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The Role ofStaphylococcus aureusAdhesins in the Pathogenesis of Ventricular Assist Device–Related Infections
Author(s) -
Carlos Arrecubieta,
Tomohiro Asai,
Manuel Prinz von Bayern,
Tony Loughman,
J. Ross Fitzgerald,
Corbett E. Shelton,
Helen Baron,
Nicholas C. Dang,
Mario C. Deng,
Yoshifumi Naka,
Timothy J. Foster,
Franklin D. Lowy
Publication year - 2006
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/501366
Subject(s) - bacterial adhesin , staphylococcus aureus , microbiology and biotechnology , biology , heterologous , pathogenesis , staphylococcal infections , immunology , bacteria , escherichia coli , gene , biochemistry , genetics
Ventricular assist devices (VADs) are an important form of therapy for end-stage congestive heart failure. However, infection of the VAD, which is often caused by Staphylococcus aureus, poses a major threat to survival. Using a novel in vitro binding assay with VAD membranes and a heterologous lactococcal system of expression, we identify 3 S. aureus proteins--clumping factor A (ClfA) and fibronectin binding proteins A and B (FnBPA and FnBPB) as the main factors involved in adherence to VAD polyurethane membranes. Adherence is greatly diminished by long implantation times, reflecting a change in topological features of the VAD membrane, and is primarily mediated by the FnBPA domains in the staphylococcal proteins. We also compare the adherence of S. aureus mutant strains and show that other staphylococcal components appear to be involved in adherence to VAD membranes. Finally, we demonstrate that ClfA, FnBPA, and FnBPB mediate bacterial infection of implanted murine intra-aortic polyurethane patches.

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