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Supplemental Oxygen Alters the Airway Microbiome in Cystic Fibrosis
Features of the airway microbiome in persons with cystic fibrosis (pwCF) are correlated with disease progression. Microbes have traditionally been classified for their ability to tolerate oxygen. It is unknown whether supplemental oxygen, a common medical intervention, affects the airway microbiome...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9601246/ https://www.ncbi.nlm.nih.gov/pubmed/36000724 http://dx.doi.org/10.1128/msystems.00364-22 |
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author | Vieira, Jacob Jesudasen, Sirus Bringhurst, Lindsay Sui, Hui-Yu McIver, Lauren Whiteson, Katrine Hanselmann, Kurt O’Toole, George A. Richards, Christopher J. Sicilian, Leonard Neuringer, Isabel Lai, Peggy S. |
author_facet | Vieira, Jacob Jesudasen, Sirus Bringhurst, Lindsay Sui, Hui-Yu McIver, Lauren Whiteson, Katrine Hanselmann, Kurt O’Toole, George A. Richards, Christopher J. Sicilian, Leonard Neuringer, Isabel Lai, Peggy S. |
author_sort | Vieira, Jacob |
collection | PubMed |
description | Features of the airway microbiome in persons with cystic fibrosis (pwCF) are correlated with disease progression. Microbes have traditionally been classified for their ability to tolerate oxygen. It is unknown whether supplemental oxygen, a common medical intervention, affects the airway microbiome of pwCF. We hypothesized that hyperoxia significantly impacts the pulmonary microbiome in cystic fibrosis. In this study, we cultured spontaneously expectorated sputum from pwCF in artificial sputum medium under 21%, 50%, and 100% oxygen conditions using a previously validated model system that recapitulates microbial community composition in uncultured sputum. Culture aliquots taken at 24, 48, and 72 h, along with uncultured sputum, underwent shotgun metagenomic sequencing with absolute abundance values obtained with the use of spike-in bacteria. Raw sequencing files were processed using the bioBakery pipeline to determine changes in taxonomy, predicted function, antimicrobial resistance genes, and mobile genetic elements. Hyperoxia reduced absolute microbial load, species richness, and diversity. Hyperoxia reduced absolute abundance of specific microbes, including facultative anaerobes such as Rothia and some Streptococcus species, with minimal impact on canonical CF pathogens such as Pseudomonas aeruginosa and Staphylococcus aureus. The effect size of hyperoxia on predicted functional pathways was stronger than that on taxonomy. Large changes in microbial cooccurrence networks were noted. Hyperoxia exposure perturbs airway microbial communities in a manner well tolerated by key pathogens. Supplemental oxygen use may enable the growth of lung pathogens and should be further studied in the clinical setting. IMPORTANCE The airway microbiome in persons with cystic fibrosis (pwCF) is correlated with lung function and disease severity. Supplemental oxygen use is common in more advanced CF, yet its role in perturbing airway microbial communities is unknown. By culturing sputum samples from pwCF under normal and elevated oxygen conditions, we found that increased oxygen led to reduced total numbers and diversity of microbes, with relative sparing of common CF pathogens such as Pseudomonas aeruginosa and Staphylococcus aureus. Supplemental oxygen use may enable the growth of lung pathogens and should be further studied in the clinical setting. |
format | Online Article Text |
id | pubmed-9601246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-96012462022-10-27 Supplemental Oxygen Alters the Airway Microbiome in Cystic Fibrosis Vieira, Jacob Jesudasen, Sirus Bringhurst, Lindsay Sui, Hui-Yu McIver, Lauren Whiteson, Katrine Hanselmann, Kurt O’Toole, George A. Richards, Christopher J. Sicilian, Leonard Neuringer, Isabel Lai, Peggy S. mSystems Research Article Features of the airway microbiome in persons with cystic fibrosis (pwCF) are correlated with disease progression. Microbes have traditionally been classified for their ability to tolerate oxygen. It is unknown whether supplemental oxygen, a common medical intervention, affects the airway microbiome of pwCF. We hypothesized that hyperoxia significantly impacts the pulmonary microbiome in cystic fibrosis. In this study, we cultured spontaneously expectorated sputum from pwCF in artificial sputum medium under 21%, 50%, and 100% oxygen conditions using a previously validated model system that recapitulates microbial community composition in uncultured sputum. Culture aliquots taken at 24, 48, and 72 h, along with uncultured sputum, underwent shotgun metagenomic sequencing with absolute abundance values obtained with the use of spike-in bacteria. Raw sequencing files were processed using the bioBakery pipeline to determine changes in taxonomy, predicted function, antimicrobial resistance genes, and mobile genetic elements. Hyperoxia reduced absolute microbial load, species richness, and diversity. Hyperoxia reduced absolute abundance of specific microbes, including facultative anaerobes such as Rothia and some Streptococcus species, with minimal impact on canonical CF pathogens such as Pseudomonas aeruginosa and Staphylococcus aureus. The effect size of hyperoxia on predicted functional pathways was stronger than that on taxonomy. Large changes in microbial cooccurrence networks were noted. Hyperoxia exposure perturbs airway microbial communities in a manner well tolerated by key pathogens. Supplemental oxygen use may enable the growth of lung pathogens and should be further studied in the clinical setting. IMPORTANCE The airway microbiome in persons with cystic fibrosis (pwCF) is correlated with lung function and disease severity. Supplemental oxygen use is common in more advanced CF, yet its role in perturbing airway microbial communities is unknown. By culturing sputum samples from pwCF under normal and elevated oxygen conditions, we found that increased oxygen led to reduced total numbers and diversity of microbes, with relative sparing of common CF pathogens such as Pseudomonas aeruginosa and Staphylococcus aureus. Supplemental oxygen use may enable the growth of lung pathogens and should be further studied in the clinical setting. American Society for Microbiology 2022-08-24 /pmc/articles/PMC9601246/ /pubmed/36000724 http://dx.doi.org/10.1128/msystems.00364-22 Text en Copyright © 2022 Vieira et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Vieira, Jacob Jesudasen, Sirus Bringhurst, Lindsay Sui, Hui-Yu McIver, Lauren Whiteson, Katrine Hanselmann, Kurt O’Toole, George A. Richards, Christopher J. Sicilian, Leonard Neuringer, Isabel Lai, Peggy S. Supplemental Oxygen Alters the Airway Microbiome in Cystic Fibrosis |
title | Supplemental Oxygen Alters the Airway Microbiome in Cystic Fibrosis |
title_full | Supplemental Oxygen Alters the Airway Microbiome in Cystic Fibrosis |
title_fullStr | Supplemental Oxygen Alters the Airway Microbiome in Cystic Fibrosis |
title_full_unstemmed | Supplemental Oxygen Alters the Airway Microbiome in Cystic Fibrosis |
title_short | Supplemental Oxygen Alters the Airway Microbiome in Cystic Fibrosis |
title_sort | supplemental oxygen alters the airway microbiome in cystic fibrosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9601246/ https://www.ncbi.nlm.nih.gov/pubmed/36000724 http://dx.doi.org/10.1128/msystems.00364-22 |
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