A metagenome-wide association study of gut microbiota in asthma in UK adults
Background Asthma, one of the most common chronic respiratory disorders, is associated with the hyper-activation of the T-cell subset of adaptive immunity. The gut microbiota may be involved in the development of asthma through the production of short-chain fatty acids (SCFAs), exhibiting modulatory...
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Published in | BMC microbiology Vol. 18; no. 1; pp. 114 - 7 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
BioMed Central
12.09.2018
BioMed Central Ltd BMC |
Subjects | |
Online Access | Get full text |
ISSN | 1471-2180 1471-2180 |
DOI | 10.1186/s12866-018-1257-x |
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Summary: | Background
Asthma, one of the most common chronic respiratory disorders, is associated with the hyper-activation of the T-cell subset of adaptive immunity. The gut microbiota may be involved in the development of asthma through the production of short-chain fatty acids (SCFAs), exhibiting modulatory effects on Th. So, we performed a metagenome-wide association study (MWAS) of the fecal microbiota from individuals with asthma and healthy controls. And that was the first case to resolve the relationship between asthma and microbiome among UK adults.
Results
The microbiota of the individuals with asthma consisted of fewer microbial entities than the microbiota of healthy individuals.
Faecalibacterium prausnitzii
,
Sutterella wadsworthensis
and
Bacteroides stercoris
were depleted in cases, whereas
Clostridiums
with
Eggerthella lenta
were over-represented in individuals with asthma. Functional analysis shows that the SCFAs might be altered in the microbiota of asthma patients.
Conclusion
In all, the adult human gut microbiome of asthma patients is clearly different from healthy controls. The functional and taxa results showed that the change of asthma patients might related to SCFAs. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1471-2180 1471-2180 |
DOI: | 10.1186/s12866-018-1257-x |