Comparison of INNO-LiPA HPV Genotyping v2 with PCR product subcloning and sequencing for identification of genital human papillomavirus genotypes in African women

被引:23
作者
Didelot-Rousseau, Marie-Noelle
Courgnaud, Valerie
Nagot, Nicolas
Ouedraogo, Abdoulaye
Konate, Issouf
Mayaud, Philippe
Weiss, Helen
Van de Perre, Philippe
Segondy, Michel
机构
[1] Montpellier Univ Hosp, Virol Lab, F-34295 Montpellier, France
[2] Univ Montpellier, UMR145, F-34295 Montpellier, France
[3] Inst Rech Dev, F-34295 Montpellier, France
[4] Bobo Dioulasso, Ctr Muraz, Burkino Faso, France
[5] London Sch Hyg & Trop Med, London WC1E 7HT, England
关键词
human papillomavirus; typing; UPA; subcloning; sequencing;
D O I
10.1016/j.jviromet.2006.03.015
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The performance characteristics of the INNO-LiPA Genotyping v2 test for human papillomavirus (HPV) identification were assessed by comparing results with those obtained by PCR product sequencing after subcloning, in genital samples from 20 highly sexually exposed African women. The INNO-LiPA HPV Genotyping v2 test identified more HPV types than subcloning/sequencing (56 versus 37, respectively). Overall, 86.5% (32/37) of the HPV types identified by subcloning/sequencing were identified by the INNO-LiPA HPV Genotyping v2 test, whereas 57.1% (32/56) of the HPV types identified by the INNO-LiPA HPV Genotyping v2 test were identified by subcloning/sequencing. Of the 20 clinical samples tested, 7 had identical types detected under both methods and a further 11 had more types detected under INNO-LiPA HPV Genotyping v2 than subcloning/sequencing. Of the remaining two samples, the same number of types were detected under both methods, but different types were detected. INNO-LiPA HPV Genotyping v2 test appears as a valid method for identifying HPV subtypes in women with multiple HPV infection. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:181 / 185
页数:5
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