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dc.creatorSchlafer, Sebastian
dc.creatorRiep, Birgit
dc.creatorGriffen, Ann
dc.creatorPetrich, Annett
dc.creatorHubner, Julia
dc.creatorBerning, Moritz
dc.creatorFriedmann, Anton
dc.creatorGobel, Ulf
dc.creatorMoter, Annette
dc.date.accessioned2010-03-25T21:32:56Z
dc.date.available2010-03-25T21:32:56Z
dc.date.issued2010-03-01
dc.identifier.citationSchlafer, Sebastian, Riep, Birgit, Griffen, Ann, Petrich, Annett, Hubner, Julia, Berning, Moritz, Friedmann, Anton, Gobel, Ulf, Moter, Annette, "Filifactor alocis - involvement in periodontal biofilms," BMC Microbiology, v10, (March, 2010), pp. 66-en_US
dc.identifier.issn1471-2180
dc.identifier.urihttp://hdl.handle.net/1811/45122
dc.description.abstractBackground. Bacteria in periodontal pockets develop complex sessile communities that attach to the tooth surface. These highly dynamic microfloral environments challenge both clinicians and researchers alike. The exploration of structural organisation and bacterial interactions within these biofilms is critically important for a thorough understanding of periodontal disease. In recent years, Filifactor alocis, a fastidious, Gram-positive, obligately anaerobic rod was repeatedly identified in periodontal lesions using DNA-based methods. It has been suggested to be a marker for periodontal deterioration. The present study investigated the epidemiology of F. alocis in periodontal pockets and analysed the spatial arrangement and architectural role of the organism in in vivo grown subgingival biofilms. Results. A species-specific oligonucleotide probe, FIAL, was designed and evaluated. A total of 490 subgingival plaque samples were submitted to PCR and subsequent dot blot hybridization to compare the prevalence of F. alocis in patients suffering from generalized aggressive periodontitis (GAP), chronic periodontitis (CP), and control subjects resistant to periodontitis. Moreover, a specially designed carrier system was used to collect in vivo grown subgingival biofilms from GAP patients. Subsequent topographic analysis was performed using fluorescence in situ hybridization. While the majority of patients suffering from GAP or CP harboured F. alocis, it was rarely detected in the control group. In the examined carrier-borne biofilms the organism predominantly colonized apical parts of the pocket in close proximity to the soft tissues and was involved in numerous structures that constitute characteristic architectural features of subgingival periodontal biofilms. Conclusions. F. alocis is likely to make a relevant contribution to the pathogenetic structure of biofilms accounting for periodontal inflammation and can be considered an excellent marker organism for periodontal disease.en_US
dc.description.sponsorshipWe thank Eva Kulik, University of Basel, and Eivind Strøm, University of Oslo, for providing clinical samples, Cindy Hefenbrock and Marie Knüver for excellent technical assistance, Derek Ramsey for proof reading, and Dr. Wolf-Ulrich Klotz for his support. This work was supported by the Sonnenfeld-Stiftung, Berlin, Germany, and by a Rahel-Hirsch grant from Charité – Universitätsmedizin to AM.en_US
dc.language.isoen_USen_US
dc.titleFilifactor alocis - involvement in periodontal biofilmsen_US
dc.typeArticleen_US
dc.identifier.doi10.1186/1471-2180-10-66
dc.identifier.osuauthorgriffen.1


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