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Quantifying fluorescent glycan uptake to elucidate strain-level variability in foraging behaviors of rumen bacteria

Gut microbiomes, such as the microbial community that colonizes the rumen, have vast catabolic potential and play a vital role in host health and nutrition. By expanding our understanding of metabolic pathways in these ecosystems, we will garner foundational information for manipulating microbiome s...

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Autores principales: Klassen, Leeann, Reintjes, Greta, Tingley, Jeffrey P., Jones, Darryl R., Hehemann, Jan-Hendrik, Smith, Adam D., Schwinghamer, Timothy D., Arnosti, Carol, Jin, Long, Alexander, Trevor W., Amundsen, Carolyn, Thomas, Dallas, Amann, Rudolf, McAllister, Tim A., Abbott, D. Wade
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7825182/
https://www.ncbi.nlm.nih.gov/pubmed/33482928
http://dx.doi.org/10.1186/s40168-020-00975-x
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author Klassen, Leeann
Reintjes, Greta
Tingley, Jeffrey P.
Jones, Darryl R.
Hehemann, Jan-Hendrik
Smith, Adam D.
Schwinghamer, Timothy D.
Arnosti, Carol
Jin, Long
Alexander, Trevor W.
Amundsen, Carolyn
Thomas, Dallas
Amann, Rudolf
McAllister, Tim A.
Abbott, D. Wade
author_facet Klassen, Leeann
Reintjes, Greta
Tingley, Jeffrey P.
Jones, Darryl R.
Hehemann, Jan-Hendrik
Smith, Adam D.
Schwinghamer, Timothy D.
Arnosti, Carol
Jin, Long
Alexander, Trevor W.
Amundsen, Carolyn
Thomas, Dallas
Amann, Rudolf
McAllister, Tim A.
Abbott, D. Wade
author_sort Klassen, Leeann
collection PubMed
description Gut microbiomes, such as the microbial community that colonizes the rumen, have vast catabolic potential and play a vital role in host health and nutrition. By expanding our understanding of metabolic pathways in these ecosystems, we will garner foundational information for manipulating microbiome structure and function to influence host physiology. Currently, our knowledge of metabolic pathways relies heavily on inferences derived from metagenomics or culturing bacteria in vitro. However, novel approaches targeting specific cell physiologies can illuminate the functional potential encoded within microbial (meta)genomes to provide accurate assessments of metabolic abilities. Using fluorescently labeled polysaccharides, we visualized carbohydrate metabolism performed by single bacterial cells in a complex rumen sample, enabling a rapid assessment of their metabolic phenotype. Specifically, we identified bovine-adapted strains of Bacteroides thetaiotaomicron that metabolized yeast mannan in the rumen microbiome ex vivo and discerned the mechanistic differences between two distinct carbohydrate foraging behaviors, referred to as “medium grower” and “high grower.” Using comparative whole-genome sequencing, RNA-seq, and carbohydrate-active enzyme fingerprinting, we could elucidate the strain-level variability in carbohydrate utilization systems of the two foraging behaviors to help predict individual strategies of nutrient acquisition. Here, we present a multi-faceted study using complimentary next-generation physiology and “omics” approaches to characterize microbial adaptation to a prebiotic in the rumen ecosystem. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-020-00975-x.
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spelling pubmed-78251822021-01-25 Quantifying fluorescent glycan uptake to elucidate strain-level variability in foraging behaviors of rumen bacteria Klassen, Leeann Reintjes, Greta Tingley, Jeffrey P. Jones, Darryl R. Hehemann, Jan-Hendrik Smith, Adam D. Schwinghamer, Timothy D. Arnosti, Carol Jin, Long Alexander, Trevor W. Amundsen, Carolyn Thomas, Dallas Amann, Rudolf McAllister, Tim A. Abbott, D. Wade Microbiome Research Gut microbiomes, such as the microbial community that colonizes the rumen, have vast catabolic potential and play a vital role in host health and nutrition. By expanding our understanding of metabolic pathways in these ecosystems, we will garner foundational information for manipulating microbiome structure and function to influence host physiology. Currently, our knowledge of metabolic pathways relies heavily on inferences derived from metagenomics or culturing bacteria in vitro. However, novel approaches targeting specific cell physiologies can illuminate the functional potential encoded within microbial (meta)genomes to provide accurate assessments of metabolic abilities. Using fluorescently labeled polysaccharides, we visualized carbohydrate metabolism performed by single bacterial cells in a complex rumen sample, enabling a rapid assessment of their metabolic phenotype. Specifically, we identified bovine-adapted strains of Bacteroides thetaiotaomicron that metabolized yeast mannan in the rumen microbiome ex vivo and discerned the mechanistic differences between two distinct carbohydrate foraging behaviors, referred to as “medium grower” and “high grower.” Using comparative whole-genome sequencing, RNA-seq, and carbohydrate-active enzyme fingerprinting, we could elucidate the strain-level variability in carbohydrate utilization systems of the two foraging behaviors to help predict individual strategies of nutrient acquisition. Here, we present a multi-faceted study using complimentary next-generation physiology and “omics” approaches to characterize microbial adaptation to a prebiotic in the rumen ecosystem. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-020-00975-x. BioMed Central 2021-01-22 /pmc/articles/PMC7825182/ /pubmed/33482928 http://dx.doi.org/10.1186/s40168-020-00975-x Text en © The Author(s) 2021 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/. 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 in a credit line to the data.
spellingShingle Research
Klassen, Leeann
Reintjes, Greta
Tingley, Jeffrey P.
Jones, Darryl R.
Hehemann, Jan-Hendrik
Smith, Adam D.
Schwinghamer, Timothy D.
Arnosti, Carol
Jin, Long
Alexander, Trevor W.
Amundsen, Carolyn
Thomas, Dallas
Amann, Rudolf
McAllister, Tim A.
Abbott, D. Wade
Quantifying fluorescent glycan uptake to elucidate strain-level variability in foraging behaviors of rumen bacteria
title Quantifying fluorescent glycan uptake to elucidate strain-level variability in foraging behaviors of rumen bacteria
title_full Quantifying fluorescent glycan uptake to elucidate strain-level variability in foraging behaviors of rumen bacteria
title_fullStr Quantifying fluorescent glycan uptake to elucidate strain-level variability in foraging behaviors of rumen bacteria
title_full_unstemmed Quantifying fluorescent glycan uptake to elucidate strain-level variability in foraging behaviors of rumen bacteria
title_short Quantifying fluorescent glycan uptake to elucidate strain-level variability in foraging behaviors of rumen bacteria
title_sort quantifying fluorescent glycan uptake to elucidate strain-level variability in foraging behaviors of rumen bacteria
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7825182/
https://www.ncbi.nlm.nih.gov/pubmed/33482928
http://dx.doi.org/10.1186/s40168-020-00975-x
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