Publication:
The detection and phylogenetic analysis of Anaplasma phagocytophilum-like 1, A. ovis and A. capra in sheep: A. capra divides into two genogroups

dc.contributor.authorAltay, Kursat
dc.contributor.authorErol, Ufuk
dc.contributor.authorŞahin, Ömer Faruk
dc.contributor.authorAytmirzakizi, Ayperi
dc.contributor.authorTemizel, Ethem Mutlu
dc.contributor.authorAydin, Mehmet Fatih
dc.contributor.authorDumanlı, Nazir
dc.contributor.authorAktaş, Münir
dc.contributor.buuauthorTEMİZEL, ETHEM MUTLU
dc.contributor.departmentBursa Uludağ Üniversitesi/Veteriner Fakültesi/İç Hastalıkları Anabilim Dalı.
dc.contributor.researcheridECV-4083-2022
dc.date.accessioned2024-11-08T12:05:24Z
dc.date.available2024-11-08T12:05:24Z
dc.date.issued2022-09-28
dc.description.abstractIn this study, the presence, prevalence, and genotypes of Anaplasma phagocytophilum, A. ovis, and A. capra in sheep were investigated based on 16 S SSU rRNA, groEL, and gtlA gene-specific polymerase chain reaction (PCR), respectively. The sequences of the genes were used for detection of the phylogenetic position of the species. Additionally, a restriction fragment length polymorphism (RFLP) were carried out for discrimination of A. phagocytophilum and related variants (A. phagocytophilum-like 1 and 2). The prevalence of Anaplasma spp. was found as 25.8% (101/391), while it was found that A. ovis, A. phagocytophilum-like 1, and A. capra are circulating in the sheep herds in Kyrgyzstan, according to the PCRs, RFLP and the partial DNA sequencing results. The positivity rates of A. phagocytophilum-like 1, A. ovis, and A. capra genotype-1 were 6.9, 22.5, and 5.3%, respectively. A total of 32 (8.2%) sheep were found to be mix infected. Moreover, phylogenetic analyses and sequence comparison with those available in the GenBank showed that A. capra formed two distinct genetic groups (A. capra genotype-1 and A. capra genotype-2). Considering the zoonotic potential of these species, it may be necessary to make changes in the interpretation of anaplasmosis cases in animals and there is a need for further studies to determine the pathogenicity of the species/genotypes circulating in animals.
dc.identifier.doi10.1007/s11259-022-09998-1
dc.identifier.endpage1279
dc.identifier.issn0165-7380
dc.identifier.issue4
dc.identifier.startpage1271
dc.identifier.urihttps://doi.org/10.1007/s11259-022-09998-1
dc.identifier.urihttps://link.springer.com/article/10.1007/s11259-022-09998-1
dc.identifier.urihttps://hdl.handle.net/11452/47643
dc.identifier.volume46
dc.identifier.wos000860413000001
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherSpringer
dc.relation.journalVeterinary Research Communications
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectMolecular survey
dc.subjectSmall ruminants
dc.subjectTicks
dc.subjectIdentification
dc.subjectInfections
dc.subjectEhrlichia
dc.subjectBovis
dc.subjectHokkaido
dc.subjectChina
dc.subjectSpp.
dc.subjectAnaplasma species
dc.subjectAnaplasma capra genotypes
dc.subject16s ssu rrna
dc.subjectGroel
dc.subjectGtla
dc.subjectSheep
dc.subjectVeterinary sciences
dc.titleThe detection and phylogenetic analysis of Anaplasma phagocytophilum-like 1, A. ovis and A. capra in sheep: A. capra divides into two genogroups
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublication32cdabad-4bba-40b7-b2b6-b36bb228ea66
relation.isAuthorOfPublication.latestForDiscovery32cdabad-4bba-40b7-b2b6-b36bb228ea66

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