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Comparison of microbial changes in early re-developing biofilms on natural teeth and dentures

Identifieur interne : 000413 ( Pmc/Curation ); précédent : 000412; suivant : 000414

Comparison of microbial changes in early re-developing biofilms on natural teeth and dentures

Auteurs : F. R. Teles [États-Unis] ; R. P. Teles [États-Unis] ; A. Sachdeo [États-Unis] ; N. G. Uzel [États-Unis] ; X. Q. Song [États-Unis] ; G. Torresyap [États-Unis] ; M. Singh ; A. Papas ; A. D. Haffajee [États-Unis] ; S. S. Socransky [États-Unis]

Source :

RBID : PMC:4041159

Abstract

Background and objective

Surfaces and fluids can affect oral bacterial colonization. The aim of this study was to compare re-developing biofilms on natural teeth and dentures.

Methods

Supragingival plaque samples were taken from 55 dentate subjects and the denture teeth of 62 edentulous subjects before and after professional cleaning. Also, samples from 7 “teeth” in randomly selected quadrants were collected after 1, 2, 4 and 7 days of no oral hygiene. Samples were analyzed using checkerboard DNA-DNA hybridization. Counts and proportions of 41 bacterial taxa were determined at each time point and significant differences were sought using the Mann-Whitney test. Ecological succession was determined using a modified moving window analysis.

Results

Mean total DNA probe counts were similar pre-cleaning but were higher in dentate subjects at all post-cleaning visits (p<0.01). Pre-cleaning edentate biofilms had higher counts and proportions of Streptococcus mitis, Streptococcus oralis and Streptococcus mutans, whereas dentate subjects had higher proportions of Tannerella forsythia, Selenomonas noxia and Neisseria mucosa. By 2 days, mean counts of all taxa were higher in natural teeth and most remained higher at 7 days (p<0.01). Succession was more rapid and complex in dentate subjects. Both groups demonstrated increased proportions of S. mitis and S. oralis by 1 day. N. mucosa, Veillonella parvula and Eikenella corrodens increased in both groups but later in edentate samples.

Conclusions

“Mature” natural and denture teeth biofilms have similar total numbers of bacteria but different species proportions. Post-cleaning biofilm re-development is more rapid and more complex on natural than denture teeth.


Url:
DOI: 10.1902/jop.2012.110506
PubMed: 22443543
PubMed Central: 4041159

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M. Singh
<affiliation>
<nlm:aff id="A6">Division of Public Health Research and Oral Medicine, Tufts University School of Dental Medicine</nlm:aff>
<wicri:noCountry code="subfield">Tufts University School of Dental Medicine</wicri:noCountry>
</affiliation>
A. Papas
<affiliation>
<nlm:aff id="A6">Division of Public Health Research and Oral Medicine, Tufts University School of Dental Medicine</nlm:aff>
<wicri:noCountry code="subfield">Tufts University School of Dental Medicine</wicri:noCountry>
</affiliation>

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<sec id="S1">
<title>Background and objective</title>
<p id="P1">Surfaces and fluids can affect oral bacterial colonization. The aim of this study was to compare re-developing biofilms on natural teeth and dentures.</p>
</sec>
<sec id="S2">
<title>Methods</title>
<p id="P2">Supragingival plaque samples were taken from 55 dentate subjects and the denture teeth of 62 edentulous subjects before and after professional cleaning. Also, samples from 7 “teeth” in randomly selected quadrants were collected after 1, 2, 4 and 7 days of no oral hygiene. Samples were analyzed using checkerboard DNA-DNA hybridization. Counts and proportions of 41 bacterial taxa were determined at each time point and significant differences were sought using the Mann-Whitney test. Ecological succession was determined using a modified moving window analysis.</p>
</sec>
<sec id="S3">
<title>Results</title>
<p id="P3">Mean total DNA probe counts were similar pre-cleaning but were higher in dentate subjects at all post-cleaning visits (p<0.01). Pre-cleaning edentate biofilms had higher counts and proportions of
<italic>Streptococcus mitis, Streptococcus oralis</italic>
and
<italic>Streptococcus mutans,</italic>
whereas dentate subjects had higher proportions of
<italic>Tannerella forsythia, Selenomonas noxia</italic>
and
<italic>Neisseria mucosa.</italic>
By 2 days, mean counts of all taxa were higher in natural teeth and most remained higher at 7 days (p<0.01). Succession was more rapid and complex in dentate subjects. Both groups demonstrated increased proportions of
<italic>S. mitis</italic>
and
<italic>S. oralis</italic>
by 1 day.
<italic>N. mucosa, Veillonella parvula</italic>
and
<italic>Eikenella corrodens</italic>
increased in both groups but later in edentate samples.</p>
</sec>
<sec id="S4">
<title>Conclusions</title>
<p id="P4">“Mature” natural and denture teeth biofilms have similar total numbers of bacteria but different species proportions. Post-cleaning biofilm re-development is more rapid and more complex on natural than denture teeth.</p>
</sec>
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<journal-id journal-id-type="nlm-journal-id">8000345</journal-id>
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<title-group>
<article-title>Comparison of microbial changes in early re-developing biofilms on natural teeth and dentures</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Teles</surname>
<given-names>F.R.</given-names>
</name>
<xref ref-type="aff" rid="A1">*</xref>
<xref ref-type="aff" rid="A2"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Teles</surname>
<given-names>R.P.</given-names>
</name>
<xref ref-type="aff" rid="A1">*</xref>
<xref ref-type="aff" rid="A2"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Sachdeo</surname>
<given-names>A.</given-names>
</name>
<xref ref-type="aff" rid="A3"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Uzel</surname>
<given-names>N.G.</given-names>
</name>
<xref ref-type="aff" rid="A4">§</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Song</surname>
<given-names>X.Q.</given-names>
</name>
<xref ref-type="aff" rid="A1">*</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Torresyap</surname>
<given-names>G.</given-names>
</name>
<xref ref-type="aff" rid="A5"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Singh</surname>
<given-names>M.</given-names>
</name>
<xref ref-type="aff" rid="A6"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Papas</surname>
<given-names>A.</given-names>
</name>
<xref ref-type="aff" rid="A6"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Haffajee</surname>
<given-names>A.D.</given-names>
</name>
<xref ref-type="aff" rid="A1">*</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Socransky</surname>
<given-names>S.S.</given-names>
</name>
<xref ref-type="aff" rid="A1">*</xref>
</contrib>
</contrib-group>
<aff id="A1">
<label>*</label>
Department of Periodontology, The Forsyth Institute, Cambridge, MA</aff>
<aff id="A2">
<label></label>
Department of Oral Medicine, Infection and Immunity, Harvard School of Dental Medicine, Boston, MA</aff>
<aff id="A3">
<label></label>
Department of Prosthodontics, Tufts University School of Dental Medicine, Boston, MA</aff>
<aff id="A4">
<label>§</label>
Private Practice, Bala Cynwyd, PA</aff>
<aff id="A5">
<label></label>
Children’s Hospital, Boston, MA</aff>
<aff id="A6">
<label></label>
Division of Public Health Research and Oral Medicine, Tufts University School of Dental Medicine</aff>
<author-notes>
<corresp id="cor1">Correspondence: Flavia R. F. Teles, Department of Periodontology, The Forsyth Institute, 245 First Street, Cambridge, MA 02142, Phone: 617-892-8562, Fax: 617-262-4021,
<email>fteles@forsyth.org</email>
</corresp>
</author-notes>
<pub-date pub-type="nihms-submitted">
<day>11</day>
<month>3</month>
<year>2013</year>
</pub-date>
<pub-date pub-type="epub">
<day>23</day>
<month>3</month>
<year>2012</year>
</pub-date>
<pub-date pub-type="ppub">
<month>9</month>
<year>2012</year>
</pub-date>
<pub-date pub-type="pmc-release">
<day>02</day>
<month>6</month>
<year>2014</year>
</pub-date>
<volume>83</volume>
<issue>9</issue>
<fpage>1139</fpage>
<lpage>1148</lpage>
<pmc-comment>elocation-id from pubmed: 10.1902/jop.2012.110506</pmc-comment>
<abstract>
<sec id="S1">
<title>Background and objective</title>
<p id="P1">Surfaces and fluids can affect oral bacterial colonization. The aim of this study was to compare re-developing biofilms on natural teeth and dentures.</p>
</sec>
<sec id="S2">
<title>Methods</title>
<p id="P2">Supragingival plaque samples were taken from 55 dentate subjects and the denture teeth of 62 edentulous subjects before and after professional cleaning. Also, samples from 7 “teeth” in randomly selected quadrants were collected after 1, 2, 4 and 7 days of no oral hygiene. Samples were analyzed using checkerboard DNA-DNA hybridization. Counts and proportions of 41 bacterial taxa were determined at each time point and significant differences were sought using the Mann-Whitney test. Ecological succession was determined using a modified moving window analysis.</p>
</sec>
<sec id="S3">
<title>Results</title>
<p id="P3">Mean total DNA probe counts were similar pre-cleaning but were higher in dentate subjects at all post-cleaning visits (p<0.01). Pre-cleaning edentate biofilms had higher counts and proportions of
<italic>Streptococcus mitis, Streptococcus oralis</italic>
and
<italic>Streptococcus mutans,</italic>
whereas dentate subjects had higher proportions of
<italic>Tannerella forsythia, Selenomonas noxia</italic>
and
<italic>Neisseria mucosa.</italic>
By 2 days, mean counts of all taxa were higher in natural teeth and most remained higher at 7 days (p<0.01). Succession was more rapid and complex in dentate subjects. Both groups demonstrated increased proportions of
<italic>S. mitis</italic>
and
<italic>S. oralis</italic>
by 1 day.
<italic>N. mucosa, Veillonella parvula</italic>
and
<italic>Eikenella corrodens</italic>
increased in both groups but later in edentate samples.</p>
</sec>
<sec id="S4">
<title>Conclusions</title>
<p id="P4">“Mature” natural and denture teeth biofilms have similar total numbers of bacteria but different species proportions. Post-cleaning biofilm re-development is more rapid and more complex on natural than denture teeth.</p>
</sec>
</abstract>
<kwd-group>
<kwd>microbiota</kwd>
<kwd>biofilms</kwd>
<kwd>supragingival</kwd>
<kwd>dental plaque</kwd>
<kwd>tooth</kwd>
<kwd>dentures</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
</record>

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