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Skin Microbiome in Prurigo Nodularis
Prurigo nodularis (PN) is a chronic condition characterized by the presence of nodular lesions accompanied by intense pruritus. The disease has been linked to several infectious factors, but data on the direct presence of microorganisms in the lesions of PN are scarce. The aim of this study was to e...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10146575/ https://www.ncbi.nlm.nih.gov/pubmed/37108838 http://dx.doi.org/10.3390/ijms24087675 |
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author | Tutka, Klaudia Żychowska, Magdalena Żaczek, Anna Maternia-Dudzik, Karolina Pawełczyk, Jakub Strapagiel, Dominik Lach, Jakub Reich, Adam |
author_facet | Tutka, Klaudia Żychowska, Magdalena Żaczek, Anna Maternia-Dudzik, Karolina Pawełczyk, Jakub Strapagiel, Dominik Lach, Jakub Reich, Adam |
author_sort | Tutka, Klaudia |
collection | PubMed |
description | Prurigo nodularis (PN) is a chronic condition characterized by the presence of nodular lesions accompanied by intense pruritus. The disease has been linked to several infectious factors, but data on the direct presence of microorganisms in the lesions of PN are scarce. The aim of this study was to evaluate the diversity and composition of the bacterial microbiome in PN lesions by targeting the region V3-V4 of 16S rRNA. Skin swabs were obtained from active nodules in 24 patients with PN, inflammatory patches of 14 patients with atopic dermatitis (AD) and corresponding skin areas of 9 healthy volunteers (HV). After DNA extraction, the V3-V4 region of the bacterial 16S rRNA gene was amplified. Sequencing was performed using the Illumina platform on the MiSeq instrument. Operational taxonomic units (OTU) were identified. The identification of taxa was carried out using the Silva v.138 database. There was no statistically significant difference in the alpha-diversity (intra-sample diversity) between the PN, AD and HV groups. The beta-diversity (inter-sample diversity) showed statistically significant differences between the three groups on a global level and in paired analyses. Staphylococcus was significantly more abundant in samples from PN and AD patients than in controls. The difference was maintained across all taxonomic levels. The PN microbiome is highly similar to that of AD. It remains unclear whether the disturbed composition of the microbiome and the domination of Staphylococcus in PN lesions may be the trigger factor of pruritus and lead to the development of cutaneous changes or is a secondary phenomenon. Our preliminary results support the theory that the composition of the skin microbiome in PN is altered and justify further research on the role of the microbiome in this debilitating condition. |
format | Online Article Text |
id | pubmed-10146575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-101465752023-04-29 Skin Microbiome in Prurigo Nodularis Tutka, Klaudia Żychowska, Magdalena Żaczek, Anna Maternia-Dudzik, Karolina Pawełczyk, Jakub Strapagiel, Dominik Lach, Jakub Reich, Adam Int J Mol Sci Article Prurigo nodularis (PN) is a chronic condition characterized by the presence of nodular lesions accompanied by intense pruritus. The disease has been linked to several infectious factors, but data on the direct presence of microorganisms in the lesions of PN are scarce. The aim of this study was to evaluate the diversity and composition of the bacterial microbiome in PN lesions by targeting the region V3-V4 of 16S rRNA. Skin swabs were obtained from active nodules in 24 patients with PN, inflammatory patches of 14 patients with atopic dermatitis (AD) and corresponding skin areas of 9 healthy volunteers (HV). After DNA extraction, the V3-V4 region of the bacterial 16S rRNA gene was amplified. Sequencing was performed using the Illumina platform on the MiSeq instrument. Operational taxonomic units (OTU) were identified. The identification of taxa was carried out using the Silva v.138 database. There was no statistically significant difference in the alpha-diversity (intra-sample diversity) between the PN, AD and HV groups. The beta-diversity (inter-sample diversity) showed statistically significant differences between the three groups on a global level and in paired analyses. Staphylococcus was significantly more abundant in samples from PN and AD patients than in controls. The difference was maintained across all taxonomic levels. The PN microbiome is highly similar to that of AD. It remains unclear whether the disturbed composition of the microbiome and the domination of Staphylococcus in PN lesions may be the trigger factor of pruritus and lead to the development of cutaneous changes or is a secondary phenomenon. Our preliminary results support the theory that the composition of the skin microbiome in PN is altered and justify further research on the role of the microbiome in this debilitating condition. MDPI 2023-04-21 /pmc/articles/PMC10146575/ /pubmed/37108838 http://dx.doi.org/10.3390/ijms24087675 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Tutka, Klaudia Żychowska, Magdalena Żaczek, Anna Maternia-Dudzik, Karolina Pawełczyk, Jakub Strapagiel, Dominik Lach, Jakub Reich, Adam Skin Microbiome in Prurigo Nodularis |
title | Skin Microbiome in Prurigo Nodularis |
title_full | Skin Microbiome in Prurigo Nodularis |
title_fullStr | Skin Microbiome in Prurigo Nodularis |
title_full_unstemmed | Skin Microbiome in Prurigo Nodularis |
title_short | Skin Microbiome in Prurigo Nodularis |
title_sort | skin microbiome in prurigo nodularis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10146575/ https://www.ncbi.nlm.nih.gov/pubmed/37108838 http://dx.doi.org/10.3390/ijms24087675 |
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