Peng Zonghui, Zhu Xiaolong, Wang Zhijiao, Yan Xianting, Wang Guangbiao, Tang Meifang, Jiang Awei, Kristiansen Karsten
BGI Americas Corporation, Cambridge, MA, USA.
Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Bioinform Biol Insights. 2020 Jun 3;14:1177932220915459. doi: 10.1177/1177932220915459. eCollection 2020.
Human fecal specimens, serve as important materials, are widely used in the field of microbiome research, in which inconsistent results have been a pressing issue. The possible attribute factors have been proposed including the specimen status after preservation, extracted DNA quality, library preparation protocol, and sample DNA input. In this study, quality comparisons for shotgun metagenomics sequencing were performed between 2 DNA extraction methods for fresh and freeze-thaw samples, 2 library preparation protocols, and various sample inputs. The results indicate that Mag-Bind® Universal Metagenomics Kit (OM) outperformed DNeasy PowerSoil Kit (QP) with a higher DNA quantity. Controlling on library preparation protocol, OM detected on-average more genes than QP. For library construction comparison by controlling on the same DNA sample, KAPA Hyper Prep Kit (KH) outperformed the TruePrep DNA Library Prep Kit V2 (TP) with the higher number of detected genes number and Shannon index. No significant differences were found in taxonomy between 2 library preparation protocols using the fresh, freeze-thaw and mock community samples. No significant difference was observed between 250 and 50 ng DNA inputs for library preparation on both fresh and freeze-thaw samples. Through the preliminary study, a combined protocol is recommended for performing metagenomics studies, by using OM method plus KH protocol as well as suitable DNA quantity on either fresh or freeze-thaw samples. Our findings provide clues for potential variations from various DNA extraction methods, library protocols, and sample DNA inputs, which are critical for consistent and comprehensive profiling of the human gut microbiome.
人类粪便样本作为重要材料,在微生物组研究领域被广泛使用,然而结果不一致一直是个紧迫问题。已提出的可能影响因素包括保存后的样本状态、提取的DNA质量、文库构建方案和样本DNA投入量。在本研究中,对新鲜样本和冻融样本的两种DNA提取方法、两种文库构建方案以及不同样本投入量进行了鸟枪法宏基因组测序的质量比较。结果表明,Mag-Bind®通用宏基因组试剂盒(OM)在DNA产量上优于DNeasy PowerSoil试剂盒(QP)。在文库构建方案相同的情况下,OM平均检测到的基因比QP更多。在相同DNA样本的文库构建比较中,KAPA Hyper Prep试剂盒(KH)在检测到的基因数量和香农指数方面优于TruePrep DNA文库制备试剂盒V2(TP)。使用新鲜样本、冻融样本和模拟群落样本时,两种文库构建方案在分类学上没有显著差异。在新鲜样本和冻融样本的文库构建中,250 ng和50 ng的DNA投入量之间没有观察到显著差异。通过初步研究,推荐一种组合方案用于进行宏基因组学研究,即使用OM方法加KH方案以及在新鲜样本或冻融样本上使用合适的DNA量。我们的研究结果为不同DNA提取方法、文库方案和样本DNA投入量可能产生的差异提供了线索,这些差异对于人类肠道微生物组的一致和全面分析至关重要。