Parasitic sex ratio distorters were artificially transferred within and between crustacean host species in order to study the effects of parasitism on host fitness and sex determination and to investigate parasite–host specificity. Implantation of Nosema sp. to uninfected strains of its Gammarus duebeni host resulted in an active parasite infection in the gonad of recipient females and subsequent transovarial parasite transmission. The young of artificially infected females were feminized by the parasite, demonstrating that Nosema sp. is a cause of sex ratio distortion in its host. In contrast, we were unable to cross-infect Armadillidium vulgare with the feminizing microsporidian from G. duebeni or to cross-infect G. duebeni with the feminizing bacterium Wolbachia sp. from A. vulgare.

Newly deposited Glossina morsitans morsitans larvae were chilled over ice and inoculated with 1 μ1 of either virus suspension derived from Glossina pallidipes salivary gland homogenate or sterile tsetse physiological saline. They were allowed to pupariate and then maintained at 25°C, 70% r.h. until soon after emergence when their salivary glands were examined for enlargement and presence of virus particles. Teneral G. m. morsitans which received the virus inoculum (n = 135) as larvae all became infected as revealed by gross hypertrophy of their salivary glands and ultrastructural manifestation of virus particles within the glandular epithelial cells and lumina. In the control group, which received the tsetse physiological saline (n = 91), only 1.1% of the flies showed the salivary gland enlargement, a level equivalent to the prevalence of virus infection normally detectable in the G. morsitans colony. This technique opens the way for testing the biocontrol potential of this virus. The DNA virus from G. pallidipes is clearly infective to G. morsitans morsitans, suggesting that the hypertrophied, chalky-white salivary glands, reported in various Glossina spp., are a manifestation of infection by one and the same virus.