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Metagenomic analysis of bile salt biotransformation in the human gut microbiome

Das, Promi, 1990 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Marcisauskas, Simonas, 1988 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Ji, Boyang, 1983 (author)
Chalmers tekniska högskola,Chalmers University of Technology
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Nielsen, Jens B, 1962 (author)
Chalmers tekniska högskola,Chalmers University of Technology,Danmarks Tekniske Universitet,Technical University of Denmark
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 (creator_code:org_t)
2019-06-25
2019
English.
In: BMC Genomics. - : Springer Science and Business Media LLC. - 1471-2164. ; 20:1
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background: In the biochemical milieu of human colon, bile acids act as signaling mediators between the host and its gut microbiota. Biotransformation of primary to secondary bile acids have been known to be involved in the immune regulation of human physiology. Several 16S amplicon-based studies with inflammatory bowel disease (IBD) subjects were found to have an association with the level of fecal bile acids. However, a detailed investigation of all the bile salt biotransformation genes in the gut microbiome of healthy and IBD subjects has not been performed. Results: Here, we report a comprehensive analysis of the bile salt biotransformation genes and their distribution at the phyla level. Based on the analysis of shotgun metagenomes, we found that the IBD subjects harbored a significantly lower abundance of these genes compared to the healthy controls. Majority of these genes originated from Firmicutes in comparison to other phyla. From metabolomics data, we found that the IBD subjects were measured with a significantly low level of secondary bile acids and high levels of primary bile acids compared to that of the healthy controls. Conclusions: Our bioinformatics-driven approach of identifying bile salt biotransformation genes predicts the bile salt biotransformation potential in the gut microbiota of IBD subjects. The functional level of dysbiosis likely contributes to the variation in the bile acid pool. This study sets the stage to envisage potential solutions to modulate the gut microbiome with the objective to restore the bile acid pool in the gut.

Subject headings

NATURVETENSKAP  -- Biologi -- Evolutionsbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Evolutionary Biology (hsv//eng)
NATURVETENSKAP  -- Biologi -- Bioinformatik och systembiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Bioinformatics and Systems Biology (hsv//eng)
NATURVETENSKAP  -- Biologi -- Genetik (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Genetics (hsv//eng)

Keyword

and bile salt biotransformation genes
gut microbiota
ibd
bioinformatics
metagenomics
metabolomics
secondary bile acids

Publication and Content Type

art (subject category)
ref (subject category)

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