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Abstract
Clinical and animal studies have shown that gut microbiome disturbances can affect neural function and behaviors via the microbiota–gut–brain axis, and may be implicated in the pathogenesis of several brain diseases. However, exactly how the gut microbiome modulates nervous system activity remains obscure. Here, using a single-cell nucleus sequencing approach, we sought to characterize the cell type–specific transcriptomic changes in the prefrontal cortex and hippocampus derived from germ-free (GF), specific pathogen free, and colonized-GF mice. We found that the absence of gut microbiota resulted in cell-specific transcriptomic changes. Furthermore, microglia transcriptomes were preferentially influenced, which could be effectively reversed by microbial colonization. Significantly, the gut microbiome modulated the mutual transformation of microglial subpopulations in the two regions. Cross-species analysis showed that the transcriptome changes of these microglial subpopulations were mainly associated with Alzheimer’s disease (AD) and major depressive disorder (MDD), which were further supported by animal behavioral tests. Our findings demonstrate that gut microbiota mainly modulate the mutual transformation of microglial subtypes, which may lead to new insights into the pathogenesis of AD and MDD.
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1 The First Affiliated Hospital of Chongqing Medical University, NHC Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases, Chongqing, China (GRID:grid.452206.7) (ISNI:0000 0004 1758 417X); The Jin Feng Laboratory, Chongqing, China (GRID:grid.452206.7); The First Affiliated Hospital of Chongqing Medical University, Department of Neurology, Chongqing, China (GRID:grid.452206.7) (ISNI:0000 0004 1758 417X)
2 The First Affiliated Hospital of Chongqing Medical University, NHC Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases, Chongqing, China (GRID:grid.452206.7) (ISNI:0000 0004 1758 417X); The Jin Feng Laboratory, Chongqing, China (GRID:grid.452206.7)
3 The First Affiliated Hospital of Chongqing Medical University, NHC Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases, Chongqing, China (GRID:grid.452206.7) (ISNI:0000 0004 1758 417X); The Jin Feng Laboratory, Chongqing, China (GRID:grid.452206.7); Yongchuan Hospital of Chongqing Medical University, Department of Neurology, Chongqing, China (GRID:grid.203458.8) (ISNI:0000 0000 8653 0555)
4 The First Affiliated Hospital of Chongqing Medical University, NHC Key Laboratory of Diagnosis and Treatment on Brain Functional Diseases, Chongqing, China (GRID:grid.452206.7) (ISNI:0000 0004 1758 417X); The Jin Feng Laboratory, Chongqing, China (GRID:grid.452206.7); The First Affiliated Hospital of Chongqing Medical University, Department of Neurology, Chongqing, China (GRID:grid.452206.7) (ISNI:0000 0004 1758 417X); Stomatological Hospital of Chongqing Medical University, Key Laboratory of Psychoseomadsy, Chongqing, China (GRID:grid.459985.c)
5 SUNY Upstate Medical University, Department of Psychiatry, College of Medicine, Syracuse, USA (GRID:grid.411023.5) (ISNI:0000 0000 9159 4457)
6 The First Affiliated Hospital of Chongqing Medical University, Department of Neurology, Chongqing, China (GRID:grid.452206.7) (ISNI:0000 0004 1758 417X); Chongqing Medical University, Institute for Brain Science and Disease, Chongqing, China (GRID:grid.203458.8) (ISNI:0000 0000 8653 0555)