» Articles » PMID: 28117832

Salivary Mucins Promote the Coexistence of Competing Oral Bacterial Species

Overview
Journal ISME J
Date 2017 Jan 25
PMID 28117832
Citations 21
Authors
Affiliations
Soon will be listed here.
Abstract

Mucus forms a major ecological niche for microbiota in various locations throughout the human body such as the gastrointestinal tract, respiratory tract and oral cavity. The primary structural components of mucus are mucin glycoproteins, which crosslink to form a complex polymer network that surrounds microbes. Although the mucin matrix could create constraints that impact inhabiting microbes, little is understood about how this key environmental factor affects interspecies interactions. In this study, we develop an experimental model using gel-forming human salivary mucins to understand the influence of mucin on the viability of two competing species of oral bacteria. We use this dual-species model to show that mucins promote the coexistence of the two competing bacteria and that mucins shift cells from the mixed-species biofilm into the planktonic form. Taken together, these findings indicate that the mucus environment could influence bacterial viability by promoting a less competitive mode of growth.

Citing Articles

Structural and functional changes in the oral microbiome of patients with craniofacial microsomia.

Zang T, Zhang Z, Liu W, Yin L, Zhao S, Liu B Sci Rep. 2025; 15(1):5400.

PMID: 39948426 PMC: 11825945. DOI: 10.1038/s41598-025-86537-3.


Changes in the Composition of Unstimulated and Stimulated Saliva Due to Chewing Sour Cherry Gum and a Toothbrush Change.

Skopko B, Homoki J, Fazekas M, Paholcsek M, Fauszt P, David P Cells. 2024; 13(3.

PMID: 38334643 PMC: 10854574. DOI: 10.3390/cells13030251.


Human saliva modifies growth, biofilm architecture, and competitive behaviors of oral streptococci.

Choi A, Dong K, Williams E, Pia L, Batagower J, Bending P mSphere. 2024; 9(2):e0077123.

PMID: 38319113 PMC: 10900908. DOI: 10.1128/msphere.00771-23.


Mutualism at the leading edge: insights into the eco-evolutionary dynamics of host-symbiont communities during range expansion.

Martignoni M, Tyson R, Kolodny O, Garnier J J Math Biol. 2024; 88(2):24.

PMID: 38308102 DOI: 10.1007/s00285-023-02037-w.


Comparison of oral cavity protein abundance among caries-free and caries-affected individuals-a systematic review and meta-analysis.

da Silveira E, Prato L, Pilati S, Arthur R Front Oral Health. 2023; 4:1265817.

PMID: 37780687 PMC: 10540632. DOI: 10.3389/froh.2023.1265817.


References
1.
Smith D, Gaffney E, Gadelha H, Kapur N, Kirkman-Brown J . Bend propagation in the flagella of migrating human sperm, and its modulation by viscosity. Cell Motil Cytoskeleton. 2009; 66(4):220-36. DOI: 10.1002/cm.20345. View

2.
Turner L, Das S, Kanamoto T, Munro C, Kitten T . Development of genetic tools for in vivo virulence analysis of Streptococcus sanguinis. Microbiology (Reading). 2009; 155(Pt 8):2573-2582. PMC: 2830871. DOI: 10.1099/mic.0.024513-0. View

3.
Caldara M, Friedlander R, Kavanaugh N, Aizenberg J, Foster K, Ribbeck K . Mucin biopolymers prevent bacterial aggregation by retaining cells in the free-swimming state. Curr Biol. 2012; 22(24):2325-30. PMC: 3703787. DOI: 10.1016/j.cub.2012.10.028. View

4.
Ge X, Kitten T, Chen Z, Lee S, Munro C, Xu P . Identification of Streptococcus sanguinis genes required for biofilm formation and examination of their role in endocarditis virulence. Infect Immun. 2008; 76(6):2551-9. PMC: 2423065. DOI: 10.1128/IAI.00338-08. View

5.
Prigent-Combaret C, Vidal O, Dorel C, Lejeune P . Abiotic surface sensing and biofilm-dependent regulation of gene expression in Escherichia coli. J Bacteriol. 1999; 181(19):5993-6002. PMC: 103626. DOI: 10.1128/JB.181.19.5993-6002.1999. View