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      The oral microbiome is associated with HPA axis response to a psychosocial stressor

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          Abstract

          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.

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          Dynamics and Stabilization of the Human Gut Microbiome during the First Year of Life.

          The gut microbiota is central to human health, but its establishment in early life has not been quantitatively and functionally examined. Applying metagenomic analysis on fecal samples from a large cohort of Swedish infants and their mothers, we characterized the gut microbiome during the first year of life and assessed the impact of mode of delivery and feeding on its establishment. In contrast to vaginally delivered infants, the gut microbiota of infants delivered by C-section showed significantly less resemblance to their mothers. Nutrition had a major impact on early microbiota composition and function, with cessation of breast-feeding, rather than introduction of solid food, being required for maturation into an adult-like microbiota. Microbiota composition and ecological network had distinctive features at each sampled stage, in accordance with functional maturation of the microbiome. Our findings establish a framework for understanding the interplay between the gut microbiome and the human body in early life.
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            The ‘Trier Social Stress Test’ – A Tool for Investigating Psychobiological Stress Responses in a Laboratory Setting

            This paper describes a protocol for induction of moderate psychological stress in a laboratory setting and evaluates its effects on physiological responses. The 'Trier Social Stress Test' (TSST) mainly consists of an anticipation period (10 min) and a test period (10 min) in which the subjects have to deliver a free speech and perform mental arithmetic in front of an audience. In six independent studies this protocol has been found to induce considerable changes in the concentration of ACTH, cortisol (serum and saliva), GH, prolactin as well as significant increases in heart rate. As for salivary cortisol levels, the TSST reliably led to 2- to 4-fold elevations above baseline with similar peak cortisol concentrations. Studies are summarized in which TSST-induced cortisol increases elucidated some of the multiple variables contributing to the interindividual variation in adrenocortical stress responses. The results suggest that gender, genetics and nicotine consumption can influence the individual's stress responsiveness to psychological stress while personality traits showed no correlation with cortisol responses to TSST stimulation. From these data we conclude that the TSST can serve as a tool for psychobiological research.
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              The hierarchy quorum sensing network in Pseudomonas aeruginosa

              Pseudomonas aeruginosa causes severe and persistent infections in immune compromised individuals and cystic fibrosis sufferers. The infection is hard to eradicate as P. aeruginosa has developed strong resistance to most conventional antibiotics. The problem is further compounded by the ability of the pathogen to form biofilm matrix, which provides bacterial cells a protected environment withstanding various stresses including antibiotics. Quorum sensing (QS), a cell density-based intercellular communication system, which plays a key role in regulation of the bacterial virulence and biofilm formation, could be a promising target for developing new strategies against P. aeruginosa infection. The QS network of P. aeruginosa is organized in a multi-layered hierarchy consisting of at least four interconnected signaling mechanisms. Evidence is accumulating that the QS regulatory network not only responds to bacterial population changes but also could react to environmental stress cues. This plasticity should be taken into consideration during exploration and development of anti-QS therapeutics.
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                Author and article information

                Contributors
                jonathan.turner@lih.lu
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                9 July 2024
                9 July 2024
                2024
                : 14
                : 15841
                Affiliations
                [1 ]Immune Endocrine Epigenetics Research Group, Department of Infection and Immunity, Luxembourg Institute of Health, ( https://ror.org/012m8gv78) 29, rue Henri Koch, 4354 Esch-sur-Alzette, Luxembourg
                [2 ]Faculty of Science, Technology and Medicine, University of Luxembourg, ( https://ror.org/036x5ad56) Esch-sur Alzette, Luxembourg
                [3 ]Department of Psychiatry and Psychotherapy, University Medicine Greifswald, ( https://ror.org/025vngs54) Greisfwald, Germany
                [4 ]Department of Psychology, University of Cyprus, ( https://ror.org/02qjrjx09) 2109 Nicosia, Cyprus
                [5 ]School of Medicine, National University of Ireland, ( https://ror.org/00shsf120) Galway, Ireland
                [6 ]Ryan Institute, National University of Galway, ( https://ror.org/03bea9k73) Galway, Ireland
                [7 ]Division of Microbiology, National University of Galway, ( https://ror.org/03bea9k73) Galway, Ireland
                [8 ]APC Microbiome Ireland, Cork, Ireland
                [9 ]German Center for Cardiovascular Diseases (DZHK), Partner Site Greifswald, Greifswald, Germany
                Author information
                http://orcid.org/0000-0002-5755-0375
                http://orcid.org/0000-0002-2760-1071
                Article
                66796
                10.1038/s41598-024-66796-2
                11233668
                38982178
                d1d394f1-6604-4224-98bb-1d04e388ca0e
                © The Author(s) 2024

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 22 February 2024
                : 3 July 2024
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001866, Fonds National de la Recherche Luxembourg;
                Award ID: PRIDE/11823097/MICROH; C16/BM/11342695 “MetCOEPs”; C12/BM/3985792 “EpiPath”; INTER/ANR/16/11568350 “MADAM”
                Award ID: PRIDE/11823097/MICROH; C16/BM/11342695 “MetCOEPs”; C12/BM/3985792 “EpiPath”; INTER/ANR/16/11568350 “MADAM”
                Award ID: PRIDE/11823097/MICROH; C16/BM/11342695 “MetCOEPs”; C12/BM/3985792 “EpiPath”; INTER/ANR/16/11568350 “MADAM”
                Award ID: PRIDE/11823097/MICROH; C16/BM/11342695 “MetCOEPs”; C12/BM/3985792 “EpiPath”; INTER/ANR/16/11568350 “MADAM”
                Award ID: PRIDE/11823097/MICROH; C16/BM/11342695 “MetCOEPs”; C12/BM/3985792 “EpiPath”; INTER/ANR/16/11568350 “MADAM”
                Award ID: PRIDE/11823097/MICROH; C16/BM/11342695 “MetCOEPs”; C12/BM/3985792 “EpiPath”; INTER/ANR/16/11568350 “MADAM”
                Award ID: PRIDE/11823097/MICROH; C16/BM/11342695 “MetCOEPs”; C12/BM/3985792 “EpiPath”; INTER/ANR/16/11568350 “MADAM”
                Award Recipient :
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                © Springer Nature Limited 2024

                Uncategorized
                early life adversity,microbiome,developmental origins of health and disease,stress,hpa axis,host-microbiome interactions,microbial communities,biomarkers,neuroimmunology,social neuroscience,stress and resilience

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