The influence of genetic factors on acquired resistance to Haemonchus contortus infections in sheep was investigated. Animals whose primary infections were terminated with an anthelmintic failed to develop any immunity against subsequent challenge as judged by worm numbers. Nevertheless, all were better able to retard the development and reduce the fecundity and haematophagic activities of their parasite populations than animals undergoing primary infections. High levels of resistance, as judged by all these parameters, were observed in most animals when the challenge larvae were superimposed on existing worm populations. The patterns of worm establishment and disease indicated that genetic factors operated in determining resistance, since fewer worms became established and less severe clinical and pathophysiological changes were observed in Scottish Blackface than in Finn Dorset sheep with the same haemoglobin type. Similar advantages were displayed by animals with haemoglobin AA and to a lesser extent those with haemoglobin AB over haemoglobin BB types. The importance of breed was further indicated by the occurrence of ‘self-cure’ in the majority of the Scottish Blackfaces but in only one Finn Dorset. There was no evidence that this reaction was associated with haemoglobin type.

The number of cercariae of Transversotrema patialense which attach to the fish host Brachydanio rerio, during a fixed exposure period, is shown to be directly proportional to cercarial density within an experimental infection arena. The distribution of successful infections/host is shown to change from a random pattern to an over-dispersed form as cercarial exposure density or duration of host exposure to infection increases. A stochastic simulation model is used to demonstrate that small differences in host susceptibility to infection, within a population of hosts, can generate patterns of dispersion in parasite numbers/host similar to those observed in the experimental studies. Differences in host behaviour, during the period of exposure to infection, are thought to generate variability in host susceptibility to cercarial infection.

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.

An antiserum was raised in rabbits against a soluble extract of fresh homogenized adult Fasciola hepatica of rat origin and was then absorbed with rat and mouse tissue antigens. This antiserum reacted specifically with the surface coat of adult flukes, of both rat and mouse origin, by indirect immunofluorescence to show the detail of surface spines. When tested against juvenile stages recovered from mice the reaction was positive with all but the earliest hepatic parenchyma stages. No reaction was present on the tegumental surface of newly excysted juveniles or stages 1 or 2 days post-infection (p.i.) whether recovered from the peritoneal cavity or the hepatic parenchyma.

The antigenic composition of sequential erythrocytic stages of Plasmodium knowlesi has been compared by crossed immuno-electrophoresis using a pool of immune rhesus monkey antiserum. Eleven major parasite antigens have been identified; 9 are stage-independent, and 2 stage-dependent. Differences in the relative amount of the stage-independent antigens have been demonstrated and quantified. The distribution of antigens between parasites and schizont and infected red cell membranes has been examined. Only 6 of the 11 parasite antigens were exhibited by a schizont membrane preparation, all these antigens were also expressed by the intracellular parasite. Antigens exclusive to the schizont membrane were not demonstrated.

The essential biological features of snail infection by miracidia are incorporated into a simple model which describes the rate of change with respect to time of the number of miracidial infections/host. The model is based on the assumption that the net rate of infection is directly proportional to the density of both miracidia and hosts. Empirical evidence is provided to support this assumption. The basic framework of the model is expanded to take into account demographic stochasticity in infection and is used to predict the percentage of snails that become infected after exposure to a known number of miracidia for a set period of time. The influence of miracidial mortalities and age-dependent infectivity are examined and theoretical predictions are compared with a range of experimental results.

Underlying heterogeneity in the distribution of the number of infections/snail is shown to generate an artifactual decrease in infection rates as exposure density rises, if rate estimation procedures are based on an assumption of randomness. Empirical evidence is presented to illustrate the generation of over-dispersion in the number of miracidial infections/snail under tightly controlled laboratory conditions, using supposedly homogeneous snail populations.

Biological causes for underlying patterns of heterogeneity are discussed in relation to snail susceptibility to infection and ‘attractiveness’ to infective stages.

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.

Artificially transformed schistosomula of Schistosoma mansoni develop a consistent but small protection against the lethal effects of antibody plus complement when cultured for 24 h in a chemically defined medium. In contrast, they become rapidly resistant to antibody plus complement, when cultured in the presence of a complex medium consisting of equal parts of heat-inactivated rabbit serum and Earle's/lactalbumin or in defined medium supplemented with small amounts of heat-inactivated rabbit serum. Sephadex G-200 gel filtration revealed that the protective factor in rabbit serum is a macromolecule with a molecular weight between 7 and 19S. Parasites cultured at 10 °C or in the presence of 200 μg of puromycin show less serum-induced protection against the lethal effects of antibody plus complement than do controls.

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.

Ribosomes and high molecular weight ribosomal ribonucleic acid (rRNA) from the blood stages of Plasmodium berghei parasites were studied in preparations free from host ribosome contamination. Purified malarial ribosomes were isolated in high yield from a population of ultrastructurally intact, viable parasites by hypertonic lysis with Triton X-100 and differential centrifugation. These ribosomes were shown to be derived from active polysomes and could be dissociated into subunits by puromycin–0·5 m KCl treatment. Malarial rRNA extracted from purified 40S and 60S ribosomal subunits was characterized by electrophoretic, sedimentation and base ratio analyses. Like certain other protozoa, the P. berghei 40S ribosomal subunit possessed an exceptionally large RNA species (mol. wt 0·9 × 106), while RNA isolated from the parasite's 60S subunit (mol. wt 1·5 × 106) was specifically ‘nicked’ to produce one large component (mol.wt 1·2 × 106) and one small component (mol.wt 0·3 × 106) in equimolar quantities. These rRNA's migrate identically on polyacrylamide gels after heating to 63°C for 5 mm or under denaturing conditions in the presence of formamide, indicating an absence of aggregation and non-specific degradation of the rRNA species. Base composition studies showed P. berghei rRNA to be low in guanosine and cytosine content, as is the case for protozoa generally.

The thiamine antagonist beclotiamine showed anticoccidial activity against Eimeria tenella, although metabolites and related substances were inactive. Oocyst production in experiments employing unilateral caecal ligation suggested that the drug reached parasitized cells by downward movement through the intestinal lumen, rather than by absorption and systemic transport. In chickens given 100 p.p.m. beclotiamine in the feed over a period of 7 days, duodenal drug concentrations of approximately 5·8 p.p.m. were achieved and maintained, while concentrations in the caeca were lower, but gradually increased to 1·2 p.p.m. Caecal levels were slow to fall following drug withdrawal, whereas duodenal levels showed an immediate decrease. [3H]thiamine absorption from the caeca of normal chicks or of chicks infected with E. tenella was inhibited by oral administration of beclotiamine. Pyrithiamine showed slight anticoccidial activity at 30 p.p.m. as did 2,4-dinitrophenol (2,4-DNP) at 100 p.p.m. A combination of 40 p.p.m. beclotiamine and 200 p.p.m. 2,4-DNP was quite effective although weight gains were not as good as with 120 p.p.m. beclotiamine alone.

Haemolymph of larval blackflies Prosimulium mixtum/fuscum and Simulium venustum parasitized by the mermithid nematode Neomesomermis flumenalis was compared with that of non-parasitized hosts with respect to protein, amino acid and carbohydrate composition. The mermithid depleted most protein fractions in a non-selective manner in both host species. In P. mixtum/fuscum, the levels of most amino compounds were reduced by mermithid parasitism, but these metabolites were approximately evenly divided into three categories (decreased, increased, unaffected by parasitism) in S. venustum. The mermithid caused a significant decrease of haemolymph glucose levels in both host species but did not affect blood trehalose concentrations. These effects of parasitism are discussed in relation to the nematode's nutritional requirements.

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.

The time-course for the development of infectivity was studied in Hyalomma detritum ticks fed as pre-imagoes on calves infected with Theileria annulata. Unfed adults derived from infected nymphs were non- infectious when inoculated into susceptible calves, whereas ticks of both sexes that had fed for 2–3 days or longer on calves or rabbits were always infectious. Some adults fed for only 1–2 days were infectious, whereas others were not. As few as 2 ticks were capable of infecting susceptible calves.

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.