Functional profiling of the gut microbiome in disease-associated inflammation

被引:50
作者
Boernigen, Daniela [1 ,2 ]
Morgan, Xochitl C. [1 ,2 ]
Franzosa, Eric A. [1 ,2 ]
Ren, Boyu [1 ]
Xavier, Ramnik J. [2 ,3 ]
Garrett, Wendy S. [2 ,4 ,5 ,6 ]
Huttenhower, Curtis [1 ,2 ]
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[2] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[3] Massachusetts Gen Hosp, Gastrointestinal Unit, Boston, MA 02115 USA
[4] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
[6] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
来源
GENOME MEDICINE | 2013年 / 5卷
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
VITAMIN-D; MULTIPLE-SCLEROSIS; BOWEL-DISEASE; ANTIBIOTIC-RESISTANCE; RHEUMATOID-ARTHRITIS; ATOPIC-DERMATITIS; WIDE ASSOCIATION; RECEPTOR; ASTHMA; AUTOIMMUNE;
D O I
10.1186/gm469
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The microbial residents of the human gut are a major factor in the development and lifelong maintenance of health. The gut microbiota differs to a large degree from person to person and has an important influence on health and disease due to its interaction with the human immune system. Its overall composition and microbial ecology have been implicated in many autoimmune diseases, and it represents a particularly important area for translational research as a new target for diagnostics and therapeutics in complex inflammatory conditions. Determining the biomolecular mechanisms by which altered microbial communities contribute to human disease will be an important outcome of current functional studies of the human microbiome. In this review, we discuss functional profiling of the human microbiome using metagenomic and metatranscriptomic approaches, focusing on the implications for inflammatory conditions such as inflammatory bowel disease and rheumatoid arthritis. Common themes in gut microbial ecology have emerged among these diverse diseases, but they have not yet been linked to targetable mechanisms such as microbial gene and genome composition, pathway and transcript activity, and metabolism. Combining these microbial activities with host gene, transcript and metabolic information will be necessary to understand how and why these complex interacting systems are altered in disease-associated inflammation.
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页数:13
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