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Metabolic plasticity enables lifestyle transitions of Porphyromonas gingivalis

Our understanding of how the oral anaerobe Porphyromonas gingivalis can persist below the gum line, induce ecological changes, and promote polymicrobial infections remains limited. P. gingivalis has long been described as a highly proteolytic and asaccharolytic pathogen that utilizes protein substra...

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Autores principales: Moradali, M. Fata, Davey, Mary E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144566/
https://www.ncbi.nlm.nih.gov/pubmed/34031416
http://dx.doi.org/10.1038/s41522-021-00217-4
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author Moradali, M. Fata
Davey, Mary E.
author_facet Moradali, M. Fata
Davey, Mary E.
author_sort Moradali, M. Fata
collection PubMed
description Our understanding of how the oral anaerobe Porphyromonas gingivalis can persist below the gum line, induce ecological changes, and promote polymicrobial infections remains limited. P. gingivalis has long been described as a highly proteolytic and asaccharolytic pathogen that utilizes protein substrates as the main source for energy production and proliferation. Here, we report that P. gingivalis displays a metabolic plasticity that enables the exploitation of non-proteinaceous substrates, specifically the monocarboxylates pyruvate and lactate, as well as human serum components, for colonization and biofilm formation. We show that anabolism of carbohydrates from pyruvate is powered by catabolism of amino acids. Concomitantly, the expression of fimbrial adhesion is upregulated, leading to the enhancement of biofilm formation, stimulation of multispecies biofilm development, and increase of colonization and invasion of the primary gingival epithelial cells by P. gingivalis. These studies provide the first glimpse into the metabolic plasticity of P. gingivalis and its adaptation to the nutritional condition of the host niche. Our findings support the model that in response to specific nutritional parameters, P. gingivalis has the potential to promote host colonization and development of a pathogenic community.
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spelling pubmed-81445662021-05-26 Metabolic plasticity enables lifestyle transitions of Porphyromonas gingivalis Moradali, M. Fata Davey, Mary E. NPJ Biofilms Microbiomes Article Our understanding of how the oral anaerobe Porphyromonas gingivalis can persist below the gum line, induce ecological changes, and promote polymicrobial infections remains limited. P. gingivalis has long been described as a highly proteolytic and asaccharolytic pathogen that utilizes protein substrates as the main source for energy production and proliferation. Here, we report that P. gingivalis displays a metabolic plasticity that enables the exploitation of non-proteinaceous substrates, specifically the monocarboxylates pyruvate and lactate, as well as human serum components, for colonization and biofilm formation. We show that anabolism of carbohydrates from pyruvate is powered by catabolism of amino acids. Concomitantly, the expression of fimbrial adhesion is upregulated, leading to the enhancement of biofilm formation, stimulation of multispecies biofilm development, and increase of colonization and invasion of the primary gingival epithelial cells by P. gingivalis. These studies provide the first glimpse into the metabolic plasticity of P. gingivalis and its adaptation to the nutritional condition of the host niche. Our findings support the model that in response to specific nutritional parameters, P. gingivalis has the potential to promote host colonization and development of a pathogenic community. Nature Publishing Group UK 2021-05-24 /pmc/articles/PMC8144566/ /pubmed/34031416 http://dx.doi.org/10.1038/s41522-021-00217-4 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
Moradali, M. Fata
Davey, Mary E.
Metabolic plasticity enables lifestyle transitions of Porphyromonas gingivalis
title Metabolic plasticity enables lifestyle transitions of Porphyromonas gingivalis
title_full Metabolic plasticity enables lifestyle transitions of Porphyromonas gingivalis
title_fullStr Metabolic plasticity enables lifestyle transitions of Porphyromonas gingivalis
title_full_unstemmed Metabolic plasticity enables lifestyle transitions of Porphyromonas gingivalis
title_short Metabolic plasticity enables lifestyle transitions of Porphyromonas gingivalis
title_sort metabolic plasticity enables lifestyle transitions of porphyromonas gingivalis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144566/
https://www.ncbi.nlm.nih.gov/pubmed/34031416
http://dx.doi.org/10.1038/s41522-021-00217-4
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