Eimeria grenieri was isolated from intensively reared guinea fowl in Britain. The oocysts had average dimensions of 21·09 × 15·48 μm and a small micropyle. Three generations of schizonts were found in the small intestine. The first mature schizonts were found in the upper intestine 30 h after inoculation. Second-generation schizonts were seen 48–80 h and third-generation schizonts were present 80–96 h after inoculation. These schizonts were found in the middle and lower small intestine. It was confirmed that gametogony of this species occurs only in the caeca. The pre-patent time was 112 h and the reproductive index from a dose of 6 × 102 oocysts was 8 × 104. Doses of between 1 × 104 and 1 × 106 caused severe depression of body weight gain. Immunity to re-infection developed rapidly. Sulphaquinoxaline at a dose of 0·04% in the drinking water given after inoculation was effective in reducing the pathogenic effects of the disease. Robenidine given in the food at a concentration of 16·5 ppm (50% of the recommended concentration for chickens) was effective in preventing disease caused by E. grenieri.

The endogenous life-cycle of E. grenieri was completed in the chorioallantoic membrane of developing chicken embryos.

Vitamin K (as menaphthone sodium bisulphite) added to a deficient diet reduced mortality due to Eimeria tenella or E. necatrix, had a slight effect on haematocrit, but had no obvious effect on weight gain or faecal blood; 0·1 ppm gave a maximal response. The effect of vitamin K on mortality was not absolute; the magnitude of the effect depended on the size of the challenge dose of oocysts. Likewise, the response of an infection to anticoccidial drugs, particularly monensin, depended on the severity of challenge. The effect of adding vitamin K in the presence of drug was to effectively reduce the coccidial challenge; no other interaction of vitamin K and drug has been found. No effects with vitamin K deficiency or supplementation were seen in cases of infections with E. acervulina, E. brunetti or E. maxima. The use of a deficient diet for experimental work is therefore quite justified – particularly as it results in a 4-fold saving of oocysts for inoculation purposes in the case of the haemorrhagic species.

An investigation of the carbohydrate energy metabolism of Rhabdias bufonis, the lung-dwelling nematode parasite of the African toad, Bufo regularis, indicates that the nematode stores very little glycogen (0·137 ± 0·003% on a fresh weight basis) but does utilize oxygen in vitro. The intracellular distribution and high levels of activity observed for the enzymes phosphoenolpyruvate carboxykinase, pyruvate kinase, lactate dehydrogenase, malate dehydrogenase, malic enzyme and fumarate reductase suggest two alternative pathways of carbohydrate energy metabolism.

An in vitro investigation has been made of the relative roles of the gut and tegument in the absorption of the neutral amino acids L-alanine and L-leucine by a marine fish-gill parasite, Diclidophora merlangi. The use of ligatures to preclude oral ingestion of trace-labelled medium has proved inadequate, invariably damaging the tegument, as revealed by stereoscan electron microscopy, and resulting in artifactual levels of absorption. Three alternative procedures have given consistently reliable data on the route of entry of low molecular weight substrates. (1) Ultrastructural examination of worms previously incubated in electron-dense cationic tracers has shown that, in vitro, there is no oral intake of sea water. (2) The suspending of worms in trace-labelled medium with the mouth out of the medium and comparing amino acid uptake with that of worms totally immersed in medium has revealed no statistically significant difference in the absorption levels. (3) Application of section (freeze-dried) auto-radiography to detect diffusible isotope has demonstrated directly transtegumental absorption of a neutral amino acid. It is concluded from these experiments that Diclidophora has a tegumental transport system for absorbing certain neutral amino acids, and whilst, clearly, the worm is sanguinivorous and digests blood in a well-developed gut, it may also be capable of supplementing this diet with low molecular weight organic nutrient absorbed directly from sea water via the tegument.

Gametogenesis in Plasmodium gallinaceum involves bicarbonate-dependent processes and requires a continuous supply of glucose (presumably as an energy source). Emergence and exflagellation of gametocytes, in vitro, occur independently of the CO2 tension but are rigidly correlated with the pH of the external medium. In bicarbonate-saline gametogenesis is initiated only if the pH exceeds 7·7. Our results suggest that gamete development of malaria parasites is stimulated when infected blood is exposed to air because the decrease in the CO2 tension of the blood causes its pH to rise.

Mice which have recovered from infections with the avirulent piroplasm Babesia microti are also resistant to challenge with the virulent malaria parasite Plasmodium vinckei. In mice infected with P. vinckei before the peak of the B. microti infection the numbers of malaria parasites in the blood increase until that peak and are then eliminated at the same time as the piroplasms. In mice infected with P. vinckei at or after the peak there is no apparent multiplication and the malaria parasites begin to disappear from the blood immediately. The malaria parasites in doubly infected mice show signs of degeneration similar to those seen in mice pre-treated with Corynebacterium parvum and it is suggested that a common mechanism exists in homologous and heterologous immunity and in immunity following pre-treatment with C. parvum or BCG.

After hamsters have been infected with Dipetalonema viteae for about 4 months, microfilariae disappear from the circulation but the adult worms remain alive and active. Such hamsters are said to harbour a ‘latent’ infection. Additional adult worms implanted into such hamsters produce no microfilariae, but adult worms recovered from hamsters with latent infections resume microfilariae production when surgically transplanted into new hosts. In vitro, worms from hamsters with latent infections renewed microfilariae production in the presence of serum from uninfected but not infected hamsters. Serum from infected animals had a marked suppressive effect on the microfilariae production of adult worms implanted into passively immunized hamsters. This suggests that microfilarial release is regulated by a serum factor. Microfilarial production in in vitro and in vivo experiments was more strongly inhibited by serum taken from hamsters with latent infections and hamsters infected for only 30 days (pre-patent) than by serum taken 90 days after infection (whilst microfilariae were in the circulation of the serum donors). A cytotoxic effect of sera from infected hamsters on the microfilariae could not be demonstrated.

In animals immunized by extracts of adult worms or microfilariae, microfilaraemia was considerably reduced. In contrast, animals immunized repeatedly with the extract from small numbers of microfilariae during the pre-patent phase of an infection had an enhanced microfilaraemia. Adult worm numbers were not affected by immunization except in animals given extract from a single female worm which harboured fewer worms than controls.

Mature male Dipetalonema viteae released a substance(s) which caused eahanced microfilaraemia in infected hamsters. In hamsters implanted with female D. viteae, the microfilaraemia of a subsequent infection was suppressed. The microfilaraemia of female worms implanted in hamsters was depressed within 5 days when the animals were given a further infection with infective larvae.

The ultrastructure of the apical surface of the gastrodermal cells of Fasciola hepatica has been investigated by transmission (TEM) and scanning electron microscopy (SEM). The surface is composed of triangular or rhomboidal lamellae which may be subdivided at their margins. The lamellae may have a smooth or wrinkled surface and apical microvilli of varied length and number. Spherical bodies may be attached to the sides or tips of the lamellae.

The lamellae of individual cells are grouped to form either a series of overlapping, concentrically arranged leaflets or a series of sinuous lamellae running parallel with the cell's long axis. Lamellae may also divide, anastomose, or cross from one cell to an adjacent cell.

The lamellae have an internal skeleton consisting of laterally orientated ‘fibres’ which are more or less evenly spaced and parallel with the cell's apical plasma membrane. There is some evidence that the ‘fibres’ are composed of a number of very small tubules in a dense matrix. The ‘fibres’ are connected to the plasma membrane and to each other by dense amorphous material.

Groups of the snail Lymnaea truncatula, maintained at a range of spatial densities, were exposed to different densities of miracidia of Fasciola hepatica. The resulting degree of parasitization was measured 3–4 weeks after infection. The relationship between parasite densities and parasitization appeared to be curvilinear. The lower than expected parasitization at high parasite densities could be explained by the multiple infection of some snails by two or more miracidia.

The level of parasitization was not related exponentially to the temperature at which infection was carried out. This was thought to be due to the inverse relationship between miracidial longevity and swimming speed, with respect to temperature. A depth of free water overlying a mud surface was an absolute requirement for miracidia to successfully infect snails.

Theileria mutans (Aitong) isolated from cattle exposed in the Narok District of Kenya and blood-passaged through cattle 8 times, appeared to have lost its original pathogenicity for cattle. It was demonstrated that the parasite was trans-stadially transmissible by the tick Amblyomma variegatum but not by Rhipicephalus appendiculatus. Four tick–bovine passages were made using A. variegatum, and infective parasites were also harvested from A. variegatum nymphs which had been fed for 5 days on rabbits. Blood containing piroplasms, or lymphoid cells infected with schizonts taken from cattle, at the 2nd tick–bovine passage were shown to be infective on inoculation.

The course of the T. mutans infections in the cattle was studied. In tick-induced infections macroschizonts occurred transiently, persisting longest in circulating lymphoid cells. Microschizonts were rarely detected. The macroschizonts were morphologically distinct from those of other Theileria species described from East Africa.

In tick-induced infections, the piroplasm parasitaemia increased rapidly and there was evidence of restored pathogenicity of the parasite since high piroplasm parasitaemias were associated with a marked anaemia.