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Infant airway microbiota and topical immune perturbations in the origins of childhood asthma
Asthma is believed to arise through early life aberrant immune development in response to environmental exposures that may influence the airway microbiota. Here, we examine the airway microbiota during the first three months of life by 16S rRNA gene amplicon sequencing in the population-based Copenh...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825176/ https://www.ncbi.nlm.nih.gov/pubmed/31676759 http://dx.doi.org/10.1038/s41467-019-12989-7 |
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author | Thorsen, Jonathan Rasmussen, Morten A. Waage, Johannes Mortensen, Martin Brejnrod, Asker Bønnelykke, Klaus Chawes, Bo L. Brix, Susanne Sørensen, Søren J. Stokholm, Jakob Bisgaard, Hans |
author_facet | Thorsen, Jonathan Rasmussen, Morten A. Waage, Johannes Mortensen, Martin Brejnrod, Asker Bønnelykke, Klaus Chawes, Bo L. Brix, Susanne Sørensen, Søren J. Stokholm, Jakob Bisgaard, Hans |
author_sort | Thorsen, Jonathan |
collection | PubMed |
description | Asthma is believed to arise through early life aberrant immune development in response to environmental exposures that may influence the airway microbiota. Here, we examine the airway microbiota during the first three months of life by 16S rRNA gene amplicon sequencing in the population-based Copenhagen Prospective Studies on Asthma in Childhood 2010 (COPSAC(2010)) cohort consisting of 700 children monitored for the development of asthma since birth. Microbial diversity and the relative abundances of Veillonella and Prevotella in the airways at age one month are associated with asthma by age 6 years, both individually and with additional taxa in a multivariable model. Higher relative abundance of these bacteria is furthermore associated with an airway immune profile dominated by reduced TNF-α and IL-1β and increased CCL2 and CCL17, which itself is an independent predictor for asthma. These findings suggest a mechanism of microbiota-immune interactions in early infancy that predisposes to childhood asthma. |
format | Online Article Text |
id | pubmed-6825176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68251762019-11-04 Infant airway microbiota and topical immune perturbations in the origins of childhood asthma Thorsen, Jonathan Rasmussen, Morten A. Waage, Johannes Mortensen, Martin Brejnrod, Asker Bønnelykke, Klaus Chawes, Bo L. Brix, Susanne Sørensen, Søren J. Stokholm, Jakob Bisgaard, Hans Nat Commun Article Asthma is believed to arise through early life aberrant immune development in response to environmental exposures that may influence the airway microbiota. Here, we examine the airway microbiota during the first three months of life by 16S rRNA gene amplicon sequencing in the population-based Copenhagen Prospective Studies on Asthma in Childhood 2010 (COPSAC(2010)) cohort consisting of 700 children monitored for the development of asthma since birth. Microbial diversity and the relative abundances of Veillonella and Prevotella in the airways at age one month are associated with asthma by age 6 years, both individually and with additional taxa in a multivariable model. Higher relative abundance of these bacteria is furthermore associated with an airway immune profile dominated by reduced TNF-α and IL-1β and increased CCL2 and CCL17, which itself is an independent predictor for asthma. These findings suggest a mechanism of microbiota-immune interactions in early infancy that predisposes to childhood asthma. Nature Publishing Group UK 2019-11-01 /pmc/articles/PMC6825176/ /pubmed/31676759 http://dx.doi.org/10.1038/s41467-019-12989-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Thorsen, Jonathan Rasmussen, Morten A. Waage, Johannes Mortensen, Martin Brejnrod, Asker Bønnelykke, Klaus Chawes, Bo L. Brix, Susanne Sørensen, Søren J. Stokholm, Jakob Bisgaard, Hans Infant airway microbiota and topical immune perturbations in the origins of childhood asthma |
title | Infant airway microbiota and topical immune perturbations in the origins of childhood asthma |
title_full | Infant airway microbiota and topical immune perturbations in the origins of childhood asthma |
title_fullStr | Infant airway microbiota and topical immune perturbations in the origins of childhood asthma |
title_full_unstemmed | Infant airway microbiota and topical immune perturbations in the origins of childhood asthma |
title_short | Infant airway microbiota and topical immune perturbations in the origins of childhood asthma |
title_sort | infant airway microbiota and topical immune perturbations in the origins of childhood asthma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825176/ https://www.ncbi.nlm.nih.gov/pubmed/31676759 http://dx.doi.org/10.1038/s41467-019-12989-7 |
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