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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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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. |
format | Online Article Text |
id | pubmed-6530040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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