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Real-time PCR analysis of fungal organisms and bacterial species at peri-implantitis sites

Identifieur interne : 000D68 ( Main/Exploration ); précédent : 000D67; suivant : 000D69

Real-time PCR analysis of fungal organisms and bacterial species at peri-implantitis sites

Auteurs : Frank Schwarz [Allemagne] ; Kathrin Becker [Allemagne] ; Sebastian Rahn [Allemagne] ; Andrea Hegewald [Allemagne] ; Klaus Pfeffer [Allemagne] ; Birgit Henrich [Allemagne]

Source :

RBID : PMC:5005605

Abstract

Background

The potential role of fungal organisms and their co-aggregation with either periodontopathogens or opportunistic pathogens at peri-implantitis sites is unknown. The aim of the present study was to qualitatively/quantitatively analyze and correlate fungal organisms and bacterial species at peri-implantitis sites.

Methods

In a total of 29 patients, submucosal/subgingival plaque samples were collected at peri-implantitis and healthy implant sites as well as teeth with a history of periodontitis (controls). A real-time PCR assay was established for the qualification of fungal organisms and a TaqMan assay for the quantification of Porphyromonas gingivalis, Parvimonas micra, Tannerella forsythia, Mycoplasma salivarium, Veillonella parvula, and Staphylococcus aureus.

Results

Fungal organisms were more frequently identified at peri-implantitis (31.6%) (i.e., Candida albicans, Candida boidinii, Penicillium spp., Rhodotorula laryngis, Paelicomyces spp., Saccharomycetes, Cladosporium cladosporioides) and healthy implant sites (40% - Candida dubliniensis, C. cladosporioides) than at selected teeth (20% - C. albicans, Fusarium solani). At implant sites, fungal organisms were significantly correlated with P. micra and T. forsythia.

Conclusions

Candida spp. and other fungal organisms were frequently identified at peri-implantitis as well as healthy implant sites and co-colonized with P. micra and T. forsythia.


Url:
DOI: 10.1186/s40729-015-0010-6
PubMed: 27747631
PubMed Central: 5005605


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<title level="j">International Journal of Implant Dentistry</title>
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<sec>
<title>Background</title>
<p>The potential role of fungal organisms and their co-aggregation with either periodontopathogens or opportunistic pathogens at peri-implantitis sites is unknown. The aim of the present study was to qualitatively/quantitatively analyze and correlate fungal organisms and bacterial species at peri-implantitis sites.</p>
</sec>
<sec>
<title>Methods</title>
<p>In a total of 29 patients, submucosal/subgingival plaque samples were collected at peri-implantitis and healthy implant sites as well as teeth with a history of periodontitis (controls). A real-time PCR assay was established for the qualification of fungal organisms and a TaqMan assay for the quantification of
<italic>Porphyromonas gingivalis</italic>
,
<italic>Parvimonas micra</italic>
,
<italic>Tannerella forsythia</italic>
,
<italic>Mycoplasma salivarium</italic>
,
<italic>Veillonella parvula</italic>
, and
<italic>Staphylococcus aureus</italic>
.</p>
</sec>
<sec>
<title>Results</title>
<p>Fungal organisms were more frequently identified at peri-implantitis (31.6%) (i.e.,
<italic>Candida albicans</italic>
,
<italic>Candida boidinii</italic>
,
<italic>Penicillium</italic>
spp
<italic>.</italic>
,
<italic>Rhodotorula laryngis</italic>
,
<italic>Paelicomyces</italic>
spp
<italic>.</italic>
,
<italic>Saccharomycetes</italic>
,
<italic>Cladosporium cladosporioides</italic>
) and healthy implant sites (40% -
<italic>Candida dubliniensis</italic>
,
<italic>C. cladosporioides</italic>
) than at selected teeth (20% -
<italic>C. albicans</italic>
,
<italic>Fusarium solani</italic>
). At implant sites, fungal organisms were significantly correlated with
<italic>P. micra</italic>
and
<italic>T. forsythia</italic>
.</p>
</sec>
<sec>
<title>Conclusions</title>
<p>
<italic>Candida</italic>
spp
<italic>.</italic>
and other fungal organisms were frequently identified at peri-implantitis as well as healthy implant sites and co-colonized with
<italic>P. micra</italic>
and
<italic>T. forsythia</italic>
.</p>
</sec>
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<li>Allemagne</li>
</country>
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<li>District de Düsseldorf</li>
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<name sortKey="Becker, Kathrin" sort="Becker, Kathrin" uniqKey="Becker K" first="Kathrin" last="Becker">Kathrin Becker</name>
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<name sortKey="Henrich, Birgit" sort="Henrich, Birgit" uniqKey="Henrich B" first="Birgit" last="Henrich">Birgit Henrich</name>
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</record>

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