Human Papillomavirus Genotyping Using an Automated Film-Based Chip Array

被引:7
|
作者
Erali, Maria [1 ]
Pattison, David C. [1 ]
Wittwer, Carl T. [1 ,2 ]
Petti, Cathy A. [1 ,2 ]
机构
[1] Univ Utah, ARUP Inst Clin & Expt Pathol, Salt Lake City, UT USA
[2] Univ Utah, Dept Pathol, Salt Lake City, UT USA
来源
JOURNAL OF MOLECULAR DIAGNOSTICS | 2009年 / 11卷 / 05期
关键词
CERVICAL INTRAEPITHELIAL NEOPLASIA; WOMEN; RISK; CANCER; PERSISTENCE; TYPE-16; LESIONS; INFECTION; PRECANCER; DNA;
D O I
10.2353/jmoldx.2009.080154
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The INFINITI HPV-QUAD assay is a commercially available genotyping platform for human papillomavirus (HPV) that uses multiplex PCR, followed by automated processing for primer extension, hybridization, and detection. The analytical performance of the HPV-QUAD assay was evaluated using liquid cervical cytology specimens, and the results were compared with those results obtained using the digene High-Risk HPV hc2 Test (HC2). The specimen types included Surepath and PreservCyt transport media, as well as residual SurePath and HC2 transport media from the HC2 assay. The overall concordance of positive and negative results following the resolution of indeterminate and intermediate results was 83% among the 197 specimens tested. HC2 positive (+) and HPV-QUAD negative (-) results were noted in 24 specimens that were shown by real-time PCR and sequence analysis to contain no HPV, HPV types that were cross-reactive in the HC2 assay, or low virus levels. Conversely, HC2 (-) and HPV-QUAD (+) results were noted in four specimens and were subsequently attributed to cross-contamination. The most common HPV types to be identified in this study were HPV16, HPV18, HPV52/58, and HPV39/56. We show that the HPV-QUAD assay is a user friendly, automated system for the identification of distinct HPV genotypes. Based on its analytical performance, future studies with this platform are warranted to assess its clinical utility for HPV detection and genotyping. (J Mol Diagn 2009, 11:439-445; DOI.10.2353/jmoldx.2009.080154)
引用
收藏
页码:439 / 445
页数:7
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