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PMID: 21593810 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Responses of gut microbiota to diet composition and weight loss in lean and obese mice.

Obesity (Silver Spring, Md.) ·Vol. 20 ·No. 4 ·2012-04-00 ·Pages 738-47

Ravussin Y, Koren O, Spor A, LeDuc C, Gutman R, Stombaugh J, Knight R, Ley RE, Leibel RL

Abstract

Maintenance of a reduced body weight is accompanied by a decrease in energy expenditure beyond that accounted for by reduced body mass and composition, as well as by an increased drive to eat. These effects appear to be due--in part--to reductions in circulating leptin concentrations due to loss of body fat. Gut microbiota have been implicated in the regulation of body weight. The effects of weight loss on qualitative aspects of gut microbiota have been studied in humans and mice, but these studies have been confounded by concurrent changes in diet composition, which influence microbial community composition. We studied the impact of 20% weight loss on the microbiota of diet-induced obese (DIO: 60% calories fat) mice on a high-fat diet (HFD). Weight-reduced DIO (DIO-WR) mice had the same body weight and composition as control (CON) ad-libitum (AL) fed mice being fed a control diet (10% calories fat), allowing a direct comparison of diet and weight-perturbation effects. Microbial community composition was assessed by pyrosequencing 16S rRNA genes derived from the ceca of sacrificed animals. There was a strong effect of diet composition on the diversity and composition of the microbiota. The relative abundance of specific members of the microbiota was correlated with circulating leptin concentrations and gene expression levels of inflammation markers in subcutaneous white adipose tissue in all mice. Together, these results suggest that both host adiposity and diet composition impact microbiota composition, possibly through leptin-mediated regulation of mucus production and/or inflammatory processes that alter the gut habitat.

MeSH Terms
Adipose Tissue, White/pathology Adiposity Animals Cecum/microbiology Diet, High-Fat Energy Intake Energy Metabolism Intestinal Mucosa/microbiology Leptin/blood Male Metagenome Mice Mice, Inbred C57BL Weight Loss
Chemicals
Leptin
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Ravussin Yann
Division of Molecular Genetics and Naomi Berrie Diabetes Center, Columbia University College of Physicians and Surgeons, New York, New York, USA.
Koren Omry
Spor Ayme
LeDuc Charles
Gutman Roee
Stombaugh Jesse
Knight Rob
Ley Ruth E
Leibel Rudolph L
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Article Info
Journal
Obesity (Silver Spring, Md.)
Abbr.
Obesity (Silver Spring)
ISSN
1930-739X
Published
2012-04-00
Epub
2011-00-19
Pages
738-47
Language
English
Region
United States
NLM ID
101264860
PMCID
PMC3871199
Subset
IM
Grants
NIDDK NIH HHS · 5P30DK026687 · United States
NIDDK NIH HHS · P01 DK078669 · United States
NHGRI NIH HHS · HG4872 · United States
NIDDK NIH HHS · 5R01DK064773 · United States
NHGRI NIH HHS · U01 HG004866 · United States
NHGRI NIH HHS · HG4866 · United States
NIDDK NIH HHS · P30 DK026687 · United States
NIDDK NIH HHS · R01 DK052431 · United States
NIDDK NIH HHS · DK78669 · United States
Howard Hughes Medical Institute · United States
NIDDK NIH HHS · DK063608-08 · United States
NIDDK NIH HHS · R01 DK064773 · United States
NHGRI NIH HHS · R01 HG004872 · United States
NIDDK NIH HHS · P30 DK063608 · United States
NIDDK NIH HHS · 5R01DK052431 · United States
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