Lactobacilli and human dental caries: more than mechanical retention

Abstract

Lactobacilli have been considered as major contributors to human dental caries for over a century. Recent in vitro model studies have shown that when compared to Streptococcus mutans, a keystone pathogen of human dental caries, the ability of lactobacilli to form biofilms is poor, although differences exist between the different major species. Further studies using molecular and bioinformatics approaches provide evidence that multiple mechanisms, including adhesin-receptor mediated physical contact with S. mutans , facilitate the adherence and establishment of lactobacilli on the tooth surface. There is also evidence that under conditions like continuous sugar consumption, weak acids and other antimicrobials such as bacteriocins from lactobacilli can become detrimental to the microbial community, especially those in the proximity. Details on the underlying mechanisms of how different Lactobacillus sp. establish and persist in the highly complex microbiota on the tooth surface await further investigation.

Introduction

Lactobacilli were the first micro-organisms implicated in human dental caries over a century ago and was the main etiological candidate before the mutans streptococci became dominant in the literature in the 1950s [1, 2]. From clinical isolation and cultivation to 16S rRNA-based analysis and more recently, deep sequencing of the plaque microbiota, Lactobacillus sp. are frequently identified at active carious sites, especially in lesions with advanced caries in adult and paediatric patients [3–6]. However, unlike Streptococcus mutans , a keystone cariogenic bacterium whose pathophysiology and virulence attributes have been well characterized through extensive investigations in recent decades, major knowledge gaps remain concerning the role of Lactobacillus sp. and especially, the mechanisms how they establish and persist on the tooth surface and facilitate the development of carious lesions.

Dental caries is a clinic manifestation of continued demineralization of the tooth enamel resulting from acids produced from sugar fermentation by bacteria in the plaque microbiota on the tooth surface, under the gum and in the proximal surfaces. Recent advances, including data from the human oral microbiome project (www.homd.org), have clearly demonstrated that dental caries results from a dysbiotic plaque microbiota in response to host and environmental perturbations that include saliva deficiency, poor oral hygiene and continuous consumption of fermentable sugars. A cariogenic plaque microbiota is featured with disproportional increases of highly acidogenic and aciduric species, which include mutans streptococci, lactobacilli and bifidobacteria. It is well-known that the abilities to colonize and persist on the tooth surface, to catabolize sugars and produce weak acidic metabolites, and to tolerate the acids and the resulting low pH environment are traits considered essential for a bacterium to cause carious lesions [7]. Many studies using in vivo models, mostly prior to the mutans streptococci paradigm, have examined the roles of lactobacilli in dental caries [8–11], but questions remain inexplicit on the molecular mechanisms concerning how Lactobacillus sp. colonize and establish on the tooth surface and how they interact with the micro-environment and with other major bacterial species in the plaque microbiota, influencing the development including temporal structure and composition of the plaque microbiota. On the other hand, many studies have been done with the food and probiotic lactobacilli, and several articles have recently offered comprehensive reviews on these lactobacilli including comparative genomics and the potential of biotechnological engineering [12–18]. This review attempts to highlight recent studies on oral lactobacilli with a focus on bacterial biofilm formation and its regulation including the roles of inter-species interactions.

Major Lactobacillus species in dental caries

From over a century of extensive investigations, the connection of lactobacilli to human dental caries in children and adults has been well established [1, 5, 6]. Lactobacilli are among the micro-organisms that can be found in the oral cavity soon after babies are born. The lactobacilli in the oral cavity of infants are believed to mainly come from the mouths of their parents, especially their mothers due to close contacts, and from the foods they eat, including milk and different fermented products. There is currently no effective means to determine the definite origin of or differentiate the types of Lactobacillus sp. In the oral cavity, lactobacilli can be found mostly in saliva, on the surface of the mucosa, the hard palate and the dorsum of the tongue. They are mostly thought to be transient in the mouth and their numbers on the tooth surfaces of healthy infants and young children are usually low [5, 6, 19]. Low affinity to the tooth surface is thought to be the major factor that contributes to its low prevalence in the plaque microbiota of healthy individuals [8, 10]. However, lactobacilli tend to increase in numbers with increasing intake of fermentable sugars in the diet, a situation that is also conducive to dental caries. In individuals with active dental caries, both the diversity and prevalence of lactobacilli in dental plaque, especially the active carious sites, increase significantly, as compared to individuals who are caries-free [5, 6]. Major differences in diversity and prevalence among different studies also exist, which can be at least in part attributed to the differences in study populations, severity of the disease at the time of the study, and the methodologies used, notably cultures versus DNA-based methods [20]. Among the Lactobacillus sp. identified from carious lesions, the most dominant species in adult and childhood dental caries, including severe early childhood caries, are L. casei/paracasei, L. fermentum, L. rhamnosus, L. gasseri, L. salivarius and L. plantarum [5, 6] (Table S1, available in the online version of this article). Those with low prevalence were thought to be more likely transient contaminants from food or other sources with no major role in dental caries. A recent study of severe early childhood caries by Caufield et al. [5] also showed that most of the Lactobacillus sp. existed as cohabitants with other lactobacilli. A few species, including L. casei/paracasei, L. fermentum and L. salivarius, were identified as the single occupant of the caries lesions. It is unclear if any of these three major species are more pathogenic than the others in terms of their cariogenesis. For more information on the natural history of the lactobacilli in the oral cavity and their association to dental caries, consult recent reviews by Caufield et al. and Duar et al. [5, 21].

Sugar fermentation and acid production

Lactobacilli have been widely used as starter cultures in food preservation and production, and some are considered as probiotic conferring health benefits on the host upon consumption/application. For various reasons, these lactobacilli have been extensively studied concerning their bacterial physiology, especially carbohydrate metabolism and regulation and the potential of biotechnological engineering. Lactobacilli are strictly fermentative bacteria, known for their high capacity to utilize a variety of carbohydrates. In fact, lactobacilli were originally grouped taxonomically according to their major carbohydrate utilization patterns as homofermentative, facultatively heterofermentative, and obligate heterofermentative lactobacilli [19]. Homofermentative lactobacilli ferment hexoses with lactic acid as the primary by-products, while heterofermentative lactobacilli produce lactic acid, ethanol, acetic acid and carbon dioxide as end-products. Lactobacillus sp. are diverse, and major differences also exist within the different species (Table S1), as revealed by 16S rRNA and whole-genome sequence analyses [13, 14, 22, 23]. However, they all possess a broad repertoire of enzymes that enable them to utilize various carbohydrates, which are rich in oligosaccharides and starches in the oral cavity. To name a few, they include glucosidases, fructosidases, galactosidases, glucansucrase, levansucrases and fructansucrases for oligosaccharides and the α- and β-amylases and amyloglucosidases for starches [13, 22–27]. Different from dairy isolates, clinical and oral L. rhamnosus were found to possess l-fucisidase, which enables them to utilize various fucosyl-glycoconjugates on epithelia cell surface and intestinal mucin [22]. Lactobacilli possess rich and redundant transport systems for a variety of mono- and disaccharides, and to a less degree, trisaccharides, which include the high-affinity, sugar-specific phosphotransferase transporter systems (PTSs). Like many other bacteria, some of the PTSs possess typical enzyme II with complete subunits, while others lack one or more of the components (incomplete PTSs) [5, 13, 24]. The number of the PTSs varies significantly between different Lactobacillus sp. (Table S1) [23]. For instance, L. rhamnosus 1.0320 has the most at 51 (with 33 complete PTSs and 18 incomplete PTSs) (Huang and Wen, personal communication), while the least was found in heterofermenters L. brevis ATCC 367 (five incomplete PTSs only) and L. reuteri F275 (four incomplete PTSs only) [28]. Besides, lactobacilli also contain non-sugar-specific ABC transporters that the bacteria utilize to take up different substrates in the expense of ATP [28, 29]. For example, L. acidophilus possesses a four-gene operon encoding a LacI-type regulator, a four-component ABC transporter, a fructosidase and a sucrose phosphorylase, respectively, which was found to function similarly as the multiple sugar metabolism (MSM) system of S. mutans [30]. Lactobacilli also possess diverse groups of glucosyltransferases (Gtfs) [31–34], including glycogen synthase and glycogen phosphorylase for glycogen biosynthesis [13]. Glycogen is one of the major carbohydrate storage mechanisms for lactobacilli, a capacity believed to allow them advantage in competition over others [35]. Lactobacilli also produce extracellular polysaccharides (EPS) that are mostly α [1, 4]-linked glucose polymers and some with α [1, 6] linkages [22, 31]. Recent studies by Caufield et al. showed that about half of the L. fermentum analysed possesses the genes for the extracellular glucans, but they were remarkably absent in other species associated with severe childhood caries [5]. No evidence suggests that lactobacilli synthesize any major adhesive EPS from sucrose [8, 36], which in S. mutans is predominantly α [3,1]-linked and known to play a central role in its adherence and cariogenicity [37].

Carbohydrate metabolism in lactobacilli is highly regulated by substrate induction and catabolite repression in response to substrate availability and presence of other more readily metabolizable carbohydrate sources [29, 38]. In addition, environmental conditions, such as oxygen tension, temperature and probably presence of other bacterial species, can also have an impact on the regulation of carbohydrate metabolism. Like S. mutans, the carbon catabolite repression protein (CcpA) in lactobacilli is a multi-functional regulator that plays a central role in regulation of carbohydrate metabolism, including modulation of the fermentation pathways from homolactic fermentation to heterofermentation in response to various environmental conditions including sugar source and availability and aeration [39–44]. There is evidence that certain species of lactobacilli displayed distinctive metabolomics profiles when they were grown together with S. mutans, when compared to the respective mono-species cultures [45], although details on the mechanisms that regulate the metabolic pathways remain largely unknown.

Acid tolerance and acid-tolerance responses

Lactobacilli are well known for their ability to rapidly break down sugars to acidic end-products, of which at least half is lactic acid. Consequently, the pH value of their immediate environment can quickly plummet to levels where the metabolic processes including glycolysis and bacterial cell growth become inhibited and even completely stopped, although differences in culture pH and the ability to cope with the environmental pH exist among different species [45–47]. Since the work of Stephan and Hemmens [48], numerous studies have shown not only the acidogenic capacities of lactobacilli but also their ability to tolerate weak acids and low pH environment [45, 49–51]. Comparing to S. mutans and members of the mutans streptococci, lactobacilli were shown to be capable of growing at pH 4.0 [52]. As illustrated using the acid-killing assays, L. casei is also significantly more acid tolerant than S. mutans (Fig. 1) [45]. Unlike S. mutans that reduced its survival rate by >5 logs after 60 min at pH 2.8, L. casei survived the same pH for a long period of time. It has been suggested that lactobacilli possess multiple mechanisms to cope with the acid stresses, including passive acid efflux via the cell membrane, active proton pump via F₁F₀-ATPase, sodium-proton antiporters, and various alkali production pathways such as the glutaminase and the arginine deiminase, whose ammonia product can neutralize protons [24, 47] (Table S1). In addition, several lactobacilli also have the glutamate decarboxylase (GAD) system, one of the essential acid tolerance systems in many Gram-negative and Gram-positive bacteria [53–55], consisting of the GAD and a glutamate/gamma-aminobutyric acid (GABA) antiporter. With the GAD system, GAD catalyses the decarboxylation of glutamate to produce GABA. The antiport of glutamate and GABA consumes protons elevating intracellular pH and contributing to a proton motive force for ATP synthesis.

Fig. 1.

S. mutans and L. casei in dual-species cultures displayed altered survival rates as compared to those grown alone, when subjected to acid- (a) and hydrogen-peroxide- (b) killing assays. For acid-killing assays, L. casei was incubated in 0.1 M glycine buffer, pH 2.0 for periods as indicated, and S. mutans was incubated in buffer of pH 2.8 for the same periods. For hydrogen-peroxide-killing assays, S. mutans and L. casei were incubated in glycine buffer containing 0.2% hydrogen peroxide. *, P<0.001 vs the respective mono-species cultures. (From Wen et al., 2017. Front. Cell. Infect. Microbiol. 7 : 524. doi: 10.3389/fcimb.2017.00524).

Lactobacilli are also capable of launching adaptive acid-tolerance response, which is featured with enhanced acid tolerance, following initial exposure to a low pH condition [45, 56] (Fig. 1). Typically, when compared to cultures grown in medium with buffered pH, cultures grown in regular medium will have a reduced culture pH and a significantly enhanced survival rate when subjected to acid-killing assays. Adaptive acid-tolerance responses often result from elevated expression and activity of the F₁F₀-ATPase, molecular chaperones such as DnaK and GroEL, enzymes such as Clp protease, excinuclease, involved in repair and protection of DNA and proteins, and enzymes such as squalene synthase involved in membrane biosynthesis and thus acid efflux [47, 57–59].

Various factors have been shown to play a role in regulation of acid-tolerance response, including GadR, GlnR and two-component signal transduction systems [60–62]. GadR in L. brevis functions as a positive regulator of GAD and glutamate/GABA antiporter, thus the GABA conversion from glutamate, and is expressed at a much higher level in the strains isolated from acidic habitats [61]. Besides, nitrogen regulator GlnR is also found to play a role in glutamate-dependent acid resistance by modulating GABA conversion from glutamate [62]. In L. elbrueckii subsp. bulgaricus, the two-component signal-transduction system HPK1/RR1 was shown to regulate the acid adaptation ability of the bacterium by means of many pathways, including the proton pump-related protein, classical stress-shock proteins, carbohydrate metabolism, nucleotide biosynthesis, DNA repair, transcription and translation, peptide transport and degradation, and cell-wall biosynthesis, etc [58, 60, 63, 64].

Biofilm formation and regulation

From early studies of human volunteers, selected lactobacilli were found to possess low affinity for the tooth surface [10]. It was found that mechanical retention either directly or indirectly by incorporation of bacterial cells in food remnants play an important role in lactobacilli establishment; and that the presence of teeth and especially, carious lesions may be required for lactobacilli to establish and maintain on the tooth surface in significant numbers [10]. In a recent article, Caufield et al. also postulated that a ‘retentive niche’, which includes food remnants and early plaque biofilms and provides physical trapping, retainment and containment, is required for sustained colonization [5].

Many of the Lactobacillus strains isolated from dental plaque, comprising different major species, were examined using animal models, including a gnotobiotic rat model, and were found to be moderately or highly cariogenic when the animals were fed with a diet rich in sucrose, but not when fed with glucose and/or starch [8, 9, 11, 65]. However, the level of carious lesions in animals infected with these lactobacilli strains was significantly lower, when compared to those infected with S. mutans [11].

In vitro model studies of different lactobacilli species, mostly laboratory strains, have also showed that lactobacilli form biofilms poorly, but differences also exist between different species [45, 66]. Using an artificial mouth system, Filoche et al. [67] found that biofilm formation by L. rhamnosus and L. plantarum was poor. In 96-well plates, Wen et al. showed that of the most prevalent species analysed, all showed limited ability to form biofilms, although differences exist between the major species tested, with L. fermentum forming the best biofilms while the least being detected with L. gasseri (Fig. 2) [45, 66]. Differences in growth rates and final culture optical densities were also observed when using different carbohydrate sources and culture media, and improvement in growth was observed when a higher amount of sucrose was supplied in the culture medium, which is consistent with early animal model studies [8, 9]. Unlike S. mutans, however, none of the tested Lactobacillus strains displayed any major increases in biofilm formation, when grown in sucrose-containing medium as compared to that without; and none produced any water insoluble, adhesive EPS as the S. mutans did when grown under similar conditions [8, 9, 36].

Fig. 2.

Lactobacilli biofilms when grown alone and together with S. mutans under static (a) and continuous flowing (b) conditions. (a) shows 48 h biofilms of L. gasseri (Lg), L. fermentum (Lf), L. salivarius (Ls) and L. rhamnosus (Lr) in mono-species and dual-species with S. mutans (Sm) grown on glass slides vertically deposited in 50 ml Falcon tubes, with * and # indicating statistical difference at P<0.001 and 0.05, respectively, when compared to the respective mono-species biofilms. (b) shows 5 day biofilms of S. mutans (Sm) and L. casei (Lc) in mono- and dual-species model grown on glass slides in a drip flow biofilm reactor, with * indicating statistical difference at P<0.001 relative to its mono-species biofilms. (From Wen et al., 2017. Front. Cell. Infect. Microbiol. 7 : 524. doi: 10.3389/fcimb.2017.00524).

Biofilm formation is initiated by bacterial cell-surface interactions, and the cell-surface structure plays a vital role in colonization and persistence. Much of the current knowledge on lactobacilli cell-surface interactions is attributed to the studies of probiotic Lactobacillus isolates of the gut. Various components on the cell envelop are implicated as mediators of bacterial adherence, which include cell-wall-associated polysaccharides and teichoic acids and lipoteichoic acids, surface-layer proteins (S-layers), surface-associated adhesins, and multi-functional moonlighting proteins such as GroEL, enolase and collagen-binding proteins [68]. Many Lactobacillus sp., but not all, have a S-layer, which is a layer of two-dimensional crystalline of repeating proteinaceous subunits that covers completely the outermost surface of the cell envelop and is responsible for the surface hydrophobicity [69]. In a number of studies, the loss of S-layer has been shown to result in reduced bacterial adherence to different surfaces, although the direct role of the S-layer proteins in bacterial adherence and biofilm formation remains unclear. Lactobacilli also possess LPXTG proteins, which are anchored to the cell envelop by sortase enzymes, including the serine-rich adhesins, although the number of these anchored proteins differ between different species [13, 70–72]. Lactobacilli serine-rich proteins, such as SRRP in probiotic L. reuteri [70], share similarities with and differences from the counterparts in other Gram-positive bacteria such as Fap1 of S. parasanguinis and GspB of S. gordonii whose roles in bacterial adherence and biofilm formation have been well documented. The LPXTG proteins in some probiotic lactobacilli have been shown to play an important role in the interactions with their habitat, including mucus-binding and the associated microbial communities. Certain Lactobacillus sp., including L. rhamnosus but not L. casei , are also piliated, and the pilins are thought to be involved in mucin-binding and inter-cellular signalling [13, 73, 74]. However, currently no further information is available concerning the roles of such proteinaceous fibres in bacterial colonization and biofilm formation. Like gut lactobacilli [68], many Lactobacillus sp. from the oral cavity, such as L. casei/paracasei, L. gasseri, L. rhamnosus, L. fermentum, L. salivarius, L. oris and L. vaginalis strains isolated from patients with severe early-childhood caries, also contain genes encoding binding proteins to type I collagens [5], which become exposed during the dentinal caries progression. Consistently, majority of Lactobacillus strains tested have showed ability to adhere to surfaces coated with type I collagen, and such adherence can be competitively inhibited with collagen [75], which is consistent with a role of Lactobacillus sp. in root and/or coronal caries. This is in contrast with their cariogenic partner S. mutans, of which only about 17 % of the isolates contain the cnm and cbm genes encoding collagen-binding protein [76].

Inter-species interactions on Lactobacilli biofilm formation

Emerging data suggest that inter-species interactions in the plaque microbiota are central drivers of homeostasis and dysbiosis and thus are the critical determinants of oral health and disease development [77, 78]. Multiple mechanisms function in interactions between different species in the oral microbiota, including synergistic mechanisms such as adhesin-receptor-mediated physical contact and cross-feeding on nutrient utilization [78]. It is well documented that in in vitro models, some Lactobacillus sp. can drastically increase biofilm formation when co-cultivated with Actinomyces sp. and S. mutans [45, 66, 67]. When co-cultivated in an artificial mouth system with Actinomyces naeslundii and A. gerencseriae, L. rhamnosus increased biofilms by as many as 20 times and L. plantarum biofilms increased by up to sevenfold, when compared to their respective mono-culture biofilm [67]. In 96-well culture plates, biofilm formation by L. casei, L. gasseri and L. rhamnosus was increased by almost 2-logs after 48 h when growing in a dual-species model with S. mutans [45, 66] (Fig. 2). From recent studies by Wen et al. [45] and Huang et al. [36], the impact of inter-species interactions on biofilm formation appears to be more species-specific. In contrast, L. fermentum in co-cultivation with S. mutans decreased biofilms by >tenfold, while no significant differences were measured with L. salivarius ssp. salivarius [36, 45, 66]. Similar results were obtained on hydroxylapatite discs and glass slides, two commonly used in vitro tooth models, and when grown under continuous flowing conditions [45] (Fig. 2b). However, no such effects were measured when they grew with Veillonella parvula and V. dispar [45, 67].

In an effort to uncover the mechanisms underlying the enhanced biofilm formation, Liao et al. showed that deficiency of multi-functional adhesin P1 and glycosyltransferase B (GtfB) in S. mutans almost completely demolished the ability of S. mutans to facilitate L. casei biofilm formation [45] (Fig. 3). GtfB is known for its ability to synthesize adhesive glucans from sucrose, but it can also function as an adhesin and directly bind to other bacteria such as Candida albicans [79]. In an in vitro adherence assay, purified native GtfB protein was able to bind to L. casei cells, and when the GtfB-bound bacterial cells were incubated with sucrose, synthesized adhesive glucose polymers that were able to bind to S. mutans (Fig. 4). In support of the mechanical retention theory [5, 10], the results further suggest that biofilms of the early colonizers and especially, their extracellular polymers, which include the rich polysaccharides and deoxyribonucleic acids [80, 81], play an important role as a scaffold in the establishment and retention of Lactobacillus sp. Besides, the results also provided evidence that other factors including the intercellular interactions mediated by adhesins such as P1 and GtfB and their receptors also actively facilitate the adherence of Lactobacillus sp. and the development of inter-species multi-cellular clusters. Further studies on the adhesins and the binding ligands in S. mutans–Lactobacillus interaction will shed new light on whether such intercellular interactions are species-specific.

Fig. 3.

L. casei biofilm formation with S. mutans mutants. L. casei (Lc) was grown alone or together with S. mutans wild-type UA159 (UA) and its mutants deficient of P1, GtfB, GtfC, GtfBC or Ftf on glass slides for 48 h. Data are expressed as the ratio of L. casei biofilms (in colony-forming-units) in dual-species over those in mono-species, with * indicating significant differences at P<0.001. (From Wen et al., 2017. Front. Cell. Infect. Microbiol. 7 : 524. doi: 10.3389/fcimb.2017.00524).

Fig. 4.

Visualization of glucans synthesized in situ by GtfB adsorbed on L. casei and S. mutans binding to L. casei with and without glucans. L. casei was incubated with GtfB or buffer, and following washes, exposed to sucrose for 1 h, and glucans were imaged using a confocal microscope. (a) L. casei (in green) with GtfB in buffer alone; (b) L. casei with bound-GtfB incubated with sucrose showing rich glucans (in red) engulfed in green L. casei cells. (c) S. mutans (in blue) incubated with green L. casei with no glucans on surface; and (d) S. mutans (in blue) incubated with L. casei coated with GtfB glucans (in red). Images were obtained using an upright Olympus confocal microscope with a 100 x oil objective. (From Wen et al., 2017. Front. Cell. Infect. Microbiol. 7 : 524. doi: 10.3389/fcimb.2017.00524).

It has been known that a synergistic relationship exists between L. bulgaricus and S. thermophilus that is featured with stimulated growth and acidification of both during milk fermentation. When grown in a mixed-species consortium in rich medium (i.e. brain heart infusion), both Lactobacillus sp. and S. mutans showed altered behaviours, including enhanced acid production and acid tolerance responses [45]. When co-cultivated with S. mutans, all Lactobacillus species, except L. fermentum , had a reduced cultural pH than the respective mono-species cultures after 24 h. Metabolomics analysis showed that selected metabolites such as succinic acid in the spent culture medium of the L. casei-S. mutans dual-species cultures were significantly different from those in both S. mutans and L. casei mono-species cultures [45]. There is also evidence that growth in dual-species with S. mutans led to alterations in metabolic dynamics including changes in amino acid biosynthesis and carbohydrate metabolism [36]. However, currently there is no definitive information concerning how Lactobacillus sp. in a mixed-species community alter their metabolic dynamics.

L. casei in dual-species with S. mutans also displays a drastic enhancement in resistance to acid and low pH, as compared to its mono-species cultures. When incubated in a glycine buffer of pH 2.0, 0.1 M, the survival rate of the mono-species cultures reduced by >3 log after 30 min. In contrast, the survival rate of those grown in the dual-species cultures with S. mutans reduced by only 1-log when analysed under the same conditions. Similar trends, although in a much less degree, were also observed with S. mutans, which is known for its ability to launch adaptive acid tolerance responses [57]. However, it is currently unclear how such physiological characteristics may affect each other and ultimately the composition and the cariogenicity of the plaque microbiota.

Probiotic Lactobacilli and their potential in oral health

Lactobacilli are known to produce a variety of compounds including acids and bacteriocins that exert direct antimicrobial activities toward competing bacteria in a community [82] (Table S1). Food-borne lactobacilli have long been utilized for food preservation through production of weak acids and bacteriocins. Probiotic lactobacilli are widely used either alone or with other probiotic species for various health benefits including displacement of putrefactive organisms and restoration of microecological homeostasis. Several Lactobacillus species, including L. salivarius, L. fermentum and L. paracasei, have also been studied for their potential against cariogenic bacteria like S. mutans and dental caries [83–90], although the idea of lactobacilli being beneficial from dental cariogenesis point of view remains controversial. Nevertheless, antimicrobial effects against mutans streptococci and some other oral bacteria in both in vitro and in vivo models are well documented [8, 11, 67, 83–85, 88, 90, 91]. Such antagonistic effects have been measured with reduction of bacterial adherence, glucan production, and biofilm formation in vitro and by reduction of caries and caries severity in vivo.

When compared to the mono-species cultures, S. mutans in dual-species model with L. casei under aerobic conditions also displayed a dramatic reduction in survival rate against hydrogen peroxide challenge and consistently, had an altered transcription profile [45, 66]. Among the down-regulated genes are the ones for GtfB and alternative sigma factor ComX, which regulates competence development, bacteriocin production and biofilm formation, while the up-regulated genes include several involved in oxidative stress tolerance responses, although the factors that trigger such alterations remain unknown. In a tri-species in vitro model including S. mutans, C. albicans and probiotic Lactobacillus , Zeng et al. recently found that of the probiotic Lactobacillus strains tested, L. plantarum demonstrated superior inhibition on the growth of C. albicans and S. mutans and disruption of virulent biofilm formation with reduced bacterial cell and EPS components [90]. Inclusion of L. plantarum in the community was shown to disrupt the S. mutans and C. albicans cross-kingdom interactions and cause down expression of genes involved in the aforementioned processes including carbohydrate metabolism and EPS production in both S. mutans and C. albicans and resistance to antifungal medication in C. albicans. In addition, Lactobacillus genes for production of antimicrobial peptide plantaricin were also significantly upregulated. Interestingly, such anti-microbial effects were measured only when the community was grown in high-sucrose (1%) conditions but not in low-sucrose (0.1%) conditions. Acid production from sugar fermentation and the pH dependent antimicrobial activity of plantaricin were thought to be part of the contributing factors, since plantaricin is most active at pH 5.0.

Several Lactobacillus sp. were found to produce hydrogen peroxide, although relative to some other oral bacteria, such as S. sanguinis and S. gordonii [92], the level of hydrogen peroxide by some of the Lactobacillus sp. such as L. fermentum was found to be extremely low under the conditions studied. Like S. sanguinis and S. gordonii [92], hydrogen peroxide production by Lactobacillus sp. also appears to be regulated in response to environmental conditions including availability of fermentable sugars [93, 94] (Huang and Wen, personal communication) and probably the presence of other different bacterial species [36]. Currently, little information is available concerning the genetics and genetic regulation of hydrogen peroxide production in lactobacilli.

L. fermentum and several other Lactobacillus sp. were recently reported to possess nitric oxide synthase activity which utilizes l-arginine to produce nitric oxide [95, 96]. In addition, some L. fermentum sp. were also shown to have nitrite reductase that utilizes nitrite to generate nitric oxide [96]. A reactive nitrogen species, nitric oxide can react with superoxide anion (O₂ ^-) forming a potent oxidant peroxynitrite (ONOO^-), which is a strong oxidant with a broad spectrum of antimicrobial activity [97, 98]. However, no nitric oxide synthase gene has been identified in any of these Lactobacillus strains, and it is currently unknown if nitric oxide production is species-specific.

It is becoming clear that while many Lactobacillus sp. produce various antimicrobial activities, the efficacy differs between different species and under different environmental conditions [78, 82, 90, 93]. How production of hydrogen peroxide, nitric oxide and/or bacteriocins in L. casei and other Lactobacillus sp. is regulated in the complex plaque microbiota and what impact these antimicrobials possess on the microecology and ultimately oral health await further investigation.

Summary

Lactobacillus sp. are major contributors to dental caries, especially the development of advanced caries lesions in both adults and children. Unlike their cariogenic partner mutans streptococci, Lactobacillus sp. alone does not adhere the tooth surface efficiently. However, in the presence of S. mutans and some other primary colonizers, their ability to establish on a tooth surface can be significantly enhanced, although differences exist between the different species. Mechanical retention, including trapping in food remnants and plaque biofilms and especially the glucan scaffold of S. mutans, is a major factor contributing to Lactobacillus establishment. Besides, adhesin-receptor mediated active intercellular contact and probably metabolites associated interactions are also involved in the S. mutans-facilitated Lactobacillus adherence and persistence. On the other hand, Lactobacillus sp. also produce various broad-spectrum antimicrobials, including weak acids and bacteriocins. There is evidence that production of the antagonistic factors is regulated in response to environmental cues including presence of other bacterial species. It is hypothesized that as the lactobacilli grow to certain degree, such antagonistic activities become detrimental to the community, especially those in close proximity like S. mutans , which in turn weakens their own ability to maintain at the sites. Thus, the inter-species interaction between S. mutans and Lactobacillus sp. is a double-edged sword in terms of the development of plaque microbiota. If it is true, it also explains why neither S. mutans nor Lactobacillus is always present at caries sites [4, 97, 99]. Further studies will be needed to better understand the molecular mechanisms that govern the interactions between S. mutans and major species of Lactobacillus and how environmental conditions influence the inter-species interactions and ultimately, oral health and disease.