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Urine Microbe-Derived Extracellular Vesicles in Children With Asthma

PURPOSE: Several studies have found significant associations between asthma and microbiome. However, it is challenging to obtain-sputum and bronchoalveolar lavage samples from pediatric patients. Thus, we used voided urine to show that urine microbe-derived extracellular vesicles (EVs) in asthma are...

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Autores principales: Lee, Yeong Seok, Kim, Jeong Hee, Lim, Dae Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7680828/
https://www.ncbi.nlm.nih.gov/pubmed/33191678
http://dx.doi.org/10.4168/aair.2021.13.1.75
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author Lee, Yeong Seok
Kim, Jeong Hee
Lim, Dae Hyun
author_facet Lee, Yeong Seok
Kim, Jeong Hee
Lim, Dae Hyun
author_sort Lee, Yeong Seok
collection PubMed
description PURPOSE: Several studies have found significant associations between asthma and microbiome. However, it is challenging to obtain-sputum and bronchoalveolar lavage samples from pediatric patients. Thus, we used voided urine to show that urine microbe-derived extracellular vesicles (EVs) in asthma are an available source for clinical research. METHODS: Five urine samples were obtained at 2–3-month intervals from each patient with asthma (n = 20), and a single voided urine sample were obtained from each healthy child (n = 20). After isolating EVs, 16S rDNA pyrosequencing was performed. The Chao1 index and principal coordinate analysis (PCoA) were used to assess diversity. To predict microbiota functional capacities, Phylogenetic Investigation of Communities by Reconstruction of Unobserved States was used based on the Kyoto Encyclopedia of Genes and Genomes pathway database. Eight covariates were included in the EnvFit analysis to identify significant factors in the asthma group. RESULTS: The asthma group showed lower Chao1 bacterial richness, and PCoA-based clustering differed significantly. Two phyla, and 13 families and genera were enriched or depleted. Functional profiling revealed significant differences between the asthma and control groups. EnvFit analysis of correlation to age, sex, body mass index, infection, season, asthma phenotype, severity, and symptoms was not significant except for infections associated with visit 1 and the season of visit 2. CONCLUSIONS: This study showed that microbe-derived EVs were constantly altered in the urine of children with asthma, consistent with the findings of previous studies indicating microbiome changes in the lung and gut. The urine may reflect the specific pattern of microbiome EVs in children with asthma.
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spelling pubmed-76808282021-01-01 Urine Microbe-Derived Extracellular Vesicles in Children With Asthma Lee, Yeong Seok Kim, Jeong Hee Lim, Dae Hyun Allergy Asthma Immunol Res Original Article PURPOSE: Several studies have found significant associations between asthma and microbiome. However, it is challenging to obtain-sputum and bronchoalveolar lavage samples from pediatric patients. Thus, we used voided urine to show that urine microbe-derived extracellular vesicles (EVs) in asthma are an available source for clinical research. METHODS: Five urine samples were obtained at 2–3-month intervals from each patient with asthma (n = 20), and a single voided urine sample were obtained from each healthy child (n = 20). After isolating EVs, 16S rDNA pyrosequencing was performed. The Chao1 index and principal coordinate analysis (PCoA) were used to assess diversity. To predict microbiota functional capacities, Phylogenetic Investigation of Communities by Reconstruction of Unobserved States was used based on the Kyoto Encyclopedia of Genes and Genomes pathway database. Eight covariates were included in the EnvFit analysis to identify significant factors in the asthma group. RESULTS: The asthma group showed lower Chao1 bacterial richness, and PCoA-based clustering differed significantly. Two phyla, and 13 families and genera were enriched or depleted. Functional profiling revealed significant differences between the asthma and control groups. EnvFit analysis of correlation to age, sex, body mass index, infection, season, asthma phenotype, severity, and symptoms was not significant except for infections associated with visit 1 and the season of visit 2. CONCLUSIONS: This study showed that microbe-derived EVs were constantly altered in the urine of children with asthma, consistent with the findings of previous studies indicating microbiome changes in the lung and gut. The urine may reflect the specific pattern of microbiome EVs in children with asthma. The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease 2020-08-31 /pmc/articles/PMC7680828/ /pubmed/33191678 http://dx.doi.org/10.4168/aair.2021.13.1.75 Text en Copyright © 2021 The Korean Academy of Asthma, Allergy and Clinical Immunology • The Korean Academy of Pediatric Allergy and Respiratory Disease https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Yeong Seok
Kim, Jeong Hee
Lim, Dae Hyun
Urine Microbe-Derived Extracellular Vesicles in Children With Asthma
title Urine Microbe-Derived Extracellular Vesicles in Children With Asthma
title_full Urine Microbe-Derived Extracellular Vesicles in Children With Asthma
title_fullStr Urine Microbe-Derived Extracellular Vesicles in Children With Asthma
title_full_unstemmed Urine Microbe-Derived Extracellular Vesicles in Children With Asthma
title_short Urine Microbe-Derived Extracellular Vesicles in Children With Asthma
title_sort urine microbe-derived extracellular vesicles in children with asthma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7680828/
https://www.ncbi.nlm.nih.gov/pubmed/33191678
http://dx.doi.org/10.4168/aair.2021.13.1.75
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