An oral multispecies biofilm model for high content screening applications

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dc.identifier.uri http://dx.doi.org/10.15488/1271
dc.identifier.uri http://www.repo.uni-hannover.de/handle/123456789/1296
dc.contributor.author Kommerein, Nadine
dc.contributor.author Stumpp, Sascha N.
dc.contributor.author Musken, Matthias
dc.contributor.author Ehlert, Nina
dc.contributor.author Winkel, Andreas
dc.contributor.author Haussler, Susanne
dc.contributor.author Behrens, Peter
dc.contributor.author Buettner, Falk F.R.
dc.contributor.author Stiesch, Meike
dc.date.accessioned 2017-04-06T06:44:27Z
dc.date.available 2017-04-06T06:44:27Z
dc.date.issued 2017
dc.identifier.citation Kommerein, N.; Stumpp, S.N.; Musken, M.; Ehlert, N.; Winkel, A. et al.: An oral multispecies biofilm model for high content screening applications. In: PLoS ONE 12 (2017), Nr. 3, 173973. DOI: https://doi.org/10.1371/journal.pone.0173973
dc.description.abstract Peri-implantitis caused by multispecies biofilms is a major complication in dental implant treatment. The bacterial infection surrounding dental implants can lead to bone loss and, in turn, to implant failure. A promising strategy to prevent these common complications is the development of implant surfaces that inhibit biofilm development. A reproducible and easyto-use biofilm model as a test system for large scale screening of new implant surfaces with putative antibacterial potency is therefore of major importance. In the present study, we developed a highly reproducible in vitro four-species biofilm model consisting of the highly relevant oral bacterial species Streptococcus oralis, Actinomyces naeslundii, Veillonella dispar and Porphyromonas gingivalis. The application of live/dead staining, quantitative real time PCR (qRT-PCR), scanning electron microscopy (SEM) and urea-NaCl fluorescence in situ hybridization (urea-NaCl-FISH) revealed that the four-species biofilm community is robust in terms of biovolume, live/dead distribution and individual species distribution over time. The biofilm community is dominated by S. oralis, followed by V. dispar, A. naeslundii and P. gingivalis. The percentage distribution in this model closely reflects the situation in early native plaques and is therefore well suited as an in vitro model test system. Furthermore, despite its nearly native composition, the multispecies model does not depend on nutrient additives, such as native human saliva or serum, and is an inexpensive, easy to handle and highly reproducible alternative to the available model systems. The 96-well plate format enables high content screening for optimized implant surfaces impeding biofilm formation or the testing of multiple antimicrobial treatment strategies to fight multispecies biofilm infections, both exemplary proven in the manuscript. eng
dc.description.sponsorship VolkswagenStiftung/VWZN2860
dc.description.sponsorship DFG/EXC/REBIRTH
dc.description.sponsorship DFG/EXC/62/2
dc.language.iso eng
dc.publisher San Francisco, CA : Public Library of Science
dc.relation.ispartofseries PLoS ONE 12 (2017), Nr. 3
dc.rights CC BY 4.0 Unported
dc.rights.uri https://creativecommons.org/licenses/by/4.0/
dc.subject.ddc 570 | Biowissenschaften, Biologie ger
dc.title An oral multispecies biofilm model for high content screening applications eng
dc.type Article
dc.type Text
dc.relation.issn 1932-6203
dc.relation.doi https://doi.org/10.1371/journal.pone.0173973
dc.bibliographicCitation.issue 3
dc.bibliographicCitation.volume 12
dc.bibliographicCitation.firstPage 173973
dc.description.version publishedVersion
tib.accessRights frei zug�nglich


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