IAI FigSearch
Home Help [Feedback] [For Subscribers] [Archive] [Search] --
IAI Accepts, published online ahead of print on 11 December 2006
This Article
Right arrow Full Text (PDF)
Right arrow Other Versions of this Article:
IAI.01262-06v1
75/3/1129    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Broekhuizen, C. A.N.
Right arrow Articles by Zaat, S. A.J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Broekhuizen, C. A.N.
Right arrow Articles by Zaat, S. A.J.

 Previous Article  |  Next Article 

Infect. Immun. doi:10.1128/IAI.01262-06
Copyright (c) 2006, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.

Peri-implant tissue is an important niche for Staphylococcus epidermidis in experimental biomaterial-associated infection in mice

Corine A.N. Broekhuizen, Leonie de Boer, Kim Schipper, Christopher D. Jones, Shan Quadir, Roger G. Feldman, Jacob Dankert, Christina M.J.E. Vandenbroucke-Grauls, Jan J. Weening, and Sebastian A.J. Zaat*

Department of Medical Microbiology, CINIMA (Center for Infection and Immunity Amsterdam), Academic Medical Center, University of Amsterdam, Meibergdreef 15, 1105 AZ Amsterdam, The Netherlands; Emergent Europe, 540-545 Eskdale Road, Winnersh Triangle, Wokingham, RG41 5TU, Berkshire, UK; Department of Pathology, Academic Medical Center, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands; Department of Medical Microbiology and Infectious Diseases, VU Medical Center, Amsterdam, The Netherlands

* To whom correspondence should be addressed. Email: s.a.zaat{at}amc.uva.nl.


   Abstract

Biomaterial-associated infections (BAI), predominantly caused by Staphylococcus epidermidis, are a significant problem in modern medicine. Biofilm formation is considered the pivotal element in the pathogenesis, but in previous mouse studies we retrieved S. epidermidis from peri-implant tissue. To assess the kinetics and generality of tissue colonization, we investigated BAI using two S. epidermidis strains, two biomaterials, and two mouse strains. At low inocula all implants were culture negative whereas surrounding tissues were positive. At higher doses tissues were more often culture positive than implants, with higher numbers of CFU. This was true for the different biomaterials tested, for both S. epidermidis strains, at different time points, and for both mouse strains. S. epidermidis co-localized with host cells at a distance of >10 cell layers from the biomaterial-tissue interface. We conclude that in mouse experimental BAI S. epidermidis peri-implant tissue colonization is more important than biofim formation.




This article has been cited by other articles:




Home Help [Feedback] [For Subscribers] [Archive] [Search] --
J. Bacteriol. J. Virol. Eukaryot. Cell
Microbiol. Mol. Biol. Rev. Clin. Vaccine Immunol. All ASM Journals

Copyright © 2006 by the American Society for Microbiology. All rights reserved.