Cross Comparison of AmpFire HPV Genotyping Assay and Roche Human Papillomavirus (HPV) Linear Array for HPV Genotyping of Anal Swab Samples

2021 ◽  
pp. 114113
Author(s):  
Kaleigh A. Connors ◽  
Stephen Abbott ◽  
Kamwing Jair ◽  
Jason Daniels ◽  
Madison Lintner ◽  
...  
2009 ◽  
Vol 48 (3) ◽  
pp. 758-764 ◽  
Author(s):  
Stephanie S. Liu ◽  
Rebecca C. Y. Leung ◽  
Karen K. L. Chan ◽  
Annie N. Y. Cheung ◽  
Hextan Y. S. Ngan

2010 ◽  
Vol 134 (12) ◽  
pp. 1813-1817
Author(s):  
Candice C. Black ◽  
Heather A. Bentley ◽  
Thomas H. Davis ◽  
Gregory J. Tsongalis

Abstract Context—Tumors of the head and neck commonly arise from the squamous and respiratory mucosa that lines the nasal and oral cavity, sinuses, pharynx, and larynx. The rate of oropharyngeal cancers diagnosed among Americans younger than 50 years is increasing. Infection of the oropharynx and tonsils by the human papillomavirus (HPV) has been linked to preneoplasia and cancer. Objectives—To evaluate the Roche Linear Array HPV Genotyping test kit to identify, and then specifically genotype, HPV in formalin-fixed, paraffin-embedded tissues. Design—We evaluated the performance of this assay for accuracy, for intra-assay and interassay precision, and for its limit of detection, using materials with known HPV status. Sixteen tumor tissues with the following origins were evaluated: 1 ocular, 1 hypopharynx, 8 tonsil, 1 retromolar trigone, 3 tongue, 1 anal, and 1 lymph node. DNA from formalin-fixed, paraffin-embedded tumor sections was isolated and amplified in duplicate, with positive and negative controls, using primers specific to the polymorphic L1 region of the HPV genome. Thirty-seven genotypes were tested using the linear array. The amplified product (450 base pairs) was visualized by gel electrophoresis and, if positive, reflexed to HPV genotyping. Results—Nine of the 16 tumors analyzed were HPV positive. The detected genotypes included HPV 6, 16, and 69. Conclusions—The Roche Linear Array HPV Genotyping test is an easy-to-use method for determining HPV genotype in the routine analysis of formalin-fixed, paraffin-embedded tumors. This assay is robust and can be performed routinely in a clinical laboratory setting.


2019 ◽  
Vol 220 (10) ◽  
pp. 1609-1619 ◽  
Author(s):  
Sarah Wagner ◽  
David Roberson ◽  
Joseph Boland ◽  
Aimée R Kreimer ◽  
Meredith Yeager ◽  
...  

AbstractBackgroundHuman papillomaviruses (HPV) cause over 500 000 cervical cancers each year, most of which occur in low-resource settings. Human papillomavirus genotyping is important to study natural history and vaccine efficacy. We evaluated TypeSeq, a novel, next-generation, sequencing-based assay that detects 51 HPV genotypes, in 2 large international epidemiologic studies.MethodsTypeSeq was evaluated in 2804 cervical specimens from the Study to Understand Cervical Cancer Endpoints and Early Determinants (SUCCEED) and in 2357 specimens from the Costa Rica Vaccine Trial (CVT). Positive agreement and risks of precancer for individual genotypes were calculated for TypeSeq in comparison to Linear Array (SUCCEED). In CVT, positive agreement and vaccine efficacy were calculated for TypeSeq and SPF10-LiPA.ResultsWe observed high overall and positive agreement for most genotypes between TypeSeq and Linear Array in SUCCEED and SPF10-LiPA in CVT. There was no significant difference in risk of precancer between TypeSeq and Linear Array in SUCCEED or in estimates of vaccine efficacy between TypeSeq and SPF10-LiPA in CVT.ConclusionsThe agreement of TypeSeq with Linear Array and SPF10-LiPA, 2 well established standards for HPV genotyping, demonstrates its high accuracy. TypeSeq provides high-throughput, affordable HPV genotyping for world-wide studies of cervical precancer risk and of HPV vaccine efficacy.


2006 ◽  
Vol 44 (6) ◽  
pp. 1998-2006 ◽  
Author(s):  
F. Coutlee ◽  
D. Rouleau ◽  
P. Petignat ◽  
G. Ghattas ◽  
J. R. Kornegay ◽  
...  

2006 ◽  
Vol 44 (11) ◽  
pp. 3915-3917 ◽  
Author(s):  
P. E. Castle ◽  
M. Sadorra ◽  
F. Garcia ◽  
E. B. Holladay ◽  
J. Kornegay

2011 ◽  
Vol 49 (9) ◽  
pp. 3262-3267 ◽  
Author(s):  
Markus Schmitt ◽  
Maurits N. C. de Koning ◽  
Just A. H. Eekhof ◽  
Wim G. V. Quint ◽  
Michael Pawlita

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