Staphylococcus aureus toxin LukSF dissociates from its membrane receptor target to enable renewed ligand sequestration
backgroundStaphylococcus aureus Panton Valentine Leukocidin (PVL) is a pore-forming toxin targeting the human C5a receptor (hC5aR), enabling this pathogen to battle the immune response by destroying phagocytes through targeted lysis. The mechanisms that contribute to rapid cell lysis are largely unexplored.\n\nResultsHere we show that cell lysis may be enabled by a process of toxins targeting receptor clusters and receptor recycling which allows multiple toxin pores to be formed close together. Using live cell single-molecule super-resolution imaging, Forster resonance energy transfer (FRET) and nanoscale total internal reflection fluorescence (TIRF) colocalization microscopy we visualized toxin pore formation in the presence of its natural docking ligand.\n\nConclusionsWe demonstrate disassociation of hC5aR from toxin complexes and simultaneous binding of new ligands. This effect may free mobile receptors to amplify hyper inflammatory reactions in early stages of microbial infections and have implications for several other similar bi-component toxins and the design of new antibiotics.