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The lung microbiome in patients with pneumocystosis

BACKROUND: Pneumocystis jirovecii pneumonia (PCP) is an opportunistic fungal infection that is associated with a high morbidity and mortality in immunocompromised individuals. In this study, we analysed the microbiome of the lower respiratory tract from critically ill intensive care unit patients wi...

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Autores principales: Kehrmann, J., Veckollari, B., Schmidt, D., Schildgen, O., Schildgen, V., Wagner, N., Zeschnigk, M., Klein-Hitpass, L., Witzke, O., Buer, J., Steinmann, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715545/
https://www.ncbi.nlm.nih.gov/pubmed/29202739
http://dx.doi.org/10.1186/s12890-017-0512-5
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author Kehrmann, J.
Veckollari, B.
Schmidt, D.
Schildgen, O.
Schildgen, V.
Wagner, N.
Zeschnigk, M.
Klein-Hitpass, L.
Witzke, O.
Buer, J.
Steinmann, J.
author_facet Kehrmann, J.
Veckollari, B.
Schmidt, D.
Schildgen, O.
Schildgen, V.
Wagner, N.
Zeschnigk, M.
Klein-Hitpass, L.
Witzke, O.
Buer, J.
Steinmann, J.
author_sort Kehrmann, J.
collection PubMed
description BACKROUND: Pneumocystis jirovecii pneumonia (PCP) is an opportunistic fungal infection that is associated with a high morbidity and mortality in immunocompromised individuals. In this study, we analysed the microbiome of the lower respiratory tract from critically ill intensive care unit patients with and without pneumocystosis. METHODS: Broncho-alveolar fluids from 65 intubated and mechanically ventilated intensive care unit patients (34 PCP+ and 31 PCP- patients) were collected. Sequence analysis of bacterial 16S rRNA gene V3/V4 regions was performed to study the composition of the respiratory microbiome using the Illumina MiSeq platform. RESULTS: Differences in the microbial composition detected between PCP+ and PCP- patients were not statistically significant on class, order, family and genus level. In addition, alpha and beta diversity metrics did not reveal significant differences between PCP+ and PCP- patients. The composition of the lung microbiota was highly variable between PCP+ patients and comparable in its variety with the microbiota composition of the heterogeneous collective of PCP- patients. CONCLUSIONS: The lower respiratory tract microbiome in patients with pneumocystosis does not appear to be determined by a specific microbial composition or to be dominated by a single bacterial species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12890-017-0512-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-57155452017-12-08 The lung microbiome in patients with pneumocystosis Kehrmann, J. Veckollari, B. Schmidt, D. Schildgen, O. Schildgen, V. Wagner, N. Zeschnigk, M. Klein-Hitpass, L. Witzke, O. Buer, J. Steinmann, J. BMC Pulm Med Research Article BACKROUND: Pneumocystis jirovecii pneumonia (PCP) is an opportunistic fungal infection that is associated with a high morbidity and mortality in immunocompromised individuals. In this study, we analysed the microbiome of the lower respiratory tract from critically ill intensive care unit patients with and without pneumocystosis. METHODS: Broncho-alveolar fluids from 65 intubated and mechanically ventilated intensive care unit patients (34 PCP+ and 31 PCP- patients) were collected. Sequence analysis of bacterial 16S rRNA gene V3/V4 regions was performed to study the composition of the respiratory microbiome using the Illumina MiSeq platform. RESULTS: Differences in the microbial composition detected between PCP+ and PCP- patients were not statistically significant on class, order, family and genus level. In addition, alpha and beta diversity metrics did not reveal significant differences between PCP+ and PCP- patients. The composition of the lung microbiota was highly variable between PCP+ patients and comparable in its variety with the microbiota composition of the heterogeneous collective of PCP- patients. CONCLUSIONS: The lower respiratory tract microbiome in patients with pneumocystosis does not appear to be determined by a specific microbial composition or to be dominated by a single bacterial species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12890-017-0512-5) contains supplementary material, which is available to authorized users. BioMed Central 2017-12-04 /pmc/articles/PMC5715545/ /pubmed/29202739 http://dx.doi.org/10.1186/s12890-017-0512-5 Text en © The Author(s). 2017 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
Kehrmann, J.
Veckollari, B.
Schmidt, D.
Schildgen, O.
Schildgen, V.
Wagner, N.
Zeschnigk, M.
Klein-Hitpass, L.
Witzke, O.
Buer, J.
Steinmann, J.
The lung microbiome in patients with pneumocystosis
title The lung microbiome in patients with pneumocystosis
title_full The lung microbiome in patients with pneumocystosis
title_fullStr The lung microbiome in patients with pneumocystosis
title_full_unstemmed The lung microbiome in patients with pneumocystosis
title_short The lung microbiome in patients with pneumocystosis
title_sort lung microbiome in patients with pneumocystosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715545/
https://www.ncbi.nlm.nih.gov/pubmed/29202739
http://dx.doi.org/10.1186/s12890-017-0512-5
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