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Altered intestinal microbiota in children with bronchiolitis

OBJECTIVE: To investigate the correlation between the alteration of intestinal microbiota and disease in children with bronchiolitis. METHODS: Fifty seven children diagnosed with bronchiolitis from January 2020 to January 2022 in our pediatric department were included as the case group, and another...

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Autores principales: Wu, Xiao-bin, Wang, Jian, Tang, Yuan, Jiang, Jing, Li, Xue-mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10306280/
https://www.ncbi.nlm.nih.gov/pubmed/37389334
http://dx.doi.org/10.3389/fmicb.2023.1197092
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author Wu, Xiao-bin
Wang, Jian
Tang, Yuan
Jiang, Jing
Li, Xue-mei
author_facet Wu, Xiao-bin
Wang, Jian
Tang, Yuan
Jiang, Jing
Li, Xue-mei
author_sort Wu, Xiao-bin
collection PubMed
description OBJECTIVE: To investigate the correlation between the alteration of intestinal microbiota and disease in children with bronchiolitis. METHODS: Fifty seven children diagnosed with bronchiolitis from January 2020 to January 2022 in our pediatric department were included as the case group, and another 36 normal children were included as the control group. Stool and blood were collected from both groups for high-throughput sequencing, untargeted metabolite detection and ELISA. A mouse model of RSV infection was established to validate the results of clinical case detection. RESULTS: Body weight, passive smoking, and a host of other factors were possible as acute bronchiolitis influencing factors in the onset of acute bronchiolitis. The alpha diversity Shannon, Simpson and Pielou’s evenness indices were significantly lower in children with acute bronchiolitis than in healthy children with gated levels of Firmicutes, Bacteroidetes and genus levels of Clostridium and other short chain fatty acid-producing bacteria. The relative abundance of short-chain fatty acid (SCFAs)-producing bacteria decreased and the abundance of genus-level sphingolipid-producing bacteria Sphingomonas increased; the progression of acute bronchiolitis is likely to be associated with the abundance of Clostridium and Sphingomonas and higher fecal amino acid concentrations, including FF-MAS, L-aspartic acid, thioinosinic acid, picolinic acid; supplementation with Clostridium butyricum significantly alleviated RSV infection-induced lung inflammation. CONCLUSION: The progression of bronchiolitis may be associated with altered intestinal microbiota, decreased SCFAs and elevated sphingolipids metabolism in children. Some fecal bacteria and metabolites may predict the onset of bronchiolitis, and oral administration of Clostridium butyricum may alleviate RSV infection-induced pulmonary inflammation.
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spelling pubmed-103062802023-06-29 Altered intestinal microbiota in children with bronchiolitis Wu, Xiao-bin Wang, Jian Tang, Yuan Jiang, Jing Li, Xue-mei Front Microbiol Microbiology OBJECTIVE: To investigate the correlation between the alteration of intestinal microbiota and disease in children with bronchiolitis. METHODS: Fifty seven children diagnosed with bronchiolitis from January 2020 to January 2022 in our pediatric department were included as the case group, and another 36 normal children were included as the control group. Stool and blood were collected from both groups for high-throughput sequencing, untargeted metabolite detection and ELISA. A mouse model of RSV infection was established to validate the results of clinical case detection. RESULTS: Body weight, passive smoking, and a host of other factors were possible as acute bronchiolitis influencing factors in the onset of acute bronchiolitis. The alpha diversity Shannon, Simpson and Pielou’s evenness indices were significantly lower in children with acute bronchiolitis than in healthy children with gated levels of Firmicutes, Bacteroidetes and genus levels of Clostridium and other short chain fatty acid-producing bacteria. The relative abundance of short-chain fatty acid (SCFAs)-producing bacteria decreased and the abundance of genus-level sphingolipid-producing bacteria Sphingomonas increased; the progression of acute bronchiolitis is likely to be associated with the abundance of Clostridium and Sphingomonas and higher fecal amino acid concentrations, including FF-MAS, L-aspartic acid, thioinosinic acid, picolinic acid; supplementation with Clostridium butyricum significantly alleviated RSV infection-induced lung inflammation. CONCLUSION: The progression of bronchiolitis may be associated with altered intestinal microbiota, decreased SCFAs and elevated sphingolipids metabolism in children. Some fecal bacteria and metabolites may predict the onset of bronchiolitis, and oral administration of Clostridium butyricum may alleviate RSV infection-induced pulmonary inflammation. Frontiers Media S.A. 2023-06-15 /pmc/articles/PMC10306280/ /pubmed/37389334 http://dx.doi.org/10.3389/fmicb.2023.1197092 Text en Copyright © 2023 Wu, Wang, Tang, Jiang and Li. https://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 Microbiology
Wu, Xiao-bin
Wang, Jian
Tang, Yuan
Jiang, Jing
Li, Xue-mei
Altered intestinal microbiota in children with bronchiolitis
title Altered intestinal microbiota in children with bronchiolitis
title_full Altered intestinal microbiota in children with bronchiolitis
title_fullStr Altered intestinal microbiota in children with bronchiolitis
title_full_unstemmed Altered intestinal microbiota in children with bronchiolitis
title_short Altered intestinal microbiota in children with bronchiolitis
title_sort altered intestinal microbiota in children with bronchiolitis
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10306280/
https://www.ncbi.nlm.nih.gov/pubmed/37389334
http://dx.doi.org/10.3389/fmicb.2023.1197092
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