Neutrophils exhibit an individual response to different oral bacterial biofilms.

Oral innate immunity is led by neutrophils. It is still unclear how their main antimicrobial mechanisms against different biofilms may contribute to balance or dysregulation in the oral cavity. We investigated the capacity of commensal (Streptococcus oralis) and pathogenic (Porphyromonas gingivalis or Aggregatibacter actinomycetemcomitans) monospecies biofilms to induce or to inhibit selected antimicrobial mechanisms of neutrophils. S. oralis induced neutrophil extracellular traps (NETs) formation, reactive oxygen species (ROS) production, and matrix metalloproteinases (MMPs) 8 and 9 secretion. However, these responses were partially reduced in PMA-activated neutrophils indicating a balance-like neutrophil response, which might be important for the maintenance of oral health. P. gingivalis generally induced ROS. Reduced NET formation and significantly decreased MMP secretion were detectable in activated neutrophils highlighting P. gingivalis' nucleolytic and proteolytic activity, which might support bacterial colonization and pathogenesis of periodontitis. In contrast, A. actinomycetemcomitans did not affect the levels of antimicrobial factors in activated neutrophils and induced NET formation, ROS production, and secretion of MMP-8 and -9 in neutrophils alone, which might contribute to tissue destruction and disease progression. In summary, neutrophil responses to biofilms were species-specific and might support either maintenance of oral health or pathogenesis of periodontitis depending on the species.

Introduction

The oral microbiome consists of several hundred different bacterial species [1-4]. These are able to form three-dimensional structures with an extracellular polymeric matrix, known as ‘biofilms’ [3-6]. Bacteria within biofilms change their gene expression compared to the planktonic state and are more resistant to antimicrobial agents as well as to the host’s protective immune response [5,7-9]. The oral health-associated multispecies biofilm consists mostly of Streptococcus spp. and Actinomyces spp., where Streptococcus oralis dominate the early formation stage [10-12]. A shift in the composition of the biofilm with higher proportion of pathogenic bacteria (i.e. Porphyromonas ginigivalis, Aggregatibacter actinomycetemcomitans) can lead to periodontitis, which has a high prevalence and is a chronic multifactorial inflammatory disease [10,13,14]. Until 2018, periodontitis was divided into an aggressive and a chronic form, among others. Now, both forms are combined under a single category. Periodontitis is defined on the basis of a stage and grade system, while ‘grade’ describes the risk or evidence of the progression rate [14,15]. P. gingivalis and A. actinomycetemcomitans are convincingly implicated in this progression [16] and A. actinomycetemcomitans is often associated with an aggressive and rapid progression rate [17,18].

The main innate immune cell types in the oral cavity are polymorphonuclear neutrophils, which constantly migrate towards a chemotactic gradient of host-derived and microbial chemoattractants through the junctional epithelium – in particular in response to an inflammatory signal. They form a robust antimicrobial barrier, act as the first line of host defense against the oral microbiome, and play an important role in the maintenance of oral health as well as in the pathogenesis of periodontitis [17,19-22].

Neutrophils are the predominant effector cells that respond to periodontal bacteria through a variety of antimicrobial mechanisms, such as phagocytosis, degranulation of antimicrobial proteins, or neutrophil extracellular traps (NETs) formation (NETosis), which are closely associated with the production of reactive oxygen species (ROS) [23-25]. NETs have been found in the gingival crevicular fluid and in purulent exudates from periodontal pockets [26,27]. They are released into the extracellular environment to entrap and immobilize bacteria and thus prevent bacterial spreading and colonization [23,28]. NETs consist of DNA as the core element decorated with a huge array of antibacterial compounds, such as histones, various enzymes – including neutrophil elastase and myeloperoxidase (MPO), as well as antimicrobial peptides [24,28,29]. It has been suggested that exaggerated NETosis and the subsequent release of destructive proteins participates in the local breakdown of connective tissue leading to detrimental effects – including periodontal tissue destruction [28,30]. NETs are more detectable in periodontitis than in oral health [31].

Generation of ROS is a distinct strategy to kill bacteria intracellularly in phagolysosomes or to attack, e.g. biofilms extracellularly [23]. ROS are key components needed to efficiently fight microbes; however, ROS can directly cause tissue damage by lipid peroxidation, DNA and protein damage, and oxidation of enzymes. Although ROS can be neutralized by antioxidants, an imbalance between ROS and antioxidants generated through an excessive oxidative burst leads to ROS-mediated periodontal tissue damage [32].

In addition, neutrophils have different types of granules, which release antibacterial proteins, either into phagolysosomes or into the extracellular space [24]. Matrix metalloproteinase 8 and 9 (MMP-8, MMP-9) are included in the specific or gelatinase granules of neutrophils, respectively [33,34]. They degrade structural components of the extracellular matrix and thus accelerate neutrophil availability at inflammatory sites and also influence several other physiological processes (e.g. antibacterial defense, tissue homeostasis, and remodeling, cell migration and immune cell activation) [35]. On the other hand, their elevated expression leads to tissue destruction [36]. It has been shown that MMP-8 and -9 are the predominant MMPs and the most important enzymes that control the pathogenesis of periodontitis [36,37]. However, it is known that the total absence of MMP-8 results in extensive progression of periodontitis [38] so that it appears that a physiological MMP-level contributes to the resolution of inflammation [35].

Neutrophils play an essential role in the host response to oral biofilm [22,23]. The balance of neutrophil reaction and the constitutive neutrophil apoptosis with removal of these cells are important for maintaining oral health; correspondingly, the imbalance can lead to the development of periodontitis [21,39]. On the one hand, hyperactive neutrophils and the local accumulation of destructive enzymes released by neutrophils, such as MMPs or ROS, can lead to tissue destruction, which contributes to disease progression. On the other hand, neutrophil deficiency and their reduced antimicrobial responses may also contribute to the progression rate of periodontitis [23,40,41]. Neutrophils are able to react specifically to various bacterial species [42]. However, little is known about how the different neutrophil responses to the various bacterial species in the multispecies biofilm might contribute to periodontitis or to the maintenance of oral health. Most of the previous studies used planktonic bacteria or just their lipopolysaccharides (LPSs) as well as other pathogen-associated molecular patterns (PAMPs), which do not represent the common situation in the oral cavity [30,42-48]. Hence, the knowledge about how the main antimicrobial mechanisms, which could be implicated in tissue destruction, are affected in neutrophils by commensal and pathogenic periodontal bacteria that grow as biofilms is important to further understand the role of neutrophils in maintaining oral health or in the pathogenesis of oral diseases [44]. Therefore, on the one hand, the bacterial species-specific NETs formation of neutrophils, their ROS production as well as MMP-8 and -9 secretion in responses to commensal (S. oralis) and pathogenic (P. gingivalis or A. actinomycetemcomitans) monospecies biofilms were investigated. On the other hand, it was determined if the monospecies biofilms were able to inhibit selected antimicrobial mechanism of PMA-stimulated neutrophils.

Materials and methods

Biofilm formation

S. oralis (ATCC®9811, American Type Culture Collection) was cultivated in tryptone soya broth medium supplemented with 10% yeast extract (TSBY) under aerobic conditions at 37°C. For biofilm formation, S. oralis was diluted in TSBY supplemented with 50 mM glucose (TSBYG) to an optical density (OD600 nm) of 0.05, approximately corresponding to 2 × 1010 CFU/mL. P. gingivalis (DSM 20709, German Collection of Microorganism and Cell Cultures) was cultivated in brain heart infusion (BHI) medium supplemented with 10 µg/mL vitamin K under anaerobic conditions (80% N2, 10% H2, 10% CO2) at 37°C. For biofilm formation, P. gingivalis was diluted in fresh BHI supplemented with 10 µg/mL vitamin K to OD600 nm = 0.01, approximately corresponding to 7.38 × 104 CFU/mL. A. actinomycetemcomitans JP2 strain (HK1651, CCUG56173, Culture Collection University of Gothenburg) isolated from aggressive juvenile periodontitis was cultivated in Todd-Hewitt broth supplemented with 10% yeast extract (THBY) at 37°C in a humidified atmosphere with 5% CO2. For biofilm formation, the smooth morphotype of A. actinomycetemcomitans was diluted in fresh THBY to OD600 nm = 0.3, approximately corresponding to 1.73 × 107 CFU/mL. All biofilms were cultivated either on glass coverslips (12 mm in diameter) in a 24-well plate, or in a 96-well plate for 24 h under appropriate conditions. Samples of each biofilm were exemplarily stained with LIVE/DEAD® BacLightTM Bacterial Viability Kit (Life Technologies) and analyzed by confocal laser scanning microscope (CLSM, TCS SP8, Leica) as previously described [49].

Neutrophil isolation and cultivation with biofilm

Human peripheral blood was drawn from four healthy donors with the approval of Hannover Medical School Ethics Committee (Ethics Statement No. 3295–2016). Polymorphnuclear leucocytes which mainly consisted of neutrophils (approx. 95%) [50] were isolated by density gradient centrifugation using PolymorphPrep (Axis-Shield, Oslo, Norway), as previously described [51]. Neutrophils were then resuspended in RPMI 1640 without supplements (PAA, Freiburg, Germany) to a concentration of 1 × 106 cells/mL.

Neutrophils were

cultivated with each single biofilm to analyze selected antimicrobial responses specifically induced by the individual biofilms: biofilms were washed with phosphate-buffered saline solution (PBS) before neutrophils were added on the biofilms (24-well plate: 5 × 105 cells in 500 µL, 96-well plate: 1 × 105 cells in 100 µL) and cultivated for 3.5 h at 37°C in a humidified atmosphere with 5% CO2.

stimulated with 25 nM phorbol 12-myristate 13-acetate (PMA) [52], which was added immediately before co-incubation with individual biofilms, in order to investigate the potential of the bacteria to inhibit antimicrobial mechanisms of neutrophils.

cultivated without biofilm (with or without PMA) in the same experimental setup in order to serve as controls.

NET visualization

After neutrophil incubation with the respective biofilm, NET formation regarding their structure associated with the biofilm was visualized by immunocytochemistry (ICC) or scanning electron microscope (SEM). For ICC, the cells were fixed with 4% paraformaldehyde (PFA). NET visualization was performed as previously described [53]. In short, after permeabilization and blocking, NETs were primary stained with a rabbit polyclonal anti-human MPO antibody (1:300 in blocking buffer, Dako A0398). The secondary staining was performed using a goat anti-rabbit Alexa Fluor 568-conjugated antibody (1:500 in blocking buffer, Thermo Scientific A11031). The samples were embedded in ProlongGold® antifade with DAPI (P36931, Molecular Probes) and analyzed by CLSM (TCS SP5, Leica). For SEM, the cells were fixed with 0.1% glutaraldehyde and 4% PFA diluted in 200 mM HEPES (4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid). The samples were dried and sputtered as previously described [54] and analyzed by SEM (Crossbeam 540, Zeiss). Both techniques allowed the qualitative observation of NETs.

Nuclease activity assay

The supernatants were collected after neutrophil incubation with the respective biofilm. The nuclease activity of the supernatants was measured using a DNA molecular beacon as previously described, but with slight modifications [55]. In short, the palindrome DNA molecular beacon (5′-FAM-CGA ATT CCT TTT TGG AAT TCG-Quencher-3′, Eurofins genomics) was used at a concentration of 0.1 µmol/L in the reaction buffer (50 mM TRIS-HCl, 5 mM CaCl2, 100 µg/mL BSA, pH 7.9). The supernatants were added and the fluorescence (excitation: 485/20 nm, emission: 528/20 nm) was determined every 2 min for 90 min at 37°C.

ROS assay

ROS production of neutrophils in response to the different biofilms was determined in 96-well plates. After 30 min of neutrophil activation, 2′,7′-dichlorofluorescein diacetate (DCF-DA) was added to a final concentration of 10 µM. The amount of ROS was measured every 30 min over a time period of 3 h (excitation: 485 nm, emission 520 nm).

Quantification of matrix metalloproteinase

Matrix metalloproteinase 8 and 9 (MMP-8, MMP-9) were measured in the collected supernatants using enzyme-linked immunosorbent assays (ELISAs, R&D systems). ELISAs were performed according to the manufacturer’s protocol. The concentrations of MMP-8 and -9 were calculated using four-parameter logistic (4-PL) equation resulting from the standard curve.

Statistical analyses

All presented data were derived from four donors cultivated with four independent biofilms of each species. The statistical analysis was performed using GraphPad Prism 8.0. Statistical differences of nuclease activity compared to Staphylococcus aureus nuclease knock-out strain (Sa^nuc) were analyzed using one-way analysis of variance (ANOVA) with Bonferroni correction. Differences between the groups regarding ROS production or MMP secretion were analyzed using two-way ANOVA with Bonferroni correction. Statistical differences were considered significant at p < 0.05.

Results

The isolated human neutrophils were incubated with the different monospecies biofilms (S. oralis, A. actinomycetemcomitans, and P. gingivalis) for 3.5 h. On the one hand, neutrophils without PMA (non-activated neutrophils) were used to analyze the induced activation of neutrophils by the respective biofilm. On the other hand, neutrophils were activated with the protein kinase C activator PMA, which is a widely used experimental substance to efficiently stimulate various neutrophil reactions, such as ROS production, NETosis, apoptosis, or degranulation [56-58]. With the activated neutrophils, the capacity of each monospecies biofilm to affect the already activated antimicrobial mechanism of neutrophils was determined. After the incubation, the neutrophil responses were analyzed for NETs release, ROS production, and secretion of MMP-8 and -9.

NET formation

Neutrophils were analyzed for their NET release using immune fluorescence staining (red; anti-human MPO antibody and blue; DAPI) and SEM (scanning electron microscopy). In the absence of PMA, untreated neutrophils do not form NETs illustrated by a clear nuclei-located DAPI-staining and MPO signal closely surrounding the nuclei (Figure 1(b)) and demonstrated in the SEM picture (Figure 1(c)), too. A. actinomycetemcomitans stimulated NET formation, which was visualized by co-staining of wide-spread DNA and the NET marker MPO (Figure 1(b)) and in the SEM picture (Figure 1(c)). Additionally, NET formation was also observed after cultivation with S. oralis (Figure 1(b,c)); however, it seemed to be that A. actinomycetemcomitans induced a stronger NET formation. In contrast, no NETs were detectable after cultivation with P. gingivalis (Figure 1(b,c)).

Figure 1.

NET formation by neutrophils after challenge with the different biofilms in the presence or absence of PMA. (a) Biofilms before the cultivation with neutrophils. Representative 3D image of different biofilms (Streptococcus oralis, Porphyromonas gingivalis and Aggregatibacter actinomycetemcomitans) stained by live/dead. Viable bacteria are visualized in green and dead in orange/red. Scale bars: 40 µm. (b) The neutrophils associated with the different biofilms were fixed after incubation for 3.5 h. Immunocytochemistry was performed to visualize cell nuclei (blue; DAPI) and NETs, which were double-stained (red; anti-human MPO antibody and blue; DAPI). No NETs formation, which is illustrated by a clear nuclei-located DAPI-staining and MPO signal closely surrounding the nuclei, was observed in untreated neutrophils. NETs formation indicated by arrows, was observed after cultivation with A. actinomycetemcomitans biofilm in absence of PMA as well as in all samples treated with PMA. Representative images are shown. Scale bars: 50 µm. (c) The samples were fixed, dried, and sputtered after incubation. Representative SEM images from four donors show the bacteria, neutrophils and any formed NETs, which are indicated by arrows. Scale bars: 5 µm; Ctr = control without biofilm; So = S. oralis; Pg = P. gingivalis; Aa = A. actinomycetemcomitans.

In the presence of PMA, NETs were detected in the control without biofilm as well as in the S. oralis and in the A. actinomycetemcomitans samples. Compared to the PMA only-treated cells, the incubation of the neutrophils with P. gingivalis appeared to show slightly less NETs (Figure 1(b,c)). Noteworthy, observations from immune fluorescence staining regarding NETs formation could be confirmed by SEM.

Nuclease activity

As a response to formation of NETs, several bacteria are known to produce nuclease to degrade NETs and avoid entrapment and/or killing by NETs [59,60]. Therefore, the nuclease activity was investigated in the supernatants after co-cultivation for 3.5 h using a DNA molecular beacon and compared to S. aureus nuclease knock-out (Sa^nuc) (Figure 2). Groups with A. actinomycetemcomitans and P. gingivalis showed no nuclease activity, neither with nor without PMA treatment. However, significant nuclease activity was detected in the S. oralis group with PMA treatment.

Figure 2.

Nuclease activity in the collected supernatants after 3.5 h cultivation of the neutrophils with the different biofilms. (a) The graph shows the typical kinetics of the nuclease assay for 60 min. Km values were determined in relation to the threshold value (red line) and (b) the mean values of four samples are listed in the table. Statistical differences to S. aureus nuclease knock-out (Sa^nuc) were analyzed using one-way ANOVA with Bonferroni correction and were considered significant at *p < 0.05. Aa = A. actinomycetemcomitans; Pg = P. gingivalis; So = S. oralis; Sa wt = S. aureus wildtype; Sa ^nuc = S. aureus nuclease knock-out

ROS production

ROS levels were determined during the incubation with the different biofilms in the presence or absence of PMA (Figure 3(a) and Figure S1). The ROS kinetics showed an almost constant ROS level during the whole incubation in the respective treatment groups (Figure S1). After 3.5 h co-cultivation (Figure 3(a)), all three biofilms significantly increased ROS production in the absence of PMA. PMA-treatment resulted in ROS production as well [56]; however, A. actinomycetemcomitans significantly decreased the ROS level of PMA-stimulated neutrophils compared to the control without biofilm, and the same trend was observed for S. oralis.

Figure 3.

ROS production and MMP secretion of neutrophils in response to the different biofilms in the presence or absence of PMA. (a) ROS was determined for 3 h by DCF-DA and means (± SEM) of the 3 h time point are shown in the bar graph. (b) MMP-8 and (c) MMP-9 were measured by ELISAs in the supernatants collected after biofilm incubation for 3.5 h. The bar graphs represent the means (± SEM). ROS production and MMP secretion were determined from four donors in technical triplicates. Differences between the groups were analyzed using two-way ANOVA with Bonferroni correction. *p < 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001

MMP secretion

MMP-8 and MMP-9 levels were determined in the supernatant after co-cultivation for 3.5 h using ELISA (Figure 3(b,c)). In the absence of PMA, A. actinomycetemcomitans significantly increased the secretion of MMP-8 and -9, and S. oralis increased the secretion of MMP-9. The co-incubation with P. gingivalis showed a similar level of MMP-8 and MMP-9 compared to the control without biofilm.

After activation with PMA, P. gingivalis significantly reduced the MMP-8 levels and S. oralis the MMP-9 levels. A. actinomycetemcomitans significantly increased the MMP-9 secretion – despite PMA activation. Additionally, the amount of MMP-8 and MMP-9 release after cultivation with A. actinomycetemcomitans was similar in the presence or absence of PMA.

Discussion

Neutrophils are the main innate immune cells in the oral cavity and are important for the host’s response to oral biofilm [22,23]. The balance in function and number of neutrophils is crucial for oral health [21,22]. The imbalance can contribute to tissue destruction which can lead to periodontitis [30]. Neutrophils are able to respond specifically and differently through their antimicrobial mechanisms to various bacterial species [42] and this might play an important role for oral health or diseases development. Therefore, in order to further explore this role of neutrophils, the aim was to investigate the bacterial species-specific effects on the antimicrobial mechanisms of neutrophils by commensal (S. oralis) and pathogenic (P. gingivalis or A. actinomycetemcomitans) monospecies biofilms.

The isolated human neutrophils were incubated with the different biofilms for 3.5 h. On the one hand, the activation of neutrophils by the respective biofilm was investigated using unstimulated neutrophils. On the other hand, modification especially the inhibition of antimicrobial mechanism of neutrophils by the respective biofilm was analyzed using PMA-activated neutrophils. In order to answer the question whether the bacterial biofilms are able to inhibit the antimicrobial defense mechanisms of neutrophils, a high level of stimulation was required. For this reason, PMA as a strong stimulus of the neutrophil response, which is extensively described as such in the literature [52] and worldwide used in laboratories, was used despite the fact that it is a non-physiological stimulus. As selected neutrophil responses, NETs release, ROS production, and secretion of MMP-8 and -9 were analyzed. NET formation was depicted in representative images since the three-dimensional structure, and the considerable background fluorescence from the bacterial DNA, significantly prevents the possibility of NET-quantification, e.g. using ImageJ. NET-quantification in a 3D structure, as in the case of the bacterial biofilms, has not yet been performed successfully [61]. Therefore, NET formation was analyzed by two different imaging methods to get more accurate results. The 3.5 h time point was chosen, since only the highest possible activity of the neutrophils enables to analyze the effect (especially inhibition) on the antimicrobial mechanisms by the bacterial biofilms. Especially, for the analysis of the NET formation, this is the commonly used time point [44,53,58]. The presented data for ROS production supported the results of NETs formation. The results for the individual biofilms showed up at an early stage which was depicted in the ROS-kinetics (Figure S1). Since MMPs concentrated in the test sample due to the continuous secretion, the late 3.5 h time point was also chosen for MMP release analysis. As summarized in Table 1, specific responses of neutrophils to different biofilms were detectable, and this was reflected in all investigated antimicrobial mechanisms: NET formation, ROS production and MMP-8 and -9 releases. Generally, a species-specific response of neutrophils was observed, which is in accordance with previous studies [42,44].

Table 1.

Evaluation of the antimicrobial response of neutrophils to the different biofilms in the absence or presence of PMA

	Control		S. oralis		P. gingivalis		A. actinomycetemcomitans
	- PMA	+ PMA	- PMA	+ PMA	- PMA	+ PMA	- PMA	+ PMA
NETs	ND	D	D	D	ND	D	D	D
ROS	-	+++	++	++	+++	+++	+++	++
MMP-8	-	+++	+	+	-	+	+++	+++
MMP-9	-	++	+	+	-	++	+++	+++

- no/slight neutrophil response; + moderate neutrophil response; ++ high neutrophil response; +++ excessive neutrophil response; ND not detected; D detected

S. oralis

The commensal S. oralis monospecies biofilm slightly enhanced NET formation in the untreated neutrophils, in accordance with the results of Oveisi et al. [44]. NETs protect the host against bacterial invasion in epithelial cells [23] and are important for the maintenance of periodontal health [28]. Therefore, the NETs enhancement induced by commensals like S. oralis might correspond to protective activation of neutrophils as a part of a healthy innate immune response [44]. On the other hand, S. oralis slightly suppressed NETs in PMA-activated neutrophils. This may be explained by the nuclease activity of S. oralis, which is in accordance with previous studies [59,60]. The degradation of the NET structure by commensals may contribute to removal of excessive NETs. This phenomenon might support oral health, as impaired NET clearance leads to a high concentration of NET-bound proteins and these support tissue destruction [29]. Thus, it seems that S. oralis is able to induce both release and degradation of NETs and thereby it might support a balance in the level of NETs, which is necessary for oral health [28,29].

The S. oralis biofilm increased ROS production in the absence of PMA and showed a tendency to reduce it after PMA activation. Thereby, after cultivation with S. oralis, ROS levels were similar in the PMA-activated as well as in neutrophils without PMA. A previous study showed that S. oralis induces activation of a transcription factor for antioxidants (nuclear factor erythroid 2-related factor, Nrf2) in neutrophils in parallel with induced ROS production [44]. The resulting antioxidants from neutrophils neutralize ROS [62] and may reduce the ROS, as we observed in our study. Thus, S. oralis induced ROS production but might limit the damage in case of an excess ROS level by generation of antioxidants in the same immune cell [44]. Similar to NETs, this balance of ROS might be important to maintain oral health.

S. oralis biofilm increased the secretion of MMP-9 in the absence of PMA, but after PMA activation, the MMP-9 level was reduced to the same level as observed without PMA. The same trend was also observed for MMP-8. Hence, S. oralis created a balance of MMP-8 and -9 levels, as we observed also for NETs and ROS. The balance of MMPs is important for maintaining oral health because both absence and enhancement of MMP secretion contribute to the progression of periodontitis [35,36,38]. Taken together, our results demonstrated that the S. oralis biofilm modulated neutrophils in a way that the tissue destructive responses of neutrophils could be balanced, which might be important to maintain oral health.

P. gingivalis

The pathogen P. gingivalis monospecies biofilm seemed to reduce NETs after PMA activation and no NETs were detected in the absence of PMA. The reduction in NETs may be mediated by bacterial DNases [42,60]. The used P. gingivalis strain was shown to have a slight DNase activity [59]. However, this was not reflected in our results. It is possible that P. gingivalis DNase degraded the NETs directly after starting the incubation with the neutrophils, as NET degradation is a rapid process and may occur within 90 min [60]. During the incubation for 3.5 h, DNases were perhaps degraded by gingipains [60] and could therefore not be measured in the nuclease activity assay at the end of the incubation. The expression of bacterial DNase and degradation of NETs might support the bacterial invasion of P. gingivalis in the tissue [63]. The evasion of host defenses may lead to increased pathogenicity and might cause periodontitis [28].

P. gingivalis biofilm induced ROS production in the absence of PMA and there was no reduction in ROS after PMA activation. These observations correspond to clinical studies in which neutrophils from chronic periodontitis patients (according to the old classification) produced higher levels of ROS compared to healthy patients [64]. Bacteria possess defense mechanisms against oxidative stress. The expression of ruberythrin by P. gingivalis protects both P. gingivalis and other biofilm organisms from oxidative stress [42,65]. Thus, the elevated release of ROS can cause tissue destruction, whereas the biofilm remains protected. Both together play an important role in the pathogenesis of periodontitis and the associated tissue destruction [66].

After incubation with P. gingivalis in absence of PMA, low levels of MMP-8 and -9 were detected which were similar to controls without biofilm. Moreover, MMP-8 was reduced by P. gingivalis after PMA stimulation. These low levels of MMPs (with and without PMA) may have been caused by a suppression of the MMP release or by gingipains during the incubation of 3.5 h. These proteases are one of the main virulence factors of P. gingivalis and can cleave many host components, such as cytokines, immunoglobulins, complement factors, MMPs, or DNases, as discussed above, to overcome the host defense mechanism [40,67]. Taken together, NET formation and MMP-8 and -9 secretions were diminished by P. gingivalis, probably to evade antimicrobial mechanisms of neutrophils. Nevertheless, ROS levels were high for which P. gingivalis has a protection system. Additionally, P. gingivalis was shown to exhibit various mechanisms in order to evade neutrophil-mediated killing, which may contribute to its colonization and invasion in the tissue [40,63]. Consequently, neutrophils may not be able to clear this pathogen. The continuous presence of the pathogen may lead to persistent neutrophil recruitment and activation in a later stage of infection, which subsequently may cause hyper-activation of neutrophils leading to inflammation with tissue destruction providing nutrients for P. gingivalis [40,68]. Therefore, periodontitis might be actively supported by continuing neutrophil reaction to P. gingivalis, which causes parallel damage to host tissue. This type of neutrophil activation might be accompanied by a slow progression of periodontitis since only some tissue-destructive antimicrobial mechanisms were induced.

A. actinomycetemcomitans

The pathogen A. actinomycetemcomitans monospecies biofilm induced strong NETs formation, in accordance with previous studies [29,30,69]. This may be caused by the virulence factor leukotoxin (Ltx) [30]. The A. actinomycetemcomitans JP2 strain, which was used in our study, expresses constant high levels of Ltx [70]. Ltx lyses leukocytes – but also activates neutrophils by induction of migration, degranulation, and NETosis, which is independent of and appears before Ltx-mediated lysis [30,71,72]. The NETs were not degraded, which could be explained by the missing nuclease activity of A. actinomycetemcomitans, which is in line with findings of Doke et al. [60]. The exaggerated NETs formation, which is often found in an aggressive form of periodontitis, can cause tissue destruction by NET-bound proteins and enzymes, such as neutrophil elastase or MPO and concomitant release of cytotoxic molecules and has a crucial role in the pathogenesis of periodontitis [28-30].

ROS production was increased by A. actinomycetemcomitans in the absence of PMA, which may be caused by Ltx binding on neutrophils [30]. However, ROS level of PMA-activated neutrophils was reduced by A. actinomycetemcomitans. This bacterium has two mechanisms to avoid the toxic effect of ROS. In response to oxidative stress, specific genes in A. actinomycetemcomitans are upregulated to neutralize ROS (katA) or to escape from the toxic environment (dspB) [18]. This may explain the decreased ROS level after PMA activation. In contrast to S. oralis, A. actinomycetemcomitans has not the ability to induce the transcription factor Nrf2 [44] and thereby the production of antioxidants in neutrophils. Consequently, the important balance between ROS and antioxidants of neutrophils, which protect the tissue, may be disrupted [32]. This imbalance and the excessive level of ROS are closely associated with aggressive periodontitis [73].

MMP-8 and -9 secretions were markedly increased by the A. actinomycetemcomitans biofilm. The excessive secretion of MMP-8 and -9 leads to the degradation of collagen in the soft tissue and the alveolar bone and are associated with tissue destruction during periodontitis [74]. The high concentration of MMP-8 has been linked to the severity of inflammation in clinical studies and was associated with an aggressive form of periodontitis [37,75]. Taken together, the A. actinomycetemcomitans biofilm induced a severe neutrophil response by the release of NETs, ROS, and MMPs, which may lead to tissue destruction and contribute to the pathogenesis of periodontitis. Thus, this immediate hyperactive reaction of the neutrophils might contribute to a rapid progression of periodontitis, since different tissue-destructive antimicrobial mechanisms were induced.

Our results demonstrated that the neutrophil response was different to each species and the type of response could be associated with possible contribution to oral health or periodontitis. It should be considered that the use of monospecies biofilms does not optimally mimic the clinical situation, where a multispecies biofilm always exists [5,6]. However, in order to clarify the role of different bacterial species in the native multispecies biofilm and the specific neutrophil response to these species, it is necessary to investigate the interaction with one bacterial species alone. Compared to planktonic bacteria, the use of monospecies biofilms is one step closer to the clinical situation, as biofilm is the common way of life in the oral cavity and bacteria within the biofilm are more resistant to the host’s immune response [5,8,9,45].

Conclusion

In conclusion, the neutrophil responses, NET formation, ROS production and MMPs secretion were different to the various bacterial species grown as monospecies biofilm. The commensal S. oralis induced a balance-like neutrophil response – which is consistent with the concept that commensals protect the host against the overgrowth of pathogenic bacteria and are required to maintain oral health [23,76]. The pathogenic biofilms induced different neutrophil responses. P. gingivalis partially diminished the neutrophil response, which might support its colonization and invasion of the tissue leading to inflammation. These might contribute to the pathogenesis of periodontitis and might be accompanied with a slow progression. In contrast, A. actinomycetemcomitans induced a strong neutrophil reaction, which might cause tissue destruction and perhaps contributes to a more rapid progression of periodontitis. Thus, the different neutrophil responses and the occurrence of these bacterial species in the native multispecies biofilm might contribute to either the maintenance of oral health or the pathogenesis of periodontal disease. These findings and future investigations may provide new opportunities for future strategies for disease treatment, where immunomodulatory drugs could be one option.

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