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Disruption of the microbiota across multiple body sites in critically ill children

BACKGROUND: Despite intense interest in the links between the microbiome and human health, little has been written about dysbiosis among ICU patients. We characterized microbial diversity in samples from 37 children in a pediatric ICU (PICU). Standard measures of alpha and beta diversity were calcul...

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Autores principales: Rogers, Matthew B., Firek, Brian, Shi, Min, Yeh, Andrew, Brower-Sinning, Rachel, Aveson, Victoria, Kohl, Brittany L., Fabio, Anthony, Carcillo, Joseph A., Morowitz, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5200963/
https://www.ncbi.nlm.nih.gov/pubmed/28034303
http://dx.doi.org/10.1186/s40168-016-0211-0
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author Rogers, Matthew B.
Firek, Brian
Shi, Min
Yeh, Andrew
Brower-Sinning, Rachel
Aveson, Victoria
Kohl, Brittany L.
Fabio, Anthony
Carcillo, Joseph A.
Morowitz, Michael J.
author_facet Rogers, Matthew B.
Firek, Brian
Shi, Min
Yeh, Andrew
Brower-Sinning, Rachel
Aveson, Victoria
Kohl, Brittany L.
Fabio, Anthony
Carcillo, Joseph A.
Morowitz, Michael J.
author_sort Rogers, Matthew B.
collection PubMed
description BACKGROUND: Despite intense interest in the links between the microbiome and human health, little has been written about dysbiosis among ICU patients. We characterized microbial diversity in samples from 37 children in a pediatric ICU (PICU). Standard measures of alpha and beta diversity were calculated, and results were compared with data from adult and pediatric reference datasets. RESULTS: Bacterial 16S rRNA gene sequences were analyzed from 71 total tongue swabs, 50 skin swabs, and 77 stool samples or rectal swabs. The mean age of the PICU patients was 2.9 years (range 1–9 years), and many were chronically ill children that had previously been hospitalized in the PICU. Relative to healthy adults and children, alpha diversity was decreased in PICU GI and tongue but not skin samples. Measures of beta diversity indicated differences in community membership at each body site between PICU, adult, and pediatric groups. Taxonomic alterations in the PICU included enrichment of gut pathogens such as Enterococcus and Staphylococcus at multiple body sites and depletion of commensals such as Faecalibacterium and Ruminococcus from GI samples. Alpha and beta diversity were unstable over time in patients followed longitudinally. We observed the frequent presence of “dominant” pathogens in PICU samples at relative abundance >50%. PICU samples were characterized by loss of site specificity, with individual taxa commonly present simultaneously at three sample sites on a single individual. Some pathogens identified by culture of tracheal aspirates were commonly observed in skin samples from the same patient. CONCLUSIONS: We conclude that the microbiota in critically ill children differs sharply from the microbiota of healthy children and adults. Acknowledgement of dysbiosis associated with critical illness could provide opportunities to modulate the microbiota with precision and thereby improve patient outcomes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40168-016-0211-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-52009632016-12-30 Disruption of the microbiota across multiple body sites in critically ill children Rogers, Matthew B. Firek, Brian Shi, Min Yeh, Andrew Brower-Sinning, Rachel Aveson, Victoria Kohl, Brittany L. Fabio, Anthony Carcillo, Joseph A. Morowitz, Michael J. Microbiome Research BACKGROUND: Despite intense interest in the links between the microbiome and human health, little has been written about dysbiosis among ICU patients. We characterized microbial diversity in samples from 37 children in a pediatric ICU (PICU). Standard measures of alpha and beta diversity were calculated, and results were compared with data from adult and pediatric reference datasets. RESULTS: Bacterial 16S rRNA gene sequences were analyzed from 71 total tongue swabs, 50 skin swabs, and 77 stool samples or rectal swabs. The mean age of the PICU patients was 2.9 years (range 1–9 years), and many were chronically ill children that had previously been hospitalized in the PICU. Relative to healthy adults and children, alpha diversity was decreased in PICU GI and tongue but not skin samples. Measures of beta diversity indicated differences in community membership at each body site between PICU, adult, and pediatric groups. Taxonomic alterations in the PICU included enrichment of gut pathogens such as Enterococcus and Staphylococcus at multiple body sites and depletion of commensals such as Faecalibacterium and Ruminococcus from GI samples. Alpha and beta diversity were unstable over time in patients followed longitudinally. We observed the frequent presence of “dominant” pathogens in PICU samples at relative abundance >50%. PICU samples were characterized by loss of site specificity, with individual taxa commonly present simultaneously at three sample sites on a single individual. Some pathogens identified by culture of tracheal aspirates were commonly observed in skin samples from the same patient. CONCLUSIONS: We conclude that the microbiota in critically ill children differs sharply from the microbiota of healthy children and adults. Acknowledgement of dysbiosis associated with critical illness could provide opportunities to modulate the microbiota with precision and thereby improve patient outcomes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40168-016-0211-0) contains supplementary material, which is available to authorized users. BioMed Central 2016-12-29 /pmc/articles/PMC5200963/ /pubmed/28034303 http://dx.doi.org/10.1186/s40168-016-0211-0 Text en © The Author(s). 2016 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
Rogers, Matthew B.
Firek, Brian
Shi, Min
Yeh, Andrew
Brower-Sinning, Rachel
Aveson, Victoria
Kohl, Brittany L.
Fabio, Anthony
Carcillo, Joseph A.
Morowitz, Michael J.
Disruption of the microbiota across multiple body sites in critically ill children
title Disruption of the microbiota across multiple body sites in critically ill children
title_full Disruption of the microbiota across multiple body sites in critically ill children
title_fullStr Disruption of the microbiota across multiple body sites in critically ill children
title_full_unstemmed Disruption of the microbiota across multiple body sites in critically ill children
title_short Disruption of the microbiota across multiple body sites in critically ill children
title_sort disruption of the microbiota across multiple body sites in critically ill children
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5200963/
https://www.ncbi.nlm.nih.gov/pubmed/28034303
http://dx.doi.org/10.1186/s40168-016-0211-0
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