西亚试剂：Moonlighting bacteriophage proteins derepress staphylococca

发布时间：2025-06-15

Moonlighting bacteriophage proteins derepress staphylococcal pathogenicity islands
María ángeles Tormo-Más1Search Ignacio Mir1Search Archana Shrestha2 Sandra M. Tallent2Search Susana Campoy3  í?igo Lasa4  Jordi Barbé3  Richard P. Novick5  Gail E. Christie2 José R. Penadés

Staphylococcal superantigen-carrying pathogenicity islands (SaPIs) are discrete, chromosomally integrated units of ~15 kilobases that are induced by helper phages to excise and replicate. SaPI DNA is then efficiently encapsidated in phage-like infectious particles, leading to extremely high frequencies of intra- as well as intergeneric transfer1, 2, 3. In the absence of helper phage lytic growth, the island is maintained in a quiescent prophage-like state by a global repressor, Stl, which controls expression of most of the SaPI genes4. Here we show that SaPI derepression is effected by a specific, non-essential phage protein that binds to Stl, disrupting the Stl–DNA complex and thereby initiating the excision-replication-packaging cycle of the island. Because SaPIs require phage proteins to be packaged5, 6, this strategy assures that SaPIs will be transferred once induced. Several different SaPIs are induced by helper phage 80α and, in each case, the SaPI commandeers a different non-essential phage protein for its derepression. The highly specific interactions between different SaPI repressors and helper-phage-encoded antirepressors represent a remarkable evolutionary adaptation involved in pathogenicity island mobilization.

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