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. 2015 Nov;9(11):ZC61-5.
doi: 10.7860/JCDR/2015/14602.6829. Epub 2015 Nov 1.

The Effect of Addition of an EPS Degrading Enzyme with and without Detergent to 2% Chlorhexidine on Disruption of Enterococcus faecalis Biofilm: A Confocal Laser Scanning Microscopic Study

Arathi Ganesh  1 , Venkateshbabu Nagendrababu  2 , Aby John  3 , Kandaswamy Deivanayagam  4
Affiliations

The Effect of Addition of an EPS Degrading Enzyme with and without Detergent to 2% Chlorhexidine on Disruption of Enterococcus faecalis Biofilm: A Confocal Laser Scanning Microscopic Study

Arathi Ganesh et al. J Clin Diagn Res. 2015 Nov.

Abstract

Background: Enterococcus faecalis is one of the most commonly occurring organisms retrieved from root canal treated teeth that show refractory apical periodontitis. Though it is well known that the ability of E. faecalis to form a matrix-encased biofilm contributes to its pathogenicity, the role of extracellular dextran and DNA in biofilm formation and its effect on the susceptibility of the biofilm to chlorhexidine remains poorly understood. It was hypothesized that the addition of an Extracellular Polymeric Substance (EPS) degrading enzyme along with a detergent to chlorhexidine may increase the susceptibility of the E. faecalis biofilm.

Aim: To evaluate the sensitivity of Enterococcus faecalis biofilms treated with DNase enzyme and their susceptibility to 2% chlorhexidine used alone or in conjunction with a detergent in a dentin disinfection model and examine under confocal laser scanning microscopy (CLSM).

Materials and methods: Semi cylindrical shaped dentin specimens were infected with E. faecalis and incubated for 24 hours. Following incubation, the infected dentin specimens were exposed for 3 minutes to the four disinfecting solutions and grouped accordingly. {Group I- Sterile saline, Group II- 2% Chlorhexidine (CHX), Group III- Dnase1 Enzyme + 2% CHX, Group IV- DNase1 Enzyme + 2% CHX & Tween 80. Bacterial viability was then assessed by staining the specimens and examining under CLSM to analyse the proportion of dead and live bacteria within the dentinal tubules.

Results: The Groups II, III and IV showed statistically significant (p<0.05) percentage of dead bacteria compared to the control (Group I). However there was no significant difference in the killing effectiveness within the experimental groups (II-IV) at (p<0.05).

Conclusion: EPS degrading enzyme (DNase I) disrupts the biofilm and increases the susceptibility of E.faecalis when exposed to 2% Chlorhexidine and the use of a surfactant with this combination significantly contributes to improving the antibacterial efficacy.

Keywords: Bacterial viability; Confocal laser scanning microscope; DNase1; Dentinal tubules; Tween 80.

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Figures

[Table/Fig-1]:
[Table/Fig-1]:
Specimen preparation and disinfection
[Table/Fig-2]:
[Table/Fig-2]:
Confocal armamentarium and bacterial stains used in the study
[Table/Fig-3]:
[Table/Fig-3]:
Figures from 1-4 represent the 4 groups- Group I: Sterile Saline, Group II: 2% CHX, Group III: 2% CHX+DNase I, Group IV: 2% CHX+Tween 80+DNase I. A represents dead bacteria and B represents live bacteria
See this image and copyright information in PMC

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