Metagenome Analysis of Bodily Microbiota in a Mouse Model of Alzheimer Disease Using Bacteria-derived Membrane Vesicles in Blood.
- Author:
Jin Young PARK
1
;
Juli CHOI
;
Yunjin LEE
;
Jung Eun LEE
;
Eun Hwa LEE
;
Hye Jin KWON
;
Jinho YANG
;
Bo Ri JEONG
;
Yoon Keun KIM
;
Pyung Lim HAN
Author Information
- Publication Type:Original Article
- Keywords: Alzheimer Disease; Microbiota; Metagenomics
- MeSH: Alzheimer Disease*; Animals; Brain; Classification; DNA; Extracellular Vesicles; Gastrointestinal Microbiome; Genes, rRNA; Membranes*; Metagenome*; Metagenomics; Mice*; Microbiota*; Reading
- From:Experimental Neurobiology 2017;26(6):369-379
- CountryRepublic of Korea
- Language:English
- Abstract: Emerging evidence has suggested that the gut microbiota contribute to brain dysfunction, including pathological symptoms of Alzheimer disease (AD). Microbiota secrete membrane vesicles, also called extracellular vesicles (EVs), which contain bacterial genomic DNA fragments and other molecules and are distributed throughout the host body, including blood. In the present study, we investigated whether bacteria-derived EVs in blood are useful for metagenome analysis in an AD mouse model. Sequence readings of variable regions of 16S rRNA genes prepared from blood EVs in Tg-APP/PS1 mice allowed us to identify over 3,200 operational taxonomic units corresponding to gut microbiota reported in previous studies. Further analysis revealed a distinctive microbiota landscape in Tg-APP/PS1 mice, with a dramatic alteration in specific microbiota at all taxonomy levels examined. Specifically, at the phylum level, the occupancy of p_Firmicutes increased, while the occupancy of p_Proteobacteria and p_Bacteroidetes moderately decreased in Tg-APP/PS1 mice. At the genus level, the occupancy of g_Aerococcus, g_Jeotgalicoccus, g_Blautia, g_Pseudomonas and unclassified members of f_Clostridiale and f_Ruminococcaceae increased, while the occupancy of g_Lactobacillus, unclassified members of f_S24-7, and g_Corynebacterium decreased in Tg-APP/PS1 mice. A number of genus members were detected in Tg-APP/PS1 mice, but not in wild-type mice, while other genus members were detected in wild-type mice, but lost in Tg-APP/PS1 mice. The results of the present study suggest that the bodily microbiota profile is altered in Tg-APP/PS1 mice, and that blood EVs are useful for the metagenome analysis of bodily microbiota in AD.
