The ArlRS two-component system is a regulator of Staphylococcus aureus-induced endothelial cell damage

Eur J Clin Microbiol Infect Dis. 2018 Feb;37(2):289-292. doi: 10.1007/s10096-017-3130-5. Epub 2017 Nov 27.

Abstract

Staphylococcus aureus endovascular infections retain a high morbidity and mortality despite antibiotics and supportive care. The destruction of endothelial cells (ECs) is a critical step in the pathogenesis of S. aureus endovascular infections. In order to better understand S. aureus-induced EC damage, we systematically screened a collection of two-component regulatory system mutants of methicillin-resistant S. aureus (MRSA) USA300 strain JE2 for damage induction in human umbilical vein ECs (HUVECs). This screen revealed that the two-component regulatory system ArlRS is required for maximum damage: arlRS inactivation leads to a > 70% reduction in damage. In a different genetic S. aureus background (RN6390, MSSA strain) arlRS inactivation had a smaller but also significant effect on EC damage. In both strains, the reduction in EC damage was accompanied by a significant reduction in internalization. In conclusion, we determined a novel role of ArlRS in S. aureus-induced EC damage, which will help to better understand the pathogenesis of S. aureus endovascular infection.

MeSH terms

  • Bacterial Proteins / genetics*
  • Cells, Cultured
  • Human Umbilical Vein Endothelial Cells / pathology*
  • Humans
  • Methicillin-Resistant Staphylococcus aureus / genetics*
  • Methicillin-Resistant Staphylococcus aureus / pathogenicity*
  • Protein Kinases / genetics*
  • Staphylococcal Infections / microbiology
  • Staphylococcal Infections / pathology
  • Trans-Activators / genetics

Substances

  • Agr protein, Staphylococcus aureus
  • ArlR protein, Staphylococcus aureus
  • Bacterial Proteins
  • Trans-Activators
  • Protein Kinases
  • ArlS protein, Staphylococcus aureus