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Article

West Nile Virus Antibody Prevalence in Horses of Ukraine

by
Ute Ziegler
1,
Artem Skrypnyk
2,
Markus Keller
1,
Christoph Staubach
3,
Maksym Bezymennyi
2,
Armando M. Damiani
4,
Nikolaus Osterrieder
4 and
Martin H. Groschup
1,*
1
Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Novel and Emerging Infectious Diseases, Südufer 10, D-17493 Greifswald-Insel Riems, Germany
2
Institute of Veterinary Medicine, National Academy of Agrarian Sciences of Ukraine, Donetska Str. 30, Kyiv, 03151 Ukraine
3
Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Epidemiology, Seestraße 55, D-16868 Wusterhausen, Germany
4
Institut für Virologie, Zentrum für Infektionsmedizin, Freie Universität Berlin, Philippstr. 13, D-14163 Berlin, Germany
*
Author to whom correspondence should be addressed.
Viruses 2013, 5(10), 2469-2482; https://doi.org/10.3390/v5102469
Submission received: 23 August 2013 / Revised: 30 September 2013 / Accepted: 1 October 2013 / Published: 4 October 2013
(This article belongs to the Section Animal Viruses)
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Abstract

:
West Nile virus (WNV) is a mosquito-borne virus of global importance. Over the last two decades, it has been responsible for significant numbers of cases of illness in humans and animals in many parts of the world. In Ukraine, WNV infections in humans and birds were first reported more than 25 years ago, yet the current epidemiological status is quite unclear. In this study, serum samples from over 300 equines were collected and screened in order to detect current WNV activity in Ukraine with the goal to estimate the risk of infection for humans and horses. Sera were tested by enzyme-linked immunosorbent assay (ELISA) and virus neutralization assay (NT) to detect WNV-specific antibodies. The results clearly revealed that WNV circulates in most of the regions from which samples were obtained, shown by a WNV seroprevalence rate of 13.5% of examined horses. This is the first topical report indicating the presence of WNV infections in horses in Ukraine, and the results of this study provide evidence of a widespread WNV circulation in this country.

1. Introduction

West Nile virus (WNV) is an arbovirus that is maintained in an enzootic cycle between ornithophilic mosquitoes and certain wild bird species. WNV is the most widespread flavivirus known, was first isolated in Uganda in 1937, and has been found on all continents [1,2], except for Antarctica. Distinct wild bird species serve as major reservoir hosts, although even under natural conditions a variety of mammalian and reptilian species are susceptible [3]. Likewise, a variety of different bird and mosquito species are involved in the WNV life cycle in various regions of the world [4]. WNV infections in humans and equines can lead to febrile illness, which in some cases will progress to encephalitis, occasionally with fatal outcome [5]. Outside of the African continent, WNV usually causes clinical cases only sporadically in humans and equines in Mediterranean countries, the Middle East, Romania and Russia [1,6,7,8]. WNV encephalitis cases were first reported in humans and horses in the Camargue region of France in the early 1960s [9] and WNV has since been observed repeatedly in the central part of Europe [10]. Until the mid1990s, WNV was considered a minor risk for humans and horses as —with some regional exceptions —it occurred only sporadically [11]. The first major WNV epidemic in Eastern Europe was observed in Romania in 14 districts of the lower Danube valley and in Bucharest with more than 400 clinical cases in 1996 [6]. In the late 1990s, outbreaks of WNV fever with high numbers of infected humans were also observed in Israel and southern Russia [12]. WNV infections became a major concern for veterinary public health after its introduction into the New World and rapidly spread to almost all countries on the American continent over the following years [13]. Large WNV outbreaks affecting humans and equines have been reported most recently in Greece [14], and WNV lineage 2 sequences could be demonstrated in human blood donors, Culex mosquitoes, wild birds and sentinel chickens. In the summer of 2012, evidence of WNV circulation was also found in Slovakia [15] and in various Balkan countries, including Serbia, Kosovo, Macedonia and Croatia [16]. Major outbreaks in humans and horses have also been observed over the past few years in the Mediterranean area, e.g. in Italy; however, preferentially WNV lineage 1 sequences have been detected [17]. Recently, WNV lineage 2 viruses have also been detected in wild birds in Sardinia [18] and in northeastern Italy.
In Ukraine, the earliest reports confirming the presence of WNV infections in humans and birds date back to the 1970s. In 1974, Sidenko et al. [19] described human WNV infections and the accompanying neurological signs, as well as WNV specific antibodies in wild birds and farm animals in the southwestern USSR. In 1985, 38 human cases, 16 of them with neurological manifestations, were recorded in the Transcarpathian region (Ukrainian SSR). The course of disease was benign [20]. At the same time (1980s), a WNV strain was detected in the blood and internal organs of a wild bird (Rook, Corvus frugileus) in the territory of the Black Sea [21]. A recently conducted study on arbovirus infections showed new active natural foci in the forest-steppe zone of Ukraine and a close etiological relation was found between acute seasonal febrile diseases and the above-mentioned arbovirus. Besides tick-borne encephalitis, WNV disease, therefore, is the leading arboviral infection in the forest-steppe zone of Ukraine [22].
Recently, clinical WNV infections have been detected in patients in Ukraine in the summer of 2011 (eight WNV cases in three different regions/oblasts) and in 2012 (12 human cases in one region (Poltavska)) [23,24,25]. However, little is known about the extent of WNV infections in horses in Ukraine at present. The aim of the monitoring study (two-year-analysis) presented here was to investigate the prevalence of WNV specific antibodies in horse sera from 14 different Ukrainian regions (oblasts) by means of enzyme-linked immunosorbent assay (ELISA) and virus neutralization assays (NT). The results provide relevant information on the current WNV situation in Ukraine, involving an infection risk for humans and horses.

2. Results and Discussion

Horse sera from 310 animals kept in 14 different Ukrainian regions were collected in 2010 and 2011 (Figure 1, Table 1). Sera were screened by a commercial WNV competition ELISA, which essentially detects flavivirus antibodies. Therefore ELISA-positive results were verified by virus neutralization tests (NT) to identify WNV or cross-reactivity specific reactions.
Viruses 05 02469 g001 1024
Figure 1. Sampling sites of the horse sera with focus on known West Nile virus (WNV) risk areas.
Figure 1. Sampling sites of the horse sera with focus on known West Nile virus (WNV) risk areas.
Viruses 05 02469 g001
Table
Table 1. Distribution of serum samples by regions (oblasts).
Table 1. Distribution of serum samples by regions (oblasts).
UkraineRegionInvestigated sera by WNV-ELISAonly WNV-NT
1Donetska1111-
2Kharkivska2121-
3Khmelnytska39381
4Kyivska1181135
5Kirovohradska59527
6Luhanska2020-
7Odeska11-
8Poltavska66-
9Rivnenska13112
10Sumska22-
11Vinnytska22-
12Volynska1010-
13Zaporizka66-
14Zhytomyrska22-
Total 31029515

2.1. WNV competition Enzyme-linked immunosorbent assay (ELISA).

From the 310 sera, 295 samples were investigated using the competitive WNV ELISA. Volumes of the remaining 15 samples were so low (<50 µl) that they were only used for different NT (Table 1). The ELISA results showed a high rate of seropositive horses in different regions of Ukraine (Table 2). A total of 49 out of the 295 sera were reactive (Figure 2). Resulting in an overall ELISA prevalence rate of 16.6%., WNV antibody-positive animals were discovered in seven of the 14 investigated Ukrainian regions and high ELISA prevalence rates between 20% and 25% were determined for the Luhanska, Kharkivska and Kirovohradska regions. Even higher prevalence rates were obtained for Poltavska (33%) and Zaporizka (83%), with the caveat, however, that available sample numbers were small (n=6) (Table 2). All 49 ELISA-positive samples were investigated further by the different NT to exactly determine the virus resulting in ELISA seropositivity.
Table
Table 2. Competitive ELISA results stratified by region and regional antibody prevalence.
Table 2. Competitive ELISA results stratified by region and regional antibody prevalence.
UkraineRegionby ELISA comp. ELISA negative comp. ELISA reactive (doubtful or positive)ELISA prevalence
1Donetska1111--
2Kharkivska2116523.80 %
3Khmelnytska383712.63 %
4Kyivska113941916.81 %
5Kirovohradska52391325.00 %
6Luhanska2016420.00 %
7Odeska11--
8Poltavska64233.33 %
9Rivnenska1111--
10Sumska22--
11Vinnytska22--
12Volynska1010--
13Zaporizka61583.33 %
14Zhytomyrska22--
Total2952464916.61 %
Viruses 05 02469 g002 1024
Figure 2. Competitive ELISA (S/N%) results of all 295 investigated horse sera. (1 = reactive samples, 2 = negative samples)
Figure 2. Competitive ELISA (S/N%) results of all 295 investigated horse sera. (1 = reactive samples, 2 = negative samples)
Viruses 05 02469 g002

2.2. Virus neutralization assays (NT)

ELISA results were generally confirmed by NT results. In total, 68 horse sera (49 initially ELISA positive sera plus the 15 sera of which only small volumes were available and four additional sera, randomly selected) were investigated in a WNV neutralization assay. The ELISA results were confirmed for 42 out of the 49 ELISA-positive sera by WNV-NT, with neutralization titers ranging between 1:10 and 1:640 (Table 3). From the 15 sera with small volumes for which no ELISA results were available, three sera contained WNV-specific antibodies. One sample was excluded due to serum toxicity for cells.
Another seven sera with positive ELISA and negative WNV-NT results, as well as sera with weak positive WNV-NT results, were eventually run in a TBEV neutralization test (NT) to check for cross-reactivity. False positive ELISA results caused by TBE cross-reactive antibodies had been observed in earlier serological studies looking at horses from Germany and Austria [26,27,28] which impede the interpretation of the ELISA results. However, no TBEV-NT positive horse serum was found among the Ukrainian horse sera. Although Lozyns'kyĭ and Vynohrad (1998 [22]) described the occurrence and wide distribution of tick-borne encephalitis in the forest-steppe zone of Ukraine, our sample panel revealed no incidence of a TBEV infection.

2.3. Indirect WNV IgM ELISA

ELISA-positive sera with clear NT negative or weak positive NT results, as well as sera, of which only small sample volumes (< 50µl) were available, were also run in a commercially available IgM ELISA to detect recent WNV infections. This capture ELISA detects WNV specific IgM antibodies in horse sera for up to 3 months post infection. However, none of the 23 investigated samples contained WNV IgM antibodies (data not shown). Therefore there was no evidence for recent WNV infections in these samples.
Table
Table 3. ELISA and neutralization assay results of 68 horse samples. (* not enough serum material for comp. ELISA, < 50µl)
Table 3. ELISA and neutralization assay results of 68 horse samples. (* not enough serum material for comp. ELISA, < 50µl)
Laboratory sample no.comp. WNV-ELISA S/N%WNV-ELISA resultsNT-ND50 (WNV lineage 2)WNV-NT resultsNT-ND50 (TBEV-Neudoerfl)TBEV-NT results
ELISA and WNV-NT positive (n=42)
3314.19%positive10weak positive< 10negative
4412.28%positive15weak positive< 10negative
536.18%positive60positive< 10negative
544.98%positive480positive< 10negative
586.35%positive640positive< 10negative
595.09%positive320positive< 10negative
644.73%positive640positive< 10negative
684.94%positive160positive< 10negative
694.87%positive640positive< 10negative
714.98%positive240positive< 10negative
724.83%positive160positive< 10negative
755.90%positive30positive< 10negative
885.53%positive40positive< 10negative
965.97%positive40positive< 10negative
974.91%positive160positive< 10negative
1055.77%positive60positive< 10negative
1074.73%positive160positive< 10negative
1084.67%positive160positive< 10negative
1237.86%positive80positive< 10negative
1244.81%positive80positive< 10negative
1284.15%positive160positive< 10negative
1313.88%positive80positive< 10negative
1468.79%positive15weak positive< 10negative
1494.31%positive20positive< 10negative
1584.04%positive80positive< 10negative
1603.78%positive320positive< 10negative
1664.55%positive120positive< 10negative
1874.63%positive180positive< 10negative
2086.09%positive10weak positive< 10negative
2177.84%positive30positive< 10negative
2284.44%positive120positive< 10negative
23210.92%positive10weak positive< 10negative
2884.48%positive320positive< 10negative
2899.16%positive60positive< 10negative
2925.09%positive40positive< 10negative
2975.35%positive480positive< 10negative
3125.12%positive60positive< 10negative
3134.92%positive160positive< 10negative
3307.98%positive80positive< 10negative
3364.18%positive120positive< 10negative
3374.44%positive160positive< 10negative
3437.08%positive10weak positive< 10negative
ELISA positive and WNV-NT negative (n=7)
9834.70%positive< 10negative< 10negative
10626.64%positive< 10negative< 10negative
18314.07%positive< 10negative< 10negative
23023.58%positive< 10negative< 10negative
25030.98%positive< 10negative< 10negative
29525.88%positive< 10negative< 10negative
32839.16%positive< 10negative< 10negative
ELISA negative and WNV-NT positive (n=4)
20991.31%negative30positive< 10negative
21086.89%negative120positive< 10negative
21290.21%negative10weak positive< 10negative
21493.03%negative320positive< 10negative
Low volume ➔ no ELISA, WNV-NT positive (n=3)
126n.d.*80positive< 10negative
127n.d.*60positive< 10negative
162n.d.*60positive< 10negative
Low volume ➔ no ELISA, WNV-NT negative (n=11+1 not evaluable)
27n.d.*< 10negative< 10negative
76n.d.*< 10negative< 10negative
100n.d.*not evaluable, because of serum toxicity for cells
125n.d.*< 10negative< 10negative
129n.d.*< 10negative< 10negative
130n.d.*< 10negative< 10negative
138n.d.*< 10negative< 10negative
139n.d.*< 10negative< 10negative
163n.d.*< 10negative< 10negative
179n.d.*< 10negative< 10negative
180n.d.*< 10negative< 10negative
186n.d.*< 10negative< 10negative
In summary, our results show that WNV circulates in large parts of Ukraine. In total, 42 horse sera (Table 3) tested positive for WNV antibodies as determined by both ELISA and NT. These samples were collected in seven regions, namely Kharkivska, Khmelnytska, Kyivska, Kirovohradska, Luhanska, Poltavska and Zaporizka (Figure 3, Table 4).
Viruses 05 02469 g003 1024
Figure 3. Number of WNV positive sera (red columns = both in ELISA and neutralization test (NT)) in horses from different Ukrainian regions. ELISA negative samples are depicted in green columns.
Figure 3. Number of WNV positive sera (red columns = both in ELISA and neutralization test (NT)) in horses from different Ukrainian regions. ELISA negative samples are depicted in green columns.
Viruses 05 02469 g003
Table
Table 4. Distribution of the ELISA and NT positive samples.
Table 4. Distribution of the ELISA and NT positive samples.
Ukraineregioncomp. ELISA positive and WNV-NT positiveWNV-NT ND50 titres
1Donetska--
2Kharkivska410 - 160
3Khmelnytska110
4Kyivska1710 - 640
5Kirovohradska1130 - 160
6Luhanska315 - 120
7Odeska--
8Poltavska140
9Rivnenska--
10Sumska--
11Vinnytska--
12Volynska--
13Zaporizka560 - 480
14Zhytomyrska--
42
The overall findings reported here are consistent with those from previous WNV seroprevalence studies in horses, mosquitoes and wild birds [7,19,21,29,30] and humans [19,20,29] in Ukraine. Most recently, high infection rates have also been found in humans in Romania and the Russian Federation, which are immediate neighbors of Ukraine [6,12]. Large parts of the Ukrainian landscape (rivers, wetlands and lowlands) and the country`s climatic conditions (wet winters and springs followed by excessive heat in the summers) are commensurate with environmental conditions necessary for productive circulation of WNV in wildlife. Moreover, Ukraine is located on major migratory bird flyways connecting Africa and The Middle East with Eurasia [31]. WNV endemics establish themselves particularly in urban regions with open water drainage systems and improper basic sanitation [32]. During the time of sampling, no clinical WNV cases were reported in horses, whereas clinical cases were confirmed in humans in 2011 and 2012 in Ukraine [23,24,25].
To exclude serological cross-reactions leading to false WNV seropositivity, differential diagnostic assays were conducted. As the WNV ELISA used also detects cross-reacting antibodies induced by other flaviviruses, e.g. TBEV [26,27,28], all sera negative in the WNV NT were also screened using a TBEV NT as well as a Japanese encephalitis virus (JEV) NT, all with negative outcomes (data not shown). The reason for ELISA reactivity of the seven sera (positive WNV ELISA, but negative in all conducted NTs, Table 3) is unclear at present. Besides measuring different properties of antibodies in the assay systems, this may indicate circulation of an as-yet-unknown flavivirus in Ukraine.

3. Experimental Materials and Methods

Serum samples. Blood samples were collected from 310 randomly selected healthy horses, which were kept in 14 regions of Ukraine during 2010 and 2011 (Table 1). Horses had no known clinical history of a previous WNV infection. Sera were kept at –20 ºC until use.
ELISA. Sera were screened for WNV specific antibodies using a commercially available competition ELISA, which allows the species-independent recognition of WNV antibodies against the PrM- and E envelope protein (ID Screen® West Nile Competition, IDVet, Montpellier, France). The ELISA cut-off is defined by the residual binding ratios (S/N%-value); sera with S/N ratios of 40% and lower are positive, while samples with S/N ratios of more than 50 are considered WNV antibody-negative. S/N values of 40–50% are inconclusive. Additionally, a commercially available IgM capture ELISA was used (IDEXX IgM WNV Ab Test, IDEXX Europe B.V., Hoofddorp, the Netherlands) to detect recent WNV infection in horses.
NT. ELISA results were confirmed by virus neutralization test carried out under biosafety level 3 conditions and using Vero cells on 96-well plates as described earlier [33]. Test serum dilutions (20 µl starting heat-inactivated serum material) were pre-incubated with 100 TCID50 of WNV strain Austria (lineage 2, Accession no. HM015884, kindly provided by Dr. N. Nowotny, Institute of Virology, University of Veterinary Medicine, Vienna). All samples were run in duplicate and NT titers were calculated after inspection of the assay at 6 to 7 days after infection, depending on the cytopathic effects in the infected control wells. The neutralizing antibody titer was defined as the neutralization dose 50% (ND50), i.e. the maximum dilution, which inhibited cytopathic effects in 50% of the wells according to the Behrens-Kaerber method. ND50 values of above 10 were considered positive. The TBEV serum neutralization test was carried out following the same protocol, except that the TBEV strain Neudoerfl (kindly provided by Dr. F. Hufert, Institute for Virology, Göttingen Germany; GenBank accession no. U27495) was used. Furthermore, JEV-NT was carried out using the same procedure and using JEV strain Nakayama (GenBank accession no. EF571853).
Maps. GIS-Analysis of the sampling sites and of the results was performed by using the ArcGIS Arview 10.0 software (ESRI, Redlands, CA, USA) and displayed using a Lambert conformal conic coordinate system.

4. Conclusions

WNV specific antibodies were detected in sera from horses originating from seven Ukrainian regions, thus representing a substantial part of the country’s territory (Figure 1), and the mean sero-prevalence rate for WNV was 13.5%. However, IgM ELISA analyses on selective sera did not reveal any evidence of recent infections. Samples were unsuitable for the demonstration of WNV genomes.
This is the first up-to-date report indicating WNV infections prevalence in horses in Ukraine, and these results provide evidence of widespread WNV circulation in this country. The results will help to determine the risk of infection for humans and to control WNV transmission. Surveillance studies in humans, vectors and animals are needed to better define endemic areas.

Acknowledgments

We thank Tobias Winterfeld and Cornelia Steffen for their excellent technical assistance. This research work was financially supported in part by the EU commission (EDENext and NADIR).

Conflict of Interest

The authors declare no conflict of interest.

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MDPI and ACS Style

Ziegler, U.; Skrypnyk, A.; Keller, M.; Staubach, C.; Bezymennyi, M.; Damiani, A.M.; Osterrieder, N.; Groschup, M.H. West Nile Virus Antibody Prevalence in Horses of Ukraine. Viruses 2013, 5, 2469-2482. https://doi.org/10.3390/v5102469

AMA Style

Ziegler U, Skrypnyk A, Keller M, Staubach C, Bezymennyi M, Damiani AM, Osterrieder N, Groschup MH. West Nile Virus Antibody Prevalence in Horses of Ukraine. Viruses. 2013; 5(10):2469-2482. https://doi.org/10.3390/v5102469

Chicago/Turabian Style

Ziegler, Ute, Artem Skrypnyk, Markus Keller, Christoph Staubach, Maksym Bezymennyi, Armando M. Damiani, Nikolaus Osterrieder, and Martin H. Groschup. 2013. "West Nile Virus Antibody Prevalence in Horses of Ukraine" Viruses 5, no. 10: 2469-2482. https://doi.org/10.3390/v5102469

APA Style

Ziegler, U., Skrypnyk, A., Keller, M., Staubach, C., Bezymennyi, M., Damiani, A. M., Osterrieder, N., & Groschup, M. H. (2013). West Nile Virus Antibody Prevalence in Horses of Ukraine. Viruses, 5(10), 2469-2482. https://doi.org/10.3390/v5102469

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