Functional amplification and preservation of human gut microbiota.

Microbial Ecology in Health and Disease Pub Date : 2017-04-10 eCollection Date: 2017-01-01 DOI:10.1080/16512235.2017.1308070
Nadia Gaci, Prem Prashant Chaudhary, William Tottey, Monique Alric, Jean-François Brugère
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引用次数: 12

Abstract

Background: The availability of fresh stool samples is a prerequisite in most gut microbiota functional studies. Objective: Strategies for amplification and long-term gut microbiota preservation from fecal samples would favor sample sharing, help comparisons and reproducibility over time and between laboratories, and improve the safety and ethical issues surrounding fecal microbiota transplantations. Design: Taking advantage of in vitro gut-simulating systems, we amplified the microbial repertoire of a fresh fecal sample and assessed the viability and resuscitation of microbes after preservation with some common intracellular and extracellular acting cryoprotective agents (CPAs), alone and in different combinations. Preservation efficiencies were determined after 3 and 6 months and compared with the fresh initial microbiota diversity and metabolic activity, using the chemostat-based Environmental Control System for Intestinal Microbiota (ECSIM) in vitro model of the gut environment. Microbial populations were tested for fermentation gas, short-chain fatty acids, and composition of amplified and resuscitated microbiota, encompassing methanogenic archaea. Results: Amplification of the microbial repertoire from a fresh fecal sample was achieved with high fidelity. Dimethylsulfoxide, alone or mixed with other CPAs, showed the best efficiency for functional preservation, and the duration of preservation had little effect. Conclusions: The amplification and resuscitation of fecal microbiota can be performed using specialized in vitro gut models. Correct amplification of the initial microbes should ease the sharing of clinical samples and improve the safety of fecal microbiota transplantation. Abbreviations: CDI, Clostridium difficile infection; CPA, cryoprotective agent; D, DMSO, dimethylsulfoxide; FMT, fecal microbiota transplantation; G, glycerol; IBD, inflammatory bowel disease; P, PEG-4000, polyethylene glycol 4000 g.mol-1; SCFA, short-chain fatty acid; SNR, signal-to-noise ratio.

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人类肠道菌群的功能扩增与保存。
背景:新鲜粪便样本的可用性是大多数肠道微生物群功能研究的先决条件。目的:从粪便样本中扩增和长期保存肠道微生物群的策略将有利于样本共享,有助于不同时间和实验室之间的比较和可重复性,并改善粪便微生物群移植的安全性和伦理问题。设计:利用体外肠道模拟系统,我们扩增了新鲜粪便样本的微生物库,并评估了一些常见的细胞内和细胞外作用冷冻保护剂(CPAs)单独和不同组合保存后微生物的活力和复苏情况。采用基于ECSIM的体外肠道环境模型,测定3个月和6个月后的保存效率,并与新鲜初始微生物群多样性和代谢活性进行比较。微生物种群检测发酵气体,短链脂肪酸,以及扩增和复苏微生物群的组成,包括产甲烷的古细菌。结果:从新鲜粪便样本中扩增的微生物库具有高保真度。二甲亚砜单独使用或与其他cpa混合使用对功能保存效果最好,保存时间对功能保存效果影响不大。结论:利用专门的体外肠道模型可以进行粪便微生物群的扩增和复苏。正确扩增初始微生物,有利于临床样品的共享,提高粪便微生物群移植的安全性。缩写词:CDI,艰难梭菌感染;CPA,冷冻保护剂;D, DMSO,二甲基亚砜;FMT,粪便微生物群移植;G,甘油;IBD,炎症性肠病;P, PEG-4000,聚乙二醇4000 g.mol-1;短链脂肪酸;信噪比,信噪比。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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