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Immunometabolites Drive Bacterial Adaptation to the Airway

Pseudomonas aeruginosa and Staphylococcus aureus are both opportunistic pathogens that are frequently associated with chronic lung infections. While bacterial virulence determinants are critical in initiating infection, the metabolic flexibility of these bacteria promotes their persistence in the ai...

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Autores principales: Tomlinson, Kira L., Prince, Alice S., Wong Fok Lung, Tania
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8656696/
https://www.ncbi.nlm.nih.gov/pubmed/34899759
http://dx.doi.org/10.3389/fimmu.2021.790574
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author Tomlinson, Kira L.
Prince, Alice S.
Wong Fok Lung, Tania
author_facet Tomlinson, Kira L.
Prince, Alice S.
Wong Fok Lung, Tania
author_sort Tomlinson, Kira L.
collection PubMed
description Pseudomonas aeruginosa and Staphylococcus aureus are both opportunistic pathogens that are frequently associated with chronic lung infections. While bacterial virulence determinants are critical in initiating infection, the metabolic flexibility of these bacteria promotes their persistence in the airway. Upon infection, these pathogens induce host immunometabolic reprogramming, resulting in an airway milieu replete with immune-signaling metabolites. These metabolites are often toxic to the bacteria and create a steep selection pressure for the emergence of bacterial isolates adapted for long-term survival in the inflamed lung. In this review, we discuss the main differences in the host immunometabolic response to P. aeruginosa and S. aureus, as well as how these pathogens alter their own metabolism to adapt to airway metabolites and cause persistent lung infections.
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spelling pubmed-86566962021-12-10 Immunometabolites Drive Bacterial Adaptation to the Airway Tomlinson, Kira L. Prince, Alice S. Wong Fok Lung, Tania Front Immunol Immunology Pseudomonas aeruginosa and Staphylococcus aureus are both opportunistic pathogens that are frequently associated with chronic lung infections. While bacterial virulence determinants are critical in initiating infection, the metabolic flexibility of these bacteria promotes their persistence in the airway. Upon infection, these pathogens induce host immunometabolic reprogramming, resulting in an airway milieu replete with immune-signaling metabolites. These metabolites are often toxic to the bacteria and create a steep selection pressure for the emergence of bacterial isolates adapted for long-term survival in the inflamed lung. In this review, we discuss the main differences in the host immunometabolic response to P. aeruginosa and S. aureus, as well as how these pathogens alter their own metabolism to adapt to airway metabolites and cause persistent lung infections. Frontiers Media S.A. 2021-11-25 /pmc/articles/PMC8656696/ /pubmed/34899759 http://dx.doi.org/10.3389/fimmu.2021.790574 Text en Copyright © 2021 Tomlinson, Prince and Wong Fok Lung 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 Immunology
Tomlinson, Kira L.
Prince, Alice S.
Wong Fok Lung, Tania
Immunometabolites Drive Bacterial Adaptation to the Airway
title Immunometabolites Drive Bacterial Adaptation to the Airway
title_full Immunometabolites Drive Bacterial Adaptation to the Airway
title_fullStr Immunometabolites Drive Bacterial Adaptation to the Airway
title_full_unstemmed Immunometabolites Drive Bacterial Adaptation to the Airway
title_short Immunometabolites Drive Bacterial Adaptation to the Airway
title_sort immunometabolites drive bacterial adaptation to the airway
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8656696/
https://www.ncbi.nlm.nih.gov/pubmed/34899759
http://dx.doi.org/10.3389/fimmu.2021.790574
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