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Human Saliva Modifies Growth, Biofilm Architecture and Competitive Behaviors of Oral Streptococci
The bacteria within supragingival biofilms participate in complex exchanges with other microbes inhabiting the same niche. One example are the mutans group streptococci (Streptococcus mutans), implicated in the development of tooth decay, and other health-associated commensal streptococci species. P...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473590/ https://www.ncbi.nlm.nih.gov/pubmed/37662325 http://dx.doi.org/10.1101/2023.08.21.554151 |
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author | Choi, Allen Dong, Kevin Williams, Emily Pia, Lindsey Batagower, Jordan Bending, Paige Shin, Iris Peters, Daniel I. Kaspar, Justin R. |
author_facet | Choi, Allen Dong, Kevin Williams, Emily Pia, Lindsey Batagower, Jordan Bending, Paige Shin, Iris Peters, Daniel I. Kaspar, Justin R. |
author_sort | Choi, Allen |
collection | PubMed |
description | The bacteria within supragingival biofilms participate in complex exchanges with other microbes inhabiting the same niche. One example are the mutans group streptococci (Streptococcus mutans), implicated in the development of tooth decay, and other health-associated commensal streptococci species. Previously, our group transcriptomically characterized intermicrobial interactions between S. mutans and several species of oral bacteria. However, these experiments were carried out in a medium that was absent of human saliva. To better mimic their natural environment, we first evaluated how inclusion of saliva affected growth and biofilm formation of eight streptococci species individually, and found saliva to positively benefit growth rates while negatively influencing biomass accumulation and altering spatial arrangement. These results carried over during evaluation of 29 saliva-derived isolates of various species. Surprisingly, we also found that addition of saliva increased the competitive behaviors of S. mutans in coculture competitions against commensal streptococci that led to increases in biofilm microcolony volumes. Through transcriptomically characterizing mono- and cocultures of S. mutans and Streptococcus oralis with and without saliva, we determined that each species developed a nutritional niche under mixed-species growth, with S. mutans upregulating carbohydrate uptake and utilization pathways while S. oralis upregulated genome features related to peptide uptake and glycan foraging. S. mutans also upregulated genes involved in oxidative stress tolerance, particularly manganese uptake, which we could artificially manipulate by supplementing in manganese to give it an advantage over its opponent. Our report highlights observable changes in microbial behaviors via leveraging environmental- and host-supplied resources over their competitors. |
format | Online Article Text |
id | pubmed-10473590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-104735902023-09-02 Human Saliva Modifies Growth, Biofilm Architecture and Competitive Behaviors of Oral Streptococci Choi, Allen Dong, Kevin Williams, Emily Pia, Lindsey Batagower, Jordan Bending, Paige Shin, Iris Peters, Daniel I. Kaspar, Justin R. bioRxiv Article The bacteria within supragingival biofilms participate in complex exchanges with other microbes inhabiting the same niche. One example are the mutans group streptococci (Streptococcus mutans), implicated in the development of tooth decay, and other health-associated commensal streptococci species. Previously, our group transcriptomically characterized intermicrobial interactions between S. mutans and several species of oral bacteria. However, these experiments were carried out in a medium that was absent of human saliva. To better mimic their natural environment, we first evaluated how inclusion of saliva affected growth and biofilm formation of eight streptococci species individually, and found saliva to positively benefit growth rates while negatively influencing biomass accumulation and altering spatial arrangement. These results carried over during evaluation of 29 saliva-derived isolates of various species. Surprisingly, we also found that addition of saliva increased the competitive behaviors of S. mutans in coculture competitions against commensal streptococci that led to increases in biofilm microcolony volumes. Through transcriptomically characterizing mono- and cocultures of S. mutans and Streptococcus oralis with and without saliva, we determined that each species developed a nutritional niche under mixed-species growth, with S. mutans upregulating carbohydrate uptake and utilization pathways while S. oralis upregulated genome features related to peptide uptake and glycan foraging. S. mutans also upregulated genes involved in oxidative stress tolerance, particularly manganese uptake, which we could artificially manipulate by supplementing in manganese to give it an advantage over its opponent. Our report highlights observable changes in microbial behaviors via leveraging environmental- and host-supplied resources over their competitors. Cold Spring Harbor Laboratory 2023-08-21 /pmc/articles/PMC10473590/ /pubmed/37662325 http://dx.doi.org/10.1101/2023.08.21.554151 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Choi, Allen Dong, Kevin Williams, Emily Pia, Lindsey Batagower, Jordan Bending, Paige Shin, Iris Peters, Daniel I. Kaspar, Justin R. Human Saliva Modifies Growth, Biofilm Architecture and Competitive Behaviors of Oral Streptococci |
title | Human Saliva Modifies Growth, Biofilm Architecture and Competitive Behaviors of Oral Streptococci |
title_full | Human Saliva Modifies Growth, Biofilm Architecture and Competitive Behaviors of Oral Streptococci |
title_fullStr | Human Saliva Modifies Growth, Biofilm Architecture and Competitive Behaviors of Oral Streptococci |
title_full_unstemmed | Human Saliva Modifies Growth, Biofilm Architecture and Competitive Behaviors of Oral Streptococci |
title_short | Human Saliva Modifies Growth, Biofilm Architecture and Competitive Behaviors of Oral Streptococci |
title_sort | human saliva modifies growth, biofilm architecture and competitive behaviors of oral streptococci |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473590/ https://www.ncbi.nlm.nih.gov/pubmed/37662325 http://dx.doi.org/10.1101/2023.08.21.554151 |
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