الملخص
<p><b>OBJECTIVE</b>To study the changes of growth and biofilm formation capability of Enterococcus faecalis (Ef) in different stress conditions.</p><p><b>METHODS</b>The changes of growth of Ef in stress conditions were observed by measuring the A600 value with ultraviolet spectrophotometer. Ef was incubated on glass slide in stress conditions, biofilm formation capability of cells was investigated by colony-forming unit (CFU) counting of the culturable bacteria and fluorescence confocal laser scanning microscopy.</p><p><b>RESULTS</b>Ef couldn't growth under the conditions of 2%, 5%NaClO, pH = 11 and 12, the A600 value was unchanged in 96 hours. But the growth curve changed at different levels in other stress conditions: under 1%NaClO, the A600 value peaked at 1.461 at 16 hour (the peaked level was 1.238 at 6 hours in control group) ; under 0,0.05%,0.15% glucose, it peaked at 0.645,0.890, 1.173, respectively, at 6 hour (it was maximized to 1.195 at 6 hours in control group); the A600 value peaked at 1.704 at 6 hours at pH = 9 and 1.225 at 10 hours at pH = 10 (the peak level was 1.732 at 6 hours at pH = 7) . Biofilm assay showed that Ef were able to form biofilm in these stress conditions except 5%NaClO and pH = 12.</p><p><b>CONCLUSIONS</b>Ef could growth and form biofilms in energy starvation, low concentrations of sodium hypochlorite and weak alkaline stress.</p>
الموضوعات
Biofilms , Colony Count, Microbial , Enterococcus faecalis , Glucose , Pharmacology , Hydrogen-Ion Concentration , Microscopy, Confocal , Sodium Hypochlorite , Pharmacologyالملخص
<p><b>OBJECTIVE</b>To analyze the community in dental plaque of elder people with root caries.</p><p><b>METHODS</b>Total DNAs were extracted from the root caries dental plaques of nine elders over 60 years of age. Polymerase chaid reaction-based denaturing gradient gel electrophoresis (PCR-DGGE) was used to analyze the microbial composition, DGGE bands were excised from the gels for sequencing and identification.</p><p><b>RESULTS</b>The dominant genus in root caries dental plaque of elder people were: Acinetobacte [0.9% (1/114)], Actinobaculum [1.8% (2/114)], Actinomyces [15.8% (18/114)], Aggregatibacter [0.9% (1/114)], Capnocytophaga [14.0% (16/114)], Corynebacterium [0.9% (1/114)], Haemophilus [0.9% (1/114)], Mobiluncus [0.9% (1/114)], Naxibacter [0.9% (1/114)], Neisseriaceae [10.5% (12/114)], Porphyromonas [0.9% (1/114)], Prevotella [12.3% (14/114)], Selenomonas [6.1% (7/114)], Staphylococcus [1.8% (2/114)], Oralis streptococcus [6.1% (7/114)], Mutans streptococcu [7.9% (9/114)], Tannerella [0.9% (1/114)], Treponema [1.8% (2/114)], Veillonella [10.5% (12/114)] and two uncultured unknown genus [1.8% (2/114)]. Uncultred genotypes accounted for 19.30% of the total. Gram-positive bacteria genotype accounted for 31.6% (36/114), and Gram-negative bacteria genotype accounted for 66.7% (76/114).</p><p><b>CONCLUSIONS</b>There were many bacteria genotypes in root caries dental plaque in the elderly, which were widely distributed. Gram-negative bacteria accounted for the majority. Genotype-specific pathogenic bacteria were not found.</p>
الموضوعات
Aged , Humans , Middle Aged , Age Factors , Capnocytophaga , Genetics , DNA, Bacterial , Genetics , Denaturing Gradient Gel Electrophoresis , Dental Plaque , Microbiology , Genotype , Gram-Negative Bacteria , Genetics , Gram-Positive Bacteria , Genetics , Neisseriaceae , Genetics , Prevotella , Genetics , Root Caries , Microbiology , Selenomonas , Genetics , Streptococcus mutans , Genetics , Streptococcus oralis , Genetics , Veillonella , Geneticsالملخص
<p><b>OBJECTIVE</b>To investigate the effect of Streptococcus mutans luxS mutarotation on the early biofilm formation.</p><p><b>METHODS</b>Based on the immobilization of magnetic beads by adherent cells, an assay of biofilm quantitative analysis was developed for the kinetic quantification of biofilm formation in this study. Streptococcus mutans luxS mutant strain was constructed and subject to this biofilm luxS mutant strain were compared.</p><p><b>RESULTS</b>The delta luxS mutant started to form a biofilm from the 6th hour (delta BFI = 2.015), and the delta BFI of luxS mutant increased more quickly than that of the wild type strain, until reaching a complete immobilization of the beads after 10 hours (delta BFI = 7.025). The wild-type strain start to form a biofilm from the 10 th hour (delta BFI = 1.875) and the beads were completely immobilized between 12 and 14 hours.</p><p><b>CONCLUSIONS</b>The luxS mutation can accelerate biofilm on a polystyrene surface during the mid-exponential growth phase. And a luxS-dependent signal may play an important role in the early biofilm formation of Streptococcus mutans.</p>