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The impact of different DNA extraction kits and laboratories upon the assessment of human gut microbiota composition by 16S rRNA gene sequencing

机译:不同DNa提取试剂盒和实验室对16s rRNa基因测序评估人肠道微生物群组成的影响

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摘要

Introduction: Determining bacterial community structure in fecal samples through DNA sequencing is an important facet of intestinal health research. The impact of different commercially available DNA extraction kits upon bacterial community structures has received relatively little attention. The aim of this study was to analyze bacterial communities in volunteer and inflammatory bowel disease (IBD) patient fecal samples extracted using widely used DNA extraction kits in established gastrointestinal research laboratories. Methods: Fecal samples from two healthy volunteers (H3 and H4) and two relapsing IBD patients (I1 and I2) were investigated. DNA extraction was undertaken using MoBio Powersoil and MP Biomedicals FastDNA SPIN Kit for Soil DNA extraction kits. PCR amplification for pyrosequencing of bacterial 16S rRNA genes was performed in both laboratories on all samples. Hierarchical clustering of sequencing data was done using the Yue and Clayton similarity coefficient. Results: DNA extracted using the FastDNA kit and the MoBio kit gave median DNA concentrations of 475 (interquartile range 228-561) and 22 (IQR 9-36) ng/μL respectively (p
机译:简介:通过DNA测序确定粪便样品中的细菌群落结构是肠道健康研究的重要方面。不同的市售DNA提取试剂盒对细菌群落结构的影响受到的关注相对较少。这项研究的目的是分析已建立的胃肠道研究实验室中使用广泛使用的DNA提取试剂盒提取的志愿者和炎症性肠病(IBD)患者粪便样品中的细菌群落。方法:调查了两名健康志愿者(H3和H4)和两名复发性IBD患者(I1和I2)的粪便样本。使用MoBio Powersoil和MP Biomedicals FastDNA SPIN Kit进行土壤DNA提取试剂盒进行DNA提取。在两个实验室的所有样品上均进行了PCR扩增,用于细菌16S rRNA基因的焦磷酸测序。使用Yue和Clayton相似系数对测序数据进行分层聚类。结果:使用FastDNA试剂盒和MoBio试剂盒提取的DNA的中位DNA浓度分别为475(四分位间距228-561)和22(IQR 9-36)ng /μL(p

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