A microsporidium, isolated from echinostome and strigeid larval trematodes in Lymnaea peregra, is described as a new species Unikaryon slaptonleyi sp.nov. The nuclei isolated at all stages of development, the disporoblastic sporogony and development in contact with host cell cytoplasm are used to assign the species to the genus Unikaryon. The absence of a vacuolar membrane to isolate the meronts and stages of sporulation from the host cell cytoplasm differentiates this genus from Encephalitozoon. Spores are uninucleate, have 17–21 turns of the polar filament coil and measure 5·0 × 2·8/μm fresh. U. slaptonleyi was isolated from rediae and metacercariae of Echinoparyphium recurvatum and sporo-cysts and cercariae of an unidentified strigeid trematode in L. peregra. It was transmitted in the laboratory to unidentified echinostomes in L. peregra and to unidentified strigeids in Planorbis planorbis by feeding the spores to field-collected snails from which cercariae were already emerging. In these natural and experimental hyperinfections the snail tissues were lightly infected but, in the helminths, much of the parenchyma and germinal tissue was destroyed, so that few cercariae were released and most of those were distorted. Similar heavy infections were produced in Fasciola hepatica in Lymnaea truncatula, when spores were fed to the snails 14 days after miracidial penetration, but even high doses (106 spores/snail) produced only light infections in Schistosoma mansoni in Biomphalaria glabrata, in only 2 out of 9 snails. No infections were obtained in larvae producing xiphidiocercariae in P. planorbis although echinostomes became infected under the same conditions. Of a number of aquatic and terrestrial arthropods tested for susceptibility by feeding or by inoculation of spores into the haemocoele, only Pieris brassicae became infected. In a small proportion of pupae surviving from larvae which had been inoculated with spores at 3rd or 4th instar, there was clear evidence of spore replication.

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.

Plasmodium mexicanum is a common malarial parasite of the western fence lizard, Sceloporus occidentalis, in northern California, USA. Infected female lizards store substantially less fat during the summer activity season and produce smaller clutches of eggs than do non-infected animals. Stored fat is utilized in the production of eggs; the energy content of the decrement in stored fat is approximately equal to the energy content of the average reduction in number of eggs. Thus, there is ongoing strong selective pressure on the host to evolve appropriate anti-parasite measures.

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.

We have examined several taxonomic features of a number of strains of Eimeria from many sources world wide. The strains were isolated on the basis of their small spherical (or sub-spherical) oocysts. From a study of mean oocyst dimensions, electrophoretic variation of enzymes, ability to develop in embryonated eggs, absence of gross lesions in heavily infected chickens, and cross-immunity, all the strains were found to belong to one species. For convenience, the parasites when isolated, were referred to as strains of E. mitis/mivati-type, but after characterization they were clearly found to be E. mitis. In contrast, a laboratory strain of E. mivati supplied to one of us (M.W.S.) was found to be a mixture of E. acervulina and E. mitis. Evidence from these and other studies supports the notion that E. mivati is a nomina dubia.

One stock of each of Leishmania mexicana mexicana and L. m. amazonesis together with two stocks of L. braziliensis panamensis and L. b. braziliensis were tested for infectivity in inbred mouse strains Balb/c and CBA/H. The infectivity was compared with hamsters and the outbred CD1 mice. Balb/c mice were more susceptible than hamsters to L. mexicaba and L. braziliensis panamensis. Balb/c mice were not susceptible to L. b. braziliensis. CBA/H mice showed a low susceptibility to infection while CD1 mice showed an intermediate response

Recent studies on the motility of coccidian sporozoites have demonstrated a membrane-associated contractile system capable of moving certain intramembraneous components down the parasite surface propelling it forwards. The properties of this system resemble recorded observations on host cell invasion. In this study the invasive behaviour of Eimeria tenella and E. acervulina has been examined, with reference to the above findings, by light microscope and scanning and transmission electron microscopes. Known inhibitors of motility prevent invasion, though attachment appears unaffected. Invasion itself consists of 3 phases; attachment and orientation, induction of a parasitophorous vacuole and translocation of the parasite into the vacuole. Ultrastructural examination reveals a close membrane/membrane association maintained throughout invasion. From these results it is suggested that the parasite enters the parasitophorous vacuole by ‘capping’ the host/parasite junction down its body, so locomoting into the host cell. Such a model has two main advantages; it requires no additional modifications to either cell, and the specificity of membrane receptors would enable the one membrane-associated contractile system to be responsible for locomotion, antibody capping and host cell invasion.

Host nutrition plays a major role in the nutritional physiology of Trichoplusia ni parasitized by the hymenopterous insect parasite, Hyposoter exiguae. Severely reduced growth rate characterized the host association throughout the 4th developmental stadium. This effect of parasitization, however, was indirect and growth depression of parasitized larvae was entirely accounted for by the accompanying decreased rate of food consumption. Parallel-fed larvae, that is, unparasitized larvae feeding on nutrients at the same rate as observed in ad libitum-fed parasitized individuals, displayed lower rates of growth than parasitized larvae and the latter had higher rates of assimilation. Parasitization, therefore, directly resulted in an increased rate of assimilation over that observed in uninfected insects after accounting for the effects of altered food consumption. Similarly, differences in the pattern of response to decreased dietary protein levels between parasitized and unparasitized insects could be explained on the basis of differences in their rates of food consumption

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.

The mode of action of suramin upon Brugia pahangi has been investigated in vivo and in vitro. The drug was without effect on the glycolytic activity of worms in vitro at 2 × 10−4 M. The lack of effect was correlated with the failure of [14C]suramin to penetrate the worms in vitro. Suramin bound to the surface of worms in vitro presumably by virtue of its polyanionic nature. B. pahangi adults ingested [14C]suramin in vivo but no reduction in the rate of lactate production, of glucose utilization or in the rates of uptake of [14C]glucose, [14C]leucine or [14C]adenosine was observed in worms recovered from jirds between weeks 1 and 5 following 4 daily doses of suramin at 50 mg/kg given intraperitoneally. Worm death occurred between weeks 5 and 7 but this delayed drug effect was not the result of a progressive accumulation of suramin in the worms. Ultrastructural changes were observed in the intestinal epithelium of worms from suramin-treated jirds and parallel observations on worms exposed to Trypan blue in vivo suggest that both polyanionic compounds are restricted to the intestinal lumen of the worms. The evidence presented is consistent with the concept that, in B. pahangi, suramin acts at the surface of the intestinal epithelium and not by primarily inhibiting glucose catabolism or inhibiting phagosome and lysosome fusion as previously demonstrated for bloodstream trypanosomes and mammalian macrophages, respectively

We have previously shown the presence of various purine salvage enzymes in Trypanosoma cruzi, including phosphoribosyltransferase, aminohydrolase, kinase, phosphorylase and hydrolase activities. We now report that a similar situation occurs in Leishmania mexicana amazonensis and Trypanosoma brucei brucei. In all three organisms we found higher levels of activity for the phosphoribosyltransferase enzymes than for the nucleoside kinases, suggesting a preference for the salvage of purine bases rather than nucleosides. Similarly, absence of inosine phosphorylase activity suggests that only one route for the salvage of hypoxanthine is available to the three organisms. The most striking difference was that whereas T. cruzi and T. brucei possessed adenosine aminohydrolase activity, this was not detected in L. mexicana; instead adenine amino-hydrolase activity was found. The overall similarity, as judged by the distribution of enzyme activities, of purine salvage in these three members of the kinetoplastida suggest a broad spectrum of activity for any inhibitor acting in this area; the plethora of alternative salvage pathways, however, suggests that in no case would such inhibition be cidal.

Trypanosoma cruzi trypomastigotes occur as a mixture of morphologically distinct forms in natural and experimental infections. We have been able to separate mixed populations into slender and broad forms using a continuous gradient composed of 12·5–25·0% hypaque in culture media. Previously, comparisons could only be made by using various strains of T. cruzi which show a predominance of either form. This separation procedure gave recoveries of 88–98% and had no effect on the viability of the parasites. Infectivity studies showed that slender forms were much more infectious to cultured muscle cells than were broad forms. However, studies with macrophages from CFW mice showed both forms to be equally capable of infection. It is concluded that the mechanism by which each form infects host cells is different; slender forms being capable of infecting both by penetration and by phagocytosis, while broad forms are only capable of infecting through phagocytosis.

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.

Experimental infections of canaries with an avian trypanosome, Trypanosoma bouffardi, isolated from West Africa demonstrated that these infections can cause pathological changes in tissues. Enlargement of the spleen coincided with peak parasitaemia but no other gross changes were observed. Histopathological examination of infected and control birds revealed focal myocarditis and lymphoid hyperplasia, in infected birds, which are consistent with trypanosome infection. Avian trypanosome infections are not usually regarded as pathogenic but our results suggest that pathological changes occur which are similar to those observed in mammals infected with salivarian trypanosomes

The structure and elemental composition of the secretory products of the pre-acetabular penetration gland cells of pre-emergent cercariae of Schistosoma mansoni have been investigated at an ultrastructural level using X-ray probe microanalysis. The secretion contains 2 types of bodies, one homogeneous and one heterogeneous with electron-lucent areas. Using a variety of fixation and sectioning techniques it has been shown that the apparent electron density of the homogeneous bodies (Type B) is the result of interaction with osmium tetroxide and stain. The small electron-lucent areas of the other type of secretory body (Type A) represent regions where granules have been leached out by processing media. X-ray analysis of cercariae still within sporocysts has indicated that these granules are very rich in calcium, and it is suggested that the calcium is absorbed by the developing cercariae through the sporocyst wall from the molluscan haemolymph.

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.

The course of infection with a Malaysian dog strain of Ancylostoma ceylanicum was investigated in 15 inbred strains of mice, in outbred and inbred mice immunosuppressed with prednisolone, and in immuno-deficient hypothymic mice. Oral, percutaneous and subcutaneous routes of infection, in both sexes of mice, were assessed. In only one instance was a single small adult male worm found. Following oral infection, larvae migrated from the stomach to the large bowel and then a proportion of worms penetrated the perianal skin. This was followed by the appearance of larvae in the lungs. Living 3rd-stage larvae were seen in the anterior small intestine, perianal skin and lungs for the 6 weeks of the study, with peak recoveries being at 12 h, 8 days and 3 weeks, respectively. It is clear that systemic migration of larvae occurs after oral infection, and it is possible that recirculation may occur. Only a small percentage of larvae penetrated the abdominal skin after being administered percutaneously. In subcutaneous infections, a small proportion of larvae moved rapidly from the site of injection and were recovered from the lungs 2 h after infection. Most larvae, however, migrated from the injection site over the ensuing few days. Living 3rd-stage larvae were seen in the lungs and in the small intestine for the 4 weeks of observation. The strain of A. ceylanicum employed does not complete its development in mice. Nevertheless, this model offers significant potential for studying the immune responses, as well as investigating the means by which these parasites evade host defences.

Longitudinal muscles in adult male Schistosoma mansoni appear to remain in almost all respects functional after tegumental disruption by Triton X-100. Responses to high K+, ouabain, low temperature, praziquantel and neurotransmitters are still present. Muscle membrane potentials remain near those of control animals and lanthanum nitrate is still excluded from the muscle after the Triton treatment. Although muscle contractility remains after tegumental disruption, sodium and calcium levels, as measured by plasma emission spectroscopy, increase by 20–30% while potassium and magnesium levels decrease by 15%. 45Ca2+ accumulation is double that of control animals. Upon exposure to a bathing medium lacking Ca2+, Triton-treated animals lose responsiveness to high K+, ouabain, low temperature and praziquantel more rapidly than do control animals. D-600, which effectively blocks the high K+ response in control animals, has no measurable effect on the high K+ response in Triton-treated animals, suggesting that voltage-dependent Ca2+ channels are present in the tegument.

The migration, growth and development of Cyclocoelum oculeum Kossack, 1911 was studied in orally and parenterally exposed coots, Fulica americana (Gm.). Young flukes injected into the body cavity migrate to the sinuses from the body cavity via the air sacs and air passages. Young flukes were first found in the trachea on day 18 post-infection and in the sinuses on day 21. Migration was not synchronous and some flukes were found in the air sacs and trachea of parenterally exposed coots up to 45 days post-infection. Exponential growth and organogenesis began between days 9 and 12. Flukes in the sinuses were consistently larger than flukes of the same age in either the air sacs or trachea. Growth and organogenesis proceeded in the latter flukes but at a slower rate than those in the sinuses.