资源有限条件下新生儿肠道菌群DNA提取方案的比较评价

Chinenye Akpulu , Aditya Kumar Lankapalli , Rida Toufiq , Kate Cook , Edward AR Portal , Rashida Yakubu Khalid , Aisha Mukkadas , Safiya Gambo , Aliyu Aminu , Kenneth Iregbu , Kathryn Thomson , Timothy Walsh , Kirsty Sands
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摘要

准确和可重复的肠道微生物组分析在很大程度上取决于DNA提取方法,特别是在低生物量样本中,如新生儿粪便。在本研究中,我们评估了三种市售DNA提取试剂盒的性能;QIAamp快速粪便DNA迷你、DNeasy PowerSoil Pro和ZymoBIOMICS DNA迷你对尼日利亚卡诺一家资源有限的医院收集的新生儿粪便样本进行检测。样品在不同条件下(温度和防腐剂)保存,DNA提取和测序使用牛津纳米孔技术。DNA产率在不同的提取试剂盒和储存条件下差异很大。PowerSoil和ZymoBIOMICS基于串流的试剂盒的性能始终优于QIAamp快速DNA粪便迷你试剂盒,后者在所有条件下的产量都可以忽略不计。当样品在新鲜且不含防腐剂的情况下加工时,两种打珠试剂盒的DNA浓度最高,而仅在储存一天后产量就急剧下降。尽管PowerSoil和ZymoBIOMICS在所有时间点上的总体DNA产量相似,但PowerSoil提取物产生了更长的测序读数和更高质量的组装。具体来说,在第0天和第6周,powersoil衍生的文库产生的读取水平N50值高于ZymoBIOMICS。虽然这些差异在统计学上不显著,但在第0天的中等效应大小(秩双列相关= 0.60)表明基因组组装连续性的潜在优势。此外,PowerSoil具有更短的处理时间,增强了其在资源有限的环境下对长读元基因组学工作流程的适用性。我们的结论是,使用基于头部殴打的提取试剂盒进行当天处理可以提高产量,并可能减少新生儿肠道微生物组研究中的偏差。这些发现尤其适用于低资源环境,设备限制和延迟的样本处理会影响数据质量和研究的可扩展性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative evaluation of DNA extraction protocols for neonatal gut microbiota profiling in a resource-limited setting
Accurate and reproducible gut microbiome profiling depends heavily on the DNA extraction method, particularly in low-biomass samples such as neonatal stool. In this study, we evaluated the performance of three commercially available DNA extraction kits; QIAamp Fast DNA Stool Mini, DNeasy PowerSoil Pro, and ZymoBIOMICS DNA Miniprep on neonatal stool samples collected in a resource-limited hospital in Kano, Nigeria. Samples were stored under various conditions (temperature and preservatives), and DNA was extracted and sequenced using Oxford Nanopore Technologies. DNA yield differed substantially across extraction kits and storage conditions. The bead-beating-based kits: PowerSoil and ZymoBIOMICS, consistently outperformed the QIAamp Fast DNA Stool Mini kit, which produced negligible yields across all conditions. Both bead-beating kits achieved the highest DNA concentrations when samples were processed fresh and without preservatives, while yields declined sharply after just one day of storage. Although overall DNA yields were similar between PowerSoil and ZymoBIOMICS at all time points, PowerSoil extracts produced longer sequencing reads and higher-quality assemblies. Specifically, PowerSoil-derived libraries generated higher read-level N50 values than those from ZymoBIOMICS at both Day 0 and Week 6. While these differences were not statistically significant, a moderate effect size at Day 0 (rank-biserial correlation = 0.60) suggests a potential advantage in genome assembly continuity. Additionally, PowerSoil had a shorter processing time, enhancing its suitability for long-read metagenomics workflows in resource-limited settings. We conclude that same-day processing using bead-beating-based extraction kits improves yield and may reduce bias in neonatal gut microbiome studies. These findings are especially relevant for low-resource settings, where equipment limitations and delayed sample processing can impact data quality and study scalability.
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