» Articles » PMID: 38721621

Molecular Commensalism: How Oral Corynebacteria and Their Extracellular Membrane Vesicles Shape Microbiome Interactions

Overview
Date 2024 May 9
PMID 38721621
Authors
Affiliations
Soon will be listed here.
Abstract

Historically, the study of microbe-associated diseases has focused primarily on pathogens, guided by Koch's postulates. This pathogen-centric view has provided a mechanistic understanding of disease etiology and microbial pathogenesis. However, next-generation sequencing approaches have revealed a far more nuanced view of the roles various microbes play in disease, highlighting the importance of microbial diversity beyond individual pathogens. This broader perspective acknowledges the roles of host and microbial communities in disease development and resistance. In particular, the concept of dysbiosis, especially within the oral cavity, has gained attention for explaining the emergence of complex polymicrobial diseases. Such diseases often stem from resident microbes rather than foreign pathogens, complicating their treatment and even clouding our understanding of disease etiology. Oral health is maintained through a delicate balance between commensal microbes and the host, with diseases like caries and periodontal disease arising from pathogenic perturbations of this balance. Commensal microbes, such as certain streptococci and , play crucial roles in maintaining oral health through mechanisms involving hydrogen peroxide production and membrane vesicle secretion, which can inhibit pathogenic species and modulate host immune responses. Recent research focused upon the mechanisms of molecular commensalism has expanded our understanding of these key functions of the commensal microbiome, demonstrating their central role in promoting oral health and preventing disease. These abilities represent a largely untapped reservoir of potential innovative strategies for disease prevention and management, emphasizing the need to bolster a symbiotic microbiome that inherently suppresses pathogenesis.

Citing Articles

Illumina Sequencing in Conjunction with Propidium Monoazide to Identify Live Bacteria After Antiseptic Treatment in a Complex Oral Biofilm: A Study Using an Ex Vivo Supragingival Biofilm Model.

Sanchez M, Hernandez P, Velapatino A, Cuba E, Ciudad M, Collado L Antibiotics (Basel). 2024; 13(11).

PMID: 39596695 PMC: 11591144. DOI: 10.3390/antibiotics13111000.


Effects of Mint Oils on the Human Oral Microbiome: A Pilot Study.

Abdelrahman S, El Samak M, El-Baz L, Hanora A, Satyal P, Dosoky N Microorganisms. 2024; 12(8).

PMID: 39203382 PMC: 11356387. DOI: 10.3390/microorganisms12081538.


Periodontitis is associated with impaired olfactory function: A clinical study.

Schertel Cassiano L, Jensen A, Pajaniaye J, Lopez R, Fjaeldstad A, Nascimento G J Periodontal Res. 2024; 60(1):55-63.

PMID: 38888002 PMC: 11840459. DOI: 10.1111/jre.13315.

References
1.
Redanz S, Cheng X, Giacaman R, Pfeifer C, Merritt J, Kreth J . Live and let die: Hydrogen peroxide production by the commensal flora and its role in maintaining a symbiotic microbiome. Mol Oral Microbiol. 2018; 33(5):337-352. PMC: 6158098. DOI: 10.1111/omi.12231. View

2.
Jakubovics N, Gill S, Vickerman M, Kolenbrander P . Role of hydrogen peroxide in competition and cooperation between Streptococcus gordonii and Actinomyces naeslundii. FEMS Microbiol Ecol. 2008; 66(3):637-44. PMC: 2820160. DOI: 10.1111/j.1574-6941.2008.00585.x. View

3.
Zhang M, Whiteley M, Lewin G . Polymicrobial Interactions of Oral Microbiota: a Historical Review and Current Perspective. mBio. 2022; 13(3):e0023522. PMC: 9239150. DOI: 10.1128/mbio.00235-22. View

4.
Hajishengallis G, Lamont R . Beyond the red complex and into more complexity: the polymicrobial synergy and dysbiosis (PSD) model of periodontal disease etiology. Mol Oral Microbiol. 2012; 27(6):409-19. PMC: 3653317. DOI: 10.1111/j.2041-1014.2012.00663.x. View

5.
OToole G . We have a community problem. J Bacteriol. 2024; 206(4):e0007324. PMC: 11025320. DOI: 10.1128/jb.00073-24. View