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Biomaterial‐Associated Persistence ofStaphylococcus epidermidisin Pericatheter Macrophages
Author(s) -
Jaap Jan Boelens,
J. Dankert,
JeanLuc Murk,
Jan J. Weening,
Tom van der Poll,
K. P. Dingemans,
Léo H. Koole,
Jon D. Laman,
Sebastian A. J. Zaat
Publication year - 2000
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 - 10.1086/315369
Subject(s) - biomaterial , staphylococcus epidermidis , microbiology and biotechnology , intracellular , bacteria , adhesion , macrophage , staphylococcus aureus , persistence (discontinuity) , chemistry , cytokine , biofilm , pathogenesis , materials science , medicine , biology , immunology , in vitro , biomedical engineering , biochemistry , composite material , genetics , geotechnical engineering , engineering
Biomaterial surfaces may be modified to reduce bacterial adhesion. The susceptibility in mice to Staphylococcus epidermidis infection in tissue surrounding the commonly used catheter materials-silicon elastomer (SE), polyamide (PA), and their surface-modified polyvinylpyrrolidone (PVP)-grafted derivatives, SE-PVP and PA-PVP, respectively-was assessed. Abscesses developed around SE-PVP. Around SE, PA, and PA-PVP catheters, no signs of infection were observed, although mice carrying PA-PVP developed septicemia after 14-21 days. S. epidermidis was cultured from the tissue surrounding PA-PVP segments. Cells around PA-PVP segments containing large numbers of bacteria were identified as macrophages by use of immunohistochemistry and electron microscopy. This persistence of intracellular bacteria was also observed around SE-PVP, SE, and PA catheters, although to a lesser extent. The cytokine profiles around the 4 materials were different. Implanted biomaterial induces an inflammatory response favorable to the persistence of S. epidermidis. Intracellular persistence of bacteria inside macrophages may be a pivotal process in the pathogenesis of biomaterial-associated infection.

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