Deutsch
 
Hilfe Datenschutzhinweis Impressum
  DetailsucheBrowse

Datensatz

DATENSATZ AKTIONENEXPORT

Freigegeben

Zeitschriftenartikel

Regulation of life span by the gut microbiota in the short-lived African turquoise killifish

MPG-Autoren

Smith,  P.
Max Planck Institute for Biology of Ageing, Max Planck Society;

Willemsen,  D.
Max Planck Institute for Biology of Ageing, Max Planck Society;

Popkes,  M.
Max Planck Institute for Biology of Ageing, Max Planck Society;

Metge,  F.
Max Planck Institute for Biology of Ageing, Max Planck Society;

Gandiwa,  E.
Max Planck Institute for Biology of Ageing, Max Planck Society;

Reichard,  M.
Max Planck Institute for Biology of Ageing, Max Planck Society;

Valenzano,  D. R.
Max Planck Institute for Biology of Ageing, Max Planck Society;

Externe Ressourcen
Volltexte (beschränkter Zugriff)
Für Ihren IP-Bereich sind aktuell keine Volltexte freigegeben.
Volltexte (frei zugänglich)
Es sind keine frei zugänglichen Volltexte in PuRe verfügbar
Ergänzendes Material (frei zugänglich)
Es sind keine frei zugänglichen Ergänzenden Materialien verfügbar
Zitation

Smith, P., Willemsen, D., Popkes, M., Metge, F., Gandiwa, E., Reichard, M., et al. (2017). Regulation of life span by the gut microbiota in the short-lived African turquoise killifish. Elife, 6. doi:10.7554/eLife.27014.


Zitierlink: https://hdl.handle.net/21.11116/0000-0001-5930-5
Zusammenfassung
Gut bacteria occupy the interface between the organism and the external environment, contributing to homeostasis and disease. Yet, the causal role of the gut microbiota during host aging is largely unexplored. Here, using the African turquoise killifish (Nothobranchius furzeri), a naturally short-lived vertebrate, we show that the gut microbiota plays a key role in modulating vertebrate life span. Recolonizing the gut of middle-age individuals with bacteria from young donors resulted in life span extension and delayed behavioral decline. This intervention prevented the decrease in microbial diversity associated with host aging and maintained a young-like gut bacterial community, characterized by overrepresentation of the key genera Exiguobacterium, Planococcus, Propionigenium and Psychrobacter. Our findings demonstrate that the natural microbial gut community of young individuals can causally induce long-lasting beneficial systemic effects that lead to life span extension in a vertebrate model.