- Research article
- Open Access
Periodontal bacterial colonization in synovial tissues exacerbates collagen-induced arthritis in B10.RIII mice
© The Author(s). 2016
- Received: 11 May 2016
- Accepted: 21 June 2016
- Published: 12 July 2016
It has been previously hypothesized that oral microbes may be an etiological link between rheumatoid arthritis (RA) and periodontal disease. However, the mechanistic basis of this association is incompletely understood. Here, we investigated the role of periodontal bacteria in induction of joint inflammation in collagen-induced arthritis (CIA) in B10.RIII mice.
CIA-prone B10.RIII mice were infected orally with a polybacterial mixture of Porphyromonas gingivalis, Treponema denticola, and Tannerella forsythia for 24 weeks before induction of CIA. The ability of polybacterial mixture to colonize the periodontium and induce systemic response, horizontal alveolar bone resorption in infected B10.RIII mice was investigated. Arthritis incidence, severity of joint inflammation, pannus formation, skeletal damage, hematogenous dissemination of the infection, matrix metalloproteinase 3 (MMP3) levels, and interleukin-17 expression levels were evaluated.
B10.RIII mice had gingival colonization with all three bacteria, higher levels of anti-bacterial immunoglobulin G (IgG) and immunoglobulin M (IgM) antibodies, significant alveolar bone resorption, and hematogenous dissemination of P. gingivalis to synovial joints. Infected B10.RIII mice had more severe arthritis, and higher serum matrix metalloproteinase 3 levels and activity. Histopathological analysis showed increased inflammatory cell infiltration, destruction of articular cartilage, erosions, and pannus formation. Additionally, involved joints showed had expression levels of interleukin-17.
These findings demonstrate that physical presence of periodontal bacteria in synovial joints of B10.RIII mice with collagen-induced arthritis is associated with arthritis exacerbation, and support the hypothesis that oral bacteria, specifically P. gingivalis, play a significant role in augmenting autoimmune arthritis due to their intravascular dissemination to the joints.
- Rheumatoid arthritis
- Periodontal disease
- Periodontal bacteria
- Porphyromonas gingivalis
- B10.RIII mice
- Collagen-induced arthritis
Rheumatoid arthritis (RA) and periodontal disease (PD) are epidemiologically associated with each other [1–3], but the mechanistic basis of this association is unclear. It is known, however, that the pathogeneses of both conditions involve TNFα, T helper (Th)17 cells, and osteoclast-mediated bone damage [4, 5]. Similar to RA, the susceptibility to PD and its severity depend on overlapping environmental and genetic factors, as both RA and PD have been shown to be associated with the human leukocyte antigen (HLA) shared epitope [6–8] and cigarette smoking has been shown to increase disease risk in both conditions .
It has long been hypothesized that oral microbes may be an etiological link between PD and RA in humans [10, 11]. For example, in Native American patients with RA and their relatives, antibodies to the periodontal bacteria Porphyromonas gingivalis (P. gingivalis) were found to be associated with anti-citrullinated protein antibodies, suggesting that P. gingivalis may be breaking the immune tolerance towards citrullinated antigens . However, there is no direct causative evidence to support this or other proposed mechanisms for the long-observed association between human RA and PD.
It is worth noting that heat-killed P. gingivalis have been previously proposed as a “priming” inflammatory agent linking experimental PD and arthritis in a rat model . That study demonstrated that the presence of extra-synovial chronic inflammatory lesions, induced by heat-killed P. gingivalis, promoted the induction and severity of experimental arthritis. Further, the same group  tried to assess the influence of preexisting PD on induction and severity of collagen antibody-induced arthritis (CIA) in mice. Using pristine-induced arthritis (PIA) Trombone et al.  described the clinical association between RA and PD in the acute inflammatory reactivity maximum (AIRmax) mice. More recently, Marchesan and associates have demonstrated strain-specific immune system divergence following infection with different strains of P. gingivalis . Moreover, P. gingivalis orally-infected DBA/1 mice with CIA had more severe arthritis associated with activation of Th17-related pathways , suggesting that this T cell subset may directly contribute to the observed association between arthritis and PD. However, given the generalized nature of the Th17 activation, the mechanistic basis of the predilection of P. gingivalis-infected mice to trigger a tissue-specific inflammatory process in the joints is still unclear.
To better elucidate the mechanistic basis of the association between RA and PD, here we have taken a different experimental approach by focusing on CIA in B10.RIII mice, which are genetically susceptible to collagen type II (CII)-induced arthritis. As periodontal disease always results from the dysbiotic interaction between the oral microbiota and host immunity we have chosen the most representative microorganisms that have been established as periodontal pathogens. We induced periodontal disease in these B10.RIII mice by chronic gingival infection with a combination of P. gingivalis, T. denticola and T. forsythia for 24 weeks [17, 18]. Our data demonstrate that mice chronically infected with these PD-causing bacteria experienced aggravated clinical signs of CIA with increased metalloproteinase activity, intense immune-based inflammatory cellular infiltration, and enhanced destruction of articular cartilage and bone. Importantly, a fluorescence in situ hybridization technique revealed dissemination of the periodontal bacteria to the synovial tissues.
These findings substantiate a previously unappreciated mechanism of cause-effect relationship between periodontal infection and arthritis, and support the hypothesis that PD-causing bacteria, specifically P. gingivalis, may contribute to the susceptibility and severity of inflammatory arthritis due to their tropism to synovial tissues, where they may contribute to intensifying the inflammatory process.
Microbial strains and inocula
P. gingivalis FDC 381, T. denticola ATCC 35404, and T. forsythia ATCC 43037 were used in this study and were routinely cultured anaerobically at 37 °C as described previously [17–19]. Bacterial inocula were prepared and used for gingival infection of mice by oral lavage as described previously [17, 18, 20, 21].
Mouse infection and oral plaque sampling
Distribution of B10.RIII mice groups, polybacterial infection and collagen administration in the induction of collagen-induced arthritis
Bacterial infection (24 weeks)
Collagen-induced arthritis (25–28 weeks)
Number of mice
CII + CFA primary
CII + IFA booster
CII + CFA primary
CII + IFA booster
Induction and clinical evaluation of collagen-induced arthritis
For induction of CIA, pre-dissolved liquid bovine type II collagen (bCII; 2 mg/ml, Chondrex LLC, Redmond, WA, USA) was emulsified with an equal volume of CFA or IFA (Chondrex LLC). After 24 weeks of infection, mice were immunized intradermally at the base of the tail with 0.1 ml of emulsion containing 100 μg of CII and CFA. Three weeks after priming (day 21), the mice were boosted with 0.1 ml of bovine CII (100 μg) emulsified in an equal volume of IFA. All mice were monitored three times a week by the same person blinded to the groups and arthritis severity was assessed using criteria as follows: 0 = no swelling or redness (normal); 1 = mild erythema or swelling of the wrist or ankle or erythema and swelling of one digit; 2 = moderate erythema and swelling of the wrist or ankle or more than three inflamed digits; 3 = severe erythema and swelling of the wrist or ankle; and 4 = complete erythema and swelling of the wrist and ankle including all digits [22–24]. A paw was considered arthritic when the individual paw score was >1 and severe arthritis was defined as an arthritis score >3 for the purpose of comparing data between groups.
Detection of P. gingivalis, T. denticola, and T. forsythia genomic DNA in oral plaque
Colony PCR was performed with gingival plaque samples obtained after every infection in a Bio-Rad thermal cycler using 16S rRNA gene species-specific oligonucleotide primers. P. gingivalis: 5′-TGTAGATGACTGATGGTGAAAACC-3′ (forward), 5′-ACGTCATCCCCACCTTCCTC-3′ (reverse); T. denticola 5′-TAATACCGAATGTGCTCATTTACAT-3′ (forward), 5′-CTGCCATATCTCTATGTCATTGCTCTT-3′ (reverse); and T. forsythia 5′-AAAACAGGGGTTCCGCATGG-3′ (forward), 5′-TTCACCGCGGACTTAACAGC-3′ (reverse). Genomic DNA extracted from these three strains served as positive controls and PCR performed with no template DNA served as negative control. PCR was performed following the conditions described previously , PCR products were separated by 1.5 % agarose gel electrophoresis and the bands were visualized using the UVP BioDoc-It Imaging System (UVP, Upland, CA, USA).
Pathogen-specific immune response in mice
Sera from infected and control B10.RIII mice were used to determine immunoglobulin G (IgG) and IgM antibody concentrations against whole cells (formalin-killed) of P. gingivalis, T. denticola, and T. forsythia by ELISA [18, 20].
Morphometric analysis of alveolar bone resorption
Detection of bacterial genomic DNA in internal organs
Heart, aorta, liver, pancreas, spleen, kidney, lung and joints/synovial tissues were harvested after euthanasia of infected/sham-infected mice. Tissues were transferred to the laboratory in vials containing reduced transport fluid and were stored at –80 °C until further use. Later they were thawed, homogenized using a mechanical tissue disruptor (TissueRuptor®, QIAGEN, Valencia, CA, USA) and genomic DNA extracted using QIAGEN DNeasy blood and tissue kit (QIAGEN) per the protocol described in the kit. Subsequently PCR was performed using 16S rRNA primers specific for each of the infection bacteria as described previously .
Detection of bacteria by fluorescence in situ hybridization (FISH)
FISH was performed on formalin-fixed paraffin-embedded ankle tissue sections using oligonucleotide probes labeled with Alexa Fluor 568 (Invitrogen, Carlsbad, CA, USA) that are specific for 16S rRNA of P. gingivalis, (5′-CAATACTCGTATCGCCCGTTATTC-3′), ’T. denticola 5′- CATGACTACCGTCATCAAAGAAGC-3′), or T. forsythia (5′-CGTATCTCATTTTATTCCCCTGTA-3′) [24–26] 16S rRNA. The protocol was performed as previously described .
In vivo molecular imaging/tomography of mice
An intravenous injection of fluorescent imaging agent (MMP Sense 750 FAST, PerkinElmer, Waltham, MA, USA) specific for MMP3 was given at a recommended dose of 2 nmol/100 μl per mouse (as per the manufacturer’s instruction) to measure the progression of arthritis . MMP Sense FAST is an activatable fluorescent imaging compound that is optically silent upon injection but produces fluorescent signal after cleavage by disease-related MMPs. The signals emitted were detected using the IVIS system (Caliper Life Sciences, MA, USA) which is an optimized set of high-efficiency filters and spectral un-mixing algorithms to measure the light emission across the blue to near infrared wavelength region.
Hind limbs together with the overlying skin from mice were excised at the termination of the experiment, and fixed in 10 % neutral buffered formalin. Later they were decalcified in 10 % ethylenediaminetetraacetic acid (EDTA) and embedded in paraffin. Serial sections (5 μm) were made and stained with hematoxylin/eosin and evaluated for synovial inflammation, pannus formation, and bone erosion . Histopathological analysis was conducted by a pathologist who was blinded to the experimental study groups. Pannus formation was quantified based on a scoring criterion as follows: a score of 0 was given to no pannus formation; 1 for minimal formation; and 2 for definitive formation. Skeletal damage was quantified as 0 for none; 1 for one or two foci seen; 2 for multiple areas seen; and 3 for extensive damage among all surface areas. Synovial inflammation was scored based on scoring criteria  as follows, 0: no hyperplasia or inflammation; 1: slight hyperplasia with scattered acute inflammation; 2: multiple foci of inflammation predominantly with neutrophils; and 3: strong inflammation with inflammatory cell infiltration.
Matrix metalloproteinase 3 levels in serum from infected mice
Serum from B10.RIII mice (four groups; n = 6) was used to detect levels of MMP3 using the commercial serum MMP3 ELISA kit (Sigma-Aldrich Co, USA).
Tissues were fixed in 10 % buffered formalin, decalcified, embedded in paraffin wax and cut to 5 μm thickness, mounted on slides and air-dried at room temperature. Sections were deparaffinized, rehydrated and incubated with 3 % hydrogen peroxide in methanol for 15 minutes at room temperature to eliminate endogenous peroxidase activity. Antigen retrieval was carried out at 95 °C for 30 minutes by placing the slides in 0.01 M sodium citrate buffer (pH 6.0). The slides were then incubated with a primary rabbit polyclonal antibody for IL-17 (Abcam #ab79056) at 4 °C overnight. For immune detection, the avidin-biotin complex method was performed according to the manufacturer’s instructions. Color development was achieved with 3, 3′-diaminobenzidine, which renders positive cells brown. Photographs were taken using an Olymbus BX-60 upright microscope (Center for live-cell imaging, UM-Michigan, USA).
For immunofluorescence quantification, slides were stained with a primary rabbit polyclonal antibody for IL-17 as above, followed by secondary donkey anti-rabbit IgG antibody conjugated to Alexa Fluor® 594 (Abcam #ab150076) and stored at 4 °C until use. 4′ 6-diamidino-2-phenylindole (DAPI) was used for nuclei staining. Quantification was done by a Biotek Cytation 5 instrument, using the Gen5Image + software (Biotek), which allows for calculation of the percentage of nucleated (DAPI-positive) cells with cytoplasmic IL-17.
Group measures are expressed as mean plus SEM. Statistical analyses were performed using the two-tailed Student’s t test with GraphPad Prism 5 (GraphPad, San Diego, CA, USA), and P < 0.05 was considered statistically significant (*P < 0.05; **P < 0.01; ***P < 0.001). For multiple-group comparisons, one-way analysis of variance (P < 0.05) with Bonferroni’s multiple-comparison was performed posttest.
Gingival colonization and antibody response to periodontal-disease-associated polybacteria in mice
Gingival plaque samples positive for bacterial gDNA identified by PCR
Positive gingival plaque samples (n = 10)
Pg/Td/Tf + collagen
Periodontal-disease-associated bacteria increase periodontal disease and severity of collagen-induced arthritis
The impact of these three bacteria on PD disease severity was investigated next. To this end we determined alveolar bone resorption, the hallmark characteristic of PD, using a morphometric approach. Among the B10.RIII mice the polybacterial-infected mice had a significantly larger (P < 0.01) mandibular horizontal ABR area when compared to sham-infected mice (Fig. 1c (i) and (ii)).
There were robust differences in the polybacteria-infected mice with CIA compared to mice with CIA but without such bacterial infection, in terms of day of arthritis onset, disease incidence, and joint swelling (Fig. 2a (i) and (ii)). In vivo tomography demonstrated the rapid progression of arthritis in polybacterial-infected mice with CIA compared to uninfected mice with CIA (Fig. 2b). There were no signs of arthritis development in polybacterial-infected non-CII immunized mice or in sham-infected mice. While we observed the progression of arthritis with the emission of fluorescence signals specific for arthritis in both the polybacterial-infected plus CII-immunized mice and mice that were CII-immunized only, the degree of intensity and severity was five times greater (measured by emission of radiance) in polybacterial-infected plus CII-immunized mice than in the CII-immunized mice (Fig. 2b). Evaluation of mice for progression of severe arthritis by in vivo tomography correlated with the observed clinical signs of arthritis in polybacterial-infected plus CII-immunized mice (Fig. 2b).
Effects of polybacterial infection on arthritis biomarkers
We determined the levels of MMP3, an enzyme capable of degrading cartilage and connective tissue in joint tissues in the sera, by ELISA. A significant (P < 0.05) elevation in serum MMP3 levels was detected in mice with polybacterial infection with or without CIA compared to sham-infected controls and mice with CIA but without polymicrobial infection (Fig. 2c). In addition, polybacterial-infected mice with CIA had higher MMP3 levels than mice with polybacterial infection without CIA.
Impact of coincidental periodontal disease and collagen type II immunization on the histopathology of arthritis
Expression of IL-17 in paw tissue
Identification of oral bacteria in remote tissues
PCR detection of P. gingivalis, T. denticola and T. forsythia genomic DNA in infected B10.RIII mice tissues
Positive systemic tissue samples
n = 10
n = 10
n = 5
n = 10
n = 10
n = 10
Pg/Td/Tf + collagen
It has long been observed that patients with PD are at a higher risk of developing RA [3, 33], and patients with RA have increased likelihood of suffering from PD [34, 35]. However, the mechanistic basis of this association remains unclear. PD is triggered by bacterial gingival infection. Therefore, the realization that PD and RA share similar risk factors and pathological pathways, and the fact that effective PD treatment is associated with reduced severity of RA , prompted us to investigate the role of bacteria as a potential link between the two diseases. In contrast to other in vivo models of PD-associated arthritis, which are induced by infection with a single bacterial species, we studied the effect of polymicrobial dysbiotic bacterial interactions, involving a synergistic polybacterial infection. Our data show that this infection protocol required a shorter PD induction period and resulted in conclusive evidence of aggravation of CIA in B10.RIII mice. The protocol used here, involving chronic recurrent gingival infection with major periodontal bacteria, was highly efficient in adherence and colonization of infected mice with all three periodontal pathogens. This enhanced colonization was associated with a strong humoral immune response with production of IgG and IgM antibodies against the periodontal pathogens. Further, we observed significant alveolar bone resorption in polybacterial-infected mice, with or without concomitant CIA. Thus, the polybacterial colonization protocol described here produced synergistic induction of PD in B10.RIII mice.
Importantly, induction of PD by polybacterial infection facilitated CIA, as evidenced by earlier arthritis onset and a more severe arthritic process, including increased inflammatory cell infiltration and pannus formation. In addition, in vivo tomographic analysis using an MMP3 probe corroborated the induction of inflammation and enhanced severity of CIA in mice infected with polybacterial inocula compared to uninfected mice with CIA. Interestingly, the in vivo imaging data were corroborated by correspondingly increased MMP3 serum levels, consistent with our observation that polybacterial-infected mice with CIA developed more severe clinical arthritis.
Cytokines play a crucial role in the pathophysiology of RA as pro-inflammatory cytokines such as TNFα, IL-1, and IL-17 stimulate inflammation and degradation of bone and cartilage. Th17 lymphocytes and IL-17 have been recognized as essential mediators of cartilage and bone destruction. The number of Th17 cells is increased in the early stages of the disease and in active RA [37–39]. The mechanisms behind the factors promoting the Th17 differentiation in RA are poorly understood. With the significant role of pathogen-mediated TLR activation in shaping the T cell response, we reasoned that the interaction between PD and RA may in part be a direct result of skewing the Th17 cell balance. The aim of the current study was to investigate the influence of periodontitis on clinical severity and specific histopathologic features of T cell-dependent experimental arthritis. IL-17, in turn, is critical in stimulating the release of TNF-α and chemokines by joint tissues in arthritis .
Our IHC and immunofluorescence data supports the increased expression of IL-17 after infection with polymicrobial periodontal microflora followed by collagen administration. These observations support the hypothesis that IL-17 induces receptor activator of NF-kB ligand (RANKL) expression that is vital for osteoclastogenesis and bone resorption. The observations in the current study further authenticate the notion postulated by previous groups about the promotion of inflammation and the catabolic effects of IL-17 on cartilage and bone leading to the propagation of arthritis.
Finally, the identification of P. gingivalis in joint tissues of mice with CIA challenged with polybacterial inocula suggests that target-tissue-disseminated bacteria may contribute to the local inflammatory process, thereby augmenting the severity of arthritis in these mice. As the degree of severity, incidence, and levels of inflammatory biomarkers were all increased in polybacterial-infected mice with CIA, it is tempting to speculate that these target-tissue-seeded bacteria may be at least partly responsible for the observed association between PD and arthritis. Tissue dissemination of oral pathogens has been implicated in atherosclerotic vascular disease , another PD-associated condition. In that condition, it has been proposed that periodontal bacteria invade the bloodstream after various manipulations such as dental procedures or tooth brushing. According to this proposed mechanism, such bacteria are deposited in the atheromatous plaque and contribute to disease pathogenesis. It is worth noting, however, that recovery of viable bacteria from atheroma tissue cultures has been difficult, suggesting that active plaque infection by live bacteria is unlikely to be the causative mechanism. Instead, bacterial antigen-triggered stimulation of biochemical pathways or the immune system seems a more likely explanation.
Analogous to atherosclerotic vascular disease, in RA it has long been speculated that the disease may be triggered by indolent joint tissue infection. These hypotheses have been largely refuted based on the failure to consistently recover viable microorganisms from synovial tissues; however the possibility that non-viable microbial antigens might contribute to the inflammatory process in arthritis has remained a plausible hypothesis [41, 42]. For example, based on close similarities between their respective signaling pathways, we have previously proposed that the known arthritogenic effect of the bacterial antigen muramyl dipeptide (MDP) might be due to its ability to functionally mimic the shared epitope ligand . We have pointed out that MDP, a building block of the bacterial cell wall and a potent immune adjuvant, displays many functional similarities to the SE ligand, including production of IL-6, TNFα, nitric oxide, reactive oxygen species, activation of osteoclasts, Th17 polarization and, importantly, facilitation of inflammatory arthritis in rodents [6, 43–46]. Obviously, the definitive molecular mechanism by which synovial tissue-seeded P. gingivalis contribute to the severity of arthritis needs to be examined experimentally.
In summary, the findings reported herein suggest that oral bacteria play a significant role in augmenting autoimmune arthritis. Our observations support the two-hit model  whereby periodontopathic subgingival bacteria provide the first hit on the host immune system, leading to periodontal disease, while a second hit generated as a result of chronic inflammatory conditions in the host will eventually produce irreversible tissue damage leading to arthritis in the human host. As this model simulates the natural course of infection of oral pathogens with the naturally occurring periodontal disease in humans, it provides relevant insights into the pathogenesis of RA and could conceivably open the door to identification of new therapeutic strategies.
ABR, alveolar bone resorption; CII, collagen type II; CFA, complete Freund’s adjuvant; CIA, collagen-induced arthritis; CMC, carboxymethylcellulose; DAPI, 4′ 6-diamidino-2-phenylindole; ELISA, enzyme linked immunosorbent assay; FISH, fluorescence in situ hybridization; H&E, hematoxylin and eosin; IFA, incomplete Freund’s adjuvant; IgG, immunoglobulin G; IgM, immunoglobulin M; IHC, immunohistochemistry; IL17, interleukin-17; MDP, muramyl dipeptide; MMP3, matrix metalloproteinase 3; PCR, polymerase chain reaction; PD, periodontal disease; Pg, P. gingivalis; RA, rheumatoid arthritis; RANKL, receptor activator of NF-kB ligand; SEM, standard error of the mean; Td, T. denticola; Tf, T. forsythia; Th, T helper; TNF-α, tumor necrosis factor-alpha
Dr. Kesavalu was supported by University of Florida, Opportunity Research Fund 00095060 and R01 DE020820 from the National Institute of Health/National Institute of Dental and Craniofacial Research (NIH/NIDCR). Dr. Holoshitz was supported by R21 DE023845 from NIH/NIDCR, and R01 AR059085 from the National Institute of Health/National Institute of Arthritis Musculoskeletal and Skin Diseases (NIH/NIAMS). The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.
SC, IB, MS, EKLC, JH, and LK were involved in drafting the article, or revising it critically (LK, SC, JH) for important intellectual content. All authors approved the final version to be published. Dr. LK had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. Study conception and design: LK, SC, MS, and EKLC. Acquisition of data: SC, Rivera-Kweh, Gehlot, Velsko, IB, Calise, MS, EKLC, and LK. Analysis and interpretation of data: SC, Rivera-Kweh, Gehlot, Velsko, IB, MS, EKLC, JH, and LK.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
All mouse procedures were performed in accordance with the guidelines and the protocol (# 5673) approved by the Institutional Animal Care and Use Committee (IACUC) of the University of Florida. The University of Florida has an assurance with the Office of Laboratory Animal Welfare (OLAW) and adheres to U.S. Public Health Services (PHS) policy, the Animal Welfare Act and Animal Welfare Regulations, and the Guide for the Care and Use of Laboratory Animals. The University of Florida is accredited by the AAALAC (Association for Assessment and Accreditation of Laboratory Animal Care).
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