真核生物DNA耗竭的皂素处理通过减少宏基因组学分析中革兰氏阴性菌的丰度来改变微生物DNA谱

Giulia Longhi, Chiara Argentini, Federico Fontana, Chiara Tarracchini, Leonardo Mancabelli, Gabriele Andrea Lugli, Giulia Alessandri, Edith Lahner, Giulia Pivetta, Francesca Turroni, Marco Ventura, Christian Milani
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引用次数: 0

摘要

背景:微生物组测序技术的最新进展为微生物组对人类健康的作用提供了新的见解,具有潜在的诊断意义。然而,这些进展往往受到大量人类DNA干扰细菌含量分析的阻碍。如今,大量的科学文献集中在真核生物DNA去除方法上,这种方法在微生物组研究中成功地去除宿主DNA,即使对细菌DNA影响的精确评估经常缺失。方法:本文研究了一种基于皂苷的DNA分离方案,该方案通常适用于不同的生物基质,以消耗释放的宿主DNA。结果:获得的细菌DNA被用来评估细菌和人类DNA的相对丰度,结果表明,2.5% wt/vol的皂苷可以消耗大部分宿主DNA,有利于细菌DNA的富集。然而,霰弹枪宏基因组测序显示DNA样本的微生物谱不准确,突出了革兰氏阳性DNA的错误增加。即使0.0125%重量/体积的皂苷的应用也会通过消耗革兰氏阴性细菌来改变细菌的特征,导致革兰氏阳性细菌DNA的总体增加。结论:基于皂苷的方案的应用极大地改变了人类相关生物标本微生物组成的检测方法。在这种情况下,我们发现皂苷不仅针对宿主细胞,也针对特定的细菌细胞,从而诱导革兰氏阴性细菌DNA谱的急剧减少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Saponin treatment for eukaryotic DNA depletion alters the microbial DNA profiles by reducing the abundance of Gram-negative bacteria in metagenomics analyses
Background: Recent advances in microbiome sequencing techniques have provided new insights into the role of the microbiome on human health with potential diagnostic implications. However, these developments are often hampered by the presence of a large amount of human DNA interfering with the analysis of the bacterial content. Nowadays, extensive scientific literature focuses on eukaryotic DNA depletion methods, which successfully remove host DNA in microbiome studies, even if a precise assessment of the impact on bacterial DNA is often missing. Methods: Here, we have investigated a saponin-based DNA isolation protocol commonly applied to different biological matrices to deplete the released host DNA. Results: The bacterial DNA obtained was used to assess the relative abundance of bacterial and human DNA, revealing that the inclusion of 2.5% wt/vol saponin allowed the depletion of most of the host’s DNA in favor of bacterial DNA enrichment. However, shotgun metagenomic sequencing showed inaccurate microbial profiles of the DNA samples, highlighting an erroneous increase in Gram-positive DNA. Even the application of 0.0125% wt/vol saponin altered the bacterial profile by depleting Gram-negative bacteria, resulting in an overall increase of Gram-positive bacterial DNA. Conclusion: The application of the saponin-based protocol drastically changes the detection of the microbial composition of human-related biological specimens. In this context, we revealed that saponin targets not only host cells but also specific bacterial cells, thus inducing a drastic reduction in the profiling of Gram-negative bacterial DNA.
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