Veterinary Diagnostics

To place an order, please choose your country

Subscribe newsletter

West Nile Virus (WNV)

ID Screen® West Nile Competition Multi-species

ELISA

Competitive ELISA kit for the detection of anti-pr-E antibodies in multiple species

The kit is proven to detect a wide range of Flavivirus antibodies (WNV, JEV, TBEV, JEV, USUV, ZIKAV, and DENV) in multiple species, including humans (see References). For research use only on human samples: contact us.

Advantages

Specifications

Format

References

Downloads

  • Highly sensitive and specific detection of Flavivirus antibodies (WNV, JEV, TBEV, JEV, USUV, ZIKAV, and DENV)
  • Applicable to multiple species, including horses, birds and others. For research use only on human samples (see References).
  • Rapid and convenient protocol, with ready-to-use reagents and results in just over 2 hours

Method :

Competitive ELISA

Species :

Multiple species, including birds, horses and others. For research use only on human samples (see References)

Specimens :

Serum or plasma

Coated antigen :

pr-E antigen

Conjugate :

Anti-pr-E-HRP conjugate (concentrated 10X)

Product reference

Kit format

Reactions

Plate format

WNC-1P 1 plate 96 12 x 8-well strips
WNC-2P 2 plates 192 12 x 8-well strips

Download a summary of the publications below here

EQUINE

1) Molini U. et al. (2021) West Nile Virus Seroprevalence in a Selected Donkey Population of Namibia.Front. Vet. Sci. 8:681354

2) Assaid N. et al. (2020) Evidence of circulation of West Nile virus in Culex pipiens mosquitoes and horses in Morocco. Acta Tropica 205, 105414

3) Selim A. et al. (2020) Seroprevalence and molecular characterization of West Nile Virus in Egypt. Comparative Immunology, Microbiology and Infectious diseases 71, 101473

4) Monaco F. et al. (2019) Immunological response in horses following west Nile virus vaccination with inactivated or recombinant vaccines. Veterinaria Italiana 55 (1), 73-79

5) Benjelloun A. et al. (2017) Seroprevalence of West Nile virus in horses in different Moroccan regions. Veterinary Medicine and Science, 3, 198–207

6) Haroun M. et al. (2017) Occurrence of Equine West Nile Virus Among Horses in Qatar : A Preliminary Investigation. European Scientific Journal January 2017 /SPECIAL/ edition ISSN: 1857 – 7881 (Print) e – ISSN 1857- 7431

7) Joó K. et al. (2017) Comparison of assays for the detection of West Nile virus antibodies in equine serum after natural infection or vaccination. Veterinary Immunology and Immunopathology 183, 1–6

8) Mehmet K. et al. (2017) Serological investigation of west nile virus infection in domestic horses and donkeys in Turkey. Pak Vet J, 37(1): 51-54

9) Bahuon C. et al. (2016) West Nile virus epizootics in the Camargue (France) in 2015 and reinforcement of surveillance and control networks. Rev. Sci. Tech. Off. Int. Epiz., 35 (3), 811-824

10) Bouzalas I.et al. (2016) Emergence of Equine West Nile Encephalitis in Central Macedonia, Greece, 2010. Transboundary and Emerging Diseases. 63(6):e219-e227

11) Chaintoutis S. et al. (2015) Evaluation of cross-protection of a lineage 1 West Nile virus inactivated vaccine against natural infections from a virulent lineage 2 strain in horses, under field conditions. Clin Vaccine Immunol 22:1040 –1049

12) Zohaib A. et al. (2014) High prevalence of West Nile virus in equines from the two provinces of Pakistan . Epidemiol. Infect., Page 1 of 5

13) Barbić L. et al. (2013) West Nile virus serosurveillance in horses in Croatia during the 2012 transmission season. Medical Sciences, 39 (2013): 95-104

14) Bargaoui R. et al.(2013) Mapping the Serological Prevalence Rate of West Nile Fever in Equids, Tunisia. Blackwell Verlag GmbH-Transboundary and Emerging Diseases

15) Borujeni P.et al. (2013) A serological survey on antibodies against West Nile virus in horses of Khuzestan province. Iranian Journal of Veterinary Medicine IJVM 7(3):185-191

16) Jonquiere F.et al. (2011) West Nile Virus Vaccination in Horses –IgM and IgG responses after injection in different muscles Pferdeheilkunde 27 ,4 (July/August) 412-416

AVIAN

17) Pallari C.T. et al. (2021) Evidence of West Nile Virus seropositivity in wild birds on the island of Cyprus. Comparative immunology, microbiology and infectious diseases, 74, 101592

18) Holicki C.M. et al. (2020) Pathogenicity of West Nile Virus Lineage 1 to German Poultry. Vaccines 8, 507

19) Islam A. et al. (2020) Serological Evidence of West Nile Virus in Wild Birds in Bangladesh. Vet. Sci. 2020, 7, 164

20) Ain-Najwaa M.Y. et al. (2020) Evidence of West Nile virus infection in migratory and resident wild birds in west coast of peninsular Malaysia. One Health 10, 100134

21) Kim C-Y. et al. (2016) First detection of West Nile virus in domestic pigeon in Korea. J Vet Sci, 17(4), 587-589

22) Pastiu A. et al. (2016) Wild Birds in Romania Are More Exposed to West Nile Virus Than to Newcastle Disease Virus. Vector-Borne and Zoonotic Diseases, 16(3), 176-180

23) Hammouda A. et al. (2015) Exposure of resident sparrows to West Nile virus evidenced in South Tunisia. Epidemiol. Infect., 143, 3546–3549

24) Chaintoutis S. et al. (2014) Evaluation of a West Nile virus surveillance and early warning system in Greece, based on domestic pigeons. Comparative Immunology, Microbiology and Infectious Diseases 37, 131– 141

25) Chaskopoulou A. et al. (2013) Detection and Early Warning of West Nile Virus Circulation in Central Macedonia, Greece, Using Sentinel Chickens and Mosquitoes. Vector Borne Zoonotic Dis. 13(10):723-32

26) Ziegler et al. (2013) Pathogenesis of West Nile virus lineage 1 and 2 in experimentally infected large falcons. Veterinary microbiology, 161(3-4), 263-273

27) Sotelo E. et al. (2011) Pathogenicity of two recent Western Mediterranean West Nile virus isolates in a wild bird species indigenous to Southern Europe: the red-legged partridge. Veterinary Research 42:11

AVIAN AND HORSES

28) Raleigh P. et al. (2012) Surveillance for antibodies to West Nile virus in Ireland. Veterinary Record 170: 180

OTHER SPECIES

29) Cosseddu G.M. et al. (2021) Sero-surveillance of emerging viral diseases in camels and cattle in Nouakchott, Mauritania: an abattoir study. Tropical Animal Health and Production, 53(2), 1-6

30) Mohammed M.N. et al. (2021) Serological evidence of West Nile viral infection in archived swine serum samples from Peninsular Malaysia. J Vet Sci.22(3):e29

31) Pham-Thanh L. et al. (2021) Dogs as Sentinels for Flavivirus Exposure in Urban, Peri-Urban and Rural Hanoi, Vietnam Viruses 13, 507

32) Ain-Najwa M.Y. et al. (2020) Exposure to Zoonotic West Nile Virus in Long-Tailed Macaques and Bats in Peninsular Malaysia. Animals 2020, 10, 2367

33) Dinç E. et al. (2020) Serological Investigation of West Nile Virus (WNV) Infection in Cats and Dogs. ARRB, 35(1): 65-71

34) Selim A. et al. (2020) The first detection of anti-West Nile virus antibody in domestic ruminants in Egypt. Tropical Animal Health and Production, 52(6), 3147-3151

35) Vitaskova E. et al. (2019) Serologic Survey of Selected Viral Pathogens in Free-Ranging Eurasian Brown Bears (Ursus arctos arctos) from Slovakia. Journal of wildlife diseases, 55(2), 499-503

36) Hassine, T.B. et al. (2017) Emerging vector-borne diseases in dromedaries in Tunisia: West Nile, Blue Tongue, Epizootic Haemorrhagic disease and Rift Valley fever. Onderstepoort Journal of Veterinary Research 84(1), a1316

37) Pâslaru A. et al. (2016) West Nile Virus Serosurveillance in Wild Boars from the East of Romania. Bull. UASVM Vet. Med, 73, 144-148

38) Lan D. et al.(2011) Serological evidence of West Nile virus in dogs and cats in Chine. Arch Virol 156:893-895

HUMANS

39) Niczyporuk J.et al. (2015) Occurrence of West Nile Virus Antibodies in Wild Birds, Horses, and Humans in Poland. BioMed Research International vol 2015, Article ID 234181

OTHER FLAVIVIRUSES

40) Constant O. et al. (2022). One Health surveillance of West Nile and Usutu viruses: A repeated cross-sectional study exploring seroprevalence and endemicity in Southern France, 2016 to 2020. Eurosurveillance, 27(25), 2200068

41) Gonzalez G. et al. (2022) A One-Health Approach to Investigating an Outbreak of Alimentary Tick-Borne Encephalitis in a Non-endemic Area in France (Ain, Eastern France): A Longitudinal Serological Study in Livestock, Detection in Ticks, and the First Tick-Borne Encephalitis Virus Isolation and Molecular Characterisation. Frontiers in microbiology. 13, 863725-863725

42) Tinto B. et al. (2022) Serological Evidence of Zika Virus Circulation in Burkina Faso. Pathogens 11, 741

43) Vasic A. et al. (2022) West Nile virus in the Republic of Serbia—Diagnostic performance of five serological tests in dog and horse sera. Transbound Emerg Dis. 1–10

44) Bournez L.et al. (2020) Exposure of Wild Ungulates to the Usutu and Tick-Borne Encephalitis Viruses in France in 2009–2014: Evidence of Undetected Flavivirus Circulation a Decade Ago. Viruses 12(1), 10

45) Constant O. et al. (2020). Evidence of Exposure to USUV and WNV in Zoo Animals in France. Pathogens 9(12), 1005

46) Beck C. et al. (2019) Serological evidence of infection with dengue and Zika viruses in horses on French Pacific Islands. PLoS Negl Trop Dis 13(2): e0007162

47) Dolz G. et al. (2019). Detection of antibodies against flavivirus over time in wild non-human primates from the lowlands of Costa Rica.

48) Llorente F. et al. (2019). Influence of flavivirus co‐circulation in serological diagnostics and surveillance: A model of study using West Nile, Usutu and Bagaza viruses. Transboundary and emerging diseases, 66(5), 2100-2106

49) Montagnaro S. et al. (2019). Serological evidence of mosquito-borne flaviviruses circulation in hunting dogs in Campania Region, Italy. Vector-Borne and Zoonotic Diseases, 19(2), 142-147

50) Napp S. et al. (2019) Usefulness of Eurasian Magpies (Pica pica) for West Nile virus Surveillance in Non-Endemic and Endemic Situations. Viruses 11, 716

51) Lim S.M. et al. (2018) Serologic evidence of West Nile virus and Usutu virus infections in Eurasian Coots in the Netherlands. Zoonoses and public health, 65(1), 96-102

52) Ruget A. S. et al. (2018). Japanese encephalitis circulation pattern in swine of northern Vietnam and consequences for swine’s vaccination recommendations. Transboundary and emerging diseases. 65(6), 1485-1492

53) Beck C. et al. (2017) Improved reliability of serological tools for the diagnosis of West Nile fever in horses within Europe. PLoS Negl Trop Dis 11(9): e0005936

54) Beck C. et al. (2015) A High-Performance Multiplex Immunoassay for Serodiagnosis of Flavivirus-Associated Neurological Diseases in Horses. BioMed Research International Volume 2015, Article ID 678084

55) Rushton J. et al. (2013) Tick-borne Encephalitis Virus in Horses, Austria, 2011. Emerging Infectious Diseases Vol. 19, No 4

Associated products

Serum transport
ELISA
Internal reference material
ELISA

Freeze-dried WNV positive horse serum. Read more