Evaluation of an enzyme-linked immunoassay employing a covalently bound capture antibody for direct detection of herpes simplex virus

Author:

Needham C A1,Hurlbert P1

Affiliation:

1. Department of Laboratory Medicine, Lahey Clinic Medical Center, Burlington, Massachusetts 01805.

Abstract

The FDL enzyme-linked immunosorbent assay (ELISA; Fairleigh Dickinson Laboratories, Inc., Abilene, Tex.) for the detection of herpes simplex virus (HSV) makes use of a covalently attached antibody. This assay was compared with viral isolation and with the Ortho HSV Antigen Detection ELISA (Ortho Diagnostic Systems, Inc., Raritan, N.J.). One hundred forty-eight specimens were tested. The FDL ELISA identified 66 of 104 specimens from which HSV was isolated, yielding a sensitivity of 63% and a specificity of 95%. These results compared favorably with those obtained by using the Ortho ELISA. The total test time was shorter and the washing step was simpler than that with the Ortho assay, making the FDL assay an attractive alternative to similar methodologies.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference7 articles.

1. Foster T. L. and R. C. Casey. April 1984. U.S. patent 4 444 879.

2. Comparison of two enzyme-linked immunosorbent assays for detection of herpes simplex virus antigen;Gonik B.;J. Clin. Microbiol.,1991

3. Evaluation of an enzymelinked immunosorbent assay for the detection of herpes simplex virus antigen;Morgan M. A.;J. Clin. Microbiol.,1984

4. Evaluation of a commercial enzyme-linked immunosorbent assay for the detection of herpes simplex virus;Sewell D. L.;J. Clin. Microbiol.,1985

5. Voller A. D. Bidwell and A. Bartlett. 1980. Enzyme-linked immunosorbent assay p. 359-371. In N. R. Rose and H. Friedman (ed.) Manual of clinical immunology 2nd ed. American Society for Microbiology Washington D.C.

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