4.8 Article

Human gut-derived B. longum subsp. longum strains protect against aging in a D-galactose-induced aging mouse model

Journal

MICROBIOME
Volume 9, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s40168-021-01108-8

Keywords

Probiotics; Bifidobacterium longum; Evolution; Transmission; Aging alleviation; Genome-wide association studies (GWAS); Genomic adaptation; Arginine metabolism; Gut microbiota

Categories

Funding

  1. National Natural Science Foundation of China Program [32021005, 31820103010, 31871773]
  2. National Natural Science Foundation for Key Programs of China [81790632]
  3. Projects of Innovation and Development Pillar Program for Key Industries in Southern Xinjiang of Xinjiang Production and Construction Corps [2018DB002]
  4. National Key Research and Development Project [2018YFC1604206]
  5. National First-Class Discipline Program of Food Science and Technology [JUFSTR20180102]
  6. BBSRC Newton Fund Joint Centre Award
  7. Collaborative Innovation Center of Food Safety and Quality Control in Jiangsu Province

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This study identified geographically distinct gene pools/populations among Bifidobacterium longum strains and explored the mechanisms of probiotics on promoting host longevity. The research revealed different abilities of strains with different genotypes in combating host aging and provided new insights into the use of specific probiotics or molecules for promoting host longevity.
Background: Probiotics have been used to regulate the gut microbiota and physiology in various contexts, but their precise mechanisms of action remain unclear. Results: By population genomic analysis of 418 Bifidobacterium longum strains, including 143 newly sequenced in this study, three geographically distinct gene pools/populations, BLAsia1, BLAsia2, and BLothers, were identified. Genes involved in cell wall biosynthesis, particularly peptidoglycan biosynthesis, varied considerably among the core genomes of the different populations, but accessory genes that contributed to the carbohydrate metabolism were significantly distinct. Although active transmission was observed inter-host, inter- country, inter-city, intra-community, and intra-family, a single B. longum clone seemed to reside within each individual. A significant negative association was observed between host age and relative abundance of B. longum, while there was a strong positive association between host age and strain genotype [e.g., single nucleotide polymorphisms in the arginine biosynthesis pathway]. Further animal experiments performed with the B. longum isolates via using a D-galactose-induced aging mouse model supported these associations, in which B. longum strains with different genotypes in arginine biosynthesis pathway showed divergent abilities on protecting against host aging possibly via their different abilities to modify the metabolism of gut microbes. Conclusions: This is the first known example of research on the evolutionary history and transmission of this probiotic species. Our results propose a new mechanistic insight for promoting host longevity via the informed use of specific probiotics or molecules.

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