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Genetic variability of mutans streptococci revealed by wide whole-genome sequencing

BACKGROUND: Mutans streptococci are a group of bacteria significantly contributing to tooth decay. Their genetic variability is however still not well understood. RESULTS: Genomes of 6 clinical S. mutans isolates of different origins, one isolate of S. sobrinus (DSM 20742) and one isolate of S. ratt...

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Autores principales: Song, Lifu, Wang, Wei, Conrads, Georg, Rheinberg, Anke, Sztajer, Helena, Reck, Michael, Wagner-Döbler, Irene, Zeng, An-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751929/
https://www.ncbi.nlm.nih.gov/pubmed/23805886
http://dx.doi.org/10.1186/1471-2164-14-430
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author Song, Lifu
Wang, Wei
Conrads, Georg
Rheinberg, Anke
Sztajer, Helena
Reck, Michael
Wagner-Döbler, Irene
Zeng, An-Ping
author_facet Song, Lifu
Wang, Wei
Conrads, Georg
Rheinberg, Anke
Sztajer, Helena
Reck, Michael
Wagner-Döbler, Irene
Zeng, An-Ping
author_sort Song, Lifu
collection PubMed
description BACKGROUND: Mutans streptococci are a group of bacteria significantly contributing to tooth decay. Their genetic variability is however still not well understood. RESULTS: Genomes of 6 clinical S. mutans isolates of different origins, one isolate of S. sobrinus (DSM 20742) and one isolate of S. ratti (DSM 20564) were sequenced and comparatively analyzed. Genome alignment revealed a mosaic-like structure of genome arrangement. Genes related to pathogenicity are found to have high variations among the strains, whereas genes for oxidative stress resistance are well conserved, indicating the importance of this trait in the dental biofilm community. Analysis of genome-scale metabolic networks revealed significant differences in 42 pathways. A striking dissimilarity is the unique presence of two lactate oxidases in S. sobrinus DSM 20742, probably indicating an unusual capability of this strain in producing H(2)O(2) and expanding its ecological niche. In addition, lactate oxidases may form with other enzymes a novel energetic pathway in S. sobrinus DSM 20742 that can remedy its deficiency in citrate utilization pathway. Using 67 S. mutans genomes currently available including the strains sequenced in this study, we estimates the theoretical core genome size of S. mutans, and performed modeling of S. mutans pan-genome by applying different fitting models. An “open” pan-genome was inferred. CONCLUSIONS: The comparative genome analyses revealed diversities in the mutans streptococci group, especially with respect to the virulence related genes and metabolic pathways. The results are helpful for better understanding the evolution and adaptive mechanisms of these oral pathogen microorganisms and for combating them.
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spelling pubmed-37519292013-08-27 Genetic variability of mutans streptococci revealed by wide whole-genome sequencing Song, Lifu Wang, Wei Conrads, Georg Rheinberg, Anke Sztajer, Helena Reck, Michael Wagner-Döbler, Irene Zeng, An-Ping BMC Genomics Research Article BACKGROUND: Mutans streptococci are a group of bacteria significantly contributing to tooth decay. Their genetic variability is however still not well understood. RESULTS: Genomes of 6 clinical S. mutans isolates of different origins, one isolate of S. sobrinus (DSM 20742) and one isolate of S. ratti (DSM 20564) were sequenced and comparatively analyzed. Genome alignment revealed a mosaic-like structure of genome arrangement. Genes related to pathogenicity are found to have high variations among the strains, whereas genes for oxidative stress resistance are well conserved, indicating the importance of this trait in the dental biofilm community. Analysis of genome-scale metabolic networks revealed significant differences in 42 pathways. A striking dissimilarity is the unique presence of two lactate oxidases in S. sobrinus DSM 20742, probably indicating an unusual capability of this strain in producing H(2)O(2) and expanding its ecological niche. In addition, lactate oxidases may form with other enzymes a novel energetic pathway in S. sobrinus DSM 20742 that can remedy its deficiency in citrate utilization pathway. Using 67 S. mutans genomes currently available including the strains sequenced in this study, we estimates the theoretical core genome size of S. mutans, and performed modeling of S. mutans pan-genome by applying different fitting models. An “open” pan-genome was inferred. CONCLUSIONS: The comparative genome analyses revealed diversities in the mutans streptococci group, especially with respect to the virulence related genes and metabolic pathways. The results are helpful for better understanding the evolution and adaptive mechanisms of these oral pathogen microorganisms and for combating them. BioMed Central 2013-06-28 /pmc/articles/PMC3751929/ /pubmed/23805886 http://dx.doi.org/10.1186/1471-2164-14-430 Text en Copyright © 2013 Song et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Song, Lifu
Wang, Wei
Conrads, Georg
Rheinberg, Anke
Sztajer, Helena
Reck, Michael
Wagner-Döbler, Irene
Zeng, An-Ping
Genetic variability of mutans streptococci revealed by wide whole-genome sequencing
title Genetic variability of mutans streptococci revealed by wide whole-genome sequencing
title_full Genetic variability of mutans streptococci revealed by wide whole-genome sequencing
title_fullStr Genetic variability of mutans streptococci revealed by wide whole-genome sequencing
title_full_unstemmed Genetic variability of mutans streptococci revealed by wide whole-genome sequencing
title_short Genetic variability of mutans streptococci revealed by wide whole-genome sequencing
title_sort genetic variability of mutans streptococci revealed by wide whole-genome sequencing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751929/
https://www.ncbi.nlm.nih.gov/pubmed/23805886
http://dx.doi.org/10.1186/1471-2164-14-430
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