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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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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 |
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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 |
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