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Generation of Greater Bacterial Biofilm Biomass using PCR-Plate Deep Well Microplate Devices
Published on: April 22, 2022
Correlation between enterococcal biofilm formation in vitro and medical-device-related infection potential in vivo
Jonathan A T Sandoe1, Ian R Witherden1, Jonathan H Cove1
1Department of Microbiology, The General Infirmary at Leeds1 and University of Leeds2, Leeds LS1 3EX, UK.
Abstract:
Hospital-acquired infections caused by enterococci have increased dramatically since the 1970s. Many nosocomial enterococcal bloodstream infections are associated with medical devices such as central venous catheters. The ability to form biofilm on medical devices is a potential virulence trait that may allow enterococci to cause infections in the expanding population of patients managed with such devices. In this study, the hypothesis that increased ability to form biofilm in vitro is associated with medical-device-related infection in vivo was tested. A microplate assay was employed to assess biofilm-forming characteristics of enterococci in 0.9 % (w/v) sodium chloride, an oligotrophic environment, and BHI, a nutrient-rich environment. Results were compared in isolates from different sources of infection. One hundred and nine enterococcal bloodstream isolates were assayed. Biofilm formation on microplates was demonstrated by all Enterococcus faecalis isolates and 16/38 (42 %) Enterococcus faecium isolates. E. faecalis isolates produced significantly more biofilm than E. faecium isolates in both media (P < 0.0001, Mann-Whitney U test). E. faecalis isolates from intravascular-catheter-related bloodstream infections (CRBSIs) produced significantly more biofilm than non-CRBSI isolates (P < 0.0001), or isolates of uncertain clinical significance (P < 0.0001). Biofilm formed by E. faecium isolates was not significantly affected by culture medium and did not differ between isolates from the different clinical categories. In conclusion, there was significantly more biofilm formed by E. faecalis isolates causing CRBSI compared with isolates from other types of infection or from isolates of uncertain clinical significance. The ability of E. faecalis isolates to form biofilm in vitro appears to be a marker of a virulence trait that enhances the ability of isolates to cause CRBSI.
Insights
Enterococcus faecalis strains causing catheter-related bloodstream infections (CRBSIs) exhibit enhanced biofilm formation. This in vitro biofilm capability serves as a virulence marker for CRBSI development in patients with medical devices.
Area of Science:
- Microbiology
- Infectious Diseases
- Medical Devices
Background:
- Hospital-acquired enterococcal infections have risen significantly since the 1970s.
- Nosocomial enterococcal bloodstream infections are frequently linked to medical devices like central venous catheters.
- Biofilm formation on medical devices is a potential virulence factor for enterococci.
Purpose of the Study:
- To test the hypothesis that enhanced in vitro biofilm formation correlates with in vivo medical-device-related infections.
- To investigate the biofilm-forming characteristics of enterococcal isolates from various infection sources.
Main Methods:
- A microplate assay was used to quantify biofilm formation by 109 enterococcal bloodstream isolates.
- Biofilm assays were conducted in both oligotrophic (0.9% NaCl) and nutrient-rich (BHI) environments.
- Isolates were categorized based on their clinical source of infection.
Main Results:
- All Enterococcus faecalis isolates and 42% of Enterococcus faecium isolates formed biofilms.
- E. faecalis isolates produced significantly more biofilm than E. faecium isolates in both media.
- E. faecalis isolates from catheter-related bloodstream infections (CRBSIs) showed significantly higher biofilm formation compared to non-CRBSI isolates.
Conclusions:
- Enhanced in vitro biofilm formation by E. faecalis is associated with CRBSI.
- E. faecalis biofilm-forming ability appears to be a virulence marker for CRBSI.
- Biofilm formation in E. faecium isolates did not significantly differ between clinical categories.
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