Ergunay Koray, Gunay Filiz, Oter Kerem, Kasap Ozge Erisoz, Orsten Serra, Akkutay Ayse Zeynep, Erdem Hakan, Ozkul Aykut, Alten Bulent
1 Department of Medical Microbiology, Virology Unit, Faculty of Medicine, Hacettepe University , Sihhiye Ankara, Turkey .
Vector Borne Zoonotic Dis. 2013 Oct;13(10):744-52. doi: 10.1089/vbz.2012.1288. Epub 2013 Aug 6.
Arbovirus screening in invertebrate vectors is an important component of the vector-borne disease surveillance programs. Turkey has been shown to harbor medically important mosquito-borne arboviruses such as West Nile Virus (WNV). However, limited information about infections in vectors are currently available. This study was performed to provide preliminary data from Eastern Thrace region, Turkey, where no arbovirus vector surveillance has previously been performed.
Mosquito sampling was undertaken at 23 sites in Edirne province during July, 2012. All specimens were identified morphologically, and selected individuals were subjected to DNA barcoding via cytochrome c oxidase I (COI) sequencing. Consensus PCR for Flavivirus, Alphavirus, and Phlebovirus genera and WNV-specific nested and real-time reverse transcription PCR were employed for mosquito pool screening and/or confirmation. Viral sequences detected in pools were characterized via sequencing.
A total of 9261 mosquitoes were captured and distributed into 232 pools from the following species: Ochlerotatus caspius (90.9%), Culex pipiens sensu lato (s.l.) (4.7%), Anopheles pseudopictus (3%), and Anopheles maculipennis s.l. (1.3%). Specimens morphologically classified as Cx. pipiens s.l. were identified as Cx. pipiens pipiens via barcoding. Thirty-seven mosquito pools (15.9%) were positive in pan-flavivirus and WNV-specific assays. Viral sequences in positive pools were characterized as WNV lineage 1 clade 1a and demonstrated 1-4% divergence. No flavivirus sequences other than WNV were detected in the mosquito pools. WNV infection rates in Oc. caspius and Cx. pipiens s.l. pools were 15.6% and 36.3%, respectively. Comparison of current and previously identified WNV sequences from Turkey revealed 94.00-96.34% similarity.
WNV RNA was identified for the first time in Cx. pipiens s.l. and Oc. caspius mosquitoes in Eastern Thrace, Turkey. Our findings indicate the circulation of WNV lineage 1 strains in potential vector species and provide an epidemiological link between WNV activity in mosquitoes and vertebrate infections.
对无脊椎动物传播媒介进行虫媒病毒筛查是媒介传播疾病监测项目的重要组成部分。土耳其已被证实存在西尼罗河病毒(WNV)等具有医学重要性的蚊媒虫媒病毒。然而,目前关于传播媒介感染的信息有限。本研究旨在提供来自土耳其东色雷斯地区的初步数据,此前该地区尚未开展过虫媒病毒传播媒介监测。
2012年7月在埃迪尔内省的23个地点进行了蚊虫采样。所有标本均进行形态学鉴定,选取的个体通过细胞色素c氧化酶I(COI)测序进行DNA条形码分析。采用针对黄病毒属、甲病毒属和白蛉病毒属的通用PCR以及WNV特异性巢式和实时逆转录PCR对蚊虫混合样本进行筛查和/或确认。对混合样本中检测到的病毒序列进行测序鉴定。
共捕获9261只蚊子,分为232个混合样本,来自以下物种:里海伊蚊(90.9%)、致倦库蚊复合组(4.7%)、伪按蚊(3%)和棕褐按蚊复合组(1.3%)。形态学分类为致倦库蚊复合组的标本经条形码分析鉴定为致倦库蚊。37个蚊虫混合样本(15.9%)在通用黄病毒和WNV特异性检测中呈阳性。阳性混合样本中的病毒序列鉴定为WNV谱系1分支1a,差异为1%-4%。在蚊虫混合样本中未检测到除WNV以外的黄病毒序列。里海伊蚊和致倦库蚊复合组混合样本中的WNV感染率分别为15.6%和36.3%。将土耳其目前和先前鉴定的WNV序列进行比较,相似度为94.00%-96.34%。
在土耳其东色雷斯的致倦库蚊复合组和里海伊蚊中首次鉴定出WNV RNA。我们的研究结果表明WNV谱系1毒株在潜在传播媒介物种中循环,并为蚊虫中的WNV活动与脊椎动物感染之间提供了流行病学联系。