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Respiratory microbiome in mechanically ventilated patients: a narrative review

The respiratory microbiome has been less explored than the gut microbiome. Despite the speculated importance of dysbiosis of the microbiome in ventilator-associated pneumonia (VAP) and acute respiratory distress syndrome (ARDS), only few studies have been performed in invasively ventilated ICU patie...

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Autores principales: Fromentin, Mélanie, Ricard, Jean-Damien, Roux, Damien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7871139/
https://www.ncbi.nlm.nih.gov/pubmed/33559707
http://dx.doi.org/10.1007/s00134-020-06338-2
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author Fromentin, Mélanie
Ricard, Jean-Damien
Roux, Damien
author_facet Fromentin, Mélanie
Ricard, Jean-Damien
Roux, Damien
author_sort Fromentin, Mélanie
collection PubMed
description The respiratory microbiome has been less explored than the gut microbiome. Despite the speculated importance of dysbiosis of the microbiome in ventilator-associated pneumonia (VAP) and acute respiratory distress syndrome (ARDS), only few studies have been performed in invasively ventilated ICU patients. And only the results of small cohorts have been published. An overlap exists between bacterial populations observed in the lower respiratory tract and the oropharyngeal tract. The bacterial microbiota is characterized by relatively abundant bacteria difficult to cultivate by standard methods. Under mechanical ventilation, a dysbiosis occurs with a drop overtime in diversity. During VAP development, lung dysbiosis is characterized by a shift towards a dominant bacterial pathogen (mostly Proteobacteria) whereas enrichment of gut-associated bacteria mainly Enterobacteriaceae is the specific feature discriminating ARDS patients. However, the role of this dysbiosis in VAP and ARDS pathogenesis is not yet fully understood. A more in-depth analysis of the interplay between bacteria, virus and fungi and a better understanding of the host-microbiome interaction could provide a more comprehensive view of the role of the microbiome in VAP and ARDS pathogenesis. Priority should be given to validate a consensual and robust methodology for respiratory microbiome research and to conduct longitudinal studies. A deeper understanding of microbial interplay should be a valuable guide for care of ARDS and VAP preventive/therapeutic strategies. We present a review on the current knowledge and expose perspectives and potential clinical applications of respiratory microbiome research in mechanically ventilated patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00134-020-06338-2.
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spelling pubmed-78711392021-02-09 Respiratory microbiome in mechanically ventilated patients: a narrative review Fromentin, Mélanie Ricard, Jean-Damien Roux, Damien Intensive Care Med Review The respiratory microbiome has been less explored than the gut microbiome. Despite the speculated importance of dysbiosis of the microbiome in ventilator-associated pneumonia (VAP) and acute respiratory distress syndrome (ARDS), only few studies have been performed in invasively ventilated ICU patients. And only the results of small cohorts have been published. An overlap exists between bacterial populations observed in the lower respiratory tract and the oropharyngeal tract. The bacterial microbiota is characterized by relatively abundant bacteria difficult to cultivate by standard methods. Under mechanical ventilation, a dysbiosis occurs with a drop overtime in diversity. During VAP development, lung dysbiosis is characterized by a shift towards a dominant bacterial pathogen (mostly Proteobacteria) whereas enrichment of gut-associated bacteria mainly Enterobacteriaceae is the specific feature discriminating ARDS patients. However, the role of this dysbiosis in VAP and ARDS pathogenesis is not yet fully understood. A more in-depth analysis of the interplay between bacteria, virus and fungi and a better understanding of the host-microbiome interaction could provide a more comprehensive view of the role of the microbiome in VAP and ARDS pathogenesis. Priority should be given to validate a consensual and robust methodology for respiratory microbiome research and to conduct longitudinal studies. A deeper understanding of microbial interplay should be a valuable guide for care of ARDS and VAP preventive/therapeutic strategies. We present a review on the current knowledge and expose perspectives and potential clinical applications of respiratory microbiome research in mechanically ventilated patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00134-020-06338-2. Springer Berlin Heidelberg 2021-02-09 2021 /pmc/articles/PMC7871139/ /pubmed/33559707 http://dx.doi.org/10.1007/s00134-020-06338-2 Text en © Springer-Verlag GmbH Germany, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review
Fromentin, Mélanie
Ricard, Jean-Damien
Roux, Damien
Respiratory microbiome in mechanically ventilated patients: a narrative review
title Respiratory microbiome in mechanically ventilated patients: a narrative review
title_full Respiratory microbiome in mechanically ventilated patients: a narrative review
title_fullStr Respiratory microbiome in mechanically ventilated patients: a narrative review
title_full_unstemmed Respiratory microbiome in mechanically ventilated patients: a narrative review
title_short Respiratory microbiome in mechanically ventilated patients: a narrative review
title_sort respiratory microbiome in mechanically ventilated patients: a narrative review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7871139/
https://www.ncbi.nlm.nih.gov/pubmed/33559707
http://dx.doi.org/10.1007/s00134-020-06338-2
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