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Conference Paper: Oral treponeme phylotypes associated with periodontal health and diseas

TitleOral treponeme phylotypes associated with periodontal health and diseas
Authors
KeywordsInfection
Microbiology
Molecular biology
Periodontal organisms
Periodontics
Issue Date2012
PublisherInternational Association for Dental Research (IADR).
Citation
The 26th Annual Scientific Meeting of the International Association for Dental Research South-East Asia Division (IADR-SEA) and 23rd Annual Meeting of SEAADE, Hong Kong, 31 October-4 November 2012. How to Cite?
AbstractOBJECTIVES: There are 10 human oral treponeme ‘phylogroups’, each composed of various numbers of treponeme species and/or species-level phylotypes. The objective of this study was to analyze the composition of treponeme phylotypes present in periodontal niches in subjects with periodontitis versus healthy controls. METHODS: After scrupulous removal of supragingival plaque, pooled subgingival plaque was sampled from multiple sites from 10 periodontitis patients and 10 periodontitis-free controls. The periodontal health status was clinically assessed using standard criteria (including %BOP, %PPD 4-5mm and >6mm). Bacterial DNA was purified from each sample, and 16S rRNA genes were PCR-amplified using ‘treponeme-selective’ primers. Cloned 16S rRNA-gene libraries were constructed, and ca. 50 clones were sequenced for each subject. Treponeme species and phylotype diversity was systematically analyzed using bioinformatic, computational phylogenetic and statistical clustering methods. RESULTS: There was no statistically-significant difference in the number of 16S rRNA plasmid clones obtained from the periodontitis (n=510) and control (n=520) groups. Higher numbers of treponeme clones were obtained from the periodontitis subjects (n=365, 70.2%) versus periodontitis-free controls (n=250, 49.0%; p<0.05, Mann-Whitney U test). 7 out of 10 treponeme phylogroups were detected in both subject groups. Periodontitis subjects had a higher clonal abundance of phylogroup 2 treponemes (p<0.001). Two specific phylotypes from phylogroup 2, including one phylotype corresponding to the type strain of Treponema denticola, appear to be associated with periodontitis (p<0.01). There were significant differences in the composition of treponeme phylotypes detected in the periodontitis and control groups, with subjects clustering according to their clinical periodontal condition. CONCLUSIONS: A wide variety of treponeme species and (species-level) phylotypes are present in ‘healthy’ subgingival plaque. Specific bacterial lineages of phylogroup 2 treponemes have an increased association with periodontal disease.
DescriptionScientific Groups - Microbiology/Immunology: paper 169795
Persistent Identifierhttp://hdl.handle.net/10722/174170

 

DC FieldValueLanguage
dc.contributor.authorLeung, WKen_US
dc.contributor.authorYou, Men_US
dc.contributor.authorMo, Sen_US
dc.contributor.authorWatt, RMen_US
dc.date.accessioned2012-11-16T03:38:04Z-
dc.date.available2012-11-16T03:38:04Z-
dc.date.issued2012en_US
dc.identifier.citationThe 26th Annual Scientific Meeting of the International Association for Dental Research South-East Asia Division (IADR-SEA) and 23rd Annual Meeting of SEAADE, Hong Kong, 31 October-4 November 2012.en_US
dc.identifier.urihttp://hdl.handle.net/10722/174170-
dc.descriptionScientific Groups - Microbiology/Immunology: paper 169795-
dc.description.abstractOBJECTIVES: There are 10 human oral treponeme ‘phylogroups’, each composed of various numbers of treponeme species and/or species-level phylotypes. The objective of this study was to analyze the composition of treponeme phylotypes present in periodontal niches in subjects with periodontitis versus healthy controls. METHODS: After scrupulous removal of supragingival plaque, pooled subgingival plaque was sampled from multiple sites from 10 periodontitis patients and 10 periodontitis-free controls. The periodontal health status was clinically assessed using standard criteria (including %BOP, %PPD 4-5mm and >6mm). Bacterial DNA was purified from each sample, and 16S rRNA genes were PCR-amplified using ‘treponeme-selective’ primers. Cloned 16S rRNA-gene libraries were constructed, and ca. 50 clones were sequenced for each subject. Treponeme species and phylotype diversity was systematically analyzed using bioinformatic, computational phylogenetic and statistical clustering methods. RESULTS: There was no statistically-significant difference in the number of 16S rRNA plasmid clones obtained from the periodontitis (n=510) and control (n=520) groups. Higher numbers of treponeme clones were obtained from the periodontitis subjects (n=365, 70.2%) versus periodontitis-free controls (n=250, 49.0%; p<0.05, Mann-Whitney U test). 7 out of 10 treponeme phylogroups were detected in both subject groups. Periodontitis subjects had a higher clonal abundance of phylogroup 2 treponemes (p<0.001). Two specific phylotypes from phylogroup 2, including one phylotype corresponding to the type strain of Treponema denticola, appear to be associated with periodontitis (p<0.01). There were significant differences in the composition of treponeme phylotypes detected in the periodontitis and control groups, with subjects clustering according to their clinical periodontal condition. CONCLUSIONS: A wide variety of treponeme species and (species-level) phylotypes are present in ‘healthy’ subgingival plaque. Specific bacterial lineages of phylogroup 2 treponemes have an increased association with periodontal disease.-
dc.languageengen_US
dc.publisherInternational Association for Dental Research (IADR).-
dc.relation.ispartof26th IADR-SEA Annual Scientific Meeting & 23rd SEAADE Annual Meetingen_US
dc.subjectInfection-
dc.subjectMicrobiology-
dc.subjectMolecular biology-
dc.subjectPeriodontal organisms-
dc.subjectPeriodontics-
dc.titleOral treponeme phylotypes associated with periodontal health and diseasen_US
dc.typeConference_Paperen_US
dc.identifier.emailLeung, WK: ewkleung@hkucc.hku.hken_US
dc.identifier.emailWatt, RM: rmwatt@hku.hken_US
dc.identifier.authorityLeung, WK=rp00019en_US
dc.identifier.authorityWatt, RM=rp00043en_US
dc.description.naturelink_to_OA_fulltext-
dc.identifier.hkuros212352en_US
dc.publisher.placeUnited States-

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