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Shotgun metagenomic sequencing reveals skin microbial variability from different facial sites

Biogeography (body site) is known to be one of the main factors influencing the composition of the skin microbial community. However, site-associated microbial variability at a fine-scale level was not well-characterized since there was a lack of high-resolution recognition of facial microbiota acro...

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Autores principales: Wei, Qingzhen, Li, Zhiming, Gu, Zhenglong, Liu, Xiao, Krutmann, Jean, Wang, Jiucun, Xia, Jingjing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364038/
https://www.ncbi.nlm.nih.gov/pubmed/35966676
http://dx.doi.org/10.3389/fmicb.2022.933189
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author Wei, Qingzhen
Li, Zhiming
Gu, Zhenglong
Liu, Xiao
Krutmann, Jean
Wang, Jiucun
Xia, Jingjing
author_facet Wei, Qingzhen
Li, Zhiming
Gu, Zhenglong
Liu, Xiao
Krutmann, Jean
Wang, Jiucun
Xia, Jingjing
author_sort Wei, Qingzhen
collection PubMed
description Biogeography (body site) is known to be one of the main factors influencing the composition of the skin microbial community. However, site-associated microbial variability at a fine-scale level was not well-characterized since there was a lack of high-resolution recognition of facial microbiota across kingdoms by shotgun metagenomic sequencing. To investigate the explicit microbial variance in the human face, 822 shotgun metagenomic sequencing data from Han Chinese recently published by our group, in combination with 97 North American samples from NIH Human Microbiome Project (HMP), were reassessed. Metagenomic profiling of bacteria, fungi, and bacteriophages, as well as enriched function modules from three facial sites (forehead, cheek, and the back of the nose), was analyzed. The results revealed that skin microbial features were more alike in the forehead and cheek while varied from the back of the nose in terms of taxonomy and functionality. Analysis based on biogeographic theories suggested that neutral drift with niche selection from the host could possibly give rise to the variations. Of note, the abundance of porphyrin-producing species, i.e., Cutibacterium acnes, Cutibacterium avidum, Cutibacterium granulosum, and Cutibacterium namnetense, was all the highest in the back of the nose compared with the forehead/cheek, which was consistent with the highest porphyrin level on the nose in our population. Sequentially, the site-associated microbiome variance was confirmed in American populations; however, it was not entirely consistent. Furthermore, our data revealed correlation patterns between Propionibacterium acnes bacteriophages with genus Cutibacterium at different facial sites in both populations; however, C. acnes exhibited a distinct correlation with P. acnes bacteriophages in Americans/Chinese. Taken together, in this study, we explored the fine-scale facial site-associated changes in the skin microbiome and provided insight into the ecological processes underlying facial microbial variations.
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spelling pubmed-93640382022-08-11 Shotgun metagenomic sequencing reveals skin microbial variability from different facial sites Wei, Qingzhen Li, Zhiming Gu, Zhenglong Liu, Xiao Krutmann, Jean Wang, Jiucun Xia, Jingjing Front Microbiol Microbiology Biogeography (body site) is known to be one of the main factors influencing the composition of the skin microbial community. However, site-associated microbial variability at a fine-scale level was not well-characterized since there was a lack of high-resolution recognition of facial microbiota across kingdoms by shotgun metagenomic sequencing. To investigate the explicit microbial variance in the human face, 822 shotgun metagenomic sequencing data from Han Chinese recently published by our group, in combination with 97 North American samples from NIH Human Microbiome Project (HMP), were reassessed. Metagenomic profiling of bacteria, fungi, and bacteriophages, as well as enriched function modules from three facial sites (forehead, cheek, and the back of the nose), was analyzed. The results revealed that skin microbial features were more alike in the forehead and cheek while varied from the back of the nose in terms of taxonomy and functionality. Analysis based on biogeographic theories suggested that neutral drift with niche selection from the host could possibly give rise to the variations. Of note, the abundance of porphyrin-producing species, i.e., Cutibacterium acnes, Cutibacterium avidum, Cutibacterium granulosum, and Cutibacterium namnetense, was all the highest in the back of the nose compared with the forehead/cheek, which was consistent with the highest porphyrin level on the nose in our population. Sequentially, the site-associated microbiome variance was confirmed in American populations; however, it was not entirely consistent. Furthermore, our data revealed correlation patterns between Propionibacterium acnes bacteriophages with genus Cutibacterium at different facial sites in both populations; however, C. acnes exhibited a distinct correlation with P. acnes bacteriophages in Americans/Chinese. Taken together, in this study, we explored the fine-scale facial site-associated changes in the skin microbiome and provided insight into the ecological processes underlying facial microbial variations. Frontiers Media S.A. 2022-07-26 /pmc/articles/PMC9364038/ /pubmed/35966676 http://dx.doi.org/10.3389/fmicb.2022.933189 Text en Copyright © 2022 Wei, Li, Gu, Liu, Krutmann, Wang and Xia. https://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 Microbiology
Wei, Qingzhen
Li, Zhiming
Gu, Zhenglong
Liu, Xiao
Krutmann, Jean
Wang, Jiucun
Xia, Jingjing
Shotgun metagenomic sequencing reveals skin microbial variability from different facial sites
title Shotgun metagenomic sequencing reveals skin microbial variability from different facial sites
title_full Shotgun metagenomic sequencing reveals skin microbial variability from different facial sites
title_fullStr Shotgun metagenomic sequencing reveals skin microbial variability from different facial sites
title_full_unstemmed Shotgun metagenomic sequencing reveals skin microbial variability from different facial sites
title_short Shotgun metagenomic sequencing reveals skin microbial variability from different facial sites
title_sort shotgun metagenomic sequencing reveals skin microbial variability from different facial sites
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364038/
https://www.ncbi.nlm.nih.gov/pubmed/35966676
http://dx.doi.org/10.3389/fmicb.2022.933189
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