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Rapid amplified enzyme linked immunosorbent assay evaluated for detecting herpes simplex virus
J A Emsbroek1, P Overdiek, R A Coutinho
1Department of Infectious Diseases, Municipal Health Service, Amsterdam, The Netherlands.
Genitourinary Medicine
|April 1, 1988
Summary
A new amplified enzyme-linked immunosorbent assay (ELISA) offers a sensitive alternative for detecting herpes simplex virus (HSV) antigen, particularly in early lesions. While effective for high-prevalence populations, viral culture remains crucial for differential diagnosis.
Area of Science:
- Virology
- Immunology
- Diagnostic Assays
Background:
- Herpes simplex virus (HSV) infections require accurate and timely diagnosis.
- Traditional diagnostic methods like viral culture can be time-consuming.
- Development of rapid and sensitive diagnostic tools is crucial for effective management.
Purpose of the Study:
- To evaluate the performance of a novel amplified enzyme-linked immunosorbent assay (ELISA) kit for detecting HSV antigen.
- To compare the sensitivity and specificity of amplified ELISA with viral culture.
- To assess the utility of amplified ELISA in different clinical presentations of herpes lesions.
Main Methods:
- Evaluation of an amplified ELISA kit using swabs from 180 patients with suspected herpes lesions.
- Comparison of results from direct swab extracts and viral transport medium.
- Analysis of sensitivity based on lesion stage (early vs. late) and sample type.
Main Results:
- The amplified ELISA demonstrated high sensitivity (83.9% for extracted samples, 77.4% for transport medium) compared to viral culture.
- Sensitivity was significantly higher (90.7%) when extracted swabs were processed first.
- Early lesions showed higher sensitivity (93.8%) than late lesions (73.3%), with an overall specificity of 94.3%.
Conclusions:
- Amplified ELISA is a viable alternative to viral culture for diagnosing HSV in early lesions.
- The test is suitable for populations with a high prevalence of HSV infection due to its specificity.
- Viral culture remains the preferred method for differential diagnosis and screening in low-prevalence populations.