Sarcocystis in a bald eagle (Haliaeetus leucocephalus).
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Biomedical subjects
J V Ernst
Publications and source records attributed to J V Ernst.
Sporogony of Isospora suis Biester, 1934 of swine.
Sporogony of Isospora suis of swine is described. Unsporulated oocysts were collected immediately after defecation, mixed in 2.5% potassium dichromate solution, incubated at various temperatures, examined at different time intervals, and classified as to stage of development. The uninucleate sporont underwent nuclear division and became binucleated, and then divided to form two round, uninucleate sporoblasts. Binucleate sporoblasts elongated to form binucleate sporocysts, each of which then gave rise to four sporozoites. Sporulation was completed within 56 hr at 20 C, 40 hr at 25 C, 16 hr at 30 C, and 12 hr at 37 C. No sporulation occurred at 4, 40, 42, 45, or 50 C. The thermal death point was between 37 and 40 C.
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Endogenous stages of Eimeria tuskegeensis (Protozoa: Eimeriidae) in the cotton rat, Sigmodon hispidus.
Endogenous stages of Eimeria tuskegeensis were studied in experimentally infected cotton rats, Sigmodon hispidus. Almost all parasites were located on the basilar side of the nucleus in epithelial cells on the sides and tips of villi of the small intestine. The endogenous cycle consisted of three generations of schizogony followed by gametogony. First-, second-, third-generation schizonts could be distinguished by time of appearance, size and shape of the schizont, and number, size, shape, and arrangement of merozoites. Immature gametogonous stages appeared to 84 hr postinoculation (PI) and developed into mature microgametocytes and macrogametes by 96 hr PI. Microgametocytes had a mono-centric type of development. Intermediate macrogametes had small, basophilic wall-forming bodies and mature macrogametes had large, eosinophilic wall-forming bodies. It was not possible to determine whether these were two distinct types of wall-forming bodies or whether they were different stages of a single type. Two nuclei were seen in the host's epithelial cells parasitized by schizonts, microgematocytes, macrogametes, and oocysts. This binucleate condition was apparently parasite-induced.
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Anthelmintic efficacy of 22,23-dihydroavermectin B1 against gastrointestinal nematodes in calves.
Anthelmintic activities of 22,23-dihydroavermectin B1 (comprised to greater than or equal to 95% 22,23-dihydroavermectin B1a and less than or equal to 5% 22,23-dihydroavermectin B1b) against gastrointestinal nematodes in calves were evaluated in 2 controlled experiments. Infective larvae of Haemonchus contortus, Ostertagia ostertagi, Trichostrongylus axei, T colubriformis, Cooperia oncophora, and C punctate were given to 11-week-old calves and Oesophagostomum radiatum had been given 21 days earlier to allow all larvae to attain adulthood at the same time. Each experiment had 4 groups of 5 calves each. Treatment was given to the calves at 14 weeks of age, and 7 to 8 days after treatment, the calves were necropsied. In experiment 1, group 1 control calves had a geometric mean of 11,054 nematodes; groups 2, 3, and 4 calves (at 14 weeks of age) given 22,23-dihydroavermectin B1 orally at doses of 50, 100, or 200 microgram/kg had reductions of 73.5%, 97.3%, and 99.7%, respectively. In experiment 2, group 5 control calves had a geometric mean of 18,897 nematodes; groups 6, 7, and 8 calves given 22,23-dihydroavermectin B1 subcutaneously at doses of 50, 100, or 200 microgram/kg had reductions of 74.6%, 95.3%, and 98.8%, respectively.
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Anthelmintic efficacy of ivermectin against immature gastrointestinal pulmonary nematodes of calves.
Anthelmintic efficacy of ivermectin (greater than or equal to 80% 22,23-dihydroavermectin B1a and less than or equal to 20% 22,23-dihydroavermectin B1b) was evaluated in a controlled experiment against immature nematodes. Twenty calves raised to about 8 weeks of age under nematode-free conditions were allocated into 4 groups. Infective larvae of Haemonchus contortus, Ostertagia ostertagi, Trichostrongylus axei, T colubriformis, Cooperia oncophora, C punctata, Oesophagostomum radiatum, and Dictyocaulus viviparus were given orally to each calf on a staggered schedule 6 to 14 days before treatments. The drug was given subcutaneously when the nematodes were in the early 4th stage of development, and the calves were killed 23 or 24 days later. Group 1 nonmedicated control calves had a geometric mean of 25,102 nematodes; groups 2, 3, and 4 calves given ivermectin at dose rates of 50, 100, or 200 micrograms/kg had reductions of 88.2%, 98.0%, and 99.8%, respectively.
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Isospora suis enteritis in piglets.
A species of porcine coccidia, Isospora suis, when inoculated into piglets, produced diarrhea, dehydration, weight loss and death. Gross lesions were characterized by a fibrino-necrotic membrane within the jejunum and ileum. Villous atrophy and variable erosion, often with an adhered necrotic membrane, were seen microscopically. Asexual and sexual stages of I. suis were seen within the intestinal epithelium and oocysts were recovered from the feces. The severity of clinical disease and lesions were dose-related.
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Effects of level of nitrogen fertilization of fescue pasture on gastrointestinal parasitism of beef cattle.
Two established tall fescue pastures were used in a 4-year study of the relationship between the level of gastrointestinal parasitism in cattle and the level of nitrogen fertilization of the pasture. One pasture was fertilized with 224 kg of NH4NO3/ha each year and served as the control. A second pasture, referred to as the low-fertilized (LF) pasture, was fertilized with N at 84 kg/ha the first year and 74 kg/ha in each of the next 3 years. Both pastures were stocked with Angus cows (2.5/ha) and their calves. Rectal fecal samples obtained every 6 weeks from 10 cows and as many calves as possible in each pasture were examined for nemotode eggs and coccidia oocysts. Two calves from each group were slaughtered at the end of each of the last 3 years to determine the numbers and species of parasites. Cows had significantly lower egg counts than did the calves. Egg counts did not differ between the two groups of cows, but the control cows had higher average weights than the cows on the LF pasture. Control calves had significantly lower egg counts than the calves on the LF pasture, but only slightly higher mean adjusted 205-day weights. At necropsy, significantly fewer worms were recovered from the controls (17,977) than from the LF-pastured calves (52,332). Cooperia oncophora was the predominant species. The level of coccidia infection did not differ between the two groups of cows and calves. The greater availability of forage in the control than in the LF pasture probably was responsible for the lower level of parasitism in the control calves and for the greater weight gains made by the control cows and calves.
Animal Feed↗
Attempts to produce experimental Eimeria wyomingensis infections in calves.
Attempts were made to produce repeatable infections with Eimeria wyomingensis in 2- to 4-wk-old calves. From 0.2 million to 10 million sporulated oocysts, or sporocysts from 1 million sporulated oocysts were given orally to 50 calves. Several regimens of flumethasone and dexamethasone at excessive dosage levels were given to some to the oocyst-inoculated calves. Nine of 10 calves given flumethasone and one of 12 calves given dexamethasone treatments died. Of the 41 calves which survived past post-inoculation day 21, 32 had patent infections. The prepatent period in the 32 infections was 13 to 15 (mean 14.2) days and the patent period was 1 to 7 (mean 3.6) days. More fecal oocysts were excreted by calves given sporulated oocysts than those given sporocysts. Calves given corticosteroids passed fewer oocysts than nontreated calves.
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Endogenous development of the swine coccidium, Isospora suis Biester 1934.
The endogenous development of Isospora suis Biester 1934 is described in piglets inoculated with 150,000 or 200,000 sporulated oocysts. Endogenous stages developed within villous epithelial cells throughout the small intestine. Two distinct types of meronts were seen in tissue sections. Type I meronts, which were seen at 3 days postinoculation, were binucleate, elongate, and 10.5 by 4.7 micron. They produced two to 14 Type I merozoites per parasitophorous vacuole. Type I merozoites were 10.0 by 3.6 micron. They produced two to 14 Type I merozoites per parasitophorous vacuole. Type I merozoites were 10.0 by 3.6 micron. Type II meronts, which were seen at 4 days postinoculation, were elongate and contained three to 12 nuclei. Type II meronts were 11.4 by 5.3 micron, and one to four were found per parasitophorous vacuole. Type II merozoites were 6.3 by 2.1 micron, and three to 16 were found per parasitophorous vacuole. The peak of asexual development occurred 4 days postinoculation. Fully developed microgamonts, macrogamonts, and oocysts were seen 5 days postinoculation. The prepatent period was 5 days, and the patent period was 5 to 8 days. No extraintestinal stages were seen.
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Prevention of sporulation of bovine coccidia by the ensiling of a manure-blended diet.
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Animal Feed↗
Efficacy of salinomycin in treatment of experimental Eimeria bovis infections in calves.
The efficacy of salinomycin for treatment of experimental Eimeria bovis infections was evaluated. In experiment 1, 18 calves were placed into four groups. Group 1 calves were nonmedicated controls; groups 2, 3, and 4 calves were given salinomycin (0.33, 0.66, and 1.00 mg/kg of body weight, respectively) in daily oral divided doses starting 2 or 3 days prior to E bovis inoculations and continuing until postinoculation day (PID) 21. Calves treated with 0.66 and 1.00 mg/kg (groups 3 and 4) passed substantially fewer oocysts than did control calves (group 1) or calves treated with 0.33 mg/kg (group 2). Group 1 control calves had typical signs of severe E bovis infections, whereas signs of infection in medicated calves were almost nonexistant. Experiment 2 was conducted as before, with 15 calves. Group 5 calves were nonmedicated controls; groups 6, 7, and 8 calves were treated with 0.5, 1.0, and 2.0 mg/kg, respectively. All group 8 calves and three of four group 7 calves had nearly complete suppression of oocyst excretions. The severity of the disease in the group 5 control calves was not as extensive as it was in group 1 control calves. In experiment 3, 16 calves were used. Group 9 calves were nonmedicated controls, whereas other calves were given salinomycin (2.0 mg/kg) during PID 3 to 7 (group 10), PID 8 to 12 (group 11), and PID 13 to 17 (group 12). Salinomycin therapy in group 2 calves resulted in substantial reductions in oocyst excretions and clinical signs.
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Anthelmintic activities of B1a fraction of avermectin against gastrointestinal nematodes in calves.
Anthelmintic activities of the B1a fraction of avermectin were evaluated in a controlled experiment. Twenty 12-week-old calves artificially infected with gastrointestinal nematodes were allotted to four groups. Calves in group 1 were used as nonmedicated controls; other calves in groups 2, 3, and 4 were given (orally) B1a avermectin at dosage levels of 50, 100, and 200 microgram/kg of body weight, respectively. These treatments were given 35 days after calves were inoculated with infective nematode larvae. In groups 2, 3, and 4, overall reductions (based on geometric means) were 98.6%, 98.7%, and 98.4%, respectively. These reductions were highly significantly different (P less than 0.01) from the control calves. Nematodes in the calves were Haemonchus contortus. Ostertagia ostertagi, Trichostrongylus axei, T colubriformis, Cooperia oncophora, C punctata, and Oesophagostomum radiatum.
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Anthelmintic efficacy of albendazole against adult Dictyocaulus viviparus in experimentally infected calves.
Anthelmintic activity of albendazole against adult Dictyocaulus viviparus was evaluated in a controlled experiment. Calves were raised nematode-free to approximately 8 weeks of age and were each given 4,000 infective 3rd-stage larvae. Twenty calves with patent parasitisms were allotted to 2 groups of 10 calves each. Calves in group 1 were used as nonmedicated controls, and calves in group 2 were given albendazole in paste formulation at the dosage concentration of 7.5 mg/kg of body weight on the 30th day after administration of infective larvae. At necropsy, nonmedicated control calves had a total of 308 adult D viviparus, whereas the albendazole-treated calves had 11, for an average efficacy of 96.4%. These reductions were statistically highly significant (P less than 0.01). At necropsy, none of the treated calves was passing 1st-stage C viviparus larvae in their feces, whereas control calves were passing an average of 46 larvae/10 g of feces.
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The endogenous stages of Eimeria utahensis (Protozoa: Eimeriidae) in the kangaroo rat, Dipodomys ordii.
The endogenous life cycle of Eimeria utahensis is described from experimentally infected kangaroo rats, Dipodomys ordii. The endogenous asexual cycle consisted of 4 generations of meronts. First-generation meronts were concentrated in the anterior third of the small intestine. The succeeding generations of meronts and the sexual stages were concentrated in the middle third of the small intestine. First-generation meronts had a mean diameter of 9.7 micrometer and contained 12 to 16 merozoites. Second-generation meronts had a mean diameter of 8.0 micrometer and contained 12 to 16 merozoites and a residual body. Third-generation meronts had a mean diameter of 12.4 micrometer and contained 4 to 8 merozoites. Fourth-generation meronts had a mean diameter of 8.6 micrometer and contained 16 to 24 merozoites. Young gamonts were located in epithelial cells of the crypts of the small intestine. Shortly after the parasites entered the epithelial cells, the infected cells became displaced into the lamina propria, and most of the mature gamonts were in this location. The nuclei of host cells containing young sexual stages became greatly elongated and flattened. A few young gamonts were seen in cells in which the host cell nuclei were dividing. During development, nuclei of microgamonts became arranged on the periphery of numerous compartments. Only one type of wall-forming body could be distinguished in the macrogamonts.
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Anthelmintic activity of fenbendazole against gastrointestinal nematodes in calves.
Anthelmintic activities of fenbendazole were evaluated in a controlled experiment. Forty calves artificially infected with gastrointestinal nematodes were allotted to 4 groups. Calves in group 1 were used as nonmedicated controls; the other calves were given (orally) fenbendazole at the dose level of 5 mg/kg in the forms of a suspension (group 2), medicated feed to individual calves (group 3), and medicated feed to the group (group 4). These treatments were given on day 35 after calves were inoculated with infective nematode larvae. In groups 2, 3, and 4, overall reductions (based on geometric means) were 99.5%, 99.7%, and 99.6%, respectively. These reductions were highly significantly different (P less than 0.01) from the control calves. Nematodes present in the calves were Haemonchus contortus, Ostertagia ostertagi, Trichostrongylus axei, T colubriformis, Cooperia onchophora, C punctata, and Oesophagostomum radiatum.
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Fine structure of microgametogenesis of Eimeria ferrisi Levine and Ivens 1965 in Mus musculus.
The 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 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.
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Endogenous stages of Eimeria sigmodontis (protozoa: Eimeriidae) in the cotton rat, Sigmodon hispidus.
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Eimeria zapi sp. n. from the meadow jumping mouse, Zapus hudsonius Zimmerman in southwestern Michigan.
Four of 5 meadow jumping mice (Zapus hudsonius) captured had in their feces a previously undescribed species of Eimeria which is named Eimeria zapi sp. n. The sporulated oocysts measured 21.7 (19.5-24.0) x 20.3 (17.5-23.0) micrometer. The single-layered oocyst wall was 1.5 micrometer thick, rough, pitted and appeared clear-to-amber. Usually 2 polar granules could be seen. An oocyst residuum was not observed. Each sporocyst averaged 16.0 (12.5-18.0) x 9.7 (7.5-11.5)micrometer. A substiedal body was present. The sporocyst residuum consisted of a membrane-enclosed packet of 15 to 20 granules. This is the first species of Eimeria to be described from the genus Zapus.
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