English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

The keystone gut species Christensenella minuta boosts gut microbial biomass and voluntary physical activity in mice

MPS-Authors
/persons/resource/persons286420

Akbuğa-Schön,  T       
Department Microbiome Science, Max Planck Institute for Biology Tübingen, Max Planck Society;

/persons/resource/persons270535

Suzuki,  TA       
Department Microbiome Science, Max Planck Institute for Biology Tübingen, Max Planck Society;

/persons/resource/persons264997

Jakob,  D       
Department Microbiome Science, Max Planck Institute for Biology Tübingen, Max Planck Society;
Mass Spectrometry, Max Planck Institute for Biology Tübingen, Max Planck Society;

/persons/resource/persons275175

Vu,  DL
Mass Spectrometry, Max Planck Institute for Biology Tübingen, Max Planck Society;

/persons/resource/persons272151

Waters,  JL       
Department Microbiome Science, Max Planck Institute for Biology Tübingen, Max Planck Society;

/persons/resource/persons270516

Ley,  RE       
Department Microbiome Science, Max Planck Institute for Biology Tübingen, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

Akbuğa-Schön, T., Suzuki, T., Jakob, D., Vu, D., Waters, J., & Ley, R. (2024). The keystone gut species Christensenella minuta boosts gut microbial biomass and voluntary physical activity in mice. mBio, 15(2): e0283623. doi:10.1128/mbio.02836-23.


Cite as: https://hdl.handle.net/21.11116/0000-000E-16E8-4
Abstract
The composition of the human gut microbiome is associated with human health. Within the human gut microbiome, the relative abundance of the bacterial family Christensenellaceae has been shown to correlate with metabolic health and a lean body type. The mechanisms underpinning this effect remain unclear. Here, we show that live C. minuta influences host physical activity and metabolic energy expenditure, accompanied by changes in murine metabolism and the gut microbial community in a sex-dependent manner in comparison to heat-killed C. minuta. Importantly, live C. minuta boosts the biomass of the microbiome in the gut, and a higher level of C. minuta is associated with greater loss of energy in stool. These observations indicate that modulation of activity levels and changes to the microbiome are ways in which the Christensenellaceae can influence host energy homeostasis and health.