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Home Eurosurveillance Edition  2014: Volume 19/ Issue 16 Article 4
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Eurosurveillance, Volume 19, Issue 16, 24 April 2014
Rapid communications
West Nile virus surveillance in mosquitoes, April to October 2013, Vojvodina province, Serbia: implications for the 2014 season
  1. Virological Research Group, Szentágothai Research Center, University of Pécs, Pécs, Hungary
  2. Institute of Biology, Faculty of Sciences, University of Pécs, Pécs, Hungary
  3. Ciklonizacija Ltd., Novi Sad, Serbia
  4. Department of Biology and Ecology, Faculty of Sciences, University of Novi Sad, Novi Sad, Serbia
  5. Institute for Veterinary Medical Research, Centre for Agricultural Research, Hungarian Academy of Sciences, Budapest, Hungary

Citation style for this article: Kemenesi G, Krtinić B, Milankov V, Kutas A, Dallos B, Oldal M, Somogyi N, Németh V, Bányai K, Jakab F. West Nile virus surveillance in mosquitoes, April to October 2013, Vojvodina province, Serbia: implications for the 2014 season. Euro Surveill. 2014;19(16):pii=20779. Article DOI:
Date of submission: 09 April 2014

After the West Nile virus (WNV) outbreak in 2012, we collected mosquito samples from Vojvodina province, Serbia, in 2013. We found high WNV infection rate in two species, Culex pipiens and Anopheles maculipennis. Phylogenetic analysis showed that Serbian WNV strains from 2013 were most closely related to Italian and Greek strains isolated in 2012 and 2010, respectively. Public health authorities should be aware of a potentially increased risk of WNV activity during the 2014 season.

In this report we provide evidence for an unprecedented detection rate of West Nile virus (WNV) in competent mosquito vectors during the 2013 season. Given that these arthropods overwinter, our WNV surveillance of mosquitoes collected during the 2013 season of high mosquito activity (April to October) from Vojvodina province, Serbia, may have implications for the preparation for the WNV season in 2014.

WNV has been documented in Serbia since the 1970s by seroepidemiological surveys and was detected in Culex pipiens mosquitoes during a mosquito surveillance programme conducted in 2010 [1,2]. After the 2012 epidemic, which was associated with WNV lineage 2 and caused 58 human cases in Serbia (eight of them fatal), the virus was successfully detected and characterised in migratory bird samples [3]. Based on phylogenetic analyses it appeared likely that WNV lineage 2 was introduced on two independent occasions [3,4]. The 2012 season was followed by a more severe epidemic season in 2013 with over 300 human cases. In the absence of information about strains causing the WNV outbreak in Serbia during 2013, it was not possible to elucidate whether the 2012 strains circulated and overwintered to cause epidemics in the consecutive year. [5]. The aim of the present study was to detect and characterise WNV strains circulating in the 2013 mosquito activity season in Vojvodina.

Mosquito collection

Center for Disease Control and Prevention (CDC) light traps baited with dry ice were placed at 13 sampling sites in Vojvodina province, Serbia, between April and October, 2013. Between four and six traps were used at each sampling site and operated overnight (from 19:00 to 07:00). Altogether, 25 overnight sampling events were conducted during the study period. Sites were sampled as part of the Serbian seasonal mosquito control activities in Vojvodina. Site selection and the number of sampling events directly correlated with the human-inhabited areas or mosquito breeding sites. Sampling sites and collection dates are shown in Figure 1. To obtain the most reliable virological results, traps were emptied immediately after each 12-hour period, and collected specimens were placed on dry ice. Mosquitoes were kept frozen at −80 °C until processing in the laboratory.

Figure 1. Location of mosquito sampling sites (n=13) and collection dates for West Nile virus surveillance, Vojvodina province, Serbia, April–October 2013 


Laboratory analysis

Mosquitoes were determined by species according to their taxonomic keys [6] and female mosquitoes were finally pooled by collection site, date and species, with a maximum of 50 individuals per pool. Mosquitoes were homogenised in sterile 600 μL phosphate-buffered saline, viral RNA was extracted from 200 μL of supernatants using DiaExtract Total RNA Isolation Kit (DIAGON Ltd., Hungary). Samples were tested with a TaqMan real-time RT-PCR targeting the NS3 region of WNV, using reagents of the OneStep RT-PCR Kit (Qiagen) [7]. Representative strains from each sampling location were re-amplified with primers targeting a longer fragment of the NS3 genomic region [8]. The amplicons were directly sequenced (BigDye Terminator v1.1 Cycle Sequencing Kit in ABI Prism 310 DNA Sequencer instrument, Applied Biosystems) and the obtained sequences were used in phylogenetic analysis.

Vector detection

A total of 6,369 female mosquitoes (combined in 180 pools) representing 11 species were tested in this study (Table). Ten (5.5%) of 180 pools (minimal infection rate (MIR) value: 1.57) sampled were positive for WNV RNA. WNV was detected in nine pools of C. pipiens (MIR value: 1.61; 95% confidence interval: 0.70–3.10) and a single pool of Anopheles maculipennis (MIR value: 45; 95% confidence interval: 1.20–228.40), suggesting that these two mosquito species may play an important role of WNV transmission in the study area.

Table. West Nile virus surveillance in mosquitoes in Vojvodina province, Serbia, April–October 2013 (n=6,369) 


Mosquitoes tested positive for WNV were collected in July and August, at sampling sites in Kikinda (four positive pools) (45°48'56.51"N; 20°25'18.24"E), Novi Sad (five positive pools) (45°13'36.10"N; 19°49'30.41"E) and Srpski Krstur (one positive pool) (46° 6'39.68"N; 20° 7'51.76"E). The number of collected C. pipiens mosquitoes and the monthly distribution of WNV-positive pools followed a similar profile over time as the mean temperature (Figure 2).

Figure 2. Abundance of female Culex pipiens mosquitoes in the sampling sites versus mean temperature, Vojvodina province, Serbia, April–October 2013 (n=6,369)

Of the 10 WNV positive pools, four representative strains were selected for further phylogenetic analyses: two strains from Kikinda and one strain each from Srpski Krstur and Novi Sad. In the phylogenetic tree, the Serbian WNV strains (KJ652314–KJ652317) clustered with other WNV lineage 2 sequences, but unambiguously separated from other lineages (Figure 3). The analysis based on the NS3 gene showed that Serbian strains were distinct from each other according to geographic locations, i.e. Kikinda, Srpski Krstur and Novi Sad. WNV sequences from 2013 showed a longer phylogenetic distance from those isolates derived from the same region in 2010 and 2012. The 2013 Serbian WNV strains were most closely related to sequences from Italy and Greece with the greatest nucleotide similarity 98–100% and 98–99%, respectively.

Figure 3. Phylogenetic analyses of West Nile virus strains detected in Culex pipiens mosquitoes in Vojvodina province, Serbia, April–October 2013 (n=4)


In the present mosquito-based surveillance of WNV we found a high infection rate in two mosquito species, C. pipiens and A. maculipennis in the Vojvodina province, Serbia. These two species have previously been identified as competent vectors of WNV in Europe [9]. The overall 5.5% positivity are consistent with an MIR of 1.61 for C. pipiens and of 45 for A. maculipennis, which is higher than described in many other European mosquito-based surveillance studies [10,11]. Detection of WNV in A. maculipennis in Serbia is a valuable observation, although not unprecedented in Europe [12]. It is important to investigate the role of this species in WNV transmission in the future. The numerous cases of confirmed human infections in 2013 along with the high infection rate of mosquitoes in the same year well demonstrate remarkable activity of the virus [5]. Two WNV-positive sampling sites, Kikinda and Srpski Krstur, are close to the borders with Hungary and Romania. The situation may therefore represent a threat to human health not only in Serbia but also in neighbouring countries, if the ecological conditions in those areas are favourable for mosquito populations.

Phylogenetic analysis showed that Serbian WNV strains from 2013 were most closely related to Italian and Greek WNV strains isolated in 2012 and 2010 and were more diverse than strains identified in 2010 (KC496016) and 2012 (KC407673) in Serbia. Previous studies found at least two different genetic clusters of lineage 2 WNV that circulated simultaneously in Serbia in 2012, suggesting that WNVs were introduced to the country by at least two different events [4]. Phylogenetic analyses with the WNV strains detected from mosquitoes in the present study point to a potential third independent introduction event of the virus.

WNV is typically a seasonal disease strongly associated with mosquito activity. Surveillance of WNV relies on multiple pillars. Laboratory testing of dead birds and of horses with central nervous system disease, together with monitoring of mosquito pools before the late summer–early autumn season provide relevant information to public health authorities about the risk of human infections with WNV. Here we report a greater than expected prevalence of WNV in C. pipiens and A. maculipennis mosquitoes collected during 2013 in parts of Serbia. Our findings were consistent with the great number of human cases in Serbia during 2013 and provide a possible explanation for the explosive spread of WNV in the affected area. This high detection rate together with the mild winter and the capability of the primary mosquito vectors to overwinter in Serbia may be alarming for the upcoming WNV season.

Public health authorities should be aware of a potentially increased risk, and should educate local inhabitants and inform the public health authorities of neighbouring countries if evidence about enhanced WNV activity emerges over time.

This research was supported by the European Union and the State of Hungary, co-financed by the European Social Fund in the framework of TÁMOP 4.2.4. A/2-11-1-2012-0001 “National Excellence Program”. This study was supported by the Hungarian Scientific Research Fund (OTKA; PD77977) project. Krisztián Bányai was supported by the “Momentum program”.

Conflict of interest
None declared.

Authors’ contributions
Gábor Kemenesi: wrote the manuscript, coordinated the study, identified mosquitoes, coordinated laboratory processes. Vesna Milankov, Bosiljka Krtinić: field sampling of mosquitoes, interpretation of the study. Anna Kutas, Bianka Dallos, Viktória Németh: perform the virological tests. Miklós Oldal: sequencing, bioinformatics and phylogenetic analyses, contributed to the revision of the draft manuscript. Nóri Somogyi: mosquito identification, entomological verification. Krisztán Bányai: coordination and interpretation of the study, contribution to the revision of the draft manuscript. Ferenc Jakab: supervised the study and co-writer of the manuscript, contribution to the revision of the draft manuscript.


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