Altered diversity and composition of gut microbiota in patients with allergic rhinitis.


Journal

Microbial pathogenesis
ISSN: 1096-1208
Titre abrégé: Microb Pathog
Pays: England
ID NLM: 8606191

Informations de publication

Date de publication:
Dec 2021
Historique:
received: 28 04 2021
revised: 21 10 2021
accepted: 22 10 2021
pubmed: 7 11 2021
medline: 15 12 2021
entrez: 6 11 2021
Statut: ppublish

Résumé

Recently, multiple studies have suggested an association between gut dysbiosis and allergic rhinitis (AR) development. However, the role of gut microbiota in AR development remains obscure. The goal of this study was to compare the gut microbiota composition and short-chain fatty acid (SCFAs) differences associated with AR (N = 18) and HCs (healthy controls, N = 17). Gut microbiota 16SrRNA gene sequences were analyzed based on next-generation sequencing. SCFAs in stool samples were analyzed by gas chromatography-mass spectrometry (GC-MS). Compared with HCs, the gut microbiota composition of AR was significantly different in diversity and richness. At the phylum level, the abundance of Firmicutes in the AR group were significantly lower than those in the HCs group. At the genus level, the abundance of Blautia, Eubacterium_hallii_group, Romboutsia, Collinsella, Dorea, Subdoligranulum and Fusicatenibacter in the AR group were significantly lower than that in the HCs group. The concentrations of SCFAs were significantly lower in the AR group compared with the HCs group. Correlation analysis showed that the Eubacterium-hallii-group and Blautia correlated positively with SCFAs. Our results demonstrate compositional and functional alterations of the gut microbiome in AR.

Sections du résumé

BACKGROUND BACKGROUND
Recently, multiple studies have suggested an association between gut dysbiosis and allergic rhinitis (AR) development. However, the role of gut microbiota in AR development remains obscure.
METHODS METHODS
The goal of this study was to compare the gut microbiota composition and short-chain fatty acid (SCFAs) differences associated with AR (N = 18) and HCs (healthy controls, N = 17). Gut microbiota 16SrRNA gene sequences were analyzed based on next-generation sequencing. SCFAs in stool samples were analyzed by gas chromatography-mass spectrometry (GC-MS).
RESULTS RESULTS
Compared with HCs, the gut microbiota composition of AR was significantly different in diversity and richness. At the phylum level, the abundance of Firmicutes in the AR group were significantly lower than those in the HCs group. At the genus level, the abundance of Blautia, Eubacterium_hallii_group, Romboutsia, Collinsella, Dorea, Subdoligranulum and Fusicatenibacter in the AR group were significantly lower than that in the HCs group. The concentrations of SCFAs were significantly lower in the AR group compared with the HCs group. Correlation analysis showed that the Eubacterium-hallii-group and Blautia correlated positively with SCFAs.
CONCLUSION CONCLUSIONS
Our results demonstrate compositional and functional alterations of the gut microbiome in AR.

Identifiants

pubmed: 34740809
pii: S0882-4010(21)00546-5
doi: 10.1016/j.micpath.2021.105272
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

105272

Informations de copyright

Copyright © 2021. Published by Elsevier Ltd.

Auteurs

Mu-Shi Zhou (MS)

Department of Anatomy and Neurobiology, School of Basic Medical Science, Central South University, Changsha, Hunan, China.

Bin Zhang (B)

Shanghai Clinical Research Center, Shanghai, China.

Zhao-Lin Gao (ZL)

Department of Anatomy and Neurobiology, School of Basic Medical Science, Central South University, Changsha, Hunan, China.

Ru-Ping Zheng (RP)

Department of Anatomy and Neurobiology, School of Basic Medical Science, Central South University, Changsha, Hunan, China.

Dama Faniriantsoa Henrio Marcellin Marcellin (DFHM)

Department of Anatomy and Neurobiology, School of Basic Medical Science, Central South University, Changsha, Hunan, China.

Adonira Saro (A)

Department of Anatomy and Neurobiology, School of Basic Medical Science, Central South University, Changsha, Hunan, China.

Jing Pan (J)

Department of Anatomy and Neurobiology, School of Basic Medical Science, Central South University, Changsha, Hunan, China.

Ling Chu (L)

Department of Pathology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, China.

Tian-Sheng Wang (TS)

Department of Otolaryngology-Head and Neck, The Third Xiangya Hospital, Central South University, Changsha, Hunan, China. Electronic address: tianshengwang@csu.edu.cn.

Ju-Fang Huang (JF)

Department of Anatomy and Neurobiology, School of Basic Medical Science, Central South University, Changsha, Hunan, China. Electronic address: huangjufang@csu.edu.cn.

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