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Proteomic shifts in multi-species oral biofilms caused by Anaeroglobus geminatus

Anaeroglobus geminatus is a relatively newly discovered putative pathogen, with a potential role in the microbial shift associated with periodontitis, a disease that causes inflammatory destruction of the periodontal tissues, and eventually tooth loss. This study aimed to introduce A. geminatus into...

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Autores principales: Bao, Kai, Bostanci, Nagihan, Thurnheer, Thomas, Belibasakis, Georgios N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5493653/
https://www.ncbi.nlm.nih.gov/pubmed/28667274
http://dx.doi.org/10.1038/s41598-017-04594-9
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author Bao, Kai
Bostanci, Nagihan
Thurnheer, Thomas
Belibasakis, Georgios N.
author_facet Bao, Kai
Bostanci, Nagihan
Thurnheer, Thomas
Belibasakis, Georgios N.
author_sort Bao, Kai
collection PubMed
description Anaeroglobus geminatus is a relatively newly discovered putative pathogen, with a potential role in the microbial shift associated with periodontitis, a disease that causes inflammatory destruction of the periodontal tissues, and eventually tooth loss. This study aimed to introduce A. geminatus into a polymicrobial biofilm model of relevance to periodontitis, and monitor the proteomic responses exerted to the rest of the biofilm community. A. geminatus was grown together with another 10-species in a well-established “subgingival” in vitro biofilm model. Its effects on the other species were quantitatively evaluated by qPCR and label-free proteomics. A. geminatus caused a significant increase in P. intermedia numbers, but not the other species in the biofilm. Whole cell proteome profiling of the biofilms by LC-MS/MS identified a total of 3213 proteins. Label-free quantitative proteomics revealed that 187 proteins belonging to the other 10 species were differentially abundant when A. geminatus was present in the biofilm. The species with most up-regulated and down-regulated proteins were P. intermedia and S. oralis, respectively. Regulated proteins were of primarily of ribosomal origin, and other affected categories involved proteolysis, carbon metabolism and iron transport. In conclusion, A. geminatus can be successfully grown in a polymicrobial biofilm community, causing quantitative proteomic shifts commensurate with increased virulence properties.
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spelling pubmed-54936532017-07-05 Proteomic shifts in multi-species oral biofilms caused by Anaeroglobus geminatus Bao, Kai Bostanci, Nagihan Thurnheer, Thomas Belibasakis, Georgios N. Sci Rep Article Anaeroglobus geminatus is a relatively newly discovered putative pathogen, with a potential role in the microbial shift associated with periodontitis, a disease that causes inflammatory destruction of the periodontal tissues, and eventually tooth loss. This study aimed to introduce A. geminatus into a polymicrobial biofilm model of relevance to periodontitis, and monitor the proteomic responses exerted to the rest of the biofilm community. A. geminatus was grown together with another 10-species in a well-established “subgingival” in vitro biofilm model. Its effects on the other species were quantitatively evaluated by qPCR and label-free proteomics. A. geminatus caused a significant increase in P. intermedia numbers, but not the other species in the biofilm. Whole cell proteome profiling of the biofilms by LC-MS/MS identified a total of 3213 proteins. Label-free quantitative proteomics revealed that 187 proteins belonging to the other 10 species were differentially abundant when A. geminatus was present in the biofilm. The species with most up-regulated and down-regulated proteins were P. intermedia and S. oralis, respectively. Regulated proteins were of primarily of ribosomal origin, and other affected categories involved proteolysis, carbon metabolism and iron transport. In conclusion, A. geminatus can be successfully grown in a polymicrobial biofilm community, causing quantitative proteomic shifts commensurate with increased virulence properties. Nature Publishing Group UK 2017-06-30 /pmc/articles/PMC5493653/ /pubmed/28667274 http://dx.doi.org/10.1038/s41598-017-04594-9 Text en © The Author(s) 2017 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
Bao, Kai
Bostanci, Nagihan
Thurnheer, Thomas
Belibasakis, Georgios N.
Proteomic shifts in multi-species oral biofilms caused by Anaeroglobus geminatus
title Proteomic shifts in multi-species oral biofilms caused by Anaeroglobus geminatus
title_full Proteomic shifts in multi-species oral biofilms caused by Anaeroglobus geminatus
title_fullStr Proteomic shifts in multi-species oral biofilms caused by Anaeroglobus geminatus
title_full_unstemmed Proteomic shifts in multi-species oral biofilms caused by Anaeroglobus geminatus
title_short Proteomic shifts in multi-species oral biofilms caused by Anaeroglobus geminatus
title_sort proteomic shifts in multi-species oral biofilms caused by anaeroglobus geminatus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5493653/
https://www.ncbi.nlm.nih.gov/pubmed/28667274
http://dx.doi.org/10.1038/s41598-017-04594-9
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