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Esp-independent biofilm formation by Enterococcus faecalis
Christopher J Kristich1, Yung-Hua Li, Dennis G Cvitkovitch
1Department of Microbiology, University of Minnesota Medical School, Minneapolis, Minnesota 55455, USA.
Journal of Bacteriology
|December 18, 2003
Summary
Enterococcus faecalis forms complex biofilms independent of the Esp protein. Biofilm development is influenced by environmental factors and enhanced by the GelE metalloprotease.
Area of Science:
- Microbiology
- Bacterial pathogenesis
- Medical microbiology
Background:
- Enterococcus faecalis is an opportunistic pathogen frequently found in biofilms on medical devices.
- The molecular mechanisms governing E. faecalis biofilm formation are not fully understood.
- The Esp cell surface protein has been implicated in E. faecalis biofilm development.
Purpose of the Study:
- To investigate the role of the Esp protein in E. faecalis biofilm formation.
- To elucidate the mechanisms underlying E. faecalis biofilm development.
- To determine the influence of environmental conditions and other factors on E. faecalis biofilm formation.
Main Methods:
- Microtiter plate assays were used to assess biofilm formation.
- A chemostat-based biofilm fermentor system was employed for detailed biofilm analysis.
- Scanning electron microscopy (SEM) was utilized to visualize biofilm structure.
- Genetically modified E. faecalis strains lacking esp were examined.
Main Results:
- E. faecalis forms biofilms even in the absence of the esp gene and its associated pathogenicity island.
- Biofilm development progresses through distinct stages: attachment, microcolony formation, and maturation with water channels.
- Environmental conditions significantly modulate E. faecalis biofilm formation and maintenance.
- The secreted metalloprotease GelE was found to enhance biofilm formation.
Conclusions:
- The Esp surface protein is dispensable for Enterococcus faecalis biofilm formation.
- E. faecalis biofilm formation is a complex, environmentally sensitive process.
- GelE plays a role in enhancing E. faecalis biofilm development.