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Gut microbiota dynamics in SAMP8 mice: insights from machine learning and longitudinal analysis
Yilang Ke1, Aiping Zeng1, Dang Li1
1Fujian Key Laboratory of Vascular Aging, Department of Geriatrics, Fujian Institute of Geriatrics, Fujian Clinical Research Center for Senile Vascular Aging and Brain Aging, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.
Aging significantly alters the gut microbiota, decreasing diversity and changing bacterial composition. The study identifies Peptococcus as a potential biomarker for aging in SAMP8 mice.
Area of Science:
- Microbiology
- Gerontology
- Bioinformatics
Background:
- Gut microbiota composition changes significantly with age.
- The SAMP8 mouse model exhibits accelerated aging, making it valuable for studying age-related changes.
- Longitudinal studies on gut microbiota dynamics in aging SAMP8 mice are limited.
Purpose of the Study:
- To comprehensively analyze gut microbiota dynamics during aging in SAMP8 mice.
- To identify age-related shifts in microbial diversity, composition, and trajectories.
- To discover potential microbial biomarkers for aging.
Main Methods:
- 16S rRNA sequencing was used to profile gut microbiota in SAMP8 mice at 1, 3, 7, and 10 months.
- Alpha and beta diversity analyses were performed to assess changes in microbial community structure.
- Random Forest analysis was employed for biomarker discovery by comparing young and aged groups.
Main Results:
- Alpha diversity (Shannon index) significantly decreased with age.
- Beta diversity showed distinct clustering between young and aged mice.
- Key bacterial phyla like Firmicutes and Actinobacteria declined, while Proteobacteria and Bacteroidetes increased.
- Peptococcus was identified as a potential aging biomarker with high diagnostic accuracy (AUC = 0.78).
Conclusions:
- Gut microbiota undergoes significant restructuring during aging in SAMP8 mice.
- Specific bacterial taxa, including Peptococcus, can serve as reliable biomarkers for aging.
- These findings provide insights into microbiota-aging interactions and potential targets for interventions.
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