Prior studies on cryopreserving embryos of several non-drosophilid flies es
tablished that two Drosophila,melanogaster, embryo cryopreservation protoco
ls were not directly suitable for use with these species. This paper descri
bes our work on developing a protocol for cryopreservation of embryos of th
e housefly, Musca domestica. Significant progress was made when permeabiliz
ation of the vitelline membrane was optimized, a vitrification solution con
taining ethylene glycol, polyethylene glycol, and trehalose was formulated,
and when cooling and recovery of the cryopreservation protocol included a
step which passed the embryos through liquid nitrogen vapor. More than 70%
of housefly embryos withstand treatments of dechorionation, permeabilizatio
n, loading with cryoprotectant, and dehydration in vitrification solution,
but the cooling, warming, and poststorage rearing steps still cause a consi
derable reduction in survival. About 53% of the vitrified M. domestica embr
yos hatched into larvae. Relative to the percentage of the control adult em
ergence, about 13% of the embryos stored in liquid nitrogen developed into
fertile adults. Hatching of the F-1 progeny of adults having been cryoprese
rved as embryos was similar to control levels, (C) 2000 Academic Press.