Cited by 79Cervical Cancer and HPV ResearchReproductive tract infections researchMolecular Biology Techniques and Applications

High-throughput detection, genotyping and quantification of the human papillomavirus using real-time PCR

Micalessi, Isabel M., Boulet, Gaëlle A.V., Bogers, Johannes J., Benoy, Ina H., Depuydt, Christophe E.·2012·Clinical Chemistry and Laboratory Medicine

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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Crossref · 10.1515/cclm.2011.835

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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).”

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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
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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