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Polymicrobial synergy within oral biofilm promotes invasion of dendritic cells and survival of consortia members

Years of human microbiome research have confirmed that microbes rarely live or function alone, favoring diverse communities. Yet most experimental host-pathogen studies employ single species models of infection. Here, the influence of three-species oral microbial consortium on growth, virulence, inv...

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Autores principales: El-Awady, Ahmed, de Sousa Rabelo, Mariana, Meghil, Mohamed M., Rajendran, Mythilypriya, Elashiry, Mahmoud, Stadler, Amanda Finger, Foz, Adriana Moura, Susin, Cristiano, Romito, Giuseppe Alexandre, Arce, Roger M., Cutler, Christopher W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423025/
https://www.ncbi.nlm.nih.gov/pubmed/32179736
http://dx.doi.org/10.1038/s41522-019-0084-7
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author El-Awady, Ahmed
de Sousa Rabelo, Mariana
Meghil, Mohamed M.
Rajendran, Mythilypriya
Elashiry, Mahmoud
Stadler, Amanda Finger
Foz, Adriana Moura
Susin, Cristiano
Romito, Giuseppe Alexandre
Arce, Roger M.
Cutler, Christopher W.
author_facet El-Awady, Ahmed
de Sousa Rabelo, Mariana
Meghil, Mohamed M.
Rajendran, Mythilypriya
Elashiry, Mahmoud
Stadler, Amanda Finger
Foz, Adriana Moura
Susin, Cristiano
Romito, Giuseppe Alexandre
Arce, Roger M.
Cutler, Christopher W.
author_sort El-Awady, Ahmed
collection PubMed
description Years of human microbiome research have confirmed that microbes rarely live or function alone, favoring diverse communities. Yet most experimental host-pathogen studies employ single species models of infection. Here, the influence of three-species oral microbial consortium on growth, virulence, invasion and persistence in dendritic cells (DCs) was examined experimentally in human monocyte-derived dendritic cells (DCs) and in patients with periodontitis (PD). Cooperative biofilm formation by Streptococcus gordonii, Fusobacterium nucleatum and Porphyromonas gingivalis was documented in vitro using growth models and scanning electron microscopy. Analysis of growth rates by species-specific 16s rRNA probes revealed distinct, early advantages to consortium growth for S. gordonii and F. nucleatum with P. gingivalis, while P. gingivalis upregulated its short mfa1 fimbriae, leading to increased invasion of DCs. F. nucleatum was only taken up by DCs when in consortium with P. gingivalis. Mature consortium regressed DC maturation upon uptake, as determined by flow cytometry. Analysis of dental plaques of PD and healthy subjects by 16s rRNA confirmed oral colonization with consortium members, but DC hematogenous spread was limited to P. gingivalis and F. nucleatum. Expression of P. gingivalis mfa1 fimbriae was increased in dental plaques and hematogenous DCs of PD patients. P. gingivalis in the consortium correlated with an adverse clinical response in the gingiva of PD subjects. In conclusion, we have identified polymicrobial synergy in a three-species oral consortium that may have negative consequences for the host, including microbial dissemination and adverse peripheral inflammatory responses.
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spelling pubmed-64230252019-03-25 Polymicrobial synergy within oral biofilm promotes invasion of dendritic cells and survival of consortia members El-Awady, Ahmed de Sousa Rabelo, Mariana Meghil, Mohamed M. Rajendran, Mythilypriya Elashiry, Mahmoud Stadler, Amanda Finger Foz, Adriana Moura Susin, Cristiano Romito, Giuseppe Alexandre Arce, Roger M. Cutler, Christopher W. NPJ Biofilms Microbiomes Article Years of human microbiome research have confirmed that microbes rarely live or function alone, favoring diverse communities. Yet most experimental host-pathogen studies employ single species models of infection. Here, the influence of three-species oral microbial consortium on growth, virulence, invasion and persistence in dendritic cells (DCs) was examined experimentally in human monocyte-derived dendritic cells (DCs) and in patients with periodontitis (PD). Cooperative biofilm formation by Streptococcus gordonii, Fusobacterium nucleatum and Porphyromonas gingivalis was documented in vitro using growth models and scanning electron microscopy. Analysis of growth rates by species-specific 16s rRNA probes revealed distinct, early advantages to consortium growth for S. gordonii and F. nucleatum with P. gingivalis, while P. gingivalis upregulated its short mfa1 fimbriae, leading to increased invasion of DCs. F. nucleatum was only taken up by DCs when in consortium with P. gingivalis. Mature consortium regressed DC maturation upon uptake, as determined by flow cytometry. Analysis of dental plaques of PD and healthy subjects by 16s rRNA confirmed oral colonization with consortium members, but DC hematogenous spread was limited to P. gingivalis and F. nucleatum. Expression of P. gingivalis mfa1 fimbriae was increased in dental plaques and hematogenous DCs of PD patients. P. gingivalis in the consortium correlated with an adverse clinical response in the gingiva of PD subjects. In conclusion, we have identified polymicrobial synergy in a three-species oral consortium that may have negative consequences for the host, including microbial dissemination and adverse peripheral inflammatory responses. Nature Publishing Group UK 2019-03-18 /pmc/articles/PMC6423025/ /pubmed/32179736 http://dx.doi.org/10.1038/s41522-019-0084-7 Text en © The Author(s) 2019 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/.
spellingShingle Article
El-Awady, Ahmed
de Sousa Rabelo, Mariana
Meghil, Mohamed M.
Rajendran, Mythilypriya
Elashiry, Mahmoud
Stadler, Amanda Finger
Foz, Adriana Moura
Susin, Cristiano
Romito, Giuseppe Alexandre
Arce, Roger M.
Cutler, Christopher W.
Polymicrobial synergy within oral biofilm promotes invasion of dendritic cells and survival of consortia members
title Polymicrobial synergy within oral biofilm promotes invasion of dendritic cells and survival of consortia members
title_full Polymicrobial synergy within oral biofilm promotes invasion of dendritic cells and survival of consortia members
title_fullStr Polymicrobial synergy within oral biofilm promotes invasion of dendritic cells and survival of consortia members
title_full_unstemmed Polymicrobial synergy within oral biofilm promotes invasion of dendritic cells and survival of consortia members
title_short Polymicrobial synergy within oral biofilm promotes invasion of dendritic cells and survival of consortia members
title_sort polymicrobial synergy within oral biofilm promotes invasion of dendritic cells and survival of consortia members
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423025/
https://www.ncbi.nlm.nih.gov/pubmed/32179736
http://dx.doi.org/10.1038/s41522-019-0084-7
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