Cargando…

Dynamics of the Microbiota in Response to Host Infection

Longitudinal studies of the microbiota are important for discovering changes in microbial communities that affect the host. The complexity of these ecosystems requires rigorous integrated experimental and computational methods to identify temporal signatures that promote physiologic or pathophysiolo...

Descripción completa

Detalles Bibliográficos
Autores principales: Belzer, Clara, Gerber, Georg K., Roeselers, Guus, Delaney, Mary, DuBois, Andrea, Liu, Qing, Belavusava, Vera, Yeliseyev, Vladimir, Houseman, Andres, Onderdonk, Andrew, Cavanaugh, Colleen, Bry, Lynn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4094490/
https://www.ncbi.nlm.nih.gov/pubmed/25014551
http://dx.doi.org/10.1371/journal.pone.0095534
_version_ 1782325838118649856
author Belzer, Clara
Gerber, Georg K.
Roeselers, Guus
Delaney, Mary
DuBois, Andrea
Liu, Qing
Belavusava, Vera
Yeliseyev, Vladimir
Houseman, Andres
Onderdonk, Andrew
Cavanaugh, Colleen
Bry, Lynn
author_facet Belzer, Clara
Gerber, Georg K.
Roeselers, Guus
Delaney, Mary
DuBois, Andrea
Liu, Qing
Belavusava, Vera
Yeliseyev, Vladimir
Houseman, Andres
Onderdonk, Andrew
Cavanaugh, Colleen
Bry, Lynn
author_sort Belzer, Clara
collection PubMed
description Longitudinal studies of the microbiota are important for discovering changes in microbial communities that affect the host. The complexity of these ecosystems requires rigorous integrated experimental and computational methods to identify temporal signatures that promote physiologic or pathophysiologic responses in vivo. Employing a murine model of infectious colitis with the pathogen Citrobacter rodentium, we generated a 2-month time-series of 16S rDNA gene profiles, and quantitatively cultured commensals, from multiple intestinal sites in infected and uninfected mice. We developed a computational framework to discover time-varying signatures for individual taxa, and to automatically group signatures to identify microbial sub-communities within the larger gut ecosystem that demonstrate common behaviors. Application of this model to the 16S rDNA dataset revealed dynamic alterations in the microbiota at multiple levels of resolution, from effects on systems-level metrics to changes across anatomic sites for individual taxa and species. These analyses revealed unique, time-dependent microbial signatures associated with host responses at different stages of colitis. Signatures included a Mucispirillum OTU associated with early disruption of the colonic surface mucus layer, prior to the onset of symptomatic colitis, and members of the Clostridiales and Lactobacillales that increased with successful resolution of inflammation, after clearance of the pathogen. Quantitative culture data validated findings for predominant species, further refining and strengthening model predictions. These findings provide new insights into the complex behaviors found within host ecosystems, and define several time-dependent microbial signatures that may be leveraged in studies of other infectious or inflammatory conditions.
format Online
Article
Text
id pubmed-4094490
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-40944902014-07-15 Dynamics of the Microbiota in Response to Host Infection Belzer, Clara Gerber, Georg K. Roeselers, Guus Delaney, Mary DuBois, Andrea Liu, Qing Belavusava, Vera Yeliseyev, Vladimir Houseman, Andres Onderdonk, Andrew Cavanaugh, Colleen Bry, Lynn PLoS One Research Article Longitudinal studies of the microbiota are important for discovering changes in microbial communities that affect the host. The complexity of these ecosystems requires rigorous integrated experimental and computational methods to identify temporal signatures that promote physiologic or pathophysiologic responses in vivo. Employing a murine model of infectious colitis with the pathogen Citrobacter rodentium, we generated a 2-month time-series of 16S rDNA gene profiles, and quantitatively cultured commensals, from multiple intestinal sites in infected and uninfected mice. We developed a computational framework to discover time-varying signatures for individual taxa, and to automatically group signatures to identify microbial sub-communities within the larger gut ecosystem that demonstrate common behaviors. Application of this model to the 16S rDNA dataset revealed dynamic alterations in the microbiota at multiple levels of resolution, from effects on systems-level metrics to changes across anatomic sites for individual taxa and species. These analyses revealed unique, time-dependent microbial signatures associated with host responses at different stages of colitis. Signatures included a Mucispirillum OTU associated with early disruption of the colonic surface mucus layer, prior to the onset of symptomatic colitis, and members of the Clostridiales and Lactobacillales that increased with successful resolution of inflammation, after clearance of the pathogen. Quantitative culture data validated findings for predominant species, further refining and strengthening model predictions. These findings provide new insights into the complex behaviors found within host ecosystems, and define several time-dependent microbial signatures that may be leveraged in studies of other infectious or inflammatory conditions. Public Library of Science 2014-07-11 /pmc/articles/PMC4094490/ /pubmed/25014551 http://dx.doi.org/10.1371/journal.pone.0095534 Text en © 2014 Belzer 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Belzer, Clara
Gerber, Georg K.
Roeselers, Guus
Delaney, Mary
DuBois, Andrea
Liu, Qing
Belavusava, Vera
Yeliseyev, Vladimir
Houseman, Andres
Onderdonk, Andrew
Cavanaugh, Colleen
Bry, Lynn
Dynamics of the Microbiota in Response to Host Infection
title Dynamics of the Microbiota in Response to Host Infection
title_full Dynamics of the Microbiota in Response to Host Infection
title_fullStr Dynamics of the Microbiota in Response to Host Infection
title_full_unstemmed Dynamics of the Microbiota in Response to Host Infection
title_short Dynamics of the Microbiota in Response to Host Infection
title_sort dynamics of the microbiota in response to host infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4094490/
https://www.ncbi.nlm.nih.gov/pubmed/25014551
http://dx.doi.org/10.1371/journal.pone.0095534
work_keys_str_mv AT belzerclara dynamicsofthemicrobiotainresponsetohostinfection
AT gerbergeorgk dynamicsofthemicrobiotainresponsetohostinfection
AT roeselersguus dynamicsofthemicrobiotainresponsetohostinfection
AT delaneymary dynamicsofthemicrobiotainresponsetohostinfection
AT duboisandrea dynamicsofthemicrobiotainresponsetohostinfection
AT liuqing dynamicsofthemicrobiotainresponsetohostinfection
AT belavusavavera dynamicsofthemicrobiotainresponsetohostinfection
AT yeliseyevvladimir dynamicsofthemicrobiotainresponsetohostinfection
AT housemanandres dynamicsofthemicrobiotainresponsetohostinfection
AT onderdonkandrew dynamicsofthemicrobiotainresponsetohostinfection
AT cavanaughcolleen dynamicsofthemicrobiotainresponsetohostinfection
AT brylynn dynamicsofthemicrobiotainresponsetohostinfection