Microscopic study on Sarcocystis moulei from sheep and goats in Saudi Arabia.

The present investigation revealed that the role of natural infection with Sarcocystis in sheep was 84% in Niemy, 76% in Najdy, 89% in Sawakny sheep and 77% in goats slaughtered in Riyadh, Saudi Arabia. The distribution of infection among the examined organs was varied from the sheep strain to goats. Recorded muscle cysts were macroscopic 8-18% (mean 13.5%) and microscopic 73-85% (mean 79%). Macroscopic cysts were usually detected on the oesophagus. EM showed an ultrastructural similarities in the cyst walls and their parasite contents (metrocytes and merozoites) for all macroscopic cysts examined from sheep and goats. These were also enclosed by a secondary cyst wall. The primary cyst wall had many cauliflower-like protrusions supported by many fibellar structures, while the ground substance underneath them contained many dark, dense granules and usually extended into the cyst cavity dividing it into many compartments containing the parasites. The cyst parasites were the peripheral globular to spherical metrocytes, which were divided by endodyogeny and the central banana-shaped merozoites. Both metrocytes and merozoites had all characteristics of the Apicomplexa. Experimental transmission of Sarcocystis to the definitive host, revealed that kittens were the only suitable final host. Thus, gamogony and zygote formation (fertilization) occurred 2-8 days post infection (p.i.) while sporulation took place within this final host 13-15 days p.i., where sporocysts were passed within faeces of infected kittens at that time. Also, the study indicated that the prepatent period was 13-15 days, while the patent period was 37-42 days.

Life-cycle of Isospora mehlhornii sp. nov. (Apicomplexa : Eimeriidae), parasite of the Egyptian swallow Hirundo rubicola savignii.

Fifty-seven Hirundo rubicola savignii swallows were collected from Damietta, Tanta, Dakahlyia and Sharkia Provinces, Egypt. They were examined for coccidian parasites. The percentage of infection with Isospora stages was 12.3%. After diagnosis it was noted that the parasites belong to a new species. The unsporulated oocysts were spherical, measuring 25.7-31.9 microm in diameter with a mean of 28.3 microm. A micropyle, polar granule and oocyst residuum were absent. Sporocysts appeared lemon-shaped and measured 19.6-24.5 microm x 12.5-17.5 microm with a mean of 22.9 x 14.4 microm. Stieda body and the sporocyst's residual body were clearly visible. Sporozoites measured 11-14.2 x 4.4-5.1 microm with a mean of 11.4 x 4.7 microm. Sporulation time was 72 h at room temperature (25 degrees C). Endogenous stages including schizogony and gamogony were detected in epithelial cells of the duodenum, jejunum and ileum of the host. Schizogony consisted of two generations. Mature first generation schizonts reached up to 11 microm in diameter and produced merozoites measuring 3.5 x 1.7 microm. Mature second generation schizonts measured 17.2 x 12.3 microm and produced merozoites measuring 11.8 x 2.2 microm. Gamogonic stages were differentiated into microgamonts and macrogamonts. Mature microgamonts were spherical and measured 23.2 microm in diameter, producing curved microgametes measuring 4.5 x 0.7 microm. The ovoid macrogametes measured 19.6 x 14.7 microm and were characterized by a large nucleus and nucleolus. Early, more or less spherical, oocysts were detected inside the intestinal epithelial cells and in the intestinal lumen. They measured 19.6 microm in diameter. The sporont measured 17.2 microm in diameter. Cytochemical studies on schizogony, gamogony and oocysts were accomplished and showed distribution of polysaccharides and composition of the oocyst wall.