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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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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. |
format | Online Article Text |
id | pubmed-10518590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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