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肠道微生物失调与炎症性肠病及其治疗。

Dysfunction of the intestinal microbiome in inflammatory bowel disease and treatment.

机构信息

Department of Biostatistics, Harvard School of Public Health, Boston, MA 02115, USA.

出版信息

Genome Biol. 2012 Apr 16;13(9):R79. doi: 10.1186/gb-2012-13-9-r79.

Abstract

BACKGROUND

The inflammatory bowel diseases (IBD) Crohn's disease and ulcerative colitis result from alterations in intestinal microbes and the immune system. However, the precise dysfunctions of microbial metabolism in the gastrointestinal microbiome during IBD remain unclear. We analyzed the microbiota of intestinal biopsies and stool samples from 231 IBD and healthy subjects by 16S gene pyrosequencing and followed up a subset using shotgun metagenomics. Gene and pathway composition were assessed, based on 16S data from phylogenetically-related reference genomes, and associated using sparse multivariate linear modeling with medications, environmental factors, and IBD status.

RESULTS

Firmicutes and Enterobacteriaceae abundances were associated with disease status as expected, but also with treatment and subject characteristics. Microbial function, though, was more consistently perturbed than composition, with 12% of analyzed pathways changed compared with 2% of genera. We identified major shifts in oxidative stress pathways, as well as decreased carbohydrate metabolism and amino acid biosynthesis in favor of nutrient transport and uptake. The microbiome of ileal Crohn's disease was notable for increases in virulence and secretion pathways.

CONCLUSIONS

This inferred functional metagenomic information provides the first insights into community-wide microbial processes and pathways that underpin IBD pathogenesis.

摘要

背景

炎症性肠病(IBD)包括克罗恩病和溃疡性结肠炎,是由肠道微生物和免疫系统的改变引起的。然而,IBD 患者胃肠道微生物组中微生物代谢的确切功能障碍仍不清楚。我们通过 16S 基因焦磷酸测序分析了 231 例 IBD 患者和健康受试者的肠道活检和粪便样本中的微生物群,并使用 shotgun 宏基因组学对其中一部分进行了随访。根据与系统发育相关的参考基因组的 16S 数据评估基因和途径组成,并使用稀疏多元线性模型将其与药物、环境因素和 IBD 状态相关联。

结果

厚壁菌门和肠杆菌科的丰度与疾病状态相关,这是预期的,但也与治疗和受试者特征相关。然而,微生物功能比组成更一致地受到干扰,与 2%的属相比,有 12%的分析途径发生了变化。我们确定了氧化应激途径的主要变化,以及碳水化合物代谢和氨基酸生物合成的减少,有利于营养物质的运输和摄取。回肠克罗恩病的微生物组以毒力和分泌途径的增加为特征。

结论

这种推断的功能宏基因组信息首次提供了对支持 IBD 发病机制的全社区微生物过程和途径的深入了解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21f2/3506950/8778a926e769/gb-2012-13-9-r79-1.jpg

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