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Synthesis of ppGpp impacts type IX secretion and biofilm matrix formation in Porphyromonas gingivalis

In order to persist, bacteria need to adjust their physiological state in response to external and internal cues. External stimuli are often referred to as stressors. The stringent response, mediated by the alarmone (p)ppGpp, is central to the stress response in many bacteria; yet, there is limited...

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Autores principales: Kim, Hey-Min, Davey, Mary E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994654/
https://www.ncbi.nlm.nih.gov/pubmed/32005827
http://dx.doi.org/10.1038/s41522-020-0115-4
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author Kim, Hey-Min
Davey, Mary E.
author_facet Kim, Hey-Min
Davey, Mary E.
author_sort Kim, Hey-Min
collection PubMed
description In order to persist, bacteria need to adjust their physiological state in response to external and internal cues. External stimuli are often referred to as stressors. The stringent response, mediated by the alarmone (p)ppGpp, is central to the stress response in many bacteria; yet, there is limited knowledge regarding the role of (p)ppGpp signaling in bacteria belonging to the phylum Bacteroidetes. Like its counterparts in the gut (e.g., Bacteroides thetaiotaomicron and Bacteroides fragilis), Porphyromonas gingivalis persists in close association with its human host. Given the potential for numerous perturbations in the oral cavity, and the fact that P. gingivalis can enter and replicate within host cells, we hypothesized that (p)ppGpp is a key signaling molecule for stress adaptation and persistence. Here, we show that accumulation of ppGpp in P. gingivalis is governed by two homologous enzymes, designated Rel, and RshB, and that ppGpp signaling affects growth rate, survival, biofilm formation, production of outer membrane vesicles, and expression of genes encoding type IX secretion structural and cargo proteins. Overall, our findings provide a potential mechanism by which biofilm formation and virulence of P. gingivalis are integrated via ppGpp signaling, a regulatory mechanism central to bacterial survival in dynamic environments.
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spelling pubmed-69946542020-02-05 Synthesis of ppGpp impacts type IX secretion and biofilm matrix formation in Porphyromonas gingivalis Kim, Hey-Min Davey, Mary E. NPJ Biofilms Microbiomes Article In order to persist, bacteria need to adjust their physiological state in response to external and internal cues. External stimuli are often referred to as stressors. The stringent response, mediated by the alarmone (p)ppGpp, is central to the stress response in many bacteria; yet, there is limited knowledge regarding the role of (p)ppGpp signaling in bacteria belonging to the phylum Bacteroidetes. Like its counterparts in the gut (e.g., Bacteroides thetaiotaomicron and Bacteroides fragilis), Porphyromonas gingivalis persists in close association with its human host. Given the potential for numerous perturbations in the oral cavity, and the fact that P. gingivalis can enter and replicate within host cells, we hypothesized that (p)ppGpp is a key signaling molecule for stress adaptation and persistence. Here, we show that accumulation of ppGpp in P. gingivalis is governed by two homologous enzymes, designated Rel, and RshB, and that ppGpp signaling affects growth rate, survival, biofilm formation, production of outer membrane vesicles, and expression of genes encoding type IX secretion structural and cargo proteins. Overall, our findings provide a potential mechanism by which biofilm formation and virulence of P. gingivalis are integrated via ppGpp signaling, a regulatory mechanism central to bacterial survival in dynamic environments. Nature Publishing Group UK 2020-01-31 /pmc/articles/PMC6994654/ /pubmed/32005827 http://dx.doi.org/10.1038/s41522-020-0115-4 Text en © The Author(s) 2020 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
Kim, Hey-Min
Davey, Mary E.
Synthesis of ppGpp impacts type IX secretion and biofilm matrix formation in Porphyromonas gingivalis
title Synthesis of ppGpp impacts type IX secretion and biofilm matrix formation in Porphyromonas gingivalis
title_full Synthesis of ppGpp impacts type IX secretion and biofilm matrix formation in Porphyromonas gingivalis
title_fullStr Synthesis of ppGpp impacts type IX secretion and biofilm matrix formation in Porphyromonas gingivalis
title_full_unstemmed Synthesis of ppGpp impacts type IX secretion and biofilm matrix formation in Porphyromonas gingivalis
title_short Synthesis of ppGpp impacts type IX secretion and biofilm matrix formation in Porphyromonas gingivalis
title_sort synthesis of ppgpp impacts type ix secretion and biofilm matrix formation in porphyromonas gingivalis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994654/
https://www.ncbi.nlm.nih.gov/pubmed/32005827
http://dx.doi.org/10.1038/s41522-020-0115-4
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