粪便微生物组并不代表整个肠道的微生物组

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Ji-Seon Ahn, Enkhchimeg Lkhagva, Sunjun Jung, Hyeon-Jin Kim, Hea-Jong Chung, Seong-Tshool Hong
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引用次数: 2

摘要

目前的肠道微生物组研究依赖于粪便微生物组,认为粪便微生物组代表了整个胃肠道的微生物组。然而,越来越多的人担心使用粪便作为研究肠道微生物组的代理。在这里,我们综合分析了遗传同质兄弟猪粪便和胃肠道14个不同位置的微生物组和代谢物的组成,以评估将粪便作为整个肠道微生物组的替代品的有效性。分别通过宏基因组测序和高性能LC-MS/MS对各肠内容物和粪便中构成肠道微生物组的肠道微生物组成及其代谢组成进行了深入研究。胃和小肠微生物组组成的波动从大肠到粪便趋于稳定,可分为3组。利用ACE(丰度覆盖估计器)丰富度和Shannon多样性测量的分类α-多样性表明,大肠微生物组的多样性远高于小肠和粪便。胃和小肠中高度独立的肠道微生物在大肠中蓬勃发展,并融合成一个紧密相连的网络群落。通过NMDS图、PCA和无监督分层聚类分析的β-多样性分析均显示,粪便中微生物组的多样性最低,而大肠中微生物组的多样性最高。肠道微生物组的组成随胃肠道的变化而变化,代谢组成也随胃肠道的变化而完全不同。粪便微生物组和代谢产物与全胃肠道的比较分析表明,粪便微生物组不足以代表全肠道微生物组。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fecal Microbiome Does Not Represent Whole Gut Microbiome
The current gut microbiome research relies on the fecal microbiome under the assumption that the fecal microbiome represents the microbiome of the entire gastrointestinal (GI) tract. However, there have been growing concerns about using feces as a proxy to study the gut microbiome. Here, we comprehensively analyzed the composition of microbiome and metabolites in the feces and at 14 different locations of GI tracts of genetically homogenous sibling pigs to evaluate the validity of using feces as a proxy to the whole gut microbiome. The composition of intestinal microbes constituting the gut microbiome at each intestinal content and feces and their metabolic compositions were thoroughly investigated through metagenome sequencing and an ultraperformance LC-MS/MS, respectively. The fluctuation in the composition of the microbiome in the stomach and the small intestine became stabilized from the large intestine to feces and was able to be categorized into 3 groups. The taxonomic α-diversities measured by ACE (abundance-based coverage estimator) richness and Shannon diversity indicated that the microbiome in the large intestine was much more diverse than those of the small intestine and feces. The highly independent intestinal microbes in the stomach and the small intestine became flourished in the large intestine and converged into a community with tightly connected networks. β-Diversity analyses by NMDS plots, PCA, and unsupervised hierarchical clustering all showed that the diversities of microbiome compositions were lowest in feces while highest in the large intestine. In accordance with fluctuation of the composition of gut microbiome along with the GI tract, the metabolic composition also completely differed in a location-specific manner along with the GI tract. Comparative analysis of the fecal microbiome and metabolites with those of the whole GI tract indicated that fecal microbiome is insufficient to represent the whole gut microbiome.
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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