Early development of the coccidium Sarcocystis muriviperae Matuschka, Heydom, Mehlhom, Abd-Al-Aal, Diesing et Bichler, 1987 is described from experimentally infected white mice fed sporocysts from naturally infected Vipera palaestinae and Coluber jugularis. Although the course of infection was similar, mice infected with the sporocysts from the first host survived an inoculum of up to 200,000 sporocysts, while others infected with the second, succumbed to inocula exceeding 40,000 sporocysts in 7-10 days post infection (p,i,). Histological and ultrastructural studies revealed merogony in the hepatocytes during days 7-10 p.i. and onset of sarcocyst development by days 19-21 p.i. The livers of infected mice are grossly enlarged and of a mottled whitish colour due to severe neutrophil inflammatory infiltration, apparently stimulated by host cell residues or from defunct disaggregating meronts at the end of the merogony cycle. Early sarcocysts undergo a further division by endopolygeny before proceeding to division by endodyogeny.
Six young tortoises Testudo marginata Schoepff, 1792 were experimentally infected with Hemolivia mauritanica (Sergent et Sergent, 1904). The prepatent period ranged from 6 to 8 weeks. Young, smaller, club-like forms (6-9 × 3-6 µm) of gametocytes appeared in the peripheral blood first, whereas mature, elongated, cylindrical forms (9-12 × 5-7 µm) were detected after 1-2 weeks and predominated during later patency. Three of the infected tortoises were euthanized and dissected to study the endogenous stages. Meronts occurred in the cells of the reticulo-endothelial system and in the erythrocytes; these were observed mostly in parenchymatous organs. Mature forms measured 14.2 × 9.3 µm and contained 7-12 merozoites. Cysts with two (exceptionally one) cystozoites were also found predominantly in parenchymatous organs and measured 14.8 × 7.9 µm. Pathological changes attributable to Hemolivia were mild and limited to liver and kidneys. The role of individual developmental stages of haemogregarines is discussed with respect to evolution of heteroxenous life cycle and long-term persistence of parasites in their intermediate hosts.
The fine structure is described of the merogonic stages and gametocytes of a Plasmodium tropiduri Aragão et Neiva, 1909-like parasite infecting the teiid lizard Kentropyx calcarata Spix from North Brazil. The trophozoites are bordered by two membranes, and with growth a pellicle is formed by the addition of an inner, thick double layer and fragmented membrane. The same type of inner membrane occurs in the pellicle of the merozoites differentiating from the meronts. Merozoites contained a large electron-dense body, sometimes seen to be embraced by a tubular mitochondrion with a dense matrix. Micro- and macrogametocytes are bounded by a double membrane, closely apposed by the detached wall of the parasitophorous vacuole. Both contain osmiophilic bodies. The microgametocyte contains an electron-dense aggregate, and the macrogametocyte has a large mitochondrion and a complex of tubuli and cisternae. These features are compared with those described in other malarial parasites.
Mabuya vitatta (Olivier) (Scincidae) and Agama stellio (L.) (Agamidae) were infected with Hemolivia mariae Smallridge et Paperna, 1997 by ingestion of tick viscera from Amblyomma limbatum Neumann, fed as nymphs on naturally infected Australian sleepy lizards, Tiliqua rugosa Gray. The unnatural infection apparently interfered with the developmental schedule of the parasites. Transmission electron microscopic images of merogonic stages were obtained, as well as images of early developing gametocytes. Tissue and intraerythrocytic meronts were bound by a hardened wall. Intraerythrocytic gametocytes were lodged in a parasitophorous vacuole, which was filled with granular material, and were bound by a two-membrane wall. Small and large osmiophilic bodies were located in a sub-pellicular position. With differentiation, the wall membranes tightened with the parasitophorous vacuole wall, and the osmiophilic bodies disappeared. The outer parasite membrane consolidated into a thick encasing with distinct sutures. Late infection in A. stellio comprised gametocytes only.