Guangdong Provincial Key Laboratory of Animal Molecular Design and Precise Breeding, College of Life Science and Engineering, Foshan University, Foshan, China; School of Laboratory Medicine/Sichuan Provincial Engineering Laboratory for Prevention and Control Technology of Veterinary Drug Residue in Animal-origin Food, Chengdu Medical College, Chengdu 610500, China; Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, Sichuan Agricultural University, Chengdu, China.
Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, Sichuan Agricultural University, Chengdu, China.
Gene. 2021 May 5;779:145510. doi: 10.1016/j.gene.2021.145510. Epub 2021 Feb 16.
The human gut microbiota in long-living people has been characterized, however, its metabolic potential is still largely unknown in this group. In this study, the gut microbiota was assessed in 37 Chinese long-living participants (aged 90 + years) by metagenomic sequencing of stool samples. Participants were categorized into two groups, healthy long-living (n = 28) and unhealthy long-living (n = 9). Gut microbiota composition and function were compared among these two groups. We found that the gut microbiota in the healthy long-living group was significantly separated from the unhealthy group. The healthy long-living group contained a higher abundance of Bacteroidetes and more functional pathways in energy metabolism, glycan biosynthesis and metabolism, metabolism of cofactors and vitamins, and biosynthesis of other secondary metabolites. The unhealthy group contained a higher abundance of Streptococcus and other pathogenic bacteria, and also contained more functional pathways for xenobiotics biodegradation and metabolism than the healthy group. Additionally, the unhealthy group had decreased levels of carbohydrate-active enzymes, including host-glycan and fiber degrading enzymes, and an increase in starch-degrading enzymes. In conclusion, the gut microbiota of unhealthy long-living people contains more pathogenic bacteria, and the overall gut microbiota may be in an unhealthy state, "dysbiosis", which leads to a decrease in carbohydrate digestion, glycan and thiamine (B1) metabolites, and fatty acid biosynthesis.
尽管已经对长寿人群的肠道微生物群进行了描述,但在这一人群中,其代谢潜能在很大程度上仍然未知。在这项研究中,通过对 37 名中国长寿参与者(年龄在 90 岁以上)的粪便样本进行宏基因组测序,评估了他们的肠道微生物群。参与者被分为两组,健康长寿组(n=28)和不健康长寿组(n=9)。比较了这两组之间的肠道微生物群组成和功能。我们发现,健康长寿组的肠道微生物群与不健康组有明显的分离。健康长寿组中厚壁菌门的丰度更高,在能量代谢、聚糖生物合成和代谢、辅因子和维生素代谢以及其他次生代谢物的生物合成方面有更多的功能途径。不健康组中链球菌和其他致病菌的丰度更高,并且比健康组有更多的外源化学物质生物降解和代谢功能途径。此外,不健康组碳水化合物活性酶的水平降低,包括宿主聚糖和纤维降解酶,淀粉降解酶的水平增加。总之,不健康长寿人群的肠道微生物群含有更多的致病菌,整个肠道微生物群可能处于不健康状态,即“生态失调”,这导致碳水化合物消化、聚糖和硫胺素(B1)代谢物以及脂肪酸生物合成减少。