Medical School, Quzhou College of Technology, Quzhou, China.
People's Hospital of Kaihua, Quzhou, China.
OMICS. 2024 Sep;28(9):461-469. doi: 10.1089/omi.2024.0120. Epub 2024 Aug 16.
The study of longevity and its determinants has been revitalized with the rise of microbiome scholarship. The gut microbiota have been established to play essential protective, metabolic, and physiological roles in human health and disease. The gut dysbiosis has been identified as an important factor contributing to the development of multiple diseases. Accordingly, it is reasonable to hypothesize that the gut microbiota of long-living individuals have healthy antiaging-associated gut microbes, which, by extension, might provide specific molecular targets for antiaging treatments and interventions. In the present study, we compared the gut microbiota of Chinese individuals in two different age groups, long-living adults (aged over 90 years) and elderly adults (aged 65-74 years) who were free of major diseases. We found significantly lower relative abundances of bacteria in the genera and in the long-living individuals. Furthermore, we established that while biological processes such as autophagy (GO:0006914) and telomere maintenance through semiconservative replication (GO:0032201) were enhanced in the long-living group, response to lipopolysaccharide (GO:0032496), nicotinamide adenine dinucleotide oxidation (GO:0006116), and -adenosyl methionine metabolism (GO:0046500) were weakened. Moreover, the two groups were found to differ with respect to amino acid metabolism. We suggest that these compositional and functional differences in the gut microbiota may potentially be associated with mechanisms that contribute to determining longevity or aging.
随着微生物组研究的兴起,对长寿及其决定因素的研究重新活跃起来。肠道微生物群已被证实对人类健康和疾病发挥着重要的保护、代谢和生理作用。肠道菌群失调已被确定为导致多种疾病发展的重要因素。因此,合理假设长寿个体的肠道微生物群具有健康的抗衰老相关肠道微生物,这些微生物可能为抗衰老治疗和干预提供特定的分子靶点。在本研究中,我们比较了两组不同年龄的中国个体的肠道微生物群,分别是长寿成年人(年龄超过 90 岁)和无重大疾病的老年成年人(年龄 65-74 岁)。我们发现长寿个体中属 和 的相对丰度显著降低。此外,我们还确定,虽然长寿组的生物过程如自噬(GO:0006914)和通过半保守复制维持端粒(GO:0032201)增强,但对脂多糖(GO:0032496)、烟酰胺腺嘌呤二核苷酸氧化(GO:0006116)和 -腺苷甲硫氨酸代谢(GO:0046500)的反应减弱。此外,两组在氨基酸代谢方面存在差异。我们认为,肠道微生物群的这些组成和功能差异可能与决定长寿或衰老的机制有关。