Fifty-day-old fry of tilapia hybrids (Oreochromis aureus x niloticus) were placed in aquaria containing sediment with oocysts of Eimeria (sensu lato) vanasi Landsberg et Paperna. In the first 29 h after exposure sporulated oocysts in the stomach and free sporozoites in the gut could be found in examined fish. By 7 to 56 h after exposure, sporozoites, with their characteristic crystalloid body, were detected in intraepithélial lymphocyte-like and other leucocyte-like cells, but never in the epithelial cells. Infected cells were confined to the epithelial layer and did not enter the lamina propria. Within this time, some of the sporo-zoitcs divided by endodyogeny, once or twice in succession, to form daughter sporozoites. The parent’s sporozoite crystalline body was divided between the offspring of the primary and secondary divisions.
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.
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.
A greater blue-eared glossy starling Lamprotornis chalybaeus Ehrenburg from a large flight aviary in Hong Kong was found on post mortem to be infected with Plasmodium octamerium Manwell, 1968, Plasmodium cf. relictum (Grassi et Feletti, 1891) and Haemoproteus cf. pastoris Mello, 1935. Descriptions of their morphology are provided as none of the examined parasites fully concord with their type (or neotype) material descriptions. Plasmodium octamerium has been recorded in avian hosts from geographically distant locations, suggesting that infection in imported hosts may persist in a chronic state for a long period. This Plasmodium species as well as P. relictum are evidently not fastidious in choice of passeriform hosts and are transmitted by ubiquitous domestic mosquito vectors, apparently facilitating their proliferation among zoo and aviary inhabitants. The Haemoproteus infection appears to be conspecific with H. cf. pastoris reported from a myna (Acridotheres tristis) in Singapore. Mynas are also common in Hong Kong, which suggests a possible cross-transmission of infection between these two starlings.
Isospora carliae sp. n. is described from the blue-throated rainbow skink Carlia rhomboidalis (Peters), from Daintree Forest, North Queensland, Australia. Oocysts are ellipsoidal, 16.8-21.0 × 12.6-15.4 µm in size, with their two sporocysts, 9.0-14.0 × 7.0-9.24 µm in size, positioned along the wide axis. Sporozoites contain a distinct refractile body and are accompanied by a residuum. All endogenous development occurs within the host-cell nucleus. Nuclei are sometimes invaded by several merozoites, but only infections by a single parasite persist. Nuclei lodging meronts, mature microgamonts and premature macrogamonts have an elongate shape. Some meronts exhibit a membrane-bound cytoplasmic inclusion that contains many micronemes.
Schellackia ptyodactyli sp. n. is described from the fan-footed gecko Ptyodactylus hasselquistii (Donndorf) found the lower Jordan Valley, Cis-Jordan. Endogenous development was studied in geckoes necropsied 7-11 days after being inoculated with blood containing sporozoites from naturally infected geckoes of the same species. Merogony and gamogony/oogony stages, as well as sporozoites, are described by light and electron microscopy. Merogony stages, microgamonts and sporozoites conformed in fine structure to that of other eimerian coccidia. whereas wall forming bodies of the macrogamonts showed some divergence from the general pattern characteristic of eimerians and Schellackia cf. agamae. Merogony stages occurred simultaneously with gamonts and sporozoites. In the blood, sporozoites entered leucocytes, thrombocytes and erythrocytes. Parasitaemia persisted for up to 2 years in some naturally infected geckoes in captivity.
One of four Hoplobatrachus occipitalis (Günther, 1859) frogs received from Niger, West Africa was heavily infected with Lankesterella blood and pre-erythrocytic stages. Infected blood and tissues from this frog were force-fed to the remaining three frogs. Two survived to necropsy on days 14 and 27 post-feeding and were found to be infected with gamogonic and oogonic stages, respectively. The source of infection is inconclusive, as a natural origin cannot be excluded. Microgamont, macrogamont, oocyst and sporozoite structure and fine structure are described and found to conform in general, but not in detail, to previous descriptions. Gamonts and oocysts occurred predominantly in the liver and spleen. Walled sporulating oocysts were situated within macrophage centres. Oocysts yielded a progeny of 32 sporozoites. Pre-erythrocytic sporozoites developed within expanded inclusions, within their host cell, from which they massively invaded the liver and spleen, and to a lesser extent the lungs and kidneys. Sporozoites occurred in a parasitophorous vacuole in the erythrocytes. Conspecificity with Lankesterella dicroglossi Paperna et Ogara, 1996 reported from the same host species in Kenya remains uncertain due to several structural and developmental differences.
Eimeria jamescooki sp. n. was recovered from the skink Cryptoblepharus virgatus (Garman) found on the grounds of James Cook University, Townsville (type locality), North Queensland, Australia. Oocysts were 17.5-25.0 (22.1 ± 1.9) × 15-22.5 (17.7 ± 1.6) µm and sporocysts 6.25-10.0 (7.9 ± 1.15) × 3.75-6.25 (5.3 ± 1.0) µm in size. Endogenous stages are described from histological material examined by light microscope and by transmission electron microscope. Both merogony stages and gamonts were found to develop in the cytoplasm of the anterior gut mucosal epithelium. Meront progeny were comprised of 10 to 21 merozoites. Premature macrogamonts were elongate; some host cells contained two elongate macrogamonts. Unique to the presently described species were the Golgi ''plaques'' and an enclosure of tubuli. Mature macrogamonts and young oocysts ranged in size from 14 x 7 to 21 × 11 µm and contained two types of wall-forming bodies, canaliculi and amylopectin granules. Differentiating microgamonts conformed in fine structure with that observed in other eimerians. Their sizes increased from 15.4 × 4.2 to 28 × 8.4 µm while dividing to over 70 nuclei, which formed a corresponding yield of microgametes.
Endogenous development of Choleoeimeria rochalimai (Carini et Pinto, 1926) Lainson et Paperna, 1999 in the gall bladder of Hemidactylus mabouia (Moreau de Jonnes, 1818) front Belem, Brazil is reported at the fine structural level. Meronts and gamonts develop in the epithelial cells of the gall bladder. Infected cells become enlarged and displaced above the epithelial layer. Developing merozoites, dividing meronts and succession of developing microgamonts from initial nuclear division up to final microgamete differentiation are described. In addition to wall forming bodies, mature macrogamonts possess a large inclusion or cisterna with fine granular contents.