Subgingival microbiome in patients with healthy and ailing dental implants

Hui Zheng, Lixin Xu, Zicheng Wang, Lianshuo Li, Jieni Zhang, Qian Zhang, Ting Chen, Jiuxiang Lin, Feng Chen, Hui Zheng, Lixin Xu, Zicheng Wang, Lianshuo Li, Jieni Zhang, Qian Zhang, Ting Chen, Jiuxiang Lin, Feng Chen

Abstract

Dental implants are commonly used to replace missing teeth. However, the dysbiotic polymicrobial communities of peri-implant sites are responsible for peri-implant diseases, such as peri-implant mucositis and peri-implantitis. In this study, we analyzed the microbial characteristics of oral plaque from peri-implant pockets or sulci of healthy implants (n = 10), peri-implant mucositis (n = 8) and peri-implantitis (n = 6) sites using pyrosequencing of the 16S rRNA gene. An increase in microbial diversity was observed in subgingival sites of ailing implants, compared with healthy implants. Microbial co-occurrence analysis revealed that periodontal pathogens, such as Porphyromonas gingivalis, Tannerella forsythia, and Prevotella intermedia, were clustered into modules in the peri-implant mucositis network. Putative pathogens associated with peri-implantitis were present at a moderate relative abundance in peri-implant mucositis, suggesting that peri-implant mucositis an important early transitional phase during the development of peri-implantitis. Furthermore, the relative abundance of Eubacterium was increased at peri-implantitis locations, and co-occurrence analysis revealed that Eubacterium minutum was correlated with Prevotella intermedia in peri-implantitis sites, which suggests the association of Eubacterium with peri-implantitis. This study indicates that periodontal pathogens may play important roles in the shifting of healthy implant status to peri-implant disease.

Figures

Figure 1. Sample collection and microbial community…
Figure 1. Sample collection and microbial community variation within groups.
(A) A diagrammatic representation of our sample collection procedure. Plaque from healthy implant, peri-implant mucositis, and peri-implantitis sites was sampled from the deepest pockets or sulci. (B) The average weighted UniFrac distance values (the beta diversities) of healthy implant (HC), peri-implant mucositis (PM), and peri-implantitis (PI) sites. Healthy implant sites tended to host diverse bacterial communities, whereas peri-implantitis sites showed the greatest similarity in microbial communities. *P < 0.05, **P < 0.01 by two-tailed t-test.
Figure 2. Calculation of alpha diversity values…
Figure 2. Calculation of alpha diversity values for comparison of the total microbial diversity of healthy implant (HC), peri-implant mucositis (PM), and peri-implantitis (PI) sites.
Alpha diversity values were calculated based on a subsample of 8000 sequences from each dataset. *P t-test. (A) The numbers of observed OTUs increased in both PM and PI. (B) The estimated OTU numbers (Chao1) of PM and PI were significantly greater than that of HC. (C) Microbial community diversity analysis (Shannon index) showed that the PI microbial community exhibited the greatest diversity. (D) Phylogenetic diversity (PD) measures of community diversity.
Figure 3. OTUs and taxa differing between…
Figure 3. OTUs and taxa differing between healthy implant (HC) and peri-implantitis (PI) sites.
(A) A total of 29 OTUs exhibited significant differences in mean relative abundances between HC and PI sites (Wilcoxon rank-sum test, P < 0.05). The bars show mean ± SEM relative abundances. In total, levels of 27 OTUs were higher in PI. (B) OTUs differing in terms of detection frequency between HC and PI sites (Fisher’s exact test, P < 0.05). (C) Species differing in terms of relative abundance between HC and PI sites (Wilcoxon rank-sum test, P < 0.05). The bars show mean ± SEM relative abundances. (D) Species differing in terms of detection frequency between HC and PI sites (Fisher’s exact test, P < 0.05). OTUs or species marked with stars (★) differed significantly in terms of both relative abundance and detection frequency. (E) A heat map of the relative abundances of OTUs that differed significantly between health and disease. The diagram shows OTUs that differed both in relative abundance (Wilcoxon rank-sum test, P < 0.05) and frequency of detection (Fisher’s exact test, P < 0.05) in HC and PI sites. Peri-implant mucositis sites were intermediate in terms of both relative abundance and prevalence.
Figure 4. Members of the genus Eubacterium…
Figure 4. Members of the genus Eubacterium in healthy implant (HC) and peri-implantitis (PI) sites.
(A) The relative abundances of Eubacterium species were compared. Bars represent the means ± SEMs of the relative abundances of detected species. *P < 0.05 by the Wilcoxon rank-sum test. (B) Total abundances, measured via real-time qPCR, of the Eubacterium brachy subgroup (including E. brachy, E. infirmum, E. nodatum, and E. tardum). **P < 0.01 by Wilcoxon rank-sum test. (C) Positive correlation between Eubacterium minutum and Prevotella intermedia.
Figure 5. Co-occurring network modules in PM…
Figure 5. Co-occurring network modules in PM site and corresponding OTUs in HC and PI sites.
Edges between each pair of OTUs indicate significant correlations (P A) Module in PM network consisted of OTUs with at least five degrees. Periodontal pathogens were marked red. (B, C) Corresponding OTUs did not cluster into pairwise modules in HC and PI sites.
Figure 6. Venn diagram of the core…
Figure 6. Venn diagram of the core microbiome of peri-implant sites.
Each circle (red, green or blue) contains OTUs present in at least 50% of subjects within a group. OTUs in the overlapping regions were shared by two or three groups. Numerically dominant OTUs with mean relative abundances >0.5% are shown in bold.

References

    1. Barber A. J., Butterworth C. J. & Rogers S. N. Systematic review of primary osseointegrated dental implants in head and neck oncology. Br J Oral Maxillofac Surg 49, 29–36, 10.1016/j.bjoms.2009.12.007 (2011).
    1. Demarosi F., Leghissa G. C., Sardella A., Lodi G. & Carrassi A. Localised maxillary ridge expansion with simultaneous implant placement: a case series. Br J Oral Maxillofac Surg 47, 535–540, 10.1016/j.bjoms.2008.11.012 (2009).
    1. Klinge B., Hultin M. & Berglundh T. Peri-implantitis. Dent Clin North Am 49, 661–676, vii–viii, 10.1016/j.cden.2005.03.007 (2005).
    1. Jepsen S., Ruhling A., Jepsen K., Ohlenbusch B. & Albers H. K. Progressive peri-implantitis. Incidence and prediction of peri-implant attachment loss. Clin Oral Implants Res 7, 133–142 (1996).
    1. Lindhe J., Meyle J. & Group D. o. E. W. o. P. Peri-implant diseases: Consensus Report of the Sixth European Workshop on Periodontology. J Clin Periodontol 35, 282–285, 10.1111/j.1600-051X.2008.01283.x (2008).
    1. Renvert S., Roos-Jansaker A. M., Lindahl C., Renvert H. & Rutger Persson G. Infection at titanium implants with or without a clinical diagnosis of inflammation. Clin Oral Implants Res 18, 509–516, 10.1111/j.1600-0501.2007.01378.x (2007).
    1. Sanz M., Chapple I. L. & Working Group 4 of the, V. E. W. o. P. Clinical research on peri-implant diseases: consensus report of Working Group 4. J Clin Periodontol 39 (Suppl 12), 202–206, 10.1111/j.1600-051X.2011.01837.x (2012).
    1. Zitzmann N. U. & Berglundh T. Definition and prevalence of peri-implant diseases. J Clin Periodontol 35, 286–291, 10.1111/j.1600-051X.2008.01274.x (2008).
    1. Sanz M. et al. Characterization of the subgingival microbial flora around endosteal sapphire dental implants in partially edentulous patients. Int J Oral Maxillofac Implants 5, 247–253 (1990).
    1. Quirynen M. et al. Dynamics of initial subgingival colonization of ‘pristine’ peri-implant pockets. Clin Oral Implants Res 17, 25–37, 10.1111/j.1600-0501.2005.01194.x (2006).
    1. Esposito M., Hirsch J. M., Lekholm U. & Thomsen P. Biological factors contributing to failures of osseointegrated oral implants. (II). Etiopathogenesis. Eur J Oral Sci 106, 721–764 (1998).
    1. Berglundh T., Persson L. & Klinge B. A systematic review of the incidence of biological and technical complications in implant dentistry reported in prospective longitudinal studies of at least 5 years. J Clin Periodontol 29 (Suppl 3), 197–212; discussion 232-193 (2002).
    1. Kistler J. O., Booth V., Bradshaw D. J. & Wade W. G. Bacterial community development in experimental gingivitis. PLoS One 8, e71227, 10.1371/journal.pone.0071227 (2013).
    1. Socransky S. S. & Haffajee A. D. Periodontal microbial ecology. Periodontol 2000 38, 135–187, 10.1111/j.1600-0757.2005.00107.x (2005).
    1. Salvi G. E. et al. Reversibility of experimental peri-implant mucositis compared with experimental gingivitis in humans. Clin Oral Implants Res 23, 182–190, 10.1111/j.1600-0501.2011.02220.x (2012).
    1. Kumar P. S., Mason M. R., Brooker M. R. & O’Brien K. Pyrosequencing reveals unique microbial signatures associated with healthy and failing dental implants. J Clin Periodontol 39, 425–433, 10.1111/j.1600-051X.2012.01856.x (2012).
    1. Meffert R. M. Periodontitis vs. peri-implantitis: the same disease? The same treatment? Crit Rev Oral Biol Med 7, 278–291 (1996).
    1. Algraffee H., Borumandi F. & Cascarini L. Peri-implantitis. Br J Oral Maxillofac Surg 50, 689–694, 10.1016/j.bjoms.2011.11.020 (2012).
    1. Shchipkova A. Y., Nagaraja H. N. & Kumar P. S. Subgingival microbial profiles of smokers with periodontitis. J Dent Res 89, 1247–1253, 10.1177/0022034510377203 (2010).
    1. Charlson E. S. et al. Disordered microbial communities in the upper respiratory tract of cigarette smokers. PLoS One 5, e15216, 10.1371/journal.pone.0015216 (2010).
    1. Keijser B. J. et al. Pyrosequencing analysis of the oral microflora of healthy adults. J Dent Res 87, 1016–1020 (2008).
    1. Shibli J. A. et al. Composition of supra- and subgingival biofilm of subjects with healthy and diseased implants. Clin Oral Implants Res 19, 975–982, 10.1111/j.1600-0501.2008.01566.x (2008).
    1. Maximo M. B. et al. Short-term clinical and microbiological evaluations of peri-implant diseases before and after mechanical anti-infective therapies. Clin Oral Implants Res 20, 99–108, 10.1111/j.1600-0501.2008.01618.x (2009).
    1. Schloss P. D. et al. Introducing mothur: open-source, platform-independent, community-supported software for describing and comparing microbial communities. Appl Environ Microbiol 75, 7537–7541, 10.1128/AEM.01541-09 (2009).
    1. Caporaso J. G. et al. QIIME allows analysis of high-throughput community sequencing data. Nat Methods 7, 335–336, 10.1038/nmeth.f.303 (2010).
    1. Spratt D. A., Weightman A. J. & Wade W. G. Diversity of oral asaccharolytic Eubacterium species in periodontitis--identification of novel phylotypes representing uncultivated taxa. Oral Microbiol Immunol 14, 56–59 (1999).
    1. Socransky S. S., Haffajee A. D., Cugini M. A., Smith C. & Kent R. L. Jr. Microbial complexes in subgingival plaque. J Clin Periodontol 25, 134–144 (1998).
    1. Tabanella G., Nowzari H. & Slots J. Clinical and microbiological determinants of ailing dental implants. Clin Implant Dent Relat Res 11, 24–36, 10.1111/j.1708-8208.2008.00088.x (2009).
    1. Koyanagi T., Sakamoto M., Takeuchi Y., Ohkuma M. & Izumi Y. Analysis of microbiota associated with peri-implantitis using 16S rRNA gene clone library. J Oral Microbiol 2, 10.3402/jom.v2i0.5104 (2010).
    1. Zijnge V. et al. Oral biofilm architecture on natural teeth. PLoS One 5, e9321, 10.1371/journal.pone.0009321 (2010).
    1. Dabdoub S. M., Tsigarida A. A. & Kumar P. S. Patient-specific analysis of periodontal and peri-implant microbiomes. J Dent Res 92, 168S–175S, 10.1177/0022034513504950 (2013).
    1. Botero J. E., Gonzalez A. M., Mercado R. A., Olave G. & Contreras A. Subgingival microbiota in peri-implant mucosa lesions and adjacent teeth in partially edentulous patients. J Periodontol 76, 1490–1495, 10.1902/jop.2005.76.9.1490 (2005).
    1. Mombelli A. & Decaillet F. The characteristics of biofilms in peri-implant disease. J Clin Periodontol 38 (Suppl 11), 203–213, 10.1111/j.1600-051X.2010.01666.x (2011).
    1. Heitz-Mayfield L. J. & Lang N. P. Comparative biology of chronic and aggressive periodontitis vs. peri-implantitis. Periodontol 2000 53, 167–181, 10.1111/j.1600-0757.2010.00348.x (2010).
    1. Li Y. et al. Phylogenetic and functional gene structure shifts of the oral microbiomes in periodontitis patients. ISME J, 10.1038/ismej.2014.28 (2014).
    1. Abusleme L. et al. The subgingival microbiome in health and periodontitis and its relationship with community biomass and inflammation. ISME J 7, 1016–1025, 10.1038/ismej.2012.174 (2013).
    1. Hultin M. et al. Microbiological findings and host response in patients with peri-implantitis. Clin Oral Implants Res 13, 349–358 (2002).
    1. Alcoforado G. A., Rams T. E., Feik D. & Slots J. Microbial aspects of failing osseointegrated dental implants in humans. J Parodontol 10, 11–18 (1991).
    1. Persson G. R. & Renvert S. Cluster of Bacteria Associated with Peri-Implantitis. Clin Implant Dent Relat Res, 10.1111/cid.12052 (2013).
    1. Leonhardt A., Renvert S. & Dahlen G. Microbial findings at failing implants. Clin Oral Implants Res 10, 339–345 (1999).
    1. Koyanagi T. et al. Comprehensive microbiological findings in peri-implantitis and periodontitis. J Clin Periodontol 40, 218–226, 10.1111/jcpe.12047 (2013).
    1. Haffajee A. D., Teles R. P. & Socransky S. S. Association of Eubacterium nodatum and Treponema denticola with human periodontitis lesions. Oral Microbiol Immunol 21, 269–282, 10.1111/j.1399-302X.2006.00287.x (2006).
    1. Booth V., Downes J., Van den Berg J. & Wade W. G. Gram-positive anaerobic bacilli in human periodontal disease. J Periodontal Res 39, 213–220, 10.1111/j.1600-0765.2004.00726.x (2004).
    1. Barberan A., Bates S. T., Casamayor E. O. & Fierer N. Using network analysis to explore co-occurrence patterns in soil microbial communities. ISME J 6, 343–351, 10.1038/ismej.2011.119 (2012).
    1. Hajishengallis G., Darveau R. P. & Curtis M. A. The keystone-pathogen hypothesis. Nat Rev Microbiol 10, 717–725, 10.1038/nrmicro2873 (2012).
    1. Lang N. P., Berglundh T. & Working Group 4 of Seventh European Workshop on, P. Periimplant diseases: where are we now?–Consensus of the Seventh European Workshop on Periodontology. J Clin Periodontol 38 (Suppl 11), 178–181, 10.1111/j.1600-051X.2010.01674.x (2011).
    1. Berglundh T., Zitzmann N. U. & Donati M. Are peri-implantitis lesions different from periodontitis lesions? J Clin Periodontol 38 (Suppl 11), 188–202, 10.1111/j.1600-051X.2010.01672.x (2011).
    1. Lang N. P., Schatzle M. A. & Loe H. Gingivitis as a risk factor in periodontal disease. J Clin Periodontol 36 (Suppl 10), 3–8, 10.1111/j.1600-051X.2009.01415.x (2009).

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