Sung Yong Park , Gina Faraci , Kevin Ganesh , Michael P. Dubé , Ha Youn Lee
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By producing more than 500 full-length HIV pol gene sequences in a single portable sequencing run, we detected Protease Inhibitor (PI), Nucleoside Reverse Transcriptase Inhibitor (NRTI), NNRTI and INSTI resistance mutations. 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引用次数: 0
摘要
背景应对 HIV 耐药性是结束艾滋病流行的主要挑战之一,但尖端基因组学的高昂费用阻碍了临床护理中 HIV 基因型检测的发展。通过与固定点 Pacbio 测序获得的平行数据进行比较,验证了准确性。我们将完整的多基因测序策略与便携式高通量测序技术相结合,对来自接受抗逆转录病毒疗法治疗的洛杉矶综合医疗中心兰德-施拉德诊所(LARSC)队列(7 人 7 份样本)和接受抗逆转录病毒疗法治疗的艾滋病疫苗免疫学中心(CHAVI)队列(38 人 51 份样本)的 58 份样本进行耐药性突变鉴定。结果 通过便携式 Nanopore 测序技术获得的 140 多万个碱基序列中,共产生了 472 个 HIV 共识序列,每个序列都标有唯一的分子标识符,这些序列与通过 Pacbio 测序技术独立获得的序列相匹配。有了这种理想的准确性,我们首次记录了在第二代 INSTI 方案失败的个体中,整合酶链转移抑制剂(INSTIs)和非核苷逆转录酶抑制剂(NNRTIs)之间的多药交叉耐药性突变联系。通过在一次便携式测序中生成 500 多个全长 HIV pol 基因序列,我们检测到了蛋白酶抑制剂 (PI)、核苷类逆转录酶抑制剂 (NRTI)、NNRTI 和 INSTI 的耐药性突变。通过便携式测序发现的所有耐药性突变都经过了固定点 Pacbio 测序的交叉验证。
Portable Nanopore sequencing solution for next-generation HIV drug resistance testing
Background
Tackling HIV drug resistance is one of major challenges for ending AIDS epidemic, but the elevated expense of cutting-edge genomics hampers the advancement of HIV genotype testing for clinical care.
Methods
We developed a HIV genotype testing pipeline that centers on a cost-efficient portable Nanopore sequencer. Accuracy verification was conducted through comparison with parallel data obtained via fixed-site Pacbio sequencing. Our complete pol-gene sequencing strategy coupled with portable high-throughput sequencing was applied to identify drug resistance mutations across 58 samples sourced from the ART-treated Los Angeles General Medical Center Rand Schrader Clinic (LARSC) cohort (7 samples from 7 individuals) and the ART-naïve Center for HIV/AIDS Vaccine Immunology (CHAVI) cohort (51 samples from 38 individuals).
Results
A total of 472 HIV consensus sequences, each tagged with a unique molecular identifier, were produced from over 1.4 million bases acquired through portable Nanopore sequencing, which matched those obtained independently via Pacbio sequencing. With this desirable accuracy, we first documented the linkage of multidrug cross-resistance mutations across Integrase Strand Transfer inhibitors (INSTIs) and Non-Nucleoside Reverse Transcriptase Inhibitors (NNRTIs) from an individual failing a second-generation INSTI regimen. By producing more than 500 full-length HIV pol gene sequences in a single portable sequencing run, we detected Protease Inhibitor (PI), Nucleoside Reverse Transcriptase Inhibitor (NRTI), NNRTI and INSTI resistance mutations. All drug resistance mutations identified through portable sequencing were cross-validated using fixed-site Pacbio sequencing.
Conclusions
Our accurate and affordable HIV drug resistance testing solution is adaptable for both individual patient care and large-scale surveillance initiatives.
期刊介绍:
The Journal of Clinical Virology, an esteemed international publication, serves as the official journal for both the Pan American Society for Clinical Virology and The European Society for Clinical Virology. Dedicated to advancing the understanding of human virology in clinical settings, the Journal of Clinical Virology focuses on disseminating research papers and reviews pertaining to the clinical aspects of virology. Its scope encompasses articles discussing diagnostic methodologies and virus-induced clinical conditions, with an emphasis on practicality and relevance to clinical practice.
The journal publishes on topics that include:
• new diagnostic technologies
• nucleic acid amplification and serologic testing
• targeted and metagenomic next-generation sequencing
• emerging pandemic viral threats
• respiratory viruses
• transplant viruses
• chronic viral infections
• cancer-associated viruses
• gastrointestinal viruses
• central nervous system viruses
• one health (excludes animal health)