One of a large number of Lymnaea peregra (Mull.) from a pond near Glasgow was found to be infested with Cercaria diplostomi gasterostei.

C. d. gastrostei has been found to penetrate Gasterosteus aculeatus and develop into a diplostomulum in the retina of the eyes.

Large numbers of G. aculeatus from the pond have been found with Diplostomulum gasterostei occurring in the retina.

Infested heads of fish were fed to domestic ducklings and pigeons, and adult stages of a worm considered to be a new species and named D. gasterostei were obtained.

Morphological details of the cercaria, diplostomulum and the adult worm are described.

The author wishes to thank Dr C. A. Hopkins for reading and criticising the manuscript, Dr D. A. Erasmus and Dr G. Rees for valuable suggestions. My thanks are due also to the technical staff of the Department who assisted me in the collection of snails and fishes, and to Mr Francis Deen who did the sectioning of the specimens. This work was in part supported by a grant from Shell Oil Company (London).

Parasitic infections in man and domestic animals exhibit two striking characteristics (a) their prevalence is high, but infections are unequally distributed among individuals within populations and (b) immunity is often slow to develop and appears, at best, only partially effective. Recent immunological and epidemiological studies suggest that effective immunity can develop, but that high prevalence within populations reflects the operation, not only of socio-economic and climatic factors, or husbandry practices, but also of powerful environmentally induced constraints upon the development of resistance. Immunogenetic studies suggest the operation of additional constraints which reflect individual genetic characteristics, and which influence the ability to develop and express effective immunity. A full understanding of all constraints is necessary before levels of population and individual resistance to infection can be increased; the need for such understanding has become more pressing with the prospect that anti-parasite vaccines may become available. Two aspects of environmentally induced constraints are considered, those arising from nutritional inadequacies and those resulting from exposure to infection in early life. Both are discussed primarily in terms of helminth parasites. Genetically determined constraints are discussed with reference to MHC-restricted recognition of malarial peptide vaccines and in terms of Class II molecule-directed control of T-cell function in Leishmania infections. Genetic influences are also considered from the standpoint of inflammatory cell function, in immunity against intestinal nematodes and in vaccine-induced immunity against Schistosoma. Finally, parasite-induced constraints, particularly those which down-regulate protective responses are discussed briefly.

The toxicity of the active oxygen species hydrogen peroxide, superoxide radical, hydroxyl radical and singlet oxygen to microfilariae (mf) has been studied in vitro, using active oxygen-generating systems and scavengers/inhibitors. Mf viability was monitored by uptake of the radiolabel, [3H]2-deoxy-D-glouse. Hydrogen peroxide and singlet oxygen, but not superoxide radical or hydroxyl radical, are toxic for mf. Hydrogen peroxide was toxic for mf within 2 h at concentrations as low as 5 ¼, an amount eosinophils have been shown to release in vitro (Weiss et al. 1986). Catalase and thiourea, but not inactivated catalase, superoxide dismutase (SOD), singlet oxygen scavengers, or hydroxyl radical scavengers, protected mf. Mf have relatively high levels of endogenous SOD but no measurable glutathione peroxidase and low levels of catalase when compared with other parasites (Callahan, Crouch & James, 1988). The low levels of hydrogen peroxide-scavenging enzymes correlate well with mf sensitivity to hydrogen peroxide and the protective effect of exogenous catalase.

When Prof. E. Hindle took over the direction of the Biological Laboratory of the Egyptian Government School of Medicine, Cairo, he found there a large collection of parasitic worms, most of which had been accumulated by Prof. Looss while in charge of the Laboratory for a number of years prior to the Great War. As a large proportion of this material was unnamed, and as the named portion of it contained many specimens possibly of considerable value as original types or co-types, which had been in a neglected condition for some time, it was thought advisable to send duplicates of the collection to England, in order that part of it might be kept there in safer custody. It was also felt to be desirable that arrangements should be made for the examination and determination of the contents of the unnamed part of the collection.

Entobdella diadema produces spermatophores from a pair of follicular glands lying one on each side of the body alongside the main nerve cord, and the secretion of these glands is stored in a two-chambered reservoir within the cirrus-sac.

The vagina is made up of two regions, a wide distal part to receive, accommodate and digest the spermatophores, and a proximal narrow part connected through the vitelline reservoir with the oviduct.

E. diadema Monticelli, 1901, is shown to be distinct from E. bumpusii Linton, 1900, and has been recorded from two new hosts, Dasyatis pastinaca at Plymouth, and Myliobatis aquila at Naples.

We wish to thank the directors and staffs at the Plymouth Marine Laboratory and at the Stazione Zoologica, Naples, for providing excellent facilities for the above studies to be carried out. The work was assisted by a grant to one of us (J. L.) from the Trustees of the Browne Fund, to whom grateful acknowledgement is made.

Toxocara canis larvae infecting dogs undergo tracheal migration following their ingestion in an experimental intermediate host. Development of the parasite then proceeds to the adult stage in the small intestine. Adult dogs are therefore capable of distributing fertile T. canis ova which, if ingested, could cause larva mirans in humans and other animals.

This work was financed by research grants from the University of Queensland and the National Health and Medical Research Council of Australia. The writer wishes to acknowledge the encouragement and criticism of Professor J. F. A. Sprent.

Plasmodium vinckei infections, which usually kill mice within 7 days, can be terminated in the majority of cases by a single injection of chloroquine phosphate equivalent to 10 mg/100 g body weight. After such drug treatment the parasites disappear from the blood for 6–11 days, after which a recrudescence with a low peak occurs. Most animals overcome this second parasitaemia and the parasites finally disappear completely. After recovery, mice exhibit an immune response to a challenge infection and, after a short period of parasitaemia during which a low peak is reached, the animals recover completely. This immunity, once acquired, apparently persists for the lifetime of the host. The establishment of the immune state depends on the period of patent parasitaemia during the primary infection and the longer this period the greater is the chance of a solid immunity developing. Immunity may be exhibited by mice treated with chloroquine as early as the 3rd day of infection. Killed parasites have no immunizing effect. Mice splenectomized before infection are capable of an immune response, and mice splenectomized after radical cure are also able to overcome a challenge infection. In both these cases more than one injection of chloroquine is required. The immunity produced in mice is that of the true sterile type, equivalent to that produced against P. berghei in rats, and is species-specific, conferring no resistance to infection with P. berghei. P. vinckei infections in mice provide a useful immunological model for laboratory studies. The immune response is predictable and easy to induce, and this parasite is therefore superior to P. berghei for immunological studies. Attention is drawn to the fact that in P. vinckei the infection is brought under control by the immune response and not by the antimalarial drug; therefore this ought to be taken into consideration in the assessment of drug trials.

Worm free lambs 2–4 months old were given a single infection of 50 000 Haemonchus contortus larvae. The changes in packed red cell volume were compared with those of uninfected sheep and the infected sheep were divided into two groups according to the rate of change of packed cell volume. In group 1, packed cell volume fell sharply from the 10th day of infection and the sheep eventually died. In group 2, the fall was less marked and the packed cell volume returned to normal after about 40 days. The rates of increase of parasite body length and dry weight were compared for the two groups. Parasites in group 1 sheep grew more slowly than their group 2 contemporaries. Accurate planning of metabolic studies on H. contortus was made possible by using this information to predict the course of an infection and the size of the worms. Parasite development was also measured in sheep for which the packed cell volume was not recorded. Computer analysis showed that adult worm length increase did not follow a simple growth pattern starting from the last ecdysis, but consisted of a rapid elongation followed by a simple negative exponential increase. Dry weight increase also followed a negative exponential during the second phase. Measurements of dry weight as a percentage of wet weight indicated that the rapid elongation was possibly linked with cell enlargement by the uptake of water.

The uptake of thiamine by isolated second-generation schizonts of Eimeria tenella and by host intestinal cells was found to consist of two components. One was passive and the other apparently an active process. The kinetic constants of the latter were compared in host (Km = 0·36 μm) and parasite (Km = 0·07 μm) and found to be significantly different. Both systems were competitively inhibited by amprolium but showed different affinities for the drug. (Host Ki = 326 μm; parasite Ki = 7·6 μm). Further differences were observed in schizonts of a drug-resistant line of E. tenella. These findings are discussed in terms of the inhibition of thiamine uptake being the basis of the anticoccidial activity of amprolium.

(1) Female Ixodes ricinus ticks which feed on a sheep infected with tick-borne fever are not capable of transmitting the infective agent to their progeny. Only the nymphs and females, therefore, can be infective to sheep. In the case of an infective female, the infection may have been acquired, (a) in the immediately preceding stage, or (b) in the larval stage, the infective agent remaining in the tissues of the tick during the nymphal engorgement and subsequent moult. This appears to occur irrespective of whether the host on which the nymph feeds is a susceptible or an insusceptible. animal.

(2) Ticks which have acquired infection are infective as soon after moulting to the next stage as they are able to attach to hosts. Unfed ticks were not found to be infective after a period of about 14 months.

(3) Infection is transmitted to the sheep in the course of the 2nd day after attachment of infective nymphs.

(4) The disease may be transmitted to sheep by inoculation of emulsions of infective ticks, if these have been allowed to commence engorgement. The use of saline for such emulsions appears to be inadvisable.

Methodology is described for the laboratory maintenance of the life-cycle of Sanguinicola inermis, using common carp (Cyprinus carpio) as the definitive host and Lymnaea peregra as the intermediate host. Lymnaea auricularia was also infected but is not considered to be a suitable laboratory host. Tench (Tinca tinca) were susceptible to infection at high cercarial doses but subsequent infection rates were low. Goldfish (Carassius auratus) and Lymnaea stagnalis were refractory to laboratory infection.

A reproducible and standardized assay for measuring the cytoadherence of knobby Plasmodium falciparum-infected red cells to amelanotic melanoma cells was developed. Adhesion was dependent on temperature, haematocrit, and parasitaemia. Addition of EDTA to the binding medium reduced adhesion. Removal of protease-sensitive molecules on the surface of the infected cell abolished cytoadherence, whereas removal of carbohydrate residues by treatment of cells with neuraminidase or galactosidase promoted adhesion. Calcium, magnesium, fibrinogen or fibronectin in the medium had no effect on adhesion nor was there any enhancement of adhesion by pre-loading infected cells with calcium. Serum was essential for good adhesion. Adhesion was species specific for target cells; human endothelial or amelanotic melanoma cells were suitable target cells whereas bovine cells were not. The amelanotic melanoma cell could be formalin-fixed and still retain its adhesion properties. The binding properties of formalin-fixed amelanotic melanoma cells were not identical to those of endothelial or unfixed target cells.

The activation of the peptidergic neurosecretory system in Diphyllobothrium dendriticum was studied following cultivation of plerocercoids for short times in vitro and in vivo. In the plerocercoid the neurosecretory cells gave a very weak reaction with paraldehyde fuchsin (PAF). After cultivation for 1 h large numbers of neurosecretory cells filled with PAF-positive granules were evident. The significance of the activation of the neurosecretory system during the transfer of the worm from the cold-blooded fish host to the warm-blooded final host is discussed.

Angiostrongylus cantonensis (rat lungworm), a parasitic nematode, is expanding its distribution. Human infection, known as angiostrongyliasis, may manifest as eosinophilic meningitis, an emerging infectious disease. The range and incidence of this disease are expanding throughout the tropics and subtropics. Recently, the Hawaiian Islands have experienced an increase in reported cases. This study addresses factors affecting the parasite's distribution and projects its potential future distribution, using Hawaii as a model for its global expansion. Specimens of 37 snail species from the Hawaiian Islands were screened for the parasite using PCR. It was present on five of the six largest islands. The data were used to generate habitat suitability models for A. cantonensis, based on temperature and precipitation, to predict its potential further spread within the archipelago. The best current climate model predicted suitable habitat on all islands, with greater suitability in regions with higher precipitation and temperatures. Projections under climate change (to 2100) indicated increased suitability in regions with estimated increased precipitation and temperatures, suitable habitat occurring increasingly at higher elevations. Analogously, climate change could facilitate the spread of A. cantonensis from its current tropical/subtropical range into more temperate regions of the world, as is beginning to be seen in the continental USA.

The virulence of the malaria parasite Plasmodium falciparum is due, in part, to its ability to cytoadhere in deep vascular beds. Our inability to quantify the load of sequestered parasites hampers our understanding of the pathophysiological mechanisms involved in disease progression and complicates diagnosis. In this study we evaluate potential biochemical markers of sequestered load by comparing them with estimates of the sequestered load from a statistical model fitted to longitudinal patterns of peripheral parasite densities in a series of 22 patients with severe Plasmodium falciparum malaria. The markers comprised the host factors: haematocrit, circulating host DNA, sTNF-R75 and parasite derived products HRP2, pLDH, pigments and circulating parasite DNA. We investigated the suitability of these markers in determining sequestered loads in patients on quinine treatment. Observed peripheral parasitaemia, plasma levels of sTNF-R75 and circulating parasite DNA were most strongly correlated with estimates of sequestered loads on admission. However the dynamics of both sTNF-R75 and circulating parasite DNA during follow-up were very different from those of the estimated sequestered mass. These analyses suggest that none of the markers gave reliable estimates of the current sequestered load, though they may reflect the history of infection. Longitudinal analyses are needed that allow for the clearance rates of the marker molecules and for variations between hosts in the history of parasitaemia.

Toxoplasmosis is a significant public health threat for Inuit in the Canadian Arctic. This study aimed to investigate arctic seals as a possible food-borne source of infection. Blood samples collected from 828 seals in 7 Canadian Arctic communities from 1999 to 2006 were tested for Toxoplasma gondii antibodies using a direct agglutination test. Polymerase chain reaction (PCR) was used to detect T. gondii DNA in tissues of a subsample of seals. Associations between seal age, sex, species, diet, community and year of capture, and serological test results were investigated by logistic regression. Overall seroprevalence was 10·4% (86/828). All tissues tested were negative by PCR. In ringed seals, seroprevalence was significantly higher in juveniles than in adults (odds ratio=2·44). Overall, seroprevalence varied amongst communities (P=0·0119) and by capture year (P=0·0001). Our study supports the hypothesis that consumption of raw seal meat is a significant source of infection for Inuit. This work raises many questions about the mechanism of transfer of this terrestrial parasite to the marine environment, the preponderance of infection in younger animals and the natural course of infection in seals. Further studies to address these questions are essential to fully understand the health risks for Inuit communities.

The sex ratios of malaria and related Apicomplexan parasites play a major role in transmission success. Here, we address 2 fundamental issues in the sex ratios of the rodent malaria parasite, Plasmodium chabaudi. First we test the accuracy of empirical methods for estimating sex ratios in malaria parasites, and show that sex ratios made with standard thin smears may overestimate the proportion of female gametocytes. Secondly, we test whether the mortality rate differs between male and female gametocytes, as assumed by sex ratio theory. Conventional application of sex ratio theory to malaria parasites assumes that the primary sex ratio can be accurately determined from mature gametocytes circulating in the peripheral circulation. We stopped gametocyte production with chloroquine in order to study a cohort of gametocytes in vitro. The mortality rate was significantly higher for female gametocytes, with an average half-life of 8 h for female gametocytes and 16 h for male gametocytes.

TaqMan minor groove binder probes were evaluated as to their suitability for the real-time allelic discrimination of the β-tubulin codon 200 TTC/TAC single nucleotide polymorphism in cyathostomin species. Amplification of titrated cloned full-length β-tubulin cDNA revealed that the TaqMan minor groove binder PCR is capable of specifically detecting as few as 10 copies. Testing of DNA from single adult and larval stages of several different species of cyathostomin allowed reproducible genotyping of individual worms. Using the real-time PCR approach, the throughput of samples was considerably increased compared with conventional post-PCR readout procedure. Only 7·8% homozygous TAC L3 were found among 102 L3 which were genotyped from phenotypically BZ-resistant small strongyle populations. The percentages of the homozygous TTC and heterozygous TTC/TAC were 41·3% and 50·9%, respectively. This resulted in a total TAC-allele percentage of only 33·3%. These findings correspond to data obtained by genotyping of an experimentally selected BZ-resistant cyathostomin population. It is concluded that the β-tubulin codon 200 polymorphism is not the sole mechanism involved in the process of BZ resistance in cyathostomins.

Phylogenetic relationships within the Capsalidae (Monogenea) were examined using large subunit ribosomal DNA sequences from 17 capsalid species (representing 7 genera, 5 subfamilies), 2 outgroup taxa (Monocotylidae) plus Udonella caligorum (Udonellidae). Trees were constructed using maximum likelihood, minimum evolution and maximum parsimony algorithms. An initial tree, generated from sequences 315 bases long, suggests that Capsalinae, Encotyllabinae, Entobdellinae and Trochopodinae are monophyletic, but that Benedeniinae is paraphyletic. Analyses indicate that Neobenedenia, currently in the Benedeniinae, should perhaps be placed in a separate subfamily. An additional analysis was made which omitted 3 capsalid taxa (for which only short sequences were available) and all outgroup taxa because of alignment difficulties. Sequence length increased to 693 bases and good branch support was achieved. The Benedeniinae was again paraphyletic. Higher-level classification of the Capsalidae, evolution of the Entobdellinae and issues of species identity in Neobenedenia are discussed.