The life-cycle of Isospora ohioensis in dogs is described. Eight dogs were killed 6, 16, 24, 48, 72, 96, 114 and 120 h after feeding 106I. ohioensis sporocysts to each. First divisional stages occurred in the jejunum at 48 h post-inoculation (p.i.). At 48 h, zoites occurred in pairs in parasitophorous vacuoles of surface epithelial cells of the jejunum. The parasitophorous vacuoles were 7–9 × 6 μm and the zoites were 7–9 × 2·5 μm in sections. At 72 h, uninucleated zoites, multinucleated zoites and meronts containing fully formed merozoites occurred in surface epithelial cells of the jejunum. At 96, 114 and 120 h asexual multiplication occurred throughout the small and large intestine, mostly in the ileum. The number of asexual generations was not determined. At least 2 structurally distinct meronts were identified at 96–120 h p.i. Type I meronts contained larger merozoites (11 × 3 μm) than those (7·5 × 1·5 μm) in Type II meronts. Meronts were merozoite-shaped and contained up to 8 nuclei. Uninucleated, binucleated and multinucleated zoites occurred within the same parasitophorous vacuole. Gamonts occurred in surface epithelial cells of the small intestine, caecum and colon, but predominantly in the ileum, 96–120 h p.i. Macrogamonts were 13–17 × 11–12 (14·5 × 12·8) μm in sections and 21–26 × 17–25 (21·7 × 17·6) μm in smears. Microgamonts were 13–17 × 8–15 (15·3 × 11·4) μm in sections and 24–30 × 15–24 (27 × 19) μm in smears and contained up to 50 microgametes. The cycle was also studied in 6 dogs killed 6, 12, 24, 48, 96 and 120 h after feeding tissues of laboratory mice that had been infected with I. ohioensis oocysts 17 days earlier. Stages were not seen in the dogs killed at 6 and 12 h p.i. Asexual and sexual stages were structurally similar in size and location to the oocyst-induced cycle but their development was faster by 24 h in the mouse-induced cycle. Extra-intestinal stages were not found in sections of mesenteric lymph nodes, spleen, lung, liver, heart, skeletal muscle and brain. However, biological evidence indicated that I. ohioensis invaded the spleens and mesenteric lymph nodes of dogs fed oocysts.

A line of Eimeria maxima acquired resistance to Lerbek (a mixture of clopidol and methyl benzoquate) after serial passage against rising drug levels. Abnormal bisporocystic oocysts which appeared throughout this series were picked out individually and these produced infections in further groups of chicks. Serial passages of selected bisporocystic forms raised their proportion in oocyst yields to about 80% after 10–14 passages, but a few normal oocysts were still present.

Eupolystoma anterorchis Tinsley, 1978, infects the urinary bladder of Bufo pardalis at the Cape, South Africa. Reproduction occurs throughout the year but the eggs are not deposited continuously: up to 300 are retained in the long uterus of the parasite and may develop to the point of hatching. The eggs are deposited intermittently en masse. The stimulus for deposition appeared to be osmotic, since worms transferred from the host's bladder into freshwater released their stored eggs. However, in simple experiments where hosts were transferred from dry land to water such egg deposition did not follow and the stimulus requires further investigation. Once discharged from the uterus the oncomiracidia hatch rapidly both in water and in host urine. Those eggs immediately expelled from the bladder at urination release larvae which can infect the same or other host individuals via the cloaca. But when eggs are deposited in the bladder between successive host urinations larvae can emerge and attach themselves directly to the bladder wall. These larvae develop to maturity alongside their parents, and this internal re-infection can give rise to massive levels of infestation. The distributions of the tegumental ciliated cells and sensillae of the oncomiracidium have been determined with silver impregnation. There are 55 ciliated cells whose pattern corresponds with that of Polystoma species except for the orientation of three dorsal cephalic cells. The distributions of their tegumental sensillae show greater divergence and the Eupolystoma larva lacks the hamulus primordia typical of Polystoma.

The distribution of Paragonimus kellicotti metacercariae in a mixed population of crayfish from a small central Ohio stream was studied for two seasons. The distribution of worms in crayfish approximates the negative binomial distribution. Prevalence and intensity of infection increased with crayfish body weight. Although no difference in intensity of infection was noted between male and female crayfish, the prevalence of infection was higher in males. The data demonstrate a seasonal recruitment of metacercariae into the crayfish only during late summer and autumn. Metacercariae can live for over 1 year but some die and become mineralized. There is no apparent detrimental effect of P. kellicotti infection on the crayfish. The seasonal timing of life-cycle events is postulated.

A morphological and histochemical study has been made of atresia in oocytes in the ovarian balls of an acanthocephalan (Centrorhynchus corvi). Growing oocytes and mature oocytes have been observed to undergo atresia. With the start of atresia, the nuclear and cytoplasmic components are observed to be greatly altered. The atretic oocytes develop abnormal aggregations of cell components, which contain proteins, phospholipids and lipoproteins. It is suggested that the cellular products of degenerating oocytes are gradually absorbed by the supporting syncytium. The atresia of growing oocytes is greater in uninseminated than in inseminated females, which indicates that in the absence of a mating stimulus atresia occurs more frequently.

On examination of a house mouse (Mus musculus) trapped in Rifa village (Assiut Governorate), a Trypanosoma cruzi-like trypanosome was encountered which differed from the cruzi-like trypanosomes of local bats. It appeared to be a hitherto unknown species for which the name Trypanosoma (Schizotrypanum) assiutis sp.nov. is suggested.

A comparison was made of the major excretory products when adult Haemonchus contortus worms were incubated with D-[U-14C]glucose under aerobic and anaerobic conditions. Catabolites measured were propan-1-ol, acetate, n-propionate and CO2 and the only major difference was that nearly twice as much CO2 both in terms of quantity and radioactivity was excreted under aerobic than anaerobic conditions. The worms were also much more physically active under aerobic conditions. When worms were incubated under aerobic conditions with increasing amounts of fluoroacetate their CO2 production was progressively reduced to the anaerobic level. Their movement and their ability to clump together was also progressively reduced. After aerobic incubation with fluoroacetate and D-[U-14C]g1ucose the quantity and radioactivity of citrate within worms increased greatly. When worms were similarly incubated anaerobically no increase in citrate occurred, no radioactivity was associated with the citrate and the worms appeared physically unaffected. When worms were incubated aerobically with fluoro[1-14C]acetate they produced radioactive fluorocitrate.

Euzetrema knoepffleri (Monogenea, Monopisthocotylea), an endoparasite of Euproctus montanus (Amphibia, Urodela), has a partially haematophagous diet, resembling that of the Polyopisthocotylea. In spite of this, the ultrastructural characteristics of the gastrodermis are typical of Monopisthocotylea. As in the Monogenea already described, digestion is intracellular with a lysosomal process, but two original features are evident. First, there is a cyclic activity of all the digestive cells during digestion with a synchronization of events, which enables two characteristic stages to be distinguished. Secondly, the elimination of the waste is similar to an ‘apocrine’ process, in which the apical portion of cytoplasm filled with residual bodies or the entire cell is released into the caecal lumen.

Aspects of the ovicidal activity of the fungus Verticillium chlamydosporium Goddard on the eggs of Ascaris lumbricoides were observed in the laboratory using a scanning electron microscope. The hyphae of the fungus form structures which are considered to be penetration organs. The hyphae also form a network over the surface of the eggs. After penetration of the eggs, the hypha or hyphae ramify and the embryos are destroyed.

A short list of terms has been compiled which provides for the discussion of variation of coccidia of the genus Eimeria at infrasubspecific levels. Based upon this list, guidelines are given for the designation of strains and lines.

The unlabelled antibody method was used in the ultrastructural localization of two hydatid fluid antigens, antigen 5 and antigen B, in brood capsules and protoscoleces of Echinococcus granulosus and E. multilocularis. Antigen 5 was found in the parenchyma cells of the protoscolex and brood capsule wall and to a lesser extent in the walls of the flame cells and collecting ducts of the excretory system and in the surrounding interstitial material. It is suggested that, while some excretion of this antigen may occur from the protoscolex, it could also be liberated into the cystic cavity by degeneration of protoscoleces and parenchymal cells of the brood capsule wall. Antigen B was found mainly in the distal cytoplasm and perinuclear cytoplasm of the tegument anterior to the suckers. It is apparently secreted to the outside and was present in the brood capsule contents; it adheres to the anterior surface and the posterior periodic acid–Schiff (PAS)-positive glycocalyx of the protoscolex and to the inner surface of the brood capsule wall. The protoscolex tegument posterior to the suckers was negative. The parenchyma cells of the protoscolex and brood capsule wall were also positive although the intensity of the reaction product was variable.

The intestinal changes brought about by rejection of Trichinella spiralis from mice were studied in relation to their effects on a concurrent infection with Hymenolepis microstoma, a cestode not normally rejected from mice. The rejection phase of T. spiralis was associated with a marked stunting of growth of H. microstoma given just before, during, or just after rejection of the nematode. The survival of H. microstoma was affected only when rejection of T. spiralis coincided with the intestinal phase of the cestode: if T. spiralis rejection was timed to occur after the scolex of the cestode had entered the bile duct there was no loss of H. microstoma. It is suggested that the adverse effects on growth and establishment of H. microstoma were due to the non-specific inflammatory component of the host's response to infection with T. spiralis.

Using the ability to sporulate as a measure of viability, the effects of exposure of unsporulated oocysts of 10 species of coccidia of chickens, rabbits and cattle to saturated NaCl solution has been studied. Although appreciable deformation and collapse of the oocyst occurred after 1–2 days contact, the effect was reversible after washing free from salt and incubating. Some reduction in ability to sporulate following several days contact with saturated salt was noted in most species, although no effect was seen with Eimeria stiedai following 7 days exposure, Eimeria tenella was one of the more sensitive species studied. Culture titration experiments in chickens with E. tenella indicated that oocysts which had sporulated following prolonged exposure to salt were in no way inferior in virulence or ability to retain virulence on prolonged storage to oocysts prepared with minimal contact with salt. No evidence was obtained to contra-indicate the use of salt-flotation methods for the separation of oocysts from faeces.

The number of schistosomula recovered from abdominal skin declined exponentially with time after infection. However, this decline was shown to be an untrue reflection of the numbers present because of changes in recoverability on days subsequent to infection. Digestion of skin by the enzymes collagenase and hyaluronidase produced a small increase in the number of schistosomula recovered. The number of schistosomula present in abdominal skin and capable of reaching maturity was estimated by exciting the area to which cercariae had been applied, from groups of hosts at daily intervals after exposure. The number of worms maturing in each group of hosts was then determined. The mean duration of stay of schistosomula in mouse, hamster and rat abdominal skin was estimated at 88, 64·5 and 70 h, respectively. The fluid content of abdominal skin to which cercariae had been applied, increased following infection but it was concluded that this alone was not the predominant factor controlling exit of worms. The stimulation of a delayed hypersensitivity response not directed against schistosomes (in mice previously sensitized with 1-chloro,2–4-dinitrobenzene (DNB)) 1 day after exposure to cercariae, produced a significant increase in the number of schistosomula leaving the skin and reaching maturity. Schistosomula can be recovered from the axial lymph nodes of mice, hamsters and rats. If the schistosomula from mice are injected into the tail vein of uninfected mouse hosts, they have the same chance of maturing as comparable skin schistosomula. They are therefore apparently unharmed by their passage through the nodes. Interference with lymphatic drainage by surgical removal of lymph nodes has no effect on the number of schistosomula recovered from the lungs, but the peak recovery is delayed by 24 h. The hamster cheek-pouch, a site with no afferent lymphatic drainage, was also used to investigate the importance of the lymphatic exit route. There was no reduction in the number of adult worms recovered following infection at this site compared with the normal abdominal skin site. The migration of schistosomula to deeper tissues and their entry into blood vessels was followed using the cheek-pouch preparation. It was concluded that the major route of exit from the skin is the blood vascular system.

Virgin females of Brugia malayi, B. pahangi and B. patei were mated with males of species other than their own to determine whether they would hybridize. Microfilariae were produced in all but one cross (that between B. pahangi males and B. malayi females). Hybrid infective larvae, produced in mosquitoes and inoculated intraperitoneally into jirds, grew to adults but these were unable to produce microfilariae because hybrid males did not produce spermatozoa. Hybrid females were fertile and produced microfilariae when crossed with males of their parental species.

The administration of an antihistomonal drug, dimetridazole, at a dose of 0·08% in feed, controlled experimental infections with Histomonas meleagridis in chickens. The treated birds developed no lesions and the duration of infection with H. meleagridis was reduced. This drug regimen, however, did not always prevent incorporation of H. meleagridis into eggs of Heterakis gallinarum; heterakid eggs pooled from medicated chickens in which H. meleagridis had never been detected transmitted the protozoan to 1 of 10 turkeys fed the eggs. Thus, therapeutic treatment of chickens with dimetridazole may reduce, but not eliminate, transmission of H. meleagridis by eggs of H. gallinarum from medicated birds.

The possible existence of strain and breed differences in the response of sheep to primary infections with Haemonchus contortus was examined by comparing the establishment and pathogenic effects of the parasite in Scottish Blackface and Finn Dorset sheep grouped according to haemoglobin type and infected with 7–10000 3rd-stage larvae. Homozygous haemoglobin A-type sheep of both breeds had lower worm burdens and faecal egg outputs, and suffered less severe clinical and pathophysiological disturbances than animals homozygous for haemoglobin B. In addition, Scottish Blackface sheep displayed similar advantages over Finn Dorsets with the same haemoglobin type and variations in the severity of the disease as judged by a variety of pathophysiological indices correlated closely with parasite numbers. It was therefore concluded that genetic resistance operated primarily against worm establishment and that, barring the unlikely involvement of non-specific physiological factors, this was controlled by the immune response elicited. The nature of this response is unknown, but appeared to operate only against the larval stages, since the size and metabolic activities of the surviving worms were similar in all animals. In a subsequent experiment, designed to examine the response of Scottish Blackface sheep to heavy infection (45000 larvae), there was no correlation between worm establishment and haemoglobin type. This was possibly due to a delayed immune response arising from exposure to excessive amounts of antigen.

Fourteen 9-month-old zebu calves were immunized with 10000 irradiated Schistosoma bovis schistosomula given in 1–3 intramuscular or subcutaneous doses, and 4 more calves were immunized with 10000 irradiated cercariae administered percutaneously in a single dose. Eight weeks after the beginning of the experiment these calves, together with four non-immunized controls were challenged percutaneously with 10000 normal S. bovis cercariae/calf. Comparative clinical, parasitological, pathological and pathophysiological observations subsequently revealed significant differences between the vaccinated and non-vaccinated calves. The vaccinated calves showed significantly higher growth rates, and a superior body composition as indicated by their lower total body water content. The beneficial effects of vaccination were also shown by significantly lower faecal egg outputs in the vaccinated calves and by their lower tissue egg and adult worm counts. The reduced tissue egg counts were also reflected in the milder histopathological changes seen in the vaccinated calves. The vaccinated calves had significantly higher packed cell and circulating red blood cell volumes than the challenged controls, longer red blood cell half lives, and somewhat lower blood volumes and rates of red blood cell synthesis. No untoward clinical effects that could be attributed to vaccination were recorded. These results indicate that zebu cattle can be effectively protected against S. bovis by vaccination with irradiated organisms. We are now evaluating this type of vaccine in a field trial in an enzootic area in the Sudan.

Domestic chicks were infected with Zygocotyle lunata to determine gross and histopathological effects on the caecal tissues, to observe the method of feeding by worms and to examine the effects of crowding on the growth and development of the worm. Caecal weights and dimensions were significantly reduced in infected chicks. Caecal debris, abundant in control chicks, stained positive for proteins, polysaccharides, acid mucopolysaccharides and neutral fats. Caecal debris was rarely seen in infected chicks. The lumen of the intestinal caeca of the worms contained acellular material which showed protease activity and stained positive for proteins, polysaccharides and acid mucopolysaccharides. Histopathological effects of the infection showed a disruption of the architecture of host caecal mucosa, worm to worm attachment, tissue plugs in the worm acetabulum, and an engorgement of host mucosal tissue with erythrocytes. Stunting due to worm crowding was very evident and by 2 weeks post-infection, worms from single-worm infections were sexually mature and more than twice the length of immature flukes obtained from chicks infected with 100–500 cysts.

Rat peritoneal eosinophils adhere to live Schistosoma mansoni schistosomula in vitro in the presence of fresh normal rat serum, or in heat-inactivated serum from rats immune to the parasite. When the eosinophils are present in sufficient numbers the worms show ultrastructural evidence of surface damage and are ultimately killed. It is believed that the appearance of focal lesions in the tegument of the schistosomulum follows the secretion of enzymes by the eosinophils onto the parasite surface. The cells have been observed within these lesions and later between the basal plasma membrane of the tegument and the underlying interstitial material. It is suggested that the cells are responsible for prising the tegument away from the body of the worm. The detached tegument shows evidence of further degradation. Adherent eosinophils which have released their secretions appear to degenerate and are eventually replaced by macrophages. Remnants of both the expended eosinophils and the disrupted tegument have been identified within the macrophages. Adherence of eosinophils through C3–C3 receptor interaction results in earlier and more severe damage to the schistosomula than when adherence occurs through Fe receptors. Rat eosinophils also adhere to C3-coated, glutaraldehyde-flxed schistosomula and C3-coated Sepharose beads. However, evidence of enzyme secretion is only obtained when the target is a schistosomulum.