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Foraging on host synthesized metabolites enables the bacterial symbiont Snodgrassella alvi to colonize the honey bee gut

View ORCID ProfileAndrew Quinn, Yassine El Chazli, Stéphane Escrig, View ORCID ProfileJean Daraspe, Nicolas Neuschwander, Aoife McNally, View ORCID ProfileChristel Genoud, View ORCID ProfileAnders Meibom, View ORCID ProfilePhilipp Engel
doi: https://doi.org/10.1101/2023.01.23.524906
Andrew Quinn
1Department of Fundamental Microbiology, University of Lausanne, Lausanne, Switzerland
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Yassine El Chazli
1Department of Fundamental Microbiology, University of Lausanne, Lausanne, Switzerland
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Stéphane Escrig
2Laboratory of Biological Geochemistry, Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland
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Jean Daraspe
3Electron Microscopy Facility, University of Lausanne, Lausanne, Switzerland
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Nicolas Neuschwander
1Department of Fundamental Microbiology, University of Lausanne, Lausanne, Switzerland
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Aoife McNally
1Department of Fundamental Microbiology, University of Lausanne, Lausanne, Switzerland
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Christel Genoud
3Electron Microscopy Facility, University of Lausanne, Lausanne, Switzerland
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Anders Meibom
2Laboratory of Biological Geochemistry, Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland
4Center for Advanced Surface Analysis, Institute of Earth Sciences, University of Lausanne, Lausanne, Switzerland
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Philipp Engel
1Department of Fundamental Microbiology, University of Lausanne, Lausanne, Switzerland
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  • For correspondence: phillipp.engel@unil.ch
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Summary

Nutrients from the host diet and microbial cross-feeding allow diverse bacteria to colonize the animal gut. Less is known about the role of host-derived nutrients in enabling gut bacterial colonization. We examined metabolic interactions within the evolutionary ancient symbiosis between the honey bee (Apis mellifera) and the core gut microbiota member Snodgrassella alvi. This Betaproteobacteria is incapable of metabolizing saccharides, yet colonizes the honey bee gut in the presence of only a sugar diet. Using comparative metabolomics, 13C tracers, and Nanoscale secondary ion mass spectrometry (NanoSIMS), we show in vivo that S. alvi grows on host-derived organic acids, including citrate, glycerate and 3-hydroxy-3-methylglutarate which are actively secreted by the host into the gut lumen. S. alvi additionally modulates tryptophan metabolism in the gut, primarily by converting kynurenine to anthranilate. These results suggest that Snodgrassella is adapted to a specific metabolic niche in the gut that depends on host-derived nutritional resources.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • https://github.com/Yelchazli/Foraging-on-host-synthesized-metabolites-enables-S.-alvi-to-colonize-the-honey-bee-gut

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
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Posted January 23, 2023.
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Foraging on host synthesized metabolites enables the bacterial symbiont Snodgrassella alvi to colonize the honey bee gut
Andrew Quinn, Yassine El Chazli, Stéphane Escrig, Jean Daraspe, Nicolas Neuschwander, Aoife McNally, Christel Genoud, Anders Meibom, Philipp Engel
bioRxiv 2023.01.23.524906; doi: https://doi.org/10.1101/2023.01.23.524906
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Foraging on host synthesized metabolites enables the bacterial symbiont Snodgrassella alvi to colonize the honey bee gut
Andrew Quinn, Yassine El Chazli, Stéphane Escrig, Jean Daraspe, Nicolas Neuschwander, Aoife McNally, Christel Genoud, Anders Meibom, Philipp Engel
bioRxiv 2023.01.23.524906; doi: https://doi.org/10.1101/2023.01.23.524906

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