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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
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.
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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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