Abstract

Lifespan costs to reproduction are common across multiple species, and such costs could potentially arise through a number of mechanisms. In the nematode Caenorhabditis elegans, it has been suggested that part of the lifespan cost to hermaphrodites from mating results from physical damage owing to the act of copulation itself. Here, we examine whether mating damages the surface of the hermaphrodite cuticle via scanning electron microscopy. It is found that mated hermaphrodites suffered delamination of cuticle layers surrounding the vulva, and that the incidence of such damage depends on genetic background. Unmated hermaphrodites demonstrated almost no such damage, even when cultured in soil with potentially abrasive particles. Thus, a consequence of mating for C. elegans hermaphrodites is physical cuticle damage. These experiments did not assess the consequences of cuticle damage for lifespan, and the biological significance of this damage remains unclear. We further discuss our results within the context of recent studies linking the lifespan cost to mating in C. elegans hermaphrodites to male secretions.

Highlights

  • Tradeoffs between lifespan and reproduction are thought to play a crucial role in the evolution of life history traits [1]

  • To evaluate the hypothesis that mating promotes physical damage in hermaphrodites, hermaphrodites either unmated or continuously mated with males for five days were examined under scanning electron microscopy (SEM)

  • We have used SEM to demonstrate that prolonged mating is associated with vulval cuticle damage in C. elegans hermaphrodites

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Summary

Introduction

Tradeoffs between lifespan and reproduction are thought to play a crucial role in the evolution of life history traits [1]. Such tradeoffs are widespread in metazoans [2,3,4], and have been traditionally framed within a theoretical context of limited organismal energetic resources. It is often presumed that use of energetic resources on lifespan (or the soma) has a detrimental consequence on reproduction (or the germline), and vice-versa [5,6,7]. Lifespan costs to reproduction are not always limited to such metabolic tradeoffs. Lifespan costs to reproduction take many forms and must entail a variety of specific mechanisms across species

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