Evidence of West Nile Virus (WNV) Circulation in Wild Birds and WNV RNA Negativity in Mosquitoes of the Danube Delta Biosphere Reserve, Romania, 2016

<b> </b>West Nile virus (WNV) is a zoonotic flavivirus whose transmission cycle in nature includes wild birds as amplifying hosts and ornithophilic mosquito vectors. Bridge vectors can transmit WNV to mammal species potentially causing West Nile Fever. Wild bird migration is a mode of WN...

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Bibliographic Details
Main Authors: Ana Vasić, Luanda Elena Oșlobanu, Mihai Marinov, Luciana Alexandra Crivei, Ioana Alexandra Rățoi, Adriana Aniță, Dragoș Aniță, Alexandru Doroșencu, Vasile Alexe, Ștefan Răileanu, Predrag Simeunović, Cristian Raileanu, Elena Falcuța, Florian Liviu Prioteasa, Jovan Bojkovski, Ivan Pavlović, Alexander Mathis, Birke Andrea Tews, Gheorghe Savuţa, Eva Veronesi, Cornelia Silaghi, the SCOPES AMSAR training group
Format: Article
Language:English
Published: MDPI AG 2019-08-01
Series:Tropical Medicine and Infectious Disease
Subjects:
VNT
Online Access:https://www.mdpi.com/2414-6366/4/3/116
Description
Summary:<b> </b>West Nile virus (WNV) is a zoonotic flavivirus whose transmission cycle in nature includes wild birds as amplifying hosts and ornithophilic mosquito vectors. Bridge vectors can transmit WNV to mammal species potentially causing West Nile Fever. Wild bird migration is a mode of WNV introduction into new areas. The Danube Delta Biosphere Reserve (DDBR) is a major stopover of wild birds migrating between Europe and Africa. The aim of this study was to investigate the presence of WNV in the DDBR during the 2016 transmission season in wild birds and mosquitoes. Blood from 68 wild birds (nine different species) trapped at four different locations was analyzed by competitive ELISA and Virus Neutralization Test (VNT), revealing positive results in 8/68 (11.8%) of the wild birds by ELISA of which six samples (three from juvenile birds) were confirmed seropositive by VNT. Mosquitoes (<i>n</i> = 6523, 5 genera) were trapped with CDC Mini Light traps at two locations and in one location resting mosquitoes were caught. The presence of WNV RNA was tested in 134 pools by reverse transcription quantitative PCR (RT-qPCR). None of the pools was positive for WNV-specific RNA. Based on the obtained results, WNV was circulating in the DDBR during 2016.
ISSN:2414-6366