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Türkiye'de bir alaca baykuş'ta (Strix aluco) Haemoproteus türünün saptanmasi{dotless} ve moleküler karakterizasyonu

Yildirim, Alparslan ; Aysul, Nuran ; Bayramli, Goksel ; Inci, Abdullah ; Eren, Hasan ; Aypak, Suleyman ; Duzlu, Onder ; Ciloglu, Arif LU and Onder, Zuhal (2013) In Ankara Universitesi Veteriner Fakultesi Dergisi 60(3). p.179-183
Abstract

Avian blood parasites have been intensively studied using morphological methods with limited information on their host specificity and species taxonomic status. Now the analysis of gene sequences, especially the mitochondrial cytochrome b (mt-cytb) gene of the avian haemosporidian species of Plasmodium, Haemoproteus, Fallisia and Leucocytozoon, offers a new tool to review the parasite specificity and status. The material of this study was a Tawny Owl (Strix aluco) which brought to an animal hospital with broken wings in Mugla province. Meanwhile blood smears were prepared from peripheral blood sample which was taken from the wing vein. Blood sample for genetic analyses was obtained by brachial venipuncture and genomic DNA extraction was... (More)

Avian blood parasites have been intensively studied using morphological methods with limited information on their host specificity and species taxonomic status. Now the analysis of gene sequences, especially the mitochondrial cytochrome b (mt-cytb) gene of the avian haemosporidian species of Plasmodium, Haemoproteus, Fallisia and Leucocytozoon, offers a new tool to review the parasite specificity and status. The material of this study was a Tawny Owl (Strix aluco) which brought to an animal hospital with broken wings in Mugla province. Meanwhile blood smears were prepared from peripheral blood sample which was taken from the wing vein. Blood sample for genetic analyses was obtained by brachial venipuncture and genomic DNA extraction was conducted. The extracted genomic DNA was analyzed by Nested Polymerase Chain Reaction (PCR) for the amplification of partial avian haemosporidian mt-cytb gene. The final PCR product was gel purified and sequenced. The obtained isolate was deposited in GenBank International Nucleotide Sequence Database with the accession number JQ768232. Intraerytrocytic stages of Haemoproteus sp. were detected in the examination of the blood smears. The phylogenetic analyses of the amplified sequence confirmed that the owl was infected with Haemoproteus sp. According to the phylogenetic comparisons the Haemoproteus lineage showed the highest identity (99.8%) with the "H-STAL2" lineage isolated from an owl (Strix aluco) in Germany among the Haemoproteus lineages available in GenBank. In conclusion, this study reports the first microscopic and molecular detection of Haemoproteus infection in an owl in Turkey. The lineage characteristics and phylogenetic relationships among several Haemoproteus lineages were also evaluated in this study.

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author
; ; ; ; ; ; ; and
alternative title
Detection and molecular characterization of a Haemoproteus lineage in a Tawny Owl (Strix aluco) in Turkey
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Avian, Haemoproteus, Haemosporidian, Owl, Turkey
in
Ankara Universitesi Veteriner Fakultesi Dergisi
volume
60
issue
3
pages
5 pages
publisher
Chartered Institution of Building Services Engineers
external identifiers
  • scopus:84877287120
ISSN
1300-0861
DOI
10.1501/Vetfak_0000002575
language
Turkish
LU publication?
no
id
0d4f012f-3d24-438f-81f8-8d43e35489af
date added to LUP
2017-12-04 15:18:27
date last changed
2022-04-01 21:05:24
@article{0d4f012f-3d24-438f-81f8-8d43e35489af,
  abstract     = {{<p>Avian blood parasites have been intensively studied using morphological methods with limited information on their host specificity and species taxonomic status. Now the analysis of gene sequences, especially the mitochondrial cytochrome b (mt-cytb) gene of the avian haemosporidian species of Plasmodium, Haemoproteus, Fallisia and Leucocytozoon, offers a new tool to review the parasite specificity and status. The material of this study was a Tawny Owl (Strix aluco) which brought to an animal hospital with broken wings in Mugla province. Meanwhile blood smears were prepared from peripheral blood sample which was taken from the wing vein. Blood sample for genetic analyses was obtained by brachial venipuncture and genomic DNA extraction was conducted. The extracted genomic DNA was analyzed by Nested Polymerase Chain Reaction (PCR) for the amplification of partial avian haemosporidian mt-cytb gene. The final PCR product was gel purified and sequenced. The obtained isolate was deposited in GenBank International Nucleotide Sequence Database with the accession number JQ768232. Intraerytrocytic stages of Haemoproteus sp. were detected in the examination of the blood smears. The phylogenetic analyses of the amplified sequence confirmed that the owl was infected with Haemoproteus sp. According to the phylogenetic comparisons the Haemoproteus lineage showed the highest identity (99.8%) with the "H-STAL2" lineage isolated from an owl (Strix aluco) in Germany among the Haemoproteus lineages available in GenBank. In conclusion, this study reports the first microscopic and molecular detection of Haemoproteus infection in an owl in Turkey. The lineage characteristics and phylogenetic relationships among several Haemoproteus lineages were also evaluated in this study.</p>}},
  author       = {{Yildirim, Alparslan and Aysul, Nuran and Bayramli, Goksel and Inci, Abdullah and Eren, Hasan and Aypak, Suleyman and Duzlu, Onder and Ciloglu, Arif and Onder, Zuhal}},
  issn         = {{1300-0861}},
  keywords     = {{Avian; Haemoproteus; Haemosporidian; Owl; Turkey}},
  language     = {{tur}},
  number       = {{3}},
  pages        = {{179--183}},
  publisher    = {{Chartered Institution of Building Services Engineers}},
  series       = {{Ankara Universitesi Veteriner Fakultesi Dergisi}},
  title        = {{Türkiye'de bir alaca baykuş'ta (Strix aluco) Haemoproteus türünün saptanmasi{dotless} ve moleküler karakterizasyonu}},
  url          = {{http://dx.doi.org/10.1501/Vetfak_0000002575}},
  doi          = {{10.1501/Vetfak_0000002575}},
  volume       = {{60}},
  year         = {{2013}},
}