Cargando…

Genome-scale metabolic reconstructions of Bifidobacterium adolescentis L2-32 and Faecalibacterium prausnitzii A2-165 and their interaction

BACKGROUND: The gut microbiota plays an important role in human health and disease by acting as a metabolic organ. Metagenomic sequencing has shown how dysbiosis in the gut microbiota is associated with human metabolic diseases such as obesity and diabetes. Modeling may assist to gain insight into t...

Descripción completa

Detalles Bibliográficos
Autores principales: El-Semman, Ibrahim E, Karlsson, Fredrik H, Shoaie, Saeed, Nookaew, Intawat, Soliman, Taysir H, Nielsen, Jens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108055/
https://www.ncbi.nlm.nih.gov/pubmed/24708835
http://dx.doi.org/10.1186/1752-0509-8-41
_version_ 1782327701462319104
author El-Semman, Ibrahim E
Karlsson, Fredrik H
Shoaie, Saeed
Nookaew, Intawat
Soliman, Taysir H
Nielsen, Jens
author_facet El-Semman, Ibrahim E
Karlsson, Fredrik H
Shoaie, Saeed
Nookaew, Intawat
Soliman, Taysir H
Nielsen, Jens
author_sort El-Semman, Ibrahim E
collection PubMed
description BACKGROUND: The gut microbiota plays an important role in human health and disease by acting as a metabolic organ. Metagenomic sequencing has shown how dysbiosis in the gut microbiota is associated with human metabolic diseases such as obesity and diabetes. Modeling may assist to gain insight into the metabolic implication of an altered microbiota. Fast and accurate reconstruction of metabolic models for members of the gut microbiota, as well as methods to simulate a community of microorganisms, are therefore needed. The Integrated Microbial Genomes (IMG) database contains functional annotation for nearly 4,650 bacterial genomes. This tremendous new genomic information adds new opportunities for systems biology to reconstruct accurate genome scale metabolic models (GEMs). RESULTS: Here we assembled a reaction data set containing 2,340 reactions obtained from existing genome-scale metabolic models, where each reaction is assigned with KEGG Orthology. The reaction data set was then used to reconstruct two genome scale metabolic models for gut microorganisms available in the IMG database Bifidobacterium adolescentis L2-32, which produces acetate during fermentation, and Faecalibacterium prausnitzii A2-165, which consumes acetate and produces butyrate. F. prausnitzii is less abundant in patients with Crohn’s disease and has been suggested to play an anti-inflammatory role in the gut ecosystem. The B. adolescentis model, iBif452, comprises 699 reactions and 611 unique metabolites. The F. prausnitzii model, iFap484, comprises 713 reactions and 621 unique metabolites. Each model was validated with in vivo data. We used OptCom and Flux Balance Analysis to simulate how both organisms interact. CONCLUSIONS: The consortium of iBif452 and iFap484 was applied to predict F. prausnitzii’s demand for acetate and production of butyrate which plays an essential role in colonic homeostasis and cancer prevention. The assembled reaction set is a useful tool to generate bacterial draft models from KEGG Orthology.
format Online
Article
Text
id pubmed-4108055
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-41080552014-08-04 Genome-scale metabolic reconstructions of Bifidobacterium adolescentis L2-32 and Faecalibacterium prausnitzii A2-165 and their interaction El-Semman, Ibrahim E Karlsson, Fredrik H Shoaie, Saeed Nookaew, Intawat Soliman, Taysir H Nielsen, Jens BMC Syst Biol Research Article BACKGROUND: The gut microbiota plays an important role in human health and disease by acting as a metabolic organ. Metagenomic sequencing has shown how dysbiosis in the gut microbiota is associated with human metabolic diseases such as obesity and diabetes. Modeling may assist to gain insight into the metabolic implication of an altered microbiota. Fast and accurate reconstruction of metabolic models for members of the gut microbiota, as well as methods to simulate a community of microorganisms, are therefore needed. The Integrated Microbial Genomes (IMG) database contains functional annotation for nearly 4,650 bacterial genomes. This tremendous new genomic information adds new opportunities for systems biology to reconstruct accurate genome scale metabolic models (GEMs). RESULTS: Here we assembled a reaction data set containing 2,340 reactions obtained from existing genome-scale metabolic models, where each reaction is assigned with KEGG Orthology. The reaction data set was then used to reconstruct two genome scale metabolic models for gut microorganisms available in the IMG database Bifidobacterium adolescentis L2-32, which produces acetate during fermentation, and Faecalibacterium prausnitzii A2-165, which consumes acetate and produces butyrate. F. prausnitzii is less abundant in patients with Crohn’s disease and has been suggested to play an anti-inflammatory role in the gut ecosystem. The B. adolescentis model, iBif452, comprises 699 reactions and 611 unique metabolites. The F. prausnitzii model, iFap484, comprises 713 reactions and 621 unique metabolites. Each model was validated with in vivo data. We used OptCom and Flux Balance Analysis to simulate how both organisms interact. CONCLUSIONS: The consortium of iBif452 and iFap484 was applied to predict F. prausnitzii’s demand for acetate and production of butyrate which plays an essential role in colonic homeostasis and cancer prevention. The assembled reaction set is a useful tool to generate bacterial draft models from KEGG Orthology. BioMed Central 2014-04-03 /pmc/articles/PMC4108055/ /pubmed/24708835 http://dx.doi.org/10.1186/1752-0509-8-41 Text en Copyright © 2014 El-Semman et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
El-Semman, Ibrahim E
Karlsson, Fredrik H
Shoaie, Saeed
Nookaew, Intawat
Soliman, Taysir H
Nielsen, Jens
Genome-scale metabolic reconstructions of Bifidobacterium adolescentis L2-32 and Faecalibacterium prausnitzii A2-165 and their interaction
title Genome-scale metabolic reconstructions of Bifidobacterium adolescentis L2-32 and Faecalibacterium prausnitzii A2-165 and their interaction
title_full Genome-scale metabolic reconstructions of Bifidobacterium adolescentis L2-32 and Faecalibacterium prausnitzii A2-165 and their interaction
title_fullStr Genome-scale metabolic reconstructions of Bifidobacterium adolescentis L2-32 and Faecalibacterium prausnitzii A2-165 and their interaction
title_full_unstemmed Genome-scale metabolic reconstructions of Bifidobacterium adolescentis L2-32 and Faecalibacterium prausnitzii A2-165 and their interaction
title_short Genome-scale metabolic reconstructions of Bifidobacterium adolescentis L2-32 and Faecalibacterium prausnitzii A2-165 and their interaction
title_sort genome-scale metabolic reconstructions of bifidobacterium adolescentis l2-32 and faecalibacterium prausnitzii a2-165 and their interaction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4108055/
https://www.ncbi.nlm.nih.gov/pubmed/24708835
http://dx.doi.org/10.1186/1752-0509-8-41
work_keys_str_mv AT elsemmanibrahime genomescalemetabolicreconstructionsofbifidobacteriumadolescentisl232andfaecalibacteriumprausnitziia2165andtheirinteraction
AT karlssonfredrikh genomescalemetabolicreconstructionsofbifidobacteriumadolescentisl232andfaecalibacteriumprausnitziia2165andtheirinteraction
AT shoaiesaeed genomescalemetabolicreconstructionsofbifidobacteriumadolescentisl232andfaecalibacteriumprausnitziia2165andtheirinteraction
AT nookaewintawat genomescalemetabolicreconstructionsofbifidobacteriumadolescentisl232andfaecalibacteriumprausnitziia2165andtheirinteraction
AT solimantaysirh genomescalemetabolicreconstructionsofbifidobacteriumadolescentisl232andfaecalibacteriumprausnitziia2165andtheirinteraction
AT nielsenjens genomescalemetabolicreconstructionsofbifidobacteriumadolescentisl232andfaecalibacteriumprausnitziia2165andtheirinteraction