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      Confocal Raman microscopy to identify bacteria in oral subgingival biofilm models

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          Abstract

          The study of oral disease progression, in relation to the accumulation of subgingival biofilm in gingivitis and periodontitis is limited, due to either the ability to monitor plaque in vitro. When compared, optical spectroscopic techniques offer advantages over traditional destructive or biofilm staining approaches, making it a suitable alternative for the analysis and continued development of three-dimensional structures. In this work, we have developed a confocal Raman spectroscopy analysis approach towards in vitro subgingival plaque models. The main objective of this study was to develop a method for differentiating multiple oral subgingival bacterial species in planktonic and biofilm conditions, using confocal Raman microscopy. Five common subgingival bacteria ( Fusobacterium nucleatum, Streptococcus mutans, Veillonella dispar, Actinomyces naeslundii and Prevotella nigrescens) were used and differentiated using a 2-way orthogonal Partial Least Square with Discriminant Analysis (O2PLS-DA) for the collected spectral data. In addition to planktonic growth, mono-species biofilms cultured using the ‘Zürich Model’ were also analyzed. The developed method was successfully used to predict planktonic and mono-species biofilm species in a cross validation setup. The results show differences in the presence and absence of chemical bands within the Raman spectra. The O2PLS-DA model was able to successfully predict 100% of all tested planktonic samples and 90% of all mono-species biofilm samples. Using this approach we have shown that Confocal Raman microscopy can analyse and predict the identity of planktonic and mono-species biofilm species, thus enabling its potential as a technique to map oral multi-species biofilm models.

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

          The goals of this study were to better understand the ecology of oral subgingival communities in health and periodontitis and elucidate the relationship between inflammation and the subgingival microbiome. Accordingly, we used 454-pyrosequencing of 16S rRNA gene libraries and quantitative PCR to characterize the subgingival microbiome of 22 subjects with chronic periodontitis. Each subject was sampled at two sites with similar periodontal destruction but differing in the presence of bleeding, a clinical indicator of increased inflammation. Communities in periodontitis were also compared with those from 10 healthy individuals. In periodontitis, presence of bleeding was not associated with different α-diversity or with a distinct microbiome, however, bleeding sites showed higher total bacterial load. In contrast, communities in health and periodontitis largely differed, with higher diversity and biomass in periodontitis. Shifts in community structure from health to periodontitis resembled ecological succession, with emergence of newly dominant taxa in periodontitis without replacement of primary health-associated species. That is, periodontitis communities had higher proportions of Spirochetes, Synergistetes, Firmicutes and Chloroflexi, among other taxa, while the proportions of Actinobacteria, particularly Actinomyces, were higher in health. Total Actinomyces load, however, remained constant from health to periodontitis. Moreover, an association existed between biomass and community structure in periodontitis, with the proportion of specific taxa correlating with bacterial load. Our study provides a global-scale framework for the ecological events in subgingival communities that underline the development of periodontitis. The association, in periodontitis, between inflammation, community biomass and community structure and their role in disease progression warrant further investigation.
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            Reference database of Raman spectra of biological molecules

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              Exopolysaccharides produced by Streptococcus mutans glucosyltransferases modulate the establishment of microcolonies within multispecies biofilms.

              Streptococcus mutans is a key contributor to the formation of the extracellular polysaccharide (EPS) matrix in dental biofilms. The exopolysaccharides, which are mostly glucans synthesized by streptococcal glucosyltransferases (Gtfs), provide binding sites that promote accumulation of microorganisms on the tooth surface and further establishment of pathogenic biofilms. This study explored (i) the role of S. mutans Gtfs in the development of the EPS matrix and microcolonies in biofilms, (ii) the influence of exopolysaccharides on formation of microcolonies, and (iii) establishment of S. mutans in a multispecies biofilm in vitro using a novel fluorescence labeling technique. Our data show that the ability of S. mutans strains defective in the gtfB gene or the gtfB and gtfC genes to form microcolonies on saliva-coated hydroxyapatite surfaces was markedly disrupted. However, deletion of both gtfB (associated with insoluble glucan synthesis) and gtfC (associated with insoluble and soluble glucan synthesis) is required for the maximum reduction in EPS matrix and biofilm formation. S. mutans grown with sucrose in the presence of Streptococcus oralis and Actinomyces naeslundii steadily formed exopolysaccharides, which allowed the initial clustering of bacterial cells and further development into highly structured microcolonies. Concomitantly, S. mutans became the major species in the mature biofilm. Neither the EPS matrix nor microcolonies were formed in the presence of glucose in the multispecies biofilm. Our data show that GtfB and GtfC are essential for establishment of the EPS matrix, but GtfB appears to be responsible for formation of microcolonies by S. mutans; these Gtf-mediated processes may enhance the competitiveness of S. mutans in the multispecies environment in biofilms on tooth surfaces.
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                Author and article information

                Contributors
                Role: Formal analysisRole: MethodologyRole: Project administrationRole: ResourcesRole: SoftwareRole: ValidationRole: VisualizationRole: Writing – original draft
                Role: ConceptualizationRole: SupervisionRole: Writing – review & editing
                Role: MethodologyRole: SupervisionRole: Writing – review & editing
                Role: ConceptualizationRole: Project administrationRole: SupervisionRole: Writing – review & editing
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                11 May 2020
                2020
                : 15
                : 5
                : e0232912
                Affiliations
                [1 ] Fraunhofer Institute for Interfacial Engineering and Biotechnology, Stuttgart, Germany
                [2 ] Procter & Gamble, Egham, England, United Kingdom
                [3 ] Procter & Gamble, Kronberg, Germany
                University of Hong Kong, HONG KONG
                Author notes

                Competing Interests: There are no conflicts of interest declared for this paper beyond the affiliations of the coauthors with P&G, with Renzo Alberto Ccahuana-Vasquez being a recognized expert in Oral Care and Kevin Wright an R&D microbiologist. There is no IP associated with this publication for any of the partners and no technologies pertaining to products either in development or on the market have been used in this work. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

                Author information
                http://orcid.org/0000-0001-6077-8314
                Article
                PONE-D-20-03132
                10.1371/journal.pone.0232912
                7213720
                32392236
                02d206b7-fd9e-4ad6-a756-72b1e8f8ae67
                © 2020 Kriem et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 3 February 2020
                : 23 April 2020
                Page count
                Figures: 4, Tables: 2, Pages: 13
                Funding
                Funded by: funder-id http://dx.doi.org/10.13039/501100007601, Horizon 2020;
                Award ID: 722871
                Award Recipient :
                This work is funded by the European Union’s Horizon 2020 research innovation programme under grant agreement No. 722871 in the scope of the Marie Skłodowska-Curie Action ITN BioClean to LSK. P&G and other partners contributed time, industrial supervision, training and technical guidance/expertise, access to equipment, placements in industry and co-authored and reviewed associated papers, including this submission all in line with EU Horizon 2020 funding rules. More details can be found on the Horizon 2020 website ( http://www.biocleanh2020.eu/index.php). The funders had no role in study design, data collection and analysis, or decision to publish the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Microbiology
                Bacteriology
                Bacterial Biofilms
                Biology and Life Sciences
                Microbiology
                Biofilms
                Bacterial Biofilms
                Biology and Life Sciences
                Microbiology
                Biofilms
                Biology and Life Sciences
                Organisms
                Eukaryota
                Animals
                Invertebrates
                Plankton
                Biology and Life Sciences
                Organisms
                Bacteria
                Biology and Life Sciences
                Developmental Biology
                Cell Differentiation
                Engineering and Technology
                Equipment
                Laboratory Equipment
                Laboratory Glassware
                Medicine and Health Sciences
                Oral Medicine
                Oral Diseases
                Periodontal Diseases
                Periodontitis
                Research and Analysis Methods
                Microscopy
                Light Microscopy
                Confocal Microscopy
                Confocal Laser Microscopy
                Custom metadata
                All relevant data are within the paper and its Supporting Information files.

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                Uncategorized

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