Published April 1, 2019 | Version v1
Journal article Open

Single cell fluorescence imaging of glycan uptake by intestinal bacteria

  • 1. Max Planck-Institute for Marine Microbiology, 28359, Bremen, Germany
  • 2. Lethbridge Research and Development Centre, Agriculture and Agri-Food Canada, 5403-1st Avenue South, Lethbridge, AB, T1J 4B1, Canada
  • 3. Didier Ndeh Department of Marine Sciences, University of North Carolina, Chapel Hill, NC, USA Carol Arnosti Corresponding authors Correspondence to Jan-Hendrik Hehemann or D. Wade Abbott. Ethics declarations Conflict of interest The authors declare that they have no conflict of interest. Additional information Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Supplementary information Sup4 Supplementary Figure captions Sup1 Sup2 Sup3 Rights and permissions Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. Reprints and Permissions About this article Verify currency and authenticity via CrossMark Cite this article Hehemann, JH., Reintjes, G., Klassen, L. et al. Single cell fluorescence imaging of glycan uptake by intestinal bacteria. ISME J 13, 1883–1889 (2019). https://doi.org/10.1038/s41396-019-0406-z Download citation Received 20 February 2018 Revised 03 December 2018 Accepted 27 February 2019 Published 01 April 2019 Issue Date July 2019 DOI https://doi.org/10.1038/s41396-019-0406-z Share this article Anyone you share the following link with will be able to read this content: Get shareable link Provided by the Springer Nature SharedIt content-sharing initiative Subjects Biological techniques Metabolomics Further reading Quantifying fluorescent glycan uptake to elucidate strain-level variability in foraging behaviors of rumen bacteria Leeann Klassen, Greta Reintjes[…] & D. Wade Abbott Microbiome (2021) Synthesis of glycoconjugates utilizing the regioselectivity of a lytic polysaccharide monooxygenase Bjørge Westereng, Stjepan K. Kračun[…] & Vincent G. H. Eijsink Scientific Reports (2020) Download PDF
  • 4. Department of Marine Sciences, University of North Carolina, Chapel Hill, NC, USA

Description

Microbes in the intestines of mammals degrade dietary glycans for energy and growth. The pathways required for polysaccharide utilization are functionally diverse; moreover, they are unequally dispersed between bacterial genomes. Hence, assigning metabolic phenotypes to genotypes remains a challenge in microbiome research. Here we demonstrate that glycan uptake in gut bacteria can be visualized with fluorescent glycan conjugates (FGCs) using epifluorescence microscopy. Yeast α-mannan and rhamnogalacturonan-II, two structurally distinct glycans from the cell walls of yeast and plants, respectively, were fluorescently labeled and fed to Bacteroides thetaiotaomicron VPI-5482. Wild-type cells rapidly consumed the FGCs and became fluorescent; whereas, strains that had deleted pathways for glycan degradation and transport were non-fluorescent. Uptake of FGCs, therefore, is direct evidence of genetic function and provides a direct method to assess specific glycan metabolism in intestinal bacteria at the single cell level.

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Funding

European Commission
RUMIC - Prebiotic Functional Enhancement of Rumen Microbiomes 840804