Intracellular persistence of Staphylococcus aureus in endothelial cells is promoted by the absence of phenol-soluble modulins

Virulence. 2021 Dec;12(1):1186-1198. doi: 10.1080/21505594.2021.1910455.

Abstract

A large proportion of clinical S. aureus isolates that carry an inactive Agr system are associated with persistent infection that is difficult to treat. Once S. aureus is inside the bloodstream, it can cross the endothelial barrier and invade almost every organ in the human body. Endothelial cells can either be lysed by this pathogen or they serve as a niche for its intracellular long-term survival. Following phagocytosis, several vesicles such as phagosomes and autophagosomes, target intracellular S. aureus for elimination. S. aureus can escape from these vesicles into the host cytoplasm through the activation of phenol-soluble modulins (PSMs) αβ. Thereafter, it replicates and lyses the host cell to disseminate to adjacent tissues. Herein we demonstrate that staphylococcal strains which lack the expression of PSMs employ an alternative pathway to better persist within endothelial cells. The intracellular survival of S. aureus is associated with the co-localization of the autophagy marker LC3. In cell culture infection models, we found that the absence of psmαβ decreased the host cell lysis and increased staphylococcal long-term survival. This study explains the positive selection of agr-negative strains that lack the expression of psmαβ in chronic infection due to their advantage in surviving and evading the clearance system of the host.

Keywords: Staphylococcus aureus; chronic infections; intracellular persistence; lc3-vesicles; phenol-soluble modulins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Toxins
  • Endothelial Cells
  • Humans
  • Persistent Infection
  • Phagosomes
  • Staphylococcal Infections*
  • Staphylococcus aureus*

Substances

  • Bacterial Toxins
  • staphylococcal delta toxin

Grants and funding

This work was supported by the Bundesministerium für Bildung und Forschung [01EC1901B (MESINFLAME)]; Bundesministerium für Bildung und Forschung [FKZ 01EO1502]; Deutsche Forschungsgemeinschaft [HU 800/10-1, HU 800/13-1 and FOR 2625]; Deutsche Forschungsgemeinschaft [SPP1879]; Deutsche Forschungsgemeinschaft [TR156 (A2)]; Deutsche Forschungsgemeinschaft [TR34 (Projects C12 and B1)]; Deutsche Forschungsgemeinschaft [HU 800/10-1]; Deutsche Forschungsgemeinschaft [RTG2581 (Project 6)].