Next-generation sequencing of HIV-1 single genome amplicons

Q1 Biochemistry, Genetics and Molecular Biology Biomolecular Detection and Quantification Pub Date : 2019-03-01 DOI:10.1016/j.bdq.2019.01.002
Gustavo H. Kijak , Eric Sanders-Buell , Phuc Pham , Elizabeth A. Harbolick , Celina Oropeza , Anne Marie O’Sullivan , Meera Bose , Charmagne G. Beckett , Mark Milazzo , Merlin L. Robb , Sheila A. Peel , Paul T. Scott , Nelson L. Michael , Adam W. Armstrong , Jerome H. Kim , David M. Brett-Major , Sodsai Tovanabutra
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引用次数: 8

Abstract

The analysis of HIV-1 sequences has helped understand the viral molecular epidemiology, monitor the development of antiretroviral drug resistance, and design candidate vaccines. The introduction of single genome amplification (SGA) has been a major advancement in the field, allowing for the characterization of multiple sequences per patient while preserving linkage among polymorphisms in the same viral genome copy. Sequencing of SGA amplicons is performed by capillary Sanger sequencing, which presents low throughput, requires a high amount of template, and is highly sensitive to template/primer mismatching. In order to meet the increasing demand for HIV-1 SGA amplicon sequencing, we have developed a platform based on benchtop next-generation sequencing (NGS) (IonTorrent) accompanied by a bioinformatics pipeline capable of running on computer resources commonly available at research laboratories. During assay validation, the NGS-based sequencing of 10 HIV-1 env SGA amplicons was fully concordant with Sanger sequencing. The field test was conducted on plasma samples from 10 US Navy and Marine service members with recent HIV-1 infection (sampling interval: 2005–2010; plasma viral load: 5,884–194,984 copies/ml). The NGS analysis of 101 SGA amplicons (median: 10 amplicons/individual) showed within-individual viral sequence profiles expected in individuals at this disease stage, including individuals with highly homogeneous quasispecies, individuals with two highly homogeneous viral lineages, and individuals with heterogeneous viral populations. In a scalability assessment using the Ion Chef automated system, 41/43 tested env SGA amplicons (95%) multiplexed on a single Ion 318 chip showed consistent gene-wide coverage >50×. With lower sample requirements and higher throughput, this approach is suitable to support the increasing demand for high-quality and cost-effective HIV-1 sequences in fields such as molecular epidemiology, and development of preventive and therapeutic strategies.

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HIV-1单基因组扩增子的新一代测序
HIV-1序列的分析有助于了解病毒的分子流行病学,监测抗逆转录病毒耐药性的发展,以及设计候选疫苗。单基因组扩增(SGA)的引入是该领域的一个重大进步,它允许对每个患者的多个序列进行表征,同时保留同一病毒基因组拷贝中多态性之间的联系。SGA扩增子的测序采用毛细管Sanger测序,其通量低,需要大量的模板,对模板/引物错配高度敏感。为了满足对HIV-1 SGA扩增子测序日益增长的需求,我们开发了一个基于台式下一代测序(NGS) (IonTorrent)的平台,并配有能够在研究实验室常用的计算机资源上运行的生物信息学管道。在实验验证中,基于ngs的10个HIV-1 env SGA扩增子测序与Sanger测序完全一致。现场试验是对10名最近感染HIV-1的美国海军和海军陆战队成员的血浆样本进行的(采样间隔:2005-2010;血浆病毒载量:5884 - 194984拷贝/ml)。对101个SGA扩增子(中位数:10个扩增子/个体)的NGS分析显示,在该疾病阶段的个体中,包括具有高度同质准种的个体、具有两个高度同质病毒谱系的个体和具有异质病毒群体的个体,预计会出现个体内病毒序列谱。在使用Ion Chef自动化系统的可扩展性评估中,41/43测试的env SGA扩增子(95%)在单个Ion 318芯片上复用,显示出一致的基因全覆盖>50倍。该方法具有较低的样品要求和较高的通量,适合支持分子流行病学等领域对高质量和高成本效益的HIV-1序列的不断增长的需求,以及预防和治疗策略的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biomolecular Detection and Quantification
Biomolecular Detection and Quantification Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
14.20
自引率
0.00%
发文量
0
审稿时长
8 weeks
期刊最新文献
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