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PubMed1976

[A contribution to the physiology of movement of gregarines: elements and modus of cellular movement (author's transl)].

1. Cytochalasin B (= CCB, Phomin) in several concentrations inhibits the visible movement of gregarines. The fine structure of the cell is simultaneously changed, fibrillar bundles are desorganized. These fibrils are regarded as myonemes. 2. These myonemes are directed peripherally of the cell longitudinal and transverse to its axis. The longitudinal myonemes are organized in separated strings stretching along the top of the epicyte folds, between the plasmalemm and the secondary membranous layer. Fibrils under this layer serve as skeleton and as thus antagonist. The skeleton fibrils remain unaltered after CCB inhibition. They are located in a parallel direction to the myonemes. Their number corresponds together in one epicyte fold. The transverse myonemata surround the central plasma nearby the basal lamella, which cannot be found in some of the regarded species. 3. The co-work of skeleton-fibrils, stiff pellicle and myonemes allows to describe the modus of all known types of movement. Only change of coordination yields the multitude of these kinds of movement.

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PubMed1976

[Contributions to the life-cycle of Frenkelia. II. The asexual development of Frenkelia clethrionomyobuteonis in the bank vole (author's transl)].

A description of the asexual development of Frenkelia clethrionomyobuteonis in the European bank vole (Clethrionomys glareolus) is given as observed in experimental infections with sporocysts from buzzards' faeces. Between the 5th and the 8th day following the oral administration of sporocysts a first schizogony could be observed in liver parenchymal cells of the mammalian host. In impression smears the banana-shaped merozoites measured on an average 7.6 X 2.2 mum. Only after the 18th day were small round cysts filled with metrocytes detected in the brain and spinal cord. During the first month after infection the cysts increased their size only gradually measuring 15 to 40 mum. After 2 months they accelerated their growth and reached in the course of 3-4 months a diameter of 300 to 400 mum. Cyst formation could not be observed in organs other than the central nervous system. Cysts older than half a year frequently showed central degeneration, but in all cases viable cystozoites persisted in the peripheral zones. The infection could be transmitted from vole to vole by intraperitoneal injection of merozoites in a suspension of liver cells from the 7th day p.i. Congential infections did not occur in the offspring of mothers infected during or before pregnancy. The infectivity of the final products of the sexual development in the buzzard is limited to the bank vole.

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PubMed1976

[Electron microscopic investigation on the evolution stages of the trophozoite of Didymophyes gigantea (Sporozoa, Gregarinida). I. The fine structure of the proto- and epimerite and the relationship between host and parasite (author's transl)].

The fine structure of the epimerite and the protomerite of D. gigantea was investigated following the different stages of the evolution of the trophozoite. The first stage is mononucleate and very poor of cytoplasmic structures (Fig. 1). All following stages are polynucleate (Fig. 3). The septum between protomerite and deutomerite appears at the third stage (Fig. 22). The body of the gregarine is in all stages surrounded by a thick cell-wall constituted of three membranes. The limit between epimerite and protomerite is indicated by the existence of an osmiophilic basal ring just under the parasite's cell-wall. This basal ring has a transverse substructure with a periodical distance of 450 A (Fig. 12). The two inner membranes join together just beneath the basal ring, whereas the outer membrane continues and forms the single cell membrane of the epimerite (Fig.9). The epimerite displays a large number of microvillosities and evaginations of the membrane which increase considerably its surface (Figs. 11-14). The epimerite essentially contains ribosomes and mitochondria (Fig.6). The protomerite contains in addition to the usual cell organites cytoplasmic agglomerations consisting of endoplasmic reticulum, ribonucleoprotein and peripheric mitochondria. During evolution from stage IV to V, these agglomerations produce osmiophilic granula of different form and size, most of which are surrounded by an elementary membrane (Fig. 18). Beside these granula one can observe sometimes small spherical or lamellar structures (Fig. 21). Large bundles of microtubules run from the protomerite into the epimerite where they generally branch off and penetrate into the mitochondrial layer (Figs. 6, 19, 20). Between the parasite and the host-cell exists a space, the periparasitic space, without any cytoplasmic inclusions. The cell membrane of the host-cell has in the periparasitic space an outer cell-coat with a ripped pattern (Fig. 13). The microvillosities of the cell membrane disappear at this place. The host-cell cytoplasm displays a large number of microtubules and a fibrillar network (Figs. 13, 14). The importance of these structures for the relationship between parasite and host-cell is discussed.

Animals↗
PubMed1978

[Investigations into the fire structure of the asexual developmental stages of Frenkelia in the liver of the bank vole (author's transl)].

Bank voles (Clethrionomys glareolus) were infected by stomach tube with Frenkelia sporocysts from the faeces of buzzards (Buteo buteo). The voles were sacrificed at regular intervals and their livers examined electronmicroscopically. Seven days p.i. developmental stages of Frenkelia could be detected in liver parenchymal cells. The youngest schizonts detected are enveloped by a pellicle consisting of two membranes. This pellicle, which is in direct contact with the host cell mitochondria, shows marked invaginations which increase with the development of the schizont. A parasitophorous vacuole is not detectable. In developing schizonts numerous sections through nuclei with nucleic spindles and merozoite anlagen (dome-shaped) structures) are visible. It is not clear whether there are several nuclei or a section through one large and lobed nucleus. Within the merozoite anlagen the conoid and the subpellicular microtubules are formed first. By the prolongation of the dome-shaped structures towards the posterior pole, the nucleus and the other newly formed cell organelles are incorporated into the forming merozoite. The posterior pole of the merozoite still remains open at this stage of development. With increasing differentiation the merozoites become lancet-shaped, their apical poles bing always directed towards the periphery of the schizont. The outer membrane of the pellicle of the schizont forms the outer part of the pellicle of the merozoites by invaginating around them. At this stage of development the inner membrane of the pellicle of the schizont is no longer detectable. Thus the typical pellicle of the motile stages of sporozoaonsisting of three membranes is formed. In the centre of the merozoites which lie freely in the liver cell a residual body is present. The host cell reacts against the parasites by forming a thick border of mitochondria and distinct endoplasmic reticulum.

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PubMed1975

Hammondia hammondi gen. nov., sp.nov., from domestic cats, a new coccidian related to Toxoplasma and Sarcocystis.

Hammondia hammondi gen.nov.,sp.nov (Eimeriorina:Sarcocystidae) is described as an obligate heteroxenous protozoon of domestic cats (final host) and laboratory mice (experimental intermediate host). Oocysts from the final host are infectious only for the intermediate host; and cysts from the intermediate host are infectious only for the final host. Intracellular cysts develop principally in striated muscle of mice that ingest oocysts, with a few cysts in the brain and perhaps elsewhere. Cysts are without septa or radial spines; bradyzoites are slender, there is no evidence of metrocytes. Cysts are not infectious for mice. After the ingestion of cysts by cats, a multiplicative cycle precedes the development of gametocytes in the epithelium of the samll intestine. Oocysts are shed unsporulated, sporogony is outside of the host, resulting in two sporocysts with four sporozoites each. Oocysts of the species average 11 x 13 mum. The prepatent period i 5s 5 to 8 days, and oocyst shedding persists for 10 to 28 days followed by immunity. Cysts in skeletal muscle measured between 100 and 340 mum in length and 40 and 95 mu-m in width. Experimental intermediate hosts are laboratory mice, rats, hamsters, guinea pigs, Peromyscus and Mastomys. Some of the intermediate hosts develop low levels of antibody and some cross-immunity against Toxoplasma; however, this has not been observed in cats.

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