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Integrated fecal microbiome-metabolome signatures reflect stress and serotonin metabolism in irritable bowel syndrome.肠道微生物组-代谢组综合特征反映了肠易激综合征中的应激和 5-羟色胺代谢。
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本文引用的文献

1
Diet rapidly and reproducibly alters the human gut microbiome.饮食可快速且可重复地改变人类肠道微生物组。
Nature. 2014 Jan 23;505(7484):559-63. doi: 10.1038/nature12820. Epub 2013 Dec 11.
2
Do gut microbial communities differ in pediatric IBS and health?肠道微生物群落是否存在于小儿 IBS 与健康的差异?
Gut Microbes. 2013 Jul-Aug;4(4):347-52. doi: 10.4161/gmic.24827. Epub 2013 May 2.
3
Alterations in the colonic microbiota in response to osmotic diarrhea.肠道微生物群落对渗透性腹泻的反应变化。
PLoS One. 2013;8(2):e55817. doi: 10.1371/journal.pone.0055817. Epub 2013 Feb 8.
4
Quantitative profiling of gut microbiota of children with diarrhea-predominant irritable bowel syndrome.腹泻型肠易激综合征患儿肠道微生物群的定量分析。
Am J Gastroenterol. 2012 Nov;107(11):1740-51. doi: 10.1038/ajg.2012.287.
5
A global perspective on irritable bowel syndrome: a consensus statement of the World Gastroenterology Organisation Summit Task Force on irritable bowel syndrome.从全球视角看肠易激综合征:世界胃肠病组织峰会肠易激综合征工作组的共识声明。
J Clin Gastroenterol. 2012 May-Jun;46(5):356-66. doi: 10.1097/MCG.0b013e318247157c.
6
Increase in fecal primary bile acids and dysbiosis in patients with diarrhea-predominant irritable bowel syndrome.腹泻型肠易激综合征患者粪便初级胆汁酸增加和肠道菌群失调。
Neurogastroenterol Motil. 2012 Jun;24(6):513-20, e246-7. doi: 10.1111/j.1365-2982.2012.01893.x. Epub 2012 Feb 22.
7
Recognition and degradation of plant cell wall polysaccharides by two human gut symbionts.人体肠道共生菌对植物细胞壁多糖的识别与降解。
PLoS Biol. 2011 Dec;9(12):e1001221. doi: 10.1371/journal.pbio.1001221. Epub 2011 Dec 20.
8
Characterization of Phascolarctobacterium succinatutens sp. nov., an asaccharolytic, succinate-utilizing bacterium isolated from human feces.鉴定一株来自人粪便的非淀粉水解、利用琥珀酸的细菌 Phascolarctobacterium succinatutens sp. nov.
Appl Environ Microbiol. 2012 Jan;78(2):511-8. doi: 10.1128/AEM.06035-11. Epub 2011 Nov 11.
9
Bacterial proteases in IBD and IBS.炎症性肠病和肠易激综合征中的细菌蛋白酶。
Gut. 2012 Nov;61(11):1610-8. doi: 10.1136/gutjnl-2011-300775. Epub 2011 Sep 7.
10
Functional analyses of multiple lichenin-degrading enzymes from the rumen bacterium Ruminococcus albus 8.从瘤胃菌 Ruminococcus albus 8 中多种几丁质降解酶的功能分析。
Appl Environ Microbiol. 2011 Nov;77(21):7541-50. doi: 10.1128/AEM.06088-11. Epub 2011 Sep 2.

健康状态和肠易激综合征患者的人体肠道微生物-代谢物关联网络存在差异。

The networks of human gut microbe-metabolite associations are different between health and irritable bowel syndrome.

作者信息

Shankar Vijay, Homer Daniel, Rigsbee Laura, Khamis Harry J, Michail Sonia, Raymer Michael, Reo Nicholas V, Paliy Oleg

机构信息

Department of Biochemistry and Molecular Biology, Wright State University, Dayton, OH, USA.

Department of Mathematics and Statistics, Wright State University, Dayton, OH, USA.

出版信息

ISME J. 2015 Aug;9(8):1899-903. doi: 10.1038/ismej.2014.258. Epub 2015 Jan 30.

DOI:10.1038/ismej.2014.258
PMID:25635640
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4511929/
Abstract

The goal of this study was to determine if fecal metabolite and microbiota profiles can serve as biomarkers of human intestinal diseases, and to uncover possible gut microbe-metabolite associations. We employed proton nuclear magnetic resonance to measure fecal metabolites of healthy children and those diagnosed with diarrhea-predominant irritable bowel syndrome (IBS-D). Metabolite levels were associated with fecal microbial abundances. Using several ordination techniques, healthy and irritable bowel syndrome (IBS) samples could be distinguished based on the metabolite profiles of fecal samples, and such partitioning was congruent with the microbiota-based sample separation. Measurements of individual metabolites indicated that the intestinal environment in IBS-D was characterized by increased proteolysis, incomplete anaerobic fermentation and possible change in methane production. By correlating metabolite levels with abundances of microbial genera, a number of statistically significant metabolite-genus associations were detected in stools of healthy children. No such associations were evident for IBS children. This finding complemented the previously observed reduction in the number of microbe-microbe associations in the distal gut of the same cohort of IBS-D children.

摘要

本研究的目的是确定粪便代谢物和微生物群谱是否可作为人类肠道疾病的生物标志物,并揭示可能的肠道微生物-代谢物关联。我们采用质子核磁共振技术测量健康儿童以及被诊断为腹泻型肠易激综合征(IBS-D)儿童的粪便代谢物。代谢物水平与粪便微生物丰度相关。使用几种排序技术,基于粪便样本的代谢物谱可以区分健康和肠易激综合征(IBS)样本,并且这种划分与基于微生物群的样本分离一致。个体代谢物的测量表明,IBS-D中的肠道环境具有蛋白水解增加、不完全厌氧发酵以及甲烷产生可能变化的特征。通过将代谢物水平与微生物属的丰度相关联,在健康儿童的粪便中检测到许多具有统计学意义的代谢物-属关联。IBS儿童中没有明显的此类关联。这一发现补充了先前在同一队列的IBS-D儿童远端肠道中观察到的微生物-微生物关联数量减少的情况。