Munyuza Chantal, Ji Hezhao, Lee Emma R
National HIV and Retrovirology Laboratories, National Microbiology Laboratory at JC Wilt Infectious Diseases Research Centre, Public Health Agency of Canada, Winnipeg, MB R3E 3R2, Canada.
Department of Medical Microbiology and Infectious Diseases, University of Manitoba, Winnipeg, MB R3E 0J9, Canada.
Pathogens. 2022 Jun 16;11(6):693. doi: 10.3390/pathogens11060693.
Human immunodeficiency virus (HIV) infections remain a significant public health concern worldwide. Over the years, sophisticated sequencing technologies such as next-generation sequencing (NGS) have emerged and been utilized to monitor the spread of HIV drug resistance (HIVDR), identify HIV drug resistance mutations, and characterize transmission dynamics. Similar applications also apply to the Hepatitis C virus (HCV), another bloodborne viral pathogen with significant intra-host genetic diversity. Several advantages to using NGS over conventional Sanger sequencing include increased data throughput, scalability, cost-effectiveness when batched sample testing is performed, and sensitivity for quantitative detection of minority resistant variants. However, NGS alone may fail to detect genomes from pathogens present in low copy numbers. As with all sequencing platforms, the primary determinant in achieving quality sequencing data is the quality and quantity of the initial template input. Samples containing degraded RNA/DNA and/or low copy number have been a consistent sequencing challenge. To overcome this limitation probe capture enrichment is a method that has recently been employed to target, enrich, and sequence the genome of a pathogen present in low copies, and for compromised specimens that contain poor quality nucleic acids. It involves the hybridization of sequence-specific DNA or RNA probes to a target sequence, which is followed by an enrichment step via PCR to increase the number of copies of the targeted sequences after which the samples are subjected to NGS procedures. This method has been performed on pathogens such as bacteria, fungus, and viruses and allows for the sequencing of complete genomes, with high coverage. Post NGS, data analysis can be performed through various bioinformatics pipelines which can provide information on genetic diversity, genotype, virulence, and drug resistance. This article reviews how probe capture enrichment helps to increase the likelihood of sequencing HIV and HCV samples that contain low viral loads and/or are compromised.
人类免疫缺陷病毒(HIV)感染仍是全球重大的公共卫生问题。多年来,诸如新一代测序(NGS)等先进的测序技术不断涌现,并被用于监测HIV耐药性(HIVDR)的传播、识别HIV耐药突变以及描述传播动态。类似的应用也适用于丙型肝炎病毒(HCV),这是另一种具有显著宿主内遗传多样性的血源病毒病原体。与传统的桑格测序相比,使用NGS有几个优点,包括数据通量增加、可扩展性、批量样本检测时的成本效益以及对少数耐药变体进行定量检测的灵敏度。然而,仅靠NGS可能无法检测到低拷贝数病原体的基因组。与所有测序平台一样,获得高质量测序数据的主要决定因素是初始模板输入的质量和数量。含有降解的RNA/DNA和/或低拷贝数的样本一直是测序面临的挑战。为了克服这一限制,探针捕获富集是一种最近采用的方法,用于靶向、富集和测序低拷贝数存在的病原体基因组,以及处理含有低质量核酸的受损样本。它涉及将序列特异性DNA或RNA探针与目标序列杂交,随后通过PCR进行富集步骤,以增加目标序列的拷贝数,之后对样本进行NGS程序。该方法已应用于细菌、真菌和病毒等病原体,能够对完整基因组进行测序,且覆盖度高。在NGS之后,可以通过各种生物信息学管道进行数据分析,这些管道可以提供有关遗传多样性、基因型、毒力和耐药性的信息。本文综述了探针捕获富集如何有助于提高对低病毒载量和/或受损的HIV和HCV样本进行测序的可能性。