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The Role of Exopolysaccharides in Oral Biofilms
Open accessAbstract
The oral cavity contains a rich consortium of exopolysaccharide-producing microbes. These extracellular polysaccharides comprise a major component of the oral biofilm. Together with extracellular proteins, DNA, and lipids, they form the biofilm matrix, which contributes to bacterial colonization, biofilm formation and maintenance, and pathogenesis. While a number of oral microbes have been studied in detail with regard to biofilm formation and pathogenesis, the exopolysaccharides have been well characterized for only select organisms, namely Streptococcus mutans and Aggregatibacter actinomycetemcomitans. Studies on the exopolysaccharides of other oral organisms, however, are in their infancy. In this review, we present the current research on exopolysaccharides of oral microbes regarding their biosynthesis, regulation, contributions to biofilm formation and stability of the matrix, and immune evasion. In addition, insight into the role of exopolysaccharides in biofilms is highlighted through the evaluation of emerging techniques such as pH probing of biofilm colonies, solid-state nuclear magnetic resonance for macromolecular interactions within biofilms, and super-resolution microscopy analysis of biofilm development. Finally, exopolysaccharide as a potential nutrient source for species within a biofilm is discussed.
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“Furthermore, exopolysaccharides create chemical and metabolic gradients within biofilms that affect chemical and nutrient cycling as well as diffusion, thus altering the microenvironment and pH within biofilms consortium.”
From The oral microbiome: Role of key organisms and complex networks in oral health and disease (2021) · cites this paper as [187]
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ZccE, a P‐type ATPase contributing to biofilm formation and competitiveness in Streptococcus mutans
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Bertl, K., Geissberger, C., Zinndorf, D., Johansson, P. E., Alshammari, H. D., Eick, S., & Stavropoulos, A. (2021) · Clinical Oral Investigations · doi:10.1007/s00784-021-04167-1 · Cited by 6
Microbiological Impact of Antimicrobial Photodynamic Therapy in Non-Surgical Periodontal Treatment
Sousa, F. P., Assunção, M. A., Bessa, L. J., & Alves, R. C. (2025) · Pharmaceutics · doi:10.3390/pharmaceutics17081070 · Cited by 5
“Oral microorganisms are organized in biofilms, surface-associated communities embedded in a self-produced extracellular polymeric substance (EPS) matrix that are highly structured physically and functionally [4,5].”
Recent perspectives on precision-targeting therapy against oral biofilm
Wu, L., Tu, Y., Xiao, S., Zeng, J., Sun, G., & Li, Y. (2026) · Journal of Oral Microbiology · doi:10.1080/20002297.2026.2662093 · Cited by 5
“Finally, the mature biofilm is characterized by a resilient three-dimensional architecture embedded within a protective EPS matrix, which confers its enhanced resistance to both antimicrobials and host defences [3,4].”
Nuclear magnetic resonance to study bacterial biofilms structure, formation, and resilience
Abreu, A. C., & Fernández, I. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819497-3.00002-7 · Cited by 5
Microscale analyses of the effect of arginine on oral biofilms
Assar, S., Kristensen, M. F., Rey, Y. C. D., Lund, M., Raittio, E. J., Schramm, A., Meyer, R. L., & Schlafer, S. (2025) · Journal of Dentistry · doi:10.1016/j.jdent.2025.105863 · Cited by 4
Deficiency of dltD contributes to increased autolysis in Streptococcus mutans
Du, J., Huang, S. H., Li, Y., Wu, M., Chen, S., Zhan, L., & Huang, X. (2023) · Journal of Oral Microbiology · doi:10.1080/20002297.2023.2290221 · Cited by 4
“Bacterial autolysis can release substantial amounts of eDNA, which is a crucial component of the extracellular matrix of bacterial biofilms [22].”
smu_1558c-mediated regulation of growth and biofilm formation in Streptococcus mutans
Zhou, J., Ma, Q., Liang, J., Pan, Y., Chen, Y., Yu, S., Liu, Y., Zhang, Q., Li, Y., & Zou, J. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1507928 · Cited by 4
Sun, L., Wang, D., Yin, Z., Zhang, C., Bible, A. N., & Xie, Z. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.744268 · Cited by 4
Antimicrobial Peptide in Oral Health: A Therapeutic Approach
Kumari, A., & Kumari, S. (2024) · Springer eBooks · doi:10.1007/978-3-031-67515-7_3 · Cited by 3
Fastidious or rarely isolated gram-negative rods with a particular focus on Kingella kingae
Zbinden, R., & Yagupsky, P. (2025) · Clinical Microbiology Reviews · doi:10.1128/cmr.00048-25 · Cited by 3
Dental plaque biofilm-targeting composite nanomaterials: advances and outlook
Zhao, J., Huang, S., Yang, Y., Wang, J., Guo, Q., Xu, Y., Jiang, B., & Lin, J. (2025) · Biomaterials Science · doi:10.1039/d5bm01747e · Cited by 5
Biofilm formation: A well-played game in bacterial pathogenesis
Thite, V. S., Bharathi, R. K., & Srinandan, C. S. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-99977-9.00009-0 · Cited by 3
Ren, S., Cheng, Y., Deng, Y., Xia, M., Yang, Y., Lei, L., & Hu, T. (2023) · Journal of Applied Microbiology · doi:10.1093/jambio/lxad298 · Cited by 3
Qiu, B., Deng, Y., Yi, Z., Yang, Y., Lei, L., & Hu, T. (2025) · Molecular Oral Microbiology · doi:10.1111/omi.70006 · Cited by 2
“The exopolysaccharide (EPS) matrix synthesized by S. mutans is a critical virulence factor of cariogenic biofilms (Cugini et al. 2019; Klein et al. 2015).”
Shi, Q., Li, F., Peng, Y., Sun, Q., Zhao, H., Lu, F., & Zhao, H. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26199510 · Cited by 4
“Collectively, these protective functions contribute to the persistence of a localized low-pH microenvironment [16,17].”
Streptococcus mutans Extracellular Vesicles Regulate Early Streptococcus sanguinis Nanoadhesion
Leiva‐Sabadini, C., Levesque, C. M., Bozec, L., Schuh, C. M. A. P., & Aguayo, S. D. (2026) · Journal of Dental Research · doi:10.1177/00220345261417246 · Cited by 2
“However, the potential influence of S. mutans bEVs on other key virulence factors such as EPS production, biofilm nanomechanical stability, and bacterial viability remains to be elucidated (Cugini et al 2019; Gloag et al 2020).”
Kaur, P., Vyas, M., Verma, S., Sharma, S., Rathore, K., Kamboj, S., & Satija, S. (2025) · Letters in Drug Design & Discovery · doi:10.1016/j.lddd.2026.100327 · Cited by 2
Surface-related factors affecting bacterial adhesion on dental implants: a short literature review
Choi, S. (2026) · The Journal of Advanced Prosthodontics · doi:10.4047/jap.2026.18.3.261 · Cited by 3
“47,48 This increased resilience is a key factor in the persistence of biofilms on dental implant surfaces and contributes to the pathogenesis of peri-implant mucositis and peri-implantitis.”
Multispecies metabolomics interactions resulting in the development of resistance
Anavadiya, B., Acharya, D., Saraf, M. S., & Goswami, D. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-95715-1.00016-9 · Cited by 2
Jung, E., Hwang, G., & Kim, K. (2025) · Nutrients · doi:10.3390/nu17182999 · Cited by 1
“This finding suggests that 6-shogaol can weaken the mechanical stability and reduce the pathogenicity of biofilms [22].”
Du, J., Huang, S., Li, Y., Qiu, Z., Hao, Y., Huang, J., Zhan, L., Chen, S., & Huang, X. (2026) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2025.1741359 · Cited by 1
Balkrishna, A., Varshney, Y., Verma, S., Nain, P., Srivastava, J., & Varshney, A. (2026) · Results in Chemistry · doi:10.1016/j.rechem.2026.103226 · Cited by 1
Zhang, Y., Chen, Z., Jing, M., Huang, Z., & Mao, M. (2026) · Molecular Oral Microbiology · doi:10.1111/omi.70027 · Cited by 1
“EPS also contributes to limiting the diffusion of lactic acid, resulting in tooth demineralization and thus promoting the occurrence and development of dental caries (Cugini et al. 2019 ).”
Buprenorphine enhances Streptococcus mutans virulence and biofilm formation
Pedrosa, M. D. S., Iannaccone, L. L., Schuls, C. S., & Ribeiro, A. A. (2026) · Journal of Oral Microbiology · doi:10.1080/20002297.2026.2652173 · Cited by 1
“These genes are a key virulence trait of S. mutans because they enable persistence on tooth surfaces and resistance to environmental stress [45,49,58].”
Influential
Metadata
- Authors
- Cugini, C., Shanmugam, M., Landge, N., & Ramasubbu, N.
- Affiliations
- Rutgers, The State University of New Jersey (US)
- Corresponding author
- Ramasubbu, N.
- Venue
- Journal of Dental Research
- Publisher
- SAGE Publications
- Published
- 2019-04-22
- Volume
- 98
- Issue
- 7
- Pages
- 739-745
- ISSN
- 0022-0345 (ISSN-L)
- 1544-0591
- PMC
- PMC6589894
- OpenAlex
- W2941974751
- Cited by
- 124
- References
- 59
- Citations by year
- 2026: 14 · 2025: 25 · 2024: 15 · 2023: 26 · 2022: 17 · 2021: 19 · 2020: 6 · 2019: 2
- FWCI
- 0.97
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Dental Research (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Dental and Craniofacial Research (R21DE027125, DE022544)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bacterial biofilms and quorum sensing
- Health Sciences › Dentistry › Periodontics › Oral microbiology and periodontitis research
- Life Sciences › Agricultural and Biological Sciences › Food Science › Polysaccharides Composition and Applications
- Keywords
- exopolysaccharides, dental plaque, biofilm matrix, Streptococcus mutans, Aggregatibacter actinomycetemcomitans, exopolysaccharide biosynthesis, gene expression regulation, bacterial colonization, pathogenesis, immune evasion, solid-state NMR, super-resolution microscopy
- MeSH terms
- Humans, Mouth, Polysaccharides, Bacterial, Streptococcus mutans, Aggregatibacter actinomycetemcomitans, Biofilms
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