Ocorrência de Actinobacillus actinomycetemcomitans em pacientes com periodontite crônica, periodontite agressiva, pessoas saudáveis e crianças com gengivite em duas cidades do Estado de São Paulo, Brasil

The aim of this study was to determine the frequency of isolation of Actinobacillus actinomycetemcomitans (Aa) in 100 patients with chronic periodontitis, 14 patients with aggressive periodontitis, 142 pre-school children with gingivitis and 134 periodontally healthy subjects. Samples of subgingival plaque were taken using sterilized paper points introduced into periodontal pockets or gingival crevice for 60 seconds and inoculated on TSBV agar, which was incubated under anaerobiosis at 37ºC, for 4 days. Microbial identification was performed through biochemical methods and morphocellular and morphocolonial analysis. Aa was detected in 40.3% of healthy subjects, 68% of patients with chronic periodontitis, 92.86% of patients with aggressive periodontitis and 40.14% of children with gingivitis. The rate of recovery of Aa in the tested human groups proved to be higher than previously reported and in agreement with participation of this facultative anaerobe as a member of native microbiota of the periodontium and its relation with aggressive and chronic periodontitis in Brazil.Avaliou-se a ocorrência de Actinobacillus actinmycetemcomitans (Aa) em pacientes 100 pacientes com periodontite crônica, 14 com doença periodontal agressiva, 142 crianças com gengivite em idade pré-escolar e 134 indivíduos adultos saudáveis. Amostras de placa subgengival foram coletadas usando cones de papel estéreis introduzidos nas bolsas periodontais ou no sulco gengival por 60 segundos e inoculadas em ágar TSBV, que foram incubadas em anaerobiose a 37ºC, por 4 dias. A identificação microbiana foi realizada através de análises bioquímicas, morfocelulares e morfocoloniais. Aa foi detectado em 40,3% de indivíduos saudáveis, 68% de pacientes com periodontite crônica, 92,86% de pacientes com periodontite agressiva e 40,14% das crianças com gengivite. A taxa de ocorrência de Aa nos grupos testados provou ser mais alta do que a previamente descrita na literatura e que esse microrganismo é membro freqüente da microbiota de indivíduos adultos periodontalmente sadios e de crianças com idade pré-escolar com gengivite além de sua relação com a periodontite crônica e agressiva no Brasil

Influência de aplicações do laser érbio:YAG sobre a viabilidade microbiana, sua resistência a drogas e atividade hemolítica

A atividade antimicrobiana do laser Er:YAG foi avaliada sobre biofilme bacteriano constituído por Escherichia coli ATCC 8739, Escherichia coli ATCC 25922, Staphylococcus aureus ATCC 6538 e 3 cepas de Fusobacterium nucleatum e sobre biofilme de microrganismos salivares. Os biofilmes foram submetidos à ação do laser a 1,2 W e 10 Hz por 5, 10, 15, 20, 30 e 60 s e fez-se a avaliação da microbiota residual em ágar sangue, em anaerobiose. O biofilme salivar se mostrou mais sensível nos primeiros tempos de irradiação. A redução microbiana em relação ao controle foi estatisticamente significativa entre todos os tempos testados. Avaliou-se também a ação do laser Er:YAG sobre 7 cepas de Fusobacterium nucleatum inoculadas sobre a superfície de corpos-de-prova (5mmX4mm) de dentes extraídos. Fez-se a aplicação do laser nos mesmos parâmetros físicos mencionados anteriormente, durante 15 s, levando à eliminação total do conteúdo séptico. O estudo avaliou também a irradiação do laser de Er:YAG durante tempos subinibitórios sobre a atividade hemolítica e susceptibilidade de 9 cepas de Fusobacterium nucleatum a amoxicilina, eritromicina, metronidazol e tetraciclina. Após a irradiação do laser, determinou-se a concentração inibitória mínima (CIM) para as drogas através do método de diluição em ágar. A ação do laser sobre a atividade hemolítica foi determinada em sangue humano. Verificou-se que o laser Er:YAG não afetou a atividade hemolítica de Fusobacterium nucleatum, que se mostrou α-hemolítica, tampouco a susceptibilidade a drogas dos isolados testados.Antimicrobial activity of Er:YAG laser was evaluated on a bacterial biofilm constituted by Escherichia coli ATCC 8739, Escherichia coli ATCC 25922, Staphylococcus aureus ATCC 6538 and 3 strains of Fusobacterium nucleatum and on biofilm produced by salivary microorganisms. Biofilms were irradiated by Er:YAG laser, 1,2 W and 10 Hz, for 5, 10, 15, 20, 30, and 60 s and the evaluation of residual contamination was performed on blood agar, under anaerobiosis. It was verified that salivary biofilm showed to be more susceptibility to the Er:YAG laser in shorter periods of laser irradiation. Bacterial reduction was significative in all tested periods of irradiation. The activity of Er:YAG laser was also evaluated on 7 strains of Fusobacterium nucleatum inoculated on samples of human dentin (5mm X 4mm), obtained from extracted teeth. The laser was used following the same physical parameters, as previously described, for 15 s, leading to complete elimination of their septic content. The study also evaluated the effects of subinibitory irradiation of Er:YAG laser on bacterial susceptibility of 9 strains of Fusobacterium nucleatum to antimicrobial drugs (amoxicillin, erythromycin, metronidazole, tetracycline) and hemolysis. Thus, after laser irradiation, the minimal inhibitory concentration of antimicrobial drugs was determined by using an agar dilution method. The influence of laser on hemolysis was carried out on human blood. It was verified that Er:YAG laser did not produce any measurable effect on hemolytic activity and the microbial susceptibility to tested antimicrobial drugs

Apical gaps after apicoectomy procedures performed on teeth filled with gutta-percha or ResilonTM

Aim: This ex vivo study compared, under scanning electron microscopy (SEM), the marginal adaptation of root canal obturation with either ResilonTM or gutta-percha cones following root-end resection. Methods: Thirty human single-rooted teeth with fully formed apices were collected and decoronated. The root canals were instrumented up to a size 45 taper .04 and obturated with laterally condensed gutta-percha (Group 1; n=15) or ResilonTM (Group 2; n=15). AH Plus sealer was used in both groups. After 48-h storage in saline, the apical 3 mm of each root were resected with a water-cooled high-speed plain fissure #170L carbide bur. Epoxy resin replicas of the resected root ends were examined by SEM. The total area of apical gap in each replica was measured using UTHSCSA ImageTool software. Data were analyzed statistically by the Mann- Whitney U-test (α=5%). Results: The mean area of apical gap in groups 1 and 2 was 0.0042 mm2 and 0.0015 mm2, respectively, with no statistically significant difference (P = 0.83). Conclusions: The type of material did not influence at the apical adaptation of root canal obturation after apicoectomy, and the misfit may be related to anatomic factors

Occurrence of Actinobacillus actinomycetemcomitans in patients with chronic periodontitis, aggressive periodontitis, healthy subjects and children with gingivitis in two cities of the state of São Paulo, Brazil

The aim of this study was to determine the frequency of isolation of Actinobacillus actinomycetemcomitans (Aa) in 100 patients with chronic periodontitis, 14 patients with aggressive periodontitis, 142 pre-school children with gingivitis and 134 periodontally healthy subjects. Samples of subgingival plaque were taken using sterilized paper points introduced into periodontal pockets or gingival crevice for 60 seconds and inoculated on TSBV agar, which was incubated under anaerobiosis at 37°C, for 4 days. Microbial identification was performed through biochemical methods and morphocellular and morphocolonial analysis. Aa was detected in 40.3% of healthy subjects, 68% of patients with chronic periodontitis, 92.86% of patients with aggressive periodontitis and 40.14% of children with gingivitis. The rate of recovery of Aa in the tested human groups proved to be higher than previously reported and in agreement with participation of this facultative anaerobe as a member of native microbiota of the periodontium and its relation with aggressive and chronic periodontitis in Brazil