Integrated Multiomics Analysis of Salivary Exosomes to Identify Biomarkers Associated with Changes in Mood States and Fatigue

• Published in: International journal of molecular sciences Vol. 23; no. 9; p. 5257
• Main Authors: Cohn, Whitaker, Zhu, Chunni, Campagna, Jesus, Bilousova, Tina, Spilman, Patricia, Teter, Bruce, Li, Feng, Guo, Rong, Elashoff, David, Cole, Greg M, Avidan, Alon, Faull, Kym Francis, Whitelegge, Julian, Wong, David T W, John, Varghese
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 09.05.2022; MDPI
• Subjects: Aircraft performance; Alzheimer's disease; Biomarkers; Biomarkers - metabolism; Chronic fatigue syndrome; Cognitive ability; cognitive impairment; Exosomes; Exosomes - genetics; Exosomes - metabolism; Fatigue; Gene expression; Hypotheses; MicroRNAs; MicroRNAs - metabolism; Mood; multiomics; Nervous system; Phosphoglycerate kinase; Phosphoglycerate kinase 1; Physiology; Proteins; Proteomics; Questionnaires; Saliva; Saliva - metabolism; Vigilance; saliva; fatigue; proteomics; biomarkers; exosomes; microRNA; cognitive impairment; multiomics
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms23095257

Fatigue and other deleterious mood alterations resulting from prolonged efforts such as a long work shift can lead to a decrease in vigilance and cognitive performance, increasing the likelihood of errors during the execution of attention-demanding activities such as piloting an aircraft or performing medical procedures. Thus, a method to rapidly and objectively assess the risk for such cognitive fatigue would be of value. The objective of the study was the identification in saliva-borne exosomes of molecular signals associated with changes in mood and fatigue that may increase the risk of reduced cognitive performance. Using integrated multiomics analysis of exosomes from the saliva of medical residents before and after a 12 h work shift, we observed changes in the abundances of several proteins and miRNAs that were associated with various mood states, and specifically fatigue, as determined by a Profile of Mood States questionnaire. The findings herein point to a promising protein biomarker, phosphoglycerate kinase 1 (PGK1), that was associated with fatigue and displayed changes in abundance in saliva, and we suggest a possible biological mechanism whereby the expression of the PGK1 gene is regulated by miR3185 in response to fatigue. Overall, these data suggest that multiomics analysis of salivary exosomes has merit for identifying novel biomarkers associated with changes in mood states and fatigue. The promising biomarker protein presents an opportunity for the development of a rapid saliva-based test for the assessment of these changes.