Social interactions among animals mediate essential behaviors, including mating, nurturing, and defense. Social behavior provides benefits such as increases survival, offers security, reduces energy expenditure. The deficit in social interaction is often observed in people with psychiatric disorders, such as autism, schizophrenia, depression, social anxiety, etc. While the intestinal bacteria contribute to social behavior in mice, gut-brain connections that regulate this complex behavior and its underlying neural basis remain poorly understood. The NCKU-Caltech team reveals that the microbiota modulates neuronal activity in specific brain regions in male mice to regulate stress responses and social behavior. Social deficit in mice without gut bacteria is associated with elevated levels of the stress hormone corticosterone, which is primarily produced by activating the hypothalamus-pituitary-adrenal (HPA) axis, a well-known system for stress response. Accordingly, removal of the adrenal gland, blockade of the glucocorticoid receptor, and pharmacological inhibition of corticosterone synthesis effectively correct social deficits modulated by gut bacteria. Genetic deletion of the glucocorticoid receptor in specific brain regions and chemogenetic inactivation of corticotrophin-releasing hormone (CRH)-expressing neurons in the paraventricular nucleus of the hypothalamus (PVN) rescue social impairments caused by microbiome depletion. Conversely, specific activation of CRH-expressing neurons in the PVN of mice is sufficient to induce social deficits. Finally, the team identifies a specific bacterial species, Enterococcus faecalis, that promotes social activity and reduces stress hormone in mice following social stress. These discoveries demonstrate that the gut microbiome can modulate social interactions via specific neuronal circuits that control stress responses in the brain.
This study was partially supported by the Ministry of Science and Technology, College of Medicine, and Higher Education Sprout Project at NCKU, Taiwan. The research was conducted by Prof. Wei-Li Wu and his team in the Department of Physiology at NCKU in collaboration with the team led by Prof. Sarkis Mazmanian of the Division of Biology and Biological Engineering at Caltech.
Prof. Wei-Li Wu (the lead and corresponding author of this paper), assistant professor in the Department of Physiology, College of Medicine at NCKU and visiting associate in the Division of Biology and Biological Engineering at Caltech.
Prof. Sarkis Mazmanian, Luis B. and Nelly Soux Professor of Microbiology in the Division of Biology and Biological Engineering at Caltech, faculty member with Tianqiao and Chrissy Chen Institute for Neuroscience at Caltech, and Heritage Medical Research Institute Investigator.
Underline: Authors from NCKU
Co-authors are Mark D. Adame, formerly of Caltech and now at the MD-PhD program of University of Michigan-Ann Arbor; PhD graduate student Chia-Wei Liou (third author) of Institute of Basic Biomedical Sciences, NCKU; graduate student Jacob T. Barlow of Caltech; MS graduate student Tzu-Ting Lai (fifth author) (MS '21); Gil Sharon formerly a postdoc at Caltech and now at the Emerald Cloud Lab; Catherine E. Schretter, formerly a graduate student at Caltech and now at the Janelia Research Campus; Postdoc Brittany D. Needham of Caltech; Madelyn I. Wang, formerly of Caltech and now at the MD program of Stony Brook University; graduate students Weiyi Tang and James Ousey of Caltech; MS graduate student Yuan-Yuan Lin (twelfth author) and BS undergraduate student Tzu-Hsuan Yao (thirteenth author) of Department of Physiology, NCKU; graduate student Reem Abdel-Haq of Caltech; Keith Beadle, formerly of Caltech and now at the Oregon Health and Science University; Professors Viviana Gradinaru and Rustem F. Ismagilov of Caltech; and Sarkis Mazmanian.
Prof. Wei-Li Wu, PhD
Department of Physiology, College of Medicine
National Cheng Kung University
TEL: +886-6-235-3535 ext 5458
Department of Life Sciences
Ministry of Science and Technology