Evidence map›Paper›PMID 41697396›Full record

ArticleApplied microbiology and biotechnology2026

Identification of fecal microbiome signatures associated with longevity through 16S rRNA sequencing in different age groups in China.

Yuexia Wang, Jie Liu, Wenjing Wang, Gefang Xu, Ying Lin, Pengxia Song, Xingchen Zhou, Kunhua Zheng

Abstract read
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Article in Applied microbiology and biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Yuexia Wang *People's Hospital of Kaihua, 59 Fenghuang Middle Road, Quzhou, 324300, PR China.
Jie Liu *Medical School, Quzhou College of Technology, 18 Jiangyuan Road, Quzhou, 324000, PR China.
Wenjing WangPeople's Hospital of Kaihua, 59 Fenghuang Middle Road, Quzhou, 324300, PR China.
Gefang XuPeople's Hospital of Kaihua, 59 Fenghuang Middle Road, Quzhou, 324300, PR China.
Ying LinPeople's Hospital of Kaihua, 59 Fenghuang Middle Road, Quzhou, 324300, PR China.
Pengxia SongMedical School, Quzhou College of Technology, 18 Jiangyuan Road, Quzhou, 324000, PR China.
Xingchen ZhouCollege of Chemical and Biological Engineering, Zhejiang University, 866 Yuhangtang Road, Hangzhou, 310058, PR China.
Kunhua ZhengPeople's Hospital of Kaihua, 59 Fenghuang Middle Road, Quzhou, 324300, PR China. kunhuazheng@sina.com.

Funding

Quzhou Science and Technology Research Project 2023K200
6 · The paper itself

Abstract

The gut microbiota plays a key role in aging and longevity. Therefore, identifying longevity-associated microbes in healthy and long-lived individuals and elucidating the molecular mechanisms through which they influence longevity are essential steps toward developing effective anti-aging interventions. In this study, we performed 16S rRNA sequencing on 301 fecal samples collected across three age groups. Long-lived individuals (≥ 90 years) had more diverse gut microbiota than typical older individuals (60-89 years), with diversity comparable to that of younger adults (45-59 years). Compared with typical older individuals, long-lived individuals exhibited a marked increase in the relative abundance of Bacteroidota and Akkermansia, accompanied by a decreased abundance of Prevotella_9 and Megamonas. Additionally, the microbiota from this age group showed significant enrichment in unsaturated fatty acid metabolism, ketone body synthesis and degradation, and tryptophan metabolism, suggesting that differences in microbiota composition and function may contribute to longevity. Finally, we developed a qPCR-based method to detect differentially abundant microbiota and established a classification model capable of distinguishing between age groups. In conclusion, the unique composition and function of the gut microbiota in long-lived individuals offer insights for identifying methods and targets for anti-aging interventions. KEY POINTS: • Long-lived individuals exhibited a marked increase in Bacteroidota and Akkermansia • Long-lived individuals exhibited enrichment in unsaturated fatty acid metabolism • We developed a qPCR-based method to detect differentially abundant microbiota.

Indexed as

BacteriaFecesGastrointestinal MicrobiomeLongevityRNA, Ribosomal, 16SChinaDNA, BacterialDNA, RibosomalHumansMiddle AgedSequence Analysis, DNADNA, BacterialDNA, RibosomalRNA, Ribosomal, 16S16S rRNA sequencingAgingGut microbiotaLongevity

Identifiers

PMID41697396
PMCPMC12909319

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.