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dc.contributor.authorPenzhorn, Barend L.
dc.contributor.authorNetherlands, Edward C.
dc.contributor.authorCook, Courtney A.
dc.contributor.authorSmit, Nico J.
dc.contributor.authorVorster, Ilse
dc.date.accessioned2018-04-13T11:35:47Z
dc.date.available2018-04-13T11:35:47Z
dc.date.issued2018
dc.identifier.citationPenzhorn, B.L. et al. 2018. Occurrence of Hepatozoon canis (Adeleorina: Hepatozoidae) and Anaplasma spp. (Rickettsiales: Anaplasmataceae) in black-backed jackals (Canis mesomelas) in South Africa. Parasites and vectors, 11(1): Article no 158. [https://doi.org/10.1186/s13071-018-2714-y]en_US
dc.identifier.issn1756-3305 (Online)
dc.identifier.urihttp://hdl.handle.net/10394/26696
dc.identifier.urihttps://doi.org/10.1186/s13071-018-2714-y
dc.identifier.urihttps://parasitesandvectors.biomedcentral.com/track/pdf/10.1186/s13071-018-2714-y
dc.description.abstractBackground: Domestic dogs are not native to sub-Saharan Africa, which may account for their susceptibility to Babesia rossi , of which endemic black-backed jackals ( Canis mesomelas ) are natural reservoirs. There is virtually no information on the occurrence of potentially pathogenic haemogregarines (e.g. Hepatozoon canis ) or even rickettsial bacteria (e.g. Ehrlichia spp. and Anaplasma spp.) in indigenous canids in sub-Saharan Africa. Such organisms could pose a risk to domestic dogs, as well as to populations of endangered indigenous canid species. Results: Genomic DNA extracted from blood samples taken from 126 free-ranging and 16 captive black-backed jackals was subjected to reverse line blot (RLB) hybridization assay; 82 (57.8%) specimens reacted only with the Ehrlichia / Anaplasma genera-specific probe. Full-length bacterial 16S rRNA gene of five of these specimens was cloned and the recombinants sequenced. The ten 16S rDNA sequences obtained were most closely related, with approximately 99% identity, to Anaplasma sp. South African Dog, various uncultured Anaplasma spp., as well as various Anaplasma phagocytophilum genotypes. Ninety-one specimens were screened for haemogregarines through PCR amplification using the 18S rRNA gene; 20 (21.9%) specimens reacted positively, of which 14 (15.4%) were confirmed positive for Hepatozoon genotypes from within H. canis . Two (2.2%) specimens were found positive for two different Hepatozoon genotypes. Conclusions: Sequence analyses confirmed the presence of 16S rDNA sequences closely related to A. phagocytophilum and Anaplasma sp. South African Dog as well as two H. canis genotypes in both free-ranging and captive black-backed jackals. Distinguishing between closely related lineages may provide insight into differences in pathogenicity and virulence of various Anaplasma and H. canis genotypes. By building up a more comprehensive understanding of the range and diversity of the bacteria and eukaryotic organisms (piroplasms and haemogregarines) in the blood of indigenous canids, we may gain insight to such infections in these often-endangered species and the potential for horizontal transmission to and from domestic dogs via ticks where favourable conditions existen_US
dc.language.isoenen_US
dc.publisherBioMed Centralen_US
dc.subjectAnaplasmaen_US
dc.subjectBlack-backed jackalen_US
dc.subjectCanis mesomelasen_US
dc.subjectHepatozoon canisen_US
dc.subjectSouthAfricaen_US
dc.titleOccurrence of Hepatozoon canis (Adeleorina: Hepatozoidae) and Anaplasma spp. (Rickettsiales: Anaplasmataceae) in black-backed jackals (Canis mesomelas) in South Africaen_US
dc.typeArticleen_US
dc.contributor.researchID24492272 - Cook, Courtney Antonia
dc.contributor.researchID21714363 - Netherlands, Edward Charles
dc.contributor.researchID21250545 - Smit, Nicholas Jacobus


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