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In-depth validation of total HIV-1 DNA assays for quantification of various HIV-1 subtypes

HIV-1 DNA quantification serves as an important reservoir biomarker in HIV cure trials. However, the high genetic diversity of HIV-1 represented by different subtypes may bring inaccuracy in quantifying HIV-1 DNA and a sensitive and validated assay covering diverse HIV-1 subtypes is lacking. Therefo...

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Autores principales: Rutsaert, Sofie, De Spiegelaere, Ward, Van Hecke, Clarissa, De Scheerder, Marie-Angélique, Kiselinova, Maja, Vervisch, Karen, Trypsteen, Wim, Vandekerckhove, Linos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6250682/
https://www.ncbi.nlm.nih.gov/pubmed/30467426
http://dx.doi.org/10.1038/s41598-018-35403-6
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author Rutsaert, Sofie
De Spiegelaere, Ward
Van Hecke, Clarissa
De Scheerder, Marie-Angélique
Kiselinova, Maja
Vervisch, Karen
Trypsteen, Wim
Vandekerckhove, Linos
author_facet Rutsaert, Sofie
De Spiegelaere, Ward
Van Hecke, Clarissa
De Scheerder, Marie-Angélique
Kiselinova, Maja
Vervisch, Karen
Trypsteen, Wim
Vandekerckhove, Linos
author_sort Rutsaert, Sofie
collection PubMed
description HIV-1 DNA quantification serves as an important reservoir biomarker in HIV cure trials. However, the high genetic diversity of HIV-1 represented by different subtypes may bring inaccuracy in quantifying HIV-1 DNA and a sensitive and validated assay covering diverse HIV-1 subtypes is lacking. Therefore, we cross-validated total HIV-1 DNA assays described in literature using a three-step comparative analysis. First, a bioinformatics tool was developed in-house to perform an in silico evaluation of 67 HIV-1 DNA assays. Secondly, these selected assays were in vitro validated using a panel of different HIV-1 subtypes and, finally, ex vivo assessed on selected patient samples with different HIV-1 subtypes. Our results show that quantification of HIV-1 DNA substantially differs between assays and we advise five best performing HIV-1 DNA assays for ddPCR and qPCR (Schvachsa_2007, Viard_2004, Heeregrave_2009, Van_der_Sluis_2013, Yu_2008 and Yun_2002). This in-depth analysis of published HIV-1 DNA assays indicates that not all assays guarantee an optimal measurement of HIV-1 DNA, especially when looking across subtypes. Using an in-depth cross-validation, we were able to validate HIV-1 DNA assays that are suitable for quantification of HIV-1 DNA in a wide variety of HIV-1 infected patients.
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spelling pubmed-62506822018-11-28 In-depth validation of total HIV-1 DNA assays for quantification of various HIV-1 subtypes Rutsaert, Sofie De Spiegelaere, Ward Van Hecke, Clarissa De Scheerder, Marie-Angélique Kiselinova, Maja Vervisch, Karen Trypsteen, Wim Vandekerckhove, Linos Sci Rep Article HIV-1 DNA quantification serves as an important reservoir biomarker in HIV cure trials. However, the high genetic diversity of HIV-1 represented by different subtypes may bring inaccuracy in quantifying HIV-1 DNA and a sensitive and validated assay covering diverse HIV-1 subtypes is lacking. Therefore, we cross-validated total HIV-1 DNA assays described in literature using a three-step comparative analysis. First, a bioinformatics tool was developed in-house to perform an in silico evaluation of 67 HIV-1 DNA assays. Secondly, these selected assays were in vitro validated using a panel of different HIV-1 subtypes and, finally, ex vivo assessed on selected patient samples with different HIV-1 subtypes. Our results show that quantification of HIV-1 DNA substantially differs between assays and we advise five best performing HIV-1 DNA assays for ddPCR and qPCR (Schvachsa_2007, Viard_2004, Heeregrave_2009, Van_der_Sluis_2013, Yu_2008 and Yun_2002). This in-depth analysis of published HIV-1 DNA assays indicates that not all assays guarantee an optimal measurement of HIV-1 DNA, especially when looking across subtypes. Using an in-depth cross-validation, we were able to validate HIV-1 DNA assays that are suitable for quantification of HIV-1 DNA in a wide variety of HIV-1 infected patients. Nature Publishing Group UK 2018-11-22 /pmc/articles/PMC6250682/ /pubmed/30467426 http://dx.doi.org/10.1038/s41598-018-35403-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Rutsaert, Sofie
De Spiegelaere, Ward
Van Hecke, Clarissa
De Scheerder, Marie-Angélique
Kiselinova, Maja
Vervisch, Karen
Trypsteen, Wim
Vandekerckhove, Linos
In-depth validation of total HIV-1 DNA assays for quantification of various HIV-1 subtypes
title In-depth validation of total HIV-1 DNA assays for quantification of various HIV-1 subtypes
title_full In-depth validation of total HIV-1 DNA assays for quantification of various HIV-1 subtypes
title_fullStr In-depth validation of total HIV-1 DNA assays for quantification of various HIV-1 subtypes
title_full_unstemmed In-depth validation of total HIV-1 DNA assays for quantification of various HIV-1 subtypes
title_short In-depth validation of total HIV-1 DNA assays for quantification of various HIV-1 subtypes
title_sort in-depth validation of total hiv-1 dna assays for quantification of various hiv-1 subtypes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6250682/
https://www.ncbi.nlm.nih.gov/pubmed/30467426
http://dx.doi.org/10.1038/s41598-018-35403-6
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