ABSTRACT
More virulent strains may result from the acquisition of genes by genetic exchange, pathogenicity islands in several species encoding toxins, adhesion factors and other factors associated with virulence. The aim of this study was to investigate the prevalence of E. faecalis strains in secondary endodontic/ persistent using endodontic infection by culture and PCR technqiues; and to investigate for the presence of virulence factor genes of gelatinase (gelE), cytolysin activator (Cyla), surface adhesion of Enterococcus (ESP) and collagen adhesin of Enterococcus (ACE). Material and methods: Microbial samples were obtained from 12 teeth with secondary/ persistent endodontic infection showing apical periodontitis. Culture techniques were used including serial dilution, plating, incubation, and biochemical identification. For PCR detection, samples were analyzed using a species-specific primer of the 16S rDNA and the downstream intergenic spacer region. Results: Culture and PCR detected the test species in 3/12 (25%) and 5/12 (41.6%) of teeth,respectively. A total of 38 Enterococcus faecalis strains were isolated and submitted to the virulence factor genes analysis. PCR products consistent with genes encoding surface adhesion (ESP), gelatinase (gelE) and collagen binding antigen (ACE) were found in 26/38 (68%), 31/38 (81%) and 38/38 (100%) of the isolates. The Cytolysin activator (Cyla) gene was not recovered from E. faecalis isolates. Conclusions: In conclusion, the present study revealed by culture and molecular methods revealed a high prevalence of E. faecalis in teeth with secondary/ persistent endodontic infection. Moreover, of a clinical relevance, we found different E. faecalis strains carrying different virulence determinants.
Objetivos: O objetivo deste estudo foi investigar a prevalência de cepas de E. faecalis em canais com infecções endodônticas secundárias/persistentes por meio de cultura e PCR, além de analisar a presença de fatores de virulência genéticos como: gelatinase (gelE), ativador de citolisina (Cyla), adesina de superfície (ESP) e adesina de colágeno (ACE). Material e métodos: Foram coletadas amostras de 12 canais radiculares com infecção endodôntica secundária/persistente e presença de lesão periapical. Para a cultura microbiológica foi realizada diluição em série, incubação e identificação bioquímica dos microrganismos, enquanto que no PCR as amostras foram analisadas através de primers específicos 16S rDNA. Os casos com presença de Enterococcus faecalis foram selecionadas para realização de análise quanto aos fatores de virulência: gelE, Cyla, ESP e ACE. Resultados: Enterococcus faecalis foi detectado através de cultura e PCR em 3/12 (25%) e 5/12 (41,6%) dos casos, respectivamente. No total, foram isoladas 38 amostras com presença de E. faecalis. Os produtos de PCR consistentes com os genes ESP, gelE e ACE foram encontrados em 26 /38 (68%), 31 /38 (81%) e 38/38 (100%) dos isolados. Cyla não foi recuperado a partir de E. faecalis em nenhum dos isolados. Conclusões: O presente estudo revelou alta prevalência de E. faecalis em dentes com infecção endodôntica secundária/ persistente. Estes microrganismos apresentaram elevado índice de diferentes fatores de virulência.
Subject(s)
Bacteria , Dental Pulp Cavity , Enterococcus faecalis , Virulence FactorsABSTRACT
O objetivo deste trabalho foi verificar a efetividade na descontaminação de cones de guta-percha e de resilon com os seguintes grupos: hipoclorito de sódio 5,25% durante 1 minuto; hipoclorito de sódio 2,5% durante 1 minuto; clorexidina 2% durante 1 minuto; glicerina fenicada durante 24 horas. Os agentes apresentaram-se eficazes, sem diferença estatística significativa, embora a clorexidina a 2% tenha apresentado um percentual de 20% de amostras positivas tanto na guta-percha como no resilon, o que pode ser considerado relevante clinicamente. Concluiu-se que o hipoclorito de sódio e a glicerina fenicada podem ser indicados para a descontaminação de ambos os tipos de cone, nas duas concentrações testadas.
The aim of this study was to assess the effectiveness in decontamination of gutta-percha and Resilon with the following groups: 5.25% sodium hypochlorite for 1 minute; 2.5% sodium hypochlorite for 1 minute, 2% chlorhexidine during 1 minute; glycerin fenicada for 24 hours. The agents had been effective, not statistically significant, although the 2% chlorhexidine presented a higher percentage of 20% of positive samples in both the gutta-percha and Resilon in what can be considered clinically relevant. It was concluded that sodium hypochlorite and glycerin fenicada may be indicated for the decontamination of both types of cone, at the concentrations tested.
Subject(s)
Solutions , Decontamination , Enterococcus faecalis , Gutta-PerchaABSTRACT
Background: Sodium hypochlorite (NaOCl) is the most widely used endodontic irrigant because of its excellent antimicrobial, organic tissue dissolving, and lubricating properties. However, it is highly cytotoxic to the periapical tissues. Aim: This study evaluated in vitro the extrusion of 5.25% NaOCl through the apical foramina of mesiobuccal (MB) root canals of maxillary first molars in two experimental conditions: Before apical debridement and after apical debridement with different instrument sizes to ensure direct access to the apical foramen (apical patency). Materials and Methods: Coronal accesses were prepared in 17 teeth and the apical foramina of the distobuccal and palatal root canals were sealed. The teeth were held in acrylic receptacles with the roots turned upwards to reproduce their position in the maxillary dental arch. The receptacles were filled with a starch/KI solution (a reagent that changes its color to blue after contacting NaOCl) covering the roots. The experiment had two phases: P1: Irrigation of the MB canals with 5.25% NaOCl without previous establishment of apical patency; P2: Canal irrigation after use of size 10 K-file and size 15 Flexofile as patency files. Only specimens with no NaOCl extrusion in P1 were assigned to P2. NaOCl was delivered pressureless at the canal entrance. The moment that the starch/KI solution contacted NaOCl was captured on digital photographs. Results and Conclusions: There was no NaOCl extrusion in nine specimens in P1, but all of these teeth had irrigant extrusion in P2. The 5.25% NaOCl used as an endodontic irrigant showed great capacity to extrude beyond both intact and small-sized apical foramina of MB root canals of maxillary first molars.