31
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Porphyromonas gingivalis disturbs host–commensal homeostasis by changing complement function

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          ABSTRACT

          Porphyromonas gingivalis is a Gram-negative anaerobic rod that has been proposed as an orchestrator of complement-dependent dysbiotic inflammation. This notion was suggested from its capacities to manipulate the complement–Toll-like receptor crosstalk in ways that promote dysbiosis and periodontal disease in animal models. Specifically, while at low colonization levels, P. gingivalis interferes with innate immunity and leads to changes in the counts and composition of the oral commensal microbiota. The resulting dysbiotic microbial community causes disruption of host–microbial homeostasis, leading to inflammatory bone loss. These findings suggested that P. gingivalis can be considered as a keystone pathogen. The concept of keystone pathogens is one where their effects have community-wide significance and are disproportionate of their abundance. The present review summarizes the relevant literature and discusses whether the results from the animal models can be extrapolated to man.

          Related collections

          Most cited references69

          • Record: found
          • Abstract: found
          • Article: found
          Is Open Access

          Defining the healthy "core microbiome" of oral microbial communities

          Background Most studies examining the commensal human oral microbiome are focused on disease or are limited in methodology. In order to diagnose and treat diseases at an early and reversible stage an in-depth definition of health is indispensible. The aim of this study therefore was to define the healthy oral microbiome using recent advances in sequencing technology (454 pyrosequencing). Results We sampled and sequenced microbiomes from several intraoral niches (dental surfaces, cheek, hard palate, tongue and saliva) in three healthy individuals. Within an individual oral cavity, we found over 3600 unique sequences, over 500 different OTUs or "species-level" phylotypes (sequences that clustered at 3% genetic difference) and 88 - 104 higher taxa (genus or more inclusive taxon). The predominant taxa belonged to Firmicutes (genus Streptococcus, family Veillonellaceae, genus Granulicatella), Proteobacteria (genus Neisseria, Haemophilus), Actinobacteria (genus Corynebacterium, Rothia, Actinomyces), Bacteroidetes (genus Prevotella, Capnocytophaga, Porphyromonas) and Fusobacteria (genus Fusobacterium). Each individual sample harboured on average 266 "species-level" phylotypes (SD 67; range 123 - 326) with cheek samples being the least diverse and the dental samples from approximal surfaces showing the highest diversity. Principal component analysis discriminated the profiles of the samples originating from shedding surfaces (mucosa of tongue, cheek and palate) from the samples that were obtained from solid surfaces (teeth). There was a large overlap in the higher taxa, "species-level" phylotypes and unique sequences among the three microbiomes: 84% of the higher taxa, 75% of the OTUs and 65% of the unique sequences were present in at least two of the three microbiomes. The three individuals shared 1660 of 6315 unique sequences. These 1660 sequences (the "core microbiome") contributed 66% of the reads. The overlapping OTUs contributed to 94% of the reads, while nearly all reads (99.8%) belonged to the shared higher taxa. Conclusions We obtained the first insight into the diversity and uniqueness of individual oral microbiomes at a resolution of next-generation sequencing. We showed that a major proportion of bacterial sequences of unrelated healthy individuals is identical, supporting the concept of a core microbiome at health.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Challenges in the Quest for Keystones

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              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.
                Bookmark

                Author and article information

                Journal
                J Oral Microbiol
                J Oral Microbiol
                ZJOM
                zjom20
                Journal of Oral Microbiology
                Taylor & Francis
                2000-2297
                2017
                30 June 2017
                : 9
                : 1
                : 1340085
                Affiliations
                [ a ] Department of Oral Biology, Faculty of Dentistry, University of Oslo , Oslo, Norway
                [ b ] Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania , PA, USA
                [ c ] Department of Microbiology, School of Dental Medicine; University of Pennsylvania , PA, USA
                Author notes
                Article
                1340085
                10.1080/20002297.2017.1340085
                5508361
                28748042
                034c8cb8-2c0d-4558-9112-81d064809ae2
                © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 22 February 2017
                : 6 June 2017
                Page count
                Figures: 2, References: 93, Pages: 12
                Funding
                Funded by: European Commmission 10.13039/501100000780
                Award ID: FP7-HEALTH-306029 ‘TRIGGER’
                Funded by: U.S. National Institutes of Health
                Award ID: DE015254
                Award ID: DE021685
                Award ID: DE024153
                Award ID: DE024716
                Award ID: DE026152
                Funded by: European Community’s Seventh Framework Programme
                Award ID: 602699 (DIREKT)
                Funded by: U.S. National Institutes of Health
                Award ID: AI003040
                Award ID: AI068730
                IO acknowledges funding through the European Commission (FP7-HEALTH-306029 ‘TRIGGER’). JDL acknowledges funding through the U.S. National Institutes of Health AI003040 and AI068730 and the European Community’s Seventh Framework Programme under grant agreement number 602699 (DIREKT). GH acknowledges funding through the US National Institutes of Health (DE015254, DE021685, DE024153, DE024716, and DE026152).
                Categories
                Review Article
                Review Article

                Microbiology & Virology
                p. gingivalis,keystone pathogen,commensal microbiota,complement,animal model,periodontitis

                Comments

                Comment on this article