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Kayseri yöresinden toplanmi{dotless}ş Culex pipiens örneklerinde Wolbachia Endobakterisinin belirlenmesi ve moleküler karakterizasyonu

Yildirim, Alparslan ; Inci, Abdullah ; Duzlu, Onder ; Onder, Zuhal and Ciloglu, Arif LU (2013) In Ankara Universitesi Veteriner Fakultesi Dergisi 60(3). p.189-194
Abstract

This study was performed to investigate Wolbachia endobacteria in Culex pipiens specimens collected from Kayseri province of Turkey. For this aim, totally 10 genomic DNA pools each including 6-15 Cx. pipiens specimens which were collected and identified within the scope of a project (No: 107O533) supported by TUBITAK, were examined by using the amplification of surface protein gene (wsp) region of the Wolbachia. The sequences from this gene were highly variable and could be used to resolve the phylogenetic relationships of different Wolbachia strains. After the genomic DNA extraction from the pools, PCR analyses were carried out with Wolbachia specific primer pair which was amplified a 590-632 bp region of the wsp gene. Out of 6 of the... (More)

This study was performed to investigate Wolbachia endobacteria in Culex pipiens specimens collected from Kayseri province of Turkey. For this aim, totally 10 genomic DNA pools each including 6-15 Cx. pipiens specimens which were collected and identified within the scope of a project (No: 107O533) supported by TUBITAK, were examined by using the amplification of surface protein gene (wsp) region of the Wolbachia. The sequences from this gene were highly variable and could be used to resolve the phylogenetic relationships of different Wolbachia strains. After the genomic DNA extraction from the pools, PCR analyses were carried out with Wolbachia specific primer pair which was amplified a 590-632 bp region of the wsp gene. Out of 6 of the 10 examined genomic DNA pools were found to be positive (60.0%) by PCR analyses. The minimum infection rate of Wolbachia spp. in the totally analyzed 118 Cx. pipens specimens was determined as 5.08. One of the amplicon from the positive isolates was gel purified and sequenced in terms of wsp gene region of Wolbachia by using the same primers. Pair wise analyses of the obtained DNA sequences and multiple alignments with some other Wolbachia strains available in the GenBank were done and phylogenies were investigated. The obtained isolate (WolKys1) was deposited in GenBank International Nucleotide Sequence Database with the accession number JX474753. The phylogenetic analyses revealed that the obtained WolKys1 isolate belongs to Wolbachia Super Group B and wPIP group. According to the phylogenetic comparisons the WolKys1 showed 100.0% identity with some other Wolbachia isolates under the Group B. In conclusion, this study reports the first molecular detection and characterization of Wolbachia endobacteria in Cx. pipiens populations in Turkey.

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author
; ; ; and
alternative title
Detection and molecular characterization of the Wolbachia endobacteria in the Culex pipiens (Diptera: Culicidae) specimens collected from Kayseri province of Turkey
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Cx. pipiens, Molecular characterization, Turkey, Wolbachia
in
Ankara Universitesi Veteriner Fakultesi Dergisi
volume
60
issue
3
pages
6 pages
publisher
Chartered Institution of Building Services Engineers
external identifiers
  • scopus:84877279915
ISSN
1300-0861
DOI
10.1501/Vetfak_0000002577
language
Turkish
LU publication?
no
id
ec8cae54-e584-4c71-9085-abef671a573f
date added to LUP
2017-12-04 15:17:47
date last changed
2022-02-22 07:05:17
@article{ec8cae54-e584-4c71-9085-abef671a573f,
  abstract     = {{<p>This study was performed to investigate Wolbachia endobacteria in Culex pipiens specimens collected from Kayseri province of Turkey. For this aim, totally 10 genomic DNA pools each including 6-15 Cx. pipiens specimens which were collected and identified within the scope of a project (No: 107O533) supported by TUBITAK, were examined by using the amplification of surface protein gene (wsp) region of the Wolbachia. The sequences from this gene were highly variable and could be used to resolve the phylogenetic relationships of different Wolbachia strains. After the genomic DNA extraction from the pools, PCR analyses were carried out with Wolbachia specific primer pair which was amplified a 590-632 bp region of the wsp gene. Out of 6 of the 10 examined genomic DNA pools were found to be positive (60.0%) by PCR analyses. The minimum infection rate of Wolbachia spp. in the totally analyzed 118 Cx. pipens specimens was determined as 5.08. One of the amplicon from the positive isolates was gel purified and sequenced in terms of wsp gene region of Wolbachia by using the same primers. Pair wise analyses of the obtained DNA sequences and multiple alignments with some other Wolbachia strains available in the GenBank were done and phylogenies were investigated. The obtained isolate (WolKys1) was deposited in GenBank International Nucleotide Sequence Database with the accession number JX474753. The phylogenetic analyses revealed that the obtained WolKys1 isolate belongs to Wolbachia Super Group B and wPIP group. According to the phylogenetic comparisons the WolKys1 showed 100.0% identity with some other Wolbachia isolates under the Group B. In conclusion, this study reports the first molecular detection and characterization of Wolbachia endobacteria in Cx. pipiens populations in Turkey.</p>}},
  author       = {{Yildirim, Alparslan and Inci, Abdullah and Duzlu, Onder and Onder, Zuhal and Ciloglu, Arif}},
  issn         = {{1300-0861}},
  keywords     = {{Cx. pipiens; Molecular characterization; Turkey; Wolbachia}},
  language     = {{tur}},
  number       = {{3}},
  pages        = {{189--194}},
  publisher    = {{Chartered Institution of Building Services Engineers}},
  series       = {{Ankara Universitesi Veteriner Fakultesi Dergisi}},
  title        = {{Kayseri yöresinden toplanmi{dotless}ş Culex pipiens örneklerinde Wolbachia Endobakterisinin belirlenmesi ve moleküler karakterizasyonu}},
  url          = {{http://dx.doi.org/10.1501/Vetfak_0000002577}},
  doi          = {{10.1501/Vetfak_0000002577}},
  volume       = {{60}},
  year         = {{2013}},
}