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The phageome in normal and inflamed human skin
Dysbiosis of skin microbiota drives the progression of atopic dermatitis (AD). The contribution of bacteriophages to bacterial community compositions in normal and inflamed skin is unknown. Using shotgun metagenomics from skin swabs of healthy individuals and patients with AD, we found 13,586 potent...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541010/ https://www.ncbi.nlm.nih.gov/pubmed/37774017 http://dx.doi.org/10.1126/sciadv.adg4015 |
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author | Wielscher, M. Pfisterer, K. Samardzic, D. Balsini, P. Bangert, C. Jäger, K. Buchberger, M. Selitsch, B. Pjevac, P. Willinger, B. Weninger, W. |
author_facet | Wielscher, M. Pfisterer, K. Samardzic, D. Balsini, P. Bangert, C. Jäger, K. Buchberger, M. Selitsch, B. Pjevac, P. Willinger, B. Weninger, W. |
author_sort | Wielscher, M. |
collection | PubMed |
description | Dysbiosis of skin microbiota drives the progression of atopic dermatitis (AD). The contribution of bacteriophages to bacterial community compositions in normal and inflamed skin is unknown. Using shotgun metagenomics from skin swabs of healthy individuals and patients with AD, we found 13,586 potential viral contiguous DNA sequences, which could be combined into 164 putative viral genomes including 133 putative phages. The Shannon diversity index for the viral metagenome-assembled genomes (vMAGs) did not correlate with AD. In total, we identified 28 vMAGs that differed significantly between normal and AD skin. Quantitative polymerase chain reaction validation of three complete vMAGs revealed their independence from host bacterium abundance. Our data indicate that normal and inflamed skin harbor distinct phageomes and suggest a causative relationship between changing viral and bacterial communities as a driver of skin pathology. |
format | Online Article Text |
id | pubmed-10541010 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-105410102023-10-01 The phageome in normal and inflamed human skin Wielscher, M. Pfisterer, K. Samardzic, D. Balsini, P. Bangert, C. Jäger, K. Buchberger, M. Selitsch, B. Pjevac, P. Willinger, B. Weninger, W. Sci Adv Biomedicine and Life Sciences Dysbiosis of skin microbiota drives the progression of atopic dermatitis (AD). The contribution of bacteriophages to bacterial community compositions in normal and inflamed skin is unknown. Using shotgun metagenomics from skin swabs of healthy individuals and patients with AD, we found 13,586 potential viral contiguous DNA sequences, which could be combined into 164 putative viral genomes including 133 putative phages. The Shannon diversity index for the viral metagenome-assembled genomes (vMAGs) did not correlate with AD. In total, we identified 28 vMAGs that differed significantly between normal and AD skin. Quantitative polymerase chain reaction validation of three complete vMAGs revealed their independence from host bacterium abundance. Our data indicate that normal and inflamed skin harbor distinct phageomes and suggest a causative relationship between changing viral and bacterial communities as a driver of skin pathology. American Association for the Advancement of Science 2023-09-29 /pmc/articles/PMC10541010/ /pubmed/37774017 http://dx.doi.org/10.1126/sciadv.adg4015 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Wielscher, M. Pfisterer, K. Samardzic, D. Balsini, P. Bangert, C. Jäger, K. Buchberger, M. Selitsch, B. Pjevac, P. Willinger, B. Weninger, W. The phageome in normal and inflamed human skin |
title | The phageome in normal and inflamed human skin |
title_full | The phageome in normal and inflamed human skin |
title_fullStr | The phageome in normal and inflamed human skin |
title_full_unstemmed | The phageome in normal and inflamed human skin |
title_short | The phageome in normal and inflamed human skin |
title_sort | phageome in normal and inflamed human skin |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541010/ https://www.ncbi.nlm.nih.gov/pubmed/37774017 http://dx.doi.org/10.1126/sciadv.adg4015 |
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