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Function of alanine racemase in the physiological activity and cariogenicity of Streptococcus mutans
The enzyme alanine racemase (Alr) has been a new target for the development of antibacterial drugs based on the involvement of D-Ala in bacterial cell wall biosynthesis. Our previous study noted that Alr is essential for the growth and interspecies competitiveness of S. mutans, the major causative o...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5899142/ https://www.ncbi.nlm.nih.gov/pubmed/29654290 http://dx.doi.org/10.1038/s41598-018-24295-1 |
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author | Liu, Shiyu Wei, Yuan Zhou, Xuedong Zhang, Keke Peng, Xian Ren, Biao Chen, Vivian Cheng, Lei Li, Mingyun |
author_facet | Liu, Shiyu Wei, Yuan Zhou, Xuedong Zhang, Keke Peng, Xian Ren, Biao Chen, Vivian Cheng, Lei Li, Mingyun |
author_sort | Liu, Shiyu |
collection | PubMed |
description | The enzyme alanine racemase (Alr) has been a new target for the development of antibacterial drugs based on the involvement of D-Ala in bacterial cell wall biosynthesis. Our previous study noted that Alr is essential for the growth and interspecies competitiveness of S. mutans, the major causative organism of dental caries. However, physiological activity and cariogenicity of S. mutans affected by Alr remains unknown. The current study examined the biofilm biomass, biofilm structure, extracellular polysaccharide (EPS) synthesis, glucosyltransferase (gtf) gene expression, acid production and acid tolerance in the alr-mutant strain. We found that biofilm formation, biofilm structure, and EPS synthesis was in a D-Ala dose-dependent manner. Biofilm structure was loose in alr-mutant group and the ratio of EPS/bacteria was also elevated. Additionally, the expression levels of multiple gtfs were up-regulated, and acid tolerance was decreased. We also established in vivo models of dental caries and found that the incidence and severity of the caries were decreased in the alr-mutant group in comparison to the parental S. mutans group. Our in vivo and in vitro experiments demonstrate that Alr is essential for the cariogenicity of S. mutans and that Alr might be a potential target for the prevention and treatment of caries. |
format | Online Article Text |
id | pubmed-5899142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58991422018-04-20 Function of alanine racemase in the physiological activity and cariogenicity of Streptococcus mutans Liu, Shiyu Wei, Yuan Zhou, Xuedong Zhang, Keke Peng, Xian Ren, Biao Chen, Vivian Cheng, Lei Li, Mingyun Sci Rep Article The enzyme alanine racemase (Alr) has been a new target for the development of antibacterial drugs based on the involvement of D-Ala in bacterial cell wall biosynthesis. Our previous study noted that Alr is essential for the growth and interspecies competitiveness of S. mutans, the major causative organism of dental caries. However, physiological activity and cariogenicity of S. mutans affected by Alr remains unknown. The current study examined the biofilm biomass, biofilm structure, extracellular polysaccharide (EPS) synthesis, glucosyltransferase (gtf) gene expression, acid production and acid tolerance in the alr-mutant strain. We found that biofilm formation, biofilm structure, and EPS synthesis was in a D-Ala dose-dependent manner. Biofilm structure was loose in alr-mutant group and the ratio of EPS/bacteria was also elevated. Additionally, the expression levels of multiple gtfs were up-regulated, and acid tolerance was decreased. We also established in vivo models of dental caries and found that the incidence and severity of the caries were decreased in the alr-mutant group in comparison to the parental S. mutans group. Our in vivo and in vitro experiments demonstrate that Alr is essential for the cariogenicity of S. mutans and that Alr might be a potential target for the prevention and treatment of caries. Nature Publishing Group UK 2018-04-13 /pmc/articles/PMC5899142/ /pubmed/29654290 http://dx.doi.org/10.1038/s41598-018-24295-1 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Liu, Shiyu Wei, Yuan Zhou, Xuedong Zhang, Keke Peng, Xian Ren, Biao Chen, Vivian Cheng, Lei Li, Mingyun Function of alanine racemase in the physiological activity and cariogenicity of Streptococcus mutans |
title | Function of alanine racemase in the physiological activity and cariogenicity of Streptococcus mutans |
title_full | Function of alanine racemase in the physiological activity and cariogenicity of Streptococcus mutans |
title_fullStr | Function of alanine racemase in the physiological activity and cariogenicity of Streptococcus mutans |
title_full_unstemmed | Function of alanine racemase in the physiological activity and cariogenicity of Streptococcus mutans |
title_short | Function of alanine racemase in the physiological activity and cariogenicity of Streptococcus mutans |
title_sort | function of alanine racemase in the physiological activity and cariogenicity of streptococcus mutans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5899142/ https://www.ncbi.nlm.nih.gov/pubmed/29654290 http://dx.doi.org/10.1038/s41598-018-24295-1 |
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