Dental Plaque Biofilms
By: Anna Frutiger
Introduction
Dental plaque is commonly known as the primary cause of dental caries and other oral infections. Rightly so, as despite the ever increasing knowledge in oral health care, the average adult in the United States has between 10 and 17 decayed, missing or filled permanent teeth [4]. Additionally, the majority of the population has at least minor gingivitis, with a much smaller percentage suffering from moderate to severe periodontitis [4]. Dental plaque, which exists not only on the tooth surface but also under the gums, can be defined as a diverse community of microorganisms in the form of a biofilm. The microorganisms bind tightly to one another in addition to the solid tooth surface by means of an extracellular matrix consisting of polymers of both host and microbial origin [1][2]. Only recently has dental plaque begun to be considered a biofilm, which has further contributed to a better understanding common oral diseases and has helped to find the best ways to prevent and control these for the future [3].
As a biofilm, dental plaque exhibits an open architecture much like that of other biofilms. The open architechture, which consists of channels and voids, helps to achieve the flow of nutrients, waste products, metabolites, enzymes, and oxygen through the biofilm[4]. Because of this structure, a variety of microbial organisms can make up biofilms, including both aerobic and anaerobic bacteria. The microbial composition of dental biofilms includes over 700 species of bacteria and archaea, which all exist in a relatively stable environment called microbial homeostasis [2]. Dental plaque biofilms are responsible for many of the diseases common to the oral cavity including dental caries, periodontitis, gingivitis, and the less common peri-implantitis (similar to periodontitis, but with dental implants), however biofilms are also present on healthy teeth as well [5].
The microbial make-up of the normal plaque biofilm, however, differs immensely from the biofilm formed in carious regions and in the sub-gingival regions associated with periodontal disease. Because bacteria in dental biofilms (and other biofilms) express an entirely different set of genes than free-floating bacteria, they are of particular interest to researchers and thus much is currently being done to explore the diverse nature of these microbial structures. The biofilm state brings about major changes in bacteria behavior such as interactions with other microbes and the host, in addition to their response to environmental conditions [5]. Because of these behavioral changes, in addition to the microbial differences present between healthy and diseased biofilms, much of the research currently being done is in relation to plaque-related diseases and cell-cell communication within the dental biofilm and the oral cavity. This is of major concern to the medical community, because it is being realized that oral pathologies have a major impact not only on the health of the oral cavity, but also on the overall health of the human body.
Formation of Dental Biofilms
The formation of dental plaque biofilms includes a series of steps that begins with the initial colonization of the pellicle and ends with the complex formation of a mature biofilm. Dental plaque biofilms exist on a variety of tooth surfaces including fissues, smooth surfaces and gingival crevices, however they are most likely to be seen in their mature state in more stagnant sites like fissures and crevices, as these places provide protection from the forces of removal, like a toothbrush [1][5]. Additionally, through the growth process of the plaque biofilm, the microbial composition changes from one that is primarily gram-positive and streptococcus-rich to a structure filled with gram-negative anaerobes in its more mature state [6].
Adsorption of Host and Bacterial Molecules to the Tooth Surface
The first step in plaque biofilm development is the adsorption of host and bacterial molecules to the tooth surface. Within minutes of tooth eruption or a cleaning, pellicle formation begins, which can be defined as a thin coat of salivary proteins [3]. The pellicle acts like an adhesive by sticking to the tooth surface and encouraging a conditioning film of bacteria to attach to the pellicle [1]. This conditioning film directly influences the initial microbial colonization, and continues to adsorb bacteria to the tooth surface.
Healthy tooth surfaces and gingivae tend to only be associated with this first phase of biofilm development. It consists of an initial few layers (1-20) of mostly gram-positive cocci bacteria, followed by some gram-positive rods and fillaments and a very small amount of gram-negative cocci. The gram-positive cocci species involved in this conditioning layer include, but are not limited to, Streptococcus mutans, Streptococcus mitis, Streptococcus sanguis, Streptococcus oralis, Rothia dentocariosa, and Staphylococcus epidermidis. The gram-negative rod and filament species include Actinomyces viscosus, Actinomyces israelis. Actinomyces gerencseriae and the Corynebacterium species. Veillonella parvula and the Neisseria species make up some of the few gram-negative cocci, which are aerobes or facultative aerobes and are able to adhere to the non-exfoliating hard tooth surfaces [5]. This early composition of the biofilm is able to withstand many of the frequent mechanisms of the oral cavity that contribute to bacterial removal such as swallowing, nose blowing, chewing, and salivary fluid outflow. The early colonizers are also able to survive in the high oxygen concentrations present in the oral cavity, without having much protection from other bacteria [5]. Thus, this thin, initial biofilm is almost always present on the tooth surface as it forms immediately after cleaning.
Passive Transport of Oral Bacteria to the Tooth Surface
Following pellicle formation, there is passive transport of oral bacteria to the tooth surface, which involves a reversible adhesion process [2]. By using weak, long-range physicochemical interactions between the pellicle coated tooth surface and the microbial cell surface, an area of weak attraction is formed that encourages the microbes to reverse their previous adhesion to the pellicle and come off the tooth surface (hence the term "reversible adhesion") [1]. This reversible adhesion then leads to a much stronger, irreversible attachment, as short-range interactions between specific molecules on the bacterial cells and the complementary receptor proteins on the pellicle surface occur. Because many oral microbial species have multiple adhesion types on their cell surface, they can thus participate in a plethora of interactions with both other microbes and with the host surface molecules [1].
Co-Adhesion of later colonizers to already attached early colonizers
The co-adhesion of the later colonizers to the already present biofilm continues to involve many specific interactions between bacterial receptors and adhesions. These interactions continue to build up the biofilm to create a more diverse environment. Further, the development of unusual morphological structures like corn-cobs and rosettes are formed during this phase [1].
The many interactions between these diverse bacterial species begin to create a number of synergistic and antagonistic biochemical interactions. For example, bacterial residing in food chains may help to contribute metabolically with other bacteria if they are located physically close to one another. Similarly, when obligate anaerobes and aerobes are involved in co-adhesion, these interactions can ensure the anaerobic bacteria’s survival in the oxygen-rich oral cavity [1].
Multiplication of the Attached Microorganisms
Eventually, the bacterial cells continue to divide until a three-dimensional mixed-culture biofilm forms that is spacially and functionally organized. Polymer production causes the development of the extracellular matrix, which consists of soluble and insoluble glucans, fructans, and heteropolymers [1]. This matrix is one of the key structural aspects of the plaque biofilm, much like that of other biofilms. Biofilms such as this are very thick, consisting of 100-300 cell layers. The bacterial stratification is arranged according to metabolism and aerotolerance, with the number of gram-negative cocci, rods and filaments increasing as more anaerobic bacteria appear [5]. As the biofilm thickens and becomes more mature, these anaerobic bacteria can live deeper within the biofilm, to further protect them from the oxygen rich environment within the oral cavity.
Inter-species Communication
The discovery that communication between cells in biofilm communities occurs has been key in understanding how dental plaque acts as a single unit. Communication can occur in a variety of ways, including gene expression, cell-cell signaling (ex. quorum sensing), and antibiotic resistance, among others. Specific bacteria within the biofilm community are able to act with other species to both help and impair the host, in addition to providing a positive cooperation between the different species of the biofilm [5]. Further, the patterns observed of microbial colonization and coaggregation appear to be primarily uni-directional, thus indicating that many of the bacterial species in dental biofilms require an environment that has been previously habituated by other microbiota in order to properly colonize [5]. These specific cell-cell interactions have proven to be very important topics of current research involving dental plaque biofilms.
Sigmund Socransky and Anne Haffajee have been able to explain much of the unique colonization patterns and positive cooperation observed in plaque biofilm. The method that has helped explain this is one involving “clustered” groups of bacteria, where each cluster is created based on nutritional and atmospheric environments [5][7]. Each of the clusters is said to influence the other clusters, in addition to being related to a specific periodontal state, thus showing that these microbes are very closely associated with one another [5]. Socransky and Haffajee found that within different periodontal states, either all or none of the species belonging to a particular cluster were found. Very few individual species or pairs of species were found, which further helped show that biofilms were a community of microbes. Certain clusters were also found to interact particularly well with other specific clusters. For example, microbial species found in the red cluster were rarely observed without the presence of the orange cluster species [5]. Because of these associations found by Socransky and Haffajee and their cluster analysis, it provided further knowledge to idea that the microbial communities in plaque biofilms were involved in a great deal of inter-species communication.
One such example of this involves the gram-negative, anaerobic bacteria Porphyromonas gingivalis. P. gingivalis is a predominant pathogen found in severe cases of adult periodontitis that attaches to the tooth surface after the initial colonization of the gram-positive Streptococcus species. The colonization of P. gingivalis is key in the transformation of the bacterial biofilm from a commensal plaque to the pathogenic form observed in periodontitis [6]. Its colonization is also dependent on its attachment to oral surfaces, which is accomplished via a fimbriae-mediated adhesion. The fimA gene encodes for this fimbriae subunit protein, which can be regulated environmentally [6]. Interestingly, the P. gingivalis fimA gene expression was found to be severely downregulated by the unrelated, gram-positive Streptococcus cristatus CC5A, which can be found in the initial colonization of dental biofilms. By interfering with the gene that encodes for the fimbriae-subunit protein, S. cristatus is able to prevent P. gingivalis fimbriae attachment to the biofilm, thus resulting in an easier removal of P. gingivalis from the biofilm by salivary flow. After further testing, it was discovered that the S. cristatus signaling activity was specific to the fimA gene, and is also associated with a 59-kDa surface protein. The size of the surface protein, however, suggests that it is inherently distinct from the signaling peptides that are secreted via other gram-positive bacteria [6].
Through these findings, it was clear that some signaling mechanisms between P. gingivalis and S. cristatus were occurring, which were preventing the colonization of P. gingivalis on the plaque biofilm. Of course, it is likely that other microbial species also contribute to the upregulation of this gene, and thus may negatively affect the downregulation of fimA caused by S. cristatus. It is also known that Fusobacterium nucleatum is involved with some type of cell-sigaling interaction with P. gingivalis, but in a different way. Rather than affecting fimbriae attachment, F. nucleatum is instead required for the P. gingivalis aggregation with the facultative aerobes already present on the biofilm [5]. This directly shows that inter-species communication between the different microbial species on dental plaque biofilm is required for proper biofilm maturation and is thus directly involved in oral disease propagation as well. This research should give us a better understanding of the regulation of P. gingivalis via cell-cell interactions within the dental plaque biofilm.
Yet another interesting aspect of cell-cell signaling on dental plaque biofilm deals with quorum sensing in Streptococcus mutans. Quorum sensing, in the general sense, is a mechanism that bacteria employ to control gene expression in response to the population size [8]. While it had been previously known that quorum sensing in gram-positive bacteria regulates genetic competence development, it was unclear what the involvement of this was during signaling in biofilm initiation and formation. In particular, it was unclear whether biofilm formation of S. mutans, which has particular importance in dental plaque biofilms, was involved in any type of coordinated activity through cell-cell communication [8]. By mutating various aspects of the quorum-sensing and signal-transduction systems, it was discovered that the competence-stimulating peptide (CSP) was necessary for proper biofilm formation of S. mutans. In particular, the comC mutant, which was unable to produce or secrete CSP, resulted in biofilms formed with an altered architecture. Additionally, comD, comE and comX mutants also resulted in abnormal biofilm formation, as they were formed with a reduced biomass. Because four different CSP mutants caused an improper biofilm formation by S. mutans, it is likely that CSP affects multiple signal-transduction pathways. It was also shown that this CSP-mediated quorum-sensing causes the transformation frequency of S. mutans be 10- to 600- fold greater in biofilms than in planktonic cells [1][8]. This shows that the quorum-sensing pathway in S. mutans needed for genetic competence is key in the proper formation of dental plaque biofilms [8].
Microbial Biofilm Composition of Oral Disease States
Many studies have been performed to attempt to determine which bacterial species are directly involved in oral pathology. Because many of the plaque-mediated oral diseases occur at regions already containing an extremely diverse microflora, it is difficult to specifically determine which of these species are pathogenic. Additionally, the bacterial traits associated with cariogenicity, such as acid production, acid tolerant, and intracellular and extracellular polysaccharide production, point to more than one single bacterial species [2]. We do know, however, that many of the desirable bacterial species include Streptococcus sanguis, S. gordonii, S. oralis, and the Actinomyces species, in addition to other related bacteria with a low acid tolerance [9]. Therefore, it seems that healthy dental biofilm microflora consists of species with limited tolerance for acid, as we do know that the cause of dental caries are bacteria with a very high acid tolerance.
Caries
Despite the lack of exact knowledge on every pathogen involved in caries production, the factors responsible for the microbial homeostasis within the biofilm are known and recognized [2]. The initial change in environment is due to an increased amount of fermentable carbohydrates in the diet of the host. The anaerobic, acid-producing bacteria present in the plaque biofilm thus produce an increased amount of acid, and thus the pH of the biofilm is lowered [2][9]. When the pH drops, there is an increase in acid-tolerant bacteria, as they are the only ones that can survive and perform glycolysis in such an acidic environment. Some of the more common bacterial species responsible for this include Streptococcus mutans, S. sorbrinus, and Lactobacillus casei which can perform glycolysis at a pH level as low as 3.2 [9]. At this low, acidic pH, these bacteria are capable of demineralizing the tooth enamel, with greater degrees of acidity causing a faster rate of demineralization. Of course, the acidification is caused by sugar ingestion, so if this ingestion is only occasional, the pH value of the biofilm will rise again and alkalinization and remineralization of the enamel can occur. Caries will result, however, if the acidification-demineralization phase is more damaging than the alkalinization-remineralization phase can fix the damage [9]. In short, when sugar is ingested and acid is produced as a metabolic biproduct, those bacteria that can survive in these acidic environments will thrive. These are the key pathogens to caries production. It is important to recognize, however, that some of the known bacterial species involved in caries production, like S. mutans, are also present in healthy plaque biofilm, in addition to also being absent from some sites of caries production. Thus, we know that there is not one particular bacterial species responsible for caries production, but a collection of several, exhibiting similar characteristics [2].
Periodontitis and Peri-implantitis
Some sort of periodontal disease affects a majority of the adult population of the United States. Because of this, it is of great importance to the medical and dental community and can thus be considered a public health problem [5]. Periodontitis, if not treated early, can lead to alveolar bone and tooth loss. Periodontitis is defined by deep pockets formed between the tooth surface and the gum [9]. This deep pocket is easily colonized by microbes due to the small dentinal tubules and enamel fissues that lead directly into the gums from the open space of the mouth. This area is incredibly difficult to reach via typical oral health care mechanisms (tooth brush, floss, etc.), which often leads to the diseased states of gingivitis or periodontitis, which has varying levels of severity.
Much of the microflora existing in these deep periodontal pockets are gram-negative anaerobes, with a very diverse population of spirochetes. In the early stages of periodontal disease, known as gingivitis, the initial microbial colonization of the plaque biofilm seems to involve members of the yellow, green and purple “clusters” (see figure above)[7]. Secondary colonization occurs with members of the orange and red clusters, and these become more dominant. The increased levels of the red and orange cluster bacteria lead to proliferation by members of all the original and secondary colonizing species. At a certain point, the organisms must disperse to other locations within the oral cavity to ensure survival. A study found that spirochetes and P. gingivalis were more prevalent in diseased sites of diseased patients than in healthy sites of diseased patients. It was also found that the organisms were also found more frequently in health sites of diseased patients than in healthy sites of healthy patients, which is evidence for the dispersal mechanism previously mentioned[7].
As the periodontal disease gets more severe, checkerboard DNA-DNA hybridization experiments have been performed to give a better idea of the species involved in periodontitis. Further analysis has been performed from this, to show that the most prevalent bacterial species involved in periodontitis is Actinomyces naeslundii.
Peri-Implantitis. These tests were performed on 40 species of which there were molecular probes. Unfortunately, there is no real way to find every single bacterial species involved in the plaque biofilm of periodontitis patients [7].
Peri-implantitis is very similar to periodontitis, however, it does differ in some aspects. Because dental implants are not surrounded by periodontal ligaments, they have differing biomechanics and defensive cell-recruitment [5]. Peri-implantitis refers to the destruction of the supporting peri-implant tissue due to a microbial infection. These infections tend to occur around places where residual teeth or failing implants can act as reservoirs for bacteria and form biofilm colonies. Interestingly, the bacterial species involved in peri-implantitis are very similar to those that play a key role in periodontitis[5]. The two diseases differ in some key ways, but they are quite similar and research in both can help lead to better treatment and prevention.
Conclusion
Dental plaque biofilm is a diverse, functioning microbial community that is found on every organism on earth that has teeth. Because of the wide diversity of organisms involved in the development and proper function of plaque biofilm, it is difficult to know everything there is to know about these fascinating microbial communities. These biofilms employ a great deal of inter-cell communication to not only keep themselves alive, but also to protect the host. Their existence, while involved in many pathogenic oral diseases, is of much benefit to the host at the early stages of development, as it provides the teeth with a layer of protection, which cannot be matched. In time, we will continue to discover more about the biochemical and developmental functions involved in dental plaque biofilms, which can help us to not only learn about microbiology, but also to improve oral health, which is of great importance to our overall well-being.
References
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Edited by Anna Frutiger, student of Joan Slonczewski for BIOL 238 Microbiology, 2009, Kenyon College.
