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A comparison of the efficiency of five different commercial DNA extraction kits for extraction of DNA from faecal samples

机译:比较五种不同的商业DNA提取试剂盒从粪便样品中提取DNA的效率

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摘要

Differences in the composition of the gut microbiota have been associated with a range of diseases using culture-independent methods. Reliable extraction of nucleic acid is a key step in identifying the composition of the faecal microbiota. Five widely used commercial deoxyribonucleic acid (DNA) extraction kits (QIAsymphony® Virus/Bacteria Midi Kit (kit QS), ZR Fecal DNA MiniPrep™ (kit Z), QIAamp® DNA Stool Mini Kit (kit QA), Ultraclean® Fecal DNA Isolation Kit (kit U) and PowerSoil® DNA Isolation Kit (kit P)) were evaluated, using human faecal samples. Yield, purity and integrity of total genomic DNA were compared spectrophotometrically and using gel electrophoresis. Three bacteria, commonly found in human faeces were quantified using real time polymerase chain reaction (qPCR) and total bacterial diversity was studied using denaturing gradient gel electrophoresis (DGGE) as well as terminal restriction fragment length polymorphism (T-RFLP). The measurements of DNA yield and purity exhibited variations between the five kits tested in this study. Automated kit QS exhibited the best quality and highest quantity of DNA. All kits were shown to be reproducible with CV values ≤ 0.46 for DNA extraction. qPCR results showed that all kits were uniformly efficient for extracting DNA from the selected target bacteria. DGGE and T-RFLP produced the highest diversity scores for DNA extracted using kit Z (H′ = 2.30 and 1.27) and kit QS (H′ = 2.16 and 0.94), which also extracted the highest DNA yields compared to the other kits assessed.
机译:肠道菌群组成的差异已通过使用与培养无关的方法与多种疾病相关联。可靠地提取核酸是鉴定粪便微生物群组成的关键步骤。五种广泛使用的商业脱氧核糖核酸(DNA)提取试剂盒(QIAsymphony®病毒/细菌Midi试剂盒(QS试剂盒),ZR Fecal DNA MiniPrep™(Z试剂盒),QIAamp®DNA Stool迷你试剂盒(QA试剂盒),Ultraclean®粪便DNA分离试剂盒使用人类粪便样品对试剂盒(试剂盒U)和PowerSoil®DNA分离试剂盒(试剂盒P)进行了评估。用分光光度法和凝胶电泳比较总基因组DNA的产量,纯度和完整性。使用实时聚合酶链反应(qPCR)对人类粪便中常见的三种细菌进行定量,并使用变性梯度凝胶电泳(DGGE)和末端限制性片段长度多态性(T-RFLP)研究总细菌多样性。在本研究中测试的五种试剂盒之间,DNA产量和纯度的测量结果有所不同。自动化试剂盒QS表现出最好的质量和最高的DNA量。所有试剂盒均可用于DNA提取,CV值≤0.46可重现。 qPCR结果表明,所有试剂盒均能有效地从选定的靶细菌中提取DNA。 DGGE和T-RFLP对使用试剂盒Z(H'= 2.30和1.27)和试剂盒QS(H'= 2.16和0.94)提取的DNA产生了最高的多样性评分,与其他评估试剂盒相比,DNA产量也最高。

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