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Cutibacterium acnes Phylotype I and II Strains Interact Differently With Human Skin Cells

Acne vulgaris is one of the most common skin disorders and affects the pilosebaceous units. Although the exact pathogenesis of acne is still unknown, Cutibacterium acnes (formerly known as Propionibacterium acnes) is considered one of the key contributing factors. In fact, a significant association...

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Autores principales: Spittaels, Karl-Jan, Ongena, Ruben, Zouboulis, Christos C., Crabbé, Aurélie, Coenye, Tom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7717938/
https://www.ncbi.nlm.nih.gov/pubmed/33330124
http://dx.doi.org/10.3389/fcimb.2020.575164
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author Spittaels, Karl-Jan
Ongena, Ruben
Zouboulis, Christos C.
Crabbé, Aurélie
Coenye, Tom
author_facet Spittaels, Karl-Jan
Ongena, Ruben
Zouboulis, Christos C.
Crabbé, Aurélie
Coenye, Tom
author_sort Spittaels, Karl-Jan
collection PubMed
description Acne vulgaris is one of the most common skin disorders and affects the pilosebaceous units. Although the exact pathogenesis of acne is still unknown, Cutibacterium acnes (formerly known as Propionibacterium acnes) is considered one of the key contributing factors. In fact, a significant association exists between C. acnes strains belonging to phylotype I and acne. However, there is still heavy debate on the exact role of C. acnes in acne and its behavior in the pilosebaceous unit, and more specifically its interactions with the human skin cells. In this study, key elements of the host-pathogen interaction were studied for a collection of C. acnes strains, belonging to phylotype I and II, including association with HaCaT keratinocytes and SZ95 sebocytes, the effect of C. acnes on keratinocyte tight junctions in a HaCaT monoculture and in an additional keratinocyte-sebocyte co-culture model, and C. acnes invasion through the keratinocyte cell layer. Our data showed association of all C. acnes strains to both skin cell lines, with a significantly higher association of type I strains compared to type II strains. Microscopic imaging and western blot analysis of the tight junction protein ZO-1, together with transepithelial electrical resistance (TEER) measurements revealed an initial induction of keratinocyte tight junctions after 24 h infection but a degradation after 48 h, demonstrating a decline in cell lining integrity during infection. Subsequently, C. acnes was able to invade after 48 h of infection, although invasion frequency was significantly higher for type II strains compared to type I strains.
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spelling pubmed-77179382020-12-15 Cutibacterium acnes Phylotype I and II Strains Interact Differently With Human Skin Cells Spittaels, Karl-Jan Ongena, Ruben Zouboulis, Christos C. Crabbé, Aurélie Coenye, Tom Front Cell Infect Microbiol Cellular and Infection Microbiology Acne vulgaris is one of the most common skin disorders and affects the pilosebaceous units. Although the exact pathogenesis of acne is still unknown, Cutibacterium acnes (formerly known as Propionibacterium acnes) is considered one of the key contributing factors. In fact, a significant association exists between C. acnes strains belonging to phylotype I and acne. However, there is still heavy debate on the exact role of C. acnes in acne and its behavior in the pilosebaceous unit, and more specifically its interactions with the human skin cells. In this study, key elements of the host-pathogen interaction were studied for a collection of C. acnes strains, belonging to phylotype I and II, including association with HaCaT keratinocytes and SZ95 sebocytes, the effect of C. acnes on keratinocyte tight junctions in a HaCaT monoculture and in an additional keratinocyte-sebocyte co-culture model, and C. acnes invasion through the keratinocyte cell layer. Our data showed association of all C. acnes strains to both skin cell lines, with a significantly higher association of type I strains compared to type II strains. Microscopic imaging and western blot analysis of the tight junction protein ZO-1, together with transepithelial electrical resistance (TEER) measurements revealed an initial induction of keratinocyte tight junctions after 24 h infection but a degradation after 48 h, demonstrating a decline in cell lining integrity during infection. Subsequently, C. acnes was able to invade after 48 h of infection, although invasion frequency was significantly higher for type II strains compared to type I strains. Frontiers Media S.A. 2020-11-16 /pmc/articles/PMC7717938/ /pubmed/33330124 http://dx.doi.org/10.3389/fcimb.2020.575164 Text en Copyright © 2020 Spittaels, Ongena, Zouboulis, Crabbé and Coenye 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
Spittaels, Karl-Jan
Ongena, Ruben
Zouboulis, Christos C.
Crabbé, Aurélie
Coenye, Tom
Cutibacterium acnes Phylotype I and II Strains Interact Differently With Human Skin Cells
title Cutibacterium acnes Phylotype I and II Strains Interact Differently With Human Skin Cells
title_full Cutibacterium acnes Phylotype I and II Strains Interact Differently With Human Skin Cells
title_fullStr Cutibacterium acnes Phylotype I and II Strains Interact Differently With Human Skin Cells
title_full_unstemmed Cutibacterium acnes Phylotype I and II Strains Interact Differently With Human Skin Cells
title_short Cutibacterium acnes Phylotype I and II Strains Interact Differently With Human Skin Cells
title_sort cutibacterium acnes phylotype i and ii strains interact differently with human skin cells
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7717938/
https://www.ncbi.nlm.nih.gov/pubmed/33330124
http://dx.doi.org/10.3389/fcimb.2020.575164
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