Competitive-Inhibition Enzyme-Linked Immunosorbent Assay for Detection of Serum Antibodies to Caprine Arthritis-Encephalitis Virus: Diagnostic Tool for Successful Eradication

Author:

Herrmann Lynn M.1234,Cheevers William P.1234,McGuire Travis C.1234,Adams D. Scott1234,Hutton Melinda M.1234,Gavin William G.1234,Knowles Donald P.1234

Affiliation:

1. Animal Disease Research Unit, Agricultural Research Service, U.S. Department of Agriculture, Pullman, Washington 99164-6630

2. Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, Washington 99164-7040

3. VMRD, Inc., Pullman, Washington 99163

4. GTC Biotherapeutics, Framingham, Massachusetts 01701-9322

Abstract

ABSTRACT A competitive-inhibition enzyme-linked immunosorbent assay (cELISA) was evaluated for the detection of serum antibodies to the surface envelope (SU) of caprine arthritis-encephalitis virus (CAEV) in goats. This assay utilized 96-well microtiter plates containing CAEV-63 SU captured by monoclonal antibody (MAb) F7-299 and measured the competitive displacement of horseradish peroxidase-conjugated MAb GPB 74A binding by undiluted goat sera (F. Özyörük, W. P. Cheevers, G. A. Hullinger, T. C. McGuire, M. Hutton, and D. P. Knowles, Clin. Diagn. Lab. Immunol. 8:44-51, 2001). Two hundred serum samples from goats in the United States were used to determine the sensitivity and specificity of cELISA based on the immunoprecipitation (IP) of [ 35 S]methionine-labeled viral antigens as a standard of comparison. A positive cELISA was defined as >33.2% inhibition of MAb 74A binding based on 2 standard deviations above the mean percent inhibition of 140 IP-negative serum samples. At this cutoff value, there were 0 of 60 false-negative sera (100% sensitivity) and 5 of 140 false-positive sera (96.4% specificity). Additional studies utilized IP-monitored cELISA to establish a CAEV-free herd of 1,640 dairy goats.

Publisher

American Society for Microbiology

Subject

Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy

Reference17 articles.

1. Adams, D. S., P. Klevjer-Anderson, J. L. Carlson, T. C. McGuire, and J. R. Gorham. 1983. Transmission and control of caprine arthritis-encephalitis virus. Am. J. Vet. Res.44:1670-1675.

2. Cheevers, W. P., D. P. Knowles, and L. K. Norton. 1991. Neutralization-resistant antigenic variants of caprine arthritis-encephalitis lentivirus associated with progressive arthritis. J. Infect. Dis.164:679-685.

3. Cheevers, W. P., and T. C. McGuire. 1988. The lentiviruses: maedi/visna, caprine arthritis-encephalitis, and equine infectious anemia. Adv. Virus Res.34:189-215.

4. Clavijo, A., and J. Thorsen. 1995. Bacterial expression of the caprine arthritis-encephalitis virus gag and env proteins and their use in enzyme-linked immunosorbent assay. Am. J. Vet. Res.56:841-848.

5. Crawford, T. B., and D. S. Adams. 1981. Caprine arthritis-encephalitis: clinical features and presence of antibody in selected goat populations. J. Am. Vet. Med. Assoc.178:713-719.

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