Abstract
Background & Aims: Alterations in the gastrointestinal microbiota have been associated with metabolic diseases. However, little is known about host factors that induce changes in gastrointestinal bacterial populations. We investigated the role of bile acids in this process because of their strong antimicrobial activities, specifically the effects of cholic acid administration on the composition of the gut microbiota in a rat model. Methods: Rats were fed diets supplemented with different concentrations of cholic acid for 10 days. We used 16S ribosomal RNA gene clone library sequencing and fluorescence in situ hybridization to characterize the composition of the cecal microbiota of the different diet groups. Bile acids in feces, organic acids in cecal contents, and some blood parameters were also analyzed. Results: Administration of cholic acid induced phylum-level alterations in the composition of the gut microbiota; Firmicutes predominated at the expense of Bacteroidetes. Cholic acid feeding simplified the composition of the microbiota, with outgrowth of several bacteria in the classes Clostridia and Erysipelotrichi. Externally administered cholic acid was efficiently transformed into deoxycholic acid by a bacterial 7α-dehydroxylation reaction. Serum levels of adiponectin decreased significantly in rats given the cholic acid diet. Conclusions: Cholic acid regulates the composition of gut microbiota in rats, inducing similar changes to those induced by high-fat diets. These findings improve our understanding of the relationship between metabolic diseases and the composition of the gastrointestinal microbiota.
| Original language | English |
|---|---|
| Pages (from-to) | 1773-1781 |
| Number of pages | 9 |
| Journal | Gastroenterology |
| Volume | 141 |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - Jan 1 2011 |
| Externally published | Yes |
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All Science Journal Classification (ASJC) codes
- Hepatology
- Gastroenterology
Cite this
Bile acid is a host factor that regulates the composition of the cecal microbiota in rats. / Islam, K. B.M.Saiful; Fukiya, Satoru; Hagio, Masahito; Fujii, Nobuyuki; Ishizuka, Satoshi; Ooka, Tadasuke; Ogura, Yoshitoshi; Hayashi, Tetsuya; Yokota, Atsushi.
In: Gastroenterology, Vol. 141, No. 5, 01.01.2011, p. 1773-1781.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Bile acid is a host factor that regulates the composition of the cecal microbiota in rats
AU - Islam, K. B.M.Saiful
AU - Fukiya, Satoru
AU - Hagio, Masahito
AU - Fujii, Nobuyuki
AU - Ishizuka, Satoshi
AU - Ooka, Tadasuke
AU - Ogura, Yoshitoshi
AU - Hayashi, Tetsuya
AU - Yokota, Atsushi
PY - 2011/1/1
Y1 - 2011/1/1
N2 - Background & Aims: Alterations in the gastrointestinal microbiota have been associated with metabolic diseases. However, little is known about host factors that induce changes in gastrointestinal bacterial populations. We investigated the role of bile acids in this process because of their strong antimicrobial activities, specifically the effects of cholic acid administration on the composition of the gut microbiota in a rat model. Methods: Rats were fed diets supplemented with different concentrations of cholic acid for 10 days. We used 16S ribosomal RNA gene clone library sequencing and fluorescence in situ hybridization to characterize the composition of the cecal microbiota of the different diet groups. Bile acids in feces, organic acids in cecal contents, and some blood parameters were also analyzed. Results: Administration of cholic acid induced phylum-level alterations in the composition of the gut microbiota; Firmicutes predominated at the expense of Bacteroidetes. Cholic acid feeding simplified the composition of the microbiota, with outgrowth of several bacteria in the classes Clostridia and Erysipelotrichi. Externally administered cholic acid was efficiently transformed into deoxycholic acid by a bacterial 7α-dehydroxylation reaction. Serum levels of adiponectin decreased significantly in rats given the cholic acid diet. Conclusions: Cholic acid regulates the composition of gut microbiota in rats, inducing similar changes to those induced by high-fat diets. These findings improve our understanding of the relationship between metabolic diseases and the composition of the gastrointestinal microbiota.
AB - Background & Aims: Alterations in the gastrointestinal microbiota have been associated with metabolic diseases. However, little is known about host factors that induce changes in gastrointestinal bacterial populations. We investigated the role of bile acids in this process because of their strong antimicrobial activities, specifically the effects of cholic acid administration on the composition of the gut microbiota in a rat model. Methods: Rats were fed diets supplemented with different concentrations of cholic acid for 10 days. We used 16S ribosomal RNA gene clone library sequencing and fluorescence in situ hybridization to characterize the composition of the cecal microbiota of the different diet groups. Bile acids in feces, organic acids in cecal contents, and some blood parameters were also analyzed. Results: Administration of cholic acid induced phylum-level alterations in the composition of the gut microbiota; Firmicutes predominated at the expense of Bacteroidetes. Cholic acid feeding simplified the composition of the microbiota, with outgrowth of several bacteria in the classes Clostridia and Erysipelotrichi. Externally administered cholic acid was efficiently transformed into deoxycholic acid by a bacterial 7α-dehydroxylation reaction. Serum levels of adiponectin decreased significantly in rats given the cholic acid diet. Conclusions: Cholic acid regulates the composition of gut microbiota in rats, inducing similar changes to those induced by high-fat diets. These findings improve our understanding of the relationship between metabolic diseases and the composition of the gastrointestinal microbiota.
UR - http://www.scopus.com/inward/record.url?scp=80054862011&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=80054862011&partnerID=8YFLogxK
U2 - 10.1053/j.gastro.2011.07.046
DO - 10.1053/j.gastro.2011.07.046
M3 - Article
VL - 141
SP - 1773
EP - 1781
JO - Gastroenterology
JF - Gastroenterology
SN - 0016-5085
IS - 5
ER -