| Literature DB >> 24030595 |
Hannelore Daniel1, Amin Moghaddas Gholami2, David Berry3, Charles Desmarchelier1, Hannes Hahne2, Gunnar Loh4, Stanislas Mondot5, Patricia Lepage6, Michael Rothballer7, Alesia Walker8, Christoph Böhm3, Mareike Wenning9, Michael Wagner3, Michael Blaut4, Philippe Schmitt-Kopplin8, Bernhard Kuster10, Dirk Haller11, Thomas Clavel12.
Abstract
The intestinal microbiota is known to regulate host energy homeostasis and can be influenced by high-calorie diets. However, changes affecting the ecosystem at the functional level are still not well characterized. We measured shifts in cecal bacterial communities in mice fed a carbohydrate or high-fat (HF) diet for 12 weeks at the level of the following: (i) diversity and taxa distribution by high-throughput 16S ribosomal RNA gene sequencing; (ii) bulk and single-cell chemical composition by Fourier-transform infrared- (FT-IR) and Raman micro-spectroscopy and (iii) metaproteome and metabolome via high-resolution mass spectrometry. High-fat diet caused shifts in the diversity of dominant gut bacteria and altered the proportion of Ruminococcaceae (decrease) and Rikenellaceae (increase). FT-IR spectroscopy revealed that the impact of the diet on cecal chemical fingerprints is greater than the impact of microbiota composition. Diet-driven changes in biochemical fingerprints of members of the Bacteroidales and Lachnospiraceae were also observed at the level of single cells, indicating that there were distinct differences in cellular composition of dominant phylotypes under different diets. Metaproteome and metabolome analyses based on the occurrence of 1760 bacterial proteins and 86 annotated metabolites revealed distinct HF diet-specific profiles. Alteration of hormonal and anti-microbial networks, bile acid and bilirubin metabolism and shifts towards amino acid and simple sugars metabolism were observed. We conclude that a HF diet markedly affects the gut bacterial ecosystem at the functional level.Entities:
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Year: 2013 PMID: 24030595 PMCID: PMC3906816 DOI: 10.1038/ismej.2013.155
Source DB: PubMed Journal: ISME J ISSN: 1751-7362 Impact factor: 10.302