Cargando…

Early-Life Adversity Leaves Its Imprint on the Oral Microbiome for More Than 20 Years and Is Associated with Long-Term Immune Changes

The early-life microbiome (ELM) interacts with the psychosocial environment, in particular during early-life adversity (ELA), defining life-long health trajectories. The ELM also plays a significant role in the maturation of the immune system. We hypothesised that, in this context, the resilience of...

Descripción completa

Detalles Bibliográficos
Autores principales: Charalambous, Eleftheria G., Mériaux, Sophie B., Guebels, Pauline, Muller, Claude P., Leenen, Fleur A. D., Elwenspoek, Martha M. C., Thiele, Ines, Hertel, Johannes, Turner, Jonathan D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8657988/
https://www.ncbi.nlm.nih.gov/pubmed/34884490
http://dx.doi.org/10.3390/ijms222312682
_version_ 1784612627366805504
author Charalambous, Eleftheria G.
Mériaux, Sophie B.
Guebels, Pauline
Muller, Claude P.
Leenen, Fleur A. D.
Elwenspoek, Martha M. C.
Thiele, Ines
Hertel, Johannes
Turner, Jonathan D.
author_facet Charalambous, Eleftheria G.
Mériaux, Sophie B.
Guebels, Pauline
Muller, Claude P.
Leenen, Fleur A. D.
Elwenspoek, Martha M. C.
Thiele, Ines
Hertel, Johannes
Turner, Jonathan D.
author_sort Charalambous, Eleftheria G.
collection PubMed
description The early-life microbiome (ELM) interacts with the psychosocial environment, in particular during early-life adversity (ELA), defining life-long health trajectories. The ELM also plays a significant role in the maturation of the immune system. We hypothesised that, in this context, the resilience of the oral microbiomes, despite being composed of diverse and distinct communities, allows them to retain an imprint of the early environment. Using 16S amplicon sequencing on the EpiPath cohort, we demonstrate that ELA leaves an imprint on both the salivary and buccal oral microbiome 24 years after exposure to adversity. Furthermore, the changes in both communities were associated with increased activation, maturation, and senescence of both innate and adaptive immune cells, although the interaction was partly dependent on prior herpesviridae exposure and current smoking. Our data suggest the presence of multiple links between ELA, Immunosenescence, and cytotoxicity that occur through long-term changes in the microbiome.
format Online
Article
Text
id pubmed-8657988
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-86579882021-12-10 Early-Life Adversity Leaves Its Imprint on the Oral Microbiome for More Than 20 Years and Is Associated with Long-Term Immune Changes Charalambous, Eleftheria G. Mériaux, Sophie B. Guebels, Pauline Muller, Claude P. Leenen, Fleur A. D. Elwenspoek, Martha M. C. Thiele, Ines Hertel, Johannes Turner, Jonathan D. Int J Mol Sci Article The early-life microbiome (ELM) interacts with the psychosocial environment, in particular during early-life adversity (ELA), defining life-long health trajectories. The ELM also plays a significant role in the maturation of the immune system. We hypothesised that, in this context, the resilience of the oral microbiomes, despite being composed of diverse and distinct communities, allows them to retain an imprint of the early environment. Using 16S amplicon sequencing on the EpiPath cohort, we demonstrate that ELA leaves an imprint on both the salivary and buccal oral microbiome 24 years after exposure to adversity. Furthermore, the changes in both communities were associated with increased activation, maturation, and senescence of both innate and adaptive immune cells, although the interaction was partly dependent on prior herpesviridae exposure and current smoking. Our data suggest the presence of multiple links between ELA, Immunosenescence, and cytotoxicity that occur through long-term changes in the microbiome. MDPI 2021-11-24 /pmc/articles/PMC8657988/ /pubmed/34884490 http://dx.doi.org/10.3390/ijms222312682 Text en © 2021 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
Charalambous, Eleftheria G.
Mériaux, Sophie B.
Guebels, Pauline
Muller, Claude P.
Leenen, Fleur A. D.
Elwenspoek, Martha M. C.
Thiele, Ines
Hertel, Johannes
Turner, Jonathan D.
Early-Life Adversity Leaves Its Imprint on the Oral Microbiome for More Than 20 Years and Is Associated with Long-Term Immune Changes
title Early-Life Adversity Leaves Its Imprint on the Oral Microbiome for More Than 20 Years and Is Associated with Long-Term Immune Changes
title_full Early-Life Adversity Leaves Its Imprint on the Oral Microbiome for More Than 20 Years and Is Associated with Long-Term Immune Changes
title_fullStr Early-Life Adversity Leaves Its Imprint on the Oral Microbiome for More Than 20 Years and Is Associated with Long-Term Immune Changes
title_full_unstemmed Early-Life Adversity Leaves Its Imprint on the Oral Microbiome for More Than 20 Years and Is Associated with Long-Term Immune Changes
title_short Early-Life Adversity Leaves Its Imprint on the Oral Microbiome for More Than 20 Years and Is Associated with Long-Term Immune Changes
title_sort early-life adversity leaves its imprint on the oral microbiome for more than 20 years and is associated with long-term immune changes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8657988/
https://www.ncbi.nlm.nih.gov/pubmed/34884490
http://dx.doi.org/10.3390/ijms222312682
work_keys_str_mv AT charalambouseleftheriag earlylifeadversityleavesitsimprintontheoralmicrobiomeformorethan20yearsandisassociatedwithlongtermimmunechanges
AT meriauxsophieb earlylifeadversityleavesitsimprintontheoralmicrobiomeformorethan20yearsandisassociatedwithlongtermimmunechanges
AT guebelspauline earlylifeadversityleavesitsimprintontheoralmicrobiomeformorethan20yearsandisassociatedwithlongtermimmunechanges
AT mullerclaudep earlylifeadversityleavesitsimprintontheoralmicrobiomeformorethan20yearsandisassociatedwithlongtermimmunechanges
AT leenenfleurad earlylifeadversityleavesitsimprintontheoralmicrobiomeformorethan20yearsandisassociatedwithlongtermimmunechanges
AT elwenspoekmarthamc earlylifeadversityleavesitsimprintontheoralmicrobiomeformorethan20yearsandisassociatedwithlongtermimmunechanges
AT thieleines earlylifeadversityleavesitsimprintontheoralmicrobiomeformorethan20yearsandisassociatedwithlongtermimmunechanges
AT herteljohannes earlylifeadversityleavesitsimprintontheoralmicrobiomeformorethan20yearsandisassociatedwithlongtermimmunechanges
AT turnerjonathand earlylifeadversityleavesitsimprintontheoralmicrobiomeformorethan20yearsandisassociatedwithlongtermimmunechanges