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Metabolic cooperativity between Porphyromonas gingivalis and Treponema denticola
BACKGROUND: Porphyromonas gingivalis and Treponema denticola are proteolytic periodontopathogens that co-localize in polymicrobial subgingival plaque biofilms, display in vitro growth symbiosis and synergistic virulence in animal models of disease. These symbioses are underpinned by a range of meta...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482830/ https://www.ncbi.nlm.nih.gov/pubmed/32944158 http://dx.doi.org/10.1080/20002297.2020.1808750 |
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author | Kin, Lin Xin Butler, Catherine A. Slakeski, Nada Hoffmann, Brigitte Dashper, Stuart G. Reynolds, Eric C. |
author_facet | Kin, Lin Xin Butler, Catherine A. Slakeski, Nada Hoffmann, Brigitte Dashper, Stuart G. Reynolds, Eric C. |
author_sort | Kin, Lin Xin |
collection | PubMed |
description | BACKGROUND: Porphyromonas gingivalis and Treponema denticola are proteolytic periodontopathogens that co-localize in polymicrobial subgingival plaque biofilms, display in vitro growth symbiosis and synergistic virulence in animal models of disease. These symbioses are underpinned by a range of metabolic interactions including cooperative hydrolysis of glycine-containing peptides to produce free glycine, which T. denticola uses as a major energy and carbon source. OBJECTIVE: To characterize the P. gingivalis gene products essential for these interactions. Methods: The P. gingivalis transcriptome exposed to cell-free T. denticola conditioned medium was determined using RNA-seq. P. gingivalis proteases potentially involved in hydrolysis of glycine-containing peptides were identified using a bioinformatics approach. RESULTS: One hundred and thirty-twogenes displayed differential expression, with the pattern of gene expression consistent with succinate cross-feeding from T. denticola to P. gingivalis and metabolic shifts in the P. gingivalis folate-mediated one carbon superpathway. Interestingly, no P. gingivalis proteases were significantly up-regulated. Three P. gingivalis proteases were identified as candidates and inactivated to determine their role in the release of free glycine. P. gingivalis PG0753 and PG1788 but not PG1605 are involved in the hydrolysis of glycine-containing peptides, making free glycine available for T. denticola utilization. CONCLUSION: Collectively these metabolic interactions help to partition resources and engage synergistic interactions between these two species. |
format | Online Article Text |
id | pubmed-7482830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-74828302020-09-16 Metabolic cooperativity between Porphyromonas gingivalis and Treponema denticola Kin, Lin Xin Butler, Catherine A. Slakeski, Nada Hoffmann, Brigitte Dashper, Stuart G. Reynolds, Eric C. J Oral Microbiol Original Article BACKGROUND: Porphyromonas gingivalis and Treponema denticola are proteolytic periodontopathogens that co-localize in polymicrobial subgingival plaque biofilms, display in vitro growth symbiosis and synergistic virulence in animal models of disease. These symbioses are underpinned by a range of metabolic interactions including cooperative hydrolysis of glycine-containing peptides to produce free glycine, which T. denticola uses as a major energy and carbon source. OBJECTIVE: To characterize the P. gingivalis gene products essential for these interactions. Methods: The P. gingivalis transcriptome exposed to cell-free T. denticola conditioned medium was determined using RNA-seq. P. gingivalis proteases potentially involved in hydrolysis of glycine-containing peptides were identified using a bioinformatics approach. RESULTS: One hundred and thirty-twogenes displayed differential expression, with the pattern of gene expression consistent with succinate cross-feeding from T. denticola to P. gingivalis and metabolic shifts in the P. gingivalis folate-mediated one carbon superpathway. Interestingly, no P. gingivalis proteases were significantly up-regulated. Three P. gingivalis proteases were identified as candidates and inactivated to determine their role in the release of free glycine. P. gingivalis PG0753 and PG1788 but not PG1605 are involved in the hydrolysis of glycine-containing peptides, making free glycine available for T. denticola utilization. CONCLUSION: Collectively these metabolic interactions help to partition resources and engage synergistic interactions between these two species. Taylor & Francis 2020-08-24 /pmc/articles/PMC7482830/ /pubmed/32944158 http://dx.doi.org/10.1080/20002297.2020.1808750 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kin, Lin Xin Butler, Catherine A. Slakeski, Nada Hoffmann, Brigitte Dashper, Stuart G. Reynolds, Eric C. Metabolic cooperativity between Porphyromonas gingivalis and Treponema denticola |
title | Metabolic cooperativity between Porphyromonas gingivalis and Treponema denticola |
title_full | Metabolic cooperativity between Porphyromonas gingivalis and Treponema denticola |
title_fullStr | Metabolic cooperativity between Porphyromonas gingivalis and Treponema denticola |
title_full_unstemmed | Metabolic cooperativity between Porphyromonas gingivalis and Treponema denticola |
title_short | Metabolic cooperativity between Porphyromonas gingivalis and Treponema denticola |
title_sort | metabolic cooperativity between porphyromonas gingivalis and treponema denticola |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482830/ https://www.ncbi.nlm.nih.gov/pubmed/32944158 http://dx.doi.org/10.1080/20002297.2020.1808750 |
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