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Niche, not phylogeny, governs the response to oxygen availability among diverse Pseudomonas aeruginosa strains
Pseudomonas aeruginosa, a ubiquitous opportunistic pathogen, is a leading cause of chronic infection of airways in cystic fibrosis (CF) patients. Chronic infections typically arise from colonization by environmental strains, followed by adaptation of P. aeruginosa to the conditions within the CF air...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428489/ https://www.ncbi.nlm.nih.gov/pubmed/36060748 http://dx.doi.org/10.3389/fmicb.2022.953964 |
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author | Shewaramani, Sonal Kassen, Rees |
author_facet | Shewaramani, Sonal Kassen, Rees |
author_sort | Shewaramani, Sonal |
collection | PubMed |
description | Pseudomonas aeruginosa, a ubiquitous opportunistic pathogen, is a leading cause of chronic infection of airways in cystic fibrosis (CF) patients. Chronic infections typically arise from colonization by environmental strains, followed by adaptation of P. aeruginosa to the conditions within the CF airway. It has been suggested that oxygen availability can be an important source of selection causing trait changes associated with the transition to chronic infection, but little data exist on the response of P. aeruginosa to varying levels of oxygen. Here, we use a diverse collection of P. aeruginosa strains recovered from both CF patients and environmental sources to evaluate the role of oxygen availability in driving adaptation to the CF lung while also accounting for phylogenetic relatedness. While we can detect a signal of phylogeny in trait responses to oxygen availability, niche of origin is a far stronger predictor. Specifically, strains isolated from the lungs of CF patients are more sensitive to external oxidative stress but more resistant to antibiotics under anoxic conditions. Additionally, many, though not all, patho-adaptive traits we assayed are insensitive to oxygen availability. Our results suggest that inferences about trait expression, especially those associated with the transition to chronic infection, depend on both the available oxygen and niche of origin of the strains being studied. |
format | Online Article Text |
id | pubmed-9428489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94284892022-09-01 Niche, not phylogeny, governs the response to oxygen availability among diverse Pseudomonas aeruginosa strains Shewaramani, Sonal Kassen, Rees Front Microbiol Microbiology Pseudomonas aeruginosa, a ubiquitous opportunistic pathogen, is a leading cause of chronic infection of airways in cystic fibrosis (CF) patients. Chronic infections typically arise from colonization by environmental strains, followed by adaptation of P. aeruginosa to the conditions within the CF airway. It has been suggested that oxygen availability can be an important source of selection causing trait changes associated with the transition to chronic infection, but little data exist on the response of P. aeruginosa to varying levels of oxygen. Here, we use a diverse collection of P. aeruginosa strains recovered from both CF patients and environmental sources to evaluate the role of oxygen availability in driving adaptation to the CF lung while also accounting for phylogenetic relatedness. While we can detect a signal of phylogeny in trait responses to oxygen availability, niche of origin is a far stronger predictor. Specifically, strains isolated from the lungs of CF patients are more sensitive to external oxidative stress but more resistant to antibiotics under anoxic conditions. Additionally, many, though not all, patho-adaptive traits we assayed are insensitive to oxygen availability. Our results suggest that inferences about trait expression, especially those associated with the transition to chronic infection, depend on both the available oxygen and niche of origin of the strains being studied. Frontiers Media S.A. 2022-08-17 /pmc/articles/PMC9428489/ /pubmed/36060748 http://dx.doi.org/10.3389/fmicb.2022.953964 Text en Copyright © 2022 Shewaramani and Kassen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Shewaramani, Sonal Kassen, Rees Niche, not phylogeny, governs the response to oxygen availability among diverse Pseudomonas aeruginosa strains |
title | Niche, not phylogeny, governs the response to oxygen availability among diverse Pseudomonas aeruginosa strains |
title_full | Niche, not phylogeny, governs the response to oxygen availability among diverse Pseudomonas aeruginosa strains |
title_fullStr | Niche, not phylogeny, governs the response to oxygen availability among diverse Pseudomonas aeruginosa strains |
title_full_unstemmed | Niche, not phylogeny, governs the response to oxygen availability among diverse Pseudomonas aeruginosa strains |
title_short | Niche, not phylogeny, governs the response to oxygen availability among diverse Pseudomonas aeruginosa strains |
title_sort | niche, not phylogeny, governs the response to oxygen availability among diverse pseudomonas aeruginosa strains |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428489/ https://www.ncbi.nlm.nih.gov/pubmed/36060748 http://dx.doi.org/10.3389/fmicb.2022.953964 |
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