Genome Institute of Singapore (GIS), Agency for Science, Technology and Research (A*STAR), 60 Biopolis Street, Genome, Singapore, 138672, Republic of Singapore.
Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Republic of Singapore.
Nat Commun. 2024 Sep 5;15(1):7751. doi: 10.1038/s41467-024-52097-9.
While rapid demographic changes in Asia are driving the incidence of chronic aging-related diseases, the limited availability of high-quality in vivo data hampers our ability to understand complex multi-factorial contributions, including gut microbial, to healthy aging. Leveraging a well-phenotyped cohort of community-living octogenarians in Singapore, we used deep shotgun-metagenomic sequencing for high-resolution taxonomic and functional characterization of their gut microbiomes (n = 234). Joint species-level analysis with other Asian cohorts identified distinct age-associated shifts characterized by reduction in microbial richness, and specific Alistipes and Bacteroides species enrichment (e.g., Alistipes shahii and Bacteroides xylanisolvens). Functional analysis confirmed these changes correspond to metabolic potential expansion in aging towards alternate pathways synthesizing and utilizing amino-acid precursors, vis-à-vis dominant microbial guilds producing butyrate in gut from pyruvate (e.g., Faecalibacterium prausnitzii, Roseburia inulinivorans). Extending these observations to key clinical markers helped identify >10 robust microbial associations to inflammation, cardiometabolic and liver health, including potential probiotic species (e.g., Parabacteroides goldsteinii) and pathobionts (e.g., Klebsiella pneumoniae), highlighting the microbiome's role as biomarkers and potential targets for promoting healthy aging.
尽管亚洲人口结构的快速变化正在推动慢性与衰老相关疾病的发病率上升,但高质量的体内数据的有限可用性,限制了我们对复杂的多因素(包括肠道微生物)对健康衰老的影响的理解能力。利用新加坡一个具有良好表型的 80 岁以上社区居住者队列,我们使用深度 shotgun 宏基因组测序,对其肠道微生物组(n=234)进行高分辨率的分类和功能特征描述。与其他亚洲队列的联合物种水平分析确定了与年龄相关的独特变化,其特征是微生物丰富度降低,以及特定的 Alistipes 和 Bacteroides 物种富集(例如,Alistipes shahii 和 Bacteroides xylanisolvens)。功能分析证实,这些变化对应于衰老过程中代谢潜力的扩展,向利用氨基酸前体合成和利用的替代途径发展,而不是由肠道中丙酮酸产生丁酸盐的主要微生物群(例如,Faecalibacterium prausnitzii、Roseburia inulinivorans)。将这些观察结果扩展到关键的临床标志物,有助于确定与炎症、心血管代谢和肝脏健康相关的 10 多种稳健的微生物关联,包括潜在的益生菌物种(例如,Parabacteroides goldsteinii)和病原体(例如,Klebsiella pneumoniae),突出了微生物组作为生物标志物和促进健康衰老的潜在靶点的作用。