TY - JOUR
T1 - The oral microbiome is associated with HPA axis response to a psychosocial stressor
AU - Charalambous, Eleftheria G.
AU - Mériaux, Sophie B.
AU - Guebels, Pauline
AU - Muller, Claude P.
AU - Leenen, Fleur A.D.
AU - Elwenspoek, Martha M.C.
AU - Thiele, Ines
AU - Hertel, Johannes
AU - Turner, Jonathan D.
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/7/9
Y1 - 2024/7/9
N2 - Intense psychosocial stress during early life has a detrimental effect on health-disease balance in later life. Simultaneously, despite its sensitivity to stress, the developing microbiome contributes to long-term health. Following stress exposure, HPA-axis activation regulates the “fight or flight” response with the release of glucose and cortisol. Here, we investigated the interaction between the oral microbiome and the stress response. We used a cohort of 115 adults, mean age 24, who either experienced institutionalisation and adoption (n = 40) or were non-adopted controls (n = 75). Glucose and cortisol measurements were taken from participants following an extended socially evaluated cold pressor test (seCPT) at multiple time points. The cohort´s oral microbiome was profiled via 16S-V4 sequencing on microbial DNA from saliva and buccal samples. Using mixed-effect linear regressions, we identified 12 genera that exhibited an interaction with host’s cortisol-glucose response to stress, strongly influencing intensity and clearance of cortisol and glucose following stress exposure. Particularly, the identified taxa influenced the glucose and cortisol release profiles and kinetics following seCPT exposure. In conclusion, our study provided evidence for the oral microbiome modifying the effect of stress on the HPA-axis and human metabolism, as shown in glucose-cortisol time series data.
AB - Intense psychosocial stress during early life has a detrimental effect on health-disease balance in later life. Simultaneously, despite its sensitivity to stress, the developing microbiome contributes to long-term health. Following stress exposure, HPA-axis activation regulates the “fight or flight” response with the release of glucose and cortisol. Here, we investigated the interaction between the oral microbiome and the stress response. We used a cohort of 115 adults, mean age 24, who either experienced institutionalisation and adoption (n = 40) or were non-adopted controls (n = 75). Glucose and cortisol measurements were taken from participants following an extended socially evaluated cold pressor test (seCPT) at multiple time points. The cohort´s oral microbiome was profiled via 16S-V4 sequencing on microbial DNA from saliva and buccal samples. Using mixed-effect linear regressions, we identified 12 genera that exhibited an interaction with host’s cortisol-glucose response to stress, strongly influencing intensity and clearance of cortisol and glucose following stress exposure. Particularly, the identified taxa influenced the glucose and cortisol release profiles and kinetics following seCPT exposure. In conclusion, our study provided evidence for the oral microbiome modifying the effect of stress on the HPA-axis and human metabolism, as shown in glucose-cortisol time series data.
KW - Developmental origins of health and disease
KW - Early life adversity
KW - Host-microbiome interactions
KW - HPA axis
KW - Microbiome
KW - Stress
UR - http://www.scopus.com/inward/record.url?scp=85198091208&partnerID=8YFLogxK
UR - https://pubmed.ncbi.nlm.nih.gov/38982178/
U2 - 10.1038/s41598-024-66796-2
DO - 10.1038/s41598-024-66796-2
M3 - Article
C2 - 38982178
AN - SCOPUS:85198091208
SN - 2045-2322
VL - 14
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 15841
ER -