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Staphylococcus aureus Targets the Duffy Antigen Receptor for Chemokines (DARC) to Lyse Erythrocytes

  • András N. Spaan
  • , Tamara Reyes-Robles
  • , Cédric Badiou
  • , Sylvie Cochet
  • , Kristina M. Boguslawski
  • , Pauline Yoong
  • , Christopher J. Day
  • , Carla J C Gosselaar-de Haas
  • , Kok P M van Kessel
  • , François Vandenesch
  • , Michael P. Jennings
  • , Caroline Le Van Kim
  • , Yves Colin
  • , Jos A G Van Strijp
  • , Thomas Henry*
  • , Victor J. Torres
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

1 Citation (Scopus)

Abstract

In order for Staphylococcus aureus to thrive inside the mammalian host, the bacterium has to overcome iron scarcity. S. aureus is thought to produce toxins that lyse erythrocytes, releasing hemoglobin, the most abundant iron source in mammals. Here we identify the Duffy antigen receptor for chemokines (DARC) as the receptor for the S. aureus hemolytic leukocidins LukED and HlgAB. By assessing human erythrocytes with DARC polymorphisms, we determined that HlgAB- and LukED-mediated lysis directly relates to DARC expression. DARC is required for S. aureus-mediated lysis of human erythrocytes, and DARC overexpression is sufficient to render cells susceptible to toxin-mediated lysis. HlgA and LukE bind directly to DARC through different regions, and by targeting DARC, HlgAB and LukED support S. aureus growth in a hemoglobin-acquisition-dependent manner. These findings elucidate how S. aureus targets and lyses erythrocytes to release one of the scarcest nutrients within the mammalian host.

Original languageEnglish
Pages (from-to)363-370
Number of pages8
JournalCell Host & Microbe
Volume18
Issue number3
DOIs
Publication statusPublished - 1 Jan 2015

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