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Evaluating DNA Extraction Methods for Community Profiling of Pig Hindgut Microbial Community

机译:猪后肠微生物群落群落分析的DNA提取方法评价

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摘要

Recovery of high quality PCR-amplifiable DNA has been the general minimal requirement for DNA extraction methods for bulk molecular analysis. However, modern high through-put community profiling technologies are more sensitive to representativeness and reproducibility of DNA extraction method. Here, we assess the impact of three DNA extraction methods (with different levels of extraction harshness) for assessing hindgut microbiomes from pigs fed with different diets (with different physical properties). DNA extraction from each sample was performed in three technical replicates for each extraction method and sequenced by 16S rRNA amplicon sequencing. Host was the primary driver of molecular sequencing outcomes, particularly on samples analysed by wheat based diets, but higher variability, with one failed extraction occurred on samples from a barley fed pig. Based on these results, an effective method will enable reproducible and quality outcomes on a range of samples, whereas an ineffective method will fail to generate extract, but host (rather than extraction method) remains the primary factor.
机译:高质量PCR可扩增DNA的回收一直是用于大分子分析的DNA提取方法的一般最低要求。但是,现代高通量社区分析技术对DNA提取方法的代表性和可重复性更为敏感。在这里,我们评估了三种DNA提取方法(不同程度的提取刺激性)对评估饲喂不同日粮(具有不同物理特性)的猪后肠微生物群的影响。从每种样品的DNA提取中,对每种提取方法进行三次技术重复,并通过16S rRNA扩增子测序进行测序。寄主是分子测序结果的主要驱动力,尤其是在以小麦为基础的日粮分析的样品上,但变异性更高,大麦饲喂猪的样品提取失败。基于这些结果,一种有效的方法将在一系列样品上实现可重现和高质量的结果,而无效的方法将无法生成提取物,但宿主(而非提取方法)仍然是主要因素。

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