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Effect of γ-lactones and γ-lactams compounds on Streptococcus mutans biofilms
Considering oral diseases, antibiofilm compounds can decrease the accumulation of pathogenic species such as Streptococcus mutans at micro-areas of teeth, dental restorations or implant-supported prostheses. OBJECTIVE: To assess the effect of thirteen different novel lactam-based compounds on the in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Faculdade De Odontologia De Bauru - USP
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5831975/ https://www.ncbi.nlm.nih.gov/pubmed/29489934 http://dx.doi.org/10.1590/1678-7757-2017-0065 |
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author | Sordi, Mariane Beatriz Moreira, Thaís Altoé Montero, Juan Felipe Dumes Barbosa, Luis Cláudio Benfatti, César Augusto Magalhães Magini, Ricardo de Souza Pimenta, Andréa de Lima de Souza, Júlio César Matias |
author_facet | Sordi, Mariane Beatriz Moreira, Thaís Altoé Montero, Juan Felipe Dumes Barbosa, Luis Cláudio Benfatti, César Augusto Magalhães Magini, Ricardo de Souza Pimenta, Andréa de Lima de Souza, Júlio César Matias |
author_sort | Sordi, Mariane Beatriz |
collection | PubMed |
description | Considering oral diseases, antibiofilm compounds can decrease the accumulation of pathogenic species such as Streptococcus mutans at micro-areas of teeth, dental restorations or implant-supported prostheses. OBJECTIVE: To assess the effect of thirteen different novel lactam-based compounds on the inhibition of S. mutans biofilm formation. MATERIAL AND METHODS: We synthesized compounds based on γ-lactones analogues from rubrolides by a mucochloric acid process and converted them into their corresponding γ-hydroxy-γ-lactams by a reaction with isobutylamine and propylamine. Compounds concentrations ranging from 0.17 up to 87.5 μg mL-1 were tested against S. mutans. We diluted the exponential cultures in TSB and incubated them (37°C) in the presence of different γ-lactones or γ-lactams dilutions. Afterwards, we measured the planktonic growth by optical density at 630 nm and therefore assessed the biofilm density by the crystal violet staining method. RESULTS: Twelve compounds were active against biofilm formation, showing no effect on bacterial viability. Only one compound was inactive against both planktonic and biofilm growth. The highest biofilm inhibition (inhibition rate above 60%) was obtained for two compounds while three other compounds revealed an inhibition rate above 40%. CONCLUSIONS: Twelve of the thirteen compounds revealed effective inhibition of S. mutans biofilm formation, with eight of them showing a specific antibiofilm effect. |
format | Online Article Text |
id | pubmed-5831975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Faculdade De Odontologia De Bauru - USP |
record_format | MEDLINE/PubMed |
spelling | pubmed-58319752018-03-07 Effect of γ-lactones and γ-lactams compounds on Streptococcus mutans biofilms Sordi, Mariane Beatriz Moreira, Thaís Altoé Montero, Juan Felipe Dumes Barbosa, Luis Cláudio Benfatti, César Augusto Magalhães Magini, Ricardo de Souza Pimenta, Andréa de Lima de Souza, Júlio César Matias J Appl Oral Sci Original Article Considering oral diseases, antibiofilm compounds can decrease the accumulation of pathogenic species such as Streptococcus mutans at micro-areas of teeth, dental restorations or implant-supported prostheses. OBJECTIVE: To assess the effect of thirteen different novel lactam-based compounds on the inhibition of S. mutans biofilm formation. MATERIAL AND METHODS: We synthesized compounds based on γ-lactones analogues from rubrolides by a mucochloric acid process and converted them into their corresponding γ-hydroxy-γ-lactams by a reaction with isobutylamine and propylamine. Compounds concentrations ranging from 0.17 up to 87.5 μg mL-1 were tested against S. mutans. We diluted the exponential cultures in TSB and incubated them (37°C) in the presence of different γ-lactones or γ-lactams dilutions. Afterwards, we measured the planktonic growth by optical density at 630 nm and therefore assessed the biofilm density by the crystal violet staining method. RESULTS: Twelve compounds were active against biofilm formation, showing no effect on bacterial viability. Only one compound was inactive against both planktonic and biofilm growth. The highest biofilm inhibition (inhibition rate above 60%) was obtained for two compounds while three other compounds revealed an inhibition rate above 40%. CONCLUSIONS: Twelve of the thirteen compounds revealed effective inhibition of S. mutans biofilm formation, with eight of them showing a specific antibiofilm effect. Faculdade De Odontologia De Bauru - USP 2018-02-15 /pmc/articles/PMC5831975/ /pubmed/29489934 http://dx.doi.org/10.1590/1678-7757-2017-0065 Text en https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Sordi, Mariane Beatriz Moreira, Thaís Altoé Montero, Juan Felipe Dumes Barbosa, Luis Cláudio Benfatti, César Augusto Magalhães Magini, Ricardo de Souza Pimenta, Andréa de Lima de Souza, Júlio César Matias Effect of γ-lactones and γ-lactams compounds on Streptococcus mutans biofilms |
title | Effect of γ-lactones and γ-lactams compounds on Streptococcus mutans biofilms |
title_full | Effect of γ-lactones and γ-lactams compounds on Streptococcus mutans biofilms |
title_fullStr | Effect of γ-lactones and γ-lactams compounds on Streptococcus mutans biofilms |
title_full_unstemmed | Effect of γ-lactones and γ-lactams compounds on Streptococcus mutans biofilms |
title_short | Effect of γ-lactones and γ-lactams compounds on Streptococcus mutans biofilms |
title_sort | effect of γ-lactones and γ-lactams compounds on streptococcus mutans biofilms |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5831975/ https://www.ncbi.nlm.nih.gov/pubmed/29489934 http://dx.doi.org/10.1590/1678-7757-2017-0065 |
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