| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Previous Article | Next Article ![]()
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.
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.
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
![]()
Abstract
This article has been cited by other articles:
| J. Bacteriol. | J. Virol. | Eukaryot. Cell |
|---|
| Microbiol. Mol. Biol. Rev. | Clin. Vaccine Immunol. | All ASM Journals |
|---|