Facile, comprehensive, high-throughput genotyping of human genital papillomaviruses using spectrally addressable liquid bead microarrays
| dc.contributor.author | Wallace, Jan | |
| dc.contributor.author | Woda, Bruce A. | |
| dc.contributor.author | Pihan, German A. | |
| dc.date | 2022-08-11T08:09:31.000 | |
| dc.date.accessioned | 2022-08-23T16:34:14Z | |
| dc.date.available | 2022-08-23T16:34:14Z | |
| dc.date.issued | 2005-02-01 | |
| dc.date.submitted | 2009-03-10 | |
| dc.identifier.citation | J Mol Diagn. 2005 Feb;7(1):72-80. | |
| dc.identifier.issn | 1525-1578 (Print) | |
| dc.identifier.pmid | 15681477 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.14038/38285 | |
| dc.description.abstract | Human papillomavirus (HPV) is the worldwide cause of carcinoma of the uterine cervix, a cancer that is the second most common neoplasm in women, resulting in nearly 250,000 deaths a year. The magnitude of the risk of cancer after HPV infection, however, is virus type-specific. Over 40 HPV types can infect the genital tract. Comprehensive, high-throughput typing assays for HPV, however, are not currently available. Blending multiplex PCR and multiplex hybridization using spectrally addressable liquid bead microarrays we have developed a high-throughput, fast, single-tube-typing assay capable of simultaneously typing 45 HPV. The overall incidence of HPV in 429 women tested using this new assay was 72.2% for those with squamous intraepithelial lesions, 51.5% for those with atypical squamous cells of undetermined significance and 15.4% for women with normal cytology, respectively. This compared well with the incidence of HPV detected by a parallel non-typing generic high-risk assay. The new assay detected a wide spectrum of HPV types and a high incidence of mixed infections. We believe our assay may find widespread applications in areas requiring virus type-specific information, such as in epidemiological studies, cancer screening programs, monitoring therapeutic interventions, and evaluating the efficacy of HPV vaccine trials. | |
| dc.language.iso | en_US | |
| dc.relation | <a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=15681477&dopt=Abstract">Link to Article in PubMed</a> | |
| dc.relation.url | http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1867512/?tool=pubmed | |
| dc.subject | DNA, Viral | |
| dc.subject | Female | |
| dc.subject | Genotype | |
| dc.subject | Humans | |
| dc.subject | Microspheres | |
| dc.subject | Oligonucleotide Array Sequence Analysis | |
| dc.subject | Papillomaviridae | |
| dc.subject | Papillomavirus Infections | |
| dc.subject | Polymerase Chain Reaction | |
| dc.subject | Uterine Cervical Neoplasms | |
| dc.subject | Life Sciences | |
| dc.subject | Medicine and Health Sciences | |
| dc.title | Facile, comprehensive, high-throughput genotyping of human genital papillomaviruses using spectrally addressable liquid bead microarrays | |
| dc.type | Journal Article | |
| dc.source.journaltitle | The Journal of molecular diagnostics : JMD | |
| dc.source.volume | 7 | |
| dc.source.issue | 1 | |
| dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/oapubs/1157 | |
| dc.identifier.contextkey | 770135 | |
| html.description.abstract | <p>Human papillomavirus (HPV) is the worldwide cause of carcinoma of the uterine cervix, a cancer that is the second most common neoplasm in women, resulting in nearly 250,000 deaths a year. The magnitude of the risk of cancer after HPV infection, however, is virus type-specific. Over 40 HPV types can infect the genital tract. Comprehensive, high-throughput typing assays for HPV, however, are not currently available. Blending multiplex PCR and multiplex hybridization using spectrally addressable liquid bead microarrays we have developed a high-throughput, fast, single-tube-typing assay capable of simultaneously typing 45 HPV. The overall incidence of HPV in 429 women tested using this new assay was 72.2% for those with squamous intraepithelial lesions, 51.5% for those with atypical squamous cells of undetermined significance and 15.4% for women with normal cytology, respectively. This compared well with the incidence of HPV detected by a parallel non-typing generic high-risk assay. The new assay detected a wide spectrum of HPV types and a high incidence of mixed infections. We believe our assay may find widespread applications in areas requiring virus type-specific information, such as in epidemiological studies, cancer screening programs, monitoring therapeutic interventions, and evaluating the efficacy of HPV vaccine trials.</p> | |
| dc.identifier.submissionpath | oapubs/1157 | |
| dc.contributor.department | Department of Pathology | |
| dc.contributor.department | Laboratory of Diagnostic Molecular Oncology | |
| dc.source.pages | 72-80 |