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Autotrophic biofilms sustained by deeply-sourced groundwater host diverse CPR bacteria implicated in sulfur and hydrogen metabolism

View ORCID ProfileLuis E. Valentin Alvarado, View ORCID ProfileSirine C. Fakra, View ORCID ProfileAlexander J. Probst, Jonathan R. Giska, View ORCID ProfileAlexander L. Jaffe, View ORCID ProfileLuke M. Oltrogge, View ORCID ProfileJacob West-Roberts, View ORCID ProfileJoel Rowland, View ORCID ProfileMichael Manga, View ORCID ProfileDavid F. Savage, View ORCID ProfileChris Greening, View ORCID ProfileBrett J. Baker, View ORCID ProfileJillian F. Banfield
doi: https://doi.org/10.1101/2022.11.17.516901
Luis E. Valentin Alvarado
1Graduate Group in Microbiology, University of California, Berkeley, CA, USA
2Innovative Genomics Institute, University of California, Berkeley, CA, USA
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Sirine C. Fakra
3Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, CA, USA
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Alexander J. Probst
4Earth and Planetary Science, University of California, Berkeley, CA, USA
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Jonathan R. Giska
4Earth and Planetary Science, University of California, Berkeley, CA, USA
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Alexander L. Jaffe
1Graduate Group in Microbiology, University of California, Berkeley, CA, USA
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Luke M. Oltrogge
5Department of Molecular and Cell Biology, University of California, Berkeley, CA, USA
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Jacob West-Roberts
6Environmental Science, Policy and Management, University of California, Berkeley, CA, USA
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Joel Rowland
4Earth and Planetary Science, University of California, Berkeley, CA, USA
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  • ORCID record for Joel Rowland
Michael Manga
4Earth and Planetary Science, University of California, Berkeley, CA, USA
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David F. Savage
2Innovative Genomics Institute, University of California, Berkeley, CA, USA
5Department of Molecular and Cell Biology, University of California, Berkeley, CA, USA
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Chris Greening
7Department of Microbiology, Biomedicine Discovery Institute, Monash University, Clayton, Australia
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Brett J. Baker
8Department of Integrative Biology, University of Texas, Austin, USA
9Department of Marine Science, University of Texas, Austin, USA
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Jillian F. Banfield
2Innovative Genomics Institute, University of California, Berkeley, CA, USA
4Earth and Planetary Science, University of California, Berkeley, CA, USA
6Environmental Science, Policy and Management, University of California, Berkeley, CA, USA
9Department of Marine Science, University of Texas, Austin, USA
10Energy Geoscience Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA
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  • For correspondence: jbanfield@berkeley.edu
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Abstract

Background Candidate Phyla Radiation (CPR) bacteria are commonly detected yet enigmatic members of diverse microbial communities. Their host associations, metabolic capabilities, and potential roles in biogeochemical cycles remain under-explored. We studied chemoautotrophically-based biofilms that host diverse CPR bacteria and grow in sulfide-rich springs using bulk geochemical analysis, genome-resolved metagenomics and scanning transmission x-ray microscopy (STXM) at room temperature and 87° K.

Results CPR-affiliated Gracilibacteria, Absconditabacteria, Saccharibacteria, Peregrinibacteria, Berkelbacteria, Microgenomates, and Parcubacteria are members of two biofilm communities dominated by chemolithotrophic sulfur-oxidizing bacteria including Thiothrix or Beggiatoa. STXM imaging revealed ultra-small cells along the surfaces of filamentous bacteria that we interpret are CPR bacterial episymbionts. STXM and NEXAFS spectroscopy at carbon K and sulfur L2,3 edges show protein-encapsulated elemental sulfur spherical granules associated with filamentous bacteria, indicating that they are sulfur-oxidizers, likely Thiothrix. Berkelbacteria and Moranbacteria in the same biofilm sample are predicted to have a novel electron bifurcating group 3b [NiFe]-hydrogenase, putatively a sulfhydrogenase, potentially linked to sulfur metabolism via redox cofactors. This complex could potentially underpin a symbiosis involving Berkelbacteria and/or Moranbacteria and filamentous sulfur-oxidizing bacteria such as Thiothrix that is based on cryptic sulfur cycling. One Doudnabacteria genome encodes adjacent sulfur dioxygenase and rhodanese genes that may convert thiosulfate to sulfite. We find similar conserved genomic architecture associated with CPR bacteria from other sulfur-rich subsurface ecosystems.

Conclusions Our combined metagenomic, geochemical, spectromicroscopic and structural bioinformatics analyses link some CPR bacteria to sulfur-oxidizing Proteobacteria, likely Thiothrix, and indicate roles for CPR bacteria in sulfur and hydrogen cycling.

Competing Interest Statement

JFB is a co-founder of Metagenomi.

Copyright 
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 November 17, 2022.
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Autotrophic biofilms sustained by deeply-sourced groundwater host diverse CPR bacteria implicated in sulfur and hydrogen metabolism
Luis E. Valentin Alvarado, Sirine C. Fakra, Alexander J. Probst, Jonathan R. Giska, Alexander L. Jaffe, Luke M. Oltrogge, Jacob West-Roberts, Joel Rowland, Michael Manga, David F. Savage, Chris Greening, Brett J. Baker, Jillian F. Banfield
bioRxiv 2022.11.17.516901; doi: https://doi.org/10.1101/2022.11.17.516901
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Autotrophic biofilms sustained by deeply-sourced groundwater host diverse CPR bacteria implicated in sulfur and hydrogen metabolism
Luis E. Valentin Alvarado, Sirine C. Fakra, Alexander J. Probst, Jonathan R. Giska, Alexander L. Jaffe, Luke M. Oltrogge, Jacob West-Roberts, Joel Rowland, Michael Manga, David F. Savage, Chris Greening, Brett J. Baker, Jillian F. Banfield
bioRxiv 2022.11.17.516901; doi: https://doi.org/10.1101/2022.11.17.516901

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