Farraj Suha A, El-Kafrawy Shreif A, Kumosani Taha A, Yousef Jehad M, Azhar Esam I
Biochemistry Department, Faculty of Sciences, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Special Infectious Agents Unit, King Fahd Medical Research Center, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Microorganisms. 2020 Jul 27;8(8):1128. doi: 10.3390/microorganisms8081128.
(1) Background: Clinical metagenomics is a promising approach that helps to identify etiological agents in cases of unknown infections. For the efficient detection of an unknown pathogen, the extraction method must be carefully selected for the maximum recovery of nucleic acid from different microorganisms. The aim of this study was to evaluate different extraction methods that have the ability to isolate nucleic acids from different types of pathogens with good quality and quantity for efficient use in clinical metagenomic identification. (2) Methods: A mock sample spiked with five different pathogens was used for the comparative evaluation of different commercial extraction kits. Extracted samples were subjected to library preparation and run on MiSeq. The selected extraction method based on the outcome of the comparative evaluation was used subsequently for the nucleic acid isolation of all infectious agents in clinical respiratory samples with multiple infections. (3) Results: The protocol using the PowerViral Environmental RNA-DNA Isolation Kit with a 5-min bead beating step achieved the best results with a low starting volume. The analysis of the tested clinical specimens showed the ability to successfully identify different types of pathogens. (4) Conclusions: The optimized extraction protocol in this study is recommended for clinical metagenomics application in specimens with multiple infections from different taxa.
(1)背景:临床宏基因组学是一种很有前景的方法,有助于在不明感染病例中识别病原体。为了有效检测未知病原体,必须谨慎选择提取方法,以便从不同微生物中最大程度地回收核酸。本研究的目的是评估不同的提取方法,这些方法能够从不同类型的病原体中分离出高质量和高数量的核酸,以便在临床宏基因组鉴定中有效使用。(2)方法:使用添加了五种不同病原体的模拟样本对不同的商业提取试剂盒进行比较评估。将提取的样本进行文库制备并在MiSeq上运行。随后,根据比较评估结果选择的提取方法用于对多重感染的临床呼吸道样本中的所有感染因子进行核酸分离。(3)结果:使用PowerViral Environmental RNA-DNA Isolation试剂盒并进行5分钟珠磨步骤的方案在起始体积较低的情况下取得了最佳结果。对测试的临床标本进行分析表明,该方法能够成功识别不同类型的病原体。(4)结论:本研究中优化的提取方案推荐用于不同分类群多重感染标本的临床宏基因组学应用。