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Fine scale transitions of the microbiota and metabolome along the gastrointestinal tract of herbivorous fishes

BACKGROUND: Gut microorganisms aid in the digestion of food by providing exogenous metabolic pathways to break down organic compounds. An integration of longitudinal microbial and chemical data is necessary to illuminate how gut microorganisms supplement the energetic and nutritional requirements of...

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Autores principales: Sparagon, Wesley J., Gentry, Emily C., Minich, Jeremiah J., Vollbrecht, Lisa, Laurens, Lieve M. L., Allen, Eric E., Sims, Neil A., Dorrestein, Pieter C., Kelly, Linda Wegley, Nelson, Craig E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9128220/
https://www.ncbi.nlm.nih.gov/pubmed/35606844
http://dx.doi.org/10.1186/s42523-022-00182-z
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author Sparagon, Wesley J.
Gentry, Emily C.
Minich, Jeremiah J.
Vollbrecht, Lisa
Laurens, Lieve M. L.
Allen, Eric E.
Sims, Neil A.
Dorrestein, Pieter C.
Kelly, Linda Wegley
Nelson, Craig E.
author_facet Sparagon, Wesley J.
Gentry, Emily C.
Minich, Jeremiah J.
Vollbrecht, Lisa
Laurens, Lieve M. L.
Allen, Eric E.
Sims, Neil A.
Dorrestein, Pieter C.
Kelly, Linda Wegley
Nelson, Craig E.
author_sort Sparagon, Wesley J.
collection PubMed
description BACKGROUND: Gut microorganisms aid in the digestion of food by providing exogenous metabolic pathways to break down organic compounds. An integration of longitudinal microbial and chemical data is necessary to illuminate how gut microorganisms supplement the energetic and nutritional requirements of animals. Although mammalian gut systems are well-studied in this capacity, the role of microbes in the breakdown and utilization of recalcitrant marine macroalgae in herbivorous fish is relatively understudied and an emerging priority for bioproduct extraction. Here we use a comprehensive survey of the marine herbivorous fish gut microbial ecosystem via parallel 16S rRNA gene amplicon profiling (microbiota) and untargeted tandem mass spectrometry (metabolomes) to demonstrate consistent transitions among 8 gut subsections across five fish of the genus of Kyphosus. RESULTS: Integration of microbial phylogenetic and chemical diversity data reveals that microbial communities and metabolomes covaried and differentiated continuously from stomach to hindgut, with the midgut containing multiple distinct and previously uncharacterized microenvironments and a distinct hindgut community dominated by obligate anaerobes. This differentiation was driven primarily by anaerobic gut endosymbionts of the classes Bacteroidia and Clostridia changing in concert with bile acids, small peptides, and phospholipids: bile acid deconjugation associated with early midgut microbiota, small peptide production associated with midgut microbiota, and phospholipid production associated with hindgut microbiota. CONCLUSIONS: The combination of microbial and untargeted metabolomic data at high spatial resolution provides a new view of the diverse fish gut microenvironment and serves as a foundation to understand functional partitioning of microbial activities that contribute to the digestion of complex macroalgae in herbivorous marine fish. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-022-00182-z.
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spelling pubmed-91282202022-05-25 Fine scale transitions of the microbiota and metabolome along the gastrointestinal tract of herbivorous fishes Sparagon, Wesley J. Gentry, Emily C. Minich, Jeremiah J. Vollbrecht, Lisa Laurens, Lieve M. L. Allen, Eric E. Sims, Neil A. Dorrestein, Pieter C. Kelly, Linda Wegley Nelson, Craig E. Anim Microbiome Research Article BACKGROUND: Gut microorganisms aid in the digestion of food by providing exogenous metabolic pathways to break down organic compounds. An integration of longitudinal microbial and chemical data is necessary to illuminate how gut microorganisms supplement the energetic and nutritional requirements of animals. Although mammalian gut systems are well-studied in this capacity, the role of microbes in the breakdown and utilization of recalcitrant marine macroalgae in herbivorous fish is relatively understudied and an emerging priority for bioproduct extraction. Here we use a comprehensive survey of the marine herbivorous fish gut microbial ecosystem via parallel 16S rRNA gene amplicon profiling (microbiota) and untargeted tandem mass spectrometry (metabolomes) to demonstrate consistent transitions among 8 gut subsections across five fish of the genus of Kyphosus. RESULTS: Integration of microbial phylogenetic and chemical diversity data reveals that microbial communities and metabolomes covaried and differentiated continuously from stomach to hindgut, with the midgut containing multiple distinct and previously uncharacterized microenvironments and a distinct hindgut community dominated by obligate anaerobes. This differentiation was driven primarily by anaerobic gut endosymbionts of the classes Bacteroidia and Clostridia changing in concert with bile acids, small peptides, and phospholipids: bile acid deconjugation associated with early midgut microbiota, small peptide production associated with midgut microbiota, and phospholipid production associated with hindgut microbiota. CONCLUSIONS: The combination of microbial and untargeted metabolomic data at high spatial resolution provides a new view of the diverse fish gut microenvironment and serves as a foundation to understand functional partitioning of microbial activities that contribute to the digestion of complex macroalgae in herbivorous marine fish. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-022-00182-z. BioMed Central 2022-05-23 /pmc/articles/PMC9128220/ /pubmed/35606844 http://dx.doi.org/10.1186/s42523-022-00182-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Sparagon, Wesley J.
Gentry, Emily C.
Minich, Jeremiah J.
Vollbrecht, Lisa
Laurens, Lieve M. L.
Allen, Eric E.
Sims, Neil A.
Dorrestein, Pieter C.
Kelly, Linda Wegley
Nelson, Craig E.
Fine scale transitions of the microbiota and metabolome along the gastrointestinal tract of herbivorous fishes
title Fine scale transitions of the microbiota and metabolome along the gastrointestinal tract of herbivorous fishes
title_full Fine scale transitions of the microbiota and metabolome along the gastrointestinal tract of herbivorous fishes
title_fullStr Fine scale transitions of the microbiota and metabolome along the gastrointestinal tract of herbivorous fishes
title_full_unstemmed Fine scale transitions of the microbiota and metabolome along the gastrointestinal tract of herbivorous fishes
title_short Fine scale transitions of the microbiota and metabolome along the gastrointestinal tract of herbivorous fishes
title_sort fine scale transitions of the microbiota and metabolome along the gastrointestinal tract of herbivorous fishes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9128220/
https://www.ncbi.nlm.nih.gov/pubmed/35606844
http://dx.doi.org/10.1186/s42523-022-00182-z
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