The role of Staphylococcus aureus adhesins in the pathogenesis of ventricular assist device-related infections

被引:44
作者
Arrecubieta, C
Asai, T
Bayern, M
Loughman, A
Fitzgerald, JR
Shelton, CE
Baron, HM
Dang, NC
Deng, MC
Naka, Y
Foster, TJ
Lowy, FD
机构
[1] Columbia Univ, Coll Phys & Surg, Dept Med, Div Infect Dis, New York, NY 10032 USA
[2] Columbia Univ, Coll Phys & Surg, Dept Med, Div Cardiol, New York, NY 10032 USA
[3] Columbia Univ, Coll Phys & Surg, Dept Pathol, New York, NY 10032 USA
[4] Columbia Univ, Coll Phys & Surg, Dept Surg, New York, NY 10032 USA
[5] Trinity Coll Dublin, Moyne Inst Prevent Med, Dept Microbiol, Dublin, Ireland
关键词
D O I
10.1086/501366
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:1109 / 1119
页数:11
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