Structure and host specificity of Staphylococcus epidermidis bacteriophage Andhra
Open accessPublished version of a preprint
Abstract
Staphylococcus epidermidis is an opportunistic pathogen of the human skin, often associated with infections of implanted medical devices. Staphylococcal picoviruses are a group of strictly lytic, short-tailed bacteriophages with compact genomes that are attractive candidates for therapeutic use. Here, we report the structure of the complete virion of S. epidermidis –infecting phage Andhra, determined using high-resolution cryo–electron microscopy, allowing atomic modeling of 11 capsid and tail proteins. The capsid is a T = 4 icosahedron containing a unique stabilizing capsid lining protein. The tail includes 12 trimers of a unique receptor binding protein (RBP), a lytic protein that also serves to anchor the RBPs to the tail stem, and a hexameric tail knob that acts as a gatekeeper for DNA ejection. Using structure prediction with AlphaFold, we identified the two proteins that comprise the tail tip heterooctamer. Our findings elucidate critical features for virion assembly, host recognition, and penetration.
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Cites
Highly accurate protein structure prediction with AlphaFold
Jumper, J., Evans, R., Pritzel, A., Green, T., Figurnov, M., Ronneberger, O., Tunyasuvunakool, K., Bates, R., Žídek, A., Potapenko, A., et al. (2021) · Nature · doi:10.1038/s41586-021-03819-2 · Cited by 43,764 · see citing works
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Host defense and pathogenesis in Staphylococcus aureus infections
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- Authors
- Hawkins, N. C., Kizziah, J. L., Hatoum-Aslan, A., & Dokland, T.
- Affiliations
- University of Alabama at Birmingham (US)
- University of Illinois Urbana-Champaign (US)
- Corresponding author
- Dokland, Terje
- Venue
- Science Advances
- Published
- 2022-12-02
- Volume
- 8
- Issue
- 48
- Pages
- eade0459-eade0459
- ISSN
- 2375-2548 (ISSN-L)
- PMC
- PMC9710869
- OpenAlex
- W4310437436
- Cited by
- 25
- References
- 4
- Citations by year
- 2026: 6 · 2025: 7 · 2024: 7 · 2023: 5
- FWCI
- 2.53
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Science Advances (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- National Institute of General Medical Sciences (U24GM116789)
- National Institute of Allergy and Infectious Diseases (R21AI156636, R01AI083255)
- Topics
- Physical Sciences › Environmental Science › Ecology › Bacteriophages and microbial interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Structural Biology › Advanced Electron Microscopy Techniques and Applications
- Physical Sciences › Materials Science › Materials Chemistry › Enzyme Structure and Function
- Keywords
- Staphylococcus epidermidis, phage structure, viral assembly, capsid, receptor binding protein, lytic proteins, host specificity, host recognition, DNA ejection, AlphaFold structure prediction, cryo-electron microscopy
- MeSH terms
- Capsid, Humans, Staphylococcus Phages, Staphylococcus epidermidis, Cryoelectron Microscopy, Capsid Proteins, Host Specificity
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