John V. Ernst

Coccidia in cows and calves on pasture in North Georgia (U.S.A.)

The prevalence and abundance of coccidian oocysts were determined in a herd of beef cows and calves on fescue pastures in the Piedmont area of Georgia during 4-consecutive grazing seasons. Twelve species of Eimeria were found in the feces of the calves and 10 species were found in the feces of the cows. Eimeria bovis was the most prevalent species found in both the calves and cows. It occurred in 72.5% of 1090 samples from the calves and 10.2% of 719 samples from cows. Eimeria bovis also comprised the majority of oocysts present in the fecal samples from the calves and cows. The greatest number of E. bovis in a sample was 45 800 oocysts per gram of feces (OPG) from a calf and 1900 OPG from a cow. No cases of clinical coccidiosis were seen in any of the animals sampled during the survey.

A fine structural study of asexual stages of the murine coccidium Eimeria ferrisi levine and ivens 1965

SummaryThe schizogony of Eimeria ferrisi was studied in experimentally infected Mus musculus. Developmental stages occurred in epithelial cells of the cecum and colon. During transformation of invasive stages into schizonts the inner membrane complex of the pellicle, the conoid, subpellicular microtubules and micronemes gradually disappeared. The micropore, however, seemed to persist. Dividing nuclei had eccentric intranuclear spindles consisting of microtubules which extended between 2 centrocones, in close relationship with centrioles. During the last nuclear division anlagen of merozoites appeared as extensions on the surface of schizonts. The outer single membrane of the schizont became the outer membrane of the merozoite pellicle. Cytoplasmic organelles, typical of eimerian merozoites were incorporated into the developing merozoites. Finally the merozoite became detached leaving behind a residual cytoplasm. Fully developed merozoites had a 3-layered pellicle, the outer single unit membrane was continuous around the merozoite with the inner complex having interruptions at the anterior and posterior poles and at the micropores. Thirty-two subpellicular microtubules, originating at the anterior polar ring extended to the posterior region of each merozoite. The apical complex consisted of a conoid, preceded by 2 rings and surrounded by a polar ring. Two rhoptries were present having club-shaped terminal ends and slender ductules in the conoid region. Some merozoites had enlarged rhoptries, with the distal vesical appearing dense and osmiophilic. The Golgi complex, endoplasmic reticulum, mitochondria, polysaccharide granules were similar to those seen in other eimerian merozoites.

The ultrastructure of macrogametes of Eimeria ferrisi Levine and Ivens 1965 in Mus musculus

SummaryMacrogametes of Eimeria ferrisi occurred in epithelial cells of the cecum and colon of Mus musculus and were studied by electron microscopy. Young stages were identified as macrogamonts by the presence of wall-forming bodies. At first an ou terlimiting membrane and remnants of the inner membrane complex of the former merozoite pellicle were present; the latter was later lost but in mature macrogametes 3 limiting membranes were observed. Type II wall-forming bodies appeared before type I; the former developed in expanded cisternae of the endoplasmic reticulum whereas the latter were smaller in size and appeared in the ground substance of the cytoplasm. After formation of the oocyst wall the bodies of the 2 types were no longer visible. The persistence of micronemes in mature macrogametes and the presence of numerous layers of rough endoplasmic reticulum during wall formation have not been previously reported.

Ultrastructure of macrogametogenesis of Eimeria mivati

SummaryThe development of the macrogamete of Eimeria mivati Edgar and Seibold 1964 was studied with the electron microscope. Development of the young gamont was characterized by a loss of organelles such as the apical complex, subpellicular microtubules, rhoptries and micronemes, followed by an increase in micropores, mitochondria, rough endoplasmic reticulum (rER), and Golgi complexes. Nuclear detachment bodies and canaliculi were present in maturing macrogamonts. Amylopectin was first observed as small electron-dense rod-like bodies that eventually became large electron-transparent bodies. Type II wall-forming bodies developed in the cisternae of the rER. Type I wall-forming bodies appeared shortly thereafter in close association with numerous Golgi complexes. Many small vesicles located between the cisternae of the rER and the Golgi complexes formed what appeared to be a secretory pathway whereby protein formed in the cisternae and, modified by the Golgi complex, may produce the type I wall body material. The outer wall of the oocyst developed between two distal membranes on the surface of the macrogamete. Although the actual mechanism of deposition of the wall material was not seen, it was probably by some secretory process. Wall-forming bodies did not fuse.

Excystation ofIsospora suis Biester, 1934 of swine

The in vitro excystation of sporozoites ofIsospora suis Biester 1934 is described. Sporocysts ofI. suis lack a Stieda body. Upon incubation in 0.75% sodium taurocholate or in 0.25% trypsin+0.75% sodium taurocholate excystation solutions, sporozoites were released by separation of the sporocyst wall into four plates. Occasionally, the sporocyst wall did not separate completely but opened partially and released the sporozoite. At the time of excystation, sporozoites were short and broad but became elongated after 5 to 10 min in the excystation fluids. Elongate sporozoites measuring 11.7×3.8 μm, had a pointed anterior end and a nucleus located in the posterior half of the cell. Living sporozoites exhibited gliding movements, side-to-side flexion, and probed with their anterior ends. Incubation in 5.25% sodium hypochlorite removed the oocyst walls from most oocysts. Sporozoites did not excyst from sporocysts that were released during treatment with sodium hypochlorite.

Fine structure of microgametogenesis of Eimeria ferrisi Levine and Ivens 1965 in Mus musculus

SummaryThe microgamogony of Eimeria ferrisi from experimentally infected mice was investigated with the electron microscope. Microgamonts were recognizable by the presence of peripherally arranged nuclei and the presence of single or paired centrioles between each nucleus and the limiting membrane of the parasite. Often an intranuclear centrocone directed toward the centriole was present. Differentiation of the microgamete began when elevations of the limiting membrane, which indicated the commencement of flagellar development, appeared above the centrioles. This event was accompanied by the segregation of nuclear content into a dense osmiophilic portion and an electron-pale portion. Then followed a gradual protrusion of the dense portion of the nucleus and developing flagella into the parasitophorous vacuole. A dense ring developed at the base of the differentiating microgamete, resulting in the formation of a stalk which was occupied by the residual portion of the nucleus. Fully developed microgametes became detached and occupied the parasitophorous vacuole along with the residual cytoplasm. Microgametes had an anterior perforatorium, a dense elongate nucleus, with an anteriorly positioned mitochondrion in a small groove of the nucleus. Usually two flagella were present but one microgamete appeared to have three. Polysaccharide first appeared when differentiation was in progress and increased until large numbers of granules were present in the microgamont cytoplasm.

The prepatent and patent periods of Eimeria alabamensis and further description of the exogenous stages

Abstract Eimeria alabamensis infections were established in calves 5 to 6 weeks of age by adminestering 10 million, 80 million, or 100 million sporulated oocysts. The prepatent period was 6 to 8 days (mean 6.6). Oocyst discharges usually lasted for 2 to 3 days although a few calves passed oocysts throughout the rest of the 3-week observation period. Calves with oocyst discharge exceeding 1 million oocysts per g of feces had a moderate diarrhea at the time of peak oocyst discharge. No other clinical signs were observed in any of the infected calves. Reinoculations with 100 million sporulated oocysts given 3 weeks after the initial inoculations of 10 million or 80 million oocysts resulted in infections characterized by greatly reduced oocyst discharges. Sporulated oocysts of E. alabamensis were 16 to 24 μ by 12 to 16 μ and were usually ovoid. The oocyst wals consisted of two layers. Sporocysts were elongate-ellipsoid, had a distinct Stieda body, and were 10 to 12 μ by 4 to 6 μ. Completely sporulated oocysts were first observed after 5 days at 25 °C, and most were sporulated after 8 days. Oocysts did not sporulate at 4 °C, 33 °C, and 37 °C.