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Gut microbiome signature and nasal lavage inflammatory markers in young people with asthma.

Sampaio Dotto Fiuza, B; Machado de Andrade, C; Meirelles, PM; Santos da Silva, J; de Jesus Silva, M; Vila Nova Santana, C; Pimentel Pinheiro, G; Mpairwe, H; Cooper, P; Brooks, C; et al. Sampaio Dotto Fiuza, B; Machado de Andrade, C; Meirelles, PM; Santos da Silva, J; de Jesus Silva, M; Vila Nova Santana, C; Pimentel Pinheiro, G; Mpairwe, H; Cooper, P; Brooks, C; Pembrey, L; Taylor, S; Douwes, J; Cruz, ÁA; Barreto, ML; Pearce, N; Figueiredo, CAV (2024) Gut microbiome signature and nasal lavage inflammatory markers in young people with asthma. J Allergy Clin Immunol Glob, 3 (2). p. 100242. ISSN 2772-8293 https://doi.org/10.1016/j.jacig.2024.100242
SGUL Authors: Cooper, Philip John

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Abstract

BACKGROUND: Asthma is a complex disease and a severe global public health problem resulting from interactions between genetic background and environmental exposures. It has been suggested that gut microbiota may be related to asthma development; however, such relationships needs further investigation. OBJECTIVE: This study aimed to characterize the gut microbiota as well as the nasal lavage cytokine profile of asthmatic and nonasthmatic individuals. METHODS: Stool and nasal lavage samples were collected from 29 children and adolescents with type 2 asthma and 28 children without asthma in Brazil. Amplicon sequencing of the stool bacterial V4 region of the 16S rRNA gene was performed using Illumina MiSeq. Microbiota analysis was performed by QIIME 2 and PICRUSt2. Type 2 asthma phenotype was characterized by high sputum eosinophil counts and positive skin prick tests for house dust mite, cockroach, and/or cat or dog dander. The nasal immune marker profile was assessed using a customized multiplex panel. RESULTS: Stool microbiota differed significantly between asthmatic and nonasthmatic participants (P = .001). Bacteroides was more abundant in participants with asthma (P < .05), while Prevotella was more abundant in nonasthmatic individuals (P < .05). In people with asthma, the relative abundance of Bacteroides correlated with IL-4 concentration in nasal lavage samples. Inference of microbiota functional capacity identified differential fatty acid biosynthesis in asthmatic compared to nonasthmatic subjects. CONCLUSION: The stool microbiota differed between asthmatic and nonasthmatic young people in Brazil. Asthma was associated with higher Bacteroides levels, which correlated with nasal IL-4 concentration.

Item Type: Article
Additional Information: © 2024 Published by Elsevier Inc. on behalf of the American Academy of Allergy, Asthma & Immunology. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Keywords: Asthma, gut microbiota, microbiome, stool
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: J Allergy Clin Immunol Glob
ISSN: 2772-8293
Language: eng
Dates:
DateEvent
29 March 2024Published
11 March 2023Published Online
24 December 2023Accepted
Publisher License: Creative Commons: Attribution-Noncommercial-No Derivative Works 4.0
Projects:
Project IDFunderFunder ID
668954European Research Councilhttp://dx.doi.org/10.13039/501100000781
101020088European Research Councilhttp://dx.doi.org/10.13039/501100000781
001Coordenação de Aperfeiçoamento de Pessoal de Nível Superior–BrasilUNSPECIFIED
PNE0003/2014Fundação de Amparo à Pesquisa do Estado da Bahiahttp://dx.doi.org/10.13039/501100006181
PNX0001/2014Fundação de Amparo à Pesquisa do Estado da Bahiahttp://dx.doi.org/10.13039/501100006181
BOL0281/2020Fundação de Amparo à Pesquisa do Estado da BahiaUNSPECIFIED
40314Conselho Nacional de Desenvolvimento Científico e Tecnológicohttp://dx.doi.org/10.13039/501100003593
308521/2019-6Conselho Nacional de Desenvolvimento Científico e Tecnológicohttp://dx.doi.org/10.13039/501100003593
PubMed ID: 38585449
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/116433
Publisher's version: https://doi.org/10.1016/j.jacig.2024.100242

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