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.

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.

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.

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.

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 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.

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.

The activity patterns and changes in shape of schistosomula recovered from various locations during migration, are described. There is no significant increase in length during the period which worms remain in the skin. Rhythmic cycles of extension and contraction of the worm body are established soon after penetration. Worms newly arrived at the lungs are identical with skin worms of the same age. Within the lungs their maximum length increases to four times that of skin worms, an adaptation which is believed to facilitate migration through the lumina of blood capillaries. Worms recovered from the lungs and systemic organs on, and subsequent to, day 8 post-infection retain this capacity for elongation. When worms arrive at the hepatic portal system they undergo a process of shortening and there is a transient doubling in the duration of cycles of activity. It is suggested that this shape and activity change terminates migration by preventing escape of worms from the hepatic portal system via the liver sinuses. The stimulus which triggers the response is thought to be the high nutrient levels present in hepatic portal blood, but not in peripheral blood. The stimulus which terminates migration also probably initiates growth. Worms cultured in vitro undergo some increase in length, but have a significantly lower maximum length than lung worms of a corresponding age. Although cultured worms were active, the cycles of extension and contraction were much more erratic than those of in vivo worms. The worms shortened spontaneously after 8–10 days in culture. This shortening occurred marginally later than in the most rapidly migrating worms in vivo.

Homogenates of adult Schistosoma mansoni contain enzymes which are capable of transferring [14C]mannose from GDP[U-14C]mannose to a lipid acceptor which migrates as a single peak on a silica gel thin-layer plate. This lipid may belong to the class of polyprenol monophosphates which are intermediate elements in the glycosylation of nascent proteins. The schistosome mannosyl transferase activity is associated with membranous particles and is dependent on the presence of Mn2+. However, other divalent metals such as Mg2+ or Ca2+ can, in decreasing order of efficiency, replace Mn2+. When UDP[U-14C]glucose was incubated with the homogenates in the same conditions, relatively little label was transferred to the lipid acceptor. Live worms incubated in a medium containing GDP[U-14C]mannose seem to incorporate the label preferentially on the tegument and on adjacent subtegumental structures. By adding foetal calf serum to the medium, incorporation of the label can be stimulated.

Eight days after mother rats were injected with 4000 infective larvae of Strongyloides ratti at different stages of lactation the numbers of adult worms in their intestines were uniformly low (< 3% of the dose) compared with unmated controls (mean = 25%). Those in their litters varied from 12% on day 5 to a maximum of 47% on day 17 post partum. These data, which do not correlate with lactational performance, imply that parasite movements in lactating rats are controlled by qualitative, not quantitative, consequences of humoral events. The numbers of worms in litters are concluded to be the result of the interaction of dynamic determinants of larval routes in the mother and changes in the suitability of the neonatal gut as an environment for worm development. The timing of events leading to milk-borne infection is defined. Injected larvae were closely synchronized in their movements, which were completed in 36 h. Larvae experimentally diverted into the mother's tissues during her first lactation were not available for the infection of a second litter.

The muscle of Ascaris suum contains sorbitol dehydrogenase [EC 1.1.1. 14] and the apparent Km values indicate that the enzymefavours fructose formation. Aldose reductase [EC 1.1.1.21] is also present and like the mammalian enzyme it has a very high apparent Km for glucose. Possible functions of the sorbitol pathway in Ascaris muscle are discussed.

Metabolic studies in vitro and studies on chemical composition indicate basic biochemical differences between the horse and sheep strains of Echinococcus granulosus and between these and the closely related species, E. multilocularis. The horse strain of E. granulosus has a similar level of DNA, but significantly more polysaccharides and lipids, with less RNA and protein than the sheep strain. E. multilocularis has significantly more lipids and DNA but less polysaccharides than the horse and sheep strains of E. granulosus, more RNA and protein than the horse strain but similar protein to and less RNA than the sheep strain. Incubations under air and under 95% N2-5% CO2 for 3 h show that only E. multilocularis takes up glucose, that all three forms consume different amounts of oxygen and endogenous glycogen and produce different concentrations of lactate, succinate, acetate, malate, pyruvate, propionate and ethanol as end products of carbohydrate metabolism.

When Diphyllobothrium latum develops from larva to adult in a definitive host, it first sheds the entire larval ‘body’ before growth of an adult strobila starts. This process of shedding off the entire larval abothrial extremity, piece by piece, takes about 48 h. By this time the larva has usually reached the anterior third of the small intestine of the host. D. dendriticum and D. ditremum develop quite differently, although exhibiting similar anterior migrations. In these two species the larvae develop directly into adults without the larval ‘bodyRsquo; first being shed. The implications of the observed differences in growth pattern between these three species of Diphyllobothrium to the classification of diphyllobothriid cestodes is discussed briefly.