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Inactivation of Streptococcus mutans genes lytST and dltAD impairs its pathogenicity in vivo
Background: Streptococcus mutans orchestrates the development of a biofilm that causes dental caries in the presence of dietary sucrose, and, in the bloodstream, S. mutans can cause systemic infections. The development of a cariogenic biofilm is dependent on the formation of an extracellular matrix...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6522913/ https://www.ncbi.nlm.nih.gov/pubmed/31143407 http://dx.doi.org/10.1080/20002297.2019.1607505 |
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author | Castillo Pedraza, Midian C. Rosalen, Pedro L. de Castilho, Aline Rogéria Freire Freires, Irlan de Almeida de Sales Leite, Luana Faustoferri, Roberta C. Quivey Jr, Robert G. Klein, Marlise I. |
author_facet | Castillo Pedraza, Midian C. Rosalen, Pedro L. de Castilho, Aline Rogéria Freire Freires, Irlan de Almeida de Sales Leite, Luana Faustoferri, Roberta C. Quivey Jr, Robert G. Klein, Marlise I. |
author_sort | Castillo Pedraza, Midian C. |
collection | PubMed |
description | Background: Streptococcus mutans orchestrates the development of a biofilm that causes dental caries in the presence of dietary sucrose, and, in the bloodstream, S. mutans can cause systemic infections. The development of a cariogenic biofilm is dependent on the formation of an extracellular matrix rich in exopolysaccharides, which contains extracellular DNA (eDNA) and lipoteichoic acids (LTAs). While the exopolysaccharides are virulence markers, the involvement of genes linked to eDNA and LTAs metabolism in the pathogenicity of S. mutans remains unclear. Objective and Design: In this study, a parental strain S. mutans UA159 and derivative strains carrying single gene deletions were used to investigate the role of eDNA (ΔlytS and ΔlytT), LTA (ΔdltA and ΔdltD), and insoluble exopolysaccharides (ΔgtfB) in virulence in a rodent model of dental caries (rats) and a systemic infection model (Galleria mellonella larvae). Results: Fewer carious lesions were observed on smooth and sulcal surfaces of enamel and dentin of the rats infected with ∆lytS, ∆dltD, and ΔgtfB (vs. the parental strain). Moreover, strains carrying gene deletions prevented the killing of larvae (vs. the parental strain). Conclusions: Altogether, these findings indicate that inactivation of lytST and dltAD impaired S. mutans cariogenicity and virulence in vivo. |
format | Online Article Text |
id | pubmed-6522913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-65229132019-05-29 Inactivation of Streptococcus mutans genes lytST and dltAD impairs its pathogenicity in vivo Castillo Pedraza, Midian C. Rosalen, Pedro L. de Castilho, Aline Rogéria Freire Freires, Irlan de Almeida de Sales Leite, Luana Faustoferri, Roberta C. Quivey Jr, Robert G. Klein, Marlise I. J Oral Microbiol Original Article Background: Streptococcus mutans orchestrates the development of a biofilm that causes dental caries in the presence of dietary sucrose, and, in the bloodstream, S. mutans can cause systemic infections. The development of a cariogenic biofilm is dependent on the formation of an extracellular matrix rich in exopolysaccharides, which contains extracellular DNA (eDNA) and lipoteichoic acids (LTAs). While the exopolysaccharides are virulence markers, the involvement of genes linked to eDNA and LTAs metabolism in the pathogenicity of S. mutans remains unclear. Objective and Design: In this study, a parental strain S. mutans UA159 and derivative strains carrying single gene deletions were used to investigate the role of eDNA (ΔlytS and ΔlytT), LTA (ΔdltA and ΔdltD), and insoluble exopolysaccharides (ΔgtfB) in virulence in a rodent model of dental caries (rats) and a systemic infection model (Galleria mellonella larvae). Results: Fewer carious lesions were observed on smooth and sulcal surfaces of enamel and dentin of the rats infected with ∆lytS, ∆dltD, and ΔgtfB (vs. the parental strain). Moreover, strains carrying gene deletions prevented the killing of larvae (vs. the parental strain). Conclusions: Altogether, these findings indicate that inactivation of lytST and dltAD impaired S. mutans cariogenicity and virulence in vivo. Taylor & Francis 2019-05-09 /pmc/articles/PMC6522913/ /pubmed/31143407 http://dx.doi.org/10.1080/20002297.2019.1607505 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Castillo Pedraza, Midian C. Rosalen, Pedro L. de Castilho, Aline Rogéria Freire Freires, Irlan de Almeida de Sales Leite, Luana Faustoferri, Roberta C. Quivey Jr, Robert G. Klein, Marlise I. Inactivation of Streptococcus mutans genes lytST and dltAD impairs its pathogenicity in vivo |
title | Inactivation of Streptococcus mutans genes lytST and dltAD impairs its pathogenicity in vivo |
title_full | Inactivation of Streptococcus mutans genes lytST and dltAD impairs its pathogenicity in vivo |
title_fullStr | Inactivation of Streptococcus mutans genes lytST and dltAD impairs its pathogenicity in vivo |
title_full_unstemmed | Inactivation of Streptococcus mutans genes lytST and dltAD impairs its pathogenicity in vivo |
title_short | Inactivation of Streptococcus mutans genes lytST and dltAD impairs its pathogenicity in vivo |
title_sort | inactivation of streptococcus mutans genes lytst and dltad impairs its pathogenicity in vivo |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6522913/ https://www.ncbi.nlm.nih.gov/pubmed/31143407 http://dx.doi.org/10.1080/20002297.2019.1607505 |
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