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RESEARCH PAPER / 2025-08-25

A hierarchy of causes of death in senescent C. elegans.

Hongyuan Wang, Carina C Kern, Chiminh Nguyen Hong, Alis Saez Allende, Jiayi Qiao, Aihan Zhang, Yimu Fan, Marina Ezcurra, David Gems

Institute of Healthy Ageing, and Research Department of Genetics, Evolution and Environment, University College London, London, UK.Institute of Healthy Ageing, and Research Department of Genetics, Evolution and Environment, University College London, London, UK. · pubmed

Abstract

Interventions that extend lifespan in animal models could, in principle, decelerate the aging process as a whole. Alternatively, they could act by suppressing one or more individual late-life pathologies that contribute to mortality. Here we show how, in the nematode Caenorhabditis elegans, late-life pathologies can compete in a hierarchical fashion to cause death, such that removal of one cause of death can unmask another. Under standard culture conditions, a major cause of death in elderly C. elegans is infection by their bacterial food source. We report that only when such infection is prevented is lifespan extended by suppression of a second senescent pathology, teratoma-like uterine tumors. Thus, as in mammals, lifespan in wild-type C. elegans can be limited by naturally-occurring neoplasia. By contrast, blocking bacterial infection attenuated the life-shortening effects of vitellogenesis, and did not unmask a life-shortening effect of distal gonad degeneration. Thus, depending on the masking or unmasking of competing causes of mortality in the hierarchy of causes of death, nematode lifespan limitation in different contexts can reflect action of distinct life-limiting senescent pathologies. This underscores how increases in lifespan do not necessarily reflect a reduction in overall aging rate.

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Research summary

The paper claims that different late-life pathologies in C. elegans can compete hierarchically to cause death, influencing lifespan extension strategies. This research is relevant as it explores the mechanisms underlying aging and lifespan limitation, contributing to our understanding of the root causes of aging rather than merely addressing symptoms.

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