Oral Microbiome in Oral and Systemic Disease: Association or Causation?

A special issue of Cells (ISSN 2073-4409). This special issue belongs to the section "Cellular Pathology".

Deadline for manuscript submissions: closed (31 March 2024) | Viewed by 5317

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Guest Editor
School of Dentistry, University of Queensland, Herston, QLD, Australia
Interests: OMICS biology; microbiome
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Special Issue Information

Dear Colleagues,

Our understanding of oral microbiology has evolved significantly from the first observation of “living animalcules” in dental plaque by Antonie van Leeuwenhoek in 1683 to metagenomics studies on the oral microbiome in the 21st century. Next-generation sequencing (NGS) data on the oral microbiome in health and disease conditions have challenged the oversimplified concept of specific oral microorganisms being the main causative pathogens for oral diseases. As we progress our understanding through NGS approaches, we are gaining insight into the extended role of novel microorganisms in disease causation; this knowledge has unraveled only recently. 

The oral–systemic disease link has been an area of great interest since the pioneering publication Micro-organisms of the Human Mouth: the Local and General Diseases Which are Caused by Them by the ‘first oral microbiologist’, W.D. Miller. To date, oral health and various oral microorganisms have been linked to systemic diseases such as cardiovascular diseases, pregnancy complications, rheumatoid arthritis, Alzheimer’s, and various forms of cancer. With the support of the latest metagenomics studies, oral microbiome signatures are being investigated as diagnostic and prognostic tools for various systemic diseases. 

However, a considerable debate still exists over the precise role of the dysbiotic oral microbiome and dysbiosis-induced inflammation in the pathogenesis of oral diseases, as well as the oral–systemic disease link. There is a need for more compelling evidence from clinical studies, as well as molecular studies, to ascertain whether the role of the oral microbiome in oral–systemic diseases is merely an association or a true causation. This Special Issue of Cells aims to provide a critical platform for both proponents and opponents of this theory to enable a healthy, constructive debate on the role of the oral microbiome in oral and systemic diseases. Both original research articles focusing on molecular mechanisms and clinical studies, as well as comprehensive reviews on specific topics on the oral microbiome, are invited. I hope that this Special Issue will provide an opportunity to obtain greater insights into this interesting and clinically relevant topic.

Dr. Jaya Seneviratne
Guest Editor

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Keywords

  • oral microbiome
  • oral diseases
  • oral–systemic link

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Published Papers (2 papers)

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28 pages, 6072 KiB  
Article
Changes in the Composition of Unstimulated and Stimulated Saliva Due to Chewing Sour Cherry Gum and a Toothbrush Change
by Boglárka Emese Skopkó, Judit Rita Homoki, Mónika Éva Fazekas, Melinda Paholcsek, Péter Fauszt, Péter Dávid, László Stündl, Piroska Bíróné Molnár, Ildikó Noémi Forgács, Judit Váradi, Kinga Ágnes Bágyi and Judit Remenyik
Cells 2024, 13(3), 251; https://doi.org/10.3390/cells13030251 - 29 Jan 2024
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Abstract
Background: Our previous studies demonstrated that sour cherry anthocyanins (AC) reduce the salivary count of Streptococcus mutans and inhibit salivary amylase activity within 30 minutes after chewing AC gum. AC gum and changing toothbrushes after scaling reduced the Gram-negative species in the unstimulated [...] Read more.
Background: Our previous studies demonstrated that sour cherry anthocyanins (AC) reduce the salivary count of Streptococcus mutans and inhibit salivary amylase activity within 30 minutes after chewing AC gum. AC gum and changing toothbrushes after scaling reduced the Gram-negative species in the unstimulated salivary microbiota. The present study examined the effect of AC gums on salivary factors, including changes in microbiome. Methods: The study was conducted over three weeks with two groups; young adults (18–30) and adults (30–45). Ten participants changed their toothbrushes, while the other 10 participants did not change after the control period. After scaling, all participants received three doses of AC gum daily. The salivary mRNA and protein levels of cytokines, mucins, melatonin, and the microbiota of unstimulated and stimulated saliva were determined by polymerase chain reaction, enzyme-linked immunosorbent assay, and 16S rRNA gene sequencing. Results: Significantly higher levels of tumor necrosis factor α (TNFα), interleukin-1β (IL-1β), mucin5B (MUC5B), mucin7 (MUC7), and melatonin were detected in stimulated saliva. Correlation analysis of these factors with the microbiota showed positive correlations with the genera Lachnospiraceae, Eikenella, Saccharibacteria_(TM7), Streptococcus, Prevotella, and Haemophilus. Conclusions: AC chewing gum has a beneficial effect on the composition of the oral microbiome, and toothbrush replacement leads to changes in the levels of salivary pro-inflammatory cytokines. Full article
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16 pages, 1040 KiB  
Review
A Mapping Review of the Pathogenesis of Peri-Implantitis: The Biofilm-Mediated Inflammation and Bone Dysregulation (BIND) Hypothesis
by Ethan Ng, John Rong Hao Tay, Nikos Mattheos, Nagihan Bostanci, Georgios N. Belibasakis and Chaminda Jayampath Seneviratne
Cells 2024, 13(4), 315; https://doi.org/10.3390/cells13040315 - 8 Feb 2024
Cited by 3 | Viewed by 2693
Abstract
This mapping review highlights the need for a new paradigm in the understanding of peri-implantitis pathogenesis. The biofilm-mediated inflammation and bone dysregulation (BIND) hypothesis is proposed, focusing on the relationship between biofilm, inflammation, and bone biology. The close interactions between immune and bone [...] Read more.
This mapping review highlights the need for a new paradigm in the understanding of peri-implantitis pathogenesis. The biofilm-mediated inflammation and bone dysregulation (BIND) hypothesis is proposed, focusing on the relationship between biofilm, inflammation, and bone biology. The close interactions between immune and bone cells are discussed, with multiple stable states likely existing between clinically observable definitions of peri-implant health and peri-implantitis. The framework presented aims to explain the transition from health to disease as a staged and incremental process, where multiple factors contribute to distinct steps towards a tipping point where disease is manifested clinically. These steps might be reached in different ways in different patients and may constitute highly individualised paths. Notably, factors affecting the underlying biology are identified in the pathogenesis of peri-implantitis, highlighting that disruptions to the host–microbe homeostasis at the implant–mucosa interface may not be the sole factor. An improved understanding of disease pathogenesis will allow for intervention on multiple levels and a personalised treatment approach. Further research areas are identified, such as the use of novel biomarkers to detect changes in macrophage polarisation and activation status, and bone turnover. Full article
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