Abstract

Mating plugs are produced by many sexually reproducing animals and are hypothesized to promote male fertilization success under promiscuous mating. However, tests of this hypothesis have been constrained by an inability to discriminate ejaculates of different males in direct competition. Here, we use stable isotope labeling in vivo and proteomics to achieve this in a promiscuous rodent, Myodes glareolus We show that, although the first male's plug is usually dislodged, it can be retained throughout the second male's copulation. Retained plugs did not completely block rival sperm but did significantly limit their numbers. Differences in the number of each male's sperm progressing through the female reproductive tract were also explained by natural variation in the size of mating plugs and reproductive accessory glands from which major plug proteins originate. Relative sperm numbers in turn predicted the relative fertilization success of rival males. Our application of stable isotopes to label ejaculates resolves a longstanding debate by revealing how rodent mating plugs promote fertilization success under competitive conditions. This approach opens new opportunities to reveal cryptic mechanisms of postcopulatory sexual selection among diverse animal taxa.

Highlights

  • Mating plugs are produced by diverse sexually reproducing animals, from worms to primates [1,2,3,4,5]

  • By employing differential stable isotope labeling and proteomics [14, 15], we are able to distinguish the proteins present in competing ejaculates (Fig. 1 A and B) and quantify the consequences of natural variation in mating plug retention and size on sperm numbers progressing through the female reproductive tract

  • Following sequential copulations with two males, our goals were to determine: 1) the origin of the mating plug(s) remaining in the female reproductive tract, and Promiscuous mating by females leads to competition between males for fertilization success

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Summary

Introduction

Mating plugs are produced by diverse sexually reproducing animals, from worms to primates [1,2,3,4,5]. By employing differential stable isotope labeling and proteomics [14, 15], we are able to distinguish the proteins present in competing ejaculates (Fig. 1 A and B) and quantify the consequences of natural variation in mating plug retention and size on sperm numbers progressing through the female reproductive tract. This proteomic labeling approach reveals insight into mating plug function in a model promiscuous rodent, the bank vole (Myodes glareolus)

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