Abstract
A high-throughput polymerase chain reaction (PCR)-based enzyme-linked oligonucleotide-sorbent assay (ELOSA) was developed for use in the diagnostic testing of serum from patients who may be infected with different hepatitis C virus (HCV) genotypes. Twelve genotype-specific 5′-aminated DNA-coated probes were designed based on the variable 5′-untranslated region sequences of the HCV genotypes 1-6. Using 100 clinical serum samples, the performance of the PCR-ELOSA method was compared with Roche's COBAS Amplicor HCV Monitor V2.0 assay and the VERSANT HCV genotype assay (LiPA), and the overall agreement was 99% at the level of HCV genotypes with a detection range of 2.0 × 102 to 1.0 × 107 IU/ml for PCR-ELOSA. The PCR-ELOSA was more comprehensive as demonstrated by the fact that ∼20% of the samples with different subtypes could be discriminated by this method but not by LiPA. In addition, the PCR-ELOSA system showed high accuracy (CV ≤ 6.36%) and even higher reproducibility (CV ≤ 5.55%). Thus, this novel PCR-ELOSA system provides a sensitive and versatile alternative to current HCV detection assays.
| Original language | English |
|---|---|
| Pages (from-to) | 211-216 |
| Number of pages | 6 |
| Journal | Journal of Virological Methods |
| Volume | 151 |
| Issue number | 2 |
| DOIs | |
| State | Published - Aug 2008 |
Bibliographical note
Funding Information:This work was supported by General Biologicals Co., Ltd., grants to M. D.-T. Chang and a China Medical University grant (CMU96-255) to H.-T. Chang.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Genotyping
- HCV
- Hepatitis C virus
- PCR-ELOSA
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