HPV Genotyping of Modified General Primer-Amplicons Is More Analytically Sensitive and Specific by Sequencing than by Hybridization
Author(s) -
Roger Meisal,
Trine B. Rounge,
Irene Kraus Christiansen,
Alexander Kirkeby Eieland,
Merete Molton Worren,
Tor Molden,
Øyvind Kommedal,
Eivind Hovig,
Truls Michael Leegaard,
Ole Herman Ambur
Publication year - 2017
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0169074
Subject(s) - genotyping , amplicon , biology , dna sequencing , computational biology , genetics , population , dna–dna hybridization , primer (cosmetics) , polymerase chain reaction , dna , genotype , gene , medicine , chemistry , environmental health , organic chemistry
Sensitive and specific genotyping of human papillomaviruses (HPVs) is important for population-based surveillance of carcinogenic HPV types and for monitoring vaccine effectiveness. Here we compare HPV genotyping by Next Generation Sequencing (NGS) to an established DNA hybridization method. In DNA isolated from urine, the overall analytical sensitivity of NGS was found to be 22% higher than that of hybridization. NGS was also found to be the most specific method and expanded the detection repertoire beyond the 37 types of the DNA hybridization assay. Furthermore, NGS provided an increased resolution by identifying genetic variants of individual HPV types. The same Modified General Primers (MGP)-amplicon was used in both methods. The NGS method is described in detail to facilitate implementation in the clinical microbiology laboratory and includes suggestions for new standards for detection and calling of types and variants with improved resolution.
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