In situ imaging of bacterial outer membrane projections and associated protein complexes using electron cryo-tomography

Author:

Kaplan Mohammed1ORCID,Chreifi Georges1ORCID,Metskas Lauren Ann1ORCID,Liedtke Janine2ORCID,Wood Cecily R3,Oikonomou Catherine M1ORCID,Nicolas William J1ORCID,Subramanian Poorna1,Zacharoff Lori A4,Wang Yuhang1ORCID,Chang Yi-Wei5ORCID,Beeby Morgan6ORCID,Dobro Megan J7ORCID,Zhu Yongtao8ORCID,McBride Mark J9ORCID,Briegel Ariane2ORCID,Shaffer Carrie L31011ORCID,Jensen Grant J112ORCID

Affiliation:

1. Division of Biology and Biological Engineering, California Institute of Technology

2. Leiden University, Sylvius Laboratories

3. Department of Veterinary Science, University of Kentucky

4. Department of Physics and Astronomy, University of Southern California

5. Department of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania

6. Department of Life Sciences, Imperial College London

7. Hampshire College

8. Department of Biological Sciences, Minnesota State University

9. Department of Biological Sciences, University of Wisconsin-Milwaukee

10. Department of Microbiology, Immunology, and Molecular Genetics, University of Kentucky

11. Department of Pharmaceutical Sciences, University of Kentucky

12. Department of Chemistry and Biochemistry, Brigham Young University

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.

Funder

National Institutes of Health

California Institute of Technology

Nederlandse Organisatie voor Wetenschappelijk Onderzoek

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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