Integrated metabolic and microbial analysis reveals host–microbial interactions in IgE-mediated childhood asthma

Abstract A metabolomics-based approach to address the molecular mechanism of childhood asthma with immunoglobulin E (IgE) or allergen sensitization related to microbiome in the airways remains lacking. Fifty-three children with lowly sensitized non-atopic asthma (n = 15), highly sensitized atopic as...

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Autores principales: Chih-Yung Chiu, Mei-Ling Cheng, Meng-Han Chiang, Chia-Jung Wang, Ming-Han Tsai, Gigin Lin
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/1cd9764a17434d0183b72be2c4c4d22b
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spelling oai:doaj.org-article:1cd9764a17434d0183b72be2c4c4d22b2021-12-05T12:16:21ZIntegrated metabolic and microbial analysis reveals host–microbial interactions in IgE-mediated childhood asthma10.1038/s41598-021-02925-52045-2322https://doaj.org/article/1cd9764a17434d0183b72be2c4c4d22b2021-12-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-02925-5https://doaj.org/toc/2045-2322Abstract A metabolomics-based approach to address the molecular mechanism of childhood asthma with immunoglobulin E (IgE) or allergen sensitization related to microbiome in the airways remains lacking. Fifty-three children with lowly sensitized non-atopic asthma (n = 15), highly sensitized atopic asthma (n = 13), and healthy controls (n = 25) were enrolled. Blood metabolomic analysis with 1H-nuclear magnetic resonance (NMR) spectroscopy and airway microbiome composition analysis by bacterial 16S rRNA sequencing were performed. An integrative analysis of their associations with allergen-specific IgE levels for lowly and highly sensitized asthma was also assessed. Four metabolites including tyrosine, isovalerate, glycine, and histidine were uniquely associated with lowly sensitized asthma, whereas one metabolite, acetic acid, was strongly associated with highly sensitized asthma. Metabolites associated with highly sensitized asthma (valine, isobutyric acid, and acetic acid) and lowly sensitized asthma (isovalerate, tyrosine, and histidine) were strongly correlated each other (P < 0.01). Highly sensitized asthma associated metabolites were mainly enriched in pyruvate and acetyl-CoA metabolisms. Metabolites associated with highly sensitized atopic asthma were mostly correlated with microbiota in the airways. Acetic acid, a short-chain fatty acid (SCFA), was negatively correlated with the genus Atopobium (P < 0.01), but positively correlated with the genus Fusobacterium (P < 0.05). In conclusion, metabolomics reveals microbes-related metabolic pathways associated with IgE responses to house dust mite allergens in childhood asthma. A strong correlation of metabolites related to highly sensitized atopic asthma with airway microbiota provides linkages between the host–microbial interactions and asthma endotypes.Chih-Yung ChiuMei-Ling ChengMeng-Han ChiangChia-Jung WangMing-Han TsaiGigin LinNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-7 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Chih-Yung Chiu
Mei-Ling Cheng
Meng-Han Chiang
Chia-Jung Wang
Ming-Han Tsai
Gigin Lin
Integrated metabolic and microbial analysis reveals host–microbial interactions in IgE-mediated childhood asthma
description Abstract A metabolomics-based approach to address the molecular mechanism of childhood asthma with immunoglobulin E (IgE) or allergen sensitization related to microbiome in the airways remains lacking. Fifty-three children with lowly sensitized non-atopic asthma (n = 15), highly sensitized atopic asthma (n = 13), and healthy controls (n = 25) were enrolled. Blood metabolomic analysis with 1H-nuclear magnetic resonance (NMR) spectroscopy and airway microbiome composition analysis by bacterial 16S rRNA sequencing were performed. An integrative analysis of their associations with allergen-specific IgE levels for lowly and highly sensitized asthma was also assessed. Four metabolites including tyrosine, isovalerate, glycine, and histidine were uniquely associated with lowly sensitized asthma, whereas one metabolite, acetic acid, was strongly associated with highly sensitized asthma. Metabolites associated with highly sensitized asthma (valine, isobutyric acid, and acetic acid) and lowly sensitized asthma (isovalerate, tyrosine, and histidine) were strongly correlated each other (P < 0.01). Highly sensitized asthma associated metabolites were mainly enriched in pyruvate and acetyl-CoA metabolisms. Metabolites associated with highly sensitized atopic asthma were mostly correlated with microbiota in the airways. Acetic acid, a short-chain fatty acid (SCFA), was negatively correlated with the genus Atopobium (P < 0.01), but positively correlated with the genus Fusobacterium (P < 0.05). In conclusion, metabolomics reveals microbes-related metabolic pathways associated with IgE responses to house dust mite allergens in childhood asthma. A strong correlation of metabolites related to highly sensitized atopic asthma with airway microbiota provides linkages between the host–microbial interactions and asthma endotypes.
format article
author Chih-Yung Chiu
Mei-Ling Cheng
Meng-Han Chiang
Chia-Jung Wang
Ming-Han Tsai
Gigin Lin
author_facet Chih-Yung Chiu
Mei-Ling Cheng
Meng-Han Chiang
Chia-Jung Wang
Ming-Han Tsai
Gigin Lin
author_sort Chih-Yung Chiu
title Integrated metabolic and microbial analysis reveals host–microbial interactions in IgE-mediated childhood asthma
title_short Integrated metabolic and microbial analysis reveals host–microbial interactions in IgE-mediated childhood asthma
title_full Integrated metabolic and microbial analysis reveals host–microbial interactions in IgE-mediated childhood asthma
title_fullStr Integrated metabolic and microbial analysis reveals host–microbial interactions in IgE-mediated childhood asthma
title_full_unstemmed Integrated metabolic and microbial analysis reveals host–microbial interactions in IgE-mediated childhood asthma
title_sort integrated metabolic and microbial analysis reveals host–microbial interactions in ige-mediated childhood asthma
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/1cd9764a17434d0183b72be2c4c4d22b
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