Conflicts of interest: A Chinese patent (application number: 201010567951.9) has been filed for the combination of all of the primers specific to 11 human papillomaviruses listed in this study and the experimental parameters used for the PCR assay. The author Xue-jun Ma is the inventor on the patent application. This technology is available for research only.
Genotyping of 11 human papillomaviruses by multiplex PCR with a GeXP analyzer†
Version of Record online: 12 APR 2012
Copyright © 2012 Wiley Periodicals, Inc.
Journal of Medical Virology
Volume 84, Issue 6, pages 957–963, June 2012
How to Cite
Yang, M.-J., Luo, L., Nie, K., Wang, M., Zhang, C., Li, J. and Ma, X.-j. (2012), Genotyping of 11 human papillomaviruses by multiplex PCR with a GeXP analyzer. J. Med. Virol., 84: 957–963. doi: 10.1002/jmv.23275
- Issue online: 12 APR 2012
- Version of Record online: 12 APR 2012
- Manuscript Accepted: 20 FEB 2012
- China Mega-Project for Infectious Disease. Grant Numbers: 2011ZX10004-001, 2009ZX10004-101
- State Key Laboratory for Genetic Engineering and Molecular Virology
- human papillomavirus (HPV);
- GenomeLab Gene Expression Profiler (GeXP);
- polymerase chain reaction (PCR);
A new, rapid, and high-throughput method was developed for simultaneous detection of 11 human papillomavirus (HPV) genotypes including nine high-risk types (HPV16, 18, 31, 33, 35, 39, 52, 58, and 66) and two low-risk types (HPV6 and 11) in a single tube by multiplex PCR based on a GenomeLab Gene Expression Profiler (GeXP) analyzer (GeXP-PCR). Eleven sets of chimeric primers were used to initiate the PCR, and one pair of universal primers was used for the subsequent cycles of the PCR. The specificity of GeXP-PCR for each HPV type was examined with clinical samples of single type HPV infection tested previously. The sensitivity of GeXP-PCR was evaluated by performing the assay on serial 10-fold dilutions of cloned PCR products. The GeXP-PCR achieved a sensitivity of 100 copies when all of the 11 pre-mixed plasmids containing HPV targets were present. Analyses of 124 clinical specimens using the GeXP-PCR demonstrated that the GeXP-PCR assay had comparable sensitivity and specificity to those of reported multiple PCR assay and an increased detection of HPV 11 in samples with mixed infections. In conclusion, the GeXP-PCR is a fast, sensitive, and high throughput method for the detection of multiple HPV infections. J. Med. Virol. 84:957–963, 2012. © 2012 Wiley Periodicals, Inc.