Previous attempts have been made to change the natural reactivity of Biomphalaria glabrata toward invasion by the trematode Schistosoma mansoni. Lie et al. (1983) observed that snails previously exposed to irradiated miracidia presented a lower infection rate (23%) when later challenged with non-irradiated miracidia, as compared with intact controls (73%). Sire et al. (1998) used instead infection with one single live miracidium and observed that this was enough to induce several degrees of alterations in the parasites derived from a challenge infection. Others have used different experimental models to investigate the development of resistance in B. glabrata. Sullivan et al. (1982) subjected B. glabrata to irradiated Ribeiroia marini miracidia and observed the development of resistance to Echinostoma paraensei. Lemos and Andrade (2001) investigated the reason for a finding already known by others, that cercarial elimination presents a progressively decreasing curve with passing time. Their data disclosed that histological changes similarly and progressively varied from no-reaction at the beginning of cercarial elimination, to diffuse hemocyte proliferation, with formation of encapsulating reactions around sporocysts and developing cercariae, at the final period of observation. This strongly suggested that a kind of adaptative To find out whether this type of reactivity could be artificially induced, we executed a series of experiments so designed in order to stimulate the internal defense system of a highly susceptible B. glabrata strain.
MATERIALS AND METHODSSnails -Adult B. glabrata snails from the Feira de Santana (FS) strain, measuring 11 to 13 mm in diameter were maintained under controlled conditions of room temperature (around 26ºC), with free access to appropriated feed. This strain has been maintained in the Laboratory for more than 20 years.
Experimental groups and proceduresGroup 1 -Thirty snails were inoculated with ± 20 ml of distilled water containing 15 S. mansoni miracidia, which had been previously irradiated with 4000 rads from a Cesio 137 irradiator, IBL 937C, type H, from Cis Bio International, Gif-sur-Yvette, France. Injection was made at the exposed cephalo-podal region Ten days later the snails were challenged with exposition to 20 freshly eliminated non-irradiated S. mansoni miracidia. The snails were killed 35 and 42 days later.A control for this group was represented by another 30 snails in which the irradiated miracidia were replaced by non-irradiated, recently eliminated ones. All the other steps were exactly the same as for the above Group.Group 2 -Thirty snails were inoculated at the cephalopodal region with 20 ml of a S. mansoni whole worm antigen in PBS, which contained 0.5 mg/ml protein concentra-