Oral Biofilms. Группа авторов

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Å, Dahlen G: The cleaning and disinfection of water systems in dental units according to the UnitClean method. Tandläkartidningen 2007;99:52–56.

      Gunnar Dahlen

      Department Oral Microbiology and Immunology, Institute of Odontology

      Sahlgrenska Academy, University of Gothenburg, Box 450

      SE–405 30 Gothenburg (Sweden)

      [email protected]

       Biofilm in General

      Published online: December 21, 2020

      Eick S (ed): Oral Biofilms. Monogr Oral Sci. Basel, Karger, 2021, vol 29, pp 19–29 (DOI: 10.1159/000510196)

      ______________________

      Lara B. Schultzea Alejandra Maldonadoa Adrian Lussib, c Anton Sculeana Sigrun Eicka

      a Department of Periodontology, Laboratory of Oral Microbiology, School of Dental Medicine, University of Bern, Bern, Switzerland; b School of Dental Medicine, University of Bern, Bern, Switzerland; c Department of Operative Dentistry and Periodontology, University Medical Center, Freiburg, Germany

      ______________________

      Abstract

      The pH value of a biofilm influences the pathogenesis and therapy of oral diseases such as caries and periodontitis. This study aimed to investigate the influence of different initial pH values on the microbial composition, bacterial counts, metabolic activity, and quantity of three defined biofilms representing oral health, caries, and periodontal disease. Respective bacterial suspensions in the nutrient broth were initially adjusted to pH values between 5 and 8. Then biofilms were cultured on polystyrene surfaces coated with a proteinaceous solution for 2 h (“healthy” biofilm), 6 h (“healthy,” and “cariogenic” biofilms), 24 h (“cariogenic,” and “periodontitis” biofilms), and 48 h (“periodontitis” biofilm). In all biofilms, total bacterial counts were lower at an initial pH of 5 or 5.5 than at higher pH values. In the biofilm representing caries, the percentage of cariogenic bacteria (Streptococcus mutans, S. sobrinus, Lactobacillus acidophilus) was higher at a low pH, the metabolic activity was highest at pH 6–6.5, and biofilm mass was greatest at pH 7–7.5. In the biofilm representing periodontitis, the percentage of Porphyromonas gingivalis increased with the pH. Also, the metabolic activity was highest at pH 8, whereas mass had the highest value at pH 7. In conclusion, the initial pH value influences biofilm formation. In particular, metabolic activity and the amount of bacteria associated with disease correlated with the respective pH known to be of importance in the development of caries (relatively low pH) and periodontitis (higher pH). Modifying the pH level in oral biofilms might be an alternative concept in (primary) prevention and treatment, not only of caries but also of periodontitis.

      © 2021 S. Karger AG, Basel

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      The aim of this study was to investigate the influence of initially different pH values on biofilm formation. For this, nutrient media containing buffers were adjusted to pH values in a range from 5 to 8 in increments of 0.5. Defined microbial strains representing oral health, caries, and periodontal disease were studied for their ability to form biofilms regarding bacterial counts, microbial composition, biofilm mass, and metabolic activity.

      Materials and Methods

      The strains were passaged 48–24 h before the experiments on tryptic-soy agar plates with 5% sheep blood. For T. forsythia, N-acetylmuramic acid (10 mg/L) was added. T. denticola was cultivated in modified mycoplasma broth (BD, Franklin Lakes, NJ, USA) added with 5 mg/mL of cocarboxylase in anaerobic conditions.

      Thereafter, the bacteria were suspended in 0.9% w/v NaCl to McFarland 4. The mixed suspension for the “healthy” biofilm consisted of two parts S. gordonii and three parts Actinomyces naeslundii. The cariogenic biofilm was mixed with one part S. gordonii and S. mutans, two parts A. naeslundii and S. sobrinus, and three parts Lactobacillus acidophilus. For the periodontal biofilm, the respective mixture was prepared with one part S. gordonii and three parts each of the other seven bacteria. These mixed suspensions were added 1:20 to the nutrient broth (Wilkins-Chalgren Broth; Oxoid, Basingstoke, UK) with 5 mg/L β-NAD (Sigma-Aldrich, Buchs, Switzerland) which had been adjusted to an approximate pH with two different buffers (citrate buffer and phosphate buffer) and precisely


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