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Patterns in the longitudinal oropharyngeal microbiome evolution related to ventilator-associated pneumonia

BACKGROUND: The aim of the study was to evaluate the composition and the temporal evolution of the oropharyngeal microbiome in antibiotic-naïve patients requiring mechanical ventilation and to gain new insights into the pathogenesis of ventilator-associated pneumonia (VAP). METHODS: Prospective, obs...

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Autores principales: Sommerstein, Rami, Merz, Tobias M., Berger, Sabine, Kraemer, Julia G., Marschall, Jonas, Hilty, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6530040/
https://www.ncbi.nlm.nih.gov/pubmed/31139364
http://dx.doi.org/10.1186/s13756-019-0530-6
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author Sommerstein, Rami
Merz, Tobias M.
Berger, Sabine
Kraemer, Julia G.
Marschall, Jonas
Hilty, Markus
author_facet Sommerstein, Rami
Merz, Tobias M.
Berger, Sabine
Kraemer, Julia G.
Marschall, Jonas
Hilty, Markus
author_sort Sommerstein, Rami
collection PubMed
description BACKGROUND: The aim of the study was to evaluate the composition and the temporal evolution of the oropharyngeal microbiome in antibiotic-naïve patients requiring mechanical ventilation and to gain new insights into the pathogenesis of ventilator-associated pneumonia (VAP). METHODS: Prospective, observational single-center nested case-control study. Patients with acute critical illness and anticipated duration of mechanical ventilation > 4 days were eligible. We took oropharyngeal swabs (and if available, tracheal secretions) daily, starting at the day of intubation. The microbiota was characterized by 16S rRNA high-throughput sequencing and compared between patients developing VAP versus controls. RESULTS: Five patients developed VAP. In three patient the causative pathogens were Enterobacteriaceae and in two Haemophilus influenzae. Locally weighted polynomial regression suggested that the within diversity (=alpha) was lower in Enterobacteriaceae VAP patients between days two to five of mechanical ventilation when compared to controls. Detection of Enterobacteriaceae in the oropharynx occurred on day two of follow-up and consisted of a single operational taxonomic unit in 2/3 patients with enterobacterial VAP. CONCLUSIONS: In acutely-ill patients who developed enterobacterial VAP the causative pathogen gained access to the oropharynx early after starting mechanical ventilation and outgrew the commensal members of the microbiome. Whether a specific pattern of the oropharyngeal microbiome between days three to five of mechanical ventilation may predict VAP enterobacterial VAP has to be evaluated in further studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13756-019-0530-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-65300402019-05-28 Patterns in the longitudinal oropharyngeal microbiome evolution related to ventilator-associated pneumonia Sommerstein, Rami Merz, Tobias M. Berger, Sabine Kraemer, Julia G. Marschall, Jonas Hilty, Markus Antimicrob Resist Infect Control Research BACKGROUND: The aim of the study was to evaluate the composition and the temporal evolution of the oropharyngeal microbiome in antibiotic-naïve patients requiring mechanical ventilation and to gain new insights into the pathogenesis of ventilator-associated pneumonia (VAP). METHODS: Prospective, observational single-center nested case-control study. Patients with acute critical illness and anticipated duration of mechanical ventilation > 4 days were eligible. We took oropharyngeal swabs (and if available, tracheal secretions) daily, starting at the day of intubation. The microbiota was characterized by 16S rRNA high-throughput sequencing and compared between patients developing VAP versus controls. RESULTS: Five patients developed VAP. In three patient the causative pathogens were Enterobacteriaceae and in two Haemophilus influenzae. Locally weighted polynomial regression suggested that the within diversity (=alpha) was lower in Enterobacteriaceae VAP patients between days two to five of mechanical ventilation when compared to controls. Detection of Enterobacteriaceae in the oropharynx occurred on day two of follow-up and consisted of a single operational taxonomic unit in 2/3 patients with enterobacterial VAP. CONCLUSIONS: In acutely-ill patients who developed enterobacterial VAP the causative pathogen gained access to the oropharynx early after starting mechanical ventilation and outgrew the commensal members of the microbiome. Whether a specific pattern of the oropharyngeal microbiome between days three to five of mechanical ventilation may predict VAP enterobacterial VAP has to be evaluated in further studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13756-019-0530-6) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-22 /pmc/articles/PMC6530040/ /pubmed/31139364 http://dx.doi.org/10.1186/s13756-019-0530-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Sommerstein, Rami
Merz, Tobias M.
Berger, Sabine
Kraemer, Julia G.
Marschall, Jonas
Hilty, Markus
Patterns in the longitudinal oropharyngeal microbiome evolution related to ventilator-associated pneumonia
title Patterns in the longitudinal oropharyngeal microbiome evolution related to ventilator-associated pneumonia
title_full Patterns in the longitudinal oropharyngeal microbiome evolution related to ventilator-associated pneumonia
title_fullStr Patterns in the longitudinal oropharyngeal microbiome evolution related to ventilator-associated pneumonia
title_full_unstemmed Patterns in the longitudinal oropharyngeal microbiome evolution related to ventilator-associated pneumonia
title_short Patterns in the longitudinal oropharyngeal microbiome evolution related to ventilator-associated pneumonia
title_sort patterns in the longitudinal oropharyngeal microbiome evolution related to ventilator-associated pneumonia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6530040/
https://www.ncbi.nlm.nih.gov/pubmed/31139364
http://dx.doi.org/10.1186/s13756-019-0530-6
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