Cargando…

Gut Microbiome and Serum Metabolome Analyses Identify Unsaturated Fatty Acids and Butanoate Metabolism Induced by Gut Microbiota in Patients With Chronic Spontaneous Urticaria

Chronic urticaria (CU) is defined as the continuous or intermittent presence of urticaria for a period exceeding 6 weeks and sometimes occurring with angioedema. Between 66 and 93% of patients with CU have chronic spontaneous urticaria (CSU), the precise pathogenesis of which is largely unknown. The...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Detong, Guo, Shuping, He, Hongxia, Gong, Li, Cui, Hongzhou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7047433/
https://www.ncbi.nlm.nih.gov/pubmed/32154184
http://dx.doi.org/10.3389/fcimb.2020.00024
_version_ 1783502141038526464
author Wang, Detong
Guo, Shuping
He, Hongxia
Gong, Li
Cui, Hongzhou
author_facet Wang, Detong
Guo, Shuping
He, Hongxia
Gong, Li
Cui, Hongzhou
author_sort Wang, Detong
collection PubMed
description Chronic urticaria (CU) is defined as the continuous or intermittent presence of urticaria for a period exceeding 6 weeks and sometimes occurring with angioedema. Between 66 and 93% of patients with CU have chronic spontaneous urticaria (CSU), the precise pathogenesis of which is largely unknown. The aim of this study was to determine the relationship between gut microbiota and serum metabolites and the possible pathogenesis underlying CSU. We collected feces and blood samples from CSU patients and healthy controls and the relationship between gut microbiota and serum metabolites was assessed using 16S rRNA gene sequencing and untargeted metabolomic analyses. The CSU group exhibited decreased alpha diversity of the microbial population compared to the control group. The abundance of unidentified Enterobacteriaceae was increased, while the abundance of Bacteroides, Faecalibacterium, Bifidobacterium, and unidentified Ruminococcaceae was significantly reduced in CSU patients. The serum metabolome analysis revealed altered levels of docosahexaenoic acid, arachidonic acid, glutamate, and succinic acid, suggesting changes in unsaturated fatty acids and the butanoate metabolism pathway. The combined serum metabolomics and gut microbiome datasets were correlated; specifically, docosahexaenoic acid, and arachidonic acid were positively correlated with Bacteroides. We speculate that alterations in gut microbes and metabolites may contribute to exacerbated inflammatory responses and dysregulated immune function with or without regulatory T cell dependence in the pathogenesis of CSU.
format Online
Article
Text
id pubmed-7047433
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-70474332020-03-09 Gut Microbiome and Serum Metabolome Analyses Identify Unsaturated Fatty Acids and Butanoate Metabolism Induced by Gut Microbiota in Patients With Chronic Spontaneous Urticaria Wang, Detong Guo, Shuping He, Hongxia Gong, Li Cui, Hongzhou Front Cell Infect Microbiol Cellular and Infection Microbiology Chronic urticaria (CU) is defined as the continuous or intermittent presence of urticaria for a period exceeding 6 weeks and sometimes occurring with angioedema. Between 66 and 93% of patients with CU have chronic spontaneous urticaria (CSU), the precise pathogenesis of which is largely unknown. The aim of this study was to determine the relationship between gut microbiota and serum metabolites and the possible pathogenesis underlying CSU. We collected feces and blood samples from CSU patients and healthy controls and the relationship between gut microbiota and serum metabolites was assessed using 16S rRNA gene sequencing and untargeted metabolomic analyses. The CSU group exhibited decreased alpha diversity of the microbial population compared to the control group. The abundance of unidentified Enterobacteriaceae was increased, while the abundance of Bacteroides, Faecalibacterium, Bifidobacterium, and unidentified Ruminococcaceae was significantly reduced in CSU patients. The serum metabolome analysis revealed altered levels of docosahexaenoic acid, arachidonic acid, glutamate, and succinic acid, suggesting changes in unsaturated fatty acids and the butanoate metabolism pathway. The combined serum metabolomics and gut microbiome datasets were correlated; specifically, docosahexaenoic acid, and arachidonic acid were positively correlated with Bacteroides. We speculate that alterations in gut microbes and metabolites may contribute to exacerbated inflammatory responses and dysregulated immune function with or without regulatory T cell dependence in the pathogenesis of CSU. Frontiers Media S.A. 2020-02-21 /pmc/articles/PMC7047433/ /pubmed/32154184 http://dx.doi.org/10.3389/fcimb.2020.00024 Text en Copyright © 2020 Wang, Guo, He, Gong and Cui. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Wang, Detong
Guo, Shuping
He, Hongxia
Gong, Li
Cui, Hongzhou
Gut Microbiome and Serum Metabolome Analyses Identify Unsaturated Fatty Acids and Butanoate Metabolism Induced by Gut Microbiota in Patients With Chronic Spontaneous Urticaria
title Gut Microbiome and Serum Metabolome Analyses Identify Unsaturated Fatty Acids and Butanoate Metabolism Induced by Gut Microbiota in Patients With Chronic Spontaneous Urticaria
title_full Gut Microbiome and Serum Metabolome Analyses Identify Unsaturated Fatty Acids and Butanoate Metabolism Induced by Gut Microbiota in Patients With Chronic Spontaneous Urticaria
title_fullStr Gut Microbiome and Serum Metabolome Analyses Identify Unsaturated Fatty Acids and Butanoate Metabolism Induced by Gut Microbiota in Patients With Chronic Spontaneous Urticaria
title_full_unstemmed Gut Microbiome and Serum Metabolome Analyses Identify Unsaturated Fatty Acids and Butanoate Metabolism Induced by Gut Microbiota in Patients With Chronic Spontaneous Urticaria
title_short Gut Microbiome and Serum Metabolome Analyses Identify Unsaturated Fatty Acids and Butanoate Metabolism Induced by Gut Microbiota in Patients With Chronic Spontaneous Urticaria
title_sort gut microbiome and serum metabolome analyses identify unsaturated fatty acids and butanoate metabolism induced by gut microbiota in patients with chronic spontaneous urticaria
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7047433/
https://www.ncbi.nlm.nih.gov/pubmed/32154184
http://dx.doi.org/10.3389/fcimb.2020.00024
work_keys_str_mv AT wangdetong gutmicrobiomeandserummetabolomeanalysesidentifyunsaturatedfattyacidsandbutanoatemetabolisminducedbygutmicrobiotainpatientswithchronicspontaneousurticaria
AT guoshuping gutmicrobiomeandserummetabolomeanalysesidentifyunsaturatedfattyacidsandbutanoatemetabolisminducedbygutmicrobiotainpatientswithchronicspontaneousurticaria
AT hehongxia gutmicrobiomeandserummetabolomeanalysesidentifyunsaturatedfattyacidsandbutanoatemetabolisminducedbygutmicrobiotainpatientswithchronicspontaneousurticaria
AT gongli gutmicrobiomeandserummetabolomeanalysesidentifyunsaturatedfattyacidsandbutanoatemetabolisminducedbygutmicrobiotainpatientswithchronicspontaneousurticaria
AT cuihongzhou gutmicrobiomeandserummetabolomeanalysesidentifyunsaturatedfattyacidsandbutanoatemetabolisminducedbygutmicrobiotainpatientswithchronicspontaneousurticaria