Rapid Detection of Equine Piroplasms Using Multiplex PCR and First Genetic Characterization of Theileria haneyi in Egypt

dc.contributor.authorElsawy, Bassma S. M.
dc.contributor.authorNassar, Ahmed M.
dc.contributor.authorAlzan, Heba F.
dc.contributor.authorBhoora, Raksha, V
dc.contributor.authorOzubek, Sezayi
dc.contributor.authorMahmoud, Mona S.
dc.contributor.authorMahdy, Olfat A.
dc.date.accessioned2026-08-12T17:36:23Z
dc.date.issued2021
dc.departmentFırat Üniversitesi
dc.description.abstractEquine Piroplasmosis (EP) is an infectious disease caused by the hemoprotozoan parasites Theileria equi, Babesia caballi, and the recently identified species T. haneyi. Hereby, we used a multiplex PCR (mPCR) targeting the 18S rRNA gene of T. equi and B. caballi for the simultaneous detection of EP in Egyptian equids and examined the presence of T. haneyi infections in Egypt. Blood samples from 155 equids (79 horses and 76 donkeys) collected from different governorates of Egypt were examined by mPCR and PCR targeting T. hayeni. The mPCR method revealed a prevalence of T. equi of 20.3% in horses and of 13.1% in donkeys and a prevalence of B. caballi of 1.2% in horses. B. caballi was not detected in donkeys in the current study. The mPCR method also detected coinfections with both species (2.5% and 1.3% in horses and donkeys, respectively). Additionally, we report the presence of T. haneyi in Egypt for the first time in 53.1% of the horse and 38.1% of the donkey tested samples. Coinfection with T. haneyi and T. equi was found in 13.5% of the samples, while infection with the three EP species was found in 1.9% of the samples.
dc.description.sponsorshipB.S.M.E, National research center, (NRC) fund
dc.description.sponsorshipThis research was funded by B.S.M.E, National research center, (NRC) fund.
dc.identifier.doi10.3390/pathogens10111414
dc.identifier.issn2076-0817
dc.identifier.issue11
dc.identifier.orcid0000-0003-2377-2735
dc.identifier.orcid0000-0001-7838-6538
dc.identifier.orcid0000-0001-5231-2258
dc.identifier.orcid0000-0002-8661-5246
dc.identifier.orcid0000-0002-0260-7813
dc.identifier.pmid34832570
dc.identifier.scopus2-s2.0-85118735035
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.3390/pathogens10111414
dc.identifier.urihttps://hdl.handle.net/11508/57913
dc.identifier.volume10
dc.identifier.wosWOS:000725892600001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherMdpi
dc.relation.ispartofPathogens
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectequids
dc.subjectBabesia caballi
dc.subjectTheileria equi
dc.subjectTheileria haneyi
dc.subjectmultiplex PCR
dc.subjectcPCR
dc.subject18S rRNA gene and sequencing
dc.titleRapid Detection of Equine Piroplasms Using Multiplex PCR and First Genetic Characterization of Theileria haneyi in Egypt
dc.typeArticle

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