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2017-07-14Zeitschriftenartikel DOI: 10.1186/s13071-017-2279-1
Generic amplification and next generation sequencing reveal Crimean-Congo hemorrhagic fever virus AP92-like strain and distinct tick phleboviruses in Anatolia, Turkey
dc.contributor.authorDinçer, Ender
dc.contributor.authorBrinkmann, Annika
dc.contributor.authorHekimoğlu, Olcay
dc.contributor.authorHacıoğlu, Sabri
dc.contributor.authorFöldes, Katalin
dc.contributor.authorKarapınar, Zeynep
dc.contributor.authorPolat, Pelin Fatoş
dc.contributor.authorOğuz, Bekir
dc.contributor.authorKılınç, Özlem Orunç
dc.contributor.authorHagedorn, Peter
dc.contributor.authorÖzer, Nurdan
dc.contributor.authorÖzkul, Aykut
dc.contributor.authorNitsche, Andreas
dc.contributor.authorErgünay, Koray
dc.date.accessioned2018-05-07T20:19:19Z
dc.date.available2018-05-07T20:19:19Z
dc.date.created2017-07-28
dc.date.issued2017-07-14none
dc.identifier.otherhttp://edoc.rki.de/oa/articles/rehxvbGRbqfng/PDF/27nXF3uqkEgA.pdf
dc.identifier.urihttp://edoc.rki.de/176904/2737
dc.description.abstractBackground: Ticks are involved with the transmission of several viruses with significant health impact. As incidences of tick-borne viral infections are rising, several novel and divergent tick- associated viruses have recently been documented to exist and circulate worldwide. This study was performed as a cross-sectional screening for all major tick-borne viruses in several regions in Turkey. Next generation sequencing (NGS) was employed for virus genome characterization. Ticks were collected at 43 locations in 14 provinces across the Aegean, Thrace, Mediterranean, Black Sea, central, southern and eastern regions of Anatolia during 2014–2016. Following morphological identification, ticks were pooled and analysed via generic nucleic acid amplification of the viruses belonging to the genera Flavivirus, Nairovirus and Phlebovirus of the families Flaviviridae and Bunyaviridae, followed by sequencing and NGS in selected specimens. Results: A total of 814 specimens, comprising 13 tick species, were collected and evaluated in 187 pools. Nairovirus and phlebovirus assays were positive in 6 (3.2%) and 48 (25.6%) pools. All nairovirus sequences were closely-related to the Crimean-Congo hemorrhagic fever virus (CCHFV) strain AP92 and formed a phylogenetically distinct cluster among related strains. Major portions of the CCHFV genomic segments were obtained via NGS. Phlebovirus sequencing revealed several tick-associated virus clades, including previously-characterized Antigone, Lesvos, KarMa and Bole tick viruses, as well as a novel clade. A wider host range for tick-associated virus strains has been observed. NGS provided near-complete sequences of the L genomic segments of Antigone and KarMa clades, as well as Antigone partial S segment. Co- infections of CCHFV and KarMa or novel phlebovirus clades were detected in 2.1% of the specimens. Conclusions: Widespread circulation of various tick-associated phlebovirus clades were documented for the first time in Anatolia. Genomes of CCHFV AP92 strains were identified in previously unexplored locations. NGS provided the most detailed genomic characterization of the Antigone and KarMa viruses to date. The epidemiological and health-related consequences must be elucidated.eng
dc.language.isoeng
dc.publisherRobert Koch-Institut, Biologische Sicherheit
dc.subjectSurveillanceeng
dc.subjectAnatoliaeng
dc.subjectTurkeyeng
dc.subjectNext generation sequencingeng
dc.subjectTickeng
dc.subjectCrimean-Congo hemorrhagic fever viruseng
dc.subjectPhleboviruseng
dc.subjectAP92 Nairoviruseng
dc.subject.ddc610 Medizin
dc.titleGeneric amplification and next generation sequencing reveal Crimean-Congo hemorrhagic fever virus AP92-like strain and distinct tick phleboviruses in Anatolia, Turkey
dc.typeperiodicalPart
dc.identifier.urnurn:nbn:de:0257-10054013
dc.identifier.doi10.1186/s13071-017-2279-1
dc.identifier.doihttp://dx.doi.org/10.25646/2662
local.edoc.container-titleParasites & Vectors
local.edoc.fp-subtypeArtikel
local.edoc.type-nameZeitschriftenartikel
local.edoc.container-typeperiodical
local.edoc.container-type-nameZeitschrift
local.edoc.container-urlhttps://parasitesandvectors.biomedcentral.com/articles/10.1186/s13071-017-2279-1
local.edoc.container-publisher-nameBioMedCentral
local.edoc.container-volume10
local.edoc.container-issue335
local.edoc.container-year2017

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