüt Schwaiganger unter Berücksichtigung Aktueller Kriterien der Diagnostik. Ph.D. Dissertation. Ludwig-Maximilians-Universität München; Munich, Germany: 2016.
- Wollanke B. Untersuchungen zur Ätiologie der Equinen Rezidivierenden Uveitis. Ph.D. Dissertation. Ludwig-Maximilians-Universität München; Munich, Germany: 1995.
- Bartol J. Is Lyme disease overdiagnosed in horses?. Equine Vet. J. 2013;45:529–530.
- Divers T.J. Equine lyme disease. J. Equine Vet. Sci. 2013;33:488–492.
- Chandrashekar R, Daniluk D, Moffitt S, Lorentzen L, Williams J. Serologic diagnosis of equine borreliosis: Evaluation of an in-clinic enzyme-linked immunosorbent assay (SNAP (R) 4Dx (R)). Int. J. Appl. Res. Vet. Med. 2008;6:145–150.
- Chandrashekar R, Mainville C.A, Beall M.J, O’Connor T, Eberts M.D, Alleman A.R, Gaunt S.D, Breitschwerdt E.B. Performance of a commercially available in-clinic ELISA for the detection of antibodies against Anaplasma phagocytophilum, Ehrlichia canis, and Borrelia burgdorferi and Dirofilaria immitis antigen in dogs. Am. J. Vet. Res. 2010;71:1443–1450.
- Zöller L, Haude M, Hassler D, Burkard S, Sonntag H. Spontaneous and post-treatment antibody kinetics in late Lyme borreliosis. Serodiagn. Immunother. Infect. Dis. 1989;3:345–353.
- Preac Mursic V, Patsouris E, Wilske B, Reinhardt S, Gross B, Mehraein P. Persistence of Borrelia burgdorferi and histopathological alterations in experimentally infected animals. A comparison with histopathological findings in human Lyme disease. Infection. 1990;18:332–341.
- Van Andel A, Magnarelli L, Heimer R, Wilson M. Development and duration of antibody response against Ehrlichia equi in horses. J. Am. Vet. Med. Assoc. 1998;212:1910–1914.
- Nyindo M, Ristic M, Lewis G, Huxsoll D, Stephenson E. Immune response of ponies to experimental infection with Ehrlichia equi. Am. J. Vet. Res. 1978;39:15–18.
- Franzén P, Aspan A, Egenvall A, Gunnarsson A, Karlstam E, Pringle J. Molecular evidence for persistence of Anaplasma phagocytophilum in the absence of clinical abnormalities in horses after recovery from acute experimental infection. J. Vet. Intern. Med. 2009;23:636–642.
- Barthold S.W, Persing D, Armstrong A.L, Peeples R.A. Kinetics of Borrelia burgdorferi dissemination and evolution of disease after intradermal inoculation of mice. Am. J. Pathol. 1991;139:263.
- Krupka I, Bechtel M, Loehnert-Thiel U, Eppendorf R, Straubinger R.K. Borreliose: Möglichkeiten und Perspektiven der Diagnostik. Leipz. Blaue Hefte. 2012:319.
- Burgess E, Gendron-Fitzpatrick A. Experimental infection of equines with Borrelia burgdorferi; Proceedings of the Lyme Borreliosis. 1990; Stockholm, Sweden. 18–21 June 1990.
- Chang Y.-F, Novosol V, McDonough S, Chang C.-F, Jacobson R, Divers T, Quimby F, Shin S, Lein D. Experimental infection of ponies with Borrelia burgdorferi by exposure to Ixodid ticks. Vet. Pathol. 2000;37:68–76.
- Chang Y.-F, Ku Y.-W, Chang C.-F, Chang C.-D, McDonough S.P, Divers T, Pough M, Torres A. Antibiotic treatment of experimentally Borrelia burgdorferi-infected ponies. Vet. Microbiol. 2005;107:285–294.
- Fahrer H, van der Linden S, Sauvain M.-J, Gern L, Zhioua E, Aeschlimann A. A positive “Lyme-Serology”—What does it mean clinically? Preliminary results of a Swiss prospective study. Lyme Borreliosis II. Zbl Bakt. 1989:329–333.
- Satz N. [Immunology and diagnostic test results in Lyme borreliosis]. Schweiz. Med. Wochenschr. 1992;122:1779–1791.
- Nyarko E, Grab D.J, Dumler J.S. Anaplasma phagocytophilum-infected neutrophils enhance transmigration of Borrelia burgdorferi across the human blood brain barrier in vitro. Int. J. Parasitol. 2006;36:601–605.
- Beall M.J, Chandrashekar R, Eberts M.D, Cyr K.E, Diniz P.P, Mainville C, Hegarty B.C, Crawford J.M, Breitschwerdt E.B. Serological and molecular prevalence of Borrelia burgdorferi, Anaplasma phagocytophilum, and Ehrlichia species in dogs from Minnesota. Vector Borne Zoonotic Dis. 2008;8:455–464.
- Socoloski S.N.G, de Castro B.G, Cordeiro M.D, da Fonseca A.H, Cepeda M.B, Nicolino R.R, Lopes L.B. Epidemiological investigation of Borrelia burgdorferi in horses in the municipality of Sinop-MT, Brazil. Trop. Anim. Health Prod. 2018;50:831–836.
- Dzierzecka M, Kita J. The use of chosen serological diagnostic methods in Lyme disease in horses. Part I. Indirect immunofluorescence and enzyme-linked immunosorbent assay (ELISA). Pol. J. Vet. Sci. 2002;5:71–77.
- Straubinger R.K. Spirochäten. In: Selbitz H.-J., Truyen U., Valentin-Weigand P., editors. Tiermedizinische Mikrobiologie, Infektions-und Seuchenlehre. 10th ed. Enke Verlag; Stuttgart, Germany: 2015.
- Littman M.P, Goldstein R.E, Labato M.A, Lappin M.R, Moore G.E. ACVIM small animal consensus statement on Lyme disease in dogs: Diagnosis, treatment, and prevention. J. Vet. Intern. Med. 2006;20:422–434.
Citations
This article has been cited 3 times.- Dorrego A, Olvera-Maneu S, Jose-Cunilleras E, Gago P, Raez A, Rivera B, Oporto A, Gonzalez S, Cruz-Lopez F. Molecular Detection of Theileria equi, Babesia caballi, and Borrelia burgdorferi Sensu Lato in Hippobosca equina from Horses in Spain. Pathogens 2026 Jan 15;15(1).
- Kloster H, Stormo C, Haaland AH, Stuen S, Kjelland V. Seroprevalence of IgG Antibodies Against Borrelia burgdorferi Sensu Lato, Anaplasma phagocytophilum, and Tick-Borne Encephalitis (TBE) Virus in Horses in Southern Norway. Microorganisms 2025 Mar 28;13(4).
- Broeckl CV, Hiereth S, Straubinger RK. A comparative study evaluating three line immunoassays available for serodiagnosis of equine Lyme borreliosis: Detection of Borrelia burgdorferi sensu lato-specific antibodies in serum samples of vaccinated and non-vaccinated horses. PLoS One 2024;19(12):e0316170.
Use Nutrition Calculator
Check if your horse's diet meets their nutrition requirements with our easy-to-use tool Check your horse's diet with our easy-to-use tool
Talk to a Nutritionist
Discuss your horse's feeding plan with our experts over a free phone consultation Discuss your horse's diet over a phone consultation
Submit Diet Evaluation
Get a customized feeding plan for your horse formulated by our equine nutritionists Get a custom feeding plan formulated by our nutritionists