Staphylococcus aureus PSMα3 Cross-α Fibril Polymorphism and Determinants of Cytotoxicity

Abstract

The phenol-soluble modulin (PSM) peptide family, secreted by Staphylococcus aureus, performs various virulence activities, some mediated by the formation of amyloid fibrils of diverse architectures. Specifically, PSM1 and PSM4 structure the S. aureus biofilm by assembling into robust cross-{beta} amyloid fibrils. PSM3, the most cytotoxic member of the family, assembles into cross- fibrils in which -helices stack into tightly mated sheets, mimicking the cross-{beta} architecture. Here we demonstrated that massive T-cell deformation and death is linked with PSM3 aggregation and co-localization with cell membranes. Our extensive mutagenesis analyses supported the role of positive charges, and especially Lys17, in interactions with the membrane, and suggested their regulation by inter- and intra-helical electrostatic interactions within the cross- fibril. We hypothesize that PSM3 cytotoxicity is governed by the ability to form cross- fibrils and involves a dynamic process of co-aggregation with cell membrane, rupturing it. HighlightsO_LIThe cytotoxic S. aureus PSM3 assembles into cross- fibrils C_LIO_LICross- fibril polymorphism and mutations-induced secondary structure switching C_LIO_LIRegulation by cross- fibril inter- and intra-helical electrostatic interactions C_LIO_LIToxicity as a putative dynamic process of PSM3 co-aggregation with membranes C_LI