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A comparative study on the characterization of hepatitis B virus quasispecies by clone-based sequencing and third-generation sequencing
Hepatitis B virus (HBV) has a high mutation rate due to the extremely high replication rate and the proofreading deficiency during reverse transcription. The generated variants with genetic heterogeneity are described as viral quasispecies (QS). Clone-based sequencing (CBS) is thought to be the ‘gol...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5717089/ https://www.ncbi.nlm.nih.gov/pubmed/29116219 http://dx.doi.org/10.1038/emi.2017.88 |
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author | Li, Jing Wang, Mingjie Yu, Demin Han, Yue Yang, Zhitao Wang, Lei Zhang, Xinxin Liu, Feng |
author_facet | Li, Jing Wang, Mingjie Yu, Demin Han, Yue Yang, Zhitao Wang, Lei Zhang, Xinxin Liu, Feng |
author_sort | Li, Jing |
collection | PubMed |
description | Hepatitis B virus (HBV) has a high mutation rate due to the extremely high replication rate and the proofreading deficiency during reverse transcription. The generated variants with genetic heterogeneity are described as viral quasispecies (QS). Clone-based sequencing (CBS) is thought to be the ‘gold standard’ for assessing QS complexity and diversity of HBV, but an important issue about CBS is cost-effectiveness and laborious. In this study, we investigated the utility of the third-generation sequencing (TGS) DNA sequencing to characterize genetic heterogeneity of HBV QS and assessed the possible contribution of TGS technology in HBV QS studies. Parallel experiments including 3 control samples, which consisted of HBV full gene genotype B and genotype C plasmids, and 10 patients samples were performed by using CBS and TGS to analyze HBV whole-genome QS. Characterization of QS heterogeneity was conducted by using comprehensive statistical analysis. The results showed that TGS had a high consistency with CBS when measuring the complexity and diversity of QS. In addition, to detect rare variants, there were strong advantages conferred by TGS. In summary, TGS was considered to be practicable in HBV QS studies and it might have a relevant role in the clinical management of HBV infection in the future. |
format | Online Article Text |
id | pubmed-5717089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-57170892017-12-06 A comparative study on the characterization of hepatitis B virus quasispecies by clone-based sequencing and third-generation sequencing Li, Jing Wang, Mingjie Yu, Demin Han, Yue Yang, Zhitao Wang, Lei Zhang, Xinxin Liu, Feng Emerg Microbes Infect Original Article Hepatitis B virus (HBV) has a high mutation rate due to the extremely high replication rate and the proofreading deficiency during reverse transcription. The generated variants with genetic heterogeneity are described as viral quasispecies (QS). Clone-based sequencing (CBS) is thought to be the ‘gold standard’ for assessing QS complexity and diversity of HBV, but an important issue about CBS is cost-effectiveness and laborious. In this study, we investigated the utility of the third-generation sequencing (TGS) DNA sequencing to characterize genetic heterogeneity of HBV QS and assessed the possible contribution of TGS technology in HBV QS studies. Parallel experiments including 3 control samples, which consisted of HBV full gene genotype B and genotype C plasmids, and 10 patients samples were performed by using CBS and TGS to analyze HBV whole-genome QS. Characterization of QS heterogeneity was conducted by using comprehensive statistical analysis. The results showed that TGS had a high consistency with CBS when measuring the complexity and diversity of QS. In addition, to detect rare variants, there were strong advantages conferred by TGS. In summary, TGS was considered to be practicable in HBV QS studies and it might have a relevant role in the clinical management of HBV infection in the future. Nature Publishing Group 2017-11 2017-11-08 /pmc/articles/PMC5717089/ /pubmed/29116219 http://dx.doi.org/10.1038/emi.2017.88 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Original Article Li, Jing Wang, Mingjie Yu, Demin Han, Yue Yang, Zhitao Wang, Lei Zhang, Xinxin Liu, Feng A comparative study on the characterization of hepatitis B virus quasispecies by clone-based sequencing and third-generation sequencing |
title | A comparative study on the characterization of hepatitis B virus quasispecies by clone-based sequencing and third-generation sequencing |
title_full | A comparative study on the characterization of hepatitis B virus quasispecies by clone-based sequencing and third-generation sequencing |
title_fullStr | A comparative study on the characterization of hepatitis B virus quasispecies by clone-based sequencing and third-generation sequencing |
title_full_unstemmed | A comparative study on the characterization of hepatitis B virus quasispecies by clone-based sequencing and third-generation sequencing |
title_short | A comparative study on the characterization of hepatitis B virus quasispecies by clone-based sequencing and third-generation sequencing |
title_sort | comparative study on the characterization of hepatitis b virus quasispecies by clone-based sequencing and third-generation sequencing |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5717089/ https://www.ncbi.nlm.nih.gov/pubmed/29116219 http://dx.doi.org/10.1038/emi.2017.88 |
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