Endodontic disease has mainly a microbial origin. It is caused by biofilms capable of attaching and surviving in the root canal. Therefore, it is important to study the conditions in which those biofilms grow, develop and colonize the root canal system. However, few studies have used natural teeth a...
- Autores:
-
Díez Ortega, Hugo; Infectious Diseases Group, School of Sciences, Department of Microbiology, Pontificia Universidad Javeriana. Bogotá, Colombia.
Correa Toral, Francisco; Center for Dental Research, School of Dentistry, Pontificia Universidad Javeriana. Bogotá, Colombia.
Delgado Hernández, Leylin; Center for Dental Research, School of Dentistry, Pontificia Universidad Javeriana. Bogotá, Colombia.
Echavarría González, Carolina
Serna Varona, Fátima
Rodríguez Ciodaro, Adriana
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2017
- Institución:
- Pontificia Universidad Javeriana
- Repositorio:
- Repositorio Universidad Javeriana
- Idioma:
- eng
- OAI Identifier:
- oai:repository.javeriana.edu.co:10554/31303
- Acceso en línea:
- http://revistas.javeriana.edu.co/index.php/scientarium/article/view/15660
http://hdl.handle.net/10554/31303
- Palabra clave:
- Odontology; endodontics; microbiology
Dental Pulp Diseases, Biofilm, microbial interactions, Enterococcus faecalis, Staphylococcus aureus, Candida albicans.
- Rights
- openAccess
- License
- Atribución-NoComercial-SinDerivadas 4.0 Internacional
| Summary: | Endodontic disease has mainly a microbial origin. It is caused by biofilms capable of attaching and surviving in the root canal. Therefore, it is important to study the conditions in which those biofilms grow, develop and colonize the root canal system. However, few studies have used natural teeth as models, which would take into account the root canal anatomical complexity and simulate the clinical reality. In this study, we used human premolar root canals to standardize in vitro biofilm optimal formation conditions for microorganisms such as Enterococcus faecalis, Staphylococcus aureus and Candida albicans. 128 lower premolars underwent canal preparation using K-type files, and were treated with 5.25% sodium hypochlorite and EDTA. Samples were inoculated with microorganisms and incubated for 15, 30, 45, and 60 days under anaerobiosis (CO2 atmosphere) and aerobiosis. Microorganism presence was confirmed by Gram staining, cell culture, and electron microscopy. Exopolysaccharide matrix and microorganism aggregation were observed following 15 days of incubation. Bacterial growth towards the apical third of the root canal and biofilm maturation was detected after 30 days. CO2 atmosphere favored microbial growth the most. In vitro biofilm maturation was confirmed after 30 days of incubation under a CO2 atmosphere for both bacteria and yeast. |
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