2. Compounds with Activity against Oral Infections

Oral microbial communities are some of the most complex microbial floras in the human body, consisting of thousands of bacterial and hundreds of fungal species [25]. Culture-independent molecular methods, such as proteomics and 16S rRNA sequencing, have demonstrated that S. mutans was the dominant species, with elevated levels of other streptococci including Streptococcus sanguinis, Streptococcus mitis, and Streptococcus salivarius. Candida spp. combined with Streptococcus spp. usually increases the virulence in invasive candidiasis, early childhood caries, or peri-implantitis ^[13][26][27][13,26,27]. The interactions between the various species in these mixed biofilms may be synergistic, in that the presence of one microorganism generates a niche for other pathogenic microorganisms, which serves to facilitate organisms’ retention. Thus, Streptococcus spp. and Candida spp. create special synergistic consortia on solid oral surfaces ^[13][26][13,26].

Streptococcus mutans strains are considered the most cariogenic bacteria; however, Candida spp. can increase their cariogenicity. Bacterial and fungal cells are able to produce glucan as an extracellular polysaccharide that aids cariogenic biofilm formation [28]. Bacteria also convert dietary sucrose and free glucose or fructose into a diverse range of soluble and, particularly, insoluble extracellular polysaccharides (EPS) (e.g., water-insoluble glucans) through exoenzymes, such as Gtfs, and EPS, to build blocks of cariogenic biofilms. These structures promote the tooth surface colonization by S. mutans and additional microorganisms into dental plaque (e.g., Porphyromonas gingivalis, streptococci, Fusobacterium spp., Prevotella spp.), while forming the scaffold core or matrix of the biofilm. In addition, the EPS matrix creates a special diffusion-limiting barrier, facilitating acidic microenvironments creation at the biofilm–tooth interface, which is critical for adjacent tooth enamel dissolution [29]. Furthermore, S. mutans displays many other virulence attributes, including its ability to produce acid and to tolerate an acidic environment.

Among Candida spp., C. albicans is the most prevalent on dental tissues, reaching 60%–70%, followed by C. tropicalis and C. glabrata [30]. As indicated earlier, these yeasts are usually commensal, but in some situations they can become parasitic, causing oral candidiasis ^[30][31][30,31]. The virulence attributes of C. albicans are the acidogenicity and aciduric nature, along with the ability to develop profuse biofilms, to ferment and assimilate dietary sugars, and to produce collagenolytic proteinases [15]. Also, C. albicans modulates the pH in dual-species biofilms to values above the critical pH where enamel dissolves. Although the species present low cariogenicity, biofilms formed by mixed populations of C. albicans and S. mutans are more voluminous [32]. The presence of Candida spp. enhances S. mutans growth, fitness, and accumulation within biofilms. It is documented that C. albicans growth stimulates S. mutans development via biofilm-derived metabolites [33]. Also, C. albicans mannans mediate S. mutans exoenzyme GtfB binding to modulate cross-kingdom biofilm development [17]. Candida spp.-derived β-1,3-glucans contribute to the EPS matrix structure, while fungal mannan and β-glucan provide sites for GtfB binding and activity; thus, the coexistence of S. mutans with C. albicans can cause dental caries progression or disease recurrence in the future [34]. It was also suggested that S. mutans co-cultivation with C. albicans influences carbohydrate utilization by bacterial cells ^[35][36][35,36], and the analysis of metabolites confirmed the increase in carbohydrate metabolism, with amounts of formate elevated by co-cultured biofilms [37]. Nonetheless, biofilm biomass and metabolic activity were both strain- and growth medium-dependent [37]. Liu and co-workers showed that nicotine promotes S. mutans attachment. The enhancement of the synergistic relationship may contribute to caries development in smokers ^[38][39][38,39]. On the other hand, there are contradictory reports in this matter. It was proposed that, by definition, C. albicans is not a cariogenic microorganism; it could prevent caries by actively increasing pH and preventing mineral loss [40]. Nonetheless, a study published in 2016 concluded that children with severe early childhood caries were likely infected by their mothers, as the mothers of these children were highly infected with C. albicans [41]. In fact, genetic testing of Candida strains from children and their mothers showed that most strains were genetically related [41].

Progress in understanding the etiology, epidemiology, and microbiology of periodontal pocket flora has called for new antimicrobial therapeutic schemes for oral diseases [42]. Distinctive means and compounds may be used to prevent oral infections. Biomolecules produced by S. mutans, lactoferrin, and probiotics, applying chemicals and photodynamic therapy, can support the management of oral candidiasis [43].

2.1. Chemical Compounds with Activity against Streptococcus mutans and Candida

spp.

 Biofilms

Recently, a wide range of antimicrobial agents and methodologies have been reported to suppress the growth of dental Streptococcus mutans–Candida spp. biofilms (Table 1). Photodynamic antimicrobial therapy (aPDT) is based on a photoactive dye—a chemical photosensitizer that binds to the target cell and is activated by a specific light wavelength. During this process, oxygen species such as singlet oxygen and free radicals are formed, exerting toxicity towards the cell [30]. The influence of pre-irradiation time employed in antimicrobial photodynamic therapy with a diode laser was recently checked [79]. It was found no effect due to C. albicans biofilm therapy; however, a pre-irradiation time of 1 min was effective against a microbial load of S. mutans. The effect of aPDT using chloroaluminium phthalocyanine in a cationic nanoemulsion was evaluated against multispecies biofilms of C. albicans, C. glabrata, and S. mutans. The technique led to photoinactivation of the biofilm and reduced colony count and metabolic activity [44]. Similar effects were obtained using hypericin–glucamine [45], Rose Bengal in α-cyclodextrin [46], curcumin ^{[44][47][48][49][50]}[44,47,48,49,50], methylene blue [52], toluidine blue O [51], erythrosine with green light [55], or Photodithazine^® obtained from the cyanobacterium Spirulina platensis ^[53][54][53,54]. Another study conducted by Soria-Lozano et al. [80], using Rose Bengal, methylene blue, and curcumin with white light, showed positive effects against the S. mutans and S. sanguis strains. Although methylene blue and Rose Bengal were the most efficient, C. albicans was the most resistant to all photosensitizers, and curcumin, in this case, was ineffective. Finally, aPDT embodies an important treatment as the photodynamic inactivation seems to be promising for biofilm-associated S. mutans and Candida spp. biofilm infection management, since there is no microbial resistance observed. Chlorhexidine is the most commonly studied active agent ^[81][82][81,82]. It is widely used for preventing dental plaque or treating mouth yeast infections. Additionally, over the years, the number of studies on antibiofilm strategies using this compound or other chemicals has increased [83]. Chlorhexidine at low concentrations, but with the addition of cis-2-decenoic acid, was able to disperse single-species biofilms formed by S. mutans and C. albicans, as well as bacterial–fungal dual-species consortia [56]. Also, chlorhexidine gluconate with tyrosol was revealed to be effective against single and mixed-species oral biofilms ^[57][58][57,58]. A solution containing 2.5% sodium hypochlorite, 2% chlorhexidine, and ozonated water inhibited biofilms of S. mutans and C. albicans in mesiobuccal root canals after irrigation [25]. A chlorhexidine carrier nanosystem based on iron oxide magnetic nanoparticles and chitosan was synthesized, and its antimicrobial effect on mono- and dual-species biofilms of C. albicans and S. mutans was evaluated. The results confirmed the nanosystem potential as a preventive or therapeutic agent to fight biofilm-associated oral diseases [60]. The advantage of chlorhexidine is that its resistance is not as common as other chemicals’. Importantly, cases are being reported more often [84]. Hence, in order to reduce the number of cases, it is important to restrict its applications to indications with a strong patient benefit and to remove it from uses that are without any advantage or have doubtful value. The antimicrobial activity of chitosan, silver nanoparticles, and ozonated olive oil was evaluated against endodontic pathogens, including S. mutans and C. albicans. This combination was characterized as novel, safe, and having the potential to eradicate mature mixed-species biofilms [61]. Chitosan and carboxymethyl chitosan were also active against Candida spp. and Streptococcus spp. biofilms ^{[62][63][64][65]}[62,63,64,65]. Also, Kivanç and co-workers [72] investigated the antimicrobial and antibiofilm activities of hexagonal boron nitride nanoparticles against S. mutans, Staphylococcus pasteuri, S. mutans -Candida spp. Their results showed that, at an appropriate concentration (0.1 mg/mL), these nanoparticles could be considered a safe potential oral care product. Similarly, EPS inhibitors may enhance antibiofilm activity ^[85][86][85,86]. A combination of the antifungal fluconazole with povidone iodine showed to completely inhibit C. albicans or mixed biofilm formation [76]. It was found that the inclusion of iodine derivative enhanced fluconazole efficacy by inhibiting α-glucan synthesis in S. mutans, which participates in protective bacterial EPS formation [76]. Moreover, thiazolidinediones have been found to act as effective quorum sensing quenchers, capable of preventing the mixed biofilm formed by Candida spp. and bacterial strains. These compounds can penetrate into deeper layers of the mixed biofilm, thereby increasing the antimicrobial activity. A small molecule, thiazolidinedione-8, has been revealed to be able to impair biofilm formation of various microbial pathogens. These compounds may disturb the symbiotic balance between C. albicans and S. mutans in a dual-species biofilm [77]. The inhibitory effects of lactams in mixed oral biofilms, including S. mutans and C. glabrata, have been assessed [78]. γ-Alkylidene-γ-lactams solubilized in 3.5% dimethyl sulfoxide led to a marked reduction in biofilm biomass. Furthermore, the total protein content and the quantity of EPS declined significantly. Hence, these compounds show important antibiomass activity, which can be important for promoting the diffusion of a second drug into oral biofilms, for its total eradication. Several materials containing silver nanoparticles, alone or with polyphosphates, were evaluated as antimicrobials against C. albicans and S. mutans. These composites demonstrated significant antimicrobial activity, especially against S. mutans, which might make them a possible alternative for new dental materials ^[66][67][66,67]. Silver nanoparticles, combined with calcium glycerophosphate as well as nanostructured silver vanadate in dental acrylic resins, have also been shown to have antimicrobial and antibiofilm activities against dental prostheses-associated microorganisms ^[73][74][73,74]. Silver has found several uses since its toxicity toward human cells is considerably lower than toward bacteria; thus, this application is promising. Base resins have also shown promising bioactive responses against C. albicans and S. mutans. Dimethylaminododecyl methacrylate-modified denture base resin proved to be a favorable therapeutic system against problems triggered by denture base microbes (e.g., denture stomatitis) [68]. Likewise, poly-(2-tert-butilaminoethyl) methacrylate decreased S. mutans’ adhesion to the material surface, but did not exhibit an antimicrobial effect against C. albicans [69]. Furthermore, a novel fluoride-releasing copolymer composed of methyl methacrylate, 2-hydroxyethyl methacrylate with polymethyl methacrylate was developed by incorporating sodium fluoride. This copolymer inhibited acidogenic mixed-species biofilms, showing potential to control these diseases by limiting biofilm growth [59]. Finally, a modified pH-responsive cationic poly (ethylene glycol)-block-poly (2-(((2-aminoethyl) carbamoyl) oxy) ethyl methacrylate has been revealed to be a promising agent for dental caries therapy and provided guidelines for drug delivery system design in other acidic pathologic systems [75]. Regarding synthetic surfactants, several compounds have also shown great potential. Cetylpyridinium chloride and cetyltrimethylammonium bromide with plant terpinen-4-ol revealed antimicrobial activity against S. mutans and C. albicans [70]. Nanoparticles of amphiphilic silanes with Chlorin e6 exhibited strong antibiofilm activity against periodontitis-related pathogens belonging to the Streptococcus genus [71]. These compounds have good prospects in antimicrobial applications to inhibit both oral disease occurrence and progression, namely periodontitis, one of the most relevant oral diseases.

2.2. Natural Compounds with Bioactivity Against Streptococcus mutans and Candida spp. Biofilms

Due to the incidence of oral disease, increased resistance by bacteria and fungi to antimicrobials, and the adverse effects of some drugs currently used in dentistry (and general medicine), there is a great need for alternative prophylaxis and treatment options that are not only safer but also cost-effective. While several antimicrobial agents are commercially available, these chemicals can alter the oral microbiota and have undesirable side effects (e.g., nausea, diarrhea, vomiting, tooth staining). Henceforth, traditional medicine and the search for alternative products are still important. In fact, natural products offer an assortment of chemical structures and possess an extensive variety of biological properties; thus, they are a source for new pharmaceuticals. Bioactive secondary metabolites have been revealed to be useful as new antimicrobial and antibiofilm drugs, such as numerous furanones, alkaloids, and flavonoids, from many plants and marine organisms [87]. Table 2 presents natural compounds and plant extracts with antimicrobial potential, particularly focused on anti-Streptococcus spp. anti-Candida spp. activities.

Table 2. Natural compounds/extracts and their in vitro bioactivity against Streptococcus spp. and Candida spp.

Year	In vitro Assays	Natural Compound/Extract	Effect	Reference(s)
2018	Antibacterial and antifungal bioactivity
2017
Antibacterial and antifungal, antibiofilm and antioxidant bioactivity
Camellia japonica	and	Thuja orientalis	Significantly inhibited the microbial grow of oral pathogens	[94]
2016	Antibacterial and antifungal, antibiofilm bioactivity Cytotoxicity and anti-inflammatory effects: human oral epithelial cells	Houttuynia cordata (herbal tea)	Antibiofilm effects against S. mutans and C. albicans	[95]
2015	Antibacterial and antifungal bioactivity	Ricinus communis and sodium hypochlorite (cleanser solutions)	Effective in controlling denture biofilms	[96]
2014	Anti-adherent properties (antibiofilm)	Schinus terebinthifolius and Croton urucurana (methanol and acetate methanol extract fractions in hydroalcoholic and dimethylsulfoxide)	Antibiofilm activity against S. mutans and C. albicans	[97]

Plant-derived compounds are a good source of therapeutic agents and inhibitors of dental caries, periodontal diseases, and candidiasis. For example, α-mangostin or lawsone methyl ether showed antimicrobial, antibiofilm, and anti-inflammatory activities. Indeed, an oral spray containing these natural chemicals was effective against common oral pathogens [98]. Lupinifolin from Albizia myriophylla wood exhibits good anti-S. mutans activity by damaging bacterial membranes, resulting in cell leakage [99]. Essential oils and bioactive fractions from Aloysia gratissima, Baccharis dracunculifolia, Coriandrum sativum, Cyperus articulatus, and Lippia sidoides were also evaluated as antimicrobials against S. mutans and Candida spp. A significant reduction in extracellular polysaccharides and bacteria was observed for A. gratissima and L. sidoides, indicating that these fractions disrupted biofilm integrity. Plus, C. sativum oils drastically affected C. albicans viability [100], and might be considered as alternative anticaries agents. In turn, quercetin and kaempferol or farnesol with myricetin showed favorable properties in terms of controlling some virulence factors of S. mutans and C. albicans biofilms ^{[101][102][103][104]}[101,102,103,104]. It was suggested that tyrosol decreased the metabolic activity and number of viable cells in single and mixed-species biofilms [105]. Correspondingly, β-caryophyllene—a bicyclic sesquiterpene of numerous essential oils—may inhibit cariogenic biofilms and may be a candidate agent for the prevention of dental caries [28]. These results highlight the promising antimicrobial activity of plants for the treatment of dental caries and oral candidiasis.

Propolis, rich in flavonoids, has a long history of use as a natural treatment for a host of health problems. It is also used as an ingredient in certain medicinal products applied directly to the skin, or in mouthwash and toothpaste. Propolis is under preliminary research for the potential development of new drugs associated with the control of C. albicans and immunomodulatory effects. Propolis and miswak (Salvadora persica tree), used in toothpaste, dental varnishes, and mouthwash, led to a significant reduction in the colony-forming units of oral biofilms ^[106][107][106,107].

Antimicrobial peptides have also been widely tested for controlling bacterial biofilms. Shang and colleagues [108] tested the efficacy of peptides from Rana chensinensis skin secretions in preventing biofilm formation by cariogenic and periodontic pathogens. Peptide L-K6, a temporin-1CEb analog, exhibited high antimicrobial activity against tested oral pathogens and was able to inhibit S. mutans biofilm formation. This peptide significantly reduced cell viability within oral biofilms. Its anti-inflammatory activity was correlated with L-K6 binding to LPS and dissociating LPS aggregates. Likewise, cyclic dipeptides (CDPs) are common metabolites widely biosynthesized by cyclodipeptide synthases or nonribosomal peptide synthetases by both prokaryotic and eukaryotic cells. Examples of CDPs that inhibit biofilm formation by Streptococcus epidermidis include cyclo-(l-Leucyl-l-Tyrosyl) isolated from mold Penicillium sp. and cyclo-(l-Leucyl-l-Prolyl) isolated from Bacillus amyoliquefaciens. The antibiofilm activity of 75 synthetic CDPs was assessed against oral pathogens, allowing for the identification of five novel CDPs that inhibit biofilm formation and adherence properties. Among them, five new active compounds were identified as preventing biofilm formation by S. mutans and C. albicans on the hydroxylapatite surface [109].

Similarly, the application of probiotics and antagonistic microorganisms for oral pathogens can bring about tangible benefits, namely boosting host immunity and disturbing the pathogen’s environment via competition for space and nutrients. Krzyściak et al. [35] evaluated the anticariogenic effects of Lactobacillus salivarius by reducing pathogenic species in biofilm models. This microorganism has demonstrated the ability to secrete intermediates capable of inhibiting the formation of cariogenic S. mutans and C. albicans biofilms. In other studies, single and mixed biofilms were inhibited by probiotic lactobacilli ^[110][111][110,111]. Therefore, they seem to be useful as an adjunctive therapeutic mode against oral Candida spp. infections. Another study reported that the Candida sorbosivorans SSE-24 strain was used to stimulate erythritol production at a level of 60 g/L. It was detected a significant inhibitory effect of erythritol on the growth and biofilm formation of S. mutans [112]. Interestingly, a novel phage (ɸAPCM01) with activity against S. mutans biofilms was recently isolated from human saliva [113], and the inhibition of S. mutans biofilms was also found by the use of liamocins from Aureobasidium pullulans [114]. Chemically, liamocins are mannitol oils specific to Streptococcus spp., having the potential to act as new inhibitors of oral streptococcal biofilms that should not affect normal oral microflora.