Alterations in composition and diversity of the intestinal microbiota in patients with diarrhea-predominant irritable bowel syndrome.

IF 2.9 3区 医学 Q1 CLINICAL NEUROLOGY Neurogastroenterology and Motility Pub Date : 2012-06-01 Epub Date: 2012-02-20 DOI:10.1111/j.1365-2982.2012.01891.x
I M Carroll, T Ringel-Kulka, J P Siddle, Y Ringel
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引用次数: 363

Abstract

Background: The intestinal microbiota has been implicated in the pathophysiology of irritable bowel syndrome (IBS). Due to the variable resolutions of techniques used to characterize the intestinal microbiota, and the heterogeneity of IBS, the defined alterations of the IBS intestinal microbiota are inconsistent. We analyzed the composition of the intestinal microbiota in a defined subgroup of IBS patients (diarrhea-predominant IBS, D-IBS) using a technique that provides the deepest characterization available for complex microbial communities.

Methods: Fecal DNA was isolated from 23 D-IBS patients and 23 healthy controls (HC). Variable regions V1-V3 and V6 of the 16S rRNA gene were amplified from all samples. PCR products were sequenced using 454 high throughput sequencing. The composition, diversity and richness of microbial communities were determined and compared between D-IBS and HC using the quantitative insights into microbial ecology pipeline.

Key results: The contribution of bacterial groups to the composition of the intestinal microbiota differed between D-IBS and HC. D-IBS patients had significantly higher levels of Enterobacteriaceae (P = 0.03), and lower levels of Fecalibacterium genera (P = 0.04) compared to HC. β-Diversity values demonstrated significantly lower levels of UniFrac distances in HC compared to D-IBS patients. The richness of 16S rRNA sequences was significantly decreased in D-IBS patients (P < 0.04).

Conclusions & inferences: Our 16S rRNA sequence data demonstrates a community-level dysbiosis in D-IBS. The altered composition of the intestinal microbiota in D-IBS is associated with significant increases in detrimental and decreases in beneficial bacterial groups, and a reduction in microbial richness.

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腹泻型肠易激综合征患者肠道菌群组成和多样性的改变
背景:肠道微生物群与肠易激综合征(IBS)的病理生理有关。由于用于表征肠道微生物群的技术分辨率不同,以及IBS的异质性,IBS肠道微生物群变化的定义不一致。我们使用一种技术分析了IBS患者(腹泻型IBS, d型IBS)的肠道微生物群组成,该技术可提供复杂微生物群落的最深入表征。方法:分离23例D-IBS患者和23例健康对照(HC)的粪便DNA。从所有样本中扩增16S rRNA基因的可变区V1-V3和V6。PCR产物采用454高通量测序。利用微生物生态管道的定量洞察,对D-IBS和HC的微生物群落组成、多样性和丰富度进行了测定和比较。关键结果:肠道菌群对D-IBS和HC肠道菌群组成的贡献不同。与HC相比,D-IBS患者肠杆菌科水平显著升高(P = 0.03),粪杆菌属水平显著降低(P = 0.04)。β-多样性值显示HC患者的UniFrac距离水平明显低于D-IBS患者。D-IBS患者16S rRNA序列丰富度显著降低(P < 0.04)。结论和推论:我们的16S rRNA序列数据显示D-IBS存在社区水平的生态失调。D-IBS患者肠道菌群组成的改变与有害菌群的显著增加和有益菌群的显著减少以及微生物丰富度的减少有关。
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来源期刊
Neurogastroenterology and Motility
Neurogastroenterology and Motility 医学-临床神经学
CiteScore
7.80
自引率
8.60%
发文量
178
审稿时长
3-6 weeks
期刊介绍: Neurogastroenterology & Motility (NMO) is the official Journal of the European Society of Neurogastroenterology & Motility (ESNM) and the American Neurogastroenterology and Motility Society (ANMS). It is edited by James Galligan, Albert Bredenoord, and Stephen Vanner. The editorial and peer review process is independent of the societies affiliated to the journal and publisher: Neither the ANMS, the ESNM or the Publisher have editorial decision-making power. Whenever these are relevant to the content being considered or published, the editors, journal management committee and editorial board declare their interests and affiliations.
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