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Porphyromonas gingivalis Produce Neutrophil Specific Chemoattractants Including Short Chain Fatty Acids

Neutrophil migration from blood to tissue-residing microbes is governed by a series of chemoattractant gradients of both endogenous and microbial origin. Periodontal disease is characterized by neutrophil accumulation in the gingival pocket, recruited by the subgingival biofilm consisting mainly of...

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Autores principales: Dahlstrand Rudin, Agnes, Khamzeh, Arsham, Venkatakrishnan, Vignesh, Persson, Tishana, Gabl, Michael, Savolainen, Otto, Forsman, Huamei, Dahlgren, Claes, Christenson, Karin, Bylund, Johan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851090/
https://www.ncbi.nlm.nih.gov/pubmed/33542906
http://dx.doi.org/10.3389/fcimb.2020.620681
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author Dahlstrand Rudin, Agnes
Khamzeh, Arsham
Venkatakrishnan, Vignesh
Persson, Tishana
Gabl, Michael
Savolainen, Otto
Forsman, Huamei
Dahlgren, Claes
Christenson, Karin
Bylund, Johan
author_facet Dahlstrand Rudin, Agnes
Khamzeh, Arsham
Venkatakrishnan, Vignesh
Persson, Tishana
Gabl, Michael
Savolainen, Otto
Forsman, Huamei
Dahlgren, Claes
Christenson, Karin
Bylund, Johan
author_sort Dahlstrand Rudin, Agnes
collection PubMed
description Neutrophil migration from blood to tissue-residing microbes is governed by a series of chemoattractant gradients of both endogenous and microbial origin. Periodontal disease is characterized by neutrophil accumulation in the gingival pocket, recruited by the subgingival biofilm consisting mainly of gram-negative, anaerobic and proteolytic species such as Porphyromonas gingivalis. The fact that neutrophils are the dominating cell type in the gingival pocket suggests that neutrophil-specific chemoattractants are released by subgingival bacteria, but characterization of chemoattractants released by subgingival biofilm species remains incomplete. In the present study we characterized small (< 3 kDa) soluble chemoattractants released by growing P. gingivalis, and show that these are selective for neutrophils. Most neutrophil chemoattractant receptors are expressed also by mononuclear phagocytes, the free fatty acid receptor 2 (FFAR2) being an exception. In agreement with the selective neutrophil recruitment, the chemotactic activity found in P. gingivalis supernatants was mediated in part by a mixture of short chain fatty acids (SCFAs) that are recognized by FFAR2, and other leukocytes (including monocytes) did not respond to SCFA stimulation. Although SCFAs, produced by bacterial fermentation of dietary fiber in the gut, has previously been shown to utilize FFAR2, our data demonstrate that the pronounced proteolytic metabolism employed by P. gingivalis (and likely also other subgingival biofilm bacteria associated with periodontal diseases) may result in the generation of SCFAs that attract neutrophils to the gingival pocket. This finding highlights the interaction between SCFAs and FFAR2 in the context of P. gingivalis colonization during periodontal disease, but may also have implications for other inflammatory pathologies involving proteolytic bacteria.
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spelling pubmed-78510902021-02-03 Porphyromonas gingivalis Produce Neutrophil Specific Chemoattractants Including Short Chain Fatty Acids Dahlstrand Rudin, Agnes Khamzeh, Arsham Venkatakrishnan, Vignesh Persson, Tishana Gabl, Michael Savolainen, Otto Forsman, Huamei Dahlgren, Claes Christenson, Karin Bylund, Johan Front Cell Infect Microbiol Cellular and Infection Microbiology Neutrophil migration from blood to tissue-residing microbes is governed by a series of chemoattractant gradients of both endogenous and microbial origin. Periodontal disease is characterized by neutrophil accumulation in the gingival pocket, recruited by the subgingival biofilm consisting mainly of gram-negative, anaerobic and proteolytic species such as Porphyromonas gingivalis. The fact that neutrophils are the dominating cell type in the gingival pocket suggests that neutrophil-specific chemoattractants are released by subgingival bacteria, but characterization of chemoattractants released by subgingival biofilm species remains incomplete. In the present study we characterized small (< 3 kDa) soluble chemoattractants released by growing P. gingivalis, and show that these are selective for neutrophils. Most neutrophil chemoattractant receptors are expressed also by mononuclear phagocytes, the free fatty acid receptor 2 (FFAR2) being an exception. In agreement with the selective neutrophil recruitment, the chemotactic activity found in P. gingivalis supernatants was mediated in part by a mixture of short chain fatty acids (SCFAs) that are recognized by FFAR2, and other leukocytes (including monocytes) did not respond to SCFA stimulation. Although SCFAs, produced by bacterial fermentation of dietary fiber in the gut, has previously been shown to utilize FFAR2, our data demonstrate that the pronounced proteolytic metabolism employed by P. gingivalis (and likely also other subgingival biofilm bacteria associated with periodontal diseases) may result in the generation of SCFAs that attract neutrophils to the gingival pocket. This finding highlights the interaction between SCFAs and FFAR2 in the context of P. gingivalis colonization during periodontal disease, but may also have implications for other inflammatory pathologies involving proteolytic bacteria. Frontiers Media S.A. 2021-01-19 /pmc/articles/PMC7851090/ /pubmed/33542906 http://dx.doi.org/10.3389/fcimb.2020.620681 Text en Copyright © 2021 Dahlstrand Rudin, Khamzeh, Venkatakrishnan, Persson, Gabl, Savolainen, Forsman, Dahlgren, Christenson and Bylund http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Dahlstrand Rudin, Agnes
Khamzeh, Arsham
Venkatakrishnan, Vignesh
Persson, Tishana
Gabl, Michael
Savolainen, Otto
Forsman, Huamei
Dahlgren, Claes
Christenson, Karin
Bylund, Johan
Porphyromonas gingivalis Produce Neutrophil Specific Chemoattractants Including Short Chain Fatty Acids
title Porphyromonas gingivalis Produce Neutrophil Specific Chemoattractants Including Short Chain Fatty Acids
title_full Porphyromonas gingivalis Produce Neutrophil Specific Chemoattractants Including Short Chain Fatty Acids
title_fullStr Porphyromonas gingivalis Produce Neutrophil Specific Chemoattractants Including Short Chain Fatty Acids
title_full_unstemmed Porphyromonas gingivalis Produce Neutrophil Specific Chemoattractants Including Short Chain Fatty Acids
title_short Porphyromonas gingivalis Produce Neutrophil Specific Chemoattractants Including Short Chain Fatty Acids
title_sort porphyromonas gingivalis produce neutrophil specific chemoattractants including short chain fatty acids
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851090/
https://www.ncbi.nlm.nih.gov/pubmed/33542906
http://dx.doi.org/10.3389/fcimb.2020.620681
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