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The Journal of veterinary medical science2013; 75(6); 715-720; doi: 10.1292/jvms.12-0449

Prevalence of tick borne pathogens in horses from Italy.

Abstract: In order to investigate the prevalence of tick-borne diseases, equine piroplasmosis, equine granulocytic anaplasmosis and Lyme borreliosis in Central Italy, blood samples from 300 horses were analyzed for the presence of antibodies against Babesia caballi, Theileria equi, Anaplasma phagocytophilum and Borrelia burgdorferi using the IFAT. The blood samples were also subjected to PCR assays in order to detect pathogen DNA. A total of 78 (26.0%) and 123 (41.0%) horses were found to be seropositive for B. caballi and T. equi, respectively, while 41 (13. 4%) and 21 (7.0%) horses were, respectively, seropositive for A. phagocytophilum and B. burgdorferi. Seropositivity for more than one agent was detected in 76 horses using IFAT. The most common association observed was between T. equi and B. caballi (14.7%). In addition, 54 horses (18.0%) were found to be positive for one or more tick-borne pathogens (TBPs) using PCR testing. Among these, 28 (9.3%) harbored single infections, while 26 (8.7%) were found to be co-infected with two or more pathogens. The correlation (K value) between IFAT and PCR results was 0.32 for T. equi, 0.34 for B. caballi, 0.62 for B. burgdorferi and 0.48 for A. phagocytophilum, reflecting an unprecedented degree of multiple exposures to TBPs in horses.
Publication Date: 2013-01-18 PubMed ID: 23328633DOI: 10.1292/jvms.12-0449Google Scholar: Lookup
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  • Journal Article

Summary

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The researchers investigated the prevalence of tick-borne diseases in horses in Central Italy, finding significant evidence of multiple exposures to disease-causing pathogens in horses.

Introduction to the Study

  • The study aimed to investigate the presence of a range of tick-borne diseases, namely equine piroplasmosis, equine granulocytic anaplasmosis, and Lyme borreliosis in the horse population in Central Italy.
  • These diseases are caused by specific pathogens that are transmitted by ticks, including Babesia caballi, Theileria equi, Anaplasma phagocytophilum, and Borrelia burgdorferi.
  • The researchers took blood samples from 300 horses and analyzed them for the presence of antibodies against these pathogens using a method known as the Immune Fluorescent Antibody Test (IFAT), a reliable method for detecting antibodies that indicates past or current infection.

Findings of the Study

  • A total of 26.0% and 41.0% of horses tested in the study were found to be seropositive for B. caballi and T. equi, respectively, indicating either past or current infection.
  • In addition, 13.4% of horses had antibodies against A. phagocytophilum and 7.0% had antibodies against B. burgdorferi.
  • Furthermore, the blood samples were subjected to Polymerase Chain Reaction (PCR) tests to detect pathogen DNA. This confirmed the presence of tick-borne pathogens (TBPs) in 18.0% of the horses, with 9.3% exhibiting single infections and 8.7% co-infected with two or more pathogens.
  • It is noteworthy that seropositivity for more than one agent was detected in 76 horses owing to the common association between T. equi and B. caballi.

Implications of the Study

  • The result identifies the unprecedented degree of multiple exposures to tick-borne pathogens in horses, emphasizing the importance of implementing effective control measures.
  • A discrepancy was found between the IFAT and PCR results reflecting that the two tests might be capturing different aspects of the infection.
  • The correlation (K value) between IFAT and PCR results ranged from 0.32 to 0.62 for different pathogens, indicating a moderate agreement between IFAT and PCR testing methods.
  • The study’s findings underscore the need for continued vigilance concerning tick-borne diseases in horses, as well as more comprehensive and cross-verifiable testing strategies to ensure accurate detection of these diseases.

Cite This Article

APA
Laus F, Veronesi F, Passamonti F, Paggi E, Cerquetella M, Hyatt D, Tesei B, Fioretti DP. (2013). Prevalence of tick borne pathogens in horses from Italy. J Vet Med Sci, 75(6), 715-720. https://doi.org/10.1292/jvms.12-0449

Publication

ISSN: 1347-7439
NlmUniqueID: 9105360
Country: Japan
Language: English
Volume: 75
Issue: 6
Pages: 715-720

Researcher Affiliations

Laus, Fulvio
  • School of Veterinary Medical Sciences, University of Camerino, Via Circonvallazione 93/95, 62024 Matelica (MC), Italy. fulvio.laus@unicam.it
Veronesi, Fabrizia
    Passamonti, Fabrizio
      Paggi, Emanuele
        Cerquetella, Matteo
          Hyatt, Doreene
            Tesei, Beniamino
              Fioretti, Daniela Piergili

                MeSH Terms

                • Anaplasma phagocytophilum / isolation & purification
                • Animals
                • Babesia / isolation & purification
                • Borrelia burgdorferi / isolation & purification
                • Fluorescent Antibody Technique, Indirect
                • Horse Diseases / epidemiology
                • Horse Diseases / microbiology
                • Horse Diseases / parasitology
                • Horses
                • Italy / epidemiology
                • Polymerase Chain Reaction / veterinary
                • Prevalence
                • Theileria / isolation & purification
                • Tick-Borne Diseases / epidemiology
                • Tick-Borne Diseases / parasitology
                • Tick-Borne Diseases / veterinary

                Citations

                This article has been cited 35 times.
                1. Villa L, Cafiso A, Cialini C, Olivieri E, Allievi C, Pintore E, Garippa G, Manfredi MT, Bazzocchi C. Serological and molecular insights into tick-borne pathogens in wild donkeys from an unexplored Mediterranean nature reserve. Curr Res Parasitol Vector Borne Dis 2025;7:100267.
                  doi: 10.1016/j.crpvbd.2025.100267pubmed: 40503032google scholar: lookup
                2. Axt CW, Springer A, von Luckner J, Naucke TJ, Müller E, Strube C, Schäfer I. [Equine piroplasmosis: Case descriptions and overview of the epidemiological situation in Europe with focus on Germany]. Tierarztl Prax Ausg G Grosstiere Nutztiere 2025 Feb;53(1):49-58.
                  doi: 10.1055/a-2457-5516pubmed: 39631762google scholar: lookup
                3. Bogdan AM, Mitrea IL, Ionita M. Equine Granulocytic Anaplasmosis: A Systematic Review and Meta-Analysis on Clinico-Pathological Findings, Diagnosis, and Therapeutic Management. Vet Sci 2024 Jun 13;11(6).
                  doi: 10.3390/vetsci11060269pubmed: 38922016google scholar: lookup
                4. Koutantou M, Drancourt M, Angelakis E. Prevalence of Lyme Disease and Relapsing Fever Borrelia spp. in Vectors, Animals, and Humans within a One Health Approach in Mediterranean Countries. Pathogens 2024 Jun 17;13(6).
                  doi: 10.3390/pathogens13060512pubmed: 38921809google scholar: lookup
                5. Axt CW, Springer A, Strube C, Jung C, Naucke TJ, Müller E, Schäfer I. Molecular and Serological Detection of Vector-Borne Pathogens Responsible for Equine Piroplasmosis in Europe between 2008 and 2021. Microorganisms 2024 Apr 17;12(4).
                6. Coluccia P, Gizzarelli M, Scicluna MT, Manna G, Foglia Manzillo V, Buono F, Auletta L, Palumbo V, Pasolini MP. A cross-sectional study on performance evaluation in Italian standardbred horses' real-time PCR-positive for Theileria equi. BMC Vet Res 2024 Mar 5;20(1):79.
                  doi: 10.1186/s12917-024-03908-0pubmed: 38443906google scholar: lookup
                7. Gehlen H, Inerle K, Bartel A, Stöckle SD, Ulrich S, Briese B, Straubinger RK. Seroprevalence of Borrelia burgdorferi sensu lato and Anaplasma phagocytophilum Infections in German Horses. Animals (Basel) 2023 Jun 14;13(12).
                  doi: 10.3390/ani13121984pubmed: 37370494google scholar: lookup
                8. Traversa D, Milillo P, Maggi R, Simonato G, Di Cesare A, Pezzuto C, Grillini M, Morelli S, Colombo M, Passarelli A, Grassano A, Serio P, Losurdo M, Brueckmann R. Seroexposure to Zoonotic Anaplasma and Borrelia in Dogs and Horses That Are in Contact with Vulnerable People in Italy. Pathogens 2023 Mar 16;12(3).
                  doi: 10.3390/pathogens12030470pubmed: 36986392google scholar: lookup
                9. Defaye B, Moutailler S, Pasqualini V, Quilichini Y. Distribution of Tick-Borne Pathogens in Domestic Animals and Their Ticks in the Countries of the Mediterranean Basin between 2000 and 2021: A Systematic Review. Microorganisms 2022 Jun 16;10(6).
                10. Villa L, Gazzonis AL, Allievi C, De Maria C, Persichetti MF, Caracappa G, Zanzani SA, Manfredi MT. Seroprevalence of Tick-Borne Infections in Horses from Northern Italy. Animals (Basel) 2022 Apr 12;12(8).
                  doi: 10.3390/ani12080999pubmed: 35454246google scholar: lookup
                11. Nadal C, Marsot M, Le Metayer G, Boireau P, Guillot J, Bonnet SI. Spatial and Temporal Circulation of Babesia caballi and Theileria equi in France Based on Seven Years of Serological Data. Pathogens 2022 Feb 9;11(2).
                  doi: 10.3390/pathogens11020227pubmed: 35215171google scholar: lookup
                12. Rocafort-Ferrer G, Leblond A, Joulié A, René-Martellet M, Sandoz A, Poux V, Pradier S, Barry S, Vial L, Legrand L. Molecular assessment of Theileria equi and Babesia caballi prevalence in horses and ticks on horses in southeastern France. Parasitol Res 2022 Mar;121(3):999-1008.
                  doi: 10.1007/s00436-022-07441-7pubmed: 35128585google scholar: lookup
                13. Seo HJ, Truong AT, Kim KH, Lim JY, Min S, Kim HC, Yoo MS, Yoon SS, Klein TA, Cho YS. Molecular Detection and Phylogenetic Analysis of Tick-Borne Pathogens in Ticks Collected from Horses in the Republic of Korea. Pathogens 2021 Aug 24;10(9).
                  doi: 10.3390/pathogens10091069pubmed: 34578102google scholar: lookup
                14. Ali A, Zahid H, Zeb I, Tufail M, Khan S, Haroon M, Tufail M, Bilal M, Hussain M, Alouffi AS, Muñoz-Leal S, Labruna MB. Risk factors associated with tick infestations on equids in Khyber Pakhtunkhwa, Pakistan, with notes on Rickettsia massiliae detection. Parasit Vectors 2021 Jul 13;14(1):363.
                  doi: 10.1186/s13071-021-04836-wpubmed: 34256806google scholar: lookup
                15. Bogdan AM, Ionita M, Mitrea IL. Serological Evidence of Natural Exposure to Tick-Borne Pathogens in Horses, Romania. Microorganisms 2021 Feb 12;9(2).
                  doi: 10.3390/microorganisms9020373pubmed: 33673353google scholar: lookup
                16. Guccione C, Colomba C, Tolomeo M, Trizzino M, Iaria C, Cascio A. Rickettsiales in Italy. Pathogens 2021 Feb 8;10(2).
                  doi: 10.3390/pathogens10020181pubmed: 33567793google scholar: lookup
                17. Sazmand A, Bahari A, Papi S, Otranto D. Parasitic diseases of equids in Iran (1931-2020): a literature review. Parasit Vectors 2020 Nov 19;13(1):586.
                  doi: 10.1186/s13071-020-04472-wpubmed: 33213507google scholar: lookup
                18. Tirosh-Levy S, Gottlieb Y, Fry LM, Knowles DP, Steinman A. Twenty Years of Equine Piroplasmosis Research: Global Distribution, Molecular Diagnosis, and Phylogeny. Pathogens 2020 Nov 8;9(11).
                  doi: 10.3390/pathogens9110926pubmed: 33171698google scholar: lookup
                19. Laamari A, Azzag N, Tennah S, Derdour SY, China B, Bouabdallah R, Ghalmi F. Seroprevalence of Antibodies Against Anaplasma Phagocytophilum and Borrelia Burgdorferi in Horses (Equus Caballus) from Northern Algeria. J Vet Res 2020 Sep;64(3):413-419.
                  doi: 10.2478/jvetres-2020-0045pubmed: 32984632google scholar: lookup
                20. Dik B, Ceylan O, Ceylan C, Tekindal MA, Semassel A, Sönmez G, Derinbay Ekici Ö. Ectoparasites of feral horses [Equus ferus caballus (Linnaeus., 1758)] on Karadağ Mountain, Karaman, Turkey. J Parasit Dis 2020 Sep;44(3):590-596.
                  doi: 10.1007/s12639-020-01234-4pubmed: 32801511google scholar: lookup
                21. Dos Santos TM, Roier ECR, Pires MS, Santos HA, Vilela JAR, Peckle M, Paulino PG, Baldani CD, Massard CL. Molecular evidence of Anaplasma phagocytophilum and Theileria equi coinfection in horses from Rio de Janeiro, Brazil. Vet Anim Sci 2019 Jun;7:100055.
                  doi: 10.1016/j.vas.2019.100055pubmed: 32734076google scholar: lookup
                22. Mshelia PW, Kappmeyer L, Johnson WC, Kudi CA, Oluyinka OO, Balogun EO, Richard EE, Onoja E, Sears KP, Ueti MW. Molecular detection of Theileria species and Babesia caballi from horses in Nigeria. Parasitol Res 2020 Sep;119(9):2955-2963.
                  doi: 10.1007/s00436-020-06797-ypubmed: 32647992google scholar: lookup
                23. Houben RMAC, Meersschaert C, Hendrickx G, Pitel PH, Amory H. Modelling the probability and impact of false-positive serology for Borrelia burgdorferi sensu lato: A case study. Equine Vet J 2021 Jan;53(1):71-77.
                  doi: 10.1111/evj.13277pubmed: 32385952google scholar: lookup
                24. Seo MG, Kwon OD, Kwak D. Molecular Identification of Borrelia afzelii from Ticks Parasitizing Domestic and Wild Animals in South Korea. Microorganisms 2020 Apr 29;8(5).
                  doi: 10.3390/microorganisms8050649pubmed: 32365723google scholar: lookup
                25. Ebani VV. Serological Evidence of Anaplasma phagocytophilum and Spotted Fever Group Rickettsia spp. Exposure in Horses from Central Italy. Pathogens 2019 Jun 26;8(3).
                  doi: 10.3390/pathogens8030088pubmed: 31247976google scholar: lookup
                26. Sprong H, Azagi T, Hoornstra D, Nijhof AM, Knorr S, Baarsma ME, Hovius JW. Control of Lyme borreliosis and other Ixodes ricinus-borne diseases. Parasit Vectors 2018 Mar 6;11(1):145.
                  doi: 10.1186/s13071-018-2744-5pubmed: 29510749google scholar: lookup
                27. Afridi MJK, Mian AH, Saqib M, Abbas G, Ali J, Mansoor MK, Sial AUR, Rasheed I, Hussain MH. Seroprevalence and Risk Factors for Theileria equi Infection in Equines from Khyber Pakhtunkhwa Province, Pakistan. Iran J Parasitol 2017 Oct-Dec;12(4):597-605.
                  pubmed: 29317885
                28. Montes Cortés MG, Fernández-García JL, Habela Martínez-Estéllez MÁ. Seroprevalence of Theileria equi and Babesia caballi in horses in Spain. Parasite 2017;24:14.
                  doi: 10.1051/parasite/2017015pubmed: 28497743google scholar: lookup
                29. Izac JR, Oliver LD Jr, Earnhart CG, Marconi RT. Identification of a defined linear epitope in the OspA protein of the Lyme disease spirochetes that elicits bactericidal antibody responses: Implications for vaccine development. Vaccine 2017 May 31;35(24):3178-3185.
                  doi: 10.1016/j.vaccine.2017.04.079pubmed: 28479174google scholar: lookup
                30. Funk RA, Pleasant RS, Witonsky SG, Reeder DS, Werre SR, Hodgson DR. 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 Jul;30(4):1300-4.
                  doi: 10.1111/jvim.13973pubmed: 27214745google scholar: lookup
                31. Skotarczak B, Wodecka B, Rymaszewska A, Adamska M. Molecular evidence for bacterial pathogens in Ixodes ricinus ticks infesting Shetland ponies. Exp Appl Acarol 2016 Jun;69(2):179-89.
                  doi: 10.1007/s10493-016-0027-4pubmed: 26920921google scholar: lookup
                32. Jiménez D, Romero-Zuñiga JJ, Dolz G. Serosurveillance of infectious agents in equines of the Central Valley of Costa Rica. Open Vet J 2014;4(2):107-12.
                  pubmed: 26623349
                33. Laus F, Spaterna A, Faillace V, Veronesi F, Ravagnan S, Beribé F, Cerquetella M, Meligrana M, Tesei B. Clinical investigation on Theileria equi and Babesia caballi infections in Italian donkeys. BMC Vet Res 2015 Apr 28;11:100.
                  doi: 10.1186/s12917-015-0411-zpubmed: 25927984google scholar: lookup
                34. Wang M, Guo W, Igarashi I, Xuan X, Wang X, Xiang W, Jia H. Epidemiological investigation of equine piroplasmosis in China by enzyme-linked immunosorbent assays. J Vet Med Sci 2014 Apr;76(4):549-52.
                  doi: 10.1292/jvms.13-0477pubmed: 24292247google scholar: lookup
                35. Stuen S, Granquist EG, Silaghi C. Anaplasma phagocytophilum--a widespread multi-host pathogen with highly adaptive strategies. Front Cell Infect Microbiol 2013;3:31.
                  doi: 10.3389/fcimb.2013.00031pubmed: 23885337google scholar: lookup