2 research outputs found
Identification of Indicative Gut Microbial Guilds in a Natural Aging Mouse Model
Gut microbial dysbiosis during later life may contribute
to health
conditions, possibly due to an increase in intestinal permeability,
immune changes, and systemic inflammation. Mouse models have been
employed to determine the influence of gut microbes on aging; however,
suitable gut microbial indicators are currently lacking. Therefore,
this study aimed to determine the gut microbial indicators and their
potential guilds in a natural aging mouse model. In agreement with
previous studies, alpha diversity indicesincluding observed
OTUs, ACE, Chao1, and Simpsonwere significantly lower in aged
mice than in younger mice. The results of beta diversity analysis
revealed the compositional differences between young and aged mice,
and the MRPP, ANOSIM, and Adonis tests indicated that the results
were representative. By employing ANCOM and LEfSe analyses, Bacteroides thetaiotaomicron (Bacteroides) and Anaeroplasma were identified
as the indicators of young and aged mice, respectively. Notably, these
indicators were still present after 3 months. The result of network
analysis confirmed the negative correlation of these genera in mice,
and the potential guild members were identified based on the increased
abundance of Anaeroplasma in aged mice.
The gut microbes of aged mice tend to correspond to those involved
in human diseases, selenocompound metabolism, and glycolysis/gluconeogenesis
in functional predictions. In this study, the gut microbial indicators
in aged mice have been identified, and it is envisaged that these
findings could provide a new approach for future studies of antiaging
Identification of Indicative Gut Microbial Guilds in a Natural Aging Mouse Model
Gut microbial dysbiosis during later life may contribute
to health
conditions, possibly due to an increase in intestinal permeability,
immune changes, and systemic inflammation. Mouse models have been
employed to determine the influence of gut microbes on aging; however,
suitable gut microbial indicators are currently lacking. Therefore,
this study aimed to determine the gut microbial indicators and their
potential guilds in a natural aging mouse model. In agreement with
previous studies, alpha diversity indicesincluding observed
OTUs, ACE, Chao1, and Simpsonwere significantly lower in aged
mice than in younger mice. The results of beta diversity analysis
revealed the compositional differences between young and aged mice,
and the MRPP, ANOSIM, and Adonis tests indicated that the results
were representative. By employing ANCOM and LEfSe analyses, Bacteroides thetaiotaomicron (Bacteroides) and Anaeroplasma were identified
as the indicators of young and aged mice, respectively. Notably, these
indicators were still present after 3 months. The result of network
analysis confirmed the negative correlation of these genera in mice,
and the potential guild members were identified based on the increased
abundance of Anaeroplasma in aged mice.
The gut microbes of aged mice tend to correspond to those involved
in human diseases, selenocompound metabolism, and glycolysis/gluconeogenesis
in functional predictions. In this study, the gut microbial indicators
in aged mice have been identified, and it is envisaged that these
findings could provide a new approach for future studies of antiaging