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Optimizing protocols for extraction of bacteriophages prior to metagenomic analyses of phage communities in the human gut

机译:优化人体肠道噬菌体社区噬菌体分析前噬菌体提取的方案

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摘要

The human gut is densely populated with archaea, eukaryotes, bacteria, and their viruses, such as bacteriophages. Advances in high-throughput sequencing (HTS) as well as bioinformatics have opened new opportunities for characterizing the viral communities harbored in our gut. However, limited attention has been given to the efficiency of protocols dealing with extraction of phages from fecal communities prior to HTS and their impact on the metagenomic dataset. We describe two optimized methods for extraction of phages from fecal samples based on tangential-flow filtration (TFF) and polyethylene glycol precipitation (PEG) approaches using an adapted method from a published protocol as control (literature-adapted protocol (LIT)). To quantify phage recovery, samples were spiked with low numbers of c2, ?29, and T4 phages (representatives of the Siphoviridae, Podoviridae, and Myoviridae families, respectively) and their concentration (plaque-forming units) followed at every step during the extraction procedure. Compared with LIT, TFF and PEG had higher recovery of all spiked phages, yielding up to 16 times more phage particles (PPs) and up to 68 times more phage DNA per volume, increasing thus the chances of extracting low abundant phages. TFF- and PEG-derived metaviromes showed 10% increase in relative abundance of Caudovirales and unclassified phages infecting gut-associated bacteria (92% for TFF and PEG, 82.4% for LIT). Our methods obtained lower relative abundance of the Myoviridae family (16%) as compared to the reference protocol (22%). This decline, however, was not considered a true loss of Myoviridae phages but rather a greater level of extraction of Siphoviridae phages (TFF and PEG 32.5%, LIT 22.6%), which was achieved with the enhanced conditions of our procedures (e.g., reduced filter clogging). A high degree of phage diversity in samples extracted using TFF and PEG was documented by transmission electron microscopy. Two procedures (TFF and PEG) for extraction of bacteriophages from fecal samples were optimized using a set of spiked bacteriophages as process control. These protocols are highly efficient tools for extraction and purification of PPs prior to HTS in phage-metavirome studies. Our methods can be easily modified, being thus applicable and adjustable for in principle any solid environmental material in dissolution.
机译:人体肠道与古痤疮,真核生物,细菌及其病毒密集地填充,例如噬菌体。高通量测序(HTS)以及生物信息学的进步开辟了在我们的肠道中表征病毒社区的新机会。然而,已经有限地注意了处理HTS在HTS之前从粪便群中提取噬菌体的噬菌体的效率及其对肉质组织数据集的影响。我们描述了两种优化的方法,用于基于切向流动过滤(TFF)和聚乙二醇沉淀(PEG)方法使用从已公开的方案作为对照(文献适应的协议(LIT))来提取两种优化的方法。为了量化噬菌体恢复,掺入少量C2,β29和T4噬菌体(分别是Siphoviridae,Podoviridae的代表,Podoviridae和Myoviridae家族的代表)及其浓度(斑块形成单位),然后在提取过程中的每一步程序。与点燃相比,TFF和PEG对所有尖刺噬菌体的恢复较高,噬菌体颗粒(PPS)的噬菌体含量高达16倍,噬菌体DNA的噬菌体DNA多达68倍,因此提取低丰厚噬菌体的可能性。 TFF和PEG衍生的荟萃血小虫表现出10%的Caudovirales和未感染肠道相关细菌的噬菌体(TFF和PEG的噬菌体的噬菌体的增加10%,而LIT的82.4%)。与参考方案相比,我们的方法获得了较低的MyoViridae家族(<16%)的相对丰度(<16%)。然而,这种下降不被认为是Myoviridae噬菌体的真实损失,而是腹股沟病毒噬菌体(TFF和PEG> 32.5%,LIT 22.6%)的更大水平,这是通过我们程序的增强条件实现的(例如,减少过滤器堵塞)。通过透射电子显微镜记录使用TFF和PEG提取的样品中的高度噬菌体分集。用于从粪便样品中提取噬菌体的两种方法(TFF和PEG)使用一组尖刺的噬菌体作为过程对照进行了优化。这些方案是高效的工具,用于在噬菌体 - 美容研究中HTS之前的PPS提取和纯化。我们的方法可以很容易地修改,因此在原则上适用和可调节任何溶解中的任何固体环境材料。

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