Host–parasite associations are complex interactions dependent on aspects of hosts (e.g. traits, phylogeny or coevolutionary history), parasites (e.g. traits and parasite interactions) and geography (e.g. latitude). Predicting the permissive host set or the subset of the host community that a parasite can infect is a central goal of parasite ecology. Here we develop models that accurately predict the permissive host set of 562 helminth parasites in five different parasite taxonomic groups. We developed predictive models using host traits, host taxonomy, geographic covariates, and parasite community composition, finding that models trained on parasite community variables were more accurate than any other covariate group, even though parasite community covariates only captured a quarter of the variance in parasite community composition. This suggests that it is possible to predict the permissive host set for a given parasite, and that parasite community structure is an important predictor, potentially because parasite communities are interacting non-random assemblages.

Freshwater snails of the Bulinus forskalii group are one of four Bulinus species complexes responsible for the transmission of schistosomes in Africa and adjacent regions. The species status of these conchologically variable and widely distributed planorbids remains unclear, and parasite compatibility varies considerably amongst the eleven taxa defined, making unambiguous identification and differentiation important prerequisites for determining their distributions and evolutionary relationships. Random Amplified Polymorphic DNA (RAPD) analyses were used to investigate relationships between taxa, with particular emphasis on Central and West African representatives. RAPD-derived phylogenies were compared with those from other independent molecular markers, including partial sequences of mitochondrial cytochrome oxidase subunit I (COI) gene, and the nuclear ribosomal RNA internal transcribed spacer 1 region (ITS1). The phylogenetic reconstructions from the three approaches were essentially congruent, in that all methods of analysis gave unstable tree topologies or largely unresolved branches. There were large sequence divergence estimates between species, with few characters useful for determining relationships between species and limited within species differentiation. Nuclear and mtDNA sequence data from Central and East African representatives of the pan-African B. forskalii showed little evidence of geographical structuring. Despite the unresolved structure within the phylogenies, specimens from the same species clustered together indicating that all methods were capable of differentiating taxa but could not establish the inter-specific relationships with confidence. The limited genetic variation displayed by B. forskalii, and the evolution and speciose nature of the group, are discussed in the context of the increasingly arid climate of the late Miocene and early Pliocene of Africa.

Although previous studies have highlighted the inflammatory responses of fish infected with parasites and exposed to pollutants, very little is known about how these two stressors interact within the fish. In this review, which also contains original data, the effect of these two parameters on the fish inflammatory response is assessed and, in particular, the role of apoptosis and the acute phase protein, C reactive protein, is evaluated. In Cyprinus carpio exposed to 0·5 mg NH4+ l−1 or 0·1 mg Cd2+ l−1 and experimentally infected with the blood fluke, Sanguinicola inermis, the pollutant type and the order in which the fish experiences the parasite and toxicant, significantly affects the ultrastructural appearance and cellular content of the pronephros and thymus. This is reflected in the intensity of infection where the pollutant appears to have less effect on an established infection. Both stressors, pollutant and infection, may mediate their effects via the endocrine system. Studies have revealed that cortisol at 100 ng ml−1 is able to induce apoptosis in pronephric cells of carp and that an increase in apoptosis is associated with an increase in phagocytosis in this immune organ. In addition, C reactive protein, which is used as a biomarker of the inflammatory response in humans and other mammals, is evaluated as a possible indicator of physiological states in fish exposed to pathogens and pollutants.

Toxoplasma gondii (T. gondii) infects one-third of the world population, but its association with cognitive functions in school-aged children is unclear. We examined the relationship between Toxoplasma seropositivity and neuropsychological tests scores (including math, reading, visuospatial reasoning and verbal memory) in 1755 school-aged children 12–16 years old who participated to the Third National Health and Nutrition Examination Survey, using multiple linear regressions adjusted for covariates. Toxoplasma seroprevalence was 7·7% and seropositivity to the parasite was associated with lower reading skills (regression coefficient [β] = −5·86, 95% confidence interval [CI]: −11·11, −0·61, P = 0·029) and memory capacities (β = −0·86, 95% CI: −1·58, −0·15, P = 0·017). The interaction between T. gondii seropositivity and vitamin E significantly correlated with memory scores. In subgroup analysis, Toxoplasma-associated memory impairment was worse in children with lower serum vitamin E concentrations (β = −1·61, 95% CI: −2·44, −0·77, P < 0·001) than in those with higher values (β = −0·12, 95% CI: −1·23, 0·99, P = 0·83). In conclusion, Toxoplasma seropositivity may be associated with reading and memory impairments in school-aged children. Serum vitamin E seems to modify the relationship between the parasitic infection and memory deficiency.

Antigenic variation in malaria was discovered in Plasmodium knowlesi studies involving longitudinal infections of rhesus macaques (M. mulatta). The variant proteins, known as the P. knowlesi Schizont Infected Cell Agglutination (SICA) antigens and the P. falciparum Erythrocyte Membrane Protein 1 (PfEMP1) antigens, expressed by the SICAvar and var multigene families, respectively, have been studied for over 30 years. Expression of the SICA antigens in P. knowlesi requires a splenic component, and specific antibodies are necessary for variant antigen switch events in vivo. Outstanding questions revolve around the role of the spleen and the mechanisms by which the expression of these variant antigen families are regulated. Importantly, the longitudinal dynamics and molecular mechanisms that govern variant antigen expression can be studied with P. knowlesi infection of its mammalian and vector hosts. Synchronous infections can be initiated with established clones and studied at multi-omic levels, with the benefit of computational tools from systems biology that permit the integration of datasets and the design of explanatory, predictive mathematical models. Here we provide an historical account of this topic, while highlighting the potential for maximizing the use of P. knowlesi – macaque model systems and summarizing exciting new progress in this area of research.

Chagas infection is a major endemic disease affecting Latin American countries. The persistence of Trypanosoma cruzi generates a chronic inflammatory reactivity that induces an immune response directed to the host's tissues. The effectiveness of the treatment in the chronic phase is still unsatisfactory due, amongst other reasons, to the collateral effects of the drugs used. We investigated the effect of clomipramine, a tricyclic antidepressant that, when used as a treatment of T. cruzi-chronically infected mice, inhibits trypanothione reductase, an exclusive and vital enzyme of T. cruzi. Clomipramine improved survival (P<0·05) by diminishing the parasite intensity as demonstrated by PCR studies in the heart and skeletal muscle, and significantly prevented the evolution to fibrosis of the inflammatory infiltrates. Clomipramine could be a good candidate for the treatment of chronic Chagas disease.

Target-based approaches for human African trypanosomiasis (HAT) and related parasites can be a valuable route for drug discovery for these diseases. However, care needs to be taken in selection of both the actual drug target and the chemical matter that is developed. In this article, potential criteria to aid target selection are described. Then the physiochemical properties of typical oral drugs are discussed and compared to those of known anti-parasitics.

The composition and diversity of metazoan parasite communities in naturally depauperate ecosystems are rarely studied. This study describes the composition of helminth endoparasite communities infecting fish that are part of naturally acidic stream ecosystems in the coastal-plains region of the State of New Jersey (USA) known as the Pinelands, and compares the diversity of parasites between six streams that differ in anthropogenic disturbance. A total of 514 fish were examined representing 6 species native but restricted to the Pinelands region, 5 species native and widespread throughout the region and State, and 6 species introduced to the Pinelands and State. Fish (prevalence: 78%) were infected with 18 helminth endoparasite species. In most streams, prevalence of infection, mean abundance, and total number of individuals for the 5 most common parasites were higher in pirate perch, a native fish species. The diversity of helminth endoparasite communities measured as species richness and Shannon index was higher in degraded streams, and especially in native or introduced fish at these sites. Parasite diversity was positively correlated with anthropogenic disturbance, which was measured by water pH, water conductance, and the proportion of agricultural and developed land surrounding streams. Helminth community composition included parasites intimately tied to trophic interactions in food webs, and disturbance to these ecosystems results in changes to these communities. Understanding structure and function of animal communities from these naturally depauperate ecosystems is important before continued anthropogenic changes result in the extirpation or extinction of their unique fauna.

A hypothesis has been erected stating that in the British Isles the acanthocephalan, Pomphorhynchus laevis can be separated into 3 strains, an English, Irish and marine strain. Ecological and morphological evidence exists in support of this hypothesis. An investigation at the molecular level was conducted in order to test the validity of the existing evidence. A mitochondrial gene, subunit I of cytochrome c oxidase was partially sequenced from 3 Irish populations of P. laevis, 1 Scottish population and 3 English populations. P. laevis sequences from brown trout from Ireland, England and Scotland were very similar, showing a mean sequence divergence of 0·7%. Sequences from two populations of P. laevis from English chub and bullhead were also similar to each other (0·35% divergence). These two groups of sequences, the brown trout group and the chub/bullhead group were 2·2% different. These data confirm the existence of at least 2 strains in Ireland and Britain, although there is evidence to suggest that these strains are defined by their host species rather than by their geographical distributions.

Caraphractus cinctus Walker is a parasitoid of the eggs of Dytiscidae. The entire development of this Mymarid takes place in eggs immersed in water and attached to, or embedded in, plant tissue. The winter is passed in diapause as a full-grown resting larva (prepupa) in the host egg.

Diapause of Caraphractus has been studied in the eggs of Agabus bipustulatus. The eggs of this Agabus do not undergo diapause and since the shell is transparent, the larvae of Caraphractus (usually two to three in each egg) are clearly visible during their later stages, so the time of pupation is easily determined.

Experiments were made of chilling the maternal generation of Caraphractus at various stages of development, but this did not lead to diapause in the larvae of the chilled generation, or to any increase in the diapause in the offspring.

When the Mymarid was bred in a north room exposed to natural daylight and darkness, some diapausing larvae occurred in mid-September and by October all were in diapause.

When larvae were reared in long photoperiods (16½–24 hr. light) development was direct, but with short photoperiods (2–15 hr. light), diapause occurred. The critical period lies between 14 and 16 hr. of light.

The stage sensitive to photoperiod is the full-grown larva, and when larvae are reared to this stage under short photoperiod and then transferred to continuous light, direct development is determined within 3 days. Conversely, larvae reared under continuous light and removed to short photoperiod before reaching the sensitive stage, go into diapause.

The larvae are sensitive to light of very low intensity, developing direct with a ‘night’ of 0·03–0·05 f.c. Larvae becoming full grown in the end of August and beginning of September do not diapause and must respond to 2–3 hr. of twilight.

Diapause induced, under artificial photoperiods at any time of the year, usually lasts about as long as the normal winter diapause. If however the prepupae are subjected to temperatures below freezing for about a fortnight (provided they have already been about 15 weeks in diapause) pupation occurs as soon as the temperature is suitable. In cold weather the pupal stage may be greatly prolonged.

I am much indebted to Professor H. G. Callan for his kind permission to use the constant temperature rooms at the Natural History Department of St Andrews University. I have received most valuable help from Dr C. Muir in conducting the various photoperiod experiments, especially in regard to light measurements, and I am most grateful to him for discussing with me many of the problems that arose in the course of this research and for commenting on the typescript of this paper. To Dr H. E. Hinton I am indebted for useful advice, and to Dr Seliga of St Andrews University for his translation of Russian papers. Professor and Mrs Stibbs have been most kind in providing me with information regarding the duration of astronomical darkness in the latitude of St Andrews. I am especially grateful to Dr George Salt for his kindness in reading over my typescript and for his helpful criticisms.

The effects of metacestodes of Hymenolepis diminuta on haemolymph proteins of Tenebrio molitor are restricted to female hosts. In beetles aged 15 days post-emergence, and harbouring 12-day-old metacestodes, haemolymph concentration is 46·7% higher than in non-infected animals and similar effects are found in longer standing infections. Electrophoresis of haemolymph revealed the presence of 13 bands. Densitometric analysis showed that only band 2/3 was significantly elevated in infected hosts although band 7/8 also showed an increase. These bands were also present in egg homogenates and are thought to be vitellogenins. It is therefore proposed that the excess protein found in infected beetles is a female-specific protein resulting from an interaction between the parasite and the host endocrine system.

Proteinase activities were examined in extracts and excretory–secretory (ES) products of the infective and adult stages of the cattle lungworm, Dictyocaulus viviparus. Multiple enzyme activities were identified from each source, as defined by pH optima, substrate specificities, inhibitor effects and substrate gel electrophoresis. Serine-, cysteine- and metalloproteinases were identified, secreted materials being more active against protein substrates per unit protein than were extracts, and the particular proteinases produced varied with the developmental stage of the parasite. The antigenicity of these parasite proteinases was demonstrated by the inhibition of enzymic activity with Protein G-purified serum IgG antibody from both infected and vaccinated hosts and in the retardation of enzyme migration on electrophoresis of enzyme–antibody complexes. For the adult products, this confirmed that the enzymes concerned were of parasite origin, and not host-derived. These results argue for investigation of D. viviparus proteinases as targets for the antibody response in the limitation of parasite-mediated tissue damage and as the active principle behind the anti-D. viviparus vaccine.

Rats can be passively protected against N. brasiliensis either with antiserum or with cells. Only some pools of antiserum (15 of 48 pools) and a few batches of cells (three of 11 batches) were protective.

Protective activity was found in serum taken after one infection as frequently as after several infections and gave the same degree of protection. This suggests that second and subsequent infections do not stimulate an anamnestic increase in protective antibodies in the circulation.

Serum and cells taken from the same rats were unrelated in their protective capacity; sometimes serum protected when the cells were ineffective and the reverse also occurred.

Cells transferred from the spleen, peritoneal cavity or mesenteric lymph nodes were capable of initiating reagin formation, irrespective of their ability to protect against N. brasiliensis.

When protection was achieved with transferred cells, the parasite life-cycle was shortened by only 1–2 days.

We have found no evidence that a delayed mechanism of the homograft type is concerned in immunity to N. brasiliensis in the rat.

We thank Miss W. D. Griffiths and Mr A. J. Edwards for their willing assistance. The statistical analysis was kindly done for us by Miss M. V. Mussett of the Statistics Department at our Institute.

Eggs of Oesophagostomum dentatum in faeces deposited on grass plots from May to October developed into infective larvae. Warm wet weather facilitated development but weather conditions which caused the faeces to dry out rapidly resulted in a heavy mortality of eggs and pre-infective larvae. During the winter no development took place and the eggs died. In the early spring and late autumn a few eggs survived and developed into 1st-stage larvae but they died without developing further. In the laboratory no development took place at 4 °C but at temperatures ranging from 10 to 25 °C development into infective larvae was completed, the rate increasing as the temperature rose. Out-of-doors infective larvae survived in faeces and on herbage for 1 year under a wide range of climatic conditions including the exceptionally cold winter of 1978–79. In the laboratory, infective larvae suspended in water survived even longer at temperatures ranging from 4 to 27 °C. They were rapidly killed by continuous freezing and by desiccation when the relative humidity was less than 90%. The relationship between climatic conditions and the development and survival of the free-living stages is discussed.

The systematics and life-cycles of the helminths of a local population of Gammarus lacustris in a eutrophic lake near Edmonton, Alberta, is reported as part of a larger study of the composition and seasonal dynamics of the helminth fauna of gammarids.

A total of 12 species of helminths, including eight cestodes, one nematode and three acanthocephalans, were recovered. Of these, eleven were new host records, ten were assigned to an intermediate host species for the first time, and one, Hymenolepis albertensis sp.nov., was described for the first time.

Adults of all twelve helminths were raised in experimentally infested birds and the life-cycles of five species (Lateriporus clerci, L. skrjabini, Hymenolepis albertensis sp.nov., Fimbriaria fasciolaris and Polymorphus marilis) were completed in the laboratory. The larvae are described, and the developmental period in the gammarids, prepatent period and life span of the adults are given for many of the helminths.

The rate of development of the cysticercoids of Lateriporus skrjabini was shown to be directly related to the size of the gammarid and inversely related to the intensity of infestation.

The proboscis-hook formula was not a good diagnostic character for the separation of the three acanthocephalans, Polymorphus contortus, P. marilis and P. paradoxus; however, the size of the largest hook and the structure of the cystacanth body-wall were good diagnostic characters.

I am indebted to Dr J. C. Holmes for advice and encouragement at all stages of the study. I also wish to thank Drs S. Prudhoe and D. R. R. Burt for their editorial assistance, Mr L. Graham for many helpful suggestions and information on the natural definitive hosts of the species encountered, Mr R. Podesta for his laboratory assistance, and Miss E. D. Senio for caring for the ducklings during their first few days of life. The study was supported by the Francis F. Reeve Foundation Graduate Bursary, the Queen Elizabeth Education Scholarship Fund, by the Department of Zoology through a Teaching Assistantship, by a grant from the R. B. Miller Biological Station Fund and by an N.R.C. operating grant (A–1464) to Dr J. C. Holmes.

1. Three new species of Myxosoma (Sporozoa, Cnidosporidia, Myxosporidia) are described from freshwater fish of the genus Tilapia in East Africa.

2. Two of these, M. heterospora and M. brachyspora spp.nov., inhabit the abdominal viscera: the former was found in 41 of 43 fish examined, while the latter was less common. The third species, M. homeospora sp.nov., produces small oval or circular ‘cysts’ in the subdermal muscle and was found in two very young fish only. Spores resembling those of the first two species were also found in one Haplochromis sp.

3. The spores of M. heterospora are roughly ellipsoidal but are very variable in shape, and range from 8·5–17·0 μ in length and 6·3–11·0 μ in breadth; the two anterior polar capsules measure from 2·0–9·5 by 1·5–3·5 μ. Those of M. brachyspora are flattened antero-posteriorly, measuring from 7·0–7·5 μ long and 12·0–13·5 μ broad; their polar capsules are from 2·5–3·8 by 2·3–2·5 μ in size. M. homeospora has ovoid spores with the anterior end narrowed, measuring from 13·5–17·0 by 8·5–11·0 μ; the polar capsules measure 4·0–6·0 by 2·0–4·0 μ.

4. It is suggested that M. heterospora, at least, is pathogenic and may play a considerable part in reducing the availability of fish as food in this part of Africa.

5. A check-list is given of all species of the genus Myxosoma.

I thank Mr R. S. A. Beauchamp (then Director of E.A.F.R.O.) and his staff, also Mr G. Bowser (Manager of TUFMAC), for facilities and assistance in the examination of fish; also Dr G. D. Fryer and Dr D. J. Garrod for sending material to me in London, and Dr P. H. Greenwood for supplying the Haplochromis and checking the names of fish; also Messrs G. D. Lomax and P. E. Nesbitt for the preparation of sections. This work was commenced while I was employed at the East African Trypanosomiasis Research Organization.

The immunogenicity of the secretory exo-antigen (EXA) originating in the stichosome of Trichuris muris has been investigated. High levels of immunity to challenge were produced using EXA (100 μg) by subcutaneous administration. Vaccination with a range of doses of EXA in Freunds' Incomplete Adjuvant (FIA) showed a dose response; 1 μg of EXA reduced the worm burden by 50% and doses of 10 μg or more reduced the worm burden by 80–90% at Day 9 post-infection. Worms recovered from vaccinated mice were significantly smaller than those from controls. A precipitin line identifiable with EXA was shown to immunize mice against T. muris challenge by vaccination. The protective antigen contained in EXA has been partially isolated using gel filtration, ion exchange filtration and isoelectric focusing and has been shown to be a protein of 30000 molecular weight having a pi of 6·8–7·3.

This paper describes a study of 194 children (aged 9–13) from a mountain village in Ecuador who were infected with one or more species of intestinal helminth or protozoan parasite. In addition to parasite load, the assessment consisted of a battery of psychological and neuropsychological tests, an EEG examination, measures of iodine level, presence of goitre and level of nutrition. We found that, in general, parasite infection, as measured at the baseline level, was not associated with cognitive impairment. The intensity of infection with A. lumbricoides, however, was correlated with the level of verbal ability and with inhibition-control aspects of cognitive behaviour. Multivariate analysis with level of nutrition, EEG status and parasite burden showed a consistent main effect of the degree of nutrition on neuropsychological performance, particularly the language, problem solving and inhibition-control dimensions.

Abomasal and duodenal motility was investigated by electromyography in 4 lambs fitted with permanent abomasal and duodenal cannulae and infected twice with 25000 Haemonchus contortus larvae at an interval of 39 days. In addition, abomasal and duodenal pH, flow rate of digesta of the duodenum, and faecal water content were determined. The 80–90 min cycles of antral contractions were shortened for at least 3 weeks after infection. This was accompanied by a 26% increase in the number of duodenal migrating myoelectric complexes/day during the intra-parietal development of the larvae (10–12 days). Concomitantly, the duodenal flow of digesta increased from 215 ± 22 ml/h to 318 ± 15 ml/h 4 days after infection and was associated with a higher water content of the faeces. The frequency of the migrating myoelectric complexes, but not the duration of antral motor cycles (or the duodenal flow rate), was correlated with both gastric (P < 0·01) and duodenal (P < 0·05) pH after the first and second infections. The duodenal flow rate was correlated with the Cl− concentration of the abomasal contents (P < 0·01) and with the duodenal pH (P < 0·05). It is concluded that, (i) the duodenal motor disturbances associated with experimental H. contortus infection are related to the alterations in abomasal gastric acid secretion which occurs during the histotrophic phase of larval development and (ii) the increased duodenal flow is a consequence of ionic permeability changes of the gastro-intestinal mucosae.

A Leishmania infantum cDNA library was screened with sera from dogs with viscero-cutaneous leishmaniasis. Sequence analysis of a positive clone isolated from the library revealed that it coded for the carboxyl-terminal region of a member of the 70-kDa heat-shock protein family. The full-length sequence of the L. infantum hsp70 gene was determined after isolation of genomic clones. This protein shows a high degree of sequence conservation with the homologous protein from other organisms. To test its antigenicity a recombinant Hsp70 protein fused to the maltose-binding protein was produced in Escherichia coli using the expression vector pMAL-cRI. By FAST-ELISA assays it was observed that while the complete recombinant protein was recognized by 100% of the sera, the 20 carboxyl-terminal amino acids of the protein were only recognized by 30% of those sera. Thus, although a B-cell epitope must be present within the carboxyl terminal end of the protein other antigenic determinant(s) must reside out of this region. The analysis of the cross-reactivity with mouse Hsp70 by Western blotting strongly suggests that the anti-Hsp70 antibodies generated by infection with L. infantum are directed at specific determinants of the L. infantum Hsp70. Thus, our results indicate that anti-Hsp70 autoantibodies are not induced during Leishmania infection.