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Deciphering the Intracellular Fate of Propionibacterium acnes in Macrophages
Propionibacterium acnes is a Gram-positive bacterium that colonizes various niches of the human body, particularly the sebaceous follicles of the skin. Over the last years a role of this common skin bacterium as an opportunistic pathogen has been explored. Persistence of P. acnes in host tissue has...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3687600/ https://www.ncbi.nlm.nih.gov/pubmed/23862148 http://dx.doi.org/10.1155/2013/603046 |
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author | Fischer, Natalie Mak, Tim N. Shinohara, Debika Biswal Sfanos, Karen S. Meyer, Thomas F. Brüggemann, Holger |
author_facet | Fischer, Natalie Mak, Tim N. Shinohara, Debika Biswal Sfanos, Karen S. Meyer, Thomas F. Brüggemann, Holger |
author_sort | Fischer, Natalie |
collection | PubMed |
description | Propionibacterium acnes is a Gram-positive bacterium that colonizes various niches of the human body, particularly the sebaceous follicles of the skin. Over the last years a role of this common skin bacterium as an opportunistic pathogen has been explored. Persistence of P. acnes in host tissue has been associated with chronic inflammation and disease development, for example, in prostate pathologies. This study investigated the intracellular fate of P. acnes in macrophages after phagocytosis. In a mouse model of P. acnes-induced chronic prostatic inflammation, the bacterium could be detected in prostate-infiltrating macrophages at 2 weeks postinfection. Further studies performed in the human macrophage cell line THP-1 revealed intracellular survival and persistence of P. acnes but no intracellular replication or escape from the host cell. Confocal analyses of phagosome acidification and maturation were performed. Acidification of P. acnes-containing phagosomes was observed at 6 h postinfection but then lost again, indicative of cytosolic escape of P. acnes or intraphagosomal pH neutralization. No colocalization with the lysosomal markers LAMP1 and cathepsin D was observed, implying that the P. acnes-containing phagosome does not fuse with lysosomes. Our findings give first insights into the intracellular fate of P. acnes; its persistency is likely to be important for the development of P. acnes-associated inflammatory diseases. |
format | Online Article Text |
id | pubmed-3687600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-36876002013-07-16 Deciphering the Intracellular Fate of Propionibacterium acnes in Macrophages Fischer, Natalie Mak, Tim N. Shinohara, Debika Biswal Sfanos, Karen S. Meyer, Thomas F. Brüggemann, Holger Biomed Res Int Research Article Propionibacterium acnes is a Gram-positive bacterium that colonizes various niches of the human body, particularly the sebaceous follicles of the skin. Over the last years a role of this common skin bacterium as an opportunistic pathogen has been explored. Persistence of P. acnes in host tissue has been associated with chronic inflammation and disease development, for example, in prostate pathologies. This study investigated the intracellular fate of P. acnes in macrophages after phagocytosis. In a mouse model of P. acnes-induced chronic prostatic inflammation, the bacterium could be detected in prostate-infiltrating macrophages at 2 weeks postinfection. Further studies performed in the human macrophage cell line THP-1 revealed intracellular survival and persistence of P. acnes but no intracellular replication or escape from the host cell. Confocal analyses of phagosome acidification and maturation were performed. Acidification of P. acnes-containing phagosomes was observed at 6 h postinfection but then lost again, indicative of cytosolic escape of P. acnes or intraphagosomal pH neutralization. No colocalization with the lysosomal markers LAMP1 and cathepsin D was observed, implying that the P. acnes-containing phagosome does not fuse with lysosomes. Our findings give first insights into the intracellular fate of P. acnes; its persistency is likely to be important for the development of P. acnes-associated inflammatory diseases. Hindawi Publishing Corporation 2013 2013-06-05 /pmc/articles/PMC3687600/ /pubmed/23862148 http://dx.doi.org/10.1155/2013/603046 Text en Copyright © 2013 Natalie Fischer et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Fischer, Natalie Mak, Tim N. Shinohara, Debika Biswal Sfanos, Karen S. Meyer, Thomas F. Brüggemann, Holger Deciphering the Intracellular Fate of Propionibacterium acnes in Macrophages |
title | Deciphering the Intracellular Fate of Propionibacterium acnes in Macrophages |
title_full | Deciphering the Intracellular Fate of Propionibacterium acnes in Macrophages |
title_fullStr | Deciphering the Intracellular Fate of Propionibacterium acnes in Macrophages |
title_full_unstemmed | Deciphering the Intracellular Fate of Propionibacterium acnes in Macrophages |
title_short | Deciphering the Intracellular Fate of Propionibacterium acnes in Macrophages |
title_sort | deciphering the intracellular fate of propionibacterium acnes in macrophages |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3687600/ https://www.ncbi.nlm.nih.gov/pubmed/23862148 http://dx.doi.org/10.1155/2013/603046 |
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