Dynamic changes in ejaculatory bulb size during Drosophila melanogaster aging and mating.

The ejaculatory bulb of Drosophila melanogaster males produces proteins and pheromones that play important roles in reproduction. This tissue is also the final mixing site for the ejaculate before transfer to the female. The ejaculatory bulb's dynamics remain largely unstudied. By microscopy of the ejaculatory bulb in maturing adult males, we observed that the ejaculatory bulb expands in size as males age. Moreover, we document that when males mate, their ejaculatory bulb expands further as ejaculate transfer begins, and then contracts halfway through the course of mating as ejaculate transfer finishes. Although there is some male-to-male variation in the timing of these changes, ultimately the tissue changes in a predictable pattern that gives insight into the active mating process in Drosophila.

Retention of Ejaculate by Drosophila melanogaster Females Requires the Male-Derived Mating Plug Protein PEBme.

Within the mated reproductive tracts of females of many taxa, seminal fluid proteins (SFPs) coagulate into a structure known as the mating plug (MP). MPs have diverse roles, including preventing female remating, altering female receptivity postmating, and being necessary for mated females to successfully store sperm. The Drosophila melanogaster MP, which is maintained in the mated female for several hours postmating, is comprised of a posterior MP (PMP) that forms quickly after mating begins and an anterior MP (AMP) that forms later. The PMP is composed of seminal proteins from the ejaculatory bulb (EB) of the male reproductive tract. To examine the role of the PMP protein PEBme in D. melanogaster reproduction, we identified an EB GAL4 driver and used it to target PEBme for RNA interference (RNAi) knockdown. PEBme knockdown in males compromised PMP coagulation in their mates and resulted in a significant reduction in female fertility, adversely affecting postmating uterine conformation, sperm storage, mating refractoriness, egg laying, and progeny generation. These defects resulted from the inability of females to retain the ejaculate in their reproductive tracts after mating. The uncoagulated MP impaired uncoupling by the knockdown male, and when he ultimately uncoupled, the ejaculate was often pulled out of the female. Thus, PEBme and MP coagulation are required for optimal fertility in D. melanogaster. Given the importance of the PMP for fertility, we identified additional MP proteins by mass spectrometry and found fertility functions for two of them. Our results highlight the importance of the MP and the proteins that comprise it in reproduction and suggest that in Drosophila the PMP is required to retain the ejaculate within the female reproductive tract, ensuring the storage of sperm by mated females.