A review of sarcocystosis in camels and redescription of Sarcocystis cameli and Sarcocystis ippeni sarcocysts from the one-humped camel (Camelus dromedarius)

摘要

There is considerable confusion concerning Sarcocystis species in camels. Five species:Sarcocystis cameli, S. ippeni, S. camelicanis, S. camelocanis, and S. miescheri were named withinadequate descriptions and no type specimens. Here, we review literature on sarcocystosis incamels worldwide and redescribe structure of S. cameli and S. ippeni sarcocysts by light andtransmission electron microscopy (LM, TEM). Eight sarcocysts from the esophagi of two camels(Camelus dromedarius) from Egypt were studied. By LM all sarcocysts were thin walled with barely visible projections on the cyst walls. By TEM, two structurally distinct sarcocysts wererecognized by unique villar protrusions (vp) not found in sarcocysts from any other host.Sarcocysts of S. cameli had vp of type 9j. The sarcocyst wall had upright slender vp, up to 3.0μm long and 0.5 μm wide; the total thickness of the sarcocyst wall with ground substance layer(gs) was 3.5 μm. On each vp there were rows of knob-like protrusions that appeared to beinterconnected. The vp had microtubules that originated at mid point of the gs and continued upto the tip; microtubules were smooth, without any granules or dense areas. Bradyzoites wereapproximately 14-15 x 3-4 μm in size with typical organelles. Sarcocystis ippeni sarcocysts hadtype 32 sarcocyst wall characterized by conical villar protrusions with an electron dense knob.The total thickness of the sarcocyst wall (from the base of gs to vp tip) was 2.3-3.0 μm. The vpwere up to 1.2 μm wide at the base and 0.25 μm at the tip. Microtubules in vp originated atmidpoint of gs and continued up to tip; microtubules were criss-crossed, smooth and withoutgranules or dense areas. Bradyzoites were 12.0-13.5 x 2.0-3.0 μm in size. Sarcocystiscamelicanis, S. camelocanis, and S. miescheri are considered invalid.