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

Publication date

2015-01-01

Authors

Spaan, András NORCID 0000-0001-5981-7259ISNI 0000000419538409
Reyes-Robles, Tamara
Badiou, Cédric
Cochet, Sylvie
Boguslawski, Kristina M.
Yoong, Pauline
Day, Christopher J.
Gosselaar-de Haas, Carla J CISNI 0000000395737840
van Kessel, CPMISNI 0000000396046048
Vandenesch, François

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Advisors

Supervisors

Document Type

Article

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License

taverne

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.

Keywords

Taverne, General Immunology and Microbiology, Cancer Research, Molecular Biology, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't

Citation

Spaan, A N, Reyes-Robles, T, Badiou, C, Cochet, S, Boguslawski, K M, Yoong, P, Day, C J, Gosselaar-de Haas, C J C, van Kessel, K P M, Vandenesch, F, Jennings, M P, Le Van Kim, C, Colin, Y, Van Strijp, J A G, Henry, T & Torres, V J 2015, 'Staphylococcus aureus Targets the Duffy Antigen Receptor for Chemokines (DARC) to Lyse Erythrocytes', Cell Host & Microbe, vol. 18, no. 3, pp. 363-370. https://doi.org/10.1016/j.chom.2015.08.001