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The respiratory tract microbiome, the pathogen load, and clinical interventions define severity of bacterial pneumonia

Bacterial pneumonia is a considerable problem worldwide. Here, we follow the inter-kingdom respiratory tract microbiome (RTM) of a unique cohort of 38 hospitalized patients (n = 97 samples) with pneumonia caused by Legionella pneumophila. The RTM composition is characterized by diversity drops early...

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Autores principales: Pérez-Cobas, Ana Elena, Ginevra, Christophe, Rusniok, Christophe, Jarraud, Sophie, Buchrieser, Carmen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518590/
https://www.ncbi.nlm.nih.gov/pubmed/37633274
http://dx.doi.org/10.1016/j.xcrm.2023.101167
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author Pérez-Cobas, Ana Elena
Ginevra, Christophe
Rusniok, Christophe
Jarraud, Sophie
Buchrieser, Carmen
author_facet Pérez-Cobas, Ana Elena
Ginevra, Christophe
Rusniok, Christophe
Jarraud, Sophie
Buchrieser, Carmen
author_sort Pérez-Cobas, Ana Elena
collection PubMed
description Bacterial pneumonia is a considerable problem worldwide. Here, we follow the inter-kingdom respiratory tract microbiome (RTM) of a unique cohort of 38 hospitalized patients (n = 97 samples) with pneumonia caused by Legionella pneumophila. The RTM composition is characterized by diversity drops early in hospitalization and ecological species replacement. RTMs with the highest bacterial and fungal loads show low diversity and pathogen enrichment, suggesting high biomass as a biomarker for secondary and/or co-infections. The RTM structure is defined by a “commensal” cluster associated with a healthy RTM and a “pathogen” enriched one, suggesting that the cluster equilibrium drives the microbiome to recovery or dysbiosis. Legionella biomass correlates with disease severity and co-morbidities, while clinical interventions influence the RTM dynamics. Fungi, archaea, and protozoa seem to contribute to progress of pneumonia. Thus, the interplay of the RTM equilibrium, the pathogen load dynamics, and clinical interventions play a critical role in patient recovery.
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spelling pubmed-105185902023-09-26 The respiratory tract microbiome, the pathogen load, and clinical interventions define severity of bacterial pneumonia Pérez-Cobas, Ana Elena Ginevra, Christophe Rusniok, Christophe Jarraud, Sophie Buchrieser, Carmen Cell Rep Med Article Bacterial pneumonia is a considerable problem worldwide. Here, we follow the inter-kingdom respiratory tract microbiome (RTM) of a unique cohort of 38 hospitalized patients (n = 97 samples) with pneumonia caused by Legionella pneumophila. The RTM composition is characterized by diversity drops early in hospitalization and ecological species replacement. RTMs with the highest bacterial and fungal loads show low diversity and pathogen enrichment, suggesting high biomass as a biomarker for secondary and/or co-infections. The RTM structure is defined by a “commensal” cluster associated with a healthy RTM and a “pathogen” enriched one, suggesting that the cluster equilibrium drives the microbiome to recovery or dysbiosis. Legionella biomass correlates with disease severity and co-morbidities, while clinical interventions influence the RTM dynamics. Fungi, archaea, and protozoa seem to contribute to progress of pneumonia. Thus, the interplay of the RTM equilibrium, the pathogen load dynamics, and clinical interventions play a critical role in patient recovery. Elsevier 2023-08-25 /pmc/articles/PMC10518590/ /pubmed/37633274 http://dx.doi.org/10.1016/j.xcrm.2023.101167 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Pérez-Cobas, Ana Elena
Ginevra, Christophe
Rusniok, Christophe
Jarraud, Sophie
Buchrieser, Carmen
The respiratory tract microbiome, the pathogen load, and clinical interventions define severity of bacterial pneumonia
title The respiratory tract microbiome, the pathogen load, and clinical interventions define severity of bacterial pneumonia
title_full The respiratory tract microbiome, the pathogen load, and clinical interventions define severity of bacterial pneumonia
title_fullStr The respiratory tract microbiome, the pathogen load, and clinical interventions define severity of bacterial pneumonia
title_full_unstemmed The respiratory tract microbiome, the pathogen load, and clinical interventions define severity of bacterial pneumonia
title_short The respiratory tract microbiome, the pathogen load, and clinical interventions define severity of bacterial pneumonia
title_sort respiratory tract microbiome, the pathogen load, and clinical interventions define severity of bacterial pneumonia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518590/
https://www.ncbi.nlm.nih.gov/pubmed/37633274
http://dx.doi.org/10.1016/j.xcrm.2023.101167
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