Cited by 25Bacteriophages and microbial interactionsAdvanced Electron Microscopy Techniques and ApplicationsEnzyme Structure and Function

Structure and host specificity of Staphylococcus epidermidis bacteriophage Andhra

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Hawkins, N’Toia C., Kizziah, James L., Hatoum-Aslan, Asma, Dokland, Terje·2022·Science Advances

Published 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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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)
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
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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