Charting host-microbe co-metabolism in skin aging and application to metagenomics data.

During aging of human skin, a number of intrinsic and extrinsic factors cause the alteration of the skin's structure, function and cutaneous physiology. Many studies have investigated the influence of the skin microbiome on these alterations, but the molecular mechanisms that dictate the interp...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Wynand Alkema, Jos Boekhorst, Robyn T Eijlander, Steve Schnittger, Fini De Gruyter, Sabina Lukovac, Kurt Schilling, Guus A M Kortman
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2021
Materias:
R
Q
Acceso en línea:https://doaj.org/article/694e0ebfbe3c47d8b60c786fdeddd1fd
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:694e0ebfbe3c47d8b60c786fdeddd1fd
record_format dspace
spelling oai:doaj.org-article:694e0ebfbe3c47d8b60c786fdeddd1fd2021-12-02T20:07:39ZCharting host-microbe co-metabolism in skin aging and application to metagenomics data.1932-620310.1371/journal.pone.0258960https://doaj.org/article/694e0ebfbe3c47d8b60c786fdeddd1fd2021-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0258960https://doaj.org/toc/1932-6203During aging of human skin, a number of intrinsic and extrinsic factors cause the alteration of the skin's structure, function and cutaneous physiology. Many studies have investigated the influence of the skin microbiome on these alterations, but the molecular mechanisms that dictate the interplay between these factors and the skin microbiome are still not fully understood. To obtain more insight into the connection between the skin microbiome and the human physiological processes involved in skin aging, we performed a systematic study on interconnected pathways of human and bacterial metabolic processes that are known to play a role in skin aging. The bacterial genes in these pathways were subsequently used to create Hidden Markov Models (HMMs), which were applied to screen for presence of defined functionalities in both genomic and metagenomic datasets of skin-associated bacteria. These models were further applied on 16S rRNA gene sequencing data from skin microbiota samples derived from female volunteers of two different age groups (25-28 years ('young') and 59-68 years ('old')). The results show that the main bacterial pathways associated with aging skin are those involved in the production of pigmentation intermediates, fatty acids and ceramides. This study furthermore provides evidence for a relation between skin aging and bacterial enzymes involved in protein glycation. Taken together, the results and insights described in this paper provide new leads for intervening with bacterial processes that are associated with aging of human skin.Wynand AlkemaJos BoekhorstRobyn T EijlanderSteve SchnittgerFini De GruyterSabina LukovacKurt SchillingGuus A M KortmanPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 11, p e0258960 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Wynand Alkema
Jos Boekhorst
Robyn T Eijlander
Steve Schnittger
Fini De Gruyter
Sabina Lukovac
Kurt Schilling
Guus A M Kortman
Charting host-microbe co-metabolism in skin aging and application to metagenomics data.
description During aging of human skin, a number of intrinsic and extrinsic factors cause the alteration of the skin's structure, function and cutaneous physiology. Many studies have investigated the influence of the skin microbiome on these alterations, but the molecular mechanisms that dictate the interplay between these factors and the skin microbiome are still not fully understood. To obtain more insight into the connection between the skin microbiome and the human physiological processes involved in skin aging, we performed a systematic study on interconnected pathways of human and bacterial metabolic processes that are known to play a role in skin aging. The bacterial genes in these pathways were subsequently used to create Hidden Markov Models (HMMs), which were applied to screen for presence of defined functionalities in both genomic and metagenomic datasets of skin-associated bacteria. These models were further applied on 16S rRNA gene sequencing data from skin microbiota samples derived from female volunteers of two different age groups (25-28 years ('young') and 59-68 years ('old')). The results show that the main bacterial pathways associated with aging skin are those involved in the production of pigmentation intermediates, fatty acids and ceramides. This study furthermore provides evidence for a relation between skin aging and bacterial enzymes involved in protein glycation. Taken together, the results and insights described in this paper provide new leads for intervening with bacterial processes that are associated with aging of human skin.
format article
author Wynand Alkema
Jos Boekhorst
Robyn T Eijlander
Steve Schnittger
Fini De Gruyter
Sabina Lukovac
Kurt Schilling
Guus A M Kortman
author_facet Wynand Alkema
Jos Boekhorst
Robyn T Eijlander
Steve Schnittger
Fini De Gruyter
Sabina Lukovac
Kurt Schilling
Guus A M Kortman
author_sort Wynand Alkema
title Charting host-microbe co-metabolism in skin aging and application to metagenomics data.
title_short Charting host-microbe co-metabolism in skin aging and application to metagenomics data.
title_full Charting host-microbe co-metabolism in skin aging and application to metagenomics data.
title_fullStr Charting host-microbe co-metabolism in skin aging and application to metagenomics data.
title_full_unstemmed Charting host-microbe co-metabolism in skin aging and application to metagenomics data.
title_sort charting host-microbe co-metabolism in skin aging and application to metagenomics data.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/694e0ebfbe3c47d8b60c786fdeddd1fd
work_keys_str_mv AT wynandalkema chartinghostmicrobecometabolisminskinagingandapplicationtometagenomicsdata
AT josboekhorst chartinghostmicrobecometabolisminskinagingandapplicationtometagenomicsdata
AT robynteijlander chartinghostmicrobecometabolisminskinagingandapplicationtometagenomicsdata
AT steveschnittger chartinghostmicrobecometabolisminskinagingandapplicationtometagenomicsdata
AT finidegruyter chartinghostmicrobecometabolisminskinagingandapplicationtometagenomicsdata
AT sabinalukovac chartinghostmicrobecometabolisminskinagingandapplicationtometagenomicsdata
AT kurtschilling chartinghostmicrobecometabolisminskinagingandapplicationtometagenomicsdata
AT guusamkortman chartinghostmicrobecometabolisminskinagingandapplicationtometagenomicsdata
_version_ 1718375245897793536