Various dosages of the microsporidian parasite, Nosema fumiferanae were fed to 12-day-old larvae of Choristoneura fumiferana using a previously undescribed bioassay capsule. A spore dose of 3 × 104 resulted in 92% infection and a significant reduction in pupal weights, adult female longevity and a mean spore concentration of 1·5 × 107/living adult. Significant mortality (68%, combined larvae and pupae) did not occur until larvae ingested 3 × 107 spores; this dose produced a mean of 1·8 × 107 spores in dead larvae and 3·6 × 107 and 4·6 × 107 spores in dead male and female pupae respectively.

Amblyospora sp. is a microsporidian parasite which is transovarially transmitted from an infected female Culex salinarius to her progeny. This transmission is dependent on synchronization of sporulation of the parasite and ovarian development of the host, both of which are initiated when the mosquito takes a blood meal. We induced sporulation in the absence of a blood meal and, with or without prior ovariectomy, by injection of 20-hydroxyecdysone, a hormone whose precursor, ecdysone, is produced by the ovaries of blood-fed mosquitoes. Sporulation in response to a blood meal was prevented by ovariectomy of the host prior to blood feeding or by decapitation immediately after feeding.

Trout acclimated to 20 °C could not be infected with Cryptobia salmositica. Those acclimated to 5 °C had longer pre-patent periods and considerably lower parasitaemias than those at 10 °C. Forty days after infection, the parasitaemias in fish at 10 °C fluctuated, while this was not observed in those at 5 °C. In vitro incubation of Cryptobia in plasma from 20 °C fish did not affect the motility nor the infectivity of the parasite. Fish infected at 15 °C (low parasitaemias and 2 weeks after inoculation) lost their infections when the ambient temperature was raised to 20 °C. However, in fish with more acute infections (4 weeks after inoculation), the parasitaemias were only substantially reduced when the ambient temperature was raised to 20 °C. Trypanosoma danilewskyi were detected in goldfish acclimated to 10, 20 and 30 °C. However, the parasitaemias in goldfish at 10 and 30 °C were consistently much lower than those at 20 °C.

Apophallus brevis metacercariae localize in parasite-produced cysts mainly in the myotomes of Perca flavescens. The host response induced by this parasite is very intense and leads to the formation of an elaborate host-formed capsule of material which is very similar if not identical to host bone. This capsule is pierced by two canals situated at opposite poles in the cyst and enables the parasite to escape from this host capsule on being ingested by a definitive host. Successive layers of melanocytes and connective tissue, containing lipid droplets, are also present around the bony capsule. Histochemically this bony capsule and the fish bone are virtually identical but there are slight organizational differences in the capsule tissues compared to the fish bone. It is postulated that the formation and arrangement of the capsule may be influenced by the parasite and may not therefore be a defensive development by the host.

Oögyrodactylus farlowellae gen. et sp.nov., an oviparous monogenean, is described from the skin and fins of Farlowella amazonum, a South American loricarid catfish. The Oögyrodactylidae fam.nov., containing O. farlowellae and Phanerothecium caballeroi Kritsky and Thatcher, 1977, is placed with the Gyrodactylidae in the Gyrodactylidea. Although oviparous, the Oögyrodactylids are closely related to the viviparous gyrodactylids. Both families share a combination of characters, including haptor morphology, articulated marginal hooks and spike sensilla, which is not seen in other monogeneans. O. farlowellae is similar to a hypothetical ancestor of the gyrodactylids and shows that the family arose from monopisthocotylean rather than polyopisthocotylean stock. There is a close resemblance between the reproductive system of the immature Oögyrodactylus and that of the mature Gyrodactylus, suggesting that progenesis, involving the precocious maturation of oocytes, may have been important in the evolution of the viviparous genera. O. farlowellae retains eggs individually in the ootype until embryonation is comparatively advanced. After oviposition the eggs adhere to the substrate and hatch to give a crawling, unciliated larva. These are adaptations to a host which inhabits fast-flowing streams, where the eggs and infective larvae are exposed to a constant, uni-directional water current. The life-cycle (egg to adult) is completed in 11–13 days at 27 °C.

Coccidiosis occurs sporadically in lambs at about 6 weeks of age when oocyst output is very high in healthy as well as in diseased lambs. These experiments were designed to throw light on the source of infection and to correlate oocyst output in lambs and ewes with performance in lambs. In two experiments, one indoors on deep litter the other in outdoor paddocks, oocyst output (of different coccidial species), body weight and clinical state of lambs were recorded weekly. Oocyst output in ewes was also recorded, starting 1–4 weeks before lambing. Monensin was included in the concentrates of ewes and/or lambs, up to lambing or before and after lambing. No periparturient rise was detected in the oocyst output of ewes. Monensin drastically reduced oocyst output in animals receiving it. Oocyst output in lambs appeared to be little affected by the output of ewes around the lambing period, but was reduced if the ewes' output was kept low after lambing. Lambs receiving monensin tended to produce drier faeces but their weight gain was not significantly greater than that of controls. Eimeria crandallis was the predominant species in the lambs, followed by E. ovinoidalis and E. ovina.

Experimental procedures are described that lead to the formation of sealed red cell ghosts capable of efficient invasion by malaria parasites. Both human and monkey cells have been studied with respect to invasion by Plasmodium falciparum and P. knowlesi respectively. Resealed ghosts containing about half the normal concentration of haemoglobin are prepared by osmotic lysis and resealing at a haematocrit of 70%. When examined in the scanning electron microscope, populations of these ghosts contain few echinocytes, but have an abundance of stomatocytic forms. When undiluted haemolysate is substituted for the aqueous saline diluent, in which the cells are suspended for lysis and resealing, discocytes result, with a morphology very similar to that of the original cells. Invasion is somewhat, but not dramatically higher for this material. An investigation of the effect of intracellular potassium concentration revealed that this had no major effect on invasion. A small increase in invasion resulted from addition of 50 or 100 mg/ml of albumin to the medium in which the cells were resealed, but intra-erythrocytic protein content per se is evidently not a major factor in determining the efficiency of invasion. Augmentation of the cytoplasmic ATP concentration during lysis and resealing increased the level of parasitaemia significantly, and the parasites in these ghosts developed normally and gave rise to viable merozoites. It was found that albumin at certain concentrations passed freely into the lysed cells and reached equilibrium with that in the external medium. By contrast, the high molecular weight solute Blue Dextran 2000 was completely excluded from the lysed cells.

Asexual stages and mature gametocytes of Plasmodium falciparum have been produced in a 500 ml suspension culture system containing 6–10% red cells. Medium change was automated and was accomplished using a tangential flow filtration unit. The rate of multiplication of the parasite (isolate NF 54) was consistently high when compared with static cultures and ranged from 6·4 × to 15·3 × per cycle in 8 experiments. Mature gametocytes were present in up to 2% of red cells in 14-day-old cultures. Only minor modifications would be required to further scale-up the volume of the culture.

Snell normal and dwarf mice were infected with Spirometra erinacei plerocercoids collected in Japan, to investigate the relationship between the growth-promoting effects of plerocercoids and the growth hormone releasing factor and the somatostatin – growth hormone – somatomedin axis in the host. Infection with plerocercoids caused increases in body weight and weights of muscle, liver, spleen and heart in the normal male mice, and increases in the head–body length, body weight and weights of muscle, liver, spleen, kidney and heart in the normal female mice, but did not increase the weight of the fat pad. Infection with plerocercoids caused increases in body weights and weights of muscle, liver and spleen in the male dwarf mice, and increases in the head–body length, body weight and weights of muscle, liver, spleen and kidney in the female dwarf mice. These observations suggest that plerocercoids promote the growth of dwarf mice as well as normal mice. As the dwarfism of Snell mice is due to a defective anterior pituitary gland, it seems that plerocercoids do not stimulate secretion of growth hormone from the pituitary. Accordingly, it seems to be more probable that the larvae secrete a growth hormone-like substance.

The guinea-pig has been reassessed as a potential laboratory host for Schistosoma mansoni. Twenty-six per cent of an infective cercarial population survive to maturity in this rodent and there are no gross fluctuations in worm burden subsequent to pairing of male and female parasites. Five day, 4-week and 6-week-old schistosomes grown in guinea-pigs have topographical features that are identical to those exhibited by similarly aged mouse worms, but different from those exhibited by rat worms. Schistosome eggs are never detected in the faeces of infected guinea-pigs, but they can be observed in the pulmonary, hepatic and intestinal tissues. Only 55% of the eggs that can be recovered from the intestinal tissues are viable, and some of these can be hatched to release miracidia that penetrate the intermediate snail host. Cercariae are sometimes liberated from infected snails, but in insufficient numbers to permit infection of naive guinea-pigs. The schistosome cycle cannot, therefore, be completed in this host. Collaterals are sometimes observed in the vasculature serving the rectum and kidneys of infected guinea-pigs and the fact that schistosome eggs are deposited in the lungs of these animals indicates that portal systemic anastomosis is a feature of the model. Pathology associated with cercarial invasion or egg deposition is not dissimilar to that described for other laboratory animals infected with S. mansoni, except that basophils participate in the inflammatory response observed in the skin and intestine.

In vivo and in vitro parameters of immunity have been assessed in guinea-pigs sensitized with 500 normal or 500 radiation-attenuated cercariae of Schistosoma mansoni. High levels of resistance to a challenge infection developed in both the chronic and irradiated vaccine model, but immunity was expressed earlier (week 4) and reached higher levels (90%) in the latter case. Vaccinated guinea-pigs have thus been shown to achieve greater resistance than the more commonly used rodent hosts. In vitro cytotoxicity assays have demonstrated that antibodies capable of participating in complement-dependent (lethal antibody) or eosinophil-mediated schistosomular killing, develop in the serum of guinea-pigs immunized with either normal or irradiated cercariae. The time course of development of the eosinophil adherence promoting antibody approximated in both models, the development of immunity in vivo, but the lethal antibody response paralleled the immune status of the animal only in the irradiated vaccine model

The ability of the cercariae of Schistosoma mansoni to penetrate the tails of mice was shown to remain constant throughout their lives. However, their capacity to establish themselves and then reach maturity decreased as they aged. The abdominal route of penetration produced consistently higher maturation rates than the tail route. Significantly different maturation rates were obtained by modifying the standard tail infection technique. Evidence is presented that age-related mortality of schisto-somula occurs within 24 h of penetration and may be associated with the exhaustion of energy reserves during the penetration of the stratum corneum. The relationship of this age-related mortality to ‘mass mortality’ is discussed.

The larvae of Brugia pahangi recovered from the jird have been shown to grow continuously between moults, their length increasing at least 5-fold during the 4th instar. This intermoult growth is achieved without an increase in the surface area of larvae. The cuticle of very early 4th and 5th-stage worms is highly folded and intermoult growth is accommodated by an expansion of surface annular folds. The major increases in the surface area of larvae occur only through ecdysis, with an 8-fold increase in the surface area being achieved at the 3rd moult. The growth curve of these worms is therefore sigmoidal but the surface area curve is stepped. The relationship between the cuticles of nematodes and insects is discussed

Infections with the intestinal flagellates Giardia muris and Spironucleus muris are accompanied by a depression in the ability of mice to mount an immune response to a thymus-dependent antigen (sheep red blood cells) but not to a thymus-independent antigen (TNP-lipopolysaccharide). The number of splenic IgM plaque-forming cells and haemagglutination titres, of both IgM and IgG, to sheep red blood cells decreased between days 10 and 21, which correlated with the time of maximal trophozoite levels in the small intestine. The number of background IgM plaque-forming cells to sheep red blood cells or DNP was not significantly different from controls in either infection. No evidence for systemic macrophage activation was associated with these infections. In fact, adherent peritoneal exudate cells (PEC) from infected mice were slightly less cytostatic against target tumour cells than adherent PEC from normal mice, at a time when the parasites were being eliminated from the small intestine.

Swiss CD-1 mice infected with cysts of Giardia muris are protected against a challenge infection. A temporal study of this phenomenon was undertaken using two different approaches. First, the time needed for mice to acquire resistance was assessed by terminating the first infection using metronidazole on days 3, 6, 12, 24 or 48. These animals received a challenge infection 7 days later. Second, the duration of the protection was determined by giving mice a challenge infection on days 30, 60, 90, 120 or 150 after the primary infection. In all cases, a significant reduction in both cyst output and trophozoite numbers in the small intestine was observed after challenge. The reduction in cyst output following challenge was similar to the reduction in trophozoite numbers. The acquired resistance of some inbred strains of mice to G. muris was similar to that of CD-1 Swiss mice. These results show that mice can acquire a significant resistance against G. muris even after a short period of contact with the parasite (3 days) and that the resistance may last up to 21 weeks.

Flubendazole or thiabendazole were administered orally to mice harbouring larvae of Angiostrongylus cantonensis, Trichinella spiralis, Diphyllobothrium erinacei or Hymenolepis nana 5–10, 28–33 and 21–26 and 1–6 days post-infection respectively. All the mice infected with A. cantonensis were completely cured after treatment with flubendazole at 5 mg/kg/day for 6 days. No noticeable damage was found in the cerebral hemispheres of the mice treated with flubendazole and examined under a dissecting microscope. On the other hand, larvae were found in or on the cerebral hemispheres showing obvious haemorrhage in the control mice. The mice treated with flubendazole gained weight while the control mice lost weight. No larvicidal effect of thiabendazole on A. cantonensis was found at a dose of 10 mg/kg/day for 6 days. The mean reduction of larval T. spiralis in mice treated with flubendazole at 5, 50 and 100 mg/kg/day for 6 days was 64, 100 and 99% respectively. In comparison, thiabendazole showed no efficacy against T. spiralis larvae at 50 or 100 mg/kg/day. Mice harbouring plerocercoids of D. erinacei or H. nana larvae were not cured with either flubendazole or thiabendazole at 50 or 100 mg/kg/day for 6 days.