Analyze Diet
Zoonoses and public health2007; 54(1); 8-15; doi: 10.1111/j.1863-2378.2007.00989.x

Observed prevalence of tick-borne pathogens in domestic animals in Sicily, Italy during 2003-2005.

Abstract: The objective of this study was to characterize the observed prevalence of tick-borne pathogens (TBP) in domestic animals in Sicily, Italy during 2003-2005. Serological (competitive ELISA and indirect immunofluorescence antibody, n = 3299) and DNA tests (polymerase chain reaction and reverse line blot, n = 2565) were conducted on horse, donkey, cattle, sheep, goat, pig and dog samples. Pathogens analysed included Anaplasma, Ehrlichia, Rickettsia, Babesia and Theileria species, and Coxiella burnetii. The most prevalent TBP were Anaplasma and Babesia species. The results reported herein suggested that cattle could serve as the major reservoir for Babesia and Theileria spp. while for Anaplasma spp. cattle, dogs, sheep and goats may be the most important reservoir species. These results expanded our knowledge about the prevalence of TBP in Sicily and provided information to understand the epidemiology of tick-borne diseases and may help to implement measures to diagnose, treat and control transmission to humans and animals in this region.
Publication Date: 2007-03-16 PubMed ID: 17359441DOI: 10.1111/j.1863-2378.2007.00989.xGoogle 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
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research examined the prevalence of tick-borne diseases in domestic animals in Sicily, Italy, from 2003 to 2005. The study found that the most common diseases were Anaplasma and Babesia species, and identified cattle, dogs, sheep, and goats as the major reservoirs for these diseases.

Objective and Methodology of the Study

  • The study aimed to understand the prevalence of tick-borne pathogens (TBP) in domestic animals within Sicily, Italy, during the period of 2003-2005.
  • To achieve this, a combination of serological and DNA tests were used. These included competitive ELISA, indirect immunofluorescence antibody tests, polymerase chain reaction, and reverse line blot.
  • These tests were deployed on a variety of domestic animals: horses, donkeys, cattle, sheep, goats, pigs, and dogs. The total number of tests conducted consisted of 3299 serological and 2565 DNA samples.

Examined Pathogens

  • The research focused on several key tick-borne pathogens. These included a variety of Anaplasma, Ehrlichia, Rickettsia, Babesia and Theileria species, in addition to Coxiella burnetii.
  • Each of these is a known pathogen that can be transmitted by ticks and cause illness in a variety of domestic animals.

Results of the Study

  • The study found that the most prevalent tick-borne pathogens in these domestic animals were Anaplasma and Babesia species.
  • The research also suggested that the principal reservoir for Babesia and Theileria species could be cattle, while for Anaplasma species, the major reservoir appears to be an assortment of cattle, dogs, sheep, and goats. A ‘reservoir’ is an animal species that hosts a pathogen under natural conditions.

Conclusion

  • Overall, these findings offer insights into the state of TBP in Sicily, illuminating the epidemiology of tick-borne diseases in the region.
  • This kind of information can be useful in devising measures to diagnose, treat and control the transmission of these diseases, not only within the animal population but also to human beings.

Cite This Article

APA
Torina A, Vicente J, Alongi A, Scimeca S, Turlá R, Nicosia S, Di Marco V, Caracappa S, de la Fuente J. (2007). Observed prevalence of tick-borne pathogens in domestic animals in Sicily, Italy during 2003-2005. Zoonoses Public Health, 54(1), 8-15. https://doi.org/10.1111/j.1863-2378.2007.00989.x

Publication

ISSN: 1863-1959
NlmUniqueID: 101300786
Country: Germany
Language: English
Volume: 54
Issue: 1
Pages: 8-15

Researcher Affiliations

Torina, A
  • Instituto Zooprofilattico Sperimentale della Sicilia, Via G. Marinuzzi no. 3, 90129 Palermo, Sicily, Italy.
Vicente, J
    Alongi, A
      Scimeca, S
        Turlá, R
          Nicosia, S
            Di Marco, V
              Caracappa, S
                de la Fuente, J

                  MeSH Terms

                  • Anaplasma
                  • Anaplasmosis / epidemiology
                  • Animals
                  • Animals, Domestic
                  • Antibodies, Bacterial / blood
                  • Arachnid Vectors / microbiology
                  • Arachnid Vectors / parasitology
                  • Babesia
                  • Babesiosis / epidemiology
                  • Babesiosis / veterinary
                  • Cattle
                  • Disease Reservoirs / veterinary
                  • Ehrlichia
                  • Ehrlichiosis / epidemiology
                  • Enzyme-Linked Immunosorbent Assay / methods
                  • Enzyme-Linked Immunosorbent Assay / veterinary
                  • Goats
                  • Horses
                  • Italy / epidemiology
                  • Sentinel Surveillance / veterinary
                  • Seroepidemiologic Studies
                  • Sheep
                  • Swine
                  • Theileria
                  • Theileriasis / epidemiology
                  • Tick-Borne Diseases / epidemiology
                  • Tick-Borne Diseases / veterinary
                  • Ticks / microbiology
                  • Ticks / parasitology

                  Citations

                  This article has been cited 36 times.
                  1. Defaye B, Moutailler S, Grech-Angelini S, Galon C, Ferrandi S, Pasqualini V, Quilichini Y. Detecting zoonotic and non-zoonotic pathogens in livestock and their ticks in Corsican wetlands.. Vet Med Sci 2022 Nov;8(6):2662-2677.
                    doi: 10.1002/vms3.956pubmed: 36207820google scholar: lookup
                  2. Saratsis A, Ligda P, Aal F, Jelicic M, Polgar J, de Vries M, Mastranestasis I, Musella V, Rinaldi L, Jongejan F, Sotiraki S. The Scenario of Ticks and Tick-Borne Pathogens of Sheep on a Mediterranean Island.. Microorganisms 2022 Jul 31;10(8).
                  3. 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).
                  4. M'ghirbi Y, Oporto B, Hurtado A, Bouattour A. First Molecular Evidence for the Presence of Anaplasma phagocytophilum in Naturally Infected Small Ruminants in Tunisia, and Confirmation of Anaplasma ovis Endemicity.. Pathogens 2022 Mar 3;11(3).
                    doi: 10.3390/pathogens11030315pubmed: 35335639google scholar: lookup
                  5. Rubel W, Schoneberg C, Wolf A, Ganter M, Bauer BU. Seroprevalence and Risk Factors of Anaplasma spp. in German Small Ruminant Flocks.. Animals (Basel) 2021 Sep 25;11(10).
                    doi: 10.3390/ani11102793pubmed: 34679815google scholar: lookup
                  6. El Hamiani Khatat S, Daminet S, Duchateau L, Elhachimi L, Kachani M, Sahibi H. Epidemiological and Clinicopathological Features of Anaplasma phagocytophilum Infection in Dogs: A Systematic Review.. Front Vet Sci 2021;8:686644.
                    doi: 10.3389/fvets.2021.686644pubmed: 34250067google scholar: lookup
                  7. 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
                  8. Perrucci S, Guardone L, Altomonte I, Salari F, Nardoni S, Martini M, Mancianti F. Apicomplexan Protozoa Responsible for Reproductive Disorders: Occurrence of DNA in Blood and Milk of Donkeys (Equus asinus) and Minireview of the Related Literature.. Pathogens 2021 Jan 22;10(2).
                    doi: 10.3390/pathogens10020111pubmed: 33499205google scholar: lookup
                  9. Ebani VV. Retrospective Study on the Occurrence of Antibodies against Coxiella burnetii in Dogs from Central Italy.. Pathogens 2020 Dec 20;9(12).
                    doi: 10.3390/pathogens9121068pubmed: 33419246google scholar: lookup
                  10. Matei IA, Estrada-Peña A, Cutler SJ, Vayssier-Taussat M, Varela-Castro L, Potkonjak A, Zeller H, Mihalca AD. A review on the eco-epidemiology and clinical management of human granulocytic anaplasmosis and its agent in Europe.. Parasit Vectors 2019 Dec 21;12(1):599.
                    doi: 10.1186/s13071-019-3852-6pubmed: 31864403google scholar: lookup
                  11. Pienaar R, Josemans A, Latif AA, Mans BJ. The host-specificity of Theileria sp. (sable) and Theileria sp. (sable-like) in African Bovidae and detection of novel Theileria in antelope and giraffe.. Parasitology 2020 Feb;147(2):213-224.
                    doi: 10.1017/S003118201900132Xpubmed: 31566155google scholar: lookup
                  12. Ebani VV. Serological Survey of Ehrlichia canis and Anaplasma phagocytophilum in Dogs from Central Italy: An Update (2013⁻2017).. Pathogens 2019 Jan 4;8(1).
                    doi: 10.3390/pathogens8010003pubmed: 30621134google scholar: lookup
                  13. Zhou Z, Wu Y, Chen Y, Wang Z, Hu S, Zhou R, Dong C, Lin H, Nie K. Molecular and serological prevalence of Toxoplasma gondii and Anaplasma spp. infection in goats from Chongqing Municipality, China.. Parasite 2018;25:20.
                    doi: 10.1051/parasite/2018024pubmed: 29633708google scholar: lookup
                  14. Teshale S, Geysen D, Ameni G, Dorny P, Berkvens D. Survey of Anaplasma phagocytophilum and Anaplasma sp. 'Omatjenne' infection in cattle in Africa with special reference to Ethiopia.. Parasit Vectors 2018 Mar 9;11(1):162.
                    doi: 10.1186/s13071-018-2633-ypubmed: 29523210google scholar: lookup
                  15. Piantedosi D, Neola B, D'Alessio N, Di Prisco F, Santoro M, Pacifico L, Sgroi G, Auletta L, Buch J, Chandrashekar R, Breitschwerdt EB, Veneziano V. Seroprevalence and risk factors associated with Ehrlichia canis, Anaplasma spp., Borrelia burgdorferi sensu lato, and D. immitis in hunting dogs from southern Italy.. Parasitol Res 2017 Oct;116(10):2651-2660.
                    doi: 10.1007/s00436-017-5574-zpubmed: 28776227google scholar: lookup
                  16. Bilgic HB, Bakırcı S, Kose O, Unlu AH, Hacılarlıoglu S, Eren H, Weir W, Karagenc T. Prevalence of tick-borne haemoparasites in small ruminants in Turkey and diagnostic sensitivity of single-PCR and RLB.. Parasit Vectors 2017 Apr 27;10(1):211.
                    doi: 10.1186/s13071-017-2151-3pubmed: 28449722google scholar: lookup
                  17. Elhamiani Khatat S, Daminet S, Kachani M, Leutenegger CM, Duchateau L, El Amri H, Hing M, Azrib R, Sahibi H. Anaplasma spp. in dogs and owners in north-western Morocco.. Parasit Vectors 2017 Apr 24;10(1):202.
                    doi: 10.1186/s13071-017-2148-ypubmed: 28438220google scholar: lookup
                  18. M'ghirbi Y, Bèji M, Oporto B, Khrouf F, Hurtado A, Bouattour A. Anaplasma marginale and A. phagocytophilum in cattle in Tunisia.. Parasit Vectors 2016 Oct 20;9(1):556.
                    doi: 10.1186/s13071-016-1840-7pubmed: 27765073google scholar: lookup
                  19. Seong G, Han YJ, Chae JB, Chae JS, Yu DH, Lee YS, Park J, Park BK, Yoo JG, Choi KS. Detection of Anaplasma sp. in Korean Native Goats (Capra aegagrus hircus) on Jeju Island, Korea.. Korean J Parasitol 2015 Dec;53(6):765-9.
                    doi: 10.3347/kjp.2015.53.6.765pubmed: 26797447google scholar: lookup
                  20. 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
                  21. Solano-Gallego L, Caprì A, Pennisi MG, Caldin M, Furlanello T, Trotta M. Acute febrile illness is associated with Rickettsia spp infection in dogs.. Parasit Vectors 2015 Apr 10;8:216.
                    doi: 10.1186/s13071-015-0824-3pubmed: 25886403google scholar: lookup
                  22. Sainz Á, Roura X, Miró G, Estrada-Peña A, Kohn B, Harrus S, Solano-Gallego L. Guideline for veterinary practitioners on canine ehrlichiosis and anaplasmosis in Europe.. Parasit Vectors 2015 Feb 4;8:75.
                    doi: 10.1186/s13071-015-0649-0pubmed: 25649069google scholar: lookup
                  23. Lledó L, Domínguez-Peñafiel G, Giménez-Pardo C, Gegúndez I, González R, Saz JV. Molecular and serological study of rickettsial infection in humans, and in wild and farm animals, in the province of Burgos, Spain.. Vector Borne Zoonotic Dis 2014 Jun;14(6):383-8.
                    doi: 10.1089/vbz.2013.1513pubmed: 24866558google scholar: lookup
                  24. Ceci L, Iarussi F, Greco B, Lacinio R, Fornelli S, Carelli G. Retrospective study of hemoparasites in cattle in southern Italy by reverse line blot hybridization.. J Vet Med Sci 2014 Jun;76(6):869-75.
                    doi: 10.1292/jvms.13-0365pubmed: 24614604google scholar: lookup
                  25. Torina A, Moreno-Cid JA, Blanda V, Fernández de Mera IG, de la Lastra JM, Scimeca S, Blanda M, Scariano ME, Briganò S, Disclafani R, Piazza A, Vicente J, Gortázar C, Caracappa S, Lelli RC, de la Fuente J. Control of tick infestations and pathogen prevalence in cattle and sheep farms vaccinated with the recombinant Subolesin-Major Surface Protein 1a chimeric antigen.. Parasit Vectors 2014 Jan 8;7:10.
                    doi: 10.1186/1756-3305-7-10pubmed: 24398155google scholar: lookup
                  26. Galindo RC, Ayllón N, Smrdel KS, Boadella M, Beltrán-Beck B, Mazariegos M, García N, de la Lastra JM, Avsic-Zupanc T, Kocan KM, Gortazar C, de la Fuente J. Gene expression profile suggests that pigs (Sus scrofa) are susceptible to Anaplasma phagocytophilum but control infection.. Parasit Vectors 2012 Aug 30;5:181.
                    doi: 10.1186/1756-3305-5-181pubmed: 22935149google scholar: lookup
                  27. M'ghirbi Y, Yaïch H, Ghorbel A, Bouattour A. Anaplasma phagocytophilum in horses and ticks in Tunisia.. Parasit Vectors 2012 Aug 30;5:180.
                    doi: 10.1186/1756-3305-5-180pubmed: 22935132google scholar: lookup
                  28. Giudice E, Giannetto C, Furco V, Alongi A, Torina A. Anaplasma phagocytophilum seroprevalence in equids: a survey in Sicily (Italy).. Parasitol Res 2012 Aug;111(2):951-5.
                    doi: 10.1007/s00436-012-2854-5pubmed: 22362364google scholar: lookup
                  29. Villar M, Ayllón N, Busby AT, Galindo RC, Blouin EF, Kocan KM, Bonzón-Kulichenko E, Zivkovic Z, Almazán C, Torina A, Vázquez J, de la Fuente J. Expression of Heat Shock and Other Stress Response Proteins in Ticks and Cultured Tick Cells in Response to Anaplasma spp. Infection and Heat Shock.. Int J Proteomics 2010;2010:657261.
                    doi: 10.1155/2010/657261pubmed: 22084679google scholar: lookup
                  30. Villar M, Torina A, Nuñez Y, Zivkovic Z, Marina A, Alongi A, Scimeca S, La Barbera G, Caracappa S, Vázquez J, Fuente Jde L. Application of highly sensitive saturation labeling to the analysis of differential protein expression in infected ticks from limited samples.. Proteome Sci 2010 Aug 12;8:43.
                    doi: 10.1186/1477-5956-8-43pubmed: 20704695google scholar: lookup
                  31. Torina A, Galindo RC, Vicente J, Di Marco V, Russo M, Aronica V, Fiasconaro M, Scimeca S, Alongi A, Caracappa S, Kocan KM, Gortazar C, de la Fuente J. Characterization of Anaplasma phagocytophilum and A. ovis infection in a naturally infected sheep flock with poor health condition.. Trop Anim Health Prod 2010 Oct;42(7):1327-31.
                    doi: 10.1007/s11250-010-9580-8pubmed: 20405320google scholar: lookup
                  32. Zivkovic Z, Torina A, Mitra R, Alongi A, Scimeca S, Kocan KM, Galindo RC, Almazán C, Blouin EF, Villar M, Nijhof AM, Mani R, La Barbera G, Caracappa S, Jongejan F, de la Fuente J. Subolesin expression in response to pathogen infection in ticks.. BMC Immunol 2010 Feb 19;11:7.
                    doi: 10.1186/1471-2172-11-7pubmed: 20170494google scholar: lookup
                  33. Hansen MG, Christoffersen M, Thuesen LR, Petersen MR, Bojesen AM. Seroprevalence of Borrelia burgdorferi sensu lato and Anaplasma phagocytophilum in Danish horses.. Acta Vet Scand 2010 Jan 18;52(1):3.
                    doi: 10.1186/1751-0147-52-3pubmed: 20082693google scholar: lookup
                  34. Torina A, Alongi A, Naranjo V, Estrada-Peña A, Vicente J, Scimeca S, Marino AM, Salina F, Caracappa S, de la Fuente J. Prevalence and genotypes of Anaplasma species and habitat suitability for ticks in a Mediterranean ecosystem.. Appl Environ Microbiol 2008 Dec;74(24):7578-84.
                    doi: 10.1128/AEM.01625-08pubmed: 18978093google scholar: lookup
                  35. Estrada-Peña A, Acevedo P, Ruiz-Fons F, Gortázar C, de la Fuente J. Evidence of the importance of host habitat use in predicting the dilution effect of wild boar for deer exposure to Anaplasma spp.. PLoS One 2008 Aug 20;3(8):e2999.
                    doi: 10.1371/journal.pone.0002999pubmed: 18714379google scholar: lookup
                  36. Torina A, Caracappa S. Anaplasmosis in cattle in Italy.. Vet Res Commun 2007 Aug;31 Suppl 1:73-8.
                    doi: 10.1007/s11259-007-0072-xpubmed: 17682850google scholar: lookup