Volume 6 Supplement 1
Streptococcal Receptor Polysaccharides: Recognition Molecules for Oral Biofilm Formation
© Yoshida et al.; licensee BioMed Central Ltd. 2006
Published: 10 July 2006
Strains of viridans group streptococci that initiate colonization of the human tooth surface typically coaggregate with each other and with Actinomyces naeslundii, another member of the developing biofilm community. These interactions generally involve adhesin-mediated recognition of streptococcal receptor polysaccharides (RPS). The objective of our studies is to understand the role of these polysaccharides in oral biofilm development.
Different structural types of RPS have been characterized by their reactions with specific antibodies and lectin-like adhesins. Streptococcal gene clusters for RPS biosynthesis were identified, sequenced, characterized and compared. RPS-producing bacteria were detected in biofilm samples using specific antibodies and gene probes.
Six different types of RPS have been identified from representative viridans group streptococci that coaggregate with A. naeslundii. Each type is composed of a different hexa- or heptasaccharide repeating unit, the structures of which contain host-like motifs, either GalNAcβ1-3Gal or Galβ1-3GalNAc. These motifs account for RPS-mediated recognition, whereas other features of these polysaccharides are more closely associated with RPS antigenicity. The RPS-dependent interaction of S. oralis with A. naeslundii promotes growth of these bacteria and biofilm formation in flowing saliva. Type specific differences in RPS production have been noted among the resident streptococcal floras of different individuals, raising the possibility of RPS-based differences in the composition of oral biofilm communities.
The structural, functional and molecular properties of streptococcal RPS support a recognition role of these cell surface molecules in oral biofilm formation.
Colonization of the human tooth surface is initiated by a limited number of gram-positive species, primarily viridans group streptococci . These bacteria attach to host salivary components that coat the mineral surface and, through growth and interactions between species, form a relatively simple biofilm community (i.e. early plaque). Members of this community can activate host cells, and the biofilm itself creates a habitat for additional species, some of which are closely associated with the initiation and progression of dental caries and periodontal disease . In the current communication we summarize evidence for the hypothesis that the surface polysaccharides of certain viridans group streptococci are receptors for lectin-like adhesins present on other members of the developing oral biofilm community. Studies of how these components influence biofilm development may provide insights into the etiology and pathogenesis of biofilm-related oral diseases.
Early Biofilm Formation Involves a Limited Number of Microbial Species
An attractive experimental model for defining early events in oral biofilm formation involves the incubation of retrievable enamel chips in the human oral cavity for periods of time from 4 to 12 hrs. Scanning electron micrographs of chips removed during this period suggest that colonization is initiated by the attachment of individual microorganisms to the saliva-coated mineral surface and proceeds primarily by the growth of attached bacteria as spreading microcolonies . These microcolonies typically consist of a peripheral monolayer of dividing cocci and rods and a central region containing multiple bacterial layers. S. sanguinis, S. oralis and S. mitis were the most prominent species identified in parallel microbiological studies  and together comprised approximately 80% of the total cultivatable flora. Gram-positive pleomophic rods, mostly strains of Actinomyces naeslundii, made up another 5 to 10% of the total. Thus, primary colonization of the saliva-coated mineral surface involves the formation of a relatively simple biofilm community.
Interestingly, S. mutans, the principal agent of human dental caries, was generally not identified from early biofilms formed on enamel chips following incubation in the oral cavities of individuals with active caries . Moreover, when this species was detected, it accounted for less than 2% of the total early streptococcal flora. Differences in the relative proportions of other streptococcal species were however noted between the early flora of caries active and caries free individuals. Specifically, the proportion of S. mitis was generally elevated at the expense of S. sanguinis in caries active individuals. The ecological consequences of this population shift are not well understood. However, they may include a lowering of the early plaque pH as suggested from comparative studies of acid production by representative strains of these streptococcal species . A more acidic environment could in turn favor the succession of aciduric species such as S. mutans, resulting in rapid caries development. Thus, the etiology and pathogenesis of oral disease may well be linked to ecological properties of the early biofilm community.
Structural Basis of Receptor Polysaccharide (RPS)-Mediated Interbacterial Adhesion
Bacterial properties that contribute to development of the early biofilm community may include the surface adhesins and receptors that mediate the coaggregations observed between different strains of S. sanguinis, S. gordonii, S. oralis, S. mitis and A. naeslundii . The coaggregations between A. naeslundii and different streptococci are typically inhibited by GalNAc or Gal and result from lectin-like binding of A. naeslundii type 2 fimbriae to complementary receptors present on the streptococcal surface. These receptors occur on most strains of S. oralis and on certain strains of S. sanguinis, S. gordonii and S. mitis. Many but not all streptococci that possess such receptors also participate in coaggregations with other strains of S. sanguinis or S. gordonii. These coaggregations are inhibited by GalNAc and result from lectin-like binding of surface adhesins present on the strains of S. sanguinis or S. gordonii . Thus, an extensive network of adhesive interactions occurs among different members of the early biofilm community.
The structural basis of the coaggregations observed between different bacteria is evident from the carbohydrate-binding specificities of the surface adhesins present on strains of A. naeslundii, S. sanguinis and S. gordonii, and from the structures of the complementary receptors present on other streptococcal strains. The type 2 fimbriae of A. naeslundii, in addition to mediating coaggregations with streptococci, mediate the adhesion of A. naeslundii to surface-associated host glycoconjugates [8, 9]. Two different receptor structures have been identified, terminal GalNAcβ1-3Gal of globoside and terminal Galβ1-3GalNAc of asialo-O-linked glycoproteins and gangliosides. Consistent with these findings, soluble GalNAcβ1-3Gal- and Galβ1-3GalNAc-containing ligands are potent inhibitors of A. naeslundii type 2 fimbriae-mediated adhesion . These disaccharides differ only in the position of the N-acetyl group. Consequently, the ability of each to inhibit binding of A. naeslundii type 2 fimbriae presumably depends on common features of these structures. The GalNAc-binding surface adhesins of S. sanguinisSK1 and S. gordonii DL1 also recognize terminal GalNAcβ1-3Gal . However, these adhesins do not bind terminal Galβ1-3GalNAc of immobilized glycocongugates. In accordance with these findings, the coaggregations observed between strains of S. sanguinis or S. gordonii and other streptococci are inhibited more effectively by soluble GalNAcβ1-3Gal- than Galβ1-3GalNAc-containing ligands . Thus, the N-acetyl group of GalNAcβ1-3Gal is critical for binding of the streptococcal adhesins that mediate these interactions.
Other features of RPS that are conserved between structural types may contribute to adhesin binding of these linear polysaccharides. Such features include the flexibility of the β1–6 linkage from Galf and the anionic phosphodiester bond that flank each recognition motif [13, 14]. This region, although critical for interbacterial adhesion, contributes little to the antigenicity of different RPS structural types. Instead, other structural features such as the Rha branch present in types 2Gn and 2G RPS  form the major epitopes of anti-RPS antibodies. Consequently, the reactions of types 2Gn and 2G RPS are similar as antigens but distinct as receptors. Other structural types such as types 1Gn and 2Gn RPS react as similar receptors but different antigens. Such findings raise the possibility that the production of different antigenic types of RPS contributes to evasion of the host secretory immune response during oral biofilm formation. However, the presence of specific anti-RPS antibodies has not been detected in samples of whole human saliva. Thus, further studies of the host response (or the lack of a response) to these molecules are needed.
Molecular Basis of RPS Structure and Function
Additional genes control the synthesis of nucleotide-linked sugars that are essential precursors for RPS biosynthesis. One of these (glf) encodes galactofuranose mutase, the enzyme that catalyzes the conversion of UDP-Galactopyranose to UDP-Galactofuranose. This gene invariably occurs within the RPS gene clusters of different strains. The location of other genes for nucleotide sugar biosynthesis varies between streptococcal species. For example, in S. gordonii 38, the first three genes of the dTDP-L-Rhamnose biosynthetic pathway (i.e., rmlA, rmlC and rmlB) occur in a separate operon with galE2, the gene for a bifunctional galactose epimerase that supplies both UDP-Gal and UDP-GalNAc for polysaccharide biosynthesis . The final gene for dTDP-L-Rhamnose biosynthesis (i.e., rmlD) is transcribed independently, downstream of the rml-galE2 operon. In contrast, rmlA, rmlC and rmlB of S. oralis strains 34 and J22 occur at the 3'-end of the respective type 1Gn and 2G RPS gene clusters of these strains, while rmlD occurs immediately downstream but transcribed in the opposite direction [19, 18]. The differences that exist between the RPS gene clusters of S. gordonii and S. oralis, both in terms of their organization and nucleotide sequence homologies, raise the interesting possibility that the evolution of RPS production in these bacteria occurred following the divergence of these species. The four RPS-producing species of oral streptococci, S. sanguinis, S. gordonii, S. oralis and S. mitis, are closely related members of the mitis group . Members of this group, which includes S. pneumoniae, are all intimately associated with the oral cavity and upper respiratory tract of man. Thus, the evolution of certain species as members of the human oral biofilm community may be closely linked with the evolution of RPS production. The identification of genes for RPS structure and function provides a beginning basis for further phylogenetic studies to examine this intriguing possibility.
Role of RPS-mediated Interbacterial Adhesion in Biofilm Development
Characterization of RPS-Producing Bacteria from Different Individuals
The identification of six structural types of RPS is based on the characterization of representative strains of the four RPS-producing species. Consequently, it is unclear how many different RPS-producing strains occur within the streptococcal flora of any one individual. To address this question, we have begun to characterize these bacteria from individual volunteers. This involves the identification of RPS-producing clones from samples of 8 hr biofilms by colony immunoblotting with a cocktail of RPS-specific antibodies and the subsequent characterization of individual clones by the reactions with specific antibodies and adhesins. Initial results of these studies indicate the production of one predominant type of RPS by the resident streptococcal flora of each individual examined to date. Thus, 22 RPS-producing isolates from one volunteer all produced type 1Gn RPS while 19 RPS-producing isolates from another individual all produced type 2Gn RPS. In addition, 21 RPS-producing isolates from a third individual included 19 that produced type 2Gn RPS and two that produced type 1Gn RPS. PCR-based genotyping  of these isolates suggests the presence of from one to three different RPS-producing clones per individual. These clones appear to be S. oralis or S. gordonii based on sequencing of a housekeeping gene . Whether RPS-producing clones of different individuals are subject to replacement or to chromosomal rearrangement over time as has been described for strains of S. mitis  and S. oralis  remains to be determined.
Over 90% of the RPS-producing streptococci identified from samples of early supragingival plaque from each of five individuals are type 1Gn or 2Gn RPS producing clones. The preponderance of these bacteria in the plaque samples examined to date raises a number of intriguing possibilities concerning the occurrence and distribution of the streptococci that produce other structural types. Clearly, one possibility is that the streptococcal floras of certain individuals will be found to produce type 2G, 3G, 4Gn or 5Gn RPS, thereby indicating significant differences in RPS production between individuals. Alternatively, the RPS-producing flora of each individual, including those that have been examined, may be more complex than is presently recognized. If so, streptococci that produce structural types other than type 1Gn or 2Gn RPS may emerge as the early biofilm community matures or perhaps appear during the colonization of other oral sites. In any case, it will be important to determine whether RPS-producing streptococci, especially those that produce Gn- and G-types, exist within distinct biofilm communities. The existence of RPS-based differences in the composition of biofilm communities would firmly establish the recognition role of these polysaccharides in biofilm development and could provide important new insights into the etiology and pathogenesis of biofilm-related oral diseases, including dental caries.
Another intriguing area of investigation involves the natural history of RPS-producing streptococci in the human host. Available findings indicate that these bacteria are transmitted from adults to infants shortly after tooth eruption. It is unclear, however, whether the resident RPS-producing streptococcal flora, once acquired, is stable, or whether changes in the population of RPS-producing clones occur over the lifetime of each individual. New structural types of RPS may evolve gradually and be disseminated by transmission between individuals. Alternatively, new types may arise frequently by the horizontal transfer of genes for RPS biosynthesis between different streptococcal strains and species within the resident flora of each individual. Current molecular studies of RPS production are directed toward distinguishing these possibilities.
This work was supported by the Intramural Research Program of the NIH, NIDCR.
- Nyvad B, Kilian M: Microbiology of the early colonization of human enamel and root surfaces in vivo. Scand J Dent Res. 1987, 95 (5): 369-380.PubMedGoogle Scholar
- Gibbons RJ: Bacterial adhesion to oral tissues: a model for infectious diseases. J Dent Res. 1989, 68 (5): 750-760.View ArticlePubMedGoogle Scholar
- Nyvad B, Fejerskov O: Scanning electron microscopy of early microbial colonization of human enamel and root surfaces in vivo. Scand J Dent Res. 1987, 95 (4): 287-296.PubMedGoogle Scholar
- Nyvad B, Kilian M: Comparison of the initial streptococcal microflora on dental enamel in caries-active and in caries-inactive individuals. Caries Res. 1990, 24 (4): 267-272.View ArticlePubMedGoogle Scholar
- de Soet JJ, Nyvad B, Kilian M: Strain-related acid production by oral streptococci. Caries Res. 2000, 34 (6): 486-490. 10.1159/000016628.View ArticlePubMedGoogle Scholar
- Hsu SD, Cisar JO, Sandberg AL, Kilian M: Adhesive properties of viridans group streptococcal species. Microb Ecol Health Dis. 1994, 125-137. 7Google Scholar
- Kolenbrander PE, Andersen RN, Moore LV: Intrageneric coaggregation among strains of human oral bacteria: potential role in primary colonization of the tooth surface. Appl Environ Microbiol. 1990, 56 (12): 3890-3894.PubMed CentralPubMedGoogle Scholar
- Brennan MJ, Joralmon RA, Cisar JO, Sandberg AL: Binding of Actinomyces naeslundii to glycosphingolipids. Infect Immun. 1987, 55 (2): 487-489.PubMed CentralPubMedGoogle Scholar
- Ruhl S, Sandberg AL, Cole MF, Cisar JO: Recognition of immunoglobulin A1 by oral actinomyces and streptococcal lectins. Infect Immun. 1996, 64 (12): 5421-5424.PubMed CentralPubMedGoogle Scholar
- Cisar JO, Sandberg AL, Abeygunawardana C, Reddy GP, Bush CA: Lectin recognition of host-like saccharide motifs in streptococcal cell wall polysaccharides. Glycobiology. 1995, 5 (7): 655-662.View ArticlePubMedGoogle Scholar
- Takahashi Y, Ruhl S, Yoon JW, Sandberg AL, Cisar JO: Adhesion of viridans group streptococci to sialic acid-, galactose- and N-acetylgalactosamine-containing receptors. Oral Microbiol Immunol. 2002, 17 (4): 257-262. 10.1034/j.1399-302X.2002.170409.x.View ArticlePubMedGoogle Scholar
- Cisar JO, Sandberg AL, Reddy GP, Abeygunawardana C, Bush CA: Structural and antigenic types of cell wall polysaccharides from viridans group streptococci with receptors for oral actinomyces and streptococcal lectins. Infect Immun. 1997, 65 (12): 5035-5041.PubMed CentralPubMedGoogle Scholar
- McIntire FC, Crosby LK, Vatter AE, Cisar JO, McNeil MR, Bush CA, Tjoa SS, Fennessey PV: A polysaccharide from Streptococcus sanguis 34 that inhibits coaggregation of S. sanguis 34 with Actinomyces viscosus T14V. J Bacteriol. 1988, 170 (5): 2229-2235.PubMed CentralPubMedGoogle Scholar
- Xu Q, Bush CA: Molecular modeling of the flexible cell wall polysaccharide of Streptococcus mitis J22 on the basis of heteronuclear NMR coupling constants. Biochemistry. 1996, 35 (46): 14521-14529. 10.1021/bi961262+.View ArticlePubMedGoogle Scholar
- Reddy GP, Abeygunawardana C, Bush CA, Cisar JO: The cell wall polysaccharide of Streptococcus gordonii 38: structure and immunochemical comparison with the receptor polysaccharides of Streptococcus oralis 34 and Streptococcus mitis J22. Glycobiology. 1994, 4 (2): 183-192.View ArticlePubMedGoogle Scholar
- Xu DQ, Thompson J, Cisar JO: Genetic loci for coaggregation receptor polysaccharide biosynthesis in Streptococcus gordonii 38. J Bacteriol. 2003, 185 (18): 5419-5430. 10.1128/JB.185.18.5419-5430.2003.PubMed CentralView ArticlePubMedGoogle Scholar
- Jiang SM, Wang L, Reeves PR: Molecular characterization of Streptococcus pneumoniae type 4, 6B, 8, and 18C capsular polysaccharide gene clusters. Infect Immun. 2001, 69 (3): 1244-1255. 10.1128/IAI.69.3.1244-1255.2001.PubMed CentralView ArticlePubMedGoogle Scholar
- Yoshida Y, Ganguly S, Bush CA, Cisar JO: Molecular basis of L-rhamnise branch formation in streptococcal coaggregation receptor polysaccharides. J Bacteriol. 2006, 188 (11): 4125-4130. 10.1128/JB.01843-05.PubMed CentralView ArticlePubMedGoogle Scholar
- Yoshida Y, Ganguly S, Bush CA, Cisar JO: Carbohydrate engineering of the recognition motifs in streptococcal co-aggregation receptor polysaccharides. Mol Microbiol. 2005, 58 (1): 244-56. 10.1111/j.1365-2958.2005.04820.x.View ArticlePubMedGoogle Scholar
- Kawamura Y, Hou XG, Sultana F, Miura H, Ezaki T: Determination of 16S rRNA sequences of Streptococcus mitis and Streptococcus gordonii and phylogenetic relationships among members of the genus Streptococcus. Int J Syst Bacteriol. 1995, 45 (2): 406-408.View ArticlePubMedGoogle Scholar
- Palmer RJ, Gordon SM, Cisar JO, Kolenbrander PE: Coaggregation-mediated interactions of streptococci and actinomyces detected in initial human dental plaque. J Bacteriol. 2003, 185 (11): 3400-3409. 10.1128/JB.185.11.3400-3409.2003.View ArticlePubMedGoogle Scholar
- Palmer RJ, Kazmerzak K, Hansen MC, Kolenbrander PE: Mutualism versus independence: strategies of mixed-species oral biofilms in vitro using saliva as the sole nutrient source. Infect Immun. 2001, 69 (9): 5794-5804. 10.1128/IAI.69.9.5794-5804.2001.PubMed CentralView ArticlePubMedGoogle Scholar
- Alam S, Brailsford SR, Whiley RA, Beighton D: PCR-Based methods for genotyping viridans group streptococci. J Clin Microbiol. 1999, 37 (9): 2772-2776.PubMed CentralPubMedGoogle Scholar
- Kawamura Y, Whiley RA, Shu SE, Ezaki T, Hardie JM: Genetic approaches to the identification of the mitis group within the genus Streptococcus. Microbiology. 1999, 145 (Pt 9): 2605-2613.View ArticlePubMedGoogle Scholar
- Hohwy J, Reinholdt J, Kilian M: Population dynamics of Streptococcus mitis in its natural habitat. Infect Immun. 2001, 69 (10): 6055-6063. 10.1128/IAI.69.10.6055-6063.2001.PubMed CentralView ArticlePubMedGoogle Scholar
- Alam S, Brailsford SR, Adams S, Allison C, Sheehy E, Zoitopoulos L, Kidd EA, Beighton D: Genotypic heterogeneity of Streptococcus oralis and distinct aciduric subpopulations in human dental plaque. Appl Environ Microbiol. 2000, 66 (8): 3330-3336. 10.1128/AEM.66.8.3330-3336.2000.PubMed CentralView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.