Analyze Diet
Parasites & vectors2021; 14(1); 275; doi: 10.1186/s13071-021-04777-4

Frequency and factors associated of potential zoonotic pathogens (Borrelia spp., Rickettsia spp., Leishmania spp., and Anaplasma phagocytophilum) in equids in the state of Bahia, Brazil.

Abstract: Currently, various zoonotic diseases are classified as emerging or reemerging. Because equids have a direct relationship with various vectors, they are possibly more frequently exposed to zoonotic agents than are humans. The undeniable importance of diseases such as human granulocytic anaplasmosis, spotted fever, and leishmaniasis for both public and animal health, as well as the possibility of equids acting as sources, reservoirs, or even sentinels for these pathogens, justifies the detection of their frequency and factors associated with infection in equids from northeastern Brazil. Methods: Blood samples were collected from 569 equids (528 horses, 33 donkeys, and 8 mules), 516 from a rural area and 53 from an urban area. Pathogen detection was carried out as follows: Borrelia spp. and Rickettsia spp., serological analysis; Leishmania spp., serological analysis and polymerase chain reaction (PCR); Anaplasma phagocytophilum, PCR. Determination of associated factors was carried out through generalized linear models. Results: The frequencies of positivity for the pathogens observed in equids were as follows: Borrelia spp., 13.9% (79/569); Leishmania spp., 3.5% (20/569); Rickettsia spp. 33.4% (190/569). Regarding factors associated with infection, male sex was associated with protection against Borrelia spp.; donkeys and mules were associated with protection against Rickettsia spp., while a younger age was a risk factor. The infection of A. phagocytophilum was not detected in the sampled population. Co-infection was detected in 5.1% (29/569) of the animals. Conclusions: Most of the studied pathogenic agents are present in the prospected area, indicating a possible risk for both human and animal health. This demonstrates that equids can be considered important sentinels in the assessment of pathogens with zoonotic potential in the region.
Publication Date: 2021-05-22 PubMed ID: 34022939PubMed Central: PMC8140576DOI: 10.1186/s13071-021-04777-4Google 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.

The research article examines the prevalence and factors associated with potential zoonotic pathogens in horses, donkeys, and mules in the state of Bahia, Brazil. It further explores the role played by these animals as carriers, or sentinels, for diseases which pose a risk for both human and animal health.

Objective and Methodology

  • The study’s goal was to understand the frequency and underlying factors associated with zoonotic pathogens which include; Borrelia spp., Rickettsia spp., Leishmania spp., and Anaplasma phagocytophilum in equids (a term used to describe horses, donkeys, and mules).
  • The researchers collected blood samples from 569 equids comprising of 528 horses, 33 donkeys, and 8 mules, with most (516) from rural areas and 53 from an urban location.
  • Detection of the pathogens was achieved using serological analysis for Borrelia spp., Rickettsia spp., and Leishmania spp., while Anaplasma phagocytophilum detection was carried out via polymerase chain reaction (PCR).
  • The study further used generalized linear models to determine the factors associated with infection.

Results

  • The study noted positive results for the pathogens in the equids as follows: Borrelia spp., at 13.9% (79 out of 569); Leishmania spp., at 3.5% (20 out of 569); Rickettsia spp., at 33.4% (190 out of 569).
  • In terms of factors associated with infection, the research revealed that male sex helped protect against Borrelia spp. infection.
  • Donkeys and mules were associated with protection against Rickettsia spp., while younger age was considered a risk factor for contracting the distemper.
  • The study did not detect any A. phagocytophilum infection in the sampled population.
  • The research also noted co-infection in 5.1% (29 out of 569) of the animals.

Conclusions

  • The researchers concluded that the majority of the pathogens studied were present in the prospected area, indicating a potential risk to human and animal health.
  • The research also pointed to the role equids play in the spread of these zoonotic pathogens, hinting at the importance of considering them as critical sentinels in controlling potential outbreaks in the region.

Cite This Article

APA
Costa SCL, de Souza Freitas J, Carvalho FS, Pereira MJS, Cordeiro MD, da Fonseca AH, Gomes Jusi MM, Machado RZ, Munhoz AD. (2021). Frequency and factors associated of potential zoonotic pathogens (Borrelia spp., Rickettsia spp., Leishmania spp., and Anaplasma phagocytophilum) in equids in the state of Bahia, Brazil. Parasit Vectors, 14(1), 275. https://doi.org/10.1186/s13071-021-04777-4

Publication

ISSN: 1756-3305
NlmUniqueID: 101462774
Country: England
Language: English
Volume: 14
Issue: 1
Pages: 275

Researcher Affiliations

Costa, Sonia Carmen Lopo
  • Department of Agricultural and Environmental Sciences, State University of Santa Cruz - UESC, Soane Nazaré de Andrade Campus, Ilhéus, BA, Brazil.
de Souza Freitas, Jéssica
  • Department of Agricultural and Environmental Sciences, State University of Santa Cruz - UESC, Soane Nazaré de Andrade Campus, Ilhéus, BA, Brazil.
Carvalho, Fábio Santos
  • Department of Agricultural and Environmental Sciences, State University of Santa Cruz - UESC, Soane Nazaré de Andrade Campus, Ilhéus, BA, Brazil.
Pereira, Maria Julia Salim
  • Department of Animal Parasitology, Rural Federal University of Rio de Janeiro-UFRRJ, Seropédica, RJ, Brazil.
Cordeiro, Matheus Dias
  • Department of Epidemiology and Public Health, Rural Federal University of Rio de Janeiro-UFRRJ, Seropédica, RJ, Brazil.
da Fonseca, Adivaldo Henrique
  • Department of Epidemiology and Public Health, Rural Federal University of Rio de Janeiro-UFRRJ, Seropédica, RJ, Brazil.
Gomes Jusi, Márcia Mariza
  • Department of Animal Pathology, Julio Mesquita Filho State University, UNESP/Jaboticabal, Rod. Paulo Castelanne s/n, Jaboticabal, São Paulo, 4884-900, Brazil.
Machado, Rosangela Zacarias
  • Department of Animal Pathology, Julio Mesquita Filho State University, UNESP/Jaboticabal, Rod. Paulo Castelanne s/n, Jaboticabal, São Paulo, 4884-900, Brazil.
Munhoz, Alexandre Dias
  • Department of Agricultural and Environmental Sciences, State University of Santa Cruz - UESC, Soane Nazaré de Andrade Campus, Ilhéus, BA, Brazil. munhoz@uesc.br.

MeSH Terms

  • Anaplasma / isolation & purification
  • Anaplasma / pathogenicity
  • Anaplasmosis / epidemiology
  • Animals
  • Borrelia / isolation & purification
  • Borrelia / pathogenicity
  • Brazil / epidemiology
  • Equidae / parasitology
  • Female
  • Leishmania / isolation & purification
  • Leishmania / pathogenicity
  • Leishmaniasis / epidemiology
  • Leishmaniasis / veterinary
  • Lyme Disease / epidemiology
  • Lyme Disease / veterinary
  • Male
  • Rickettsia / isolation & purification
  • Rickettsia / pathogenicity
  • Rickettsia Infections / epidemiology
  • Rickettsia Infections / veterinary
  • Zoonoses / epidemiology
  • Zoonoses / parasitology

Grant Funding

  • 003/2014 / CAPES/FAPESB

Conflict of Interest Statement

The authors declare that they have no competing interests.

References

This article includes 82 references
  1. Butler CM, Houwers DJ, Jongejan F, van der Kolk JH. Borrelia burgdorferi infections with special reference to horses. A review.. Vet Q 2005;27:146–56.
    doi: 10.1080/01652176.2002.9695196pubmed: 16402512google scholar: lookup
  2. Ishag MY, Majid AM, Abuobeida MM. Studies on Toxoplasmosis in horses in Khartoum State-Sudan.. J Vet Med Anim Prod 2014;5:29–35.
  3. Galo KR, Fonseca AH, Madureira RC, Neto JDB. Frequência de anticorpos homólogos anti-Borrelia burgdorferi em equinos na mesorregião metropolitana de Belém. Estado do Pará. Pesqui Vet Bras 2009;29:229–232.
  4. Brooks DR, Hoberg EP. How will global climate change affect parasite-host assemblages?. Trends Parasitol 2007;23:571–574.
    doi: 10.1016/j.pt.2007.08.016pubmed: 17962073google scholar: lookup
  5. . Leishmaniose visceral: recomendações clínicas para redução da letalidade.. Ministério da Saúde. 2011;9:1–78.
  6. Naucke TJ, Menn B, Massberg D, Lorentz S. Sandflies and leishmaniasis in Germany.. Parasitol Res 2008;103:65–68.
    doi: 10.1007/s00436-008-1052-ypubmed: 19030887google scholar: lookup
  7. Rikihisa Y. Mechanisms of obligatory intracellular infection with Anaplasma phagocytophilum.. Clin Microbiol Rev 2011;24:469–489.
    doi: 10.1128/CMR.00064-10pmc: PMC3131063pubmed: 21734244google scholar: lookup
  8. Hansen MGB, Christoffersen M, Thuesen LR, Petersen MR, Bojesen AM. Seroprevalence of Borrelia burgdorferi sensu lato and Anaplasma phagocytophilum in Danish horses.. Acta Vet Scand 2010;52:3.
    doi: 10.1186/1751-0147-52-3pmc: PMC2818635pubmed: 20082693google scholar: lookup
  9. Kiss T, Cadar D, Krupaci AF, Bordeanu A, Brudaşcă GF, Mihalca AD. Serological reactivity to Borrelia burgdorferi sensu lato in dogs and horses from distinct areas in Romania.. Vector Borne Zoonotic Dis 2011;11:1259–62.
    pubmed: 21612524
  10. Maurizi L, Marie J, Aoun O, Courtin C, Gorsane S, Chal D. Seroprevalence survey of Equine Lyme Borreliosis in France and in Sub-Saharan Africa.. Vector-Borne Zoonotic Dis 2010;10:7–10.
    doi: 10.1089/vbz.2009.0083pubmed: 19877821google scholar: lookup
  11. Brüning A. Equine piroplasmosis an update on diagnosis, treatment and prevention.. Br Vet J 1996;152:139–151.
    doi: 10.1016/S0007-1935(96)80070-4pubmed: 8680838google scholar: lookup
  12. Coiro CJ, Langoni H, da Silva RC. Epidemiological aspects in the Leptospira spp. and Toxoplasma gondii infection in horses from Botucatu, São Paulo Brazil.. J Equine Vet Sci 2012;32:620–3.
  13. Reuss SM. Review of equine cutaneous leishmaniasis : not just a foreign animal disease.. Am Assoc Equine Pract 2013;59:256–60.
  14. Ribeiro AJ, Cardoso L, Maia JM, Coutinho T, Cotovio M. Prevalence of Theileria equi, Babesia caballi, and Anaplasma phagocytophilum in horses from the north of Portugal.. Parasitol Res 2013;112:2611–2617.
    doi: 10.1007/s00436-013-3429-9pubmed: 23591484google scholar: lookup
  15. Truppel JH, Otomura F, Teodoro U, Massafera R, Da Costa-Ribeiro MCV, Catarino CM. Can equids be a reservoir of Leishmania braziliensis in endemic areas?. PLoS ONE 2014;9:1–6.
  16. . Manual de Vigilância e Controle da Leishmaniose Visceral.. Ministério da Saúde. 2006;1a edição:120.
  17. DeVilbiss BA, Mohammed HO, Divers TJ. Perception of equine practitioners regarding the occurrence of selected equine neurologic diseases in the Northeast over a 10-year period.. J Equine Vet Sci 2009;29:237–46.
  18. Madureira RC, Rangel CP, Barbosa-Neto DJ, Fonseca AH. Sorologia para Borrelia Burgdorferi em equinos da ilha de Marajó e município de Castanhal, Pará. Brasil. Rev Ciências da Vida 2009;29:9–15.
  19. Parra AC. Investigação diagnóstica de doença concomitante Babesiose e Anaplasmose em rebanho equino, por técnicas de Nested PCR, c – ELISA ou ELISA indireto.. Universidade de São Paulo; 2009.
  20. Salvagni CA, Dagnone AS, Gomes TS, Mota JS, Andrade GM, Baldani CD. Serologic evidence of equine granulocytic anaplasmosis in horses from central West Brazil.. Rev Bras Parasitol Vet 2010;19:135–40.
  21. Soares IR, Silva SO, Moreira FM, Prado LG, Fantini P, Maranhão R. First evidence of autochthonous cases of Leishmania (Leishmania) infantum in horse (Equus caballus) in the Americas and mixed infection of Leishmania infantum and Leishmania (Viannia) braziliensis.. Vet Parasitol 2013;197:665–9.
    doi: 10.1016/j.vetpar.2013.06.014pubmed: 23845306google scholar: lookup
  22. Vedovello-Filho D, Jorge FA, Lonardoni MVC, Teodoro U, Silveira TGV. American cutaneous leishmaniasis in horses from endemic areas in the north-central Mesoregion of Paraná state, Brazil.. Zoonoses Public Health 2008;55:149–155.
  23. Ricketts HT. Some aspects of Rocky Moutain spotted fever as shown by recent investigations.. Med Rec 1909;76:843–845.
    pubmed: 1775857
  24. Heinemann PG, Moore JJ. Experimental therapy of Rocky Moutain spotted fever: the preventive and curative action of a serum for spotted fever, and the inefficiency of sodium cacodylate as a curative agent for this disease in guinea pigs.. J Infect Dis 1912;10:294–304.
    doi: 10.1093/infdis/10.3.294google scholar: lookup
  25. . Produção da Pecuária Municipal 2010.. Inst Bras Geogr e Estatística -IBGE [Internet]. 2010;38:1–65.
  26. . Normais Climatológicas (1961–1999), Versão Revisada e Ampliada [Internet].. Digital. INMET, editor. Ministério da Agricultura e Reforma Agrária; 2010.
  27. Aragão HB, Fonseca F. Notas de Ixodologia. VIII. Lista e chave para os representantes da fauna ixodológica brasileira.. Mem Inst Oswaldo Cruz 1961;59:115–29.
  28. Martins TF, Onofrio VC, Barros-Battesti DM, Labruna MB. Nymphs of the genus Amblyomma (Acari: Ixodidae) of Brazil: descriptions, redescriptions, and identification key.. Ticks Tick Borne Dis 2010;1:75–99.
    doi: 10.1016/j.ttbdis.2010.03.002pubmed: 21771514google scholar: lookup
  29. Barros-Battesti DM, Arzua M, Bechara GH. Carrapatos de importância médico-veterinária da região neotropical: um guia ilustrado para identificação de espécie.. São Paulo: Vox/ICTTD-3/Butantan; 2006.
  30. Cordeiro MD, De Meireles GS, Da Silva JB, De Souza MMS, Da Fonseca AH. Soroprevalência para Borrelia spp. em cães no município de Seropédica, estado do Rio de Janeiro*.. Rev Bras Med Vet 2012;34:251–6.
  31. Machado RZ, Montassier HJ, Pinto AA, Lemos EG, Machado MRF, Valadão IFF. An enzyme-linked immunosorbent assay (ELISA) for the detection of antibodies against Babesia bovis in cattle.. Vet Parasitol 1997;71:17–26.
    doi: 10.1016/S0304-4017(97)00003-4pubmed: 9231985google scholar: lookup
  32. Labruna MB, Horta MC, Aguiar DM, Cavalcante GT, Pinter A, Gennari SM. Prevalence of Rickettsia infection in dogs from the urban and rural areas of Monte Negro Municipality, Western Amazon Brazil.. Vector-Borne Zoonotic Dis 2007;7:249–255.
    doi: 10.1089/vbz.2006.0621pubmed: 17627445google scholar: lookup
  33. Pinter A, Labruna MB. Isolation of Rickettsia rickettsii and Rickettsia bellii in cell culture from the tick Amblyomma aureolatum in Brazil.. Ann N Y Acad Sci 2006;1078:523–529.
    doi: 10.1196/annals.1374.103pubmed: 17114770google scholar: lookup
  34. Silveira I, Pacheco RC, Szabó MPJ, Ramos HGC, Labruna MB. Rickettsia parkeri in Brazil.. Emerg Infect Dis 2007;13:1111–1113.
    doi: 10.3201/eid1307.061397pmc: PMC2878225pubmed: 18214195google scholar: lookup
  35. Lachaud L, Chabbert E, Dubessay P, Dereure J, Lamothe J, Dedet JP. Value of two PCR methods for the diagnosis of canine visceral leishmaniasis and the detection of asymptomatic carriers.. Parasitology 2002;125:197–207.
    doi: 10.1017/S0031182002002081pubmed: 12358417google scholar: lookup
  36. de Bruijn MHL, Barker DC. Diagnosis of New World leishmaniasis: specific detection of species of the Leishmania braziliensis complex by amplification of kinetoplast DNA.. Acta Trop 1992;52:45–58.
    doi: 10.1016/0001-706X(92)90006-Jpubmed: 1359760google scholar: lookup
  37. Massung RF, Slater K, Owens JH, Nicholson WL, Mather TN, Solberg VB. Nested PCR assay for detection of granulocytic Ehrlichiae.. J Clin Microbiol 1998;36:1090–5.
    pmc: PMC104695pubmed: 9542943
  38. Birkenheuer AJ, Levy MG, Breitschwerdt EB. Development and evaluation of a Seminested PCR for detection and differentiation of Babesia gibsoni (Asian Genotype) and B. canis DN.. J Clin Microbiol 2003;41:4172–7.
  39. Lacerda L, Silva A, Freitas J, Cruz R, Said R, Munhoz A. Feline immunodeficiency virus and feline leukemia virus: frequency and associated factors in cats in northeastern Brazil.. Genet Mol Res 2017;16:8.
    doi: 10.4238/gmr16029633pubmed: 28510253google scholar: lookup
  40. Santolin IDAC, Famadas KM, McIntosh D. Detection and identification of Rickettsia agents in ticks collected from wild birds in Brazil by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis.. Rev Bras Med Vet 2013;35:68–73.
  41. Mangold AJ, Bargues MD, Mas-Coma S. Mitochondrial 16S rDNA sequences and phylogenetic relationships of species of Rhipicephalus and other tick genera among Metastriata (Acari: Ixodidae). Parasitol Res 1998;84:478–484.
    doi: 10.1007/s004360050433pubmed: 9660138google scholar: lookup
  42. McIntosh D, Bezerra RA, Luz HR, Faccini JLH, Gaiotto FA, Giné GAF. Detection of Rickettsia bellii and Rickettsia amblyommii in Amblyomma longirostre (Acari: Ixodidae) from Bahia state, Northeast Brazil.. Brazil J Microbiol 2015;46:879–883.
  43. Starkweather J. Linear Mixed Effects Modelling using R.. 2010.
  44. Dohoo IR, Martin S. Veterinary Epidemiologic Research.. 1. Charlottrtown: University Prince Edward Island; 2003.
  45. R Development Core Team. R: a language and environment for statistical computing [Internet].. Vienna: R Foundation for Statistical Computing; 2016.
  46. Bates D, Mächler M, Bolker BM, Walker SC. Fitting linear mixed-effects models using lme4.. J Stat Softw 2015;67:1–48.
    doi: 10.18637/jss.v067.i01google scholar: lookup
  47. Krawczak FS, Nieri-Bastos FA, Nunes FP, Soares JF, Moraes-Filho J, Labruna MB. Rickettsial infection in Amblyomma cajennense ticks and capybaras (Hydrochoerus hydrochaeris) in a Brazilian spotted fever-endemic area.. Parasit Vectors 2014;7:7.
    doi: 10.1186/1756-3305-7-7pmc: PMC3892071pubmed: 24387674google scholar: lookup
  48. Basile RC, Yoshinari NH, Mantovani E, Bonoldi VN, da Macoris D, de Queiroz-Neto A. Brazilian borreliosis with special emphasis on humans and horses.. Brazil J Microbiol 2017;48:167–72.
    doi: 10.1016/j.bjm.2016.09.005pmc: PMC5220628pubmed: 27769883google scholar: lookup
  49. de Oliveira PB, Harvey TV, Fehlberg HF, Rocha JM, Martins TF, da Acosta ICL. Serologic and molecular survey of Rickettsia spp. in dogs, horses and ticks from the Atlantic rainforest of the state of Bahia Brazil.. Exp Appl Acarol 2019;78:431–42.
    doi: 10.1007/s10493-019-00397-xpubmed: 31270640google scholar: lookup
  50. Horta MC, Labruna MB, Sangione LA, Vianna MCB, Gennari SM, Galvão M a M. Prevalence of antibodies to spotted fever group Rickettsiae in humans and domestic animals in a brazilian spotted fever-endemic area in the state of São Paulo, Brazil: serologic evidence for infection by Rickettsia Rickettsii and another spotted fever group Rickettsia.. Am J Trop Med Hyg 2004;71:93–7.
    pubmed: 15238696
  51. Otomura FH, Sangioni LA, Pacheco RC, Labruna MB, Galhardo JA, Ribeiro MG. Anticorpos anti-rickettsias do grupo da febre maculosa em equídeos e caninos no norte do Estado do Paraná, Brasil.. Arq Bras Med Vet e Zootec 2010;62:761–764.
  52. Castagnolli KC, De Figueiredo LB, Santana DA, De Castro MB, Romano MA, Szabó MPJ. Acquired resistance of horses to Amblyomma cajennense (Fabricius, 1787) ticks.. Vet Parasitol 2003;117:271–283.
    doi: 10.1016/j.vetpar.2003.09.004pubmed: 14637029google scholar: lookup
  53. Lopes MG. Infecção por Rickettsia spp. em equídeos e carrapatos do Centro-Norte do Piauí.. 2012.
  54. Martins MEP, Brito WMED, Labruna MB, Moraes-Filho J. Identificação e pesquisa de Rickettsia spp. em carrapatos colhidos em cães e equinos de Quirinópolis, Goiás, Brasil.. Multi-Science J 2015;1:120–7.
    doi: 10.33837/msj.v1i1.58google scholar: lookup
  55. BRASIL. DATASUS/FEBRE MACULOSA - Casos confirmados no Sistema de Informação de Agravos de Notificação [Internet].. SinanNet 2018 [cited 2017 Dec 20].
  56. Paddock CD, Brenner O, Vaid C, Boyd DB, Berg JM, Joseph RJ. Short report: concurrent Rocky Mountain spotted fever in a dog and its owner.. Am J Trop Med Hyg 2002;66:197–199.
    doi: 10.4269/ajtmh.2002.66.197pubmed: 12135293google scholar: lookup
  57. Sangioni LA, Horta MC, Vianna MCB, Gennari SM, Soares RM, Galvão MAM. Rickettsial infection in animals and Brazilian spotted fever endemicity.. Emerg Infect Dis 2005;11:265–270.
    doi: 10.3201/eid1102.040656pmc: PMC3320454pubmed: 15752445google scholar: lookup
  58. Pinter A, Horta MC, Pacheco RC, Moraes-Filho J, Labruna MB. Serosurvey of Rickettsia spp. in dogs and humans from an endemic area for Brazilian spotted fever in State of São Paulo. Brazil.. Cad Saúde Pública 2008;24:247–52.
  59. Nasser JT, Lana RC, dos Silva CM, Lourenço RW, da Silva DC, Donalísio MR. Urbanization of Brazilian spotted fever in a municipality of the southeastern region: epidemiology and spatial distribution.. Rev Bras Epidemiol 2015;18:299–312.
    doi: 10.1590/1980-5497201500020002pubmed: 26083504google scholar: lookup
  60. Prado RFS, De CCHC, Cordeiro MD, Pires MS, Cepeda MB, Mafra C. Seroprevalence of homologous anti-Borrelia burgdorferi antibodies in horses of military use in Brazil.. Rev Bras Ciência Veterinária 2017;24:72–76.
    doi: 10.4322/rbcv.2017.015google scholar: lookup
  61. Salles RS, Fonseca AH, Madureira RC, Yoshinari NH. Sorologia para Borrelia burgdorferi latu sensu em equinos no estado do Rio de Janeiro.. Hora Veterinária 2002;127:46–49.
  62. Madureira RC, Corrêa F do N, Cunha NC da, Guedes D da S, Fonseca AH da. Ocorrência de anticorpos homólogos anti-Borrelia burgdorferi em eqüinos de propriedades dos municípios de Três Rios e Vassouras, estado do Rio de Janeiro.. Rev Bras Ciência Veterinária 2007;14:43–6.
  63. Carlos RSA, Muniz-Neta ES, Spagnol FH, Oliveira LLS, Brito RLLDE, Albuquerque GR. Frequência de anticorpos anti Erlichia canis, Borrelia burgdorferi e antígenos de Dirofilaria immitis em cães na microrregião Ilhéus-Itabuna, Bahia, Brasil.. Rev Bras Parasitol Veterinária 2007;16:117–20.
    pubmed: 18078596
  64. Yoshinari NH, Mantovani E, Bonoldi VLN, Marangoni RG, Gauditano G. Doença de Lyme-Símile Brasileira ou Síndrome Baggio-Yoshinari: Zoonose exótica e emergente transmitida por carrapatos.. Rev Assoc Med Bras 2010;56:363–369.
  65. Cordeiro MD, Bahia M, Magalhães-Matos PC, Cepeda MB, Guterres A, Fonseca AH. Morphological, molecular and phylogenetic characterization of Borrelia theileri in Rhipicephalus microplus.. Rev Bras Parasitol Vet 2018;27:555–561.
    doi: 10.1590/s1984-296120180083pubmed: 30517424google scholar: lookup
  66. Nascimento DA, da Vieira RF, Vieira TSWJ, dos Todelo R, Tamekuni K, dos Santos NJ. Serosurvey of Borrelia in dogs, horses, and humans exposed to ticks in a rural settlement of southern Brazil.. Brazil J Vet Parasitol 2016;25:418–22.
    doi: 10.1590/s1984-29612016085pubmed: 27982299google scholar: lookup
  67. Egenvall A, Franzén P, Gunnarsson A, Engvall EO, Vågsholm I, Wikström UB. 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.
    doi: 10.1016/S0167-5877(01)00187-8pubmed: 11311953google scholar: lookup
  68. 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;30:1300–1304.
    doi: 10.1111/jvim.13973pmc: PMC5089602pubmed: 27214745google scholar: lookup
  69. Lee SH, Yun SH, Choi E, Park YS, Lee SE, Cho GJ. Serological detection of Borrelia Burgdorferi among horses in Korea.. Korean J Parasitol 2016;54:97–101.
    doi: 10.3347/kjp.2016.54.1.97pmc: PMC4792323pubmed: 26951987google scholar: lookup
  70. Passamonti F, Veronesi F, Cappelli K, Capomaccio S, Reginato A, Miglio A. Polysynovitis in a horse due to Borrelia burgdorferi sensu lato infection – Case study.. Ann Agric Environ Med 2015;22:247–250.
    doi: 10.5604/12321966.1152074pubmed: 26094517google scholar: lookup
  71. Butler CM, Van O-O, Werners AH, Stout TAE. Borrelia burgdorferi and Anaplasma phagocytophilum in ticks and their equine hosts: a prospective clinical and diagnostic study of 47 horses following removal of a feeding tick.. Pferdeheilkunde 2016;32:335.
    doi: 10.21836/PEM20160406google scholar: lookup
  72. . Leishmaniose Tegumentar Americana - Casos confirmados notificados no sistema de informação de agravos de notificação.. Ministério da Saúde. 2017;26:2–3.
  73. . Produção da pecuária municipal 2015.. Inst Bras Geogr e Estatística - IBGE. 2015;43:1–49.
  74. Aguilar CM, Fernandez E, de Fernandez R, Deane LM. Study of an outbreak of cutaneous leishmaniasis in Venezuela. The role of domestic animals.. Mem Inst Oswaldo Cruz 1984;79:181–95.
  75. Benassi JC, Benvenga GU, Ferreira HL, Soares RM, Silva DT, Pereira VF. Molecular and serological detection of Leishmania spp. in horses from an endemic area for canine visceral leishmaniasis in southeastern Brazil.. Pesqui Vet Bras 2018;38:1058–63.
  76. Follador I, Araujo C, Cardoso MA, Tavares-Neto J, Barral A, Miranda JC. Surto de leishmaniose tegumentar americana em Canoa, Santo Amaro, Bahia. Brasil. Rev Soc Bras Med Trop 1999;32:497–503.
  77. Slivinska K, Víchová B, Werszko J, Szewczyk T, Wróblewski Z, Peťko B. Molecular surveillance of Theileria equi and Anaplasma phagocytophilum infections in horses from Ukraine, Poland and Slovakia.. Vet Parasitol 2016;215:35–7.
    doi: 10.1016/j.vetpar.2015.10.025pubmed: 26790735google scholar: lookup
  78. Dziegiel B, Adaszek Ł, Kalinowski M, Winiarczyk S. Equine granulocytic anaplasmosis.. Res Vet Sci 2013;95:316–320.
    doi: 10.1016/j.rvsc.2013.05.010pubmed: 23790982google scholar: lookup
  79. Franzén P, Aspan A, Egenvall A, Gunnarsson A, Åberg 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;19:232–9.
  80. Prado LG, Palhares MS, Bastos C V., da Silveira JAG, Ribeiro ÁAR, Miranda ALS. Anaplasma phagocytophilum direct detection and exposure evidence in equines from two breeding farms from Minas Gerais, Brazil.. Arq do Inst Biológico 2018;85:1–6.
  81. Lopes AP, Sousa S, Dubey JP, Ribeiro AJ, Silvestre R, Cotovio M. Prevalence of antibodies to Leishmania infantum and Toxoplasma gondii in horses from the north of Portugal.. Parasit Vectors 2013;6:178.
    doi: 10.1186/1756-3305-6-178pmc: PMC3686701pubmed: 23773870google scholar: lookup
  82. Kouam MK, Diakou A, Kanzoura V, Papadopoulos E, Gajadhar AA, Theodoropoulos G. A seroepidemiological study of exposure to Toxoplasma, Leishmania, Echinococcus and Trichinella in equids in Greece and analysis of risk factors.. Vet Parasitol 2010;170:170–5.
    doi: 10.1016/j.vetpar.2010.02.004pubmed: 20197215google scholar: lookup

Citations

This article has been cited 5 times.
  1. Badillo-Viloria M, García-Bocanegra I, de la Rosa Jaramillo S, Mattar S, Frías-Casas M, Cano-Terriza D. Molecular Characterization and Epidemiology of Anaplasmataceae in Ticks and Domestic Animals in the Colombian Caribbean. Animals (Basel) 2025 Dec 19;16(1).
    doi: 10.3390/ani16010008pubmed: 41514697google scholar: lookup
  2. Labruna MB, Faccini-Martínez ÁA, Muñoz-Leal S, Szabó MPJ, Angerami RN. Lyme borreliosis in Brazil: a critical review on the Baggio-Yoshinari syndrome (Brazilian Lyme-like disease). Clin Microbiol Rev 2024 Dec 10;37(4):e0009724.
    doi: 10.1128/cmr.00097-24pubmed: 39494872google scholar: lookup
  3. Athanasiou LV, Katsogiannou EG, Tyrnenopoulou P, Gougoulis D, Apostolidis KN, Papadakis SM, Kokkinaki KCG, Papatsiros VG, Tsokana CN. 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 Sep 11;13(9).
    doi: 10.3390/biom13091374pubmed: 37759774google scholar: lookup
  4. Bonilla-Aldana DK, Castaño-Betancourt KJ, Ortega-Martínez JM, Ulloque-Badaracco JR, Hernandez-Bustamante EA, Benites-Zapata VA, Rodriguez-Morales AJ. Prevalence of zoonotic and non-zoonotic Rickettsia in horses: A systematic review and meta-analysis. New Microbes New Infect 2023 Jan;51:101068.
    doi: 10.1016/j.nmni.2022.101068pubmed: 36632173google scholar: lookup
  5. Kamran K, Akbar A, Naseem M, Samad A, Samiullah, Achakzai JK, Rehman ZU, Sohail Sajid M, Ali A. Participatory appraisal for healthcare and welfare management strategies of donkeys (Equus ascinus) in Balochistan, Pakistan. Front Vet Sci 2022;9:1005079.
    doi: 10.3389/fvets.2022.1005079pubmed: 36118345google scholar: lookup