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Commensal and pathogenic biofilms differently modulate peri‐implant oral mucosa in an organotypic model

The impact of oral commensal and pathogenic bacteria on peri‐implant mucosa is not well understood, despite the high prevalence of peri‐implant infections. Hence, we investigated responses of the peri‐implant mucosa to Streptococcus oralis or Aggregatibacter actinomycetemcomitans biofilms using a no...

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Autores principales: Ingendoh‐Tsakmakidis, Alexandra, Mikolai, Carina, Winkel, Andreas, Szafrański, Szymon P., Falk, Christine S., Rossi, Angela, Walles, Heike, Stiesch, Meike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771885/
https://www.ncbi.nlm.nih.gov/pubmed/31270923
http://dx.doi.org/10.1111/cmi.13078
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author Ingendoh‐Tsakmakidis, Alexandra
Mikolai, Carina
Winkel, Andreas
Szafrański, Szymon P.
Falk, Christine S.
Rossi, Angela
Walles, Heike
Stiesch, Meike
author_facet Ingendoh‐Tsakmakidis, Alexandra
Mikolai, Carina
Winkel, Andreas
Szafrański, Szymon P.
Falk, Christine S.
Rossi, Angela
Walles, Heike
Stiesch, Meike
author_sort Ingendoh‐Tsakmakidis, Alexandra
collection PubMed
description The impact of oral commensal and pathogenic bacteria on peri‐implant mucosa is not well understood, despite the high prevalence of peri‐implant infections. Hence, we investigated responses of the peri‐implant mucosa to Streptococcus oralis or Aggregatibacter actinomycetemcomitans biofilms using a novel in vitro peri‐implant mucosa‐biofilm model. Our 3D model combined three components, organotypic oral mucosa, implant material, and oral biofilm, with structural assembly close to native situation. S. oralis induced a protective stress response in the peri‐implant mucosa through upregulation of heat shock protein (HSP70) genes. Attenuated inflammatory response was indicated by reduced cytokine levels of interleukin‐6 (IL‐6), interleukin‐8 (CXCL8), and monocyte chemoattractant protein‐1 (CCL2). The inflammatory balance was preserved through increased levels of tumor necrosis factor‐alpha (TNF‐α). A. actinomycetemcomitans induced downregulation of genes important for cell survival and host inflammatory response. The reduced cytokine levels of chemokine ligand 1 (CXCL1), CXCL8, and CCL2 also indicated a diminished inflammatory response. The induced immune balance by S. oralis may support oral health, whereas the reduced inflammatory response to A. actinomycetemcomitans may provide colonisation advantage and facilitate later tissue invasion. The comprehensive characterisation of peri‐implant mucosa‐biofilm interactions using our 3D model can provide new knowledge to improve strategies for prevention and therapy of peri‐implant disease.
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spelling pubmed-67718852019-10-07 Commensal and pathogenic biofilms differently modulate peri‐implant oral mucosa in an organotypic model Ingendoh‐Tsakmakidis, Alexandra Mikolai, Carina Winkel, Andreas Szafrański, Szymon P. Falk, Christine S. Rossi, Angela Walles, Heike Stiesch, Meike Cell Microbiol Research Articles The impact of oral commensal and pathogenic bacteria on peri‐implant mucosa is not well understood, despite the high prevalence of peri‐implant infections. Hence, we investigated responses of the peri‐implant mucosa to Streptococcus oralis or Aggregatibacter actinomycetemcomitans biofilms using a novel in vitro peri‐implant mucosa‐biofilm model. Our 3D model combined three components, organotypic oral mucosa, implant material, and oral biofilm, with structural assembly close to native situation. S. oralis induced a protective stress response in the peri‐implant mucosa through upregulation of heat shock protein (HSP70) genes. Attenuated inflammatory response was indicated by reduced cytokine levels of interleukin‐6 (IL‐6), interleukin‐8 (CXCL8), and monocyte chemoattractant protein‐1 (CCL2). The inflammatory balance was preserved through increased levels of tumor necrosis factor‐alpha (TNF‐α). A. actinomycetemcomitans induced downregulation of genes important for cell survival and host inflammatory response. The reduced cytokine levels of chemokine ligand 1 (CXCL1), CXCL8, and CCL2 also indicated a diminished inflammatory response. The induced immune balance by S. oralis may support oral health, whereas the reduced inflammatory response to A. actinomycetemcomitans may provide colonisation advantage and facilitate later tissue invasion. The comprehensive characterisation of peri‐implant mucosa‐biofilm interactions using our 3D model can provide new knowledge to improve strategies for prevention and therapy of peri‐implant disease. John Wiley and Sons Inc. 2019-07-17 2019-10 /pmc/articles/PMC6771885/ /pubmed/31270923 http://dx.doi.org/10.1111/cmi.13078 Text en © 2019 The Authors Cellular Microbiology Published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Ingendoh‐Tsakmakidis, Alexandra
Mikolai, Carina
Winkel, Andreas
Szafrański, Szymon P.
Falk, Christine S.
Rossi, Angela
Walles, Heike
Stiesch, Meike
Commensal and pathogenic biofilms differently modulate peri‐implant oral mucosa in an organotypic model
title Commensal and pathogenic biofilms differently modulate peri‐implant oral mucosa in an organotypic model
title_full Commensal and pathogenic biofilms differently modulate peri‐implant oral mucosa in an organotypic model
title_fullStr Commensal and pathogenic biofilms differently modulate peri‐implant oral mucosa in an organotypic model
title_full_unstemmed Commensal and pathogenic biofilms differently modulate peri‐implant oral mucosa in an organotypic model
title_short Commensal and pathogenic biofilms differently modulate peri‐implant oral mucosa in an organotypic model
title_sort commensal and pathogenic biofilms differently modulate peri‐implant oral mucosa in an organotypic model
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771885/
https://www.ncbi.nlm.nih.gov/pubmed/31270923
http://dx.doi.org/10.1111/cmi.13078
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