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Microbial community profiling shows dysbiosis in the lesional skin of Vitiligo subjects
Healthy human skin harbours a diverse array of microbes that comprise the skin microbiome. Commensal bacteria constitute an important component of resident microbiome and are intricately linked to skin health. Recent studies describe an association between altered skin microbial community and epidem...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4725359/ https://www.ncbi.nlm.nih.gov/pubmed/26758568 http://dx.doi.org/10.1038/srep18761 |
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author | Ganju, Parul Nagpal, Sunil Mohammed, MH Nishal Kumar, P Pandey, Rajesh Natarajan, Vivek T Mande, Sharmila S. Gokhale, Rajesh S. |
author_facet | Ganju, Parul Nagpal, Sunil Mohammed, MH Nishal Kumar, P Pandey, Rajesh Natarajan, Vivek T Mande, Sharmila S. Gokhale, Rajesh S. |
author_sort | Ganju, Parul |
collection | PubMed |
description | Healthy human skin harbours a diverse array of microbes that comprise the skin microbiome. Commensal bacteria constitute an important component of resident microbiome and are intricately linked to skin health. Recent studies describe an association between altered skin microbial community and epidemiology of diseases, like psoriasis, atopic dermatitis etc. In this study, we compare the differences in bacterial community of lesional and non-lesional skin of vitiligo subjects. Our study reveals dysbiosis in the diversity of microbial community structure in lesional skin of vitiligo subjects. Although individual specific signature is dominant over the vitiligo-specific microbiota, a clear decrease in taxonomic richness and evenness can be noted in lesional patches. Investigation of community specific correlation networks reveals distinctive pattern of interactions between resident bacterial populations of the two sites (lesional and non-lesional). While Actinobacterial species constitute the central regulatory nodes (w.r.t. degree of interaction) in non-lesional skin, species belonging to Firmicutes dominate on lesional sites. We propose that the changes in taxonomic characteristics of vitiligo lesions, as revealed by our study, could play a crucial role in altering the maintenance and severity of disease. Future studies would elucidate mechanistic relevance of these microbial dynamics that can provide new avenues for therapeutic interventions. |
format | Online Article Text |
id | pubmed-4725359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47253592016-01-28 Microbial community profiling shows dysbiosis in the lesional skin of Vitiligo subjects Ganju, Parul Nagpal, Sunil Mohammed, MH Nishal Kumar, P Pandey, Rajesh Natarajan, Vivek T Mande, Sharmila S. Gokhale, Rajesh S. Sci Rep Article Healthy human skin harbours a diverse array of microbes that comprise the skin microbiome. Commensal bacteria constitute an important component of resident microbiome and are intricately linked to skin health. Recent studies describe an association between altered skin microbial community and epidemiology of diseases, like psoriasis, atopic dermatitis etc. In this study, we compare the differences in bacterial community of lesional and non-lesional skin of vitiligo subjects. Our study reveals dysbiosis in the diversity of microbial community structure in lesional skin of vitiligo subjects. Although individual specific signature is dominant over the vitiligo-specific microbiota, a clear decrease in taxonomic richness and evenness can be noted in lesional patches. Investigation of community specific correlation networks reveals distinctive pattern of interactions between resident bacterial populations of the two sites (lesional and non-lesional). While Actinobacterial species constitute the central regulatory nodes (w.r.t. degree of interaction) in non-lesional skin, species belonging to Firmicutes dominate on lesional sites. We propose that the changes in taxonomic characteristics of vitiligo lesions, as revealed by our study, could play a crucial role in altering the maintenance and severity of disease. Future studies would elucidate mechanistic relevance of these microbial dynamics that can provide new avenues for therapeutic interventions. Nature Publishing Group 2016-01-13 /pmc/articles/PMC4725359/ /pubmed/26758568 http://dx.doi.org/10.1038/srep18761 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Ganju, Parul Nagpal, Sunil Mohammed, MH Nishal Kumar, P Pandey, Rajesh Natarajan, Vivek T Mande, Sharmila S. Gokhale, Rajesh S. Microbial community profiling shows dysbiosis in the lesional skin of Vitiligo subjects |
title | Microbial community profiling shows dysbiosis in the lesional skin of Vitiligo subjects |
title_full | Microbial community profiling shows dysbiosis in the lesional skin of Vitiligo subjects |
title_fullStr | Microbial community profiling shows dysbiosis in the lesional skin of Vitiligo subjects |
title_full_unstemmed | Microbial community profiling shows dysbiosis in the lesional skin of Vitiligo subjects |
title_short | Microbial community profiling shows dysbiosis in the lesional skin of Vitiligo subjects |
title_sort | microbial community profiling shows dysbiosis in the lesional skin of vitiligo subjects |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4725359/ https://www.ncbi.nlm.nih.gov/pubmed/26758568 http://dx.doi.org/10.1038/srep18761 |
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