Critical evaluation of HPV16 gene copy number quantification by SYBR green PCR

<p>Abstract</p> <p>Background</p> <p>Human papilloma virus (HPV) load and physical status are considered useful parameters for clinical evaluation of cervical squamous cell neoplasia. However, the errors implicit in HPV gene quantification by PCR are not well documented...

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Main Authors: Pett Mark R, Herdman Michael T, Stanley Margaret, Foster Nicola, Ng Grace, Roberts Ian, Teschendorff Andrew, Coleman Nicholas
Format: Article
Language:English
Published: BMC 2008-07-01
Series:BMC Biotechnology
Online Access:http://www.biomedcentral.com/1472-6750/8/57
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author Pett Mark R
Herdman Michael T
Stanley Margaret
Foster Nicola
Ng Grace
Roberts Ian
Teschendorff Andrew
Coleman Nicholas
author_facet Pett Mark R
Herdman Michael T
Stanley Margaret
Foster Nicola
Ng Grace
Roberts Ian
Teschendorff Andrew
Coleman Nicholas
author_sort Pett Mark R
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Human papilloma virus (HPV) load and physical status are considered useful parameters for clinical evaluation of cervical squamous cell neoplasia. However, the errors implicit in HPV gene quantification by PCR are not well documented. We have undertaken the first rigorous evaluation of the errors that can be expected when using SYBR green qPCR for quantification of HPV type 16 gene copy numbers. We assessed a modified method, in which external calibration curves were generated from a single construct containing HPV16 E2, HPV16 E6 and the host gene hydroxymethylbilane synthase in a 1:1:1 ratio.</p> <p>Results</p> <p>When testing dilutions of mixed HPV/host DNA in replicate runs, we observed errors in quantifying E2 and E6 amplicons of 5–40%, with greatest error at the lowest DNA template concentration (3 ng/μl). Errors in determining viral copy numbers per diploid genome were 13–53%. Nevertheless, in cervical keratinocyte cell lines we observed reasonable agreement between viral loads determined by qPCR and Southern blotting. The mean E2/E6 ratio in episome-only cells was 1.04, but with a range of 0.76–1.32. In three integrant-only lines the mean E2/E6 ratios were 0.20, 0.72 and 2.61 (values confirmed by gene-specific Southern blotting). When E2/E6 ratios in fourteen HPV16-positive cervical carcinomas were analysed, conclusions regarding viral physical state could only be made in three cases, where the E2/E6 ratio was ≤ 0.06.</p> <p>Conclusion</p> <p>Run-to-run variation in SYBR green qPCR produces unavoidable inaccuracies that should be allowed for when quantifying HPV gene copy number. While E6 copy numbers can be considered to provide a useable indication of viral loads, the E2/E6 ratio is of limited value. Previous studies may have overestimated the frequency of mixed episomal/integrant HPV infections.</p>
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spelling doaj.art-3c0de22dea6e4d36b677d3615a1ca1882022-12-22T03:05:37ZengBMCBMC Biotechnology1472-67502008-07-01815710.1186/1472-6750-8-57Critical evaluation of HPV16 gene copy number quantification by SYBR green PCRPett Mark RHerdman Michael TStanley MargaretFoster NicolaNg GraceRoberts IanTeschendorff AndrewColeman Nicholas<p>Abstract</p> <p>Background</p> <p>Human papilloma virus (HPV) load and physical status are considered useful parameters for clinical evaluation of cervical squamous cell neoplasia. However, the errors implicit in HPV gene quantification by PCR are not well documented. We have undertaken the first rigorous evaluation of the errors that can be expected when using SYBR green qPCR for quantification of HPV type 16 gene copy numbers. We assessed a modified method, in which external calibration curves were generated from a single construct containing HPV16 E2, HPV16 E6 and the host gene hydroxymethylbilane synthase in a 1:1:1 ratio.</p> <p>Results</p> <p>When testing dilutions of mixed HPV/host DNA in replicate runs, we observed errors in quantifying E2 and E6 amplicons of 5–40%, with greatest error at the lowest DNA template concentration (3 ng/μl). Errors in determining viral copy numbers per diploid genome were 13–53%. Nevertheless, in cervical keratinocyte cell lines we observed reasonable agreement between viral loads determined by qPCR and Southern blotting. The mean E2/E6 ratio in episome-only cells was 1.04, but with a range of 0.76–1.32. In three integrant-only lines the mean E2/E6 ratios were 0.20, 0.72 and 2.61 (values confirmed by gene-specific Southern blotting). When E2/E6 ratios in fourteen HPV16-positive cervical carcinomas were analysed, conclusions regarding viral physical state could only be made in three cases, where the E2/E6 ratio was ≤ 0.06.</p> <p>Conclusion</p> <p>Run-to-run variation in SYBR green qPCR produces unavoidable inaccuracies that should be allowed for when quantifying HPV gene copy number. While E6 copy numbers can be considered to provide a useable indication of viral loads, the E2/E6 ratio is of limited value. Previous studies may have overestimated the frequency of mixed episomal/integrant HPV infections.</p>http://www.biomedcentral.com/1472-6750/8/57
spellingShingle Pett Mark R
Herdman Michael T
Stanley Margaret
Foster Nicola
Ng Grace
Roberts Ian
Teschendorff Andrew
Coleman Nicholas
Critical evaluation of HPV16 gene copy number quantification by SYBR green PCR
BMC Biotechnology
title Critical evaluation of HPV16 gene copy number quantification by SYBR green PCR
title_full Critical evaluation of HPV16 gene copy number quantification by SYBR green PCR
title_fullStr Critical evaluation of HPV16 gene copy number quantification by SYBR green PCR
title_full_unstemmed Critical evaluation of HPV16 gene copy number quantification by SYBR green PCR
title_short Critical evaluation of HPV16 gene copy number quantification by SYBR green PCR
title_sort critical evaluation of hpv16 gene copy number quantification by sybr green pcr
url http://www.biomedcentral.com/1472-6750/8/57
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