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Mechanisms underlying interactions between two abundant oral commensal bacteria

Complex polymicrobial biofilm communities are abundant in nature particularly in the human oral cavity where their composition and fitness can affect health. While the study of these communities during disease is essential and prevalent, little is known about interactions within the healthy plaque c...

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Autores principales: Perera, Dasith, McLean, Anthony, Morillo-López, Viviana, Cloutier-Leblanc, Kaileigh, Almeida, Eric, Cabana, Kiana, Mark Welch, Jessica, Ramsey, Matthew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8940909/
https://www.ncbi.nlm.nih.gov/pubmed/34732850
http://dx.doi.org/10.1038/s41396-021-01141-3
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author Perera, Dasith
McLean, Anthony
Morillo-López, Viviana
Cloutier-Leblanc, Kaileigh
Almeida, Eric
Cabana, Kiana
Mark Welch, Jessica
Ramsey, Matthew
author_facet Perera, Dasith
McLean, Anthony
Morillo-López, Viviana
Cloutier-Leblanc, Kaileigh
Almeida, Eric
Cabana, Kiana
Mark Welch, Jessica
Ramsey, Matthew
author_sort Perera, Dasith
collection PubMed
description Complex polymicrobial biofilm communities are abundant in nature particularly in the human oral cavity where their composition and fitness can affect health. While the study of these communities during disease is essential and prevalent, little is known about interactions within the healthy plaque community. Here we describe interactions between two of the most abundant species in this healthy microbiome, Haemophilus parainfluenzae and Streptococcus mitis. We discovered that H. parainfluenzae typically exists adjacent to mitis group streptococci in vivo with which it is also positively correlated based on microbiome data. By comparing in vitro coculture data to ex vivo microscopy we revealed that this co-occurrence is density dependent and further influenced by H(2)O(2) production. We discovered that H. parainfluenzae utilizes a more redundant, multifactorial response to H(2)O(2) than related microorganisms and that this system’s integrity enhances streptococcal fitness. Our results indicate that mitis group streptococci are likely the in vivo source of NAD for H. parainfluenzae and also evoke patterns of carbon utilization in vitro for H. parainfluenzae similar to those observed in vivo. Our findings describe mechanistic interactions between two of the most abundant and prevalent members of healthy supragingival plaque that contribute to their in vivo survival.
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spelling pubmed-89409092022-04-08 Mechanisms underlying interactions between two abundant oral commensal bacteria Perera, Dasith McLean, Anthony Morillo-López, Viviana Cloutier-Leblanc, Kaileigh Almeida, Eric Cabana, Kiana Mark Welch, Jessica Ramsey, Matthew ISME J Article Complex polymicrobial biofilm communities are abundant in nature particularly in the human oral cavity where their composition and fitness can affect health. While the study of these communities during disease is essential and prevalent, little is known about interactions within the healthy plaque community. Here we describe interactions between two of the most abundant species in this healthy microbiome, Haemophilus parainfluenzae and Streptococcus mitis. We discovered that H. parainfluenzae typically exists adjacent to mitis group streptococci in vivo with which it is also positively correlated based on microbiome data. By comparing in vitro coculture data to ex vivo microscopy we revealed that this co-occurrence is density dependent and further influenced by H(2)O(2) production. We discovered that H. parainfluenzae utilizes a more redundant, multifactorial response to H(2)O(2) than related microorganisms and that this system’s integrity enhances streptococcal fitness. Our results indicate that mitis group streptococci are likely the in vivo source of NAD for H. parainfluenzae and also evoke patterns of carbon utilization in vitro for H. parainfluenzae similar to those observed in vivo. Our findings describe mechanistic interactions between two of the most abundant and prevalent members of healthy supragingival plaque that contribute to their in vivo survival. Nature Publishing Group UK 2021-11-03 2022-04 /pmc/articles/PMC8940909/ /pubmed/34732850 http://dx.doi.org/10.1038/s41396-021-01141-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Perera, Dasith
McLean, Anthony
Morillo-López, Viviana
Cloutier-Leblanc, Kaileigh
Almeida, Eric
Cabana, Kiana
Mark Welch, Jessica
Ramsey, Matthew
Mechanisms underlying interactions between two abundant oral commensal bacteria
title Mechanisms underlying interactions between two abundant oral commensal bacteria
title_full Mechanisms underlying interactions between two abundant oral commensal bacteria
title_fullStr Mechanisms underlying interactions between two abundant oral commensal bacteria
title_full_unstemmed Mechanisms underlying interactions between two abundant oral commensal bacteria
title_short Mechanisms underlying interactions between two abundant oral commensal bacteria
title_sort mechanisms underlying interactions between two abundant oral commensal bacteria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8940909/
https://www.ncbi.nlm.nih.gov/pubmed/34732850
http://dx.doi.org/10.1038/s41396-021-01141-3
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