The adhesive organ of Apatemon gracilis minor Yamaguti, 1933, consists of two lobes lying in a cup-shaped fore-body. The cytoplasmic tegument covering the apposing faces of the lobes is different from that covering their outer surfaces. The covering of the outer surface corresponds to the general tegument present on the rest of the body, whereas that on the inner surfaces is finely pitted and in certain regions is elevated to form a coarse reticulum. This specialized surface is covered externally by a plasma membrane and is in continuity with nucleated cell bodies lying below the basement layer. The cell bodies contain large quantities of granular endoplasmic reticulum as well as several Golgi complexes and numerous mitochondria. Masses of secretion bodies are present and these also occur in the extensions to the external tegument as well as within the external tegument of the lobes. When the parasite is attached the inner faces of the lobes come into contact with the vascular lamina propria of the host. The possible biological role of this specialized host–parasite interface is discussed and it is suggested that this surface specialization may form a morphological basis for the ‘placental’ function suggested for the adhesive organ by earlier workers.

The author wishes to acknowledge the research grant provided by the S.R.C. for the purchase of a vacuum coating unit and an AEI EM 6 electron microscope. The progress of this study was greatly facilitated by the excellent assistance of Mr T. Davies and Miss C. Green. The Stereoscan micrographs are published by permission of the Cambridge Instrument Company.

Taenia solium cysticercosis is a parasitic disease frequently affecting human health and the pig industry in many developing countries. A synthetic peptide vaccine (designated S3Pvac) against porcine cysticercosis has been developed previously as an aid to interrupt transmission and has been shown to be effective. The results of the present study support the effectiveness of the vaccine under endemic field conditions. However, given the time-frame of the vaccination trial, no changes in the local levels of transmission were detectable before and after vaccination using sentinel pigs. Thus, this investigation shows the limited usefulness of single vaccination as the sole means of interrupting Taenia solium transmission in an endemic region.

The size and fecundity of parasitic nematodes are constrained by the host immune response. For the parasitic nematode of rats, Strongyloides ratti, parasitic females infecting immunized rats are smaller and less fecund than those infecting naïve rats. Here, we investigated whether these constraints on size and fecundity are life-long. This was done by comparison of worms from different immunization and immunosuppression regimes. It was found that the per capita fecundity of parasitic females of S. ratti is fully reversed, but that their size is only partially reversed, if previously immunized hosts are subsequently immunosuppressed, suggesting that fecundity is not subject to life-long constraints. The host immune response also resulted in allometric changes in the parasitic females. The significance of these results with respect to the growth and control of nematode fecundity are discussed.

In outbred (CFLP) and inbred (NIH) mice, the inflammatory response which is thought to be party responsible for the expulsion of Trichinella spiralis from the mid-region of the small intestine, also seemed to be largely responsible fo rthe simulataneous (i.e. early) expulsion of Trichuris muris from the caecum and large intestine during concurrent primary infections. The intractive explusion operated only when the concurrent infections were timed to produce T. Spiralis expulsion before T. muris expulsion would normally occur and the effect persisted for several days after T. Spiralis has been expelled.

Interactive expulsion wasss depressed during application of the nonsteroid, anti-inflammatory drug indomethacin and by T-cell expulsion of T. spiralis. These results indicate that a T-cell mediated inflammatory response was probably the basis of the interaction.

When the timing of the infections was altered such that the expulsion of T. spiralis there was no reciprocal ecpulsion of the latter. Mice immunized againest one or the other species did not show cross-immunity on heterologus challenge, confirming that the interaction did not involve similar antigens in the two species. The interactive expulsive response is considered as an example of an indirect cross-immunity.

Forms of Trypanosoma brucei isolated from lymph nodes of cyclically or intravenously infected rats, at different stages of infection, were morphologically compared with the corresponding bloodstream forms. Unlike the pleomorphic bloodstream trypanosome population, the lymph node trypanosome population was essentially monomorphic and resembled the slender forms of the bloodstream. Values for the morphometric parameters indicated a position between the slender and the stumpy forms. The number of trypanosomes/ml of blood showed the well-known periodic fluctuations while the number of trypanosomes/g of lymph node remained fairly constant. Serology revealed that lymph node trypanosome populations differed antigenically from the trypanosome populations isolated simultaneously from the bloodstream.

Agglutination reactions between living trypanosomes and sera of experimentally infected rabbits is described.

Agglutinins in infected rabbits and in hyperimmunized rabbits with dead trypanosomes appeared between 5 and 8 days and reached their maximum within 14 days. They persisted in infected untreated rabbits until death, but in infected rabbits treated with Suramin they persisted for only 3 months. In hyperimmunized rabbits the titre of agglutinins gradually fell and disappeared 4 weeks after the last inoculation.

Agglutinins appear to be species specific; sera of rabbits infected with T. brucei agglutinated homologous and heterologous strains of the T. brucei, but failed to agglutinate heterologous species of trypanosomes. Similar results were obtained with sera of other species of trypanosomes.

Four sera from naturally occurring cases of T. rhodesiense infection in man produced agglutination reactions with titre varying from 1:80 to 1:1280 with T. rhodesiense, but did not agglutinate T. brucei.

Homologues of the mammalian multidrug resistance gene have been identified in isolates and clones of Plasmodium falciparum and designated pfmdr1 and pfmdr2. Mutations in pfmdr1 have been associated with chloroquine resistance but confirmation could not be obtained in a genetic cross. We have examined the copy number and expression of pfmdr1 and pfmdr2 in chloroquine-sensitive and -resistant P. falciparum and have found no relationship between the copy number of either gene and chloroquine resistance. However, a marked correlation was seen between levels of mRNA transcribed for each gene and chloroquine resistance. Two transcripts of pfmdr1 were detected, and in the asexual blood cycle an 8 kb transcript appeared first, followed by the appearance of a 7 kb species.

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.

A major question in the study of any parasitic disease is the relationship between infection and clinical disease. The public health importance of lymphatic filariasis has generated a large body of research in this area, both in laboratory studies (Ottesen, 1984,1989; Maizels & Lawrence, 1991) and in the field (Hayashi, 1962; Hairston & Jachowski, 1968; Denham & McGreevy, 1977; Vanamail et al. 1989 b; Bundy, Grenfell & Rajagopalan, 1991; Srividya et al. 1991 b). Despite this, there is still no conclusive explanation for the apparently complex relationship between infection and clinical disease observed in human communities. At least part of the problem may lie in the current impossibility of measuring adult worm burden in vivo (Pichon et al. 1980; Denham & Fletcher, 1987; Das et al. 1990; Grenfell et al. 1990). Although there has recently been significant progress in the development of immuno logical markers for infection status in humans (Ottesen, 1989; Day et al. 1991 a), microfilaraemia is still the most reliable measure of current infection in the field. Studies in endemic areas indicate that, far from there being any simple direct relationship between microfilaraemia and disease status, it is possible to find some individuals with microfilariae in their blood but no disease, and indeed with all other combinations of infection and disease status (Hairston & de-Meillon, 1968; Hairston & Jachowski, 1968; Beaver, 1970; Bryan & Southgate, 1976; Denham & McGreevy, 1977; Pani et al. 1991). Furthermore, the proportions of people in different categories are often observed to vary between endemic areas (Denham & McGreevy, 1977; Day et al. 1991 a).

Application of quantitative methods to the study of leishmaniasis epidemiology has allowed Dye (1992) to pinpoint important biological parameters which, if they could be accurately measured in the field, would contribute most to our knowledge of the spread of disease and key targets for control. Three areas in which laboratory-based research could impact most on leishmaniasis epidemiology were highlighted by Dye (1992): (i) the development of accurate diagnostic tools which can distinguish between current and past infection; (ii) to determine the underlying molecular/genetic basis to virulence polymorphisms in the parasite and study these in the context of field epidemiological studies; and (iii) to provide the molecular tools to measure genetic variation in resistance to infection in humans and in reservoir hosts of disease. This paper describes current progress in attaining these goals, highlighting first the work on isolation and field application of genomic and kDNA probes for species-specific diagnosis, and the development of PCR-based assays which can be performed under field conditions. At a more preliminary stage, studies are described in which variability in the major molecular determinants of virulence (lipophosphoglycan, GP63, and members of the HSP7O family of stress proteins) identified through studies of laboratory models of infection, is being measured in primary field isolates of Leishmania peruviana. To complete the picture, current progress in identifying and cloning the genes which control host resistance to leishmanial infection is described, along with field studies of multicase families of human disease in which linkage analysis using marker genes from the chromosomal regions bearing these genes can be used to find evidence for their role in determining disease phenotypes in man. The leishmaniasis epidemiology will be all down to the DNA. projected view from these studies is that the future of leishmaniasis epidemiology will be all down to the DNA.

Cadmium and lead concentrations were compared in tissues of cutlassfish, Trichiurus lepturus L., its intestinal nematode Hysterothylacium sp. type MB larvae, and in water from the same location in the Sea of Oman. Metal accumulation in hosts, parasites and sea water was measured by ICP-OES. Hysterothylacium larvae from the intestinal lumen and visceral cavity showed much higher metal concentrations than in host tissues or sea water. Statistical analyses revealed no significant differences in metal accumulation between infected and uninfected hosts. Cadmium concentration in the host muscle was lower than in intestine, liver and gonad tissues. The mean concentrations of lead and cadmium in nematodes were 289·03 and 81·5 times higher than in host intestine, 188·4 and 225 times higher than in host muscle, 108·6 and 65·3 times higher than in host gonads, 70·5 and 19·5 times higher than in host liver and 3351 and 148 times higher than in sea water. The results show the value of this and possibly related nematodes as bioindicators of heavy metals and their potential use in environmental studies.

Experiments on hybridization between Fasciola hepatica and Fasciola gigantica were carried out to clarify whether a reproductive isolating mechanism appears between the two Fasciola species. Molecular evidence for hybridization was based on the DNA sequence of the internal transcribed spacer 1 (ITS1) region in nuclear ribosomal DNA, which differs between the species. The results suggested that there were not pre-mating but post-mating isolating mechanisms between the two species. However, viable adults of the hybrids F1 and F2 were produced from both parental F. hepatica and F. gigantica. The hybrids inherited phenotypic characteristics such as ratio of body length and width and infectivity to rats from parental Fasciola hepatica and F. gigantica. These findings suggest that reproductive isolation is incomplete between Fasciola hepatica and F. gigantica. Adults of the hybrids F1 and F2 were completely different in mode of reproduction from aspermic Fasciola forms that occur in Asia and seem to be offspring originated from hybridization between F. hepatica and F. gigantica and to reproduce parthenogenetically.

The complexity and connectedness of eco-social processes have major influence on the emergence and spread of infectious diseases amongst humans and animals. The disciplinary nature of most research activity has made it difficult to improve our understanding of interactions and feedback loops within the relevant systems. Influenced by the One Health approach, increasing efforts have recently been made to address this knowledge gap. Disease emergence and spread is strongly influenced by host density and contact structures, pathogen characteristics and pathogen population and molecular evolutionary dynamics in different host species, and host response to infection. All these mechanisms are strongly influenced by eco-social processes, such as globalization and urbanization, which lead to changes in global ecosystem dynamics, including patterns of mobility, human population density and contact structures, and food production and consumption. An improved understanding of epidemiological and eco-social processes, including their interdependence, will be essential to be able to manage diseases in these circumstances. The interfaces between wild animals, domestic animals and humans need to be examined to identify the main risk pathways and put in place appropriate mitigation. Some recent examples of emerging infectious disease are described to illustrate eco-social processes that are influencing disease emergence and spread.

The European shore crab, Carcinus maenas, is one of the most successful marine invasive species. Its success has been in part attributed to the loss of parasites, rekindling an interest in host-parasite interactions and impacts on host fitness in this crab. In the present study, we investigated C. maenas populations from Europe, South Africa and Australia for parasites, and assessed their impact on the fitness of male crabs. For the shore crab, testes weight along with success in mating competition is traded off against other life-history traits. We therefore used this parameter as an indicator both for reproductive fitness and a possible resource trade-off in response to parasite infestation. In the native range, crabs infested with Sacculina carcini showed significantly lower testes weight than uninfected crabs. However, helminth parasites did not generally cause reduced testes weights. Crab populations from South Africa and Australia were either parasitized at very low prevalences, or were completely parasite free. However, no population level effect of this parasite release was reflected in testes weight. These findings do not support a severe fitness impact of helminth parasites on C. maenas, which questions the role of parasites on its population dynamics, both in the native area and for invasive success.

There are conspicuous differences in respect of hibernation among the mosquitoes; for certain species, such as Culex pipiens and Anopheles maculipennis, hibernate as adults, but others, for instance A. claviger (bifurcates), pass the winter as larvae. These differences have been the subject of many investigations and of much theoretical discussion; perusal of the literature suggests that we still lack a sufficient knowledge of the facts. It is known that an accumulation of fat in autumn is characteristic of those mosquitoes which hibernate as adults, as it is of several insects of other orders. But it seems that little is known of the quantity of fat stored, or of the rate at which it disappears as winter passes. It is my present purpose to set out certain observations on the composition of adult female Culex pipiens at different times during the period of hibernation. Later it may be possible to make an experimental study of the causes of hibernation and to discuss the relevant literature. But at the moment let it suffice to refer to the following papers, from which the reader may inform himself of the present state of knowledge and theory: de Boissezon (1930), Roubaud (1932), and Shlenova (1933). The paper by Hecht (1933) contains a valuable summary of the subject.

A consideration of the above experiments, and of the available literature dealing with the distribution of trypanosomes and tsetse flies in nature, has suggested certain general conclusions which will now be put forward.

By selection for early development of oocysts during serial passage through chickens the pre-patent period of the Houghton (H) strain of Eimeria mivati ( = mitis) was reduced by over 20 h. The precocious parasite is less pathogenic than the H strain and has a reduced reproductive potential. Chicks inoculated with the precocious parasite were protected against challenge with the H strain. The pathogenicity, immunogenicity and reproduction of precocious E. mivati and an attenuated egg-adapted line of E. mivati were compared. Although the precocious parasite produced more oocysts than the egg-adapted parasite in chickens, neither parasite induced loss of weight and both were immunogenic.

After demonstrating that rats were capable of discriminating between the same diet treated with either flavour 1 or flavour 2 and that the 2 flavours of diet were equipreferred, an experiment was carried out to see whether learned taste aversion might play a role in the reduction of food intake that is commonly observed during the course of a parasitic infection. The results showed that rats, given a subcutaneous inoculation of approximately 6000 third-stage larvae of Nippostrongylus brasiliensis (Nematoda) while feeding on a diet containing flavour 2, strongly preferred to eat diet containing flavour 1 when given simultaneous choice conditions. Uninfected rats showed no preference and ate equal amounts of both flavoured diets. This effect is interpreted as the first experimental demonstration of learned taste aversion using a eukaryotic parasite as the inductive agent.

Human parasites are often distributed in metapopulations, which makes random sampling for genetic epidemiology difficult. The typical approach to sampling Schistosoma mansoni involves laboratory passage to obtain individual worms with small sample size and selection bias as a consequence. By contrast, the naturally pooled samples from egg output in stool or urine directly represent the genetic composition of current populations. To test whether pooled samples could be used to estimate population allele frequencies, DNA from individual cloned parasites was pooled and amplified by PCR for 7 microsatellites. By polyacrylamide gel analysis, the relative band intensities of the products from the major alleles in the pooled samples differed by 0–6% from the summed intensities of the individual clones (mean=2·1%±2·1% S.D.). The number of PCR cycles (25–40) did not influence the accuracy of the estimate. Varying the frequency of 1 allele in pooled samples from 32 to 69% likewise did not affect accuracy. Allele frequency estimates from aggregate samples such as eggs will be a better foundation for studies of parasite population dynamics as well as the basis for large-scale association studies of host and parasite characteristics.