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Evidence that asthma is a developmental origin disease influenced by maternal diet and bacterial metabolites.
- Source :
-
Nature communications [Nat Commun] 2015 Jun 23; Vol. 6, pp. 7320. Date of Electronic Publication: 2015 Jun 23. - Publication Year :
- 2015
-
Abstract
- Asthma is prevalent in Western countries, and recent explanations have evoked the actions of the gut microbiota. Here we show that feeding mice a high-fibre diet yields a distinctive gut microbiota, which increases the levels of the short-chain fatty acid, acetate. High-fibre or acetate-feeding led to marked suppression of allergic airways disease (AAD, a model for human asthma), by enhancing T-regulatory cell numbers and function. Acetate increases acetylation at the Foxp3 promoter, likely through HDAC9 inhibition. Epigenetic effects of fibre/acetate in adult mice led us to examine the influence of maternal intake of fibre/acetate. High-fibre/acetate feeding of pregnant mice imparts on their adult offspring an inability to develop robust AAD. High fibre/acetate suppresses expression of certain genes in the mouse fetal lung linked to both human asthma and mouse AAD. Thus, diet acting on the gut microbiota profoundly influences airway responses, and may represent an approach to prevent asthma, including during pregnancy.
- Subjects :
- Acetates pharmacology
Acetylation drug effects
Animals
Asthma immunology
Disease Models, Animal
Epigenesis, Genetic drug effects
Fatty Acids, Volatile metabolism
Fatty Acids, Volatile pharmacology
Female
Forkhead Transcription Factors drug effects
Forkhead Transcription Factors genetics
Histone Deacetylases drug effects
Histone Deacetylases metabolism
Mice
Pregnancy
Prenatal Exposure Delayed Effects immunology
Promoter Regions, Genetic
Repressor Proteins drug effects
Repressor Proteins metabolism
T-Lymphocytes, Regulatory cytology
T-Lymphocytes, Regulatory drug effects
Acetates metabolism
Asthma metabolism
Diet
Dietary Fiber metabolism
Gastrointestinal Microbiome
Prenatal Exposure Delayed Effects metabolism
T-Lymphocytes, Regulatory immunology
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 6
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 26102221
- Full Text :
- https://doi.org/10.1038/ncomms8320