Study of the morphological characteristics of Schistosoma mansoni in mice, squirrels, and hamsters.

ABSTRACT

This study attempted to describe mophological characteristics of S. mansoni worms. In the present study, 6 hamsters, 35 squirrels and 141 mice were infected with pooled cercariae of Schistosoma mansoni by intraperitoneal and percutaneous routes. The worm recovery rate was 18.2% (257/1,412) in hamsters (Mesocricetus auratus); 10.1% (3,310/32,792) in squirrels (Callosciurus erythraeus roberti) and 16.2% (4,328/26,720) in mice (Swiss strain). There were no significant differences between the sizes of 332 adults studied from three kinds of experimental animals. However, the worms collected from the hepatic portal system were usually larger than those from the peritoneal cavity because the latter almost always remained in the immature stage. We found male S. mansoni with tandem (17-22%), non-tandem (80-83%) and unusual/irregular arrangement (3-5%) of testes. The number of S. mansoni testes found were from 3 to 15 in mice, 3 to 11 in hamsters and 4 to 15 in squirrels. Mature worms had a tendency to reduce their size with aging. The number of S. mansoni cecal loops were from 1 to 5 in mice and hamsters and 1 to 4 in squirrels. The location of the first cecal loop was usually in the anterior part of body (1/4 in females and 1/3 in males), but there were some exceptions. The number of eggs in the uterus of each female worm, were 0-3 in mice, 0-1 in squirrels and hamsters. The average number was 0.75. The location of the ovary was usually situated in the anterior part of body of the worm in the three kinds of experimental animals. A few mated male and female worms of S. mansoni being free in the peritoneal cavity were found to develop to sexual maturity, because eggs were observed in their uteri. Their size was usually found to be considerably smaller than the worms seen in the hepatic portal system, and they had no hematin in their intestinal ceca. Encapsulated eggs were found from the peritoneal cavities of a few mice following intraperitoneal and percutaneous methods of infection.