High-throughput detection, genotyping and quantification of the human papillomavirus using real-time PCR
Abstract
The establishment of the causal relationship between high-risk human papillomavirus (HR-HPV) infection and cervical cancer and its precursors has resulted in the development of HPV DNA detection systems. Currently, real-time PCR assays for the detection of HPV, such as the RealTime High Risk (HR) HPV assay (Abbott) and the cobas® 4800 HPV Test (Roche Molecular Diagnostics) are commercially available. However, none of them enables the detection and typing of all HR-HPV types in a clinical high-throughput setting. This paper describes the laboratory workflow and the validation of a type-specific real-time quantitative PCR (qPCR) assay for high-throughput HPV detection, genotyping and quantification. This assay is routinely applied in a liquid-based cytology screening setting (700 samples in 24 h) and was used in many epidemiological and clinical studies. The TaqMan-based qPCR assay enables the detection of 17 HPV genotypes and β-globin in seven multiplex reactions. These HPV types include all 12 high-risk types (HPV16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59), three probably high-risk types (HPV53, 66 and 68), one low-risk type (HPV6) and one undetermined risk type (HPV67). An analytical sensitivity of ≤100 copies was obtained for all the HPV types. The analytical specificity of each primer pair was 100% and an intra- and inter-run variability of <6.4% was observed. The type-specific real-time PCR approach enables detection of 17 HPV types, identification of the HPV type and determination of the viral load in a single sensitive assay suitable for high-throughput screening.
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Published multiplex real-time PCR assays for HPV genotyping need at least 6 different PCR wells per sample to overcome limitations of present chemistries and equipment, which distinguish at best 3 to 5 targets per well.
“Thus, published multiplex real-time PCR assays for HPV genotyping need at least 6 different PCR wells per sample to overcome the limitations of present chemistries and equipment, which distinguish at best 3 to 5 targets per well (21).”
From Comparison of Seegene Anyplex II HPV28 with the PGMY-CHUV Assay for Human Papillomavirus Genotyping (2014) · cites this paper as [21]
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VALGENT: a protocol for clinical validation of human papillomavirus assays
Arbyn, M., Depuydt, C., Benoy, I., Bogers, J., Cuschieri, K., Schmitt, M., Pawlita, M., Geraets, D., Heard, I., Gheit, T., et al. (2016) · Journal of Clinical Virology · doi:10.1016/j.jcv.2015.09.014 · Cited by 157 · see citing works
Self-citationComparison of Seegene Anyplex II HPV28 with the PGMY-CHUV Assay for Human Papillomavirus Genotyping
Estrade, C., & Sahli, R. (2014) · Journal of Clinical Microbiology · doi:10.1128/jcm.02749-13 · Cited by 57 · see citing works
Cuschieri, K., Geraets, D., Cuzick, J., Cadman, L., Moore, C., Vanden Broeck, D., Padalko, E., Quint, W., & Arbyn, M. (2016) · Journal of Clinical Microbiology · doi:10.1128/jcm.00897-16 · Cited by 55 · see citing works
Kellen, E., Benoy, I., Vanden Broeck, D., Martens, P., Bogers, J., Haelens, A., & Van Limbergen, E. (2018) · International Journal of Cancer · doi:10.1002/ijc.31391 · Cited by 48 · see citing works
Self-citation
- Authors
- Micalessi, I. M., Boulet, G. A. V., Bogers, J. J., Benoy, I. H., & Depuydt, C. E.
- Affiliations
- University of Antwerp (BE)
- Corresponding author
- Micalessi, Isabel M.
- Venue
- Clinical Chemistry and Laboratory Medicine
- Publisher
- Walter de Gruyter GmbH
- Published
- 2012-01-01
- Volume
- 50
- Issue
- 4
- Pages
- 655-61
- ISSN
- 1434-6621 (ISSN-L)
- 1437-4331
- OpenAlex
- W2075692523
- Cited by
- 79
- References
- 0
- Citations by year
- 2026: 2 · 2025: 5 · 2024: 9 · 2023: 3 · 2022: 5 · 2021: 4 · 2020: 4 · 2019: 7 · 2018: 5 · 2017: 4 · 2016: 11 · 2015: 5 · 2014: 5 · 2013: 3 · 2012: 7
- FWCI
- 4.75
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Clinical Chemistry and Laboratory Medicine (CCLM) (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Epidemiology › Cervical Cancer and HPV Research
- Life Sciences › Immunology and Microbiology › Microbiology › Reproductive tract infections research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Molecular Biology Techniques and Applications
- Keywords
- human papillomavirus, high-risk HPV genotyping, HPV testing, TaqMan real-time PCR, cervical cancer screening, viral load, assay validation, high-throughput screening
- MeSH terms
- DNA, Viral, Female, Humans, Viral Load, Papillomaviridae, Genotyping Techniques, Real-Time Polymerase Chain Reaction
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