Metabolic activity of Streptococcus mutans biofilms after treatment with different mouthwash formulations

Aim: The aim of this study was to investigate the metabolic activity of Streptococcus mutans biofilms after treatment with mouthwashes with different compositions. Methods: S. mutans biofilms were growth on polystyrene plates during 18 h, washed with sterile saline and treated with the following mou...

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Main Authors: Taciano R. Cardoso, Alexandre S. Carvalho, Marcelo E. Beletti, Marcelo H. Napimoga, Geraldo Thedei Junior
Format: Article
Language:English
Published: Universidade Estadual de Campinas 2015-11-01
Series:Brazilian Journal of Oral Sciences
Subjects:
Online Access:https://periodicos.sbu.unicamp.br/ojs/index.php/bjos/article/view/8641714
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author Taciano R. Cardoso
Alexandre S. Carvalho
Marcelo E. Beletti
Marcelo H. Napimoga
Geraldo Thedei Junior
author_facet Taciano R. Cardoso
Alexandre S. Carvalho
Marcelo E. Beletti
Marcelo H. Napimoga
Geraldo Thedei Junior
author_sort Taciano R. Cardoso
collection DOAJ
description Aim: The aim of this study was to investigate the metabolic activity of Streptococcus mutans biofilms after treatment with mouthwashes with different compositions. Methods: S. mutans biofilms were growth on polystyrene plates during 18 h, washed with sterile saline and treated with the following mouthwashes during 1 min: Listerine®, Oral B®, Parodontax® and Periogard® with and without alcohol. After the treatment, the biofilms were incubated with complete medium containing sucrose during 60, 120 or 180 min, and then samples were collected for pH measurements. In addition, biofilms were grown in microscope coverslips treated as described above, followed by staining with Propidium Iodide and Fluoresceine for visualization with a confocal laser scanning microscopy. Results: For all mouthwashes evaluated, treatment was deleterious to cell metabolism, since little or no acidification was observed at least 60 min after treatment. Mouthwashes containing 0.2% chlorhexidine (Parodontax®) or essential oils (Listerine®) induced a significant reduction in the metabolic activity of biofilms during the tested time points (120 and 180 min after treatment), being thus more effective than the mouthwashes containing 0.12% chlorhexidine (Periogard®) or cetylpyridinium plus fluoride (Oral B®). The confocal analysis overall confirmed the results observed in the analysis of metabolic activity. Conclusions: The treatment of biofilms with mouthwashes containing 0.2% chlorhexidine or essential oils induced significant reduction in S. mutans metabolism.
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spelling doaj.art-139c9a7bd06e4f0289d409fdc1721c482022-12-21T22:11:51ZengUniversidade Estadual de CampinasBrazilian Journal of Oral Sciences1677-32252015-11-0110110.20396/bjos.v10i1.8641714Metabolic activity of Streptococcus mutans biofilms after treatment with different mouthwash formulationsTaciano R. Cardoso0Alexandre S. Carvalho1Marcelo E. Beletti2Marcelo H. Napimoga3Geraldo Thedei Junior4University of UberabaUniversity of Uberaba, UberabaFederal University of UberlandiaUniversity of UberabaUniversity of Uberaba, UberabaAim: The aim of this study was to investigate the metabolic activity of Streptococcus mutans biofilms after treatment with mouthwashes with different compositions. Methods: S. mutans biofilms were growth on polystyrene plates during 18 h, washed with sterile saline and treated with the following mouthwashes during 1 min: Listerine®, Oral B®, Parodontax® and Periogard® with and without alcohol. After the treatment, the biofilms were incubated with complete medium containing sucrose during 60, 120 or 180 min, and then samples were collected for pH measurements. In addition, biofilms were grown in microscope coverslips treated as described above, followed by staining with Propidium Iodide and Fluoresceine for visualization with a confocal laser scanning microscopy. Results: For all mouthwashes evaluated, treatment was deleterious to cell metabolism, since little or no acidification was observed at least 60 min after treatment. Mouthwashes containing 0.2% chlorhexidine (Parodontax®) or essential oils (Listerine®) induced a significant reduction in the metabolic activity of biofilms during the tested time points (120 and 180 min after treatment), being thus more effective than the mouthwashes containing 0.12% chlorhexidine (Periogard®) or cetylpyridinium plus fluoride (Oral B®). The confocal analysis overall confirmed the results observed in the analysis of metabolic activity. Conclusions: The treatment of biofilms with mouthwashes containing 0.2% chlorhexidine or essential oils induced significant reduction in S. mutans metabolism.https://periodicos.sbu.unicamp.br/ojs/index.php/bjos/article/view/8641714Streptococcus mutansMouthwashesChlorhexidineBiofilm
spellingShingle Taciano R. Cardoso
Alexandre S. Carvalho
Marcelo E. Beletti
Marcelo H. Napimoga
Geraldo Thedei Junior
Metabolic activity of Streptococcus mutans biofilms after treatment with different mouthwash formulations
Brazilian Journal of Oral Sciences
Streptococcus mutans
Mouthwashes
Chlorhexidine
Biofilm
title Metabolic activity of Streptococcus mutans biofilms after treatment with different mouthwash formulations
title_full Metabolic activity of Streptococcus mutans biofilms after treatment with different mouthwash formulations
title_fullStr Metabolic activity of Streptococcus mutans biofilms after treatment with different mouthwash formulations
title_full_unstemmed Metabolic activity of Streptococcus mutans biofilms after treatment with different mouthwash formulations
title_short Metabolic activity of Streptococcus mutans biofilms after treatment with different mouthwash formulations
title_sort metabolic activity of streptococcus mutans biofilms after treatment with different mouthwash formulations
topic Streptococcus mutans
Mouthwashes
Chlorhexidine
Biofilm
url https://periodicos.sbu.unicamp.br/ojs/index.php/bjos/article/view/8641714
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AT marceloebeletti metabolicactivityofstreptococcusmutansbiofilmsaftertreatmentwithdifferentmouthwashformulations
AT marcelohnapimoga metabolicactivityofstreptococcusmutansbiofilmsaftertreatmentwithdifferentmouthwashformulations
AT geraldothedeijunior metabolicactivityofstreptococcusmutansbiofilmsaftertreatmentwithdifferentmouthwashformulations