Programa de Pós-Graduação em Genética e Biologia Molecular, Departamento de Genética, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Laboratório de Medicina Genômica, Centro de Pesquisa Experimental, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
Biopreserv Biobank. 2024 Apr;22(2):166-173. doi: 10.1089/bio.2022.0188. Epub 2023 Aug 9.
During the COVID-19 pandemic, an extraordinary number of nasopharyngeal secretion samples inoculated in viral transport medium (VTM) were collected and analyzed to detect SARS-CoV-2 infection. In addition to viral detection, those samples can also be a source of host genomic material, providing excellent opportunities for biobanking and research. To describe a simple, in-house-developed DNA extraction method to obtain high yield and quality genomic DNA from VTM samples for host genetic analysis and assess its relative efficiency by comparing its yield and suitability to downstream applications to two different commercial DNA extraction kits. In this study, 13 VTM samples were processed by two commercial silica-based kits and compared with an in-House-developed protocol for host DNA extraction. An additional 452 samples were processed by the in-House method. The quantity and quality of the differentially extracted DNA samples were assessed by Qubit and spectrophotometric measurements. The suitability of extracted samples for downstream applications was tested by polymerase chain reaction (PCR) amplification followed by amplicon sequencing and allelic discrimination in real-time PCR. The in-House method provided greater median DNA yield (0.81 μg), being significantly different from the PureLink method (0.14 μg, < 0.001), but not from the QIAamp method (0.47 μg, = 0.980). Overall satisfactory results in DNA concentrations and purity, in addition to cost, were observed using the in-House method, whose samples were able to produce clear amplification in PCR and sequencing reads, as well as effective allelic discrimination in real-time PCR TaqMan assay. The described in-House method proved to be suitable and economically viable for genomic DNA extraction from VTM samples for biobanking purposes. These results are extremely valuable for the study of the COVID-19 pandemic and other emergent infectious diseases, allowing host genetic studies to be performed in samples initially collected for diagnosis.
在 COVID-19 大流行期间,采集并分析了大量接种于病毒运输介质 (VTM) 的鼻咽分泌物样本,以检测 SARS-CoV-2 感染。除了病毒检测外,这些样本还可以作为宿主基因组材料的来源,为生物库和研究提供了极好的机会。本研究旨在描述一种简单的、内部开发的 DNA 提取方法,从 VTM 样本中获得高产量和高质量的基因组 DNA,用于宿主遗传分析,并通过比较其产量和对两种不同商业 DNA 提取试剂盒下游应用的适用性,评估其相对效率。在这项研究中,13 个 VTM 样本通过两种商业硅基试剂盒进行处理,并与内部开发的宿主 DNA 提取方案进行比较。另外 452 个样本通过内部方法进行处理。通过 Qubit 和分光光度法测量评估不同提取 DNA 样本的数量和质量。通过聚合酶链反应 (PCR) 扩增,随后进行扩增子测序和实时 PCR 等位基因鉴别,测试提取样本对下游应用的适用性。内部方法提供了更高的 DNA 产量中位数(0.81μg),与 PureLink 方法(0.14μg,<0.001)显著不同,但与 QIAamp 方法(0.47μg,=0.980)无显著差异。内部方法观察到 DNA 浓度和纯度以及成本方面的总体令人满意的结果,其样本能够在 PCR 和测序读长中产生清晰的扩增,以及在实时 PCR TaqMan 测定中有效进行等位基因鉴别。所描述的内部方法已被证明适用于从 VTM 样本中提取基因组 DNA 用于生物库目的,并且经济可行。这些结果对于 COVID-19 大流行和其他新发传染病的研究非常有价值,允许在最初为诊断而采集的样本中进行宿主遗传学研究。