Seroprevalence of IgG Antibodies Against Borrelia burgdorferi Sensu Lato, Anaplasma phagocytophilum, and Tick-Borne Encephalitis (TBE) Virus in Horses in Southern Norway.
Abstract: ticks play a crucial role as carriers of diseases, transmitting pathogens to vertebrate hosts, including horses. This study aimed to investigate the seroprevalence of IgG antibodies against sensu lato (s. l.), , and tick-borne encephalitis virus (TBE-virus) in equine sera collected in southern Norway. In total, sera from 331 horses stabled in four counties (Agder, Vestfold and Telemark, Vestland, and Viken) were analyzed by immunoblot. In total, 66% of the horses were IgG-seropositive for antibodies against one or multiple tick-borne pathogens. The highest seroprevalence was detected against s. l. (47%), followed by (34%) and TBE-virus (10%). A significant difference between the counties regarding IgG antibodies against was found, with the highest seroprevalence in horses stabled in the coastal areas of Agder and Vestland. In conclusion, the study demonstrates that horses in southern Norway are at high risk of contracting tick-borne infections.
Publication Date: 2025-03-28 PubMed ID: 40284608PubMed Central: PMC12029606DOI: 10.3390/microorganisms13040771Google Scholar: Lookup
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Summary
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Overview
- This study analyzed how common certain tick-borne infections are in horses from southern Norway by testing their blood for antibodies against the pathogens Borrelia burgdorferi sensu lato, Anaplasma phagocytophilum, and tick-borne encephalitis virus (TBE virus).
- The research found a high prevalence of antibodies indicating widespread exposure to these pathogens among horses in the region, with variation by geographic area.
Background
- Ticks are vectors that carry and transmit multiple pathogens to vertebrate hosts, including horses.
- Common tick-borne pathogens affecting horses include:
- Borrelia burgdorferi sensu lato (s.l.): the bacteria responsible for Lyme disease.
- Anaplasma phagocytophilum: causes granulocytic anaplasmosis.
- Tick-borne encephalitis (TBE) virus: a viral infection that can affect the nervous system.
- Understanding seroprevalence—the proportion of individuals with antibodies—in horses helps assess the risk of infection and informs preventive measures.
Study Design and Methods
- Samples collected: 331 serum samples from horses kept in four counties in southern Norway—Agder, Vestfold and Telemark, Vestland, and Viken.
- Analysis technique: Immunoblot assay was used to detect IgG antibodies against the three tick-borne pathogens.
- IgG antibodies indicate past exposure or infection, not necessarily current active disease.
Key Findings
- Overall, 66% of horses had IgG antibodies against one or more of the tested tick-borne pathogens, indicating high exposure rates.
- Seroprevalence rates for individual pathogens were:
- Borrelia burgdorferi s.l.: 47% of horses were seropositive.
- Anaplasma phagocytophilum: 34% seropositive.
- TBE virus: 10% seropositive.
- Geographical variation was noted:
- Significant differences in Borrelia seroprevalence between counties.
- The highest Borrelia antibody prevalence was seen in horses from coastal counties Agder and Vestland, areas likely with higher tick exposure.
Conclusions and Implications
- Horses in southern Norway are frequently exposed to multiple tick-borne pathogens.
- The high seroprevalence emphasizes the need for heightened awareness and preventive efforts against tick infestations and tick-borne diseases in equine populations in this region.
- Regional differences suggest that environmental factors such as proximity to coastlines influence tick activity and pathogen transmission risk.
- Veterinarians and horse owners should consider these risks when managing horse health and when deciding on tick control strategies.
Cite This Article
APA
Kloster H, Stormo C, Haaland AH, Stuen S, Kjelland V.
(2025).
Seroprevalence of IgG Antibodies Against Borrelia burgdorferi Sensu Lato, Anaplasma phagocytophilum, and Tick-Borne Encephalitis (TBE) Virus in Horses in Southern Norway.
Microorganisms, 13(4), 771.
https://doi.org/10.3390/microorganisms13040771 Publication
Researcher Affiliations
- Department of Natural Sciences, Faculty of Engineering and Science, University of Agder, 4630 Kristiansand, Norway.
- Department of Natural Sciences, Faculty of Engineering and Science, University of Agder, 4630 Kristiansand, Norway.
- Department of Companion Animal Clinical Sciences, Faculty of Veterinary Medicine, Norwegian University of Life Sciences, 1433 Aas, Norway.
- Norwegian Food Safety Authority, Head Office, 0170 Oslo, Norway.
- Department of Production Animal Clinical Sciences, Faculty of Veterinary Medicine, Norwegian University of Life Science, 4325 Sandnes, Norway.
- Department of Natural Sciences, Faculty of Engineering and Science, University of Agder, 4630 Kristiansand, Norway.
Conflict of Interest Statement
The authors declare no conflicts of interest.
References
This article includes 63 references
- Kjaer L.J., Soleng A., Edgar K.S., Lindstedt H.E.H., Paulsen K.M., Andreassen A.K., Korslund L., Kjelland V., Slettan A., Stuen S., et al. A large-scale screening for the taiga tick, Ixodes persulcatus, and the meadow tick, Dermacentor reticulatus, in southern Scandinavia, 2016. Parasites Vectors. 2019;12:338. doi: 10.1186/s13071-019-3596-3.
- Soleng A., Edgar K.S., Paulsen K.M., Pedersen B.N., Okbaldet Y.B., Skjetne I.E.B., Gurung D., Vikse R., Andreassen A.K. Distribution of Ixodes ricinus ticks and prevalence of tick-borne encephalitis virus among questing ticks in the Arctic Circle region of northern Norway. Ticks Tick Borne Dis. 2018;9:97–103. doi: 10.1016/j.ttbdis.2017.10.002.
- Mehl R. The distribution and host relations of Norwegian ticks (Acari, Ixodides) Fauna Nor. 1983;30:46–51.
- Hvidsten D., Stuen S., Jenkins A., Dienus O., Olsen R.S., Kristiansen B.E., Mehl R., Matussek A. Ixodes ricinus and Borrelia prevalence at the Arctic Circle in Norway. Ticks Tick Borne Dis. 2014;5:107–112. doi: 10.1016/j.ttbdis.2013.09.003.
- Jore S., Vanwambeke S.O., Viljugrein H., Isaksen K., Kristoffersen A.B., Woldehiwet Z., Johansen B., Brun E., Brun-Hansen H., Westermann S., et al. Climate and environmental change drives Ixodes ricinus geographical expansion at the northern range margin. Parasites Vectors. 2014;7:11. doi: 10.1186/1756-3305-7-11.
- Le Dortz L.L., Rouxel C., Polack B., Boulouis H.J., Lagrée A.-C., Deshuillers P.L., Haddad N. Tick-borne diseases in Europe: Current prevention, control tools and the promise of aptamers. Vet. Parasitol. 2024;328:110190. doi: 10.1016/j.vetpar.2024.110190.
- Kjelland V., Stuen S., Skarpaas T., Slettan A. Prevalence and genotypes of Borrelia burgdorferi sensu lato infection in Ixodes ricinus ticks in southern Norway. Scand. J. Infect. Dis. 2010;42:579–585. doi: 10.3109/00365541003716526.
- Kjelland V., Ytrehus B., Vikorren T., Stuen S., Skarpaas T., Slettan A. Borrelia burgdorferi sensu lato detected in skin of Norwegian mountain hares (Lepus timidus) without signs of dissemination. J. Wildl. Dis. 2011;47:293–299. doi: 10.7589/0090-3558-47.2.293.
- Kjaer L.J., Klitgaard K., Soleng A., Edgar K.S., Lindstedt H.E.H., Paulsen K.M., Andreassen A.K., Korslund L., Kjelland V., Slettan A., et al. Spatial patterns of pathogen prevalence in questing Ixodes ricinus nymphs in southern Scandinavia, 2016. Sci. Rep. 2020;10:19376. doi: 10.1038/s41598-020-76334-5.
- Rosef O., Radzijevskaja J., Paulauskas A., Haslekas C. The prevalence of Anaplasma phagocytophilum in host-seeking Ixodes ricinus ticks in Norway. Clin. Microbiol. Infect. 2009;15((Suppl. 2)):43–45. doi: 10.1111/j.1469-0691.2008.02169.x.
- Andreassen A., Jore S., Cuber P., Dudman S., Tengs T., Isaksen K., Hygen H.O., Viljugrein H., Ånestad G., Ottesen P. Prevalence of tick borne encephalitis virus in tick nymphs in relation to climatic factors on the southern coast of Norway. Parasites Vectors. 2012;5:177. doi: 10.1186/1756-3305-5-177.
- Jenkins A., Raasok C., Pedersen B.N., Jensen K., Andreassen A., Soleng A., Edgar K.S., Lindstedt H.H., Kjelland V., Stuen S., et al. Detection of Candidatus Neoehrlichia mikurensis in Norway up to the northern limit of Ixodes ricinus distribution using a novel real time PCR test targeting the groEL gene. BMC Microbiol. 2019;19:199. doi: 10.1186/s12866-019-1502-y.
- Quarsten H., Skarpaas T., Fajs L., Noraas S., Kjelland V. Tick-borne bacteria in Ixodes ricinus collected in southern Norway evaluated by a commercial kit and established real-time PCR protocols. Ticks Tick Borne Dis. 2015;6:538–544. doi: 10.1016/j.ttbdis.2015.04.008.
- Kjelland V., Rollum R., Korslund L., Slettan A., Tveitnes D. Borrelia miyamotoi is widespread in Ixodes ricinus ticks in southern Norway. Ticks Tick Borne Dis. 2015;6:516–521. doi: 10.1016/j.ttbdis.2015.04.004.
- Oines O., Radzijevskaja J., Paulauskas A., Rosef O. Prevalence and diversity of Babesia spp. in questing Ixodes ricinus ticks from Norway. Parasite Vectors. 2012;5:156. doi: 10.1186/1756-3305-5-156.
- Sacristan C., das Neves C.G., Suhel F., Sacristan I., Tengs T., Hamnes I.S., Madslien K. Bartonella spp. detection in ticks, Culicoides biting midges and wild cervids from Norway. Transbound. Emerg. Dis. 2021;68:941–951. doi: 10.1111/tbed.13762.
- Thortveit E.T., Aase A., Petersen L.B., Lorentzen A.R., Mygland A., Ljostad U. Human seroprevalence of antibodies to tick-borne microbes in southern Norway. Ticks Tick Borne Dis. 2020;11:101410. doi: 10.1016/j.ttbdis.2020.101410.
- Springer A., Glass A., Topp A.K., Strube C. Zoonotic tick-borne pathogens in temperate and cold regions of Europe-a review on the prevalence in domestic animals. Front. Vet. Sci. 2020;7:604910. doi: 10.3389/fvets.2020.604910.
- Butler C., Nijhof A., Jongejan F., Van der Kolk J. Anaplasma phagocytophilum infection in horses in the Netherlands. Vet. Rec. 2008;162:216–217. doi: 10.1136/vr.162.7.216.
- M’Ghirbi Y., Yaich H., Ghorbel A., Bouattour A. Anaplasma phagocytophilum in horses and ticks in Tunisia. Parasite Vectors. 2012;5:180. doi: 10.1186/1756-3305-5-180.
- Passamonti F., Veronesi F., Cappelli K., Capomaccio S., Coppola G., Marenzoni M.L., Piergili F.D., Verini S.A., Coletti M. Anaplasma phagocytophilum in horses and ticks: A preliminary survey of Central Italy. Comp. Immunol. Microbiol. Infect. Dis. 2010;33:73–83. doi: 10.1016/j.cimid.2008.08.002.
- Conze T.M., Bagó Z., Revilla-Fernández S., Schlegel J., Goehring L.S., Matiasek K. Tick-borne encephalitis virus (TBEV) infection in two horses. Viruses. 2021;13:1775. doi: 10.3390/v13091775.
- Divers T.J. Equine lyme disease. J. Equine Vet. Sci. 2013;33:488–492.
- de Heus P., Bagó Z., Weidinger P., Lale D., Trachsel D.S., Revilla-Fernández S., Matiasek K., Nowotny N. Severe neurologic disease in a horse caused by tick-borne encephalitis virus, Austria, 2021. Viruses. 2023;15:2022. doi: 10.3390/v15102022.
- R Core Team . R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing; Vienna, Austria: 2023.
- Wickham H., Chang W., Henry L., Pedersen T.L., Takahashi K., Wilke C., Woo K., Yutani H., Dunnington D., Brand T.v.d. ggplot2: Elegant Graphics for Data Analysis. Springer; New York, NY, USA: 2016.
- Pebesma E. Simple Features for R: Standardized support for spatial vector data. R J. 2018;10:439–446.
- Kjaer L.J., Soleng A., Edgar K.S., Lindstedt H.E.H., Paulsen K.M., Andreassen A.K., Korslund L., Kjelland V., Slettan A., Stuen S., et al. Predicting and mapping human risk of exposure to Ixodes ricinus nymphs using climatic and environmental data, Denmark, Norway and Sweden, 2016. Euro. Surveill. 2019;24:1800101. doi: 10.2807/1560-7917.ES.2019.24.9.1800101.
- Lyngholt M.C. Anaplasma Phagocytophilum hos hest: En Seroprevalensstudie hos Islandshest i Grimstad Kommune. [(accessed on 20 October 2024)]. Available online: https://www.ddd.dk/media/2090/mari-c-lyngholt.pdf.
- 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.
- 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;52:3. doi: 10.1186/1751-0147-52-3.
- Traversa D., Milillo P., Maggi R., Simonato G., Di Cesare A., Pezzuto C., Grillini M., Morelli S., Colombo M., Passarelli A., et al. Seroexposure to zoonotic Anaplasma and Borrelia in dogs and horses that are in contact with vulnerable people in Italy. Pathogens. 2023;12:470. doi: 10.3390/pathogens12030470.
- Athanasiou L.V., Katsogiannou E.G., Tyrnenopoulou P., Gougoulis D., Apostolidis K.N., Papadakis S.M., Kokkinaki K.C.G., Papatsiros V.G., Tsokana C.N. Evidence of horse exposure to Anaplasma phagocytophilum, Borrelia burgdorferi, and Leishmania infantum in Greece through the detection of IgG antibodies in serum and in an alternative diagnostic sample—The Saliva. Biomolecules. 2023;13:1374. doi: 10.3390/biom13091374.
- Schafer I., Silaghi C., Fischer S., Marsboom C., Hendrickx G., Gehlen H., Muller E. Detection of Anaplasma phagocytophilum in horses from Germany by molecular and serological testing (2008–2021) Vet. Parasitol. 2022;312:109840. doi: 10.1016/j.vetpar.2022.109840.
- Gehlen H., Inerle K., Bartel A., Stöckle S.D., Ulrich S., Briese B., Straubinger R.K. Seroprevalence of Borrelia burgdorferi sensu lato and Anaplasma phagocytophilum infections in German horses. Animals. 2023;13:1984. doi: 10.3390/ani13121984.
- Kjelland V., Paulsen K.M., Rollum R., Jenkins A., Stuen S., Soleng A., Edgar K.S., Lindstedt H.H., Vaino K., Gibory M., et al. Tick-borne encephalitis virus, Borrelia burgdorferi sensu lato, Borrelia miyamotoi, Anaplasma phagocytophilum and Candidatus Neoehrlichia mikurensis in Ixodes ricinus ticks collected from recreational islands in southern Norway. Ticks Tick Borne Dis. 2018;9:1098–1102. doi: 10.1016/j.ttbdis.2018.04.005.
- Jenkins A., Kristiansen B.E., Allum A.G., Aakre R.K., Strand L., Kleveland E.J., van de Pol I., Schouls L. Borrelia burgdorferi sensu lato and Ehrlichia spp. in Ixodes ticks from southern Norway. J. Clin. Microbiol. 2001;39:3666–3671. doi: 10.1128/JCM.39.10.3666-3671.2001.
- Stigum V.M., Jaarsma R.I., Sprong H., Rolandsen C.M., Mysterud A. Infection prevalence and ecotypes of Anaplasma phagocytophilum in moose Alces alces, red deer Cervus elaphus, roe deer Capreolus capreolus and Ixodes ricinus ticks from Norway. Parasite Vectors. 2019;12:1. doi: 10.1186/s13071-018-3256-z.
- Mysterud A., Easterday W.R., Qviller L., Viljugrein H., Ytrehus B. Spatial and seasonal variation in the prevalence of Anaplasma phagocytophilum and Borrelia burgdorferi sensu lato in questing Ixodes ricinus ticks in Norway. Parasite Vectors. 2013;6:187. doi: 10.1186/1756-3305-6-187.
- Stuen S., Pettersen K.S., Granquist E.G., Bergstrom K., Bown K.J., Birtles R.J. Anaplasma phagocytophilum variants in sympatric red deer (Cervus elaphus) and sheep in southern Norway. Ticks Tick Borne Dis. 2013;4:197–201. doi: 10.1016/j.ttbdis.2012.11.014.
- Khatat S.E.H., Kachani M., Duchateau L., Elhachimi L., Sahibi H., Daminet S. Anaplasma spp. in dogs: Is there a danger for humans? Rev. Vétérinaire Clin. 2022;57:1–15.
- Wass L., Grankvist A., Mattsson M., Gustafsson H., Krogfelt K., Olsen B., Nilsson K., Martensson A., Quarsten H., Henningsson A.J., et al. Serological reactivity to Anaplasma phagocytophilum in neoehrlichiosis patients. Eur. J. Clin. Microbiol. Infect. Dis. 2018;37:1673–1678. doi: 10.1007/s10096-018-3298-3.
- 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.
- Kiss T., Cadar D., Krupaci A.F., Bordeanu A., Brudasca G.F., Mihalca A.D., Mircean V., Gliga L., Dumitrache M.O., Spinu 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. doi: 10.1089/vbz.2010.0254.
- Strnad M., Honig V., Ruzek D., Grubhoffer L., Rego R.O.M. Europe-wide meta-analysis of Borrelia burgdorferi Sensu Lato prevalence in questing Ixodes ricinus ticks. Appl. Environ. Microbiol. 2017;83:e00609–e00617. doi: 10.1128/AEM.00609-17.
- Topp A.K., Springer A., Mischke R., Rieder J., Feige K., Ganter M., Nagel-Kohl U., Nordhoff M., Boelke M., Becker S., et al. Seroprevalence of tick-borne encephalitis virus in wild and domestic animals in northern Germany. Ticks Tick Borne Dis. 2023;14:102220. doi: 10.1016/j.ttbdis.2023.102220.
- Sikutova S., Hornok S., Hubalek Z., Dolezalkova I., Juricova Z., Rudolf I. Serological survey of domestic animals for tick-borne encephalitis and Bhanja viruses in northeastern Hungary. Vet. Microbiol. 2009;135:267–271. doi: 10.1016/j.vetmic.2008.09.082.
- Rushton J.O., Lecollinet S., Hubalek Z., Svobodova P., Lussy H., Nowotny N. Tick-borne encephalitis virus in horses, Austria, 2011. Emerg. Infect. Dis. 2013;19:635–637. doi: 10.3201/eid1904.121450.
- Csank T., Drzewnioková P., Korytár Ľ., Major P., Gyuranecz M., Pistl J., Bakonyi T. A serosurvey of flavivirus infection in horses and birds in Slovakia. Vector-Borne Zoonotic Dis. 2018;18:206–213. doi: 10.1089/vbz.2017.2216.
- Vilibic-Cavlek T., Krcmar S., Bogdanic M., Tomljenovic M., Barbic L., Roncevic D., Sabadi D., Vucelja M., Santini M., Hunjak B., et al. An overview of tick-borne encephalitis epidemiology in endemic regions of continental Croatia, 2017–2023. Microorganisms. 2024;12:386. doi: 10.3390/microorganisms12020386.
- Pautienius A., Armonaite A., Simkute E., Zagrabskaite R., Buitkuviene J., Alpizar-Jara R., Grigas J., Zakiene I., Zienius D., Salomskas A., et al. Cross-sectional study on the prevalence and factors influencing occurrence of tick-borne encephalitis in horses in Lithuania. Pathogens. 2021;10:140. doi: 10.3390/pathogens10020140.
- Gothe L.M., Ganzenberg S., Ziegler U., Obiegala A., Lohmann K.L., Sieg M., Vahlenkamp T.W., Groschup M.H., Hörügel U., Pfeffer M. Horses as sentinels for the circulation of flaviviruses in Eastern–Central Germany. Viruses. 2023;15:1108. doi: 10.3390/v15051108.
- Paulsen K.M., Stuen S., das Neves C.G., Suhel F., Gurung D., Soleng A., Stiasny K., Vikse R., Andreassen A.K., Granquist E.G. Tick-borne encephalitis virus in cows and unpasteurized cow milk from Norway. Zoonoses Public Health. 2019;66:216–222. doi: 10.1111/zph.12554.
- Paulsen K.M., Das Neves C.G., Granquist E.G., Madslien K., Stuen S., Pedersen B.N., Vikse R., Rocchi M., Laming E., Stiasny K. Cervids as sentinel-species for tick-borne encephalitis virus in Norway-A serological study. Zoonoses Public Health. 2020;67:342–351.
- Ytrehus B., Vainio K., Dudman S.G., Gilray J., Willoughby K. Tick-borne encephalitis virus and louping-ill virus may co-circulate in Southern Norway. Vector Borne Zoonotic Dis. 2013;13:762–768. doi: 10.1089/vbz.2012.1023.
- Marvik A., Tveten Y., Pedersen A.B., Stiasny K., Andreassen A.K., Grude N. Low prevalence of tick-borne encephalitis virus antibodies in Norwegian blood donors. Infect Dis. 2021;53:44–51. doi: 10.1080/23744235.2020.1819561.
- Vikse R., Paulsen K.M., Edgar K.S., Pettersson J.H.-O., Ottesen P.S., Okbaldet Y.B., Kiran N., Lamsal A., Lindstedt H.E.H., Pedersen B.N., et al. Geographical distribution and prevalence of tick-borne encephalitis virus in questing Ixodes ricinus ticks and phylogeographic structure of the Ixodes ricinus vector in Norway. Zoonoses Public Health. 2020;67:370–381. doi: 10.1111/zph.12696.
- MSIS The Norwegian Surveillance System for Communicable Dieases (MSIS) [(accessed on 15 January 2025)]. Available online: https://msis.no/
- Hjetland R., Henningsson A.J., Vainio K., Dudman S.G., Grude N., Ulvestad E. Seroprevalence of antibodies to tick-borne encephalitis virus and Anaplasma phagocytophilum in healthy adults from western Norway. Infect Dis. 2015;47:52–56. doi: 10.3109/00365548.2014.959044.
- Vikse R., Maharjan U., Soleng A., Lindstedt H.H., Rykkvin R., Alfsnes K., Andreassen A.K. TBE in Norway. Chapter 13. In: Dobler G., Erber W., Bröker M., Chitimia-Dobler L., Schmitt H.J., editors. The TBE Book. 7th ed. Global Health Press; Singapore: 2024.
- Gao G.F., Jiang W.R., Hussain M.H., Venugopal K., Gritsun T.S., Reid H.W., Gould E.A. Sequencing and antigenic studies of a Norwegian virus isolated from encephalomyelitic sheep confirm the existence of louping ill virus outside Great Britain and Ireland. J. Gen. Virol. 1993;74:109–114.
- Lamsal A., Tryland M., Paulsen K.M., Romano J.S., Nymo I.H., Stiasny K., Soleng A., Vikse R., Andreassen A.K. Serological screening for tick-borne encephalitis virus in eight Norwegian herds of semi-domesticated reindeer (Rangifer tarandus tarandus) Zoonoses Public Health. 2023;70:692–698. doi: 10.1111/zph.13060.
- Kasparkova N., Bartova E., Zakovska A., Budikova M., Sedlak K. Antibodies against Borrelia burgdorferi Sensu Lato in clinically healthy and sick horses: First report from the Czech Republic. Microorganisms. 2023;11:1706. doi: 10.3390/microorganisms11071706.
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