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  • Oral Presentation
  • OP-PMD-008

Wall teichoic acid substitution with glucose governs phage susceptibility of Staphylococcus epidermidis

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Raum 5-6

Session

Biology of Microbial Viruses

Thema

  • Phages and microbial defense systems

Mitwirkende

Christian Beck (Tübingen / DE), Janes Krusche (Tübingen / DE), Anna Notaro (Naples / IT), Axel Walter (Tübingen / DE), Lara Kränkel (Tübingen / DE), Anneli Vollert (Tübingen / DE), Regine Stemmler (Tübingen / DE), Johannes Wittmann (Brunswick / DE), Martin Schaller (Tübingen / DE), Christoph Slavetinsky (Tübingen / DE), Christoph Mayer (Tübingen / DE), Cristina De Castro (Naples / IT), Andreas Peschel (Tübingen / DE)

Abstract

The species- and clone-specific susceptibility of Staphylococcus cells for bacteriophages is governed by the structures and glycosylation patterns of wall teichoic acid (WTA) glycopolymers. The glycosylation dependent phage-WTA interactions in the opportunistic pathogen Staphylococcus epidermidis and in other coagulase-negative staphylococci (CoNS) have remained unknown. We report a new S. epidermidis WTA glycosyltransferase TagE whose deletion confers resistance to siphoviruses such as ΦE72 but enables binding of otherwise unbound podoviruses. S. epidermidis glycerolphosphate WTA was found to be modified with glucose in a tagE-dependent manner. TagE is encoded together with the enzymes PgcA and GtaB providing uridine diphosphate-activated glucose. ΦE72 transduced several other CoNS species encoding TagE homologs suggesting that WTA glycosylation via TagE is a frequent trait among CoNS that permits inter-species horizontal gene transfer. Our study unravels a crucial mechanism of phage-Staphylococcus interaction and of horizontal gene transfer and it will help in the design of anti-staphylococcal phage therapies.

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