Please use this identifier to cite or link to this item: https://doi.org/10.1590/1678-7757-2018-0699
DC FieldValue
dc.titleRole of extracellular dna in enterococcus faecalis biofilm formation and its susceptibility to sodium hypochlorite
dc.contributor.authorYu, M.-K.
dc.contributor.authorKim, M.-A.
dc.contributor.authorRosa, V.
dc.contributor.authorHwang, Y.-C.
dc.contributor.authorDel Fabbro, M.
dc.contributor.authorSohn, W.-J.
dc.contributor.authorMin, K.-S.
dc.date.accessioned2021-11-16T07:26:02Z
dc.date.available2021-11-16T07:26:02Z
dc.date.issued2019
dc.identifier.citationYu, M.-K., Kim, M.-A., Rosa, V., Hwang, Y.-C., Del Fabbro, M., Sohn, W.-J., Min, K.-S. (2019). Role of extracellular dna in enterococcus faecalis biofilm formation and its susceptibility to sodium hypochlorite. Journal of Applied Oral Science 27 : e20180699. ScholarBank@NUS Repository. https://doi.org/10.1590/1678-7757-2018-0699
dc.identifier.issn1678-7757
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/206411
dc.description.abstractObjective: This study investigated the role of extracellular deoxyribonucleic acid (eDNA) on Enterococcus faecalis (E. faecalis) biofilm and the susceptibility of E. faecalis to sodium hypochlorite (NaOCl). Methodology: E. faecalis biofilm was formed in bovine tooth specimens and the biofilm was cultured with or without deoxyribonuclease (DNase), an inhibitor of eDNA. Then, the role of eDNA in E. faecalis growth and biofilm formation was investigated using colony forming unit (CFUs) counting, eDNA level assay, crystal violet staining, confocal laser scanning microscopy, and scanning electron microscopy. The susceptibility of E. faecalis biofilm to low (0.5%) or high (5%) NaOCl concentrations was also analyzed by CFU counting. Results: CFUs and biofilm formation decreased significantly with DNase treatment (p<0.05). The microstructure of DNase-treated biofilms exhibited less structured features when compared to the control. The volume of exopolysaccharides in the DNase-treated biofilm was significantly lower than that of control (p<0.05). Moreover, the CFUs, eDNA level, biofilm formation, and exopolysaccharides volume were lower when the biofilm was treated with DNase de novo when compared to when DNase was applied to matured biofilm (p<0.05). E. faecalis in the biofilm was more susceptible to NaOCl when it was cultured with DNase (p<0.05). Furthermore, 0.5% NaOCl combined with DNase treatment was as efficient as 5% NaOCl alone regarding susceptibility (p>0.05). Conclusions: Inhibition of eDNA leads to decrease of E. faecalis biofilm formation and increase of susceptibility of E. faecalis to NaOCl even at low concentrations. Therefore, our results suggest that inhibition of eDNA would be beneficial in facilitating the efficacy of NaOCl and reducing its concentration. © 2019, Bauru School of Dentistry, University of Sao Paulo. All rights reserved.
dc.publisherBauru School of Dentistry, University of Sao Paulo
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2019
dc.typeArticle
dc.contributor.departmentDENTISTRY
dc.description.doi10.1590/1678-7757-2018-0699
dc.description.sourcetitleJournal of Applied Oral Science
dc.description.volume27
dc.description.pagee20180699
Appears in Collections:Elements
Staff Publications

Show simple item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_1590_1678-7757-2018-0699.pdf697.81 kBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


This item is licensed under a Creative Commons License Creative Commons