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Evidence that asthma is a developmental origin disease influenced by maternal diet and bacterial metabolites
- Source :
- Nature communications. 6
- 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 :
- Dietary Fiber
medicine.medical_specialty
General Physics and Astronomy
Inflammation
Biology
Gut flora
Acetates
T-Lymphocytes, Regulatory
General Biochemistry, Genetics and Molecular Biology
Histone Deacetylases
Epigenesis, Genetic
Mice
Pregnancy
Internal medicine
medicine
Animals
Epigenetics
Receptor
Promoter Regions, Genetic
Asthma
chemistry.chemical_classification
Multidisciplinary
Fatty acid
FOXP3
Acetylation
Forkhead Transcription Factors
General Chemistry
medicine.disease
biology.organism_classification
Fatty Acids, Volatile
Diet
Gastrointestinal Microbiome
Repressor Proteins
Disease Models, Animal
Endocrinology
chemistry
Prenatal Exposure Delayed Effects
Immunology
Female
medicine.symptom
Subjects
Details
- ISSN :
- 20411723
- Volume :
- 6
- Database :
- OpenAIRE
- Journal :
- Nature communications
- Accession number :
- edsair.doi.dedup.....c038e68e203844da460cec896cf23b06