Comparison of human papillomavirus detection and genotyping with four different prime sets by PCR-sequencing.
- Author:
Yu Pin CAI
1
;
Yi YANG
;
Bao Li ZHU
;
Yuan LI
;
Xiao Yu XIA
;
Rui Fen ZHANG
;
Yang XIANG
Author Information
- Publication Type:Journal Article
- MeSH: Adult; Aged; Alphapapillomavirus; genetics; isolation & purification; Female; Genotype; Humans; Middle Aged; Papillomavirus Infections; virology; Polymerase Chain Reaction; methods; Young Adult
- From: Biomedical and Environmental Sciences 2013;26(1):40-47
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo assess and compare the Human Papillomavirus (HPV) detection efficiency and the potential clinical utility of PCR sequencing-based technology.
METHODSFour HPV consensus primer sets (GP5+/6+, MGP, MY09/11, and PGMY09/11) were used in order to amplify a broad spectrum of HPV types for HPV infection in 325 cervical samples and the PCR products were sequenced afterwards for the HPV genotyping.
RESULTSThe HPV-positive rate was 75.4%, of which 35.5% harbored more than one HPV genotype. A total of 36 different genotypes was found, with HPV 16 (24.1%) being the most prevalent, followed by HPV 58 (13.3%) and HPV 52 (9.6%). There were substantial to almost perfect agreements between different primer sets regarding HPV detection efficiency, with the kappa value varying from 0.751 to 0.925, MGP, and PGMY09/11 were the most effective in detecting multiple infections (P < 0.001). With each of the primer sets, a board range of HPV types could be identified, though there were several differences for a few genotypes.
CONCLUSIONThe substantial agreement between PCR-sequencing and HC2 for the detection of high-risk HPV (kappa=0.761) indicated that PCR-sequencing is also suitable for routine HPV screening.
