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Structure, viability and bacterial kinetics of an in vitro biofilm model using six bacteria from the subgingival microbiota

dc.contributor.authorSánchez Beltrán, María Del Carmen
dc.contributor.authorLlama Palacios, María Arantxazu
dc.contributor.authorBlanc, Vanesa
dc.contributor.authorLeón, Rubén
dc.contributor.authorHerrera González, David
dc.contributor.authorSanz Alonso, Mariano
dc.date.accessioned2024-01-22T16:27:00Z
dc.date.available2024-01-22T16:27:00Z
dc.date.issued2011
dc.description.abstractBackground and Objective: There are few in vitro models available in the scientific literature for study of the structure, formation and development of the subgingival biofilm. The purpose of this study was to develop and validate an in vitro biofilm model, using representative selected bacteria from the subgingival microbiota. Material and Methods: Six standard reference strains were used to develop biofilms over sterile ceramic calcium hydroxyapatite discs coated with saliva within the wells of presterilized polystyrene tissue culture plates. The selected species represent initial (Streptococcus oralis and Actinomyces naeslundii), early (Veillonella parvula), secondary (Fusobacterium nucleatum) and late colonizers (Porphyromonas gingivalis and Aggregatibacter actinomycetemcomitans). The structure of the biofilm obtained was studied using a vital fluorescence technique in conjunction with confocal laser scanning microscopy. The biofilm bacterial kinetics were studied by terminal restriction fragment length polymorphism analysis. Results: After 12 h, initial and early colonizers were the first microorganisms detected adhering to the calcium hydroxyapatite discs. The intermediate colonizer F. nucleatum was not detected in the model until 24 h of incubation. Late colonizers A. actinomycetemcomitans and P. gingivalis could be measured inside the biofilm after 48 h. The biofilm reached its steady state between 72 and 96 h after inoculation, with bacterial vitality increasing from the hydroxyapatite surface to the central part of the biofilm. Conclusion: An in vitro biofilm model was developed and validated, demonstrating a pattern of bacterial colonization and maturation similar to the in vivo development of the subgingival biofilm.en
dc.description.departmentDepto. de Especialidades Clínicas Odontológicas
dc.description.facultyFac. de Odontología
dc.description.refereedTRUE
dc.description.statuspub
dc.identifier.citationSánchez MC, Llama-Palacios A, Blanc V, León R, Herrera D, Sanz M. Structure, viability and bacterial kinetics of an in vitro biofilm model using six bacteria from the subgingival microbiota. J Periodontal Res. 2011 Apr;46(2):252-60.
dc.identifier.doi10.1111/j.1600-0765.2010.01341.x
dc.identifier.essn1600-0765
dc.identifier.issn0022-3484
dc.identifier.officialurlhttps://doi.org/10.1111/j.1600-0765.2010.01341.x
dc.identifier.urihttps://hdl.handle.net/20.500.14352/94492
dc.issue.number2
dc.journal.titleJournal of Periodontal Research
dc.language.isoeng
dc.page.final260
dc.page.initial252
dc.publisherWilley
dc.rights.accessRightsrestricted access
dc.subject.cdu616.31-022
dc.subject.keywordSubgingival plaque
dc.subject.keywordAnaerobic biofilm
dc.subject.keywordConfocal laser scanning microscopy
dc.subject.keywordTerminal restriction fragment length polymorphism
dc.subject.ucmMicrobiología (Biología)
dc.subject.unesco3201.03 Microbiología Clínica
dc.titleStructure, viability and bacterial kinetics of an in vitro biofilm model using six bacteria from the subgingival microbiotaen
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number46
dspace.entity.typePublication
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relation.isAuthorOfPublication.latestForDiscovery27fce85c-05b6-4420-b0a4-22ef8510f4e2

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