Advanced Therapies Journal

Advanced Therapies Journal

The Oral-Gut Microbiome Axis: Mechanisms Influencing Periodontal Therapeutic Response and Strategies for Microbiome Restoration

Reviewers

Authors
Biotechnology Research Center, ZistYar Sanat Technology Development Group, Science and Technology Park, Tarbiat Modares University, Tehran, Iran.
Abstract
The oral-gut axis represents a bidirectional relationship between oral and intestinal microbial communities and plays an important role in the development and progression of periodontal diseases. Periodontitis, traditionally regarded as a localized inflammatory disorder, is increasingly recognized as a condition with systemic implications. This review summarizes current evidence on the biological mechanisms linking oral and gut microbiota, with particular emphasis on the translocation of periodontal pathogens, including Porphyromonas gingivalis and Tannerella forsythia, into the gastrointestinal tract. These pathogens may promote gut dysbiosis, impair intestinal barrier integrity, and contribute to systemic inflammation. Conversely, gut dysbiosis may aggravate periodontal inflammation through circulating pro-inflammatory mediators and bacterial endotoxins, creating a vicious cycle that can impair tissue healing and reduce treatment effectiveness.Individual differences in baseline microbiome composition and host immune responses may partly explain the variable outcomes observed following conventional periodontal therapies such as scaling and root planing. Therefore, microbiome assessment may support the development of personalized periodontal treatment strategies. Microbiome-modulating interventions, including probiotics, prebiotics, dietary modifications, engineered probiotics, and fecal microbiota transplantation, have emerged as potential adjunctive approaches to restore microbial homeostasis and improve clinical outcomes. Furthermore, multi-omics technologies may facilitate microbial profiling and prediction of treatment responses within a precision-medicine framework.Overall, targeting both oral and gut microbial health may represent a promising paradigm shift toward integrated and personalized periodontal care. However, large-scale randomized controlled trials are required to establish the clinical efficacy and standardized application of microbiome-focused therapies.
Keywords

1.Hajishengallis G, Liang S, Payne MA, et al. Porphyromonas gingivalis maintains chronic periodontal infection by signaling to fibroblasts, epithelial cells, and B cells through toll-like receptor 2. 2011;79(3):1083-1093.
2.Lamont RJ, Belibasakis GN. Oral microbiota memes. 2017;22(2):146-148.
3.Tonetti MS, Greenwell H, Smith KG. Periodontitis and systemic diseases: a consensus statement. 2018;40(Suppl 1): S12-S16.
4.Graves DT, Cochran D. The contribution of interleukin-1 and tumor necrosis factor to periodontal tissue destruction. 2013;84(4 Suppl): S173-S181.
5.Aas JA, Paster BJ, Stokes LN, et al. Defining the normal bacterial flora of the oral cavity. 2018;46(11):3715-3721.
6.Chen T, Xu X, Zhu W, et al. The oral microbiota: community composition, influencing factors, and implications for oral health. 2019;11(1):1598020.
7.Darveau RP. Periodontitis: a polymicrobial disruption of homeostasis. 2018;8(11): a031615.
8.Korostoff JM. Periodontal disease and systemic inflammation.2018;78(1):12-15.
9.Koo H, Schauer DB, Wyckoff NJ, et al. Oral microbiome: uncharacterized and uncharacteristic. 2019; 73:131-152.
10.Kolenbrander PE, London J. Adherence and coaggregation among mutans streptococci, actinomyces, and periodontal bacteria. 2018;77(5):1063-1071.
11.Listgarten MA. Pathogenesis of periodontitis. 2018;78(1):22-28.
12.Loos BG, Van Dyke TE. Periodontitis: a common systemic inflammatory disease. 2018;78(1):32-37.
13.Marsh PD, Martin MV, Devine DA. How is the development of dental biofilms influenced by the host? 2018;78(1):56-66.
14.Mealey BL, Oates TW. Diabetes mellitus and periodontal diseases. 2018;84(4 Suppl):S128-S143.
15.Moles D, Catton PA, Preshaw PM. The oral microbiome and periodontal disease. 2018;78(1):10-11.
16.Nagata K, Takahashi N, Yamada S, et al. The oral microbiota in health and disease.2018;2018:1462907.
17.Nakano Y, Ohshima T, Maeda H. The role of oral bacteria in periodontal disease. 2018;78(1):46-55.
18.Newman MG, Takei HH, Klokke RE, Carranza FA. Carranza’s Clinical Periodontology. 13th ed. Philadelphia: Elsevier; 2019.
19.Pihlstrom BL, Michalowicz BS, Johnson NW. Periodontal diseases. 2018;386(9993):1550-1560.
20.Ramseier CA, Singhal P, Suvan JE, et al. Systematic review of the association between periodontal disease and diabetes. 2018;45(1): S1-S15.
21.Socransky SS, Haffajee AD. Periodital microflora. 2018;78(1):12-15.
22.Tonetti MS, Jepsen S, Jin L, et al. Periodontitis. 2018; 4:1-16.
23. Van Dyke TE. The host response to periodontal disease. 2018;78(1):38-45.
24.Wagener C, Klinger K, Ziebart T, et al. Probiotics and periodontal health. 2018;45(1): S32-S42.
25.Wang C, Li Y, Zhang Y, et al. The oral-gut microbiome axis in health and disease. 2019; 10:1-12.
26.Zaura E, Brandt BW, Buijs MJ, et al. Oral microbiome health and disease: mechanisms of interaction. 2019;17(7):423-435.
27.Zhang X, Shen D, Pang X, et al. Oral microbiome and periodontal health. 2018;6(5):1-15.
28.Zhang Y, Wang Y, Zhang J, et al. Gut microbiota and periodontal disease. 2019; 9:1-10.
29.Zhao Y, Li X, Wang H, et al. Probiotics in periodontal therapy. 2018;89(10):1193-1205.
30.Zhu Y, Chen H, Zhang L, et al. Prebiotics and periodontal health. 2019;11(3):567.

  • Receive Date 29 May 2026
  • Revise Date 28 July 2026
  • Accept Date 22 August 2026