Bacterial community composition of chronic periodontitis and novel oral sampling sites for detecting disease indicators
- Vaia Galimanas†1,
- Michael William Hall†2,
- Natasha Singh1,
- Michael David Joseph Lynch2,
- Michael Goldberg1,
- Howard Tenenbaum1,
- Dennis Gerard Cvitkovitch1,
- Josh David Neufeld2 and
- Dilani Braziunas Senadheera1Email author
© Galimanas et al.; licensee BioMed Central Ltd. 2014
Received: 27 March 2014
Accepted: 29 July 2014
Published: 26 August 2014
Periodontitis is an infectious and inflammatory disease of polymicrobial etiology that can lead to the destruction of bones and tissues that support the teeth. The management of chronic periodontitis (CP) relies heavily on elimination or at least control of known pathogenic consortia associated with the disease. Until now, microbial plaque obtained from the subgingival (SubG) sites has been the primary focus for bacterial community analysis using deep sequencing. In addition to the use of SubG plaque, here, we investigated whether plaque obtained from supragingival (SupG) and tongue dorsum sites can serve as alternatives for monitoring CP-associated bacterial biomarkers.
Using SubG, SupG, and tongue plaque DNA from 11 healthy and 13 diseased subjects, we sequenced V3 regions (approximately 200 bases) of the 16S rRNA gene using Illumina sequencing. After quality filtering, approximately 4.1 million sequences were collapsed into operational taxonomic units (OTUs; sequence identity cutoff of >97%) that were classified to a total of 19 phyla spanning 114 genera. Bacterial community diversity and overall composition was not affected by health or disease, and multiresponse permutation procedure (MRPP) on Bray-Curtis distance measures only supported weakly distinct bacterial communities in SubG and tongue plaque depending on health or disease status (P < 0.05). Nonetheless, in SubG and tongue sites, the relative abundance of Firmicutes was increased significantly from health to disease and members of Synergistetes were found in higher abundance across all sites in disease. Taxa indicative of CP were identified in all three locations (for example, Treponema denticola, Porphyromonas gingivalis, Synergistes oral taxa 362 and 363).
For the first time, this study demonstrates that SupG and tongue dorsum plaque can serve as alternative sources for detecting and enumerating known and novel bacterial biomarkers of CP. This finding is clinically important because, in contrast with SubG sampling that requires trained professionals, obtaining plaque from SupG and tongue sites is convenient and minimally-invasive and offers a novel means to track CP-biomarker organisms during treatment outcome monitoring.
KeywordsOral microbiome 16S rRNA gene Chronic periodontitis Tongue Supragingival Subgingival Plaque Bacterial community
Bacterial communities that colonize the human body are intimately linked with host physiology, immunity, metabolism, and nutrition [1–3]. Of colonization sites, the mouth accommodates a bacterial consortium with high taxonomic richness and phylogenetic diversity [4–6]. The microbial composition of the plaque biofilm has a critical role in oral health. Disruption of plaque homeostasis can stimulate tissue destruction and inflammation, leading to infections such as dental caries, gingivitis, and periodontitis [4, 7]. A comprehensive and systematic profiling of the oral biofilm is necessary, not only to understand microbial associations with localized infections, but also because the oral microbiome has long been known as a reservoir for infections at other body sites [8, 9]. Bacterial species normally found in the oral cavity have been associated with distal infections in the lungs, heart, brain, and liver, either reflecting their involvement in opportunistic infections as a result of systemic changes in the body, or perhaps suggesting a causative link [8, 10–13]. Therefore, the plaque consortia can be a mirror and possibly even a monitor of oral and non-oral health and disease.
Periodontitis is a chronic inflammatory disease affecting tooth-supporting structures including the alveolar bone, connective tissue attachment, and gingiva [14, 15]. Although several forms of periodontal diseases have been recognized, the predominant category is chronic periodontitis (CP), which remains a primary cause of tooth loss in adults worldwide . In addition to its large socio-economic burden , CP is associated with considerable morbidity in terms of pain, uncomfortable chewing, oral malodor, and tooth migration. Although the pathogenesis of periodontitis is multifactorial and includes genetic and epigenetic factors, the development of periodontitis is modulated by microbial biofilm that forms on and around teeth, eliciting an inflammatory host reaction [18–21]. The etiology of periodontitis is polymicrobial. In particular, disease progression has been linked with the proliferation of Gram-negative anaerobic species such as Porphyromonas gingivalis, Treponema denticola, and Tannerella forsythia.
Over the past two decades, culture-based, immunohistochemistry, and molecular techniques have focused largely on a small subset of CP-associated microorganisms in the gingival sulcus and thus have overlooked the impact of potentially large numbers of other oral bacterial species in the infectious process [22–24]. Although these as-yet-unidentified organisms might not always be associated intimately with the periodontium at all times, it is still likely that several of them, at one time or another, participate in the pathophysiological processes that lead to and cause the advancement of CP. Emerging evidence of subgingival (SubG) community analysis using DNA sequencing suggests that periodontal destruction is associated with many uncultivable and uncharacterized disease indicator organisms [25–27]. However, despite the growing list of periodontitis-associated bacteria, there is slow progress in the use of this information to develop more cost-effective and sensitive methods to treat, control, or prevent disease progression. It is probable that a more complete characterization of bacterial biomarkers of CP will lead to the development of new therapeutics, improved diagnostics, and alternative methods for monitoring the outcomes of treatment success.
Recently, high-throughput sequencing approaches have assessed bacterial composition in deep and shallow SubG samples derived from patients with periodontitis compared to healthy patients . The results demonstrated that patients with periodontitis had more diverse combinations of species but also had all of the health-associated species, albeit at a lower frequency. These results agreed with another study that showed increasing diversity in diseased compared to healthy sites . However, diversity did not increase between bleeding and non-bleeding SubG sites; an increase in total bacterial load was demonstrated in the SubG samples obtained from bleeding sites. Both of these studies noted a clear distinction between healthy and diseased SubG sites when using distance metric analysis [25, 27].
In this study, we used 16S rRNA gene analyses for examining bacterial communities associated with periodontal health and CP, using plaque extracted from SubG and supragingival (SupG) as well as sites on the dorsum of the tongue. We hypothesized that consistent differences in bacterial communities of both dental and tongue plaque would exist between CP and healthy patients and that these differences would be largely due to known disease-associated taxa as well as other as-yet-uncharacterized bacteria. Another goal was to determine if SupG and tongue plaque sampling could be used as a novel and non-invasive detection method of indicator taxa for CP, instead of conventionally sampled SubG plaque. A relatively simpler alternative sampling protocol would greatly facilitate the detection of periodontitis-associated bacterial biomarkers in disease monitoring. For the first time, we provide evidence that both SupG and tongue dorsum sites may be suitable as alternative sampling sources for the detection and enumeration of selected CP-associated bacterial biomarkers. The use of tongue plaque or SupG plaque that is above the gum line to monitor oral health is convenient and circumvents the utility of specially trained personnel for the sampling procedure; in fact, samples can be provided by the patients themselves. From a clinical standpoint, this study provides important groundwork for developing a minimally invasive method to monitor CP treatment outcomes.
Demographics, clinical attributes, and sequencing
Demographics and clinical parameters of participants
Demographics, clinical parameters, and habits
Healthy group (n = 11)
Diseased group (n = 13)
3 men; 8 women
6 men; 7 women
38.4 ± 4.1
46.8 ± 4.0
146.9 ± 7.1
159.1 ± 8.2
Probing depth (mm) in > 30% of sites
Attachment loss (mm) in >30% of sites
Chronic periodontal disease (CP)
For comparing bacterial community composition between participants with a healthy periodontium and CP patients, DNA isolated from plaque was subjected to PCR amplification using primers covering an approximate 200-bp segment of the V3 region of the 16S rRNA gene. DNA sequencing yielded approximately 5.8 million sequences, with a minimum of 27,187 sequences per sample (average of 57,441 ± 23,336) and between-sample analyses rarefied all sample data to 27,187 sequences. After quality filtering and PANDAseq assembly (minimum overlap of 60 nucleotides), approximately 4.1 million sequences remained. These sequences were collapsed into operational taxonomic units (OTUs) based on a pairwise sequence identity cutoff of 97%. Of the total sequences, 49,327 formed singletons and 6,160 OTUs did not classify to the phylum level (representing 66,466 sequences, approximately 0.02% of the usable sequences). OTUs were classified to a total of 19 phyla, 114 genera, and 302 species.
Advanced periodontal disease is not correlated with changes in α-diversity
Tongue harbors a unique consortium, and periodontal destruction is associated with a weakly distinct shift relative to health
Further investigation was carried out to determine whether or not there are distinct bacterial compositions in SupG, SubG, and tongue sites depending on the health status of the periodontium. For each site, a PCoA ordination and MRPP analysis, based on Bray-Curtis distances, was performed. The PCoA ordination did not reveal strong grouping of health and disease on the primary axes (Figure 3). In addition, no clear separation of health and disease samples was seen in the UniFrac-based PCoA plots (see Additional file 2). MRPP analysis of the distance matrix suggested very weak differences between health and disease samples for the combined, SubG, and tongue sites (P < 0.05; full MRPP results available in Additional file 3), although not for the SupG site.
Relative abundance of distinct taxa is affected by periodontal destruction in oral plaque communities
Closer examination of CP-associated abundance profiles at a higher taxonomic resolution revealed many highly abundant genera in the SubG to be significantly increased in health, including Corynebacterium, Capnocytophaga, Campylobacter, Neisseria, and Kingella (shown in Additional file 4, panel A). On the other hand, the tongue harbored many highly abundant disease-associated genera such as Treponema, Synergistes, and Clostridiales (shown in Additional file 4, panel C). Examining results at the species level highlighted classic periodontal disease-associated OTUs in each of the three sites. These included T. forsythia, Filifactor alocis, and Porphyromonas endodontalis (see Additional file 5). In particular, F. alocis was found in all three sites in high abundance and significantly higher proportions in disease. Health-associated taxa included unclassified Fusobacteria and Corynebacterium matruchotii in the SubG site, Granulicatella adiacens and Selenomonas artemidis in SupG, and S. artemidis and unclassified Porphyromonas in tongue samples (significantly elevated species listed in Additional file 6).
Periodontal destruction and periodontal health are associated with indicator organisms
Quantitative PCR confirms periodontal disease indicators
There were no significant alterations in bacterial 16S rRNA gene copy numbers (per ng of DNA) in healthy versus diseased plaque (Figure 7). Using species-specific primers, qPCR was used to determine the relative abundance of three species (that is, P. gingivalis, F. alocis, and T. forsythia) in SubG, SupG, and tongue sites using healthy and diseased plaque. Of these species, P. gingivalis and T. forsythia were validated as the most significantly abundant taxa in the CP group (Figure 7), in agreement with the sequence data. In particular, levels of P. gingivalis were elevated in all three sites affected by CP, suggesting that SupG and tongue are as effective as SubG sampling sites for quantification of P. gingivalis (Figure 7). The relative number of T. forsythia was significantly elevated in diseased samples in SupG and SubG sites, but not in the tongue. The relative abundance of F. alocis was elevated significantly in SupG diseased samples, relative to controls. Although its abundance was markedly increased in diseased SubG samples, this result could not be validated on the basis of statistical analyses performed in this study. Some disagreement between the high-throughput sequencing and qPCR was seen. The sequencing results showed a significant increase in F. alocis in the disease state in all three sites, but the qPCR results suggested an increase in F. alocis in the healthy samples of the tongue site (qPCR data shown in Figure 7, Additional file 5 visualizes the differences between species, and Additional file 6 lists species with significantly different abundances and relevant statistics). An increase in P. gingivalis was indicated in all three sites by the qPCR method, but this increase could not be validated with statistical analyses of the sequence data. A significant increase in T. forsythia was reported in the SubG and SupG sites by qPCR, but sequencing results identified an increase in this organism in the SubG and tongue sites.
In this study, microbial communities associated with CP and periodontal health were characterized by examining plaque bacteria from SupG, SubG, and tongue sites, providing a comprehensive cross-sectional description of microbiota in the presence of CP and periodontal health. Findings reported here show that most OTUs are shared between periodontal health and disease. Nonetheless, a relatively small proportion of OTUs were distinct to disease and included T. denticola, T. forsythia, P. endodontalis, Synergistes OT 362, and Synergistes OT 363. Because these disease indicators were present in high abundance in tongue plaque of individuals suffering from CP, we propose that tongue plaque may be used as an easily accessible, non-invasive source to collect plaque to quantify bacterial biomarkers to monitor treatment outcomes against CP over time. In developing such methodologies, it will be useful to evaluate the ratio of selected periodontal disease-associated taxa to health-associated taxa and with larger numbers of human participants for validation. It will also be critically important to differentiate between active and inactive periodontal disease because the microbial communities under these two conditions can vary.
High-throughput sequencing studies conducted to date have examined plaque derived from SubG and SupG sites to differentiate between healthy and periodontal disease consortia [25, 27, 30]. SubG samples can be more difficult to obtain as compared to samples taken from SupG or tongue sites. Collecting plaque from SubG locations generally requires that dentally trained investigators do most of the sampling. However, if sampling of oral microbes associated with periodontitis were to be done on a larger basis and for large population samples (for example, investigations that seek to correlate periodontitis with non-oral diseases), it would be most advantageous to develop a simpler approach to microbial sampling. Here, we investigated the use of SupG and tongue samples as potential surrogate sites for bacterial biomarker detection under health and CP. The keratinized mucosal surface present in the tongue dorsum is a distinct colonization surface relative to that of tooth structures, which are comprised of highly mineralized tissues such as enamel and cementum. Tooth surfaces are colonized by different consortia depending on the distinct anatomical site and gingival surfaces [31, 32]. Not surprisingly, in our ordination plots using SupG, SubG, and tongue plaque, tongue samples clearly separated from tooth plaque samples (Figures 2 and 3A). This separation indicated that bacterial communities present in tongue sites were distinct from those found in SupG and SubG sites. Previously, Griffen and colleagues reported clustering based on disease, although only SubG plaque was sampled in their study . Similar clustering was not seen in our PCoA ordinations (Figure 3). Similar to the weak separation found in our findings, a recent metagenomic and metatranscriptomic study of SubG and SupG plaque failed to find a strong separation between health and CP . The shift from health to disease may be due to a subtle ecological shift and as a result will not appear in the primary axes of the ordination plots. An MRPP analysis, which calculates group separation based on higher dimensional data, would be able to identify a more subtle separation by utilizing all dimensions of the data. MRPP revealed small but significant differences in the community composition between health and diseased states in the combined, SubG, and tongue sites (P < 0.05; full MRPP statistics available in Additional file 3).
Previous work demonstrated that certain bacterial complexes associate with each other and potential periodontal diseases . DNA-DNA hybridization was used to monitor 40 bacterial species using 13,261 plaque samples from 185 healthy or periodontal disease patients. By examining pre- and post-therapy bacterial profiles, species prevalence, community ordination, and association with 0 to 3 mm, 4 to 6 mm, and >6 mm probing depths, disease-associated bacteria included P. gingivalis, T. forsythia, and T. denticola, which were highly prevalent in deeper sites that bled upon probing . Prior to this, it was reported that that the probability of finding oral treponemes at sites that harbored P. gingivalis was escalated as periodontal destruction was increased . Others demonstrated that species present in disease were also present in the healthy state, albeit in lower proportions , while another group demonstrated that SupG sites harbored the same species as SubG sites below the gingival margin, again in smaller proportions . The latter study postulated that this may be conducive to re-infection and individuals with ‘healthy’ sites with abundant disease-indicator organisms may be at higher risk for disease progression. As a result, it may not be unexpected that the Bray-Curtis and UniFrac distance ordinations did not show consistent group separation. Furthermore, additional statistical tests of the datasets may be more informative than ordinations for identifying disease-associated taxa.
In addition to classic periodontitis-associated pathogens mentioned above, we and others detected F. alocis in patients with increased periodontal destruction (Figure 6) [37–39]. In this study, F. alocis was detected in significantly higher abundances in disease in all three sites (differences between health and disease are visualized in Additional file 5, and statistics are available in Additional file 6). F. alocis is a rod-shaped Gram-positive facultative anaerobe that possesses trypsin proteases, invades human cells, resists oxidative stress, and forms biofilms, which are properties conducive to disease initiation and progression [38, 40, 41]. In particular, the prevalence of F. alocis was elevated in patients suffering from generalized aggressive periodontitis and CP, whereas it was rarely detected in the control group resistant to periodontitis . Although this pathogen was shown to colonize apical parts of the pocket in close proximity to the soft tissues, it was also shown to contribute to the structural integrity of these multispecies biofilms. Hence, F. alocis was suggested to be a good diagnostic marker organism for periodontal disease . Based on previous investigations, as well as the data shown here, here, we propose that F. alocis be included as a novel member in Socransky’s ‘Red complex’ of periodontal pathogens .
Comparisons within sites using the qPCR assay demonstrated an increase in bacterial abundance only in the tongue samples derived from patients with CP (Figure 7).The total bacterial abundance was not significantly altered when SubG and SupG sites were compared. This result is in contrast to recent studies that indicated a marked increase in the total bacterial abundance in SubG sites of subjects affected by periodontal disease [36, 42]. Our qPCR analysis, as well as those conducted by others, does not account for the total bacterial biomass of plaque samples. As in other studies, the total bacterial load between health and disease states were calculated by normalizing qPCR results with the total nanogram of genomic DNA in each sample. Hence, it is not possible to make inferences about the total bacterial load between health and disease samples (that is, per mg plaque dry weight) using the methods employed in this study. Further, although qPCR was useful for validating our Illumina-based indicator species and results generally agreed, observed trends could not always be statistically validated by both methods. In the case of F. alocis in the tongue site, the two methods disagreed. Importantly, differences between the qPCR assay and the high-throughput sequence data methods may have been the cause of discrepancies. The qPCR assay depends on primers that may not be entirely specific to the intended organism. The high-throughput sequence data, on the other hand, is affected by the reference dataset used to classify the sequences. Misclassifications or OTUs not having the required taxonomic resolution would cause discrepancies when compared with qPCR data.
Marked differences in α-diversity between health and disease consortia were not detected (Figure 1). These results are not in agreement with findings reported in two recent high-throughput sequencing studies that reported significant elevations in community α-diversity under health and advanced periodontal disease [25, 27]. It is likely that discrepancies in the sampling technique (i.e., curette versus paper-point methods), sampling location, and/or methods of DNA extraction can explain differences in α-diversity measures between this research and previous studies. Other issues that might have also influenced the conclusions could be related to disease activity in either the study reported here or others. In this regard, even if periodontal pockets are identified, this does not mean a priori that the disease is in an active state. In such cases, it is also possible that the microbial communities found in patients with active versus inactive periodontitis might actually be different from one another. Hence, further and more detailed study is probably needed to consider active versus inactive disease when taking microbiological samples. Indeed, it might even be possible that a particular shift in the microbiome could be used as a predictive marker for the development of active disease or for the presence of inactive disease. For a better understanding of α-diversity differences, future studies should also consider sampling both periodontal pockets and healthy tissue from the same patient, controlling for the between-patient variability observed here.
For the first time, we demonstrate that the tongue dorsum and SupG sites can be used as alternative sampling sites for detection and enumeration of bacterial biomarkers associated with CP. Use of plaque from these sites, as opposed to sampling periodontal pockets has important clinical implications. The tongue is an easily accessible body site and sampling the tongue dorsum for plaque collection is convenient and less invasive. This means that others with an interest in examining, for example, correlations between CP and certain non-oral disease (for example, respiratory disease) could conceivably perform meaningful microbiological analyses even if they have no training in the dental clinical sciences. It is also noteworthy that even within dental research settings, ongoing or post-treatment assessments of the microbial population could be carried out by almost any technologist thus reducing the costs of investigation since dentists or dental hygienists would not necessarily be needed for the procedure. Thus, the spectrum of those studying oral health and general health correlations and interactions could be widened considerably, at least where microbiological parameters are needed. Currently, 27 CP indicator organisms identified in this study are being quantified in periodontal and case-matched control samples via qPCR to identify the strongest disease biomarkers for both SupG and tongue sites.
The findings reported here add to knowledge of oral microbial communities associated with periodontitis. Of classic and novel periodontal pathogens identified to date, the role of F. alocis as a diagnostic marker for CP is noteworthy. Based on results from this study, as well as data presented by others, we propose that F. alocis be included as a novel member in Socransky’s Red complex of periodontal pathogens . Because chronic periodontal destruction was attributed predominantly to proliferation of Gram-negative pathogens, inclusion of F. alocis in the Red cluster also changes this classic perspective.
For this cross-sectional study, 24 patients were recruited through the University of Toronto Graduate Periodontology and Undergraduate Clinics. The study was approved by the University of Toronto Research Ethics Board (REB 23872), and informed consent to participate in the study was obtained from all patients. Eleven healthy and 13 patients with advanced CP (confirmed by clinical and radiographic examinations) consented to participate in this investigation (Table 1). Patients with systemic disease and/or those who had used antibiotics or had undergone a professional dental cleaning within the last six months were excluded from the study. Both SupG and SubG plaque samples were collected from interproximal sites between teeth 16/15 and 15/14 as well as 26/25 and 25/24 using separate metal curettes. After the SupG plaque was collected, the tooth was wiped with sterile gauze and the subgingival environment was accessed through the periodontal pocket. Samples from each site were placed in phosphate-buffered saline (PBS) and then subsequently pooled into SubG and SupG for each patient; samples were not pooled across patients. Plaque from the tongue was collected using a curette by making two midline scrapes of the dorsal surface. Plaque was then frozen at -80°C until DNA analysis could be carried out. All plaque samples used in this study were collected by the same clinician to limit the variability during plaque sampling. DNA was extracted using the BacReady DNA extraction kit utilizing a single enzyme lysis system as recommended by the supplier (GeneScript USA Inc., Piscataway, NJ, USA). Briefly, 1 μL of the plaque mixture was added to 20 μL of the Buffer BR-A (Genscript, NJ), mixed thoroughly by pipetting and incubated for 10 min at room temperature. These reactions containing template DNA from lysed cells were used for PCR as described below. To validate the use of BacReady DNA kit for DNA extraction, we employed a mock bacterial community that comprised equal numbers of cells of five Gram-negative and Gram-positive species that are found in the oral cavity. These included Actinomycetes actinomycetemcomitans, P. gingivalis, T. denticola, T. forsythia, and Streptococcus mutans. Lysis mixtures were used for PCR amplification using species-specific primers (not shown), whereas genomic DNA obtained from pure cultures was used as positive controls. Using agarose gel-electrophoresis, we obtained the expected amplicons for all five species (data not shown) using the BacReady kit for cell lysis, which was used to justify our DNA extraction protocol.
A 16S rRNA gene library of approximately 200-bp V3 16S rRNA genes was generated using modified bacterial 341F and 528R primers . Three PCR amplifications were performed for each sample using 50-μl reaction volumes in order to minimize potential amplification bias . Each reaction mixture contained 25 pmol of each primer, 200 μM of each dNTP, 1.5 nM MgCl2 and 1 U of Phusion Taq polymerase (New England Biolabs, Ipswich, MA, USA), and 10 ng of template DNA. Amplifications were carried out as follows: denaturation at 95°C for 5 min, 20 cycles at 95°C for 1 min, 50°C for 1 min, and 72°C for 1 min, followed by an extension step at 72°C for 7 min. A 2% agarose gel was used to separate products from primers; the correct band was recovered using a QIAquick Gel Extraction Kit as recommended by the manufacturer (Qiagen, Valencia, CA, USA). After measuring sample concentration using a NanoPhotometer (Implen, Denmark), 10 ng/μl aliquots of PCR amplicons were combined prior to paired-end sequencing with individually indexed samples . Sequencing was performed on an Illumina MiSeq (2 × 151 bp using a 300 cycle reagent kit). All sequences were deposited into the European Nucleotide Archive under the project accession number PRJEB6047.
Sequence data were analyzed in four parallel AXIOME (v1.6) analyses (i.e., SubG samples, SupG samples, tongue samples, and all three sites combined). All analyses were conducted using the same configurations. Paired-end reads were assembled using PANDAseq , then assembled sequences were clustered into operational taxonomic units (OTUs) at 97% identity using cd-hit-est (v4.5.4) . Multiple sequence alignment of representative sequences was completed with PyNAST (v1.2) via QIIME (v1.6) and FastTreeMP (v2.1.3), with default parameters, to generate a phylogenetic tree of OTUs to calculate UniFrac distances [47–50]. Classification was completed using RDP (v2.2) via QIIME with a confidence cutoff of 0.8 [48, 51]. Classifications were rank-flexible, meaning each OTU was only classified down to the lowest taxonomic rank that had 80% or greater posterior probability. A merged Greengenes (October 2012 revision) [52, 53] and OSU CORE oral database (9 February 2012 revision)  was used for classification. The final OTU table was generated by QIIME. UniFrac-based principal coordinates analysis (PCoA) which was performed through QIIME. Indicator species analysis , Bray-Curtis PCoA ordinations, and multiresponse permutation procedure (MRPP) analyses , based on nonmetric multidimensional scaling (NMDS) plots using Bray-Curtis distances, were conducted by the AXIOME pipeline . Alpha-diversity plots were generated by Phyloseq (v1.3.14) .
Validation of CP indicator species using quantitative Real-Time PCR (qPCR)
Forty nanograms of DNA from each plaque sample were amplified using qPCR with species-specific primer-pairs for Tanerella forsythia (Tf: 5′-GGATTGACCACCGGCGAAGACA-3′ and 5′-CGGACACGACGGTTACTCAAATGG-3′), P. gingivalis (Pg: 5′-CTTGACTTCAGTGGCGGCAG-3′ and 5′-AGGGAAGACGGTTTTCACCA-3′), and Filifactor alocis (Fa: 5′-TCGGTGCCGAAGTTAACACA-3′ and 5′-GGGTCCCCGTCAATTCCTTT-3′) as well as universal primers (5′-TCCTACGGGAGGCAGCAGT-3′ and 5′-GGACTACCAGGGTATCTAATCCTGTT-3′), to quantify total bacteria. Each reaction was run in duplicate using the Stratagene Mx3000P cycler (Agilent Technologies, Santa Clara, CA, USA), and reciprocal values of the mean normalized Ct values (Ctindicator species/Cttotal bacteria) were obtained. Significant differences between healthy cohorts and those with CP within each of the respective locations in the oral cavity were calculated based on use of the non-parametric Mann-Whitney test with GraphPad Prism 6 Software (La Jolla, CA, USA) and outliers removed using Grubbs’ Outlier Test (extreme studentized deviate).
- CAL :
clinical attachment loss
- CP :
- MRPP :
multiresponse permutation procedure
- NMDS :
non-metric multidimensional scaling
- OT :
- OTU :
operational taxonomic unit
- PCoA :
principal coordinates analysis
- qPCR :
quantitative polymerase chain reaction
- SubG :
- SupG :
We acknowledge funding from CIHR-IMHA OMH-134133 for DBS, as well as the Dental Research Institute (University of Toronto) to DBS, DGC, and HT. MWH, MDJL, and JDN were supported by an Early Researcher Award (Government of Ontario) and the Canadian Institutes of Health Research (CIHR).
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