Cargando…

Dynamics of metatranscription in the inflammatory bowel disease gut microbiome

Inflammatory bowel disease (IBD) is a group of chronic diseases of the digestive tract affecting millions of people worldwide. Genetic, environmental and microbial factors have been implicated in onset and exacerbation of IBD. However, the mechanisms associating gut microbial dysbioses and aberrant...

Descripción completa

Detalles Bibliográficos
Autores principales: Schirmer, Melanie, Franzosa, Eric A., Lloyd-Price, Jason, McIver, Lauren J., Schwager, Randall, Poon, Tiffany W., Ananthakrishnan, Ashwin N., Andrews, Elizabeth, Barron, Gildardo, Lake, Kathleen, Prasad, Mahadev, Sauk, Jenny, Stevens, Betsy, Wilson, Robin G., Braun, Jonathan, Denson, Lee A., Kugathasan, Subra, McGovern, Dermot P.B., Vlamakis, Hera, Xavier, Ramnik J., Huttenhower, Curtis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131705/
https://www.ncbi.nlm.nih.gov/pubmed/29311644
http://dx.doi.org/10.1038/s41564-017-0089-z
_version_ 1783354174911545344
author Schirmer, Melanie
Franzosa, Eric A.
Lloyd-Price, Jason
McIver, Lauren J.
Schwager, Randall
Poon, Tiffany W.
Ananthakrishnan, Ashwin N.
Andrews, Elizabeth
Barron, Gildardo
Lake, Kathleen
Prasad, Mahadev
Sauk, Jenny
Stevens, Betsy
Wilson, Robin G.
Braun, Jonathan
Denson, Lee A.
Kugathasan, Subra
McGovern, Dermot P.B.
Vlamakis, Hera
Xavier, Ramnik J.
Huttenhower, Curtis
author_facet Schirmer, Melanie
Franzosa, Eric A.
Lloyd-Price, Jason
McIver, Lauren J.
Schwager, Randall
Poon, Tiffany W.
Ananthakrishnan, Ashwin N.
Andrews, Elizabeth
Barron, Gildardo
Lake, Kathleen
Prasad, Mahadev
Sauk, Jenny
Stevens, Betsy
Wilson, Robin G.
Braun, Jonathan
Denson, Lee A.
Kugathasan, Subra
McGovern, Dermot P.B.
Vlamakis, Hera
Xavier, Ramnik J.
Huttenhower, Curtis
author_sort Schirmer, Melanie
collection PubMed
description Inflammatory bowel disease (IBD) is a group of chronic diseases of the digestive tract affecting millions of people worldwide. Genetic, environmental and microbial factors have been implicated in onset and exacerbation of IBD. However, the mechanisms associating gut microbial dysbioses and aberrant immune responses remain largely unknown. The integrative Human Microbiome Project (iHMP) seeks to close these gaps by examining the dynamics of microbiome functionality in disease by profiling the gut microbiomes of more than 100 individuals sampled over a one year period. Here, we present the first results based on 78 paired fecal metagenomes/metatranscriptomes and 222 additional metagenomes from 59 Crohn’s disease (CD), 34 ulcerative colitis (UC), and 24 non-IBD control patients. We demonstrate several cases in which measures of microbial gene expression in the inflamed gut can be informative relative to metagenomic profiles of functional potential. First, while many microbial organisms exhibited concordant DNA and RNA abundances, we also detected species-specific biases in transcriptional activity, revealing predominant transcription of pathways by individual microbes per host (e.g. by Faecalibacterium prausnitzii). Therefore, a loss of these organisms in disease may have more far-reaching consequences than suggested by their genomic abundances. Further, we identified organisms that were metagenomically abundant but inactive or dormant in the gut with little or no expression (e.g. Dialister invisus). Lastly, certain disease-specific microbial characteristics were more pronounced or only detectable at the transcript level, such as pathways predominantly expressed by different organisms in IBD patients (e.g. Bacteroides vulgatus and Alistipes putredinis). This provides potential insights into gut microbial pathway transcription that can vary over time, inducing phenotypic changes complementary to those linked to metagenomic abundances. The study’s results highlight the strength of analyzing both the activity and presence of gut microbes to provide insight into the role of the microbiome in IBD.
format Online
Article
Text
id pubmed-6131705
institution National Center for Biotechnology Information
language English
publishDate 2018
record_format MEDLINE/PubMed
spelling pubmed-61317052018-09-11 Dynamics of metatranscription in the inflammatory bowel disease gut microbiome Schirmer, Melanie Franzosa, Eric A. Lloyd-Price, Jason McIver, Lauren J. Schwager, Randall Poon, Tiffany W. Ananthakrishnan, Ashwin N. Andrews, Elizabeth Barron, Gildardo Lake, Kathleen Prasad, Mahadev Sauk, Jenny Stevens, Betsy Wilson, Robin G. Braun, Jonathan Denson, Lee A. Kugathasan, Subra McGovern, Dermot P.B. Vlamakis, Hera Xavier, Ramnik J. Huttenhower, Curtis Nat Microbiol Article Inflammatory bowel disease (IBD) is a group of chronic diseases of the digestive tract affecting millions of people worldwide. Genetic, environmental and microbial factors have been implicated in onset and exacerbation of IBD. However, the mechanisms associating gut microbial dysbioses and aberrant immune responses remain largely unknown. The integrative Human Microbiome Project (iHMP) seeks to close these gaps by examining the dynamics of microbiome functionality in disease by profiling the gut microbiomes of more than 100 individuals sampled over a one year period. Here, we present the first results based on 78 paired fecal metagenomes/metatranscriptomes and 222 additional metagenomes from 59 Crohn’s disease (CD), 34 ulcerative colitis (UC), and 24 non-IBD control patients. We demonstrate several cases in which measures of microbial gene expression in the inflamed gut can be informative relative to metagenomic profiles of functional potential. First, while many microbial organisms exhibited concordant DNA and RNA abundances, we also detected species-specific biases in transcriptional activity, revealing predominant transcription of pathways by individual microbes per host (e.g. by Faecalibacterium prausnitzii). Therefore, a loss of these organisms in disease may have more far-reaching consequences than suggested by their genomic abundances. Further, we identified organisms that were metagenomically abundant but inactive or dormant in the gut with little or no expression (e.g. Dialister invisus). Lastly, certain disease-specific microbial characteristics were more pronounced or only detectable at the transcript level, such as pathways predominantly expressed by different organisms in IBD patients (e.g. Bacteroides vulgatus and Alistipes putredinis). This provides potential insights into gut microbial pathway transcription that can vary over time, inducing phenotypic changes complementary to those linked to metagenomic abundances. The study’s results highlight the strength of analyzing both the activity and presence of gut microbes to provide insight into the role of the microbiome in IBD. 2018-01-08 2018-03 /pmc/articles/PMC6131705/ /pubmed/29311644 http://dx.doi.org/10.1038/s41564-017-0089-z Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Schirmer, Melanie
Franzosa, Eric A.
Lloyd-Price, Jason
McIver, Lauren J.
Schwager, Randall
Poon, Tiffany W.
Ananthakrishnan, Ashwin N.
Andrews, Elizabeth
Barron, Gildardo
Lake, Kathleen
Prasad, Mahadev
Sauk, Jenny
Stevens, Betsy
Wilson, Robin G.
Braun, Jonathan
Denson, Lee A.
Kugathasan, Subra
McGovern, Dermot P.B.
Vlamakis, Hera
Xavier, Ramnik J.
Huttenhower, Curtis
Dynamics of metatranscription in the inflammatory bowel disease gut microbiome
title Dynamics of metatranscription in the inflammatory bowel disease gut microbiome
title_full Dynamics of metatranscription in the inflammatory bowel disease gut microbiome
title_fullStr Dynamics of metatranscription in the inflammatory bowel disease gut microbiome
title_full_unstemmed Dynamics of metatranscription in the inflammatory bowel disease gut microbiome
title_short Dynamics of metatranscription in the inflammatory bowel disease gut microbiome
title_sort dynamics of metatranscription in the inflammatory bowel disease gut microbiome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131705/
https://www.ncbi.nlm.nih.gov/pubmed/29311644
http://dx.doi.org/10.1038/s41564-017-0089-z
work_keys_str_mv AT schirmermelanie dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT franzosaerica dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT lloydpricejason dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT mciverlaurenj dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT schwagerrandall dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT poontiffanyw dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT ananthakrishnanashwinn dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT andrewselizabeth dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT barrongildardo dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT lakekathleen dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT prasadmahadev dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT saukjenny dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT stevensbetsy dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT wilsonrobing dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT braunjonathan dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT densonleea dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT kugathasansubra dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT mcgoverndermotpb dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT vlamakishera dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT xavierramnikj dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome
AT huttenhowercurtis dynamicsofmetatranscriptionintheinflammatoryboweldiseasegutmicrobiome