Serveur d'exploration sur le patient édenté (maquette)

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Patient-specific analysis of periodontal and peri-implant microbiomes.

Identifieur interne : 000020 ( PubMed/Corpus ); précédent : 000019; suivant : 000021

Patient-specific analysis of periodontal and peri-implant microbiomes.

Auteurs : S M Dabdoub ; A A Tsigarida ; P S Kumar

Source :

RBID : pubmed:24158341

English descriptors

Abstract

Periodontally involved teeth have been implicated as 'microbial reservoirs' in the etiology of peri-implant diseases. Therefore, the purpose of this investigation was to use a deep-sequencing approach to identify the degree of congruence between adjacent peri-implant and periodontal microbiomes in states of health and disease. Subgingival and peri-implant biofilm samples were collected from 81 partially edentulous individuals with periodontal and peri-implant health and disease. Bacterial DNA was isolated, and the 16S rRNA gene was amplified and sequenced by pyrotag sequencing. Chimera-depleted sequences were compared against a locally hosted curated database for bacterial identification. Statistical significance was determined by paired Student's t tests between tooth-implant pairs. The 1.9 million sequences identified represented 523 species. Sixty percent of individuals shared less than 50% of all species between their periodontal and peri-implant biofilms, and 85% of individuals shared less than 8% of abundant species between tooth and implant. Additionally, the periodontal microbiome demonstrated significantly higher diversity than the implant, and distinct bacterial lineages were associated with health and disease in each ecosystem. Analysis of our data suggests that simple geographic proximity is not a sufficient determinant of colonization of topographically distinct niches, and that the peri-implant and periodontal microbiomes represent microbiologically distinct ecosystems.

DOI: 10.1177/0022034513504950
PubMed: 24158341

Links to Exploration step

pubmed:24158341

Le document en format XML

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<div type="abstract" xml:lang="en">Periodontally involved teeth have been implicated as 'microbial reservoirs' in the etiology of peri-implant diseases. Therefore, the purpose of this investigation was to use a deep-sequencing approach to identify the degree of congruence between adjacent peri-implant and periodontal microbiomes in states of health and disease. Subgingival and peri-implant biofilm samples were collected from 81 partially edentulous individuals with periodontal and peri-implant health and disease. Bacterial DNA was isolated, and the 16S rRNA gene was amplified and sequenced by pyrotag sequencing. Chimera-depleted sequences were compared against a locally hosted curated database for bacterial identification. Statistical significance was determined by paired Student's t tests between tooth-implant pairs. The 1.9 million sequences identified represented 523 species. Sixty percent of individuals shared less than 50% of all species between their periodontal and peri-implant biofilms, and 85% of individuals shared less than 8% of abundant species between tooth and implant. Additionally, the periodontal microbiome demonstrated significantly higher diversity than the implant, and distinct bacterial lineages were associated with health and disease in each ecosystem. Analysis of our data suggests that simple geographic proximity is not a sufficient determinant of colonization of topographically distinct niches, and that the peri-implant and periodontal microbiomes represent microbiologically distinct ecosystems.</div>
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<CommentsCorrectionsList>
<CommentsCorrections RefType="Cites">
<RefSource>Ann Periodontol. 1999 Dec;4(1):1-6</RefSource>
<PMID Version="1">10863370</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Clin Periodontol. 2009 Jul;36(7):604-9</RefSource>
<PMID Version="1">19538334</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Clin Oral Implants Res. 2000 Dec;11(6):511-20</RefSource>
<PMID Version="1">11168244</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Clin Oral Implants Res. 2001 Jun;12(3):189-95</RefSource>
<PMID Version="1">11359474</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Clin Periodontol. 1985 Jul;12(6):465-76</RefSource>
<PMID Version="1">3894435</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Clin Oral Implants Res. 1990 Dec;1(1):8-12</RefSource>
<PMID Version="1">2099212</PMID>
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<RefSource>Clin Oral Implants Res. 2009 Aug;20(8):817-26</RefSource>
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<CommentsCorrections RefType="Cites">
<RefSource>Nat Methods. 2010 May;7(5):335-6</RefSource>
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</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Clin Periodontol. 2011 Mar;38 Suppl 11:188-202</RefSource>
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<CommentsCorrections RefType="Cites">
<RefSource>PLoS One. 2011;6(6):e20956</RefSource>
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<RefSource>Clin Oral Implants Res. 2012 Feb;23(2):182-90</RefSource>
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<RefSource>J Clin Periodontol. 2012 May;39(5):425-33</RefSource>
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<RefSource>J Biomed Mater Res. 2000 Nov;52(2):388-94</RefSource>
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</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Clin Oral Implants Res. 1993 Sep;4(3):113-20</RefSource>
<PMID Version="1">8297958</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Clin Periodontol. 1995 Feb;22(2):124-30</RefSource>
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<RefSource>Clin Oral Implants Res. 1996 Dec;7(4):405-9</RefSource>
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<RefSource>Bull Tokyo Dent Coll. 2004 May;45(2):77-85</RefSource>
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<RefSource>Environ Microbiol. 2006 Apr;8(4):755-8</RefSource>
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<RefSource>J Clin Microbiol. 2006 Oct;44(10):3665-73</RefSource>
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<RefSource>Eur J Oral Implantol. 2012;5 Suppl:S21-41</RefSource>
<PMID Version="1">22834392</PMID>
</CommentsCorrections>
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