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Dysfunctional Gut Microbiome Networks in Childhood IgE-Mediated Food Allergy

The development of food allergy has been reported to be related with the changes in the gut microbiome, however the specific microbe associated with the pathogenesis of food allergy remains elusive. This study aimed to comprehensively characterize the gut microbiome and identify individual or group...

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Autores principales: Lee, Khui Hung, Guo, Jing, Song, Yong, Ariff, Amir, O’Sullivan, Michael, Hales, Belinda, Mullins, Benjamin J., Zhang, Guicheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7923212/
https://www.ncbi.nlm.nih.gov/pubmed/33669849
http://dx.doi.org/10.3390/ijms22042079
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author Lee, Khui Hung
Guo, Jing
Song, Yong
Ariff, Amir
O’Sullivan, Michael
Hales, Belinda
Mullins, Benjamin J.
Zhang, Guicheng
author_facet Lee, Khui Hung
Guo, Jing
Song, Yong
Ariff, Amir
O’Sullivan, Michael
Hales, Belinda
Mullins, Benjamin J.
Zhang, Guicheng
author_sort Lee, Khui Hung
collection PubMed
description The development of food allergy has been reported to be related with the changes in the gut microbiome, however the specific microbe associated with the pathogenesis of food allergy remains elusive. This study aimed to comprehensively characterize the gut microbiome and identify individual or group gut microbes relating to food-allergy using 16S rRNA gene sequencing with network analysis. Faecal samples were collected from children with IgE-mediated food allergies (n = 33) and without food allergy (n = 27). Gut microbiome was profiled by 16S rRNA gene sequencing. OTUs obtained from 16S rRNA gene sequencing were then used to construct a co-abundance network using Weighted Gene Co-expression Network Analysis (WGCNA) and mapped onto Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways. We identified a co-abundance network module to be positively correlated with IgE-mediated food allergy and this module was characterized by a hub taxon, namely Ruminococcaceae UCG-002 (phylum Firmicutes). Functional pathway analysis of all the gut microbiome showed enrichment of methane metabolism and glycerolipid metabolism in the gut microbiome of food-allergic children and enrichment of ubiquinone and other terpenoid-quinone biosynthesis in the gut microbiome of non-food allergic children. We concluded that Ruminococcaceae UCG-002 may play determinant roles in gut microbial community structure and function leading to the development of IgE-mediated food allergy.
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spelling pubmed-79232122021-03-03 Dysfunctional Gut Microbiome Networks in Childhood IgE-Mediated Food Allergy Lee, Khui Hung Guo, Jing Song, Yong Ariff, Amir O’Sullivan, Michael Hales, Belinda Mullins, Benjamin J. Zhang, Guicheng Int J Mol Sci Article The development of food allergy has been reported to be related with the changes in the gut microbiome, however the specific microbe associated with the pathogenesis of food allergy remains elusive. This study aimed to comprehensively characterize the gut microbiome and identify individual or group gut microbes relating to food-allergy using 16S rRNA gene sequencing with network analysis. Faecal samples were collected from children with IgE-mediated food allergies (n = 33) and without food allergy (n = 27). Gut microbiome was profiled by 16S rRNA gene sequencing. OTUs obtained from 16S rRNA gene sequencing were then used to construct a co-abundance network using Weighted Gene Co-expression Network Analysis (WGCNA) and mapped onto Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways. We identified a co-abundance network module to be positively correlated with IgE-mediated food allergy and this module was characterized by a hub taxon, namely Ruminococcaceae UCG-002 (phylum Firmicutes). Functional pathway analysis of all the gut microbiome showed enrichment of methane metabolism and glycerolipid metabolism in the gut microbiome of food-allergic children and enrichment of ubiquinone and other terpenoid-quinone biosynthesis in the gut microbiome of non-food allergic children. We concluded that Ruminococcaceae UCG-002 may play determinant roles in gut microbial community structure and function leading to the development of IgE-mediated food allergy. MDPI 2021-02-19 /pmc/articles/PMC7923212/ /pubmed/33669849 http://dx.doi.org/10.3390/ijms22042079 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lee, Khui Hung
Guo, Jing
Song, Yong
Ariff, Amir
O’Sullivan, Michael
Hales, Belinda
Mullins, Benjamin J.
Zhang, Guicheng
Dysfunctional Gut Microbiome Networks in Childhood IgE-Mediated Food Allergy
title Dysfunctional Gut Microbiome Networks in Childhood IgE-Mediated Food Allergy
title_full Dysfunctional Gut Microbiome Networks in Childhood IgE-Mediated Food Allergy
title_fullStr Dysfunctional Gut Microbiome Networks in Childhood IgE-Mediated Food Allergy
title_full_unstemmed Dysfunctional Gut Microbiome Networks in Childhood IgE-Mediated Food Allergy
title_short Dysfunctional Gut Microbiome Networks in Childhood IgE-Mediated Food Allergy
title_sort dysfunctional gut microbiome networks in childhood ige-mediated food allergy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7923212/
https://www.ncbi.nlm.nih.gov/pubmed/33669849
http://dx.doi.org/10.3390/ijms22042079
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