Functional profiling of the gut microbiome in disease-associated inflammation

Standard

Functional profiling of the gut microbiome in disease-associated inflammation. / Börnigen, Daniela; Morgan, Xochitl C; Franzosa, Eric A; Ren, Boyu; Xavier, Ramnik J; Garrett, Wendy S; Huttenhower, Curtis.

In: GENOME MED, Vol. 5, No. 7, 2013, p. 65.

Research output: SCORING: Contribution to journalSCORING: Review articleResearch

Harvard

Börnigen, D, Morgan, XC, Franzosa, EA, Ren, B, Xavier, RJ, Garrett, WS & Huttenhower, C 2013, 'Functional profiling of the gut microbiome in disease-associated inflammation', GENOME MED, vol. 5, no. 7, pp. 65. https://doi.org/10.1186/gm469

APA

Börnigen, D., Morgan, X. C., Franzosa, E. A., Ren, B., Xavier, R. J., Garrett, W. S., & Huttenhower, C. (2013). Functional profiling of the gut microbiome in disease-associated inflammation. GENOME MED, 5(7), 65. https://doi.org/10.1186/gm469

Vancouver

Börnigen D, Morgan XC, Franzosa EA, Ren B, Xavier RJ, Garrett WS et al. Functional profiling of the gut microbiome in disease-associated inflammation. GENOME MED. 2013;5(7):65. https://doi.org/10.1186/gm469

Bibtex

@article{43cd0b19ef2f4185ac4522fc74e1cc67,
title = "Functional profiling of the gut microbiome in disease-associated inflammation",
abstract = "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.",
keywords = "Journal Article, Review",
author = "Daniela B{\"o}rnigen and Morgan, {Xochitl C} and Franzosa, {Eric A} and Boyu Ren and Xavier, {Ramnik J} and Garrett, {Wendy S} and Curtis Huttenhower",
year = "2013",
doi = "10.1186/gm469",
language = "English",
volume = "5",
pages = "65",
journal = "GENOME MED",
issn = "1756-994X",
publisher = "BioMed Central Ltd.",
number = "7",

}

RIS

TY - JOUR

T1 - Functional profiling of the gut microbiome in disease-associated inflammation

AU - Börnigen, Daniela

AU - Morgan, Xochitl C

AU - Franzosa, Eric A

AU - Ren, Boyu

AU - Xavier, Ramnik J

AU - Garrett, Wendy S

AU - Huttenhower, Curtis

PY - 2013

Y1 - 2013

N2 - 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.

AB - 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.

KW - Journal Article

KW - Review

U2 - 10.1186/gm469

DO - 10.1186/gm469

M3 - SCORING: Review article

C2 - 23906180

VL - 5

SP - 65

JO - GENOME MED

JF - GENOME MED

SN - 1756-994X

IS - 7

ER -