Literature DB >> 1661305

Relation of counts of microbial species to clinical status at the sampled site.

S S Socransky1, A D Haffajee, C Smith, S Dibart.   

Abstract

The purpose of the present investigation was to relate clinical characteristics at a site to the frequency of detection, absolute counts and proportions of 14 subgingival species. Subgingival plaque samples were removed by curette from the mesial surface of 2299 teeth in 3 healthy and 87 subjects with periodontal attachment loss. Samples were dispersed, diluted and plated on Trypticase soy agar supplemented with 5% sheep blood. After 7 days of anaerobic incubation, colonies were lifted onto nylon filters, lysed and the DNA fixed to the filters. Digoxygenin-labeled DNA probes were used to identify colonies of each test species. Measurements of pocket depth, attachment level, recession, redness, bleeding on probing and suppuration were made at each sampled site. Total viable counts at sites ranged from 10(3) to greater than 10(8) and were strongly related to pocket depth. Mean total counts at sites less than 3 mm averaged 4.6 x 10(6), while mean counts at sites greater than 7 mm averaged 2.0 x 10(7). Species enumerated and % of sites colonized were as follows; V. parvula 44; S. sanguis II 36; B. intermedius I 33; C. ochracea 31; B. intermedius II 30; S. sanguis I 29; B. gingivalis 27; S. intermedius 25; P. micros 24; W. recta 23; F. nucleatum ss vincentii 18; B. forsythus 15; A. actinomycetemcomitans serotype a 10; A. actinomycetemcomitans serotype b 8. Counts of B. intermedius II were higher at sites which exhibited gingival redness while B. intermedius I was higher at sites which bled on probing. A. actinomycetemcomitans serotype b was more frequent and at higher mean % at sites without recession. The opposite was true for S. sanguis II. B. gingivalis was somewhat more prevalent and at higher levels at suppurating sites. B. gingivalis, B. intermedius I and II and B. forsythus were found more frequently and at higher levels at sites with deeper pockets, while V. parvula was less prevalent at sites with pocket depths less than 4 mm. B. gingivalis, B. intermedius I and A. actinomycetemcomitans serotype b increased with increasing pocket depth in both localized and widespread disease subjects, but mean counts were higher in the localized disease subjects at any pocket depth. Only W. recta was found at higher levels at deep sites in widespread disease subjects when compared with similar sites in localized disease subjects. No suspected pathogens were detected in 38% of shallow sites, 31% of intermediate sites and 22% of deep sites, 2/3 of deep pockets, but less than 1/2 of shallow pockets harbored at least 2 of the suspected pathogens.

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Year:  1991        PMID: 1661305     DOI: 10.1111/j.1600-051x.1991.tb00070.x

Source DB:  PubMed          Journal:  J Clin Periodontol        ISSN: 0303-6979            Impact factor:   8.728


  55 in total

1.  Dysbiosis and alterations in predicted functions of the subgingival microbiome in chronic periodontitis.

Authors:  Mariana E Kirst; Eric C Li; Barnett Alfant; Yueh-Yun Chi; Clay Walker; Ingvar Magnusson; Gary P Wang
Journal:  Appl Environ Microbiol       Date:  2014-11-14       Impact factor: 4.792

2.  Microbiome Profiles of Ligature-Induced Periodontitis in Nonhuman Primates across the Life Span.

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3.  The subgingival microbiome in health and periodontitis and its relationship with community biomass and inflammation.

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Review 4.  Lessons learned and unlearned in periodontal microbiology.

Authors:  Ricardo Teles; Flavia Teles; Jorge Frias-Lopez; Bruce Paster; Anne Haffajee
Journal:  Periodontol 2000       Date:  2013-06       Impact factor: 7.589

5.  Oral microbiota in Swiss adolescents.

Authors:  Sigrun Eick; Malgorzata Pietkiewicz; Anton Sculean
Journal:  Clin Oral Investig       Date:  2012-02-28       Impact factor: 3.573

6.  Relationships between subgingival microbiota and GCF biomarkers in generalized aggressive periodontitis.

Authors:  Ricardo P Teles; Lauren C Gursky; Marcelo Faveri; Edvaldo A Rosa; Flavia R F Teles; Magda Feres; Sigmund S Socransky; Anne D Haffajee
Journal:  J Clin Periodontol       Date:  2010-04       Impact factor: 8.728

7.  RgpA-Kgp peptide-based immunogens provide protection against Porphyromonas gingivalis challenge in a murine lesion model.

Authors:  N M O'Brien-Simpson; R A Paolini; E C Reynolds
Journal:  Infect Immun       Date:  2000-07       Impact factor: 3.441

8.  Relationships among gingival crevicular fluid biomarkers, clinical parameters of periodontal disease, and the subgingival microbiota.

Authors:  Ricardo Teles; Dimitra Sakellari; Flavia Teles; Antonis Konstantinidis; Ralph Kent; Sigmund Socransky; Anne Haffajee
Journal:  J Periodontol       Date:  2010-01       Impact factor: 6.993

9.  Subgingival bacterial colonization profiles correlate with gingival tissue gene expression.

Authors:  Panos N Papapanou; Jan H Behle; Moritz Kebschull; Romanita Celenti; Dana L Wolf; Martin Handfield; Paul Pavlidis; Ryan T Demmer
Journal:  BMC Microbiol       Date:  2009-10-18       Impact factor: 3.605

10.  Effect of periodontal therapy on the subgingival microbiota over a 2-year monitoring period. I. Overall effect and kinetics of change.

Authors:  Sigmund S Socransky; Anne D Haffajee; Ricardo Teles; Jan L Wennstrom; Jan Lindhe; Anna Bogren; Hatice Hasturk; Thomas van Dyke; Xiaoshan Wang; Jo Max Goodson
Journal:  J Clin Periodontol       Date:  2013-05-27       Impact factor: 8.728

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