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Actinomyces spp. gene expression in root caries lesions

BACKGROUND: The studies of the distribution of Actinomyces spp. on carious and non-carious root surfaces have not been able to confirm the association of these bacteria with root caries, although they were extensively implicated as a prime suspect in root caries. OBJECTIVE: The aim of this study was...

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Autores principales: Dame-Teixeira, Naile, Parolo, Clarissa Cavalcanti Fatturi, Maltz, Marisa, Tugnait, Aradhna, Devine, Deirdre, Do, Thuy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5027334/
https://www.ncbi.nlm.nih.gov/pubmed/27640531
http://dx.doi.org/10.3402/jom.v8.32383
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author Dame-Teixeira, Naile
Parolo, Clarissa Cavalcanti Fatturi
Maltz, Marisa
Tugnait, Aradhna
Devine, Deirdre
Do, Thuy
author_facet Dame-Teixeira, Naile
Parolo, Clarissa Cavalcanti Fatturi
Maltz, Marisa
Tugnait, Aradhna
Devine, Deirdre
Do, Thuy
author_sort Dame-Teixeira, Naile
collection PubMed
description BACKGROUND: The studies of the distribution of Actinomyces spp. on carious and non-carious root surfaces have not been able to confirm the association of these bacteria with root caries, although they were extensively implicated as a prime suspect in root caries. OBJECTIVE: The aim of this study was to observe the gene expression of Actinomyces spp. in the microbiota of root surfaces with and without caries. DESIGN: The oral biofilms from exposed sound root surface (SRS; n=10) and active root caries (RC; n=30) samples were collected. The total bacterial RNA was extracted, and the mRNA was isolated. Samples with low RNA concentration were pooled, yielding a final sample size of SRS=10 and RC=9. Complementary DNA (cDNA) libraries were prepared and sequenced on an Illumina(®) HiSeq 2500 system. Sequence reads were mapped to eight Actinomyces genomes. Count data were normalized using DESeq2 to analyse differential gene expression applying the Benjamini-Hochberg correction (false discovery rate [FDR]<0.001). RESULTS: Actinomyces spp. had similar numbers of reads (Mann-Whitney U-test; p>0.05), except for Actinomyces OT178 (p=0.001) and Actinomyces gerencseriae (p=0.004), which had higher read counts in the SRS. Genes that code for stress proteins (clp, dnaK, and groEL), enzymes of glycolysis pathways (including enolase and phosphoenolpyruvate carboxykinase), adhesion (Type-2 fimbrial and collagen-binding protein), and cell growth (EF-Tu) were highly – but not differentially (p>0.001) – expressed in both groups. Genes with the most significant upregulation in RC were those coding for hypothetical proteins and uracil DNA glycosylase (p=2.61E-17). The gene with the most significant upregulation in SRS was a peptide ABC transporter substrate-binding protein (log2FC=−6.00, FDR=2.37E-05). CONCLUSION: There were similar levels of Actinomyces gene expression in both sound and carious root biofilms. These bacteria can be commensal in root surface sites but may be cariogenic due to survival mechanisms that allow them to exist in acid environments and to metabolize sugars, saving energy.
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spelling pubmed-50273342016-09-30 Actinomyces spp. gene expression in root caries lesions Dame-Teixeira, Naile Parolo, Clarissa Cavalcanti Fatturi Maltz, Marisa Tugnait, Aradhna Devine, Deirdre Do, Thuy J Oral Microbiol Original Article BACKGROUND: The studies of the distribution of Actinomyces spp. on carious and non-carious root surfaces have not been able to confirm the association of these bacteria with root caries, although they were extensively implicated as a prime suspect in root caries. OBJECTIVE: The aim of this study was to observe the gene expression of Actinomyces spp. in the microbiota of root surfaces with and without caries. DESIGN: The oral biofilms from exposed sound root surface (SRS; n=10) and active root caries (RC; n=30) samples were collected. The total bacterial RNA was extracted, and the mRNA was isolated. Samples with low RNA concentration were pooled, yielding a final sample size of SRS=10 and RC=9. Complementary DNA (cDNA) libraries were prepared and sequenced on an Illumina(®) HiSeq 2500 system. Sequence reads were mapped to eight Actinomyces genomes. Count data were normalized using DESeq2 to analyse differential gene expression applying the Benjamini-Hochberg correction (false discovery rate [FDR]<0.001). RESULTS: Actinomyces spp. had similar numbers of reads (Mann-Whitney U-test; p>0.05), except for Actinomyces OT178 (p=0.001) and Actinomyces gerencseriae (p=0.004), which had higher read counts in the SRS. Genes that code for stress proteins (clp, dnaK, and groEL), enzymes of glycolysis pathways (including enolase and phosphoenolpyruvate carboxykinase), adhesion (Type-2 fimbrial and collagen-binding protein), and cell growth (EF-Tu) were highly – but not differentially (p>0.001) – expressed in both groups. Genes with the most significant upregulation in RC were those coding for hypothetical proteins and uracil DNA glycosylase (p=2.61E-17). The gene with the most significant upregulation in SRS was a peptide ABC transporter substrate-binding protein (log2FC=−6.00, FDR=2.37E-05). CONCLUSION: There were similar levels of Actinomyces gene expression in both sound and carious root biofilms. These bacteria can be commensal in root surface sites but may be cariogenic due to survival mechanisms that allow them to exist in acid environments and to metabolize sugars, saving energy. Co-Action Publishing 2016-09-16 /pmc/articles/PMC5027334/ /pubmed/27640531 http://dx.doi.org/10.3402/jom.v8.32383 Text en © 2016 Naile Dame-Teixeira et al. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Dame-Teixeira, Naile
Parolo, Clarissa Cavalcanti Fatturi
Maltz, Marisa
Tugnait, Aradhna
Devine, Deirdre
Do, Thuy
Actinomyces spp. gene expression in root caries lesions
title Actinomyces spp. gene expression in root caries lesions
title_full Actinomyces spp. gene expression in root caries lesions
title_fullStr Actinomyces spp. gene expression in root caries lesions
title_full_unstemmed Actinomyces spp. gene expression in root caries lesions
title_short Actinomyces spp. gene expression in root caries lesions
title_sort actinomyces spp. gene expression in root caries lesions
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5027334/
https://www.ncbi.nlm.nih.gov/pubmed/27640531
http://dx.doi.org/10.3402/jom.v8.32383
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