Serveur d'exploration sur le patient édenté (maquette)

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Functional expression of dental plaque microbiota

Identifieur interne : 000546 ( Pmc/Curation ); précédent : 000545; suivant : 000547

Functional expression of dental plaque microbiota

Auteurs : Scott N. Peterson [États-Unis] ; Tobias Meissner [États-Unis] ; Andrew I. Su [États-Unis] ; Erik Snesrud [États-Unis] ; Ana C. Ong [États-Unis] ; Nicholas J. Schork [États-Unis] ; Walter A. Bretz [États-Unis]

Source :

RBID : PMC:4132376

Abstract

Dental caries remains a significant public health problem and is considered pandemic worldwide. The prediction of dental caries based on profiling of microbial species involved in disease and equally important, the identification of species conferring dental health has proven more difficult than anticipated due to high interpersonal and geographical variability of dental plaque microbiota. We have used RNA-Seq to perform global gene expression analysis of dental plaque microbiota derived from 19 twin pairs that were either concordant (caries-active or caries-free) or discordant for dental caries. The transcription profiling allowed us to define a functional core microbiota consisting of nearly 60 species. Similarities in gene expression patterns allowed a preliminary assessment of the relative contribution of human genetics, environmental factors and caries phenotype on the microbiota's transcriptome. Correlation analysis of transcription allowed the identification of numerous functional networks, suggesting that inter-personal environmental variables may co-select for groups of genera and species. Analysis of functional role categories allowed the identification of dominant functions expressed by dental plaque biofilm communities, that highlight the biochemical priorities of dental plaque microbes to metabolize diverse sugars and cope with the acid and oxidative stress resulting from sugar fermentation. The wealth of data generated by deep sequencing of expressed transcripts enables a greatly expanded perspective concerning the functional expression of dental plaque microbiota.


Url:
DOI: 10.3389/fcimb.2014.00108
PubMed: 25177549
PubMed Central: 4132376

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PMC:4132376

Le document en format XML

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<p>Dental caries remains a significant public health problem and is considered pandemic worldwide. The prediction of dental caries based on profiling of microbial species involved in disease and equally important, the identification of species conferring dental health has proven more difficult than anticipated due to high interpersonal and geographical variability of dental plaque microbiota. We have used RNA-Seq to perform global gene expression analysis of dental plaque microbiota derived from 19 twin pairs that were either concordant (caries-active or caries-free) or discordant for dental caries. The transcription profiling allowed us to define a functional core microbiota consisting of nearly 60 species. Similarities in gene expression patterns allowed a preliminary assessment of the relative contribution of human genetics, environmental factors and caries phenotype on the microbiota's transcriptome. Correlation analysis of transcription allowed the identification of numerous functional networks, suggesting that inter-personal environmental variables may co-select for groups of genera and species. Analysis of functional role categories allowed the identification of dominant functions expressed by dental plaque biofilm communities, that highlight the biochemical priorities of dental plaque microbes to metabolize diverse sugars and cope with the acid and oxidative stress resulting from sugar fermentation. The wealth of data generated by deep sequencing of expressed transcripts enables a greatly expanded perspective concerning the functional expression of dental plaque microbiota.</p>
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<pmc article-type="research-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Front Cell Infect Microbiol</journal-id>
<journal-id journal-id-type="iso-abbrev">Front Cell Infect Microbiol</journal-id>
<journal-id journal-id-type="publisher-id">Front. Cell. Infect. Microbiol.</journal-id>
<journal-title-group>
<journal-title>Frontiers in Cellular and Infection Microbiology</journal-title>
</journal-title-group>
<issn pub-type="epub">2235-2988</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">25177549</article-id>
<article-id pub-id-type="pmc">4132376</article-id>
<article-id pub-id-type="doi">10.3389/fcimb.2014.00108</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Microbiology</subject>
<subj-group>
<subject>Original Research Article</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Functional expression of dental plaque microbiota</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Peterson</surname>
<given-names>Scott N.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>*</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://community.frontiersin.org/people/u/18540"></uri>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Meissner</surname>
<given-names>Tobias</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://community.frontiersin.org/people/u/158355"></uri>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Su</surname>
<given-names>Andrew I.</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://community.frontiersin.org/people/u/176248"></uri>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Snesrud</surname>
<given-names>Erik</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://community.frontiersin.org/people/u/175562"></uri>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ong</surname>
<given-names>Ana C.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://community.frontiersin.org/people/u/176214"></uri>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Schork</surname>
<given-names>Nicholas J.</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="author-notes" rid="fn003">
<sup></sup>
</xref>
<uri xlink:type="simple" xlink:href="http://community.frontiersin.org/people/u/22723"></uri>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Bretz</surname>
<given-names>Walter A.</given-names>
</name>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://community.frontiersin.org/people/u/60802"></uri>
</contrib>
</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Infectious Diseases, J. Craig Venter Institute</institution>
<country>Rockville, MD, USA</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Department of Molecular and Experimental Medicine at the Scripps Research Institute</institution>
<country>La Jolla, CA, USA</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>The Scripps Translational Science Institute and Scripps Health</institution>
<country>La Jolla, CA, USA</country>
</aff>
<aff id="aff4">
<sup>4</sup>
<institution>Department of Cariology and Comprehensive Care, College of Dentistry, New York University</institution>
<country>New York, NY, USA</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>Edited by: Alex Mira, Center for Advanced Research in Public Health, Spain</p>
</fn>
<fn fn-type="edited-by">
<p>Reviewed by: Jeff Banas, University of Iowa, USA; Valerio Iebba, ‘Sapienza’ University of Rome, Italy</p>
</fn>
<corresp id="fn001">*Correspondence: Scott N. Peterson, Sanford Burnham Medical Research Institute, 10901 North Torrey Pines Rd., La Jolla, CA 92037, USA e-mail:
<email xlink:type="simple">speterson@sanfordburnham.org</email>
</corresp>
<fn fn-type="other" id="fn002">
<p>This article was submitted to the journal Frontiers in Cellular and Infection Microbiology.</p>
</fn>
<fn fn-type="present-address" id="fn003">
<p>†Present address: Nicholas J. Schork, Human Biology, J. Craig Venter Institute, La Jolla, USA</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>14</day>
<month>8</month>
<year>2014</year>
</pub-date>
<pub-date pub-type="collection">
<year>2014</year>
</pub-date>
<volume>4</volume>
<elocation-id>108</elocation-id>
<history>
<date date-type="received">
<day>06</day>
<month>5</month>
<year>2014</year>
</date>
<date date-type="accepted">
<day>24</day>
<month>7</month>
<year>2014</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright © 2014 Peterson, Meissner, Su, Snesrud, Ong, Schork and Bretz.</copyright-statement>
<copyright-year>2014</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/3.0/">
<license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</license-p>
</license>
</permissions>
<abstract>
<p>Dental caries remains a significant public health problem and is considered pandemic worldwide. The prediction of dental caries based on profiling of microbial species involved in disease and equally important, the identification of species conferring dental health has proven more difficult than anticipated due to high interpersonal and geographical variability of dental plaque microbiota. We have used RNA-Seq to perform global gene expression analysis of dental plaque microbiota derived from 19 twin pairs that were either concordant (caries-active or caries-free) or discordant for dental caries. The transcription profiling allowed us to define a functional core microbiota consisting of nearly 60 species. Similarities in gene expression patterns allowed a preliminary assessment of the relative contribution of human genetics, environmental factors and caries phenotype on the microbiota's transcriptome. Correlation analysis of transcription allowed the identification of numerous functional networks, suggesting that inter-personal environmental variables may co-select for groups of genera and species. Analysis of functional role categories allowed the identification of dominant functions expressed by dental plaque biofilm communities, that highlight the biochemical priorities of dental plaque microbes to metabolize diverse sugars and cope with the acid and oxidative stress resulting from sugar fermentation. The wealth of data generated by deep sequencing of expressed transcripts enables a greatly expanded perspective concerning the functional expression of dental plaque microbiota.</p>
</abstract>
<kwd-group>
<kwd>caries</kwd>
<kwd>oral microbiota</kwd>
<kwd>dental plaque</kwd>
<kwd>biofilm</kwd>
<kwd>transcriptome</kwd>
</kwd-group>
<counts>
<fig-count count="8"></fig-count>
<table-count count="1"></table-count>
<equation-count count="0"></equation-count>
<ref-count count="43"></ref-count>
<page-count count="13"></page-count>
<word-count count="7919"></word-count>
</counts>
</article-meta>
</front>
</pmc>
</record>

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