Very variable levels of immunity to a second infection with Schistosoma mansoni were recorded in 7 strains of mice, 12–15 weeks following a small primary infection. When 2 or more strains of mice were assayed at the same time, less variation occurred within the experiment than between different experiments. This evidence suggested variation between pools of cercariae as the main cause of variability in immunity. In direct experiments in one strain of mouse, 2 different pools of cercariae stimulated widely different levels of immunity to the same challenge. Conversely, challenge infections drawn from different pools showed different susceptibility to immunity stimulated by the same primary infection. Individual clones of cercariae, from snails infected with single miracidia, showed a high level of susceptibility to immunity stimulated by a small bisexual infection, or were not susceptible at all. Antigenic polymorphism is the most likely explanation for the differences observed between clones of cercariae. However, indirect immunofluorescence showed the presence of at least 1 common antigen on the surface of schistosomula derived from different clones of cercariae and clone-specific antigens have not been detected.

Isolates of Trypanosoma cruzi from human patients, domestic and sylvatic animals and vector insects were obtained in different areas of Argentina. Electrophoretic patterns of enzymes from extracts of 95 isolates were analysed. On the basis of zymograms providing information on 10 loci, 12 zymodemes are described according to their genotypes. Data presented show fixed heterozygosity, absence of segregation of genotypes, significant departures from Hardy–Weinberg equilibrium, and over-represented genotypes. This evidence supports the hypothesis that sexual reproduction is very restricted or absent in this parasite. The proportion of polymorphic loci is 80%. The expected mean heterozygosity per locus (He) is 0·43, while the observed value (Ho) is 0·24. Differences between these values may be explained by accepting a basically clonal structure for T. cruzi. The data matrix of 12 zymodemes using 28 characters was analysed using a Wagner parsimony algorithm. Two equally most parsimonious unrooted trees were generated; both have 39 steps. The results show clusters clearly separated according to the geographical origin of the stocks. There are some indications of some correlations between genetic composition of the parasite and the clinical picture of the infection in human patients.

Trypanosomes isolated from South American bats include the human pathogen Trypanosoma cruzi. Other Trypanosoma spp. that have been found exclusively in bats are not well characterized at the DNA sequence level and we have therefore used the SL RNA gene to differentiate and characterize kinetoplastids isolated from bats in South America. A Trypanosoma sp. isolated from bats in southern Brazil was compared with the geographically diverse isolates T. cruzi marinkellei, T. vespertilionis, and T. dionisii. Analysis of the SL RNA gene repeats revealed size and sequence variability among these bat trypanosomes. We have developed hybridization probes to separate these bat isolates and have analysed the DNA sequence data to estimate their relatedness. A new species, Trypanosoma desterrensis sp. n., is proposed, for which a 5S rRNA gene was also found within the SL RNA repeat.

A new subgenus and species of avian haemocytozoon Fallisia (Plasmodioides) neotropicalis is described. The principal characteristics are the main host cells, thrombocytes and mononuclear leucocytes, where trophozoites, schizonts and gametocytes are found. Occasionally, granulocytes and very rarely reticulocytes are also parasitized. Phanerozoites very similar to those of Plasmodium of birds are also present. The host is the domestic pigeon, Columbalivia, an imported species but similar parasites have been identified, always mixed with species of Plasmodium, in several indigenous species of Ciconiiformes, which seem to be the natural hosts. This is the first report in birds of a representative of the genus Fallisia, parasites of neotropical lizards.

Parvicapsula minibicornis is a myxozoan parasite implicated in mortalities of both juvenile and pre-spawning adult salmon in the Pacific Northwest of North America. Disease severity and presentation varies between salmon species and geographical localities. To better characterize population structure of the parasite, we sought genetic markers in the P. minibicornis ribosomal RNA gene. We compared samples from California with the type specimen from British Columbia, identified sequence variations, and then sequenced 197 samples from fish, river water and the parasite's polychaete worm host. Although DNA sequences of the parasite were >98·9% similar, there was enough variation to define 15 genotypes. All genotypes were detected in fish samples, although not in all species. A single genotype only was found in sockeye and pink salmon in the Fraser River Basin, but was not detected in sockeye from the adjacent Columbia River Basin. All coho salmon, irrespective of river basin, were infected with a unique mix of 2 genotypes. These data indicated that the P. minibicornis population exhibited strong signals of structuring by both geography and salmonid host species. Particular genotypes may correlate with disease differences seen in salmon populations in the Pacific Northwest.

The infectivity of wild and laboratory strains of Heligmosomoides polygyrus (Nematospiroides dubius) in laboratory mice and in three species of wild British rodent was compared. Wild strains, of the subspecies H. p. polygyrus, were isolated from wild caught Apodemus sylvaticus. Only very low-level infections of the wild strains became established in laboratory mice. Similar worm burdens of the laboratory strain became established in laboratory mice and A. sylvaticus, although infections in A. sylvaticus were more short lived. Cortisone treatment of hosts increased the establishment and survival of the heterologous worm strain to that of the homologous strain. In contrast, neither strain of parasite established in Clethrionomys glareolus or Microtus agrestis, and cortisone treatment of C. glareolus did not increase establishment. Infection of laboratory mice with the wild-strain parasite induced significant immunity to a challenge infection with the laboratory strain.

This investigation compared the effect of two common types of diet on worm burdens and faecal egg counts of pigs inoculated with Ascaris suum and Oesophagostomum dentatum. The diets were both considered nutritionally sufficient for pigs of this age, and gave high and comparable growth rates. Pigs were inoculated with both worm species at 14 weeks of age and slaughtered 3 or 12 weeks later. At 3 weeks, A. suum larvae were numerous in the small intestine of pigs fed ground barley plus protein supplement, but were not detected from pigs fed a commercial full-constituent pelleted feed. At 12 weeks, however, average adult worm burdens were low and similar in both groups. At both slaughter times, O. dentatum worm burdens were significantly higher in pigs fed barley plus protein than in pigs given commercial feed, particularly for female worms, and the commercial diet led to worms being located further along the large intestine, and to reduced worm fecundity. The chemical composition of large intestinal contents differed significantly between pigs fed the two diets.

The distribution of Trichostrongylus colubriformis in the intestine of the non-immune guinea-pig is described. At day 10 of the primary infection the majority of larvae were found in the anterior half of the small intestine with progressively smaller numbers in all parts of the gut posterior to this. However, soon after day 10 a migration of the worm population took place so that by day 15, before there had been a reduction in the total present, the majority of worms were found in the posterior small intestine. Thereafter the posterior movement continued, but while the numbers in the large intestine increased the movement then coincided with the beginning of the expulsion of the worms.

By the irradiation of guinea-pigs prior to infection the posterior migration was prevented, indicating that the latter was the result of a host response.

The independent migration of two generations of parasites was noted and two possible explanations are put forward.

This work was carried out during the tenure of a Research Training Scholarship awarded by the Animal Health Trust.

The author would like to thank Professor W. I. B. Beveridge in whose Department this work was carried out, and also Mr King of the Department of Radio-therapeutics, University of Cambridge, who irradiated the guinea-pigs used in Expt. 3.

Two experiments were carried out in which calves reared parasite-free were infected with a single dose of 3rd-stage larvae of Cooperia oncophora. In the first experiment the calves received 20000 or 200000 infective larvae and they were autopsied 28 or 56 days after the infection. In the second experiment the doses were the same but the animals were killed 14, 84 or 140 days after infection. If a dose of 20000 was given, clinical signs were never observed, while at a dose level of 200000 the weight gain was less on 56 and 84 days after the infection compared with the low-infected groups or the control animals. After 140 days the differences in weight gain were compensated. Faecal egg output was higher in the 200000 groups only in the first period of patency, thereafter the calves in the 20000 groups produced more. No obvious differences between the two infection levels were observed with regard to the haematological data. In the low-infected groups worm counts were only slightly lower when the results after 28 days were compared with those after 56 days. Also, the worm numbers after 14 days were almost equal to those after 84 days, while at 140 days 1 animal still had the same number, the other one had lost its worm burden. In the high-infected groups the worm loss was much quicker. After 28 days a great part of the population had already been lost. Obviously, at the 200000 level the reaction of the host against the parasite was much stronger. Adult worms were expelled at a higher rate than early 4th-larval stages. In the first experiment worm measurements revealed differences between the length of females, males and spicules of males, these being significantly longer in the low-infected groups. Analysis of the distribution of worms over the small intestine showed that in the low-infected groups worms were mainly restricted to the first 6 metres. In the high-infected groups the worm population was distributed more evenly over the whole small intestine.

The properties of 4 fluorescent lipid compounds in the surface membrane of adult male Schistosoma mansoni worms were examined by fluorescent microscopy and fluorescent recovery after photobleaching (FRAP). The data suggest that the probes N-(4,4-difluoro-5,7-dimethyl-4-bora-3a,4a-diaza-s-indacene-3-pentanoyl) sphingosine (BODIPY FL ceramide) and PKH2 pass through the outer membrane and enter structures in or below the membrane. In contrast 5-(N-octadecanoyl)aminofluorescein (AF18) and N-(4,4-difluoro-5,7-dimethyl-4-bora-3a,4a-diaza-s-indacene-3-pentanoyl) sphingosylphosphocholine (BODIPY FL sphingomyelin) insert into the outer monolayer. The DL values of these latter 2 compounds, 8·83 ± 2·35 × 10−9 cm2 s−1 and 2·76 ± 0·53 × 10−9cm2 s−1, respectively, suggest that they enter different domains. Furthermore, it was observed that both BODIPY FL ceramide and BODIPY FL sphingomyelin entered particular structures in or under the surface membrane. The possible nature of these particles is discussed.

We studied a total of eight developmental stages of capped brood and newly emerged workers of Apis mellifera carnica colonies naturally parasitized with Varroa destructor. During winter and early spring four colonies were fed syrup containing 1·8 mg vitamin C kg−1 (ascorbic acid group; group AA) while four colonies were fed syrup without the vitamin C (control group C). Selected elements of the antioxidative system were analysed including total antioxidant status (TAS), glutathione content and antioxidative enzyme activities (superoxide dismutase, catalase, peroxidase and glutathione S-transferase). Body weight, protein content and indices of infestation were also determined. The prevalence (8·11%) and intensity (1·15 parasite per bee) of the infestation were lower in group AA compared with group C (11·3% and 1·21, respectively). Changes in the indicators of antioxidative stress were evidence for the strengthening of the antioxidative system in the brood by administration of vitamin C. In freshly emerged worker bees of group AA, despite the infestation, protein content, TAS, and the activity of all antioxidative enzymes had significantly higher values in relation to group C.

The tapeworm Raillietina trapezoides was studied in a Tunisian population of the fat sand rat Psammomys obesus. Seasonal changes in the abundance of parasite and host were monitored in a longitudinal field survey lasting 20 months. In total 582 intestinal samples were collected during 10 trapping sessions between May 1995 and January 1997 and examined. The impact of abiotic and biotic factors on the prevalence and parasite burden were explored, using generalized linear models. R. trapezoides showed a seasonal pattern with most transmission occurring in summer and autumn. In August–September when the rodents were at low density and most adult (90–100%) were infected. In winter, infections with R. trapezoides were highly prevalent in the cohort of adults only. The worm burden by number was also high in late summer and autumn. Prevalence and parasite burden by number or by biomass were highly age dependent. Season and age act in synergy so that the rodents were highly infected in late summer and autumn. Unusually dry conditions in winter seemed to increase prevalence and to reduce the number of worms. There was no difference between males and females in prevalence or parasite burden (by number or by biomass). Prevalence was not correlated with the relative density of the hosts whereas parasite burden depended upon their densities. The more numerous the worms were, the smaller they were individually, reflecting a crowding effect. The possibility of an immune response regulating P. obesus is discussed, in regard to the very high natural prevalence and the variation in worm burden, and compared with other parasite–host systems.

The activity of atovaquone against Plasmodium berghei ANKA during sporogonic development has been examined. Anopheles stephensi mosquitoes were fed on gametocyte infected mice which had been treated 8 h previously with atovaquone or diluent alone. Mosquito midguts were examined for oocysts, and salivary gland infections were estimated using an ELISA for the circumsporozoite protein (CSP). The number of oocysts per midgut fell by at least 97% when mosquitoes were fed on mice dosed with 0·1–10 mg atovaquone/kg body weight. This was paralleled by a decrease in the prevalence of oocyst-infected mosquitoes from 70–90% in controls to 40% or 10% respectively. No oocysts were observed at a dose of 100 mg/kg. CSP ELISA results indicated that mosquitoes fed on atovaquone failed to produce sporozoites. Mosquitoes which fed on gametocytaemic, atovaquone-treated mice (0·1–100 mg/kg) did not transmit malaria to naive mice. These results demonstrate that atovaquone has a highly potent inhibitory activity against the mosquito stages of P. berghei.

High molecular weight proteinases of Trichomonas vaginalis (with apparent Mr values 142 and > 220 kDa) and Tritrichomonas mobilensis (Mr 67, 86, 104 and 120 kDa), optimally active at pH 8, were analysed in gelatin-containing polyacrylamide gels. All of these proteinases were resistant to serine-, aspartic- as well as cysteine proteinase inhibitors. Both proteolytic bands in T. vaginalis and two proteinases in T. mobilensis (67 and 104 kDa) were inhibited by EDTA and EGTA suggesting that they belong to the metallo-proteinase class. The 67 kDa proteinase of T. mobilensis was inhibited also by o-phenanthroline. The other two bands of T. mobilensis (86, 120 kDa) were not classified to any proteinase group since they appeared to be resistant to the chelating agents tested in this study.

The aim of the study was to measure the impact of Schistosoma japonicum and Trichuris suis infections in young growing pigs fed low- or high-protein diets. Thirty-two pigs, 6–10 weeks old, were randomly allocated to 2 groups receiving either a high- or a low-protein diet. After 11 weeks half of the pigs from each group were infected with 1500 S. japonicum cercariae and 4000 T. suis eggs. The weight of the pigs was measured throughout the study, and blood and faecal samples were collected every second week from the time of infection. At the time of infection the low-protein pigs had significantly lower mean body weights, haemoglobin and albumin levels compared with the high-protein pigs, and this pattern continued throughout the study. The serum albumin concentration was further significantly reduced in the infected low-protein pigs compared to the non-infected low-protein pigs. Significantly more S. japonicum worms as well as faecal and tissue eggs were found in the low-protein pigs compared with the high-protein pigs. No differences between the 2 diet groups were observed in T. suis establishment rates or faecal egg excretion. We conclude that this low-protein diet increased the establishment rates of S. japonicum, favoured larger deposits of S. japonicum eggs in the liver and faecal egg excretion, reduced weight gains and caused anaemia and hypoalbuminaemia in younggrowing pigs as compared with a high-protein diet.

The brush border of the intestinal cells of the infective larva of Trichinella spiralis is shown to consist of microvilli. It is suggested that large vesicular complexes in association with Golgi complexes may be responsible for the production of the mucopolysaccharide or mucoprotein filling the lumen of the intestine. Indirect evidence of a latent intranuclear virus infection is presented. The cuticle lining the hind gut, although continuous with the external cuticle, is not similar in structure.

I would like to thank Dr D. L. Lee for instruction in all aspects of this work, Professor Boyd for the use of the Anatomy Department electron microscope and the Agricultural Research Council for financial support.

For the tick Hyalomma anatolicum anatolicum, at constant temperature and humidity, the pattern of oviposition is constant, and consists of a peak period, usually after 2–3 days, followed by a gradual decline.

Oviposition proceeds more rapidly in constant darkness than in continuous light.

With increased temperature the oviposition period is decreased, but with increased humidity the period is extended.

The largest eggs are laid from 0 to 48 h after the peak of egg production, and no correlation has been observed between female size and egg size.

The number of eggs produced by a tick is directly proportional to its engorged weight, and since the engorged female weight is a direct reflexion of its unfed weight, the number of eggs laid is directly dependent on the size of the unfed female.

Guinea-pigs show partial immune response to adults of H. anatolicum anatolicum when the ticks are fed on them repeatedly. This minimizes the amount of nutrients imbibed and accordingly egg-laying potential is not realized.

The material on which this study was made was presented to us by Dr R. P. Chaudhuri, and we gratefully acknowledge his kindness.

It is now slightly more than 60 years since Piaget described as Haematomyzus elephantis an extraordinary insect found by him living as an ectoparasite upon an African elephant in the Zoological Garden of Rotterdam. The insect was considered by its describer to be a sucking louse, and this assignment has been accepted by almost all of the few entomologists who have since been privileged to examine specimens. Walker, who in ignorance of Piaget'os work, redescribed the species as Idolocoris elephantis, regarded it as constituting a new family of Hemiptera Heteroptera near the bed bugs. Since that time no one has questioned the belief that it is a sucking louse and for it Enderlein named a family, the Haematomyzidae, in the Anoplura.

Equine piroplasmosis (EP) is a tick-borne disease of economic importance, relevant in the international movement of equids. The causative agents are at least two apicomplexan protozoan parasites Babesia caballi and Theileria equi. To date, there is no study that estimates global and regional exposure of equids to EP. We therefore conducted a systematic review and meta-analysis to estimate the pooled prevalence and heterogeneity of EP using random-effects model. Six electronic databases were searched for publications on EP and assessed according to Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines. A total of 66 eligible studies published between 1990 and 2019 and representing 24 041 equids were included. The overall pooled prevalence estimates (PPEs) of B. caballi was 22.3% (95% CI 21.7–22.8), while the overall PPE for T. equi was 29.4% (95% CI 28.7–30.0). The overall pooled prevalence due to co-infection with both parasites was 11.8% (95% CI 11.32–12.32). Also, subgroup analysis according to sex, age, diagnostic technique, equid species, region and publication years showed a substantial degree of heterogeneity across studies computed for both B. caballi and T. equi infections in equids. Awareness of the current status of EP globally will alert the relevant authorities and stakeholders where necessary on the need for better preventive and control strategies against the disease.

An account is given of the bacterial flora isolated from the blood-sucking Reduviid bugs, Triatoma infestans and T. protracta, and the predatory Reduviid, Sinea diadema. The micro-organisms which have been found in Triatoma spp. differ from that found in Rhodnius prolixus (Actinomyces rhodnii), in both specific identity and in their relation to the cells of the mid-gut. The symbiont occurring most frequently in T. infestans has been identified as a diphtheroid organism resembling Coryne-bacterium hofmannii, and sections show this organism inside vacuoles within some of the endothelial cells of the insect's intestine. The organism occurring in R. prolixus, on the other hand, cannot be found in this situation, but remains in the lumen of the gut. While the occurrence of the bacteria found in T. infestans in so intimate a connexion with the cells of its host seems to suggest a more highly organized state of affairs, T. infestans does not show the fixed association with one species of micro-organism which is shown by R. prolixus. Other bacteria occur commonly in T. infestans, although they do not occur in cell-vacuoles; and the range of bacterial types is so great that it seems unlikely that the species recorded in this paper are the only ones that may occur. The presence of these other bacteria may be due either to the anti-biotic action of the Corynebacterium sp. being weaker than that of A. rhodnii, or to masking of the anti-biotic action by the cell wall that encloses the organisms. The situation in R. prolixus shows clearly that a constant symbiotic association with a micro-organism can be maintained without the presence of specialized organs of the mycetome type.

With regard to the predatory species, no general conclusion can be reached on the evidence so far available. Compared with the blood-sucking Reduviids, insects of this kind usually have powerful proteolytic enzymes secreted in the anterior mid-gut, while the same region of the blood-suckers is a simple storage and concentration sac, digestion taking place lower down the intestine. Thus the region of the gut where bacteria are found in blood-suckers might not be a favourable situation for them in predatory bugs. Hence it is perhaps significant that most of the few successful isolations from a predatory type were from the rectum of the insect. It is the usual opinion that insects with a predatory diet do not need bacterial symbionts, but the aim in examining the predatory Reduviidae has been to find out whether they show a condition which might have evolved into that found in their blood-sucking relatives. The search is still in progress for a rather unspecialized type of predatory Reduviid in which the salivary and anterior mid-gut digestion is less strongly developed than in those species which have been available for study up to the present.