It has previously been shown that antibodies against the transmembrane proteins, band 3 and glycophorin A, inhibit entry of the merozoite into the red cell and, in the case of band 3, it was established that attachment of the parasite to the cell is not prevented. We have found that antibodies against the cytoplasmic domains of band 3 and of glycophorin A, when present in the interior of resealed ghosts of human red cells, also inhibit invasion by P. falciparum. It is inferred that attachment of the merozoite to the red cell causes structural effects that are transduced to the membrane cytoskeleton and the antibodies against transmembrane proteins interfere with the invasion sequence at this level.

Scanning electron microscopical studies of adult male and female Schistosoma curassoni, male S. haematobium and male S. bovis are reported. The tubercles on the dorsal and dorso-lateral surfaces of male S. bovis are devoid of spines, whereas spines are present on the tubercles of male S. curassoni and S. haematobium. Some of the tubercles of S. curassoni and S. haematobium are completely covered in spines, whereas others have a spine-free apical area. Thus, on the isolates examined from Senegal it is concluded that adult male S. bovis can be easily distinguished from S. curassoni or S. haematobium on the basis of the structure of the tubercles. The surface of female S. curassoni is smooth, with transverse striations and a pitted appearance, apart from the posterior part where anteriorly pointing spines are found.

Biomphalaria glabrata snails are known to be castrated by infection with the trematode parasite Schistosoma mansoni 4–6 weeks post-infection. The pattern of oviposition in the first 35 days post-exposure (p.e.) was investigated, in snails aged 14 weeks and measuring 7–10 mm diameter which had not commenced egg-laying, by counting the numbers of eggs laid in 7-day intervals. A group of exposed snails was compared with a control non-exposed group. The exposed group included both parasitized and non-parasitized snails, and showed a significant increase in the median number of eggs laid during the periods 14–21 and 22–28 days p.e. Throughout the entire 35-day period exposed non-parasitized snails laid significantly more eggs than control snails, while parasitized snails laid significantly more eggs than controls during days 22–28 p.e. and significantly fewer during days 29–35 p.e. Parasitized snails also laid significantly more eggs/egg mass in the period 16–28 days p.e. than did control snails. Growth of the snails was measured. By day 28 p.e. the mean diameter of the exposed group was significantly greater than that of the control group. The increase in oviposition by snails soon after exposure is discussed in terms of a compensatory response for expected future suppression of egg-laying. The fact that parasitized and non-parasitized snails both show increased oviposition indicates that normal development of the parasite is not necessary to trigger the response.

Adults of Pseudodiplorchis americanus occur in the host's urinary bladder, the typical habitat of polystomatid monogeneans in amphibians. However, larvae which invade the respiratory tract via the nostrils then migrate to the bladder through the stomach and intestine, a route which is without precedent amongst monogeneans. Parasite transmission is correlated with the spawning of the desert toad Scaphiopus couchii (June/July in Arizona, USA) and the gut migration, which takes as little as 5 min, occurs after 26 days post-infection (p.i.). Migration occurs during the host's feeding season, and therefore the parasites normally encounter maximum digestive activity along their path. Worms transferred experimentally from respiratory tract to the digestive fluids in the gut are killed within 60 s. However, natural migration is stimulated by an unidentified host factor which triggers protective adaptations, enabling parasite survival for up to 4 h in these lethal conditions. Without this essential stimulus, migration may be delayed for over 1 year and juveniles remaining in the respiratory tract undergo no development beyond that reached at 4 weeks p.i. Rapid reproductive development is resumed immediately after migration, leading to maturation around 1 month later and progressive accumulation of embryos in utero in preparation for transmission during the next summer's rains.

The structure of the ovarian tissue in juvenile Corynosoma semerme and C. strumosum from a fish paratenic host and in the cystacanth stage of Echinorhynchus gadi from an amphipod intermediate host was investigated by means of transmission electron microscopy. The species were obtained from hosts living in the Baltic Sea. The observations indicate that ovarian development was more advanced in cystacanths of E. gadi than in juveniles of C. semerme and C. strumosum. Free ovaries were present in E. gadi with an obvious supporting syncytium and surface microvilli. The biological significance of the different stages of ovarian development in these species is discussed briefly in relation to either reproductive strategies and host specificity in definitive hosts or to the attainment of infectivity by cystacanths in intermediate hosts.

The major transaminase in Heligmosomoides polygyrus, Panagrellus redivivus and rat liver was the 2-oxoglutarate-glutamate system, with relatively few amino acids acting as donors for the pyruvate-alanine and oxaloacetate–aspartate systems. The relative effectiveness of the different amino acid donors in the three transaminase systems was similar in all three tissues. Both H. polygyrus and P. redivivus can oxidatively deaminate a range of L-amino acids, although D-amino acid oxidase activity was low. Serine and threonine dehydratase activity and histidase activity were present in H. polygyrus and P. redivivus and both nematodes were also able to deaminate glutamine, asparagine and arginine. When NAD(H) was the cofactor the glutamate dehydrogenases of H. polygyrus and P. redivivus showed similar regulatory properties to the mammalian enzyme. However, with NADP(H) the results were anomalous. The capacity of both nematodes to transaminate and oxidatively deaminate amino acids was broadly similar and comparable to mammalian tissue. Glutamate dehydrogenase is probably the major route for deamination in these nematodes. A complete sequence of urea cycle enzymes could not be demonstrated in either P. redivivus or H. polygyrus.

All of the enzymes of proline catabolism were present in Heligmosomoides polygyrus and Panagrellus redivivus and the activities were, in general, similar to those found in rat liver. Both nematodes were also shown to be able to catabolize the branched-chain amino acids leucine, isoleucine and valine, by pathways similar to those found in mammalian liver. There were no significant differences in amino acid catabolism between the animal-parasitic and free-living species of nematode.

Laboratory hamsters (Mesocricetus auratus) were infected with Echinostoma revolutum (Trematoda). Hamsters developed marked and sometimes fatal echinostomiasis. Clinical signs included progressive unthriftiness, watery diarrhoea and weight loss. Packed cell volume, haemoglobin and red blood cell counts increased in those animals with severe diarrhoea. No increase in eosinophils was noted in peripheral blood smears. Examination of tissues of infected animals showed wide individual variations related to the intensity of infection. The histopathological responses of hamsters to the parasite showed erosion of intestinal villi with lymphocytic infiltration being the primary response. Periportal lymphocytic infiltration and focal hepatic necrosis were observed in livers from some infected animals. The findings of this study are discussed in terms of variations in pathogenicity of E. revolutum and as a model for the study of echinostomiasis.

Monthly samples of the leeches Erpobdella octoculata, Glossiphonia complanata and Helobdella stagnalis were taken over a two-year period from an eutrophic, English lake to detect metacercariae of the trematode, Apatemon gracilis. In each cohort of each of the three leeches, prevalence was low in young individuals, rose to a peak in autumn/winter, and then declined until the cohort had almost died out; in E. octoculata and H. stagnalis a final brief increase occurred. Mean intensity and relative density values followed a similar seasonal pattern of change to that of prevalence in these last two species, but in G. complanata values fluctuated irregularly with no distinct pattern. The frequency distribution of the parasite in G. complanata was highly over-dispersed, but less so in the other two species. Infected E. octoculata reached sexual maturity. The parasite reduced egg production in G. complanata and H. stagnalis, but only by maximum values of 2·5 and 9% respectively. This reduction in fecundity is low compared to the subsequent high mortality, at 95% or more, of newly recruited young from as yet unidentified causes. Parasite-related host mortality was difficult to assess in young leeches, but there was some evidence for its occurrence in older leeches of E. octoculata and H. stagnalis. However, this is unlikely to play a prominent role in the control and regulation of lacustrine leech populations.

An in vitro anthelmintic primary screen in which the effects of compounds on the aggregation response of newly moulted adult worms of Trichostrongylus colubriformis was monitored is described. Representatives of all the major classes of the anti-trichostrongyle anthelmintics all inhibited worm aggregation completely when present in the culture medium either at or at less than micromolar concentrations. The screen proved highly selective for these broad-spectrum agents, much higher concentrations of the narrower spectrum anthelmintics, active only against blood-sucking nematodes, trematodes and/or cestodes, having little or no effect on this response. This in vitro assay, based solely on the occurrence or absence of worm aggregation following the final moult in culture, proved very easy to interpret rapidly and accurately. It can be recommended therefore for the primary mass screening of synthetic compounds or natural products for intrinsic activity against the trichostrongylid helminths of ruminants.

Faecal blood loss was measured during Nippostrongylus brasiliensis infection in the DA rat using 51Cr-labelled red blood cells (r.b.c.s). In an initial study, faecal blood loss was measured on day 7 of primary infection with 3000 larvae administered subcutaneously (s.c), and found to be 0·03 ml/24 h in uninfected animals and 0·14 ml/24 h in infected animals. In a further experiment, blood loss was measured on the day before infection and for 13 days after primary s.c. infection with 5000 larvae. Faecal blood loss was 0·05 ml/24 h or less until day 3, began to rise from day 5, reached a peak of 0·51 ml/24 h on day 8, and fell until day 13. This was closely associated with the rise and fall of the pooled faecal egg count. Direct worm count confirmed a high worm burden on day 7 and expulsion by day 14. The effect of the worm burden on the haemoglobin concentration (Hb) was measured in a further experiment and showed a fall in Hb with a mean worm burden of 726 compared to that of 47 or 284 worms. The study concluded that there is minimal background blood loss in uninfected rats but that infection with N. brasiliensis is a cause of intestinal blood loss and this is associated with a fall in Hb concentration that is dependent on the worm burden.

The development and hatching of Ancylostoma ceylanicum and Ancylostoma tubaeforme eggs in a range of potentially inimical solutions has been examined using time-lapse video micro-recording techniques. In all compounds tested the larvae developed to the active pretzel stage. The inception of activity resulted in an increase in shell permeability to water and small molecules. In anthelmintics of molecular weight (Mr) 400 development continued normally until about the time that control eggs hatched, when there was a marked decrease in larval activity and eclosion did not occur. The addition of a low Mr surface-active agent potentiated the effect of the anthelmintic and caused larval activity to be lost earlier. The calcium inhibitor lanthanum chloride affected larval development rather than eclosion. Large Mr compounds did not affect either development or hatching and the results suggest that the egg-shell may act as a form of sieve, allowing the essential oxygen to reach the developing larva while excluding large potentially dangerous molecules. No appreciable differences were found between the two species of hookworm examined.

Adult Wuchereria bancrofti were recovered from infected Presbytis cristatus monkeys and radio-isotope labelled extrinsically with 125I and in vitro with [35S]methionine. 125I labelling of the surface of adult W. bancrofti permitted a comparison between the major surface antigens of this species and those from the related lymphatic filariae, Brugia malayi and B. pahangi. All species bear a prominent Mr 29 000 surface antigen but among the differences observed were the strongly labelled molecules with Mr 58 000 and 67 000 in W. bancrofti which are extremely faint in the Brugia species. The [35S]methionine label was effectively incorporated into somatic parasite proteins in vitro although it was not possible to identify any secreted proteins in this way. The antigenicity of these products was investigated using a variety of sera from homologous and heterologous infections and the immunoprecipitation patterns highlighted particular differences between somatic proteins of male and female worms. One secreted antigen was detected, however, by virtue of its phosphorylcholine epitopes, in the culture medium of mixed adult worms; medium from male W. bancrofti adults was negative although homogenates of either sex of adult W. bancrofti were strongly positive in the same system.

The actinomycete, Pasteuria penetrans, is a specific endoparasite of various plant-parasitic nematodes. When parasitizing the root-knot nematode (Meloidogyne javanical) the nematode's capacity to reproduce is destroyed and feeding on and stimulation of the plant host are unaffected even though the bulbous body of the female nematode becomes filled with spores. Parasitism by the actinomycete does not alter the rate of growth in the early stages of nematode development although the non-parasitized female grows more rapidly than the parasitized one for a short time immediately after the final moult. Pasteuria did not invade or inactivate the anterior oesophageal region of the female Meloidogyne or influence the morphology of the giant cells induced by these nematodes in their hosts' roots. The influence of this parasite on the developmental physiology of its nematode host is discussed.

Absorption of glucose in vitro by enteric stages of Trichinella spiralis was examined in worms isolated at different times following infection. Glucose absorption by 6-h-old worms was similar to that seen during moulting (24 h post-infection (p.i.)). As embryogenesis began (48 h p.i.) glucose absorption in vitro by the parasite rose dramatically to a peak in 72-h-old worms. Absorption of glucose in vitro remained high in 96-h-old worms but as larviposition began (120 h p.i.) glucose uptake by T. spiralis dropped significantly. Glucose absorption by worms isolated from the host during the primary immune response was unaffected. Glucose absorption in vitro remained at similar levels in worms isolated between 120 and 312 h p.i. The percentage of absorbed label incorporated into parasite tissues was greatest in 48- and 312-h-old worms. Glucose uptake in vitro by pre-adult and adult worms changed with time and these changes accompanied specific events in the biology of the parasite.

Three distinct muscle types have been identified within the metacestode of Grillotia erinaceus. These consist of peripheral somatic myofibres plus two muscle systems directly involved in parasite attachment to the host, i.e. the tentacular bulb and its antagonistic retractor muscle. In common with other cestodes the somatic muscle consists of smooth-type fibres running longitudinally and obliquely to the main body axis. The retractor muscle consists of myofibres with centrally displaced nuclei. Upon contraction these latter fibres become spirally orientated causing the muscle to coil and lateral membranes to become elevated as spikes. Definitive nerve processes have not been identified within somatic or retractor muscle. Individual tentacular bulbs form the proximal terminus for a closed hydraulic system. Each bulb consists of overlapping, contrarotating myofibres which display obvious striations; the striations appear in alternate fibres to be in transverse and oblique planes. Adjacent myofibres are separated by approximately 0·5 μm, possess abundant mitochondria and have shallow t-tubules plus associated vesicles of sarcoplasmic reticulum at each Z line. Thick myofilaments are surrounded by 13, shared, thin myofilaments. Close neuronal control for the bulb muscle is suggested by the presence of obvious motor end-plates which contain both lucent and dense neurovesicles.

Previously we reported the isolation of several Escherichia coli clones expressing fragments of Taenia taeniaeformis antigens as β-galactosidase fused proteins (Bowtell, Saint, Rickard & Mitchell, 1984). Here we describe the isolation of additional antigen-expressing clones from a larval cDNA library and the assignment of these clones to 7 antigen families. These were isolated with a polyspecific rabbit antiserum raised to the oncosphere. Since this serum was capable of reacting with a large number of antigens, it was important to develop techniques for rapidly determining the identity of the native T. taeniaeformis molecule corresponding to a cloned antigen gene. These included active immunization of rabbits with fused proteins and several techniques involving affinity purification on immobilized fused proteins. The reactivity of the antigen-positive clones with sera from humans infected with related parasites was also assessed. Finally, immunization of mice with several fused proteins failed to protect against subsequent infection, although antigens previously identified as candidate host-protective antigens (Bowtell, Mitchell, Anders, Lightowlers & Rickard, 1983) have yet to be identified in the expression library.