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Streptococcus mutans and Actinomyces naeslundii Interaction in Dual-Species Biofilm

The study of bacterial interaction between Streptococcus mutans and Actinomyces naeslundii may disclose important features of biofilm interspecies relationships. The aim of this study was to characterize—with an emphasis on biofilm formation and composition and metabolic activity—single- and dual-sp...

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Autores principales: de Oliveira, Rosa Virginia Dutra, Bonafé, Fernanda Salloume Sampaio, Spolidorio, Denise Madalena Palomari, Koga-Ito, Cristiane Yumi, de Farias, Aline Leite, Kirker, Kelly R., James, Garth A., Brighenti, Fernanda Lourenção
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074783/
https://www.ncbi.nlm.nih.gov/pubmed/32023892
http://dx.doi.org/10.3390/microorganisms8020194
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author de Oliveira, Rosa Virginia Dutra
Bonafé, Fernanda Salloume Sampaio
Spolidorio, Denise Madalena Palomari
Koga-Ito, Cristiane Yumi
de Farias, Aline Leite
Kirker, Kelly R.
James, Garth A.
Brighenti, Fernanda Lourenção
author_facet de Oliveira, Rosa Virginia Dutra
Bonafé, Fernanda Salloume Sampaio
Spolidorio, Denise Madalena Palomari
Koga-Ito, Cristiane Yumi
de Farias, Aline Leite
Kirker, Kelly R.
James, Garth A.
Brighenti, Fernanda Lourenção
author_sort de Oliveira, Rosa Virginia Dutra
collection PubMed
description The study of bacterial interaction between Streptococcus mutans and Actinomyces naeslundii may disclose important features of biofilm interspecies relationships. The aim of this study was to characterize—with an emphasis on biofilm formation and composition and metabolic activity—single- and dual-species biofilms of S. mutans or A. naeslundii, and to use a drip flow reactor (DFR) to evaluate biofilm stress responses to 0.2% chlorhexidine diacetate (CHX). Single- and dual-species biofilms were grown for 24 h. The following factors were evaluated: cell viability, biomass and total proteins in the extracellular matrix, 2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide—“XTT”—reduction and lactic acid production. To evaluate stress response, biofilms were grown in DFR. Biofilms were treated with CHX or 0.9% sodium chloride (NaCl; control). Biofilms were plated for viability assessment. Confocal laser-scanning microscopy (CLSM) was also performed. Data analysis was carried out at 5% significance level. S. mutans viability and lactic acid production in dual-species biofilms were significantly reduced. S. mutans showed a higher resistance to CHX in dual-species biofilms. Total protein content, biomass and XTT reduction showed no significant differences between single- and dual-species biofilms. CLSM images showed the formation of large clusters in dual-species biofilms. In conclusion, dual-species biofilms reduced S. mutans viability and lactic acid production and increased S. mutans’ resistance to chlorhexidine.
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spelling pubmed-70747832020-03-20 Streptococcus mutans and Actinomyces naeslundii Interaction in Dual-Species Biofilm de Oliveira, Rosa Virginia Dutra Bonafé, Fernanda Salloume Sampaio Spolidorio, Denise Madalena Palomari Koga-Ito, Cristiane Yumi de Farias, Aline Leite Kirker, Kelly R. James, Garth A. Brighenti, Fernanda Lourenção Microorganisms Article The study of bacterial interaction between Streptococcus mutans and Actinomyces naeslundii may disclose important features of biofilm interspecies relationships. The aim of this study was to characterize—with an emphasis on biofilm formation and composition and metabolic activity—single- and dual-species biofilms of S. mutans or A. naeslundii, and to use a drip flow reactor (DFR) to evaluate biofilm stress responses to 0.2% chlorhexidine diacetate (CHX). Single- and dual-species biofilms were grown for 24 h. The following factors were evaluated: cell viability, biomass and total proteins in the extracellular matrix, 2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide—“XTT”—reduction and lactic acid production. To evaluate stress response, biofilms were grown in DFR. Biofilms were treated with CHX or 0.9% sodium chloride (NaCl; control). Biofilms were plated for viability assessment. Confocal laser-scanning microscopy (CLSM) was also performed. Data analysis was carried out at 5% significance level. S. mutans viability and lactic acid production in dual-species biofilms were significantly reduced. S. mutans showed a higher resistance to CHX in dual-species biofilms. Total protein content, biomass and XTT reduction showed no significant differences between single- and dual-species biofilms. CLSM images showed the formation of large clusters in dual-species biofilms. In conclusion, dual-species biofilms reduced S. mutans viability and lactic acid production and increased S. mutans’ resistance to chlorhexidine. MDPI 2020-01-31 /pmc/articles/PMC7074783/ /pubmed/32023892 http://dx.doi.org/10.3390/microorganisms8020194 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
de Oliveira, Rosa Virginia Dutra
Bonafé, Fernanda Salloume Sampaio
Spolidorio, Denise Madalena Palomari
Koga-Ito, Cristiane Yumi
de Farias, Aline Leite
Kirker, Kelly R.
James, Garth A.
Brighenti, Fernanda Lourenção
Streptococcus mutans and Actinomyces naeslundii Interaction in Dual-Species Biofilm
title Streptococcus mutans and Actinomyces naeslundii Interaction in Dual-Species Biofilm
title_full Streptococcus mutans and Actinomyces naeslundii Interaction in Dual-Species Biofilm
title_fullStr Streptococcus mutans and Actinomyces naeslundii Interaction in Dual-Species Biofilm
title_full_unstemmed Streptococcus mutans and Actinomyces naeslundii Interaction in Dual-Species Biofilm
title_short Streptococcus mutans and Actinomyces naeslundii Interaction in Dual-Species Biofilm
title_sort streptococcus mutans and actinomyces naeslundii interaction in dual-species biofilm
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074783/
https://www.ncbi.nlm.nih.gov/pubmed/32023892
http://dx.doi.org/10.3390/microorganisms8020194
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