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Clinical and Vaccine Immunology, August 2007, p. 1024-1031, Vol. 14, No. 8
1071-412X/07/$08.00+0     doi:10.1128/CVI.00051-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Epitope-Blocking Enzyme-Linked Immunosorbent Assay To Differentiate West Nile Virus from Japanese Encephalitis Virus Infections in Equine Sera{triangledown}

Yoko Kitai,1 Mizue Shoda,1 Takashi Kondo,2 and Eiji Konishi1*

Department of Health Sciences, Kobe University School of Medicine, Kobe,1 Epizootic Research Center, Equine Research Institute, Japan Racing Association, Tochigi, Japan2

Received 20 January 2007/ Returned for modification 5 March 2007/ Accepted 13 June 2007

West Nile virus (WNV) is now widely distributed worldwide, except in most areas of Asia where Japanese encephalitis virus (JEV) is distributed. Considering the movement and migration of reservoir birds, there is concern that WNV may be introduced in Asian countries. Although manuals and guidelines for serological tests have been created in Japan in preparedness for the introduction of WNV, differential diagnosis between WNV and JEV may be complicated by antigenic cross-reactivities between these flaviviruses. Here, we generated a monoclonal antibody specific for the nonstructural protein 1 (NS1) of WNV and established an epitope-blocking enzyme-linked immunosorbent assay that can differentiate WNV from JEV infections in horse sera. Under conditions well suited for our assay system, samples collected from 95 horses in Japan (regarded as negative for WNV antibodies), including those collected from horses naturally infected with JEV, showed a mean inhibition value of 8.2% and a standard deviation (SD) of 6.5%. However, inhibition values obtained with serum used as a positive control (obtained after 28 days from a horse experimentally infected with WNV) in nine separate experiments showed a mean of 54.4% and an SD of 7.1%. We tentatively determined 27.6% (mean + 3 x SD obtained with 95 negative samples) as the cutoff value to differentiate positive from negative samples. Under this criterion, two horses experimentally infected with WNV were diagnosed as positive at 12 and 14 days, respectively, after infection.

* Corresponding author. Mailing address: Department of Health Sciences, Kobe University School of Medicine, 7-10-2 Tomogaoka, Suma-ku, Kobe 654-0142, Japan. Phone and fax: 81-78-796-4594. E-mail: ekon{at}kobe-u.ac.jp

{triangledown} Published ahead of print on 27 June 2007.

Clinical and Vaccine Immunology, August 2007, p. 1024-1031, Vol. 14, No. 8
1071-412X/07/$08.00+0     doi:10.1128/CVI.00051-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Suzuki, R., Fayzulin, R., Frolov, I., Mason, P. W. (2008). Identification of Mutated Cyclization Sequences That Permit Efficient Replication of West Nile Virus Genomes: Use in Safer Propagation of a Novel Vaccine Candidate. J. Virol. 82: 6942-6951 [Abstract] [Full Text]  
  • Chiou, S.-S., Crill, W. D., Chen, L.-K., Chang, G.-J. J. (2008). Enzyme-Linked Immunosorbent Assays Using Novel Japanese Encephalitis Virus Antigen Improve the Accuracy of Clinical Diagnosis of Flavivirus Infections. CVI 15: 825-835 [Abstract] [Full Text]  
  • Konishi, E., Kitai, Y., Kondo, T. (2008). Utilization of Complement-Dependent Cytotoxicity To Measure Low Levels of Antibodies: Application to Nonstructural Protein 1 in a Model of Japanese Encephalitis Virus. CVI 15: 88-94 [Abstract] [Full Text]  


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