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Updated: Jun 17, 2026

Biomimetic Materials to Characterize Bacteria-host Interactions
Published on: November 16, 2015
Staphylococcus aureus extracellular adherence protein serves as anti-inflammatory factor by inhibiting the
Triantafyllos Chavakis1, Muzaffar Hussain, Sandip M Kanse
1Institute for Biochemistry, Third Department of Internal Medicine, Justus-Liebig-Universität, Giessen, Germany. triantafyllos.chavakis@innere.med.uni-giessen.de
Abstract:
Staphylococcus aureus is a human pathogen that secretes proteins that contribute to bacterial colonization. Here we describe the extracellular adherence protein (Eap) as a novel anti-inflammatory factor that inhibits host leukocyte recruitment. Due to its direct interactions with the host adhesive proteins intercellular adhesion molecule 1 (ICAM-1), fibrinogen or vitronectin, Eap disrupted beta(2)-integrin and urokinase receptor mediated leukocyte adhesion in vitro. Whereas Eap-expressing S. aureus induced a 2 3-fold lower neutrophil recruitment in bacterial peritonitis in mice as compared with an Eap-negative strain, isolated Eap prevented beta(2)-integrin-dependent neutrophil recruitment in a mouse model of acute thioglycollate-induced peritonitis. Thus, the specific interactions with ICAM-1 and extracellular matrix proteins render Eap a potent anti-inflammatory factor, which may serve as a new therapeutic substance to block leukocyte extravasation in patients with hyperinflammatory pathologies.
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