The life-cycle of Theileria parva in the gut of the tick Rhipicephalus appendiculatus was investigated in Giemsa-stained smears and in wet preparations under the phase-contrast microscope. The different developmental stages of T. parva were seen in a large proportion of specially-selected R. appendiculatus tickes. After the intra-erythorcytic merozoites were engorged by the ticks during a blood meal, the following development was observed. (1) In the lumen of the gut of infected nymphs, spindle-shaped microgamonts developed out of the ring-forms. These broke up into several thread-like microgameters after nuclear division and development of thread-like cytoplasmic projections. The ring-froms developed into round-forms of 3–4 μm in diameter which are considered to be macrogametes. (2) From the 6th day after repletion, zygotes with a clear zone in the centre appeared in the epithelial cells of the tick's gut. A steady increase in size and a progressively denser cytoplasm were observed up to the 3rd day after moulting to adult ticks. (3) Subsequently a slightly angular, retort-like stage developed by invagination inside the rounded zygotes, and from the 5th day after moulting this stage developed further into a club-shaped kinete. The kinetes propelled themselves in the gut by active gliding movements.

The muscular saucer-shaped haptor of the monogenean parasite Entobdella soleae is attached to the skin of its host Solea solea by means of a suction pressure generated within the sea-water-filled cavity enclosed between the cup-shaped haptor and the skin of the fish. The suction pressure is produced by the action of a pair of extrinsic muscles which are situated in the body of the parasite. Each extrinsic muscle communicates with the haptor by means of a long tendon which passes through a fair-lead in a prop-like accessory sclerite and is inserted on the end of a girder-like anterior hamulus embedded in the roof of the concavity of the haptor. The pull exerted by the muscles lifts the girders and the roof of the suction cup in which they are embedded relative to the props, thereby producing a suction pressure.

An electron microscope was used to investigate the ultrastructure of the tendon, which was found to consist largely of unbranched banded fibrils which differed from the collagen fibrils of vertebrate tendon in their diameter and periodicity.

I would like to express my thanks to Dr J. Llewellyn for suggesting the problem and for much helpful discussion. I am also grateful to Dr M. P. Osborne for tuition on the cutting of sections for electron microscopy. The work was conducted during the tenure of a Fishery Research Training Grant from the Development Commission.

The antigenic composition of sequential erythrocytic stages of Plasmodium knowlesi has been compared by crossed immuno-electrophoresis using a pool of immune rhesus monkey antiserum. Eleven major parasite antigens have been identified; 9 are stage-independent, and 2 stage-dependent. Differences in the relative amount of the stage-independent antigens have been demonstrated and quantified. The distribution of antigens between parasites and schizont and infected red cell membranes has been examined. Only 6 of the 11 parasite antigens were exhibited by a schizont membrane preparation, all these antigens were also expressed by the intracellular parasite. Antigens exclusive to the schizont membrane were not demonstrated.

The invasion and establishment of Heterodera glycines has been studied for 0–120 h after addition to host roots using a synchronized infection system. A high degree of synchrony in development was noted, with juvenile nematodes reaching their feeding sites adjacent to the root endodermis and discharging their subventral pharyngeal glands by 24 h post-invasion (p.i.). The moult to the 3rd-stage juvenile occurred approximately 89 h after entry to the root. Using an enzyme-linked immunosorbent assay with monoclonal antibodies (MAbs) whose tissue specificities had already been defined by immuno-cytochemistry, it was found that MAbs recognizing intestinal lipid droplets and granules showed a major increase in reactivity 18–24 h p.i. before declining by 39 h p.i. In contrast, the reactivity of two MAbs recognizing adult cuticle increased significantly only after 89 h p.i., following the second moult. MAbs to the two subventral pharyngeal gland cells showed a variety of patterns of changing reactivity during the experiment. One increased within 24 h of invasion before declining whereas a second fell without any initial rise. Two further MAbs specific for the subventral glands initially declined but showed a secondary increase in reactivity after 72 h and could be detected in adult females. This pattern was also seen in a MAb specific for the dorsal pharyngeal gland cell. These changes are discussed in the context of events taking place following invasion, with particular reference to the initiation and maintenance of a feeding syncytium by the developing nematode.

Adult parasites of Schistosoma mansoni reside within vertebrate mesenteric veins where they consume immense quantities of host glucose after transporting the sugar through their surface syncytium or tegument. Previously we obtained cDNA clones encoding two functional facilitated diffusion glucose transporter proteins expressed by S. mansoni adult worms (Skelly et al. 1994). Antibodies specific for one transporter (SGTP1) have been generated against an extrafacial and an internal domain of the protein and used to localize the protein by light and electron microscopy. By light microscopy both antibodies stain a linear structure approximately 1–5 μm from the surface of the tegument of adult male and female schistosomes. Electron microscopic examination of frozen thin sections show binding of the antibodies to membranes in the base of the tegument and not to the membranes covering the outer surface or their invaginations. Analysis of the gold distribution suggests that the extrafacial domain is disposed toward the interstitial space beneath the tegument and the internal domain faces the syncytial plasm. The localization suggests that SGTP1 may function to transport free glucose from within the tegument and into the interstitial fluids that bathe the internal organs of these parasites.

In order to better comprehend the putative association between genotype Trypanosoma cruzi II and primates, an evaluation of the infection in free ranging primates and specimens born in captivity from different geographical areas, the Amazon and the Atlantic forest, was carried out. Seroprevalences of the T. cruzi infection among the primates was similar in both biomes (45·5% and 46%). The parasites were isolated from 8 and 4 different species of primates, respectively from the Amazon and Atlantic forest. Multi-locus enzyme electrophoresis (MLEE) typed the isolates from Amazon as zymodeme 1. Mini-exon gene analysis characterized all these isolates as T. cruzi I, the main genotype circulating in the region. In the Atlantic forest, primates infected with TCI and TCII, as well as a mixed infection (TCI and TCII), were detected. These findings prove that primates may maintain stable infections by both genotypes. Moreover, data show that T. cruzi can occur in a wide range of primate genera, independent of their social behaviour, niches or habitats. Considering the high seroprevalence and stability of T. cruzi infection among the primates, these animals play an important role in the maintenance of the parasite in nature.

Using a combination of morphological, life-history and molecular data, we redescribe Sphaerospora ranae (Morelle, 1929) n. comb. (previously Leptotheca ranae) and emend its taxonomic status. Renal infection was recorded in 2 spp. of frogs (out of 5 amphibian spp. examined), Rana dalmatina (proposed type host) and Rana temporaria, suggesting restricted host specifity of S. ranae. We provide a description of sporogonic stages of S. ranae for the first time and suggest possible modes of its developmental cycle. Phylogenetic analysis inferred from the small-subunit ribosomal DNA revealed a close relationship of S. ranae with piscine Sphaerospora elegans (type species of the genus) and Sphaerospora truttae, forming together with distantly related Leptotheca fugu a ‘Sphaerosporid clade’, the basal branch to all myxosporean species. The close relationship of the 3 Sphaerospora spp. is further supported by the presence of 2 areas with extensive nucleotide insertions in the V4 region of the SSU rDNA (absent in L. fugu), morphology and life-history features. We conclude, that the spore morphology of Sphaerospora s.l., is very simple and probably represents a ‘primitive’, basal morphotype retained in most myxosporean lineages. Based on presented data, we propose emendation of the genus Sphaerospora using morpological, life-history and molecular features.

Robinia aurata n. g., n. sp. is described from Liza aurata (Mugilidae), the golden grey mullet, from the Ebro Delta, Spanish Mediterranean. The new genus differs from all other hemiurid genera in the combined possession of muscular flanges and a vestigial ecsoma. Within the Bunocotylinae, which currently accommodates 2 genera, Bunocotyle and Saturnius, the new genus exhibits a unique combination of blind caeca, Juel's organ, post-ovarian bulk of the uterus in the hind-body, and tegumental papillae surrounding the oral and ventral sucker apertures. Furthermore, Robinia n. g. differs from both Bunocotyle and Saturnius in the nature of the muscular extensions around the oral sucker, with the shape of a muscular belt in the latter and numerous muscular papillae in the former. The phylogenetic hypothesis for the Bunocotylinae developed from sequence data analyses based on partial lsrDNA and complete ssrDNA combined (22 species) and V4 domain of the ssrRNA gene (37 species) supports the erection of the new genus and confirms its position within the Hemiuroidea. Both molecular analyses confirmed the monophyly of the Hemiuroidea, its division into 2 major clades and the polyphyly of the Derogenidae, as in previous studies, and suggest that the Gonocercinae (with 2 genera, Gonocerca and Hemipera), may require a distinct familial status. Finally, there was poor support for the distinct status of the Lecithasteridae and Hemiuridae, following previous suggestions based on different sequence data sets. A key to genera of the Bunocotylinae is presented.

Host tissue penetration, feeding and immune evasion by helminth parasites may be mediated by both mechanical processes and histolytic products released by the parasite. The aim of this study was to investigate potential histolytic products released during in vitro maintenance of exsheathed third (L3) and 4th larval stage (L4) and adult Ostertagia ostertagi. Therefore, the pH optima, substrate specificity, molecular size and inhibitor sensitivity of in vitro released (IVR) proteinases were analysed by spectrophotometry and substrate gel electrophoresis. It was shown that L3, L4 and adult IVR proteinases degrade a variety of protein substrates in a pH-dependent and stage-specific manner. At alkaline pH, gelatin, casein and fibrinogen were degraded by metallo- and serine proteinases. In contrast, mucin, fibrinogen, albumin and haemoglobin were degraded at acidic pH by aspartyl protease- and cathepsin L-like activity. At pH 3, the heavy chain of bovine IgG was completely degraded by an aspartyl proteinase secreted by all 3 parasitic stages. The specificity of the L3, L4 and adult Ostertagia ostertagi proteinases against the different substrates indicates variable functional requirements.

Here we report on the action of the novel cyclo-depsipeptide anthelmintic, emodepside, on the body wall muscle of the parasitic nematode, Ascaris suum. Emodepside caused (i) muscle relaxation, (ii) inhibition of muscle contraction elicited by either acetylcholine (ACh), or the neuropeptide, AF2 (KHEYLRFamide) and (iii) a rapid relaxation of muscle tonically contracted by ACh. The inhibitory action of emodepside on the response to ACh was not observed in a denervated muscle strip, indicating that it may exert this action through the nerve cord, and not directly on the muscle. Electrophysiological recordings showed emodepside elicited a Ca++-dependent hyperpolarization of muscle cells. Furthermore, the response to emodepside was dependent on extracellular K+, similar to the action of the inhibitory neuropeptides PF1 and PF2 (SDPNFLRFamide and SADPNFLRFamide). Thus emodepside may act at the neuromuscular junction to stimulate release of an inhibitory neurotransmitter or neuromodulator, with a similar action to the PF1/PF2 neuropeptides.

Three heat-induced genes of the infective-stage larvae of Trichinella spiralis were successfully identified by the suppression subtractive hybridization (SSH) technique. As indicated by reverse Northern blotting, 19 of 25 clones were scored as differentially transcribed in the heat-shocked infective-stage larvae. The sequencing data showed the presence of 12 different genes. Three were homologous to histone H3, histone H2B and translationally controlled tumour protein (TCTP). A 0.6 kb cDNA of histone H3 was generated by the RACE method and sequenced. It contained an open reading frame of 136 amino acids that demonstrated 94% identity with genes from Drosophila hydei. Semi-quantitative RT-PCR indicated that after heat-shock treatment, the expression levels of histone H3, histone H2B and TCTP increased 4.8, 27 and 5.7-fold, respectively. Northern analysis confirmed the upregulation of histone H3, histone H2B and TCTP transcripts. The upregulation of these genes during stress conditions has not been reported in parasitic organisms. The stress proteins may play an active role to sustain the parasite after exposure to hostile host factors.

Myxozoans are a group of diverse, spore-forming metazoan microparasites bound to aquatic environments. Sphaerospora dykovae (previously S. renicola) causes renal sphaerosporosis and acute swim bladder inflammation (SBI) in juvenile Cyprinus carpio carpio, in central Europe. A morphologically similar species with comparably low pathogenicity, S. angulata has been described from C. c. carpio, Carassius auratus auratus and Carassius gibelio. To clarify uncertainties and ambiguities in taxon identification in these hosts we decided to re-investigate differences in spore morphology using a statistical approach, in combination with SSU and LSU rDNA sequence analyses. We found that developing spores of S. angulata and S. dykovae cannot be distinguished morphologically and designed a duplex PCR assay for the cryptic species that demonstrated S. dykovae is specific to C. c. carpio, whereas S. angulata infects C. a. auratus and C. gibelio. The molecular identification of myxozoan blood stages in common carp and goldfish, which had previously been ascribed to Sphaerospora spp. showed that approximately 75% of blood stages were from non-sphaerosporid coelozoic species infecting these cyprinids and more than 10% were from an alien species, Myxobilatus gasterostei, developing in sticklebacks. We hereby report non-selective myxozoan host invasion and multi-species infections, whose role in SBI still requires clarification.

Toxoplasmosis is largely present in rural areas but its spatial distribution in this environment remains poorly known. In particular, it is unclear if areas of high density of cats, the only hosts excreting Toxoplasma gondii, constitute foci of high prevalence. To improve our understanding of the spatial distribution of T. gondii in rural areas, we performed a serological survey in rodents from two villages in France. We trapped 710 rodents including commensal rats and meadow or forest voles and mice. The presence of T. gondii was examined using PCR, mice inoculation and modified agglutination test for antibodies (MAT). We conducted multivariate and discriminant analyses to identify biological, ecological or spatial variables that could explain T. gondii serology in rodents. We then used a logistic regression to assess the relative influence of each explanatory variable. Overall seroprevalence was 4·1%. Commensal-rats were more infected (12·5%) than non-commensal species (3·7%). However, the major determinant of the risk of infection was the distance to the nearest farm (OR = 0·75 for 100 m), which explained the risk in all species or non-commensal species only. We contrast the role of species characteristics and that of the local environment, and discuss the risk of environmental contamination for humans.

Two new, nine little known species and nine unnamed ‘species’ of Echeneibothrium Beneden, 1850, have been investigated and observations have been made on the ‘related’ genera, Discobothrium Beneden, 1870, and Pseudanthobothrium Baer, 1956. Brief descriptions of the species are given, but a discussion of the history of each differs greatly from most previous accounts in that few or no synonyms have been listed for the species and in that nine forms are left unnamed; this approach differs greatly from that in a large number of taxonomic papers in helminthology. A detailed discussion of the reasons for adopting this procedure is, therefore, given. A provisional key to nineteen ‘species’ of Echeneibothrium is included. E. minutum sp.nov. closely resembles E. variabile var. exiguum of Euzet (1959), described in this paper as ‘Echeneibothrium sp. of R. clavata’, but occurs only in R. batis and differs in its very small size, in having only about ten proglottids, long peduncles to the bothridia and a myzorhynchus which remains evaginated in fixed specimens. It differs from E. demeusiae Euzet, 1959, mainly in the number of proglottids, testes and loculi. E. elongatum sp.nov. resembles E. dubium from which it differs in the length and form of the strobila, in having only six clearly visible loculi in each bothridium, about twenty testes and in that it occurs in R. circularis. It has, however, more characters in common with a species referred to in this paper as ‘Echeneibothrium sp. from Raja naevus’ and which possesses eight loculi. A list is given of twenty-seven species wrongly allocated by various authors to the genus Echeneibothrium. The comparative morphology of some species of the genus, their ecology and speculations on their life-histories, are described.

It is shown for the first time that Echeneibothrium from species of Raja caught off the British Isles, and presumably from rays of other localities, can be separated into two distinct biological groups. One group includes species which possess shallow open bothridia covering comparatively large areas of the host's mucosa, a variable myzorhynchus which may be either rudimentary or very large and spherical eggs laid singly or in capsules; these occur mainly in rays from shallow waters and in which the mucosa of the intestine lacks prominent villi. The other group includes species in which each bothridium possesses a small opening adapted for attachment to a single villus, the myzorhynchus is consistently cylindrical, the eggs have long polar filaments and the species occur in deep water rays with well-defined villi on the intestinal mucosa. Studies on variation in the form of the eggs in different species of Echeneibothrium in relation to the behaviour and feeding habits of the various host-species suggest that the eggs are eaten by arthropods which are most likely to form part of the diet of the final host. A general trend towards an increase in the complexity of the bothridium and a decrease in the size of the myzorhynchus in Echeneibothrium is thought to be of considerable advantage to the species and an indication that Rhinebothrium, which is restricted to the Myliobatoidea, has evolved from a form like Echeneibothrium which is restricted to the Rajoidea. This supports the view that the Myliobatoidea have evolved from the Rajoidea. The results from this study of Echeneibothrium illustrate the following general rule which can be applied to the Tetraphyllidea, namely, those species which are abundant in any given host are very well adapted for attachment to the host's gut and cause little, if any, damage while rare species are often highly pathogenic.

This work would not have been possible without generous financial aid from the Department of Scientific and Industrial Research and various kinds of other aid and encouragement from a number of persons, in particular Dr Gwendolen Rees.

It was begun in 1958 at the University College of Wales, Aberystwyth, the British Museum (Natural History), University of Montpellier, France, University of Neuchatel, Switzerland, the Plymouth Marine Laboratory and the Aberdeen Marine Laboratory during my tenure of a D.S.I.R. Fellowship. I wish to record my gratitude to Dr Rees who has also suggested improvements to the manuscript and to the following persons: the late Professor T. A. Stephenson, F.R.S., Dr E. E. Watkin, Mr S. Prudhoe, Dr L. Euzet, Professor Jean G. Baer, The Director, Dr F. S. Russell and Staff, in particular Mr J. Green and Mr A. Mattacola, of the Plymouth Marine Laboratory, and the Director and staff, in particular Dr B. B. Rae and Dr Z. Kabata, of the Aberdeen Marine Laboratory.

The work was later continued at the University College, Cardiff, and I am most grateful to Professor James Brough for providing excellent research facilities and to Mr W. O'Grady for technical assistance.

At the Bureau of Helminthology, St Albans, much encouragement from Professor R. T. Leiper, C.M.G., F.R.S., enabled me to put the work together while having free access to his invaluable collection of books and reprints on helminths; it became unnecessary to search elsewhere for the literature. Mr G. Dimmock gave technical assistance for which I am most grateful.

1. Spores of Nosema apis nearly all germinate within 30 min. after entering the ventriculus of the honeybee.

2. The cause of germination in vivo remains unknown, but is probably not a change of osmotic pressure or pH and is probably not due to anaerobic conditions or an enzyme. The agent causing germination is probably unstable and is destroyed when removed from the bee.

3. The anterior end of the ventriculus receives an initial heavy infection and the circumstantial evidence which this provides supports the theory that a free living ‘planont’ stage does not exist but that the parasite is injected directly into the host cell from the spore via the hollow polar filament.

4. The central region of the ventriculus which contains many granules of calcium phosphate receives the lowest initial infection. It is considered possible that the granules inhibit the initial rapid development of the parasite by maintaining an unfavourably high level of pH until they are eventually dissolved by the slowly developing organism.

1. Attempts, made over a period of more than 6 months, to produce a strain of Plasmodium gallinaceum resistant to mepacrine failed.

2. A strain of P. gallinaceum resistant to daily doses of 0·08 mg./20 g. of pamaquin was obtained after approximately 8 months' treatment with the drug.

3. A strain of P. gallinaceum resistant to the maximum dose of paludrine which the chicks would tolerate (1·0 mg./20 g. twice daily) was obtained after 4½ months' treatment with gradually increasing doses of the drug.

4. The exo-erythrocytic parasites of P. gallinaceum formed in chicks infected with a paludrine-resistant strain are themselves resistant to the drug. It is not, however, considered probable that the development of resistance is due to the action of the drugs upon the exo-erythrocytic parasites, as the technique used was one which reduced their number to a minimum.

5. A strain of P. gallinaceum resistant to paludrine showed a normal sensitivity to mepacrine and pamaquin, but was resistant to 4430, the methyl homologue of paludrine.

6. Chicks carrying a latent infection of the normal strain of P. gallinaceum were immune to infection with the paludrine-resistant strain; and conversely chicks carrying a latent infection of the paludrine-resistant strain were immune to infection with the normal parasite.

7. A paludrine-resistant strain of P. gallinaceum retained its resistance to this drug after five cyclical passages through mosquitoes without intervening drug treatment.

Plasmodium falciparum parasites infecting Aotus trivirgatus erythrocytes were cultured in media (Harvard and TC199) augmented with human, foetal calf, or other sera. Conditions were established which supported growth of parasites and allowed cyclical multiplication when fresh erythrocytes (from Aotus or Homo) were added in sub-culture (mean multiplication rate: x 3). Immunoglobulin G pools, prepared from plasma collected in endemic malarious areas in Africa and from unexposed Britons, were tested for effects on the in vitro growth (measured by incorporation of tritiated leucine) and multiplication of parasites. Whilst non-immune IgG was without effect, IgG from both East and West Africa inhibited the multiplication of East African (Uganda-Palo Alto strain) parasites.

In a longitudinal study in a UK upland site, 38% of adult sheep were detected as infected with the tick-borne bacterium Ehrlichia phagocytophila by PCR of blood samples. Infection prevalence declined significantly with sheep age but varied significantly and non-linearly with the number of adult Ixodes ricinus ticks feeding per sheep. These findings suggested that under conditions of natural repeated tick-borne challenge sheep remain partially susceptible to re-infections, but the likelihood of re-infection depended on the numbers of feeding ticks. Transmission efficiency from sheep to immature ticks also varied significantly and non-linearly with the number of adult ticks feeding per sheep: transmission efficiency was almost zero in sheep with low adult tick infestations rising to 30% at certain levels of adult tick infestation. Infection intensity in infected engorged immature ticks also varied with the number of adult ticks feeding per sheep, but neither prevalence nor intensity of infection in engorged ticks were related to sheep blood PCR result. These findings suggest that variation in the numbers of ticks feeding per sheep may influence E. phagocytophila transmission by direct effects on transmission at the tick–host interface.

While purine transport has been widely studied in protozoa, almost nothing is known about their capacity to salvage pyrimidines. Here, we report a Leishmania major transporter with high affinity for uracil (Km=0·32±0·07 μM) which we designated LmU1. This transporter displayed a high degree of specificity, as it had virtually no affinity for cytosine, thymine or purine nucleobases, nor did it transport pyrimidine nucleosides. Highest affinity was for 5-fluorouracil. The results show that the permeant binding site of LmU1 interacts strongly with the keto groups of uracil, as shown by a low affinity for 2-thio- and 4-thiouracil. LmU1 appears to further bind uracil through a weak hydrogen bond with N(1)H of the pyrimidine ring in addition to a stronger H-bond with N(3)H. Substrate binding and selectivity were strikingly similar to that of the U1 transporter in the related kinetoplastid Trypanosoma brucei. Uracil analogues likely to be transported by LmU1 were also screened for antileishmanial activity, with 5-fluorouracil displaying strong activity against promastigotes and intracellular amastigotes. Overall, the results show that, like purine nucleobase transport, pyrimidine nucleobase transport function is very similar in L. major and T. brucei insect forms.

A mechanism for eggshell production in Schistosoma mansoni has been proposed (Wells & Cordingley, 1991), and suggests that the release of eggshell protein globules from the vitelline cells occurs under alkaline conditions within the ootype followed by their subsequent fusion to form the eggshell. Fusion and tanning of these components produces eggshell which autofluoresces. The present study was carried out to determine whether a similar process operates in Fasciola hepatica. A number of drug treatments were used to disrupt key steps in the maturation of vitelline cells. Treatment with the calcium ionophore lasalocid (1×10−5m) led to the premature release of eggshell globules from the vitelline cells but not their fusion. Incubation in monensin (1×10−6m), a sodium ionophore and ammonium chloride (NH4Cl) (5×10−2m), a weak base, resulted in the premature fusion of eggshell protein globules within the vitelline cells and premature tanning of the eggshell protein material. The copper-containing enzyme, phenol oxidase, is thought to be involved in the tanning process during the production of eggs. Diethyldithiocarbamate (DDC, 1×10−3m) is a phenol oxidase inhibitor and treatment with this compound, in combination treatments with monensin and NH4Cl, prevented fusion of the vitelline cell globules and tanning of the shell protein material. The results of the study suggest that the mechanism for eggshell formation in F. hepatica is similar to that proposed for S. mansoni and may be common to other trematodes as well.