A diet of oxidative stress–adapted bacteria improves stress resistance and lifespan in C. elegans via p38-MAPK

Author:

Bhat Ajay1ORCID,Cox Rebecca L.1ORCID,Hendrickson Brice Graham1,Das Nupur K.1ORCID,Schaller Megan L.1,Tuckowski Angela M.2ORCID,Wang Emily1ORCID,Shah Yatrik M.13ORCID,Leiser Scott F.13ORCID

Affiliation:

1. Molecular & Integrative Physiology Department, University of Michigan, Ann Arbor, MI 48109, USA.

2. Cellular and Molecular Biology Program, University of Michigan, Ann Arbor, MI 48109, USA.

3. Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109, USA.

Abstract

Organisms across taxa face stresses including variable temperature, redox imbalance, and xenobiotics. Successfully responding to stress and restoring homeostasis are crucial for survival. Aging is associated with a decreased stress response and alterations in the microbiome, which contribute to disease development. Animals and their microbiota share their environment; however, microbes have short generation time and can rapidly evolve and potentially affect host physiology during stress. Here, we leverage Caenorhabditis elegans and its simplified bacterial diet to demonstrate how microbial adaptation to oxidative stress affects the host’s lifespan and stress response. We find that worms fed stress-evolved bacteria exhibit enhanced stress resistance and an extended lifespan. Through comprehensive genetic and metabolic analysis, we find that iron in stress-evolved bacteria enhances worm stress resistance and lifespan via activation of the mitogen-activated protein kinase pathway. In conclusion, our study provides evidence that understanding microbial stress–mediated adaptations could be used to slow aging and alleviate age-related health decline.

Publisher

American Association for the Advancement of Science (AAAS)

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