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Duplex Real-time PCR assay and SYBR green I melting curve analysis for molecular identification of HPV genotypes 16, 18, 31, 35, 51 and 66

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Autore
Tsakogiannis, D.; Papacharalampous, M.; Toska, E.; Kyriakopoulou, Z.; Dimitriou, T. G.; Ruether, I. G. A.; Komiotis, D.; Markoulatos, P.
Data
2015
DOI
10.1016/j.mcp.2014.09.003
Soggetto
HPV genotyping
Duplex Real-time PCR
Melting curve analysis
L1 gene
HUMAN-PAPILLOMAVIRUS INFECTION
CERVICAL CYTOLOGY
MULTIPLE TYPES
CANCER
RISK
DNA
CLASSIFICATION
WOMEN
Biochemical Research Methods
Biochemistry & Molecular Biology
Biotechnology & Applied Microbiology
Cell Biology
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Abstract
Long-term infection with high-risk HPV genotypes is the leading cause of cervical cancer. In the present study a Duplex Real-time PCR assay was developed in order to identify HPV types 16, 18, 31, 35, 51 and 66 in three reactions, through SYBR green I melting curve analysis. The method utilizes type-specific primer sets that allowed the amplification of highly conserved regions of L1 gene. Reconstitution experiments were conducted by using HPV DNA plasmids in order to determine the sensitivity of the assay. The newly designed assay has a limit of detection of 10 copies per reaction. The most prevalent HPV genotype in single and in multiple HPV infections was HPV16 followed by HPV18, HPV51, HPV31, HPV35 and HPV66. The proposed method is a simple, specific, sensitive and cost-effective assay that can be easily incorporated in small and medium size laboratories for the rapid identification of the most clinically important HPV genotypes. (C) 2014 Elsevier Ltd. All rights reserved.
URI
http://hdl.handle.net/11615/33761
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