Characterization and host range prediction of Staphylococcus aureus phages through receptor-binding protein analysis

Bacteriophages are crucial in bacterial communities and can be used for therapy of multidrug-resistant pathogens such as Staphylococcusaureus. However, the host range of new phages remains difficult to predict. We identified the receptor-binding proteins (RBPs) of 335 S. aureus-infecting phages, yielding 8 distinct RBP clusters. Recombinant representative RBPs of all clusters, including several subclusters, were analyzed for binding to S. aureus strains differing in potential phage receptor structures. Notably, most of the phages encoded two separate RBPs, and all RBPs used S. aureus wall teichoic acid (WTA) polymers as receptors, albeit with varying preference for WTA glycosylation patterns and backbone structures. Based on these findings, a sequence-based tool for predicting the adsorption of new phages was developed. Moreover, one of the RBPs proved useful for identifying S. aureus-type WTA in other bacterial species. These findings facilitate the characterization of phage and bacterial isolates and the development of phage therapies.

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Publication Details

Journal
Cell Reports
Published
2025-02-28
DOI
https://doi.org/10.1016/j.celrep.2025.115369
Citations
14
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
24.03

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article

Characterization and host range prediction of Staphylococcus aureus phages through receptor-binding protein analysis

Hadil Onallah, Christiane Wolz, Silvia Würstle, Janes Krusche et al.
14 citations
Cell Reports
Bacteriophages and microbial interactions
24.03
article

Characterization and host range prediction of Staphylococcus aureus phages through receptor-binding protein analysis

Hadil Onallah, Christiane Wolz, Silvia Würstle, Janes Krusche, Esther Lehmann, David Gerlach, Ellen Daiber, Christoph Mayer, Jennifer Müller, Christian Beck, Andreas Peschel
article en
14 citations

Abstract

Bacteriophages are crucial in bacterial communities and can be used for therapy of multidrug-resistant pathogens such as Staphylococcusaureus. However, the host range of new phages remains difficult to predict. We identified the receptor-binding proteins (RBPs) of 335 S. aureus-infecting phages, yielding 8 distinct RBP clusters. Recombinant representative RBPs of all clusters, including several subclusters, were analyzed for binding to S. aureus strains differing in potential phage receptor structures. Notably, most of the phages encoded two separate RBPs, and all RBPs used S. aureus wall teichoic acid (WTA) polymers as receptors, albeit with varying preference for WTA glycosylation patterns and backbone structures. Based on these findings, a sequence-based tool for predicting the adsorption of new phages was developed. Moreover, one of the RBPs proved useful for identifying S. aureus-type WTA in other bacterial species. These findings facilitate the characterization of phage and bacterial isolates and the development of phage therapies.

Cell ReportsVol. 44(3)
Goethe University Frankfurt (DE), Yale University (US), University Children's Hospital Tübingen (DE), University Hospital Frankfurt (DE), Bernstein Center for Computational Neuroscience Tübingen (DE), Institute of Medical Microbiology and Hygiene (DE), University of Tübingen (DE), Ludwig-Maximilians-Universität München (DE)
Deutsches Zentrum für Infektionsforschung, Minerva Foundation, Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung
Zero hunger
Openalex Percentile: Top 0%
Bacteriophages and microbial interactions
24.03
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