In situ imaging of bacterial outer membrane projections and associated protein complexes using electron cryo-tomography
- Creators
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Kaplan, Mohammed
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Chreifi, Georges
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Metskas, Lauren Ann
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Liedtke, Janine
- Wood, Cecily R.
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Oikonomou, Catherine M.
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Nicolas, William J.
- Subramanian, Poorna
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Zacharoff, Lori A.
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Wang, Yuhang
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Chang, Yi-Wei
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Beeby, Morgan
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Dobro, Megan J.
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Zhu, Yongtao
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McBride, Mark J.
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Briegel, Ariane
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Shaffer, Carrie L.
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Jensen, Grant J.
Abstract
The ability to produce outer membrane projections in the form of tubular membrane extensions (MEs) and membrane vesicles (MVs) is a widespread phenomenon among diderm bacteria. Despite this, our knowledge of the ultrastructure of these extensions and their associated protein complexes remains limited. Here, we surveyed the ultrastructure and formation of MEs and MVs, and their associated protein complexes, in tens of thousands of electron cryo-tomograms of ~90 bacterial species that we have collected for various projects over the past 15 years (Jensen lab database), in addition to data generated in the Briegel lab. We identified outer MEs and MVs in 13 diderm bacterial species and classified several major ultrastructures: (1) tubes with a uniform diameter (with or without an internal scaffold), (2) tubes with irregular diameter, (3) tubes with a vesicular dilation at their tip, (4) pearling tubes, (5) connected chains of vesicles (with or without neck-like connectors), (6) budding vesicles and nanopods. We also identified several protein complexes associated with these MEs and MVs which were distributed either randomly or exclusively at the tip. These complexes include a secretin-like structure and a novel crown-shaped structure observed primarily in vesicles from lysed cells. In total, this work helps to characterize the diversity of bacterial membrane projections and lays the groundwork for future research in this field.
Additional Information
© 2021 Kaplan et al. This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited. Preprinted: 13 July 2021; Received: 17 August 2021; Accepted: 23 August 2021; Published: 01 September 2021. This project was funded by the NIH (grant R35 GM122588 to GJJ, and P20 GM130456 to CLS) and a Baxter postdoctoral fellowship from Caltech to MK. Cryo-ET work was done in the Beckman Institute Resource Center for Transmission Electron Microscopy at the California Institute of Technology. We are grateful to Prof. Martin Pilhofer for collecting the P. luteoviolacea data and for critically reading the manuscript. We thank Prof. Elitza I Tocheva for collecting the D. acidovorans data. We thank Prof. Mohamed El-Naggar for insights into preparing S. oneidensis samples and Dr. Yuxi Liu for discussions. Briegel lab data was collected at the Netherlands Center for Electron Nanoscopy with support from Dr Wen Yang. This data was collected with support from the National Roadmap for Large-Scale Research Infrastructure 2017–2018 with project number 184.034.014, which is financed in part by the Dutch Research Council (NWO). This work was also supported by the NWO OCENW.GROOT.2019.063 grant. The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication. Author Contributions: Mohammed Kaplan, Conceptualization, Data curation, Formal analysis, Funding acquisition, Writing - original draft; Georges Chreifi, Lauren Ann Metskas, Cecily R Wood, Poorna Subramanian, Lori A Zacharoff, Yuhang Wang, Yi-Wei Chang, Morgan Beeby, Megan J Dobro, Yongtao Zhu, Mark J McBride, Data curation, Writing – review and editing; Janine Liedtke, Data curation, Formal analysis, Writing – review and editing; Catherine M Oikonomou, William J Nicolas, Formal analysis, Writing – review and editing; Ariane Briegel, Formal analysis, Funding acquisition, Writing – review and editing; Carrie L Shaffer, Data curation, Formal analysis, Funding acquisition, Writing – review and editing; Grant J Jensen, Conceptualization, Formal analysis, Funding acquisition, Investigation, Supervision, Writing – review and editing. The authors declare that no competing interests exist. Data availability: All data generated or analysed during this study are included in the manuscript and supporting files and movies.Attached Files
Published - elife-73099-v2.pdf
Submitted - 2021.07.13.452161v1.full.pdf
Supplemental Material - elife-73099-transrepform1-v2.docx
Supplemental Material - elife-73099-video1.mp4
Supplemental Material - elife-73099-video2.mp4
Supplemental Material - elife-73099-video3.mp4
Supplemental Material - elife-73099-video4.mp4
Supplemental Material - elife-73099-video5.mp4
Supplemental Material - elife-73099-video6.mp4
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Additional details
- Alternative title
- In situ imaging of bacterial membrane projections and associated protein complexes using electron cryo-tomography
- Eprint ID
- 109850
- Resolver ID
- CaltechAUTHORS:20210715-193000687
- NIH
- R35 GM122588
- NIH
- P20 GM130456
- Baxter Foundation
- Nederlandse Organisatie voor Wetenschappelijk Onderzoek (NWO)
- 184.034.014
- Nederlandse Organisatie voor Wetenschappelijk Onderzoek (NWO)
- OCENW.GROOT.2019.063
- Created
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2021-07-15Created from EPrint's datestamp field
- Updated
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2021-09-22Created from EPrint's last_modified field
- Caltech groups
- Division of Biology and Biological Engineering (BBE)