ABSTRACT
Knowledge of the microbial composition of abscessed primary tooth is limited. Aim: The aim was to investigate the presence of 10 oral bacterial species in samples from abscessed primary tooth root canals using microarray technology and to determine their association with clinical findings. Subjects and Methods: The samples were collected from root canals of 20 primary molars with acute primer infection. The bacterial composition of the samples was semi-quantitatively defined using a microarray system (ParoCheck®). Clinical parameters included the presence of spontaneous pain, mobility, percussion sensitivity and swelling. Statistical Analysis: Data were statistically analyzed by Student' t-test, Fisher's exact Chi-square test, Freeman–Halton–Fisher's exact test, and Spearman's rho correlation analysis. Results: All the tested species were detected in the samples. Fusobacterium nucleatum was the most frequent bacterium (100%), followed by Parvimonas micra (65%), Provetella intermedia (45%), and Treponema denticola (45%). According to paired bacterial combinations, F. nucleatum was significantly positively correlated with P. intermedia and P. micra (P < 0.05). T. denticola was significantly positively correlated with Porphyromonas gingivalis, Tannerella forsythia, Campylobacter rectus, and P. micra, while it was negatively correlated with Eikenella corrodens (P < 0.05). No statistically significant relationships were found between the presence of any bacteria and clinical findings. Conclusion: Microarray technology used in this study has demonstrated the presence of various bacteria with varying proportions in the root canals of abscessed primary teeth. The results regarding the high rate of certain bacterial combinations suggest the enhanced pathogenicity due to additive or synergistic effects of these microbial combinations.
ABSTRACT
Objective: The aim of this in vitro study was to compare the effectiveness of different final irrigant agitation techniques in the removal of Enterococcus faecalis biofilms from root canals. Material and Methods: In total, the root canals of 85 extracted single-rooted human maxillary incisors teeth were prepared using the Revo-S system to a 40/06 size. The apical foramen of each tooth was sealed by light-cured resin composite material to obstruct bacterial leakage. The specimens were sterilized in an autoclave at 121°C for 15 min and stored until further use. All teeth except five (negative control group) were inoculated with Enterococcus faecalis and incubated in a CO2 chamber at 37°C for 7 days; the trypticase soy broth was changed every 2 days. For the determination of possible biofilm formation, five of the 80 teeth were randomly selected as a positive control group; one tooth of positive control group was analysed for biofilm development by scanning electron microscope (SEM) and these teeth received no final irrigant agitation procedure. Then, the remaining 75 teeth were randomly divided into five test groups (n=15 each) and were sequentially irrigated with 5% sodium hypochlorite (NaOCl), 17% ethylenediaminetetraacetic acid and 5% NaOCl. Following each irrigant application, different final irrigant agitation techniques were introduced for 60 s (3×20-s sessions). Group 1 received manual dynamic agitation, group 2 received passive ultrasonic agitation (PUI), group 3 received EndoActivator agitation, group 4 received photoninitiated photoacoustic streaming (PIPS) with the Er:YAG laser and group 5 received conventional syringe irrigation. Colony-forming units (CFUs) were counted in samples from the positive control and test groups. Data were analysed using Kruskal Wallis and post-hoc MannWhitney U multiple comparison tests. Results: E. faecalis elimination was significantly better in the experimental groups than in the positive control groups (p < 0.001). Manualdynamic agitation and conventional syringe irrigation, with no significant differences between the two groups. Conclusion: Essentially, CFU reduction was significantly greater in the PUI, EndoActivator and PIPS groups than in the manualdynamic agitation and conventional syringe irrigation groups (p <0.001) , with no significant differences among the former three groups. (AU)
Objetivo: O objetivo deste estudo in vitro foi comparar a eficácia de diferentes técnicas finais de agitação de irrigantes na remoção de biofilmes de Enterococcus faecalis de canais radiculares. Material e Métodos: No total, os canais radiculares de 85 dentes incisivos superiores unirradiculares humanos extraídos foram preparados usando o sistema Revo-S para um tamanho 40/06. O forame apical de cada dente foi selado por material compósito de resina fotopolimerizável para obstruir o vazamento bacteriano. Os espécimes foram esterilizados em autoclave a 121 ° C por 15 min e armazenados até uso posterior. Todos os dentes, exceto cinco (grupo controle negativo), foram inoculados com Enterococcus faecalis e incubados em câmara de CO2 a 37 ° C por 7 dias; o caldo de soja tripticase foi trocado a cada 2 dias. Para a determinação da possível formação de biofilme, cinco dos 80 dentes foram selecionados aleatoriamente como grupo controle positivo; um dos dentes do grupo controle positivo foi analisado para o desenvolvimento do biofilme por microscopia eletrônica de varredura (MEV) e estes dentes não receberam nenhum procedimento final de agitação irrigante. Em seguida, os 75 dentes restantes foram aleatoriamente divididos em cinco gruposteste (n = 15 cada) e irrigados sequencialmente com hipoclorito de sódio a 5% (NaOCl), ácido etilenodiaminotetracético a 17% e NaOCl a 5%. Após cada aplicação de irrigantes, diferentes técnicas finais de agitação foram introduzidas por 60 s (3 x 20 s sessões). Grupo 1 recebeu agitação manual-dinâmica, grupo 2 recebeu agitação ultra-sônica passiva (PUI), grupo 3 recebeu agitação EndoActivator, grupo 4 recebeu fotoacústica iniciada por fóton (PIPS) com o laser Er: YAG e grupo 5 recebeu irrigação convencional com seringa. As unidades formadoras de colônia (CFUs) foram contadas em amostras dos grupos controle positivo e teste. Os dados foram analisados utilizando testes de comparação múltipla Kruskal-Wallis e post-hoc Mann-Whitney U. Resultados: A eliminação de E. faecalis foi significativamente melhor nos grupos experimentais do que nos grupos de controle positivo (p < 0,001). Agitação manual-dinâmica e irrigação com seringa convencional, sem diferenças significativas entre os dois grupos. Conclusão: Essencialmente, a redução de UFC foi significativamente maior nos grupos PUI, EndoActivator e PIPS do que nos grupos de agitação manual-dinâmica e de seringa convencional (p < 0,001), sem diferenças significativas entre os três grupos anteriores (AU)
Subject(s)
Enterococcus faecalis , Dental PlaqueABSTRACT
Aim: The purpose of this study was to analyze the presence of Aggregatibacter actinomycetemcomitans in saliva and cardiac tissue samples of children requiring cardiac surgery in Istanbul, Turkey. Subjects and Methods: Twenty‑five patients (mean age: 6.24 ± 2.93) undergoing surgery for congenital heart defects (CHDs) and an age/gender‑matched control group of 25 healthy children were enrolled in the study. Saliva samples were collected from all children; plaque index (PI) and gingival index (GI) were also determined. In CHD group, cardiac tissue samples were received during surgery. All samples were evaluated for the presence of A. actinomycetemcomitans and its highly leukotoxic JP2 clonal strains using polymerase chain reaction. The findings were analyzed by Mann–Whitney U, Chi‑square, and Fisher’s exact tests. Results: No significant differences were found in PI and GI values between the groups. A. actinomycetemcomitans was not detected in cardiac tissue samples. A. actinomycetemcomitans in saliva was detected in 2 (8%) of the CHD and 5 (20%) of the control children (p > 0.05). A. actinomycetemcomitans JP2 clonal strains were determined from 1 (4%) of the control group while it was not determined from the samples of the CHD group. Conclusions: Early colonization of A. actinomycetemcomitans in oral cavities could be assessed as a risk marker for periodontal disease. Periodontal pathogens may enter bloodstream through bacteremia; thus, the presence of periodontal pathogens in the oral cavity of children should be assessed as a risk marker for cardiac diseases in older ages.