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Formate cross‐feeding and cooperative metabolic interactions revealed by transcriptomics in co‐cultures of acetogenic and amylolytic human colonic bacteria

Interspecies cross‐feeding is a fundamental factor in anaerobic microbial communities. In the human colon, formate is produced by many bacterial species but is normally detected only at low concentrations. Ruminococcus bromii produces formate, ethanol and acetate in approximately equal molar proport...

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Autores principales: Laverde Gomez, Jenny A., Mukhopadhya, Indrani, Duncan, Sylvia H., Louis, Petra, Shaw, Sophie, Collie‐Duguid, Elaina, Crost, Emmanuelle, Juge, Nathalie, Flint, Harry J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378601/
https://www.ncbi.nlm.nih.gov/pubmed/30362296
http://dx.doi.org/10.1111/1462-2920.14454
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author Laverde Gomez, Jenny A.
Mukhopadhya, Indrani
Duncan, Sylvia H.
Louis, Petra
Shaw, Sophie
Collie‐Duguid, Elaina
Crost, Emmanuelle
Juge, Nathalie
Flint, Harry J.
author_facet Laverde Gomez, Jenny A.
Mukhopadhya, Indrani
Duncan, Sylvia H.
Louis, Petra
Shaw, Sophie
Collie‐Duguid, Elaina
Crost, Emmanuelle
Juge, Nathalie
Flint, Harry J.
author_sort Laverde Gomez, Jenny A.
collection PubMed
description Interspecies cross‐feeding is a fundamental factor in anaerobic microbial communities. In the human colon, formate is produced by many bacterial species but is normally detected only at low concentrations. Ruminococcus bromii produces formate, ethanol and acetate in approximately equal molar proportions in pure culture on RUM‐RS medium with 0.2% Novelose resistant starch (RS3) as energy source. Batch co‐culturing on starch with the acetogen Blautia hydrogenotrophica however led to the disappearance of formate and increased levels of acetate, which is proposed to occur through the routing of formate via the Wood Ljungdahl pathway of B. hydrogenotrophica. We investigated these inter‐species interactions further using RNAseq to examine gene expression in continuous co‐cultures of R. bromii and B. hydrogenotrophica. Transcriptome analysis revealed upregulation of B. hydrogenotrophica genes involved in the Wood‐Ljungdahl pathway and of a 10 gene cluster responsible for increased branched chain amino acid fermentation in the co‐cultures. Cross‐feeding between formate‐producing species and acetogens may be a significant factor in short chain fatty acid formation in the colon contributing to high rates of acetate production. Transcriptome analysis also indicated competition for the vitamin thiamine and downregulation of dissimilatory sulfate reduction and key redox proteins in R. bromii in the co‐cultures, thus demonstrating the wide‐ranging consequences of inter‐species interactions in this model system.
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spelling pubmed-63786012019-02-28 Formate cross‐feeding and cooperative metabolic interactions revealed by transcriptomics in co‐cultures of acetogenic and amylolytic human colonic bacteria Laverde Gomez, Jenny A. Mukhopadhya, Indrani Duncan, Sylvia H. Louis, Petra Shaw, Sophie Collie‐Duguid, Elaina Crost, Emmanuelle Juge, Nathalie Flint, Harry J. Environ Microbiol Research Articles Interspecies cross‐feeding is a fundamental factor in anaerobic microbial communities. In the human colon, formate is produced by many bacterial species but is normally detected only at low concentrations. Ruminococcus bromii produces formate, ethanol and acetate in approximately equal molar proportions in pure culture on RUM‐RS medium with 0.2% Novelose resistant starch (RS3) as energy source. Batch co‐culturing on starch with the acetogen Blautia hydrogenotrophica however led to the disappearance of formate and increased levels of acetate, which is proposed to occur through the routing of formate via the Wood Ljungdahl pathway of B. hydrogenotrophica. We investigated these inter‐species interactions further using RNAseq to examine gene expression in continuous co‐cultures of R. bromii and B. hydrogenotrophica. Transcriptome analysis revealed upregulation of B. hydrogenotrophica genes involved in the Wood‐Ljungdahl pathway and of a 10 gene cluster responsible for increased branched chain amino acid fermentation in the co‐cultures. Cross‐feeding between formate‐producing species and acetogens may be a significant factor in short chain fatty acid formation in the colon contributing to high rates of acetate production. Transcriptome analysis also indicated competition for the vitamin thiamine and downregulation of dissimilatory sulfate reduction and key redox proteins in R. bromii in the co‐cultures, thus demonstrating the wide‐ranging consequences of inter‐species interactions in this model system. John Wiley & Sons, Inc. 2018-11-22 2019-01 /pmc/articles/PMC6378601/ /pubmed/30362296 http://dx.doi.org/10.1111/1462-2920.14454 Text en © 2018 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Laverde Gomez, Jenny A.
Mukhopadhya, Indrani
Duncan, Sylvia H.
Louis, Petra
Shaw, Sophie
Collie‐Duguid, Elaina
Crost, Emmanuelle
Juge, Nathalie
Flint, Harry J.
Formate cross‐feeding and cooperative metabolic interactions revealed by transcriptomics in co‐cultures of acetogenic and amylolytic human colonic bacteria
title Formate cross‐feeding and cooperative metabolic interactions revealed by transcriptomics in co‐cultures of acetogenic and amylolytic human colonic bacteria
title_full Formate cross‐feeding and cooperative metabolic interactions revealed by transcriptomics in co‐cultures of acetogenic and amylolytic human colonic bacteria
title_fullStr Formate cross‐feeding and cooperative metabolic interactions revealed by transcriptomics in co‐cultures of acetogenic and amylolytic human colonic bacteria
title_full_unstemmed Formate cross‐feeding and cooperative metabolic interactions revealed by transcriptomics in co‐cultures of acetogenic and amylolytic human colonic bacteria
title_short Formate cross‐feeding and cooperative metabolic interactions revealed by transcriptomics in co‐cultures of acetogenic and amylolytic human colonic bacteria
title_sort formate cross‐feeding and cooperative metabolic interactions revealed by transcriptomics in co‐cultures of acetogenic and amylolytic human colonic bacteria
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378601/
https://www.ncbi.nlm.nih.gov/pubmed/30362296
http://dx.doi.org/10.1111/1462-2920.14454
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