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Repeated bronchoscopy in health and obstructive lung disease: is the airway microbiome stable?
OBJECTIVE: Little is known concerning the stability of the lower airway microbiome. We have compared the microbiota identified by repeated bronchoscopy in healthy subjects and patients with ostructive lung diseaseases (OLD). METHODS: 21 healthy controls and 41 patients with OLD completed two broncho...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8561866/ https://www.ncbi.nlm.nih.gov/pubmed/34727907 http://dx.doi.org/10.1186/s12890-021-01687-0 |
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author | Nielsen, Rune Xue, Yaxin Jonassen, Inge Haaland, Ingvild Kommedal, Øyvind Wiker, Harald G. Drengenes, Christine Bakke, Per S. Eagan, Tomas M. L. |
author_facet | Nielsen, Rune Xue, Yaxin Jonassen, Inge Haaland, Ingvild Kommedal, Øyvind Wiker, Harald G. Drengenes, Christine Bakke, Per S. Eagan, Tomas M. L. |
author_sort | Nielsen, Rune |
collection | PubMed |
description | OBJECTIVE: Little is known concerning the stability of the lower airway microbiome. We have compared the microbiota identified by repeated bronchoscopy in healthy subjects and patients with ostructive lung diseaseases (OLD). METHODS: 21 healthy controls and 41 patients with OLD completed two bronchoscopies. In addition to negative controls (NCS) and oral wash (OW) samples, we gathered protected bronchoalveolar lavage in two fractions (PBAL1 and PBAL2) and protected specimen brushes (PSB). After DNA extraction, we amplified the V3V4 region of the 16S rRNA gene, and performed paired-end sequencing (Illumina MiSeq). Initial bioinformatic processing was carried out in the QIIME-2 pipeline, identifying amplicon sequence variants (ASVs) with the DADA2 algorithm. Potentially contaminating ASVs were identified and removed using the decontam package in R and the sequenced NCS. RESULTS: A final table of 551 ASVs consisted of 19 × 10(6) sequences. Alpha diversity was lower in the second exam for OW samples, and borderline lower for PBAL1, with larger differences in subjects not having received intercurrent antibiotics. Permutational tests of beta diversity indicated that within-individual changes were significantly lower than between-individual changes. A non-parametric trend test showed that differences in composition between the two exams (beta diversity) were largest in the PSBs, and that these differences followed a pattern of PSB > PBAL2 > PBAL1 > OW. Time between procedures was not associated with increased diversity. CONCLUSION: The airways microbiota varied between examinations. However, there is compositional microbiota stability within a person, beyond that of chance, supporting the notion of a transient airways microbiota with a possibly more stable individual core microbiome. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12890-021-01687-0. |
format | Online Article Text |
id | pubmed-8561866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85618662021-11-03 Repeated bronchoscopy in health and obstructive lung disease: is the airway microbiome stable? Nielsen, Rune Xue, Yaxin Jonassen, Inge Haaland, Ingvild Kommedal, Øyvind Wiker, Harald G. Drengenes, Christine Bakke, Per S. Eagan, Tomas M. L. BMC Pulm Med Research OBJECTIVE: Little is known concerning the stability of the lower airway microbiome. We have compared the microbiota identified by repeated bronchoscopy in healthy subjects and patients with ostructive lung diseaseases (OLD). METHODS: 21 healthy controls and 41 patients with OLD completed two bronchoscopies. In addition to negative controls (NCS) and oral wash (OW) samples, we gathered protected bronchoalveolar lavage in two fractions (PBAL1 and PBAL2) and protected specimen brushes (PSB). After DNA extraction, we amplified the V3V4 region of the 16S rRNA gene, and performed paired-end sequencing (Illumina MiSeq). Initial bioinformatic processing was carried out in the QIIME-2 pipeline, identifying amplicon sequence variants (ASVs) with the DADA2 algorithm. Potentially contaminating ASVs were identified and removed using the decontam package in R and the sequenced NCS. RESULTS: A final table of 551 ASVs consisted of 19 × 10(6) sequences. Alpha diversity was lower in the second exam for OW samples, and borderline lower for PBAL1, with larger differences in subjects not having received intercurrent antibiotics. Permutational tests of beta diversity indicated that within-individual changes were significantly lower than between-individual changes. A non-parametric trend test showed that differences in composition between the two exams (beta diversity) were largest in the PSBs, and that these differences followed a pattern of PSB > PBAL2 > PBAL1 > OW. Time between procedures was not associated with increased diversity. CONCLUSION: The airways microbiota varied between examinations. However, there is compositional microbiota stability within a person, beyond that of chance, supporting the notion of a transient airways microbiota with a possibly more stable individual core microbiome. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12890-021-01687-0. BioMed Central 2021-11-02 /pmc/articles/PMC8561866/ /pubmed/34727907 http://dx.doi.org/10.1186/s12890-021-01687-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Nielsen, Rune Xue, Yaxin Jonassen, Inge Haaland, Ingvild Kommedal, Øyvind Wiker, Harald G. Drengenes, Christine Bakke, Per S. Eagan, Tomas M. L. Repeated bronchoscopy in health and obstructive lung disease: is the airway microbiome stable? |
title | Repeated bronchoscopy in health and obstructive lung disease: is the airway microbiome stable? |
title_full | Repeated bronchoscopy in health and obstructive lung disease: is the airway microbiome stable? |
title_fullStr | Repeated bronchoscopy in health and obstructive lung disease: is the airway microbiome stable? |
title_full_unstemmed | Repeated bronchoscopy in health and obstructive lung disease: is the airway microbiome stable? |
title_short | Repeated bronchoscopy in health and obstructive lung disease: is the airway microbiome stable? |
title_sort | repeated bronchoscopy in health and obstructive lung disease: is the airway microbiome stable? |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8561866/ https://www.ncbi.nlm.nih.gov/pubmed/34727907 http://dx.doi.org/10.1186/s12890-021-01687-0 |
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