Analyze Diet
Journal of wildlife diseases2014; 51(1); 137-147; doi: 10.7589/2013-11-316

Prevalence of Theileria equi and Babesia caballi as well as the identification of associated ticks in sympatric Grevy’s zebras (Equus grevyi) and donkeys (Equus africanus asinus) in northern Kenya.

Abstract: The role of equine piroplasmosis as a factor in the population decline of the Grevy's zebra is not known. We determined the prevalence of Babesia caballi and Theileria equi in cograzing Grevy's zebras (Equus grevyi) and donkeys (Equus africanus asinus) in northern Kenya and identified the associated tick vectors. Blood samples were taken from 71 donkeys and 16 Grevy's zebras from March to May 2011. A nested PCR reaction using 18s ribosomal (r)RNA primers on 87 blood spots showed 72% (51/71; 95% confidence interval [CI] 60.4-81.0%) of donkeys and 100% (16/16; 95% CI, 77.3-100%) of Grevy's zebras were T. equi positive. No samples were positive for B. caballi. Sequence comparison using the National Center for Biotechnology Information's basic local alignment search tool identified homologous 18s rRNA sequences with a global geographic spread. The T. equi-derived sequences were evaluated using Bayesian approaches with independent Metropolis-coupled Markov chain Monte Carlo runs. The sequences clustered with those found in Sudan, Croatia, Mongolia, and the US, with statistical support greater than 80% for the two main clades. Hyalomma tick species were found on both donkeys and Grevy's zebras, whereas Rhipicephalus pulchellus was found exclusively on Grevy's zebras and Hyalomma marginatum rupfipes on donkeys. The prevalence of T. equi was 100% in Grevy's zebras and 72% in donkeys with common tick vectors identified. Our results suggest that donkeys and Grevy's zebras can be asymptomatic carriers and that piroplasmosis is endemic in the study area.
Publication Date: 2014-11-08 PubMed ID: 25380362DOI: 10.7589/2013-11-316Google 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.

The researchers carried out a study to gauge the prevalence of the protozoan parasites, Theileria equi and Babesia caballi, in Grevy’s zebras and donkeys in northern Kenya. The study also identified the types of ticks that act as vectors for these parasites, and the preliminary findings suggest that both equine species are potential carriers of these parasites, which are endemic in the area.

Objective and Methodology of the Study

  • The study aimed to investigate the prevalence of two protozoa parasites, Theileria equi and Babesia caballi, in Grevy’s zebras and donkeys living together in northern Kenya. Moreover, it aimed to identify the tick species transmitting these parasites.
  • Blood samples were collected from a total of 87 equids – 71 donkeys and 16 zebras – between March and May 2011.
  • The researchers used a method called nested PCR, with 18s ribosomal RNA primers, to test the blood samples for the presence of the parasites.

Findings of the Study

  • The tests revealed that all zebras and 72% of the donkeys tested positive for T. equi. None of the samples were found to have B. caballi.
  • The T. equi-derived sequences matched with similar sequences in a global database, suggesting a wide geographic spread of these parasites. Statistical tools revealed these sequences were closely related to those found in Sudan, Croatia, Mongolia, and the US.
  • Various species of the Hyalomma tick were identified on both donkeys and zebras, showing them to be the likely vectors for T. equi. Rhipicephalus pulchellus ticks were found only on Grevy’s zebras, while Hyalomma marginatum rupfipes were identified only on donkeys.

Conclusion end Implications

  • The study provides strong evidence that T. equi is prevalent among the population of Grevy’s zebras and donkeys in the region, while B. caballi was not detected.
  • This occurrence, coupled with the identification of common tick vectors on both species, suggests that both may be reservoirs for these parasites, despite not showing any symptoms.
  • These findings indicate that piroplasmosis, a disease caused by these protozoan parasites, may be endemic in this part of Kenya, which might influence conservation approaches for the Grevy’s zebra.

Cite This Article

APA
Hawkins E, Kock R, McKeever D, Gakuya F, Musyoki C, Chege SM, Mutinda M, Kariuki E, Davidson Z, Low B, Skilton RA, Njahira MN, Wamalwa M, Maina E. (2014). Prevalence of Theileria equi and Babesia caballi as well as the identification of associated ticks in sympatric Grevy’s zebras (Equus grevyi) and donkeys (Equus africanus asinus) in northern Kenya. J Wildl Dis, 51(1), 137-147. https://doi.org/10.7589/2013-11-316

Publication

ISSN: 1943-3700
NlmUniqueID: 0244160
Country: United States
Language: English
Volume: 51
Issue: 1
Pages: 137-147

Researcher Affiliations

Hawkins, Elaine
  • 1 Royal Veterinary College, Hawkshead Lane, North Mymms, Hatfield, Herts AL9 7TA, UK.
Kock, Richard
    McKeever, Declan
      Gakuya, Francis
        Musyoki, Charles
          Chege, Stephen M
            Mutinda, Mathew
              Kariuki, Edward
                Davidson, Zeke
                  Low, Belinda
                    Skilton, Robert A
                      Njahira, Moses N
                        Wamalwa, Mark
                          Maina, Elsie

                            MeSH Terms

                            • Animals
                            • Babesia / isolation & purification
                            • Babesiosis / epidemiology
                            • Equidae
                            • Female
                            • Kenya / epidemiology
                            • Male
                            • Phylogeny
                            • Theileria / genetics
                            • Theileria / isolation & purification
                            • Theileriasis / epidemiology
                            • Theileriasis / parasitology
                            • Tick Infestations / epidemiology
                            • Tick Infestations / parasitology
                            • Tick Infestations / veterinary
                            • Ticks / microbiology
                            • Ticks / parasitology
                            • Ticks / physiology

                            Citations

                            This article has been cited 15 times.
                            1. Bhosale CR, Wilson KN, Ledger KJ, White ZS, Dorleans R, De Jesus CE, Wisely SM. Ticks and Tick-Borne Pathogens in Recreational Greenspaces in North Central Florida, USA. Microorganisms 2023 Mar 15;11(3).
                            2. Ledger KJ, Beati L, Wisely SM. Survey of Ticks and Tick-Borne Rickettsial and Protozoan Pathogens in Eswatini. Pathogens 2021 Aug 17;10(8).
                              doi: 10.3390/pathogens10081043pubmed: 34451507google scholar: lookup
                            3. Olivieri E, Kariuki E, Floriano AM, Castelli M, Tafesse YM, Magoga G, Kumsa B, Montagna M, Sassera D. Multi-country investigation of the diversity and associated microorganisms isolated from tick species from domestic animals, wildlife and vegetation in selected african countries. Exp Appl Acarol 2021 Mar;83(3):427-448.
                              doi: 10.1007/s10493-021-00598-3pubmed: 33646482google scholar: lookup
                            4. 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
                            5. Onyiche TE, Taioe MO, Molefe NI, Biu AA, Luka J, Omeh IJ, Yokoyama N, Thekisoe O. Equine piroplasmosis: an insight into global exposure of equids from 1990 to 2019 by systematic review and meta-analysis. Parasitology 2020 Nov;147(13):1411-1424.
                              doi: 10.1017/S0031182020001407pubmed: 32741382google scholar: lookup
                            6. Onyiche TE, Taioe MO, Ogo NI, Sivakumar T, Biu AA, Mbaya AW, Xuan X, Yokoyama N, Thekisoe O. Molecular evidence of Babesia caballi and Theileria equi in equines and ticks in Nigeria: prevalence and risk factors analysis. Parasitology 2020 Sep;147(11):1238-1248.
                              doi: 10.1017/S0031182020000992pubmed: 32605687google scholar: lookup
                            7. Bishop RP, Kappmeyer LS, Onzere CK, Odongo DO, Githaka N, Sears KP, Knowles DP, Fry LM. Equid infective Theileria cluster in distinct 18S rRNA gene clades comprising multiple taxa with unusually broad mammalian host ranges. Parasit Vectors 2020 May 19;13(1):261.
                              doi: 10.1186/s13071-020-04131-0pubmed: 32430015google scholar: lookup
                            8. King'ori E, Obanda V, Chiyo PI, Soriguer RC, Morrondo P, Angelone S. Molecular identification of Ehrlichia, Anaplasma, Babesia and Theileria in African elephants and their ticks. PLoS One 2019;14(12):e0226083.
                              doi: 10.1371/journal.pone.0226083pubmed: 31805127google scholar: lookup
                            9. Smith RM, Bhoora RV, Kotzé A, Grobler JP, Lee Dalton D. Translocation a potential corridor for equine piroplasms in Cape mountain zebra (Equus zebra zebra). Int J Parasitol Parasites Wildl 2019 Aug;9:130-133.
                              doi: 10.1016/j.ijppaw.2019.04.010pubmed: 31080728google scholar: lookup
                            10. Omar Abdallah M, Niu Q, Yu P, Guan G, Yang J, Chen Z, Liu G, Wei Y, Luo J, Yin H. Identification of piroplasm infection in questing ticks by RLB: a broad range extension of tick-borne piroplasm in China?. Parasitol Res 2016 May;115(5):2035-44.
                              doi: 10.1007/s00436-016-4947-zpubmed: 26896077google scholar: lookup
                            11. Zhang J, Kelly P, Li J, Xu C, Wang C. Molecular Detection of Theileria spp. in Livestock on Five Caribbean Islands. Biomed Res Int 2015;2015:624728.
                              doi: 10.1155/2015/624728pubmed: 26783522google scholar: lookup
                            12. Wamuyu L, Obanda V, Kariuki D, Gakuya F, Makanda M, Otiende M, Ommeh S. Molecular Detection and Characterization of Theileria Infecting Wildebeest (Connochaetes taurinus) in the Maasai Mara National Reserve, Kenya. Pathogens 2015 Aug 18;4(3):626-38.
                              doi: 10.3390/pathogens4030626pubmed: 26295263google scholar: lookup
                            13. Fachet-Lehmann K, Lindau A, Mackenstedt U. Unwanted souvenirs-import routes and pathogen detection of the non-endemic tick Rhipicephalus sanguineus s.l. in Germany. Exp Appl Acarol 2025 Mar 11;94(3):42.
                              doi: 10.1007/s10493-025-01010-0pubmed: 40067537google scholar: lookup
                            14. Onzere CK, Hassan A, Sears K, Kappmeyer LS, Villarino NF, Fry LM, Bastos RG. Transient efficacy of buparvaquone against Theileria haneyi in chronically infected horses. Parasit Vectors 2024 Aug 12;17(1):337.
                              doi: 10.1186/s13071-024-06397-0pubmed: 39129000google scholar: lookup
                            15. Cui Y, Cao M, Yu F, Zhao A, Tao D, Zhu T, Zhang Z, Qi M. Molecular detection of piroplasms in domestic donkeys in Xinjiang, China. Vet Med Sci 2024 Jul;10(4):e1468.
                              doi: 10.1002/vms3.1468pubmed: 38879882google scholar: lookup