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Dynamics of microbiota during mechanical ventilation in aspiration pneumonia

BACKGROUND: The emergence of multi-drug resistant pathogens is an urgent health-related problem, and the appropriate use of antibiotics is imperative. It is often difficult to identify the causative bacteria in patients with aspiration pneumonia because tracheal aspirate contains contaminants of ora...

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Autores principales: Otsuji, Ken, Fukuda, Kazumasa, Ogawa, Midori, Fujino, Yoshihisa, Kamochi, Masayuki, Saito, Mitsumasa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929358/
https://www.ncbi.nlm.nih.gov/pubmed/31870355
http://dx.doi.org/10.1186/s12890-019-1021-5
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author Otsuji, Ken
Fukuda, Kazumasa
Ogawa, Midori
Fujino, Yoshihisa
Kamochi, Masayuki
Saito, Mitsumasa
author_facet Otsuji, Ken
Fukuda, Kazumasa
Ogawa, Midori
Fujino, Yoshihisa
Kamochi, Masayuki
Saito, Mitsumasa
author_sort Otsuji, Ken
collection PubMed
description BACKGROUND: The emergence of multi-drug resistant pathogens is an urgent health-related problem, and the appropriate use of antibiotics is imperative. It is often difficult to identify the causative bacteria in patients with aspiration pneumonia because tracheal aspirate contains contaminants of oral bacteria. We investigated the dynamics of microbiota in mechanically ventilated patients with aspiration pneumonia to develop a treatment strategy. METHODS: Twenty-two intubated patients with aspiration pneumonia were recruited. Saliva and tracheal aspirate of the subjects were collected at three time points: (A) within 2 h after intubation, (B) just before administration of antibiotics, and (C) 48-72 h after administration of antibiotics. The microbiota in each specimen was analyzed by using the 16S rRNA gene clone library sequencing method. Bacterial floras of the samples were analyzed by principal component analysis. RESULTS: Principal component analysis based on the composition of genus revealed that although the changes of microbiota in the saliva from (A) to (B) were not clear, the composition of anaerobes in the tracheal aspirate (B) was lower than (A). In fact, the reduction of anaerobes, not in the saliva but in the tracheal aspirate from (A) to (B), was confirmed by incident rate ratios estimated by a multilevel Poisson regression model (p < 0.001). The extent of decrease in anaerobes was fully dependent on the time difference between the sampling of tracheal aspirate (A) and (B)—in particular, over 3 h of mechanical ventilation. This indicates that the alterations of microbiota (involving the reduction of anaerobes in the lower respiratory tract) occurred during mechanical ventilation prior to the administration of antibiotics. After the administration of antibiotics, Enterobacter spp., Corynebacterium spp., Pseudomonas aeruginosa, Klebsiella pneumoniae, Staphylococcus aureus, and Granulicatera adiacens were predominantly detected in the tracheal aspirate (C). CONCLUSION: The microbiota of the lower respiratory tract changes dynamically during mechanical ventilation and during the administration of antibiotics in intubated patients with aspiration pneumonia. Antibiotics should be selected on the premise that dynamic changes in microbiota (involved in the reduction of anaerobes) may occur during the mechanical ventilation in these patients.
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spelling pubmed-69293582019-12-30 Dynamics of microbiota during mechanical ventilation in aspiration pneumonia Otsuji, Ken Fukuda, Kazumasa Ogawa, Midori Fujino, Yoshihisa Kamochi, Masayuki Saito, Mitsumasa BMC Pulm Med Research Article BACKGROUND: The emergence of multi-drug resistant pathogens is an urgent health-related problem, and the appropriate use of antibiotics is imperative. It is often difficult to identify the causative bacteria in patients with aspiration pneumonia because tracheal aspirate contains contaminants of oral bacteria. We investigated the dynamics of microbiota in mechanically ventilated patients with aspiration pneumonia to develop a treatment strategy. METHODS: Twenty-two intubated patients with aspiration pneumonia were recruited. Saliva and tracheal aspirate of the subjects were collected at three time points: (A) within 2 h after intubation, (B) just before administration of antibiotics, and (C) 48-72 h after administration of antibiotics. The microbiota in each specimen was analyzed by using the 16S rRNA gene clone library sequencing method. Bacterial floras of the samples were analyzed by principal component analysis. RESULTS: Principal component analysis based on the composition of genus revealed that although the changes of microbiota in the saliva from (A) to (B) were not clear, the composition of anaerobes in the tracheal aspirate (B) was lower than (A). In fact, the reduction of anaerobes, not in the saliva but in the tracheal aspirate from (A) to (B), was confirmed by incident rate ratios estimated by a multilevel Poisson regression model (p < 0.001). The extent of decrease in anaerobes was fully dependent on the time difference between the sampling of tracheal aspirate (A) and (B)—in particular, over 3 h of mechanical ventilation. This indicates that the alterations of microbiota (involving the reduction of anaerobes in the lower respiratory tract) occurred during mechanical ventilation prior to the administration of antibiotics. After the administration of antibiotics, Enterobacter spp., Corynebacterium spp., Pseudomonas aeruginosa, Klebsiella pneumoniae, Staphylococcus aureus, and Granulicatera adiacens were predominantly detected in the tracheal aspirate (C). CONCLUSION: The microbiota of the lower respiratory tract changes dynamically during mechanical ventilation and during the administration of antibiotics in intubated patients with aspiration pneumonia. Antibiotics should be selected on the premise that dynamic changes in microbiota (involved in the reduction of anaerobes) may occur during the mechanical ventilation in these patients. BioMed Central 2019-12-23 /pmc/articles/PMC6929358/ /pubmed/31870355 http://dx.doi.org/10.1186/s12890-019-1021-5 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 Article
Otsuji, Ken
Fukuda, Kazumasa
Ogawa, Midori
Fujino, Yoshihisa
Kamochi, Masayuki
Saito, Mitsumasa
Dynamics of microbiota during mechanical ventilation in aspiration pneumonia
title Dynamics of microbiota during mechanical ventilation in aspiration pneumonia
title_full Dynamics of microbiota during mechanical ventilation in aspiration pneumonia
title_fullStr Dynamics of microbiota during mechanical ventilation in aspiration pneumonia
title_full_unstemmed Dynamics of microbiota during mechanical ventilation in aspiration pneumonia
title_short Dynamics of microbiota during mechanical ventilation in aspiration pneumonia
title_sort dynamics of microbiota during mechanical ventilation in aspiration pneumonia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929358/
https://www.ncbi.nlm.nih.gov/pubmed/31870355
http://dx.doi.org/10.1186/s12890-019-1021-5
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