Cargando…

Repeated sleep disruption in mice leads to persistent shifts in the fecal microbiome and metabolome

It has been established in recent years that the gut microbiome plays a role in health and disease, potentially via alterations in metabolites that influence host physiology. Although sleep disruption and gut dysbiosis have been associated with many of the same diseases, studies investigating the gu...

Descripción completa

Detalles Bibliográficos
Autores principales: Bowers, Samuel J., Vargas, Fernando, González, Antonio, He, Shannon, Jiang, Peng, Dorrestein, Pieter C., Knight, Rob, Wright, Kenneth P., Lowry, Christopher A., Fleshner, Monika, Vitaterna, Martha H., Turek, Fred W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7032712/
https://www.ncbi.nlm.nih.gov/pubmed/32078624
http://dx.doi.org/10.1371/journal.pone.0229001
_version_ 1783499552925417472
author Bowers, Samuel J.
Vargas, Fernando
González, Antonio
He, Shannon
Jiang, Peng
Dorrestein, Pieter C.
Knight, Rob
Wright, Kenneth P.
Lowry, Christopher A.
Fleshner, Monika
Vitaterna, Martha H.
Turek, Fred W.
author_facet Bowers, Samuel J.
Vargas, Fernando
González, Antonio
He, Shannon
Jiang, Peng
Dorrestein, Pieter C.
Knight, Rob
Wright, Kenneth P.
Lowry, Christopher A.
Fleshner, Monika
Vitaterna, Martha H.
Turek, Fred W.
author_sort Bowers, Samuel J.
collection PubMed
description It has been established in recent years that the gut microbiome plays a role in health and disease, potentially via alterations in metabolites that influence host physiology. Although sleep disruption and gut dysbiosis have been associated with many of the same diseases, studies investigating the gut microbiome in the context of sleep disruption have yielded inconsistent results, and have not assessed the fecal metabolome. We exposed mice to five days of sleep disruption followed by four days of ad libitum recovery sleep, and assessed the fecal microbiome and fecal metabolome at multiple timepoints using 16S rRNA gene amplicons and untargeted LC-MS/MS mass spectrometry. We found global shifts in both the microbiome and metabolome in the sleep-disrupted group on the second day of recovery sleep, when most sleep parameters had recovered to baseline levels. We observed an increase in the Firmicutes:Bacteroidetes ratio, along with decreases in the genus Lactobacillus, phylum Actinobacteria, and genus Bifidobacterium in sleep-disrupted mice compared to control mice. The latter two taxa remained low at the fourth day post-sleep disruption. We also identified multiple classes of fecal metabolites that were differentially abundant in sleep-disrupted mice, some of which are physiologically relevant and commonly influenced by the microbiome. This included bile acids, and inference of microbial functional gene content suggested reduced levels of the microbial bile salt hydrolase gene in sleep-disrupted mice. Overall, this study adds to the evidence base linking disrupted sleep to the gut microbiome and expands it to the fecal metabolome, identifying sleep disruption-sensitive bacterial taxa and classes of metabolites that may serve as therapeutic targets to improve health after poor sleep.
format Online
Article
Text
id pubmed-7032712
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-70327122020-02-27 Repeated sleep disruption in mice leads to persistent shifts in the fecal microbiome and metabolome Bowers, Samuel J. Vargas, Fernando González, Antonio He, Shannon Jiang, Peng Dorrestein, Pieter C. Knight, Rob Wright, Kenneth P. Lowry, Christopher A. Fleshner, Monika Vitaterna, Martha H. Turek, Fred W. PLoS One Research Article It has been established in recent years that the gut microbiome plays a role in health and disease, potentially via alterations in metabolites that influence host physiology. Although sleep disruption and gut dysbiosis have been associated with many of the same diseases, studies investigating the gut microbiome in the context of sleep disruption have yielded inconsistent results, and have not assessed the fecal metabolome. We exposed mice to five days of sleep disruption followed by four days of ad libitum recovery sleep, and assessed the fecal microbiome and fecal metabolome at multiple timepoints using 16S rRNA gene amplicons and untargeted LC-MS/MS mass spectrometry. We found global shifts in both the microbiome and metabolome in the sleep-disrupted group on the second day of recovery sleep, when most sleep parameters had recovered to baseline levels. We observed an increase in the Firmicutes:Bacteroidetes ratio, along with decreases in the genus Lactobacillus, phylum Actinobacteria, and genus Bifidobacterium in sleep-disrupted mice compared to control mice. The latter two taxa remained low at the fourth day post-sleep disruption. We also identified multiple classes of fecal metabolites that were differentially abundant in sleep-disrupted mice, some of which are physiologically relevant and commonly influenced by the microbiome. This included bile acids, and inference of microbial functional gene content suggested reduced levels of the microbial bile salt hydrolase gene in sleep-disrupted mice. Overall, this study adds to the evidence base linking disrupted sleep to the gut microbiome and expands it to the fecal metabolome, identifying sleep disruption-sensitive bacterial taxa and classes of metabolites that may serve as therapeutic targets to improve health after poor sleep. Public Library of Science 2020-02-20 /pmc/articles/PMC7032712/ /pubmed/32078624 http://dx.doi.org/10.1371/journal.pone.0229001 Text en © 2020 Bowers et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Bowers, Samuel J.
Vargas, Fernando
González, Antonio
He, Shannon
Jiang, Peng
Dorrestein, Pieter C.
Knight, Rob
Wright, Kenneth P.
Lowry, Christopher A.
Fleshner, Monika
Vitaterna, Martha H.
Turek, Fred W.
Repeated sleep disruption in mice leads to persistent shifts in the fecal microbiome and metabolome
title Repeated sleep disruption in mice leads to persistent shifts in the fecal microbiome and metabolome
title_full Repeated sleep disruption in mice leads to persistent shifts in the fecal microbiome and metabolome
title_fullStr Repeated sleep disruption in mice leads to persistent shifts in the fecal microbiome and metabolome
title_full_unstemmed Repeated sleep disruption in mice leads to persistent shifts in the fecal microbiome and metabolome
title_short Repeated sleep disruption in mice leads to persistent shifts in the fecal microbiome and metabolome
title_sort repeated sleep disruption in mice leads to persistent shifts in the fecal microbiome and metabolome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7032712/
https://www.ncbi.nlm.nih.gov/pubmed/32078624
http://dx.doi.org/10.1371/journal.pone.0229001
work_keys_str_mv AT bowerssamuelj repeatedsleepdisruptioninmiceleadstopersistentshiftsinthefecalmicrobiomeandmetabolome
AT vargasfernando repeatedsleepdisruptioninmiceleadstopersistentshiftsinthefecalmicrobiomeandmetabolome
AT gonzalezantonio repeatedsleepdisruptioninmiceleadstopersistentshiftsinthefecalmicrobiomeandmetabolome
AT heshannon repeatedsleepdisruptioninmiceleadstopersistentshiftsinthefecalmicrobiomeandmetabolome
AT jiangpeng repeatedsleepdisruptioninmiceleadstopersistentshiftsinthefecalmicrobiomeandmetabolome
AT dorresteinpieterc repeatedsleepdisruptioninmiceleadstopersistentshiftsinthefecalmicrobiomeandmetabolome
AT knightrob repeatedsleepdisruptioninmiceleadstopersistentshiftsinthefecalmicrobiomeandmetabolome
AT wrightkennethp repeatedsleepdisruptioninmiceleadstopersistentshiftsinthefecalmicrobiomeandmetabolome
AT lowrychristophera repeatedsleepdisruptioninmiceleadstopersistentshiftsinthefecalmicrobiomeandmetabolome
AT fleshnermonika repeatedsleepdisruptioninmiceleadstopersistentshiftsinthefecalmicrobiomeandmetabolome
AT vitaternamarthah repeatedsleepdisruptioninmiceleadstopersistentshiftsinthefecalmicrobiomeandmetabolome
AT turekfredw repeatedsleepdisruptioninmiceleadstopersistentshiftsinthefecalmicrobiomeandmetabolome