Disease tolerance and infection pathogenesis age-related tradeoffs in mice

Disease tolerance is a defence strategy essential for survival of infections, limiting physiological damage without killing the pathogen<sup>1,2</sup>. The disease course and pathology an infection may cause can change over the lifespan of a host due to the structural and functional physiological changes that accumulate with age. Because successful disease tolerance responses require the host to engage mechanisms that are compatible with the disease course and pathology caused by an infection, we predicted that this defence strategy would change with age. Animals infected with a 50% lethal dose (LD<sub>50</sub>) of a pathogen often show distinct health and sickness trajectories due to differences in disease tolerance<sup>1,3</sup> and can be used to define tolerance mechanisms. Here, using a polymicrobial sepsis model, we found that, despite having the same LD<sub>50</sub>, aged and young susceptible mice showed distinct disease courses. In young survivors, cardiac Foxo1 and its downstream effector Trim63 (MuRF1) protected from sepsis-induced cardiac remodelling, multi-organ injury and mortality. Conversely, in aged hosts, Foxo1 and Trim63 acted as drivers of sepsis pathogenesis and death. Our findings have implications for the tailoring of therapy to the age of an infected individual and indicate that disease tolerance genes show antagonistic pleiotropy.

Authors

Institutions

Publication Details

Journal
Nature
Published
2026-01-14
DOI
https://doi.org/10.1038/s41586-025-09923-x
Citations
2
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
Type
article
Field-Weighted Citation Impact
30.19
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Disease tolerance and infection pathogenesis age-related tradeoffs in mice

Sarah Stengel, April E. Williams, Justin L. McCarville, Janelle S. Ayres et al.
2 citations
Nature
Genetics, Aging, and Longevity in Model Organisms
30.19
article

Disease tolerance and infection pathogenesis age-related tradeoffs in mice

Sarah Stengel, April E. Williams, Justin L. McCarville, Janelle S. Ayres, Jessica M. Snyder, Karina K. Sanchez
article en
2 citations

Abstract

Disease tolerance is a defence strategy essential for survival of infections, limiting physiological damage without killing the pathogen<sup>1,2</sup>. The disease course and pathology an infection may cause can change over the lifespan of a host due to the structural and functional physiological changes that accumulate with age. Because successful disease tolerance responses require the host to engage mechanisms that are compatible with the disease course and pathology caused by an infection, we predicted that this defence strategy would change with age. Animals infected with a 50% lethal dose (LD<sub>50</sub>) of a pathogen often show distinct health and sickness trajectories due to differences in disease tolerance<sup>1,3</sup> and can be used to define tolerance mechanisms. Here, using a polymicrobial sepsis model, we found that, despite having the same LD<sub>50</sub>, aged and young susceptible mice showed distinct disease courses. In young survivors, cardiac Foxo1 and its downstream effector Trim63 (MuRF1) protected from sepsis-induced cardiac remodelling, multi-organ injury and mortality. Conversely, in aged hosts, Foxo1 and Trim63 acted as drivers of sepsis pathogenesis and death. Our findings have implications for the tailoring of therapy to the age of an infected individual and indicate that disease tolerance genes show antagonistic pleiotropy.

NatureVol. 650(8102)
Salk Institute for Biological Studies (US), Howard Hughes Medical Institute (US), University of Washington (US)
Openalex Percentile: Top 0%
Genetics, Aging, and Longevity in Model Organisms
30.19
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.