Showing papers in "Parasitology in 1978"

The regulation of host population growth by parasitic species.

Abstract: The nature of parasitism at the population level is defined in terms of the parasite's influence on the natural intrinsic growth rate of its host population. It is suggested that the influence on this rate is related to the average parasite burden/host and hence to the statistical distribution of parasites within the host population.Theoretical models of host–parasite associations are used to assess the regulatory influence of parasitic species on host population growth. Model predictions suggest that three specific groups of population processes are of particular importance: over-dispersion of parasite numbers/host, density dependence in parasite mortality or reproduction and parasite-induced host mortality that increases faster than linearly with the parasite burden. Other population mechanisms are shown to have a destabilizing influence, namely: parasite-induced reduction in host reproductive potential, direct parasite reproduction within the host and time delays in the development of transmission stages of the parasite.These regulatory and destabilizing processes are shown to be commonly observed features of natural host-parasite associations. It is argued that interactions in the real world are characterized by a degree of tension between these regulatory and destabilizing forces and that population rate parameter values in parasite life-cycles are very far from being a haphazard selection of all numerically possible values. It is suggested that evolutionary pressures in observed associations will tend to counteract a strong destabilizing force by an equally strong regulatory influence. Empirical evidence is shown to support this suggestion in, for example, associations between larval digeneans and molluscan hosts (parasite-induced reduction in host reproductive potential counteracted by tight density-dependent constraints on parasite population growth), and interactions between protozoan parasites and mammalian hosts (direct parasite reproduction counteracted by a well-developed immunological response by the host).The type of laboratory and field data required to improve our understanding of the dynamical properties of host–parasite population associations is discussed and it is suggested that quantitative measurement of rates of parasite-induced host mortality, degrees of over-dispersion, transmission rates and reproductive and mortality rates of both host and parasite would provide an important first step. The value of laboratory work in this area is demonstrated by reference to studies which highlight the regulatory influence of parasitic species on host population growth.

Haemoflagellates: commercially available liquid media for rapid cultivation

Abstract: The successful cultivation of a variety of haemoflagellates in three different liquid media is reported. These media include medium 199, Grace's insect tissue-culture medium and Schneider's drosophila medium, each in combination with 30% (v/v) foetal calf serum. These media were used to cultivate Old and New World species of visceral and cutaneous human Leishmania, as well as Leishmania species isolated from sandflies, rodents, and reptiles. Four strains of Trypanosoma cruzi, an isolate of T. R-angeli and and an isolate of T. lewisi have also been cultivated in these media. One or more of these media have been used to cultivate 121 strains of haemoflagellates, including at least 14 different species (11 Leishmania and 3 Trypanosoma) and many geographic isolates or strains. The Leishmania include L. braziliensis, L. peruviana, L. mexicana, L. tropica, L. donovani, L. chagasi, L. enriettii, L. hertigi, L. hoogstraali, L. adleri, and L. agamae. Using the Schneider's based medium, we have obtained primary isolates of both cutaneous and visceral Leishmania of man and of experimentally infected laboratory rodents and canines. Freeze-dried preparations of the Schneider's based medium that were reconsituted with distilled water after 24 months of storage at ambient temperature have proven to be suitable cultivation media. This feature makes the media valuable field tools. The various species of human Leishmania cultivated in these media have in our experience demonstrated no differences in growth rate, viability after liquid nitrogen preservation, or infectivity for laboratory animals and tissue-culture cells compared with promastigotes derived from blood-agar cultivation.

Gamete development in malaria parasites: bicarbonate-dependent stimulation by pH in vitro.

Abstract: Gametogenesis in Plasmodium gallinaceum involves bicarbonate-dependent processes and requires a continuous supply of glucose (presumably as an energy source). Emergence and exflagellation of gametocytes, in vitro, occur independently of the CO2 tension but are rigidly correlated with the pH of the external medium. In bicarbonate-saline gametogenesis is initiated only if the pH exceeds 7.7. Our results suggest that gamete development of malaria parasites is stimulated when infected blood is exposed to air because the decrease in the CO2 tension of the blood causes its pH to rise.

Studies on enzyme variation in the murine malaria parasites Plasmodium berghei, P. yoelii, P. vinckei and P. chabaudi by starch gel electrophoresis.

Abstract: Electrophoretic variation of the enzymes glucose phosphate isomerase, 6-phosphogluconate dehydrogenase, lactate dehydrogenase and glutamate dehydrogenase (NADP-dependent) has been studied in the African murine malaria parasites Plasmodium berghei, P. yoelii, P. vinckei and P. chabaudi and their subspecies. Horizontal starch gel electrophoresis was used throughout. The number of isolates examined in each subspecies varied from 1 (P. y. nigeriensis) to 24 (P. c. chabaudi). Extensive enzyme variation was found among isolates of most of the subspecies from which more than two such isolates were available for study. It is clear that the phenomenon of enzyme polymorphism is of common occurrence among malaria parasites. With the exception of P. berghei and P. yoelii, of which all isolates share an identical electrophoretic form of lactate dehydrogenase, no enzyme forms are shared between any of the 4 species of murine plasmodia. By contrast, within each species common enzyme forms are shared among each of the subspecies. The subspecies are, nevertheless, distinguished from each other by the electrophoretic forms of at least one enzyme.The distribution and reassortment of enzyme variation among isolates of a single subspecies is in accordance with the concept of malaria parasites as sexually reproducing organisms. The study of variation among parasites present in individual wild-caught rodent hosts demonstrates that natural malarial infections usually comprise genetically heterogeneous populations of parasites. Nevertheless, the number of genetically distinct types of parasite of any one species present in a single infected host appears to be small. Generally not more than 2 or 3 clones of parasite of distinct genetic constitution are present in a single infected animal.

Ultrastructural evidence for complement and antibody-dependent damage to schistosomula of Schistosoma mansoni by rat eosinophils in vitro

Abstract: Rat peritoneal eosinophils adhere to live Schistosoma mansoni schistosomula in vitro in the presence of fresh normal rat serum, or in heat-inactivated serum from rats immune to the parasite. When the eosinophils are present in sufficient numbers the worms show ultrastructural evidence of surface damage and are ultimately killed. It is believed that the appearance of focal lesions in the tegument of the schistosomulum follows the secretion of enzymes by the eosinophils onto the parasite surface. The cells have been observed within these lesions and later between the basal plasma membrane of the tegument and the underlying interstitial material. It is suggested that the cells are responsible for prising the tegument away from the body of the worm. The detached tegument shows evidence of further degradation. Adherent eosinophils which have released their secretions appear to degenerate and are eventually replaced by macrophages. Remnants of both the expended eosinophils and the disrupted tegument have been identified within the macrophages. Adherence of eosinophils through C 3 –C 3 receptor interaction results in earlier and more severe damage to the schistosomula than when adherence occurs through Fe receptors. Rat eosinophils also adhere to C 3 -coated, glutaraldehyde-flxed schistosomula and C 3 -coated Sepharose beads. However, evidence of enzyme secretion is only obtained when the target is a schistosomulum.

Differences in the chemical composition and carbohydrate metabolism of Echinococcus granulosus (horse and sheep strains) and E. multilocularis

Abstract: Metabolic studies in vitro and studies on chemical composition indicate basic biochemical differences between the horse and sheep strains of Echinococcus granulosus and between these and the closely related species, E. multilocularis. The horse strain of E. granulosus has a similar level of DNA, but significantly more polysaccharides and lipids, with less RNA and protein than the sheep strain. E. multilocularis has significantly more lipids and DNA but less polysaccharides than the horse and sheep strains of E. granulosus, more RNA and protein than the horse strain but similar protein to and less RNA than the sheep strain. Incubations under air and under 95% N2-5% CO2 for 3 h show that only E. multilocularis takes up glucose, that all three forms consume different amounts of oxygen and endogenous glycogen and produce different concentrations of lactate, succinate, acetate, malate, pyruvate, propionate and ethanol as end products of carbohydrate metabolism.

Isolation of blood and intracellular forms of Trypanosoma cruzi from rats and other rodents and preliminary studies of their metabolism

Abstract: Isolation of blood and intracellular forms of Trypanosoma cruzi was made mainly from rats (90-110 g) which had received 580 rad of whole-body gamma-irradiation not more than 24 h before subcutaneous inoculation with 10(7) trypomastigotes of the Sonya strain of T. cruzi. Unirradiated chinchillas (250-350 g) were, however, used for some experiments. Blood forms were isolated using a technique involving differential centrifugation to remove most of the erythrocytes and DEAE-cellulose chromatography to remove the remaining blood cells. Overall recoveries were usually in the range 30-70%. Parasites were mainly (approximately 98%) broad forms and were motile, metabolically active (as judged by respiratory and radio-tracer incorporation studies) and had lost none of their infectivity for mice. Intracellular forms were isolated from hind-limb muscle tissue. This was disrupted in an MSE tissue homogenizer and the homogenate incubated with DNase, collagenase and trypsin. Parasites, contaminated only by a few blood cells, were then obtained by differential centrifugation. For purer preparations, a terminal sucrose gradient step was used. Recoveries ranged between 40 and 70%. About 1-3% of the parasites isolated were epimastigotes and trypomastigotes; the remainder are probably best collectively termed 'amastigotes', though they were pointed and most had a short, free flagellum. They were undamaged as judged by light and electron microscopy and metabolically active as judged by respiratory and radio-tracer incorporation studies. However, the infectivity for mice of both these purified preparations and the initial cell homogenates could be accounted for by the epimastigotes and trypomastigotes present in them. Preliminary biochemical studies with isolated parasites have shown that blood, intracellular and culture forms of T. cruzi have a respiratory system which is in part sensitive to CN- and that all forms synthesize nucleic acids and proteins when incubated in vitro. There appears, however, to be a lack of DNA synthesis in blood stages, and thus it is not surprising that these forms do not divide.

Genetic resistance to helminths. The influence of breed and haemoglobin type on the response of sheep to re-infection with Haemonchus contortus.

Abstract: The possible existence of strain and breed differences in the response of sheep to primary infections with Haemonchus contortus was examined by comparing the establishment and pathogenic effects of the parasite in Scottish Blackface and Finn Dorset sheep grouped according to haemoglobin type and infected with 7–10000 3rd-stage larvae. Homozygous haemoglobin A-type sheep of both breeds had lower worm burdens and faecal egg outputs, and suffered less severe clinical and pathophysiological disturbances than animals homozygous for haemoglobin B. In addition, Scottish Blackface sheep displayed similar advantages over Finn Dorsets with the same haemoglobin type and variations in the severity of the disease as judged by a variety of pathophysiological indices correlated closely with parasite numbers. It was therefore concluded that genetic resistance operated primarily against worm establishment and that, barring the unlikely involvement of non-specific physiological factors, this was controlled by the immune response elicited. The nature of this response is unknown, but appeared to operate only against the larval stages, since the size and metabolic activities of the surviving worms were similar in all animals. In a subsequent experiment, designed to examine the response of Scottish Blackface sheep to heavy infection (45000 larvae), there was no correlation between worm establishment and haemoglobin type. This was possibly due to a delayed immune response arising from exposure to excessive amounts of antigen.

Schistosoma mansoni : the activity and development of the schistosomulum during migration from the skin to the hepatic portal system

Abstract: The activity patterns and changes in shape of schistosomula recovered from various locations during migration, are described. There is no significant increase in length during the period which worms remain in the skin. Rhythmic cycles of extension and contraction of the worm body are established soon after penetration. Worms newly arrived at the lungs are identical with skin worms of the same age. Within the lungs their maximum length increases to four times that of skin worms, an adaptation which is believed to facilitate migration through the lumina of blood capillaries. Worms recovered from the lungs and systemic organs on, and subsequent to, day 8 post-infection retain this capacity for elongation. When worms arrive at the hepatic portal system they undergo a process of shortening and there is a transient doubling in the duration of cycles of activity. It is suggested that this shape and activity change terminates migration by preventing escape of worms from the hepatic portal system via the liver sinuses. The stimulus which triggers the response is thought to be the high nutrient levels present in hepatic portal blood, but not in peripheral blood. The stimulus which terminates migration also probably initiates growth. Worms cultured in vitro undergo some increase in length, but have a significantly lower maximum length than lung worms of a corresponding age. Although cultured worms were active, the cycles of extension and contraction were much more erratic than those of in vivo worms. The worms shortened spontaneously after 8–10 days in culture. This shortening occurred marginally later than in the most rapidly migrating worms in vivo .

Boophilus microplus: rejection of larvae from British breed cattle.

Abstract: Larvae of Boophilus microplus were labelled with [32P] and used to study the rejection of larvae from British breed cattle with different levels of resistance. On animals of high resistance the loss of larvae due to grooming ranged from 9-54% during the first 24 h of infestation, and more time was spent grooming by these animals. Most of the grooming activity could be attributed to the presence of tick larvae and the presence of older tick stages did not increase the percentage of larvae lost. Grooming was directed to attached larvae and these could be removed. Animals of low resistance did not lose a significant number of larvae as a result of grooming, but all previously infested hosts lost a proportion of the larvae (18-39%) which could not be accounted for by grooming. This loss was greater than the total loss of larvae (11%) on animals not previously exposed to B. microplus.

A freeze fracture study of the developing tegumental outer membrane of Schistosoma mansoni

Abstract: The freeze fracture technique has been used to quantify changes in the integral components of the double outer membrane of Schistosoma mansoni during the 6-week period of development within the mouse. The intramembraneous particle (IMP) density on the P1 face begins to rise within 6 h of host penetration, reaches a maximum at day 4 and then falls rapidly after day 9, so that it is at a low level between 3 and 6 weeks. The E1 face IMP density follows the same course as that of the P1 face except that maximum particle density is recorded on day 1 and the counts begin to fall on day 5. The IMP density on the P2 face remains at a consistently low level throughout development. The E2 face IMP density rises gradually to a peak at day 4, when the parasites have migrated to the lungs, and remains thereafter at a similar level, so that by 6 weeks the E2 face has a higher IMP density than the other three fracture faces. The E2 face IMP show a marked increase in size on day 4. Morphological studies indicate that a different type of inclusion body makes a transient appearance in the tegument of the lung worms, and immunocytochemical techniques show the lung worms to be nonimmunogenic. It is suggested, therefore, that the E2 face IMP may represent complexes of parasite antigens and acquired host antigens. The tegumental membranes of cultured specimens have also been examined by freeze fracturing and the IMP densities compared with those obtained from in vivo parasites; the cultured schistosomula have a lower E2 face particle density than the in vivo specimens.

Immunization of calves against Schistosoma bovis using irradiated cercariae of schistosomula of S. bovis.

Abstract: Fourteen 9-month-old zebu calves were immunized with 10000 irradiated Schistosoma bovis schistosomula given in 1–3 intramuscular or subcutaneous doses, and 4 more calves were immunized with 10000 irradiated cercariae administered percutaneously in a single dose. Eight weeks after the beginning of the experiment these calves, together with four non-immunized controls were challenged percutaneously with 10000 normal S. bovis cercariae/calf. Comparative clinical, parasitological, pathological and pathophysiological observations subsequently revealed significant differences between the vaccinated and non-vaccinated calves. The vaccinated calves showed significantly higher growth rates, and a superior body composition as indicated by their lower total body water content. The beneficial effects of vaccination were also shown by significantly lower faecal egg outputs in the vaccinated calves and by their lower tissue egg and adult worm counts. The reduced tissue egg counts were also reflected in the milder histopathological changes seen in the vaccinated calves. The vaccinated calves had significantly higher packed cell and circulating red blood cell volumes than the challenged controls, longer red blood cell half lives, and somewhat lower blood volumes and rates of red blood cell synthesis. No untoward clinical effects that could be attributed to vaccination were recorded. These results indicate that zebu cattle can be effectively protected against S. bovis by vaccination with irradiated organisms. We are now evaluating this type of vaccine in a field trial in an enzootic area in the Sudan.

Population dynamics of snail infection by miracidia.

Abstract: The essential biological features of snail infection by miracidia are incorporated into a simple model which describes the rate of change with respect to time of the number of miracidial infections/host. The model is based on the assumption that the net rate of infection is directly proportional to the density of both miracidia and hosts. Empirical evidence is provided to support this assumption. The basic framework of the model is expanded to take into account demographic stochasticity in infection and is used to predict the percentage of snails that become infected after exposure to a known number of miracidia for a set period of time. The influence of miracidial mortalities and age-dependent infectivity are examined and theoretical predictions are compared with a range of experimental results.Underlying heterogeneity in the distribution of the number of infections/snail is shown to generate an artifactual decrease in infection rates as exposure density rises, if rate estimation procedures are based on an assumption of randomness. Empirical evidence is presented to illustrate the generation of over-dispersion in the number of miracidial infections/snail under tightly controlled laboratory conditions, using supposedly homogeneous snail populations.Biological causes for underlying patterns of heterogeneity are discussed in relation to snail susceptibility to infection and ‘attractiveness’ to infective stages.

Antigenic analysis of sequential erythrocytic stages of Plasmodium knowlesi.

Abstract: 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.

Experimental studies of infection dynamics: infection of the definitive host by the cercariae of Transversotrema patialense

Abstract: The number of cercariae of Transversotrema patialense which attach to the fish host Brachydanio rerio, during a fixed exposure period, is shown to be directly proportional to cercarial density within an experimental infection arena. The distribution of successful infections/host is shown to change from a random pattern to an over-dispersed form as cercarial exposure density or duration of host exposure to infection increases. A stochastic simulation model is used to demonstrate that small differences in host susceptibility to infection, within a population of hosts, can generate patterns of dispersion in parasite numbers/host similar to those observed in the experimental studies. Differences in host behaviour, during the period of exposure to infection, are thought to generate variability in host susceptibility to cercarial infection.

Studies on the transmission and course of infection of a Kenyan strain of Theileria mutans.

Abstract: Theileria mutans (Aitong) isolated from cattle exposed in the Narok District of Kenya and blood-passaged through cattle 8 times, appeared to have lost its original pathogenicity for cattle. It was demonstrated that the parasite was trans-stadially transmissible by the tick Amblyomma variegatum but not by Rhipicephalus appendiculatus. Four tick–bovine passages were made using A. variegatum, and infective parasites were also harvested from A. variegatum nymphs which had been fed for 5 days on rabbits. Blood containing piroplasms, or lymphoid cells infected with schizonts taken from cattle, at the 2nd tick–bovine passage were shown to be infective on inoculation.The course of the T. mutans infections in the cattle was studied. In tick-induced infections macroschizonts occurred transiently, persisting longest in circulating lymphoid cells. Microschizonts were rarely detected. The macroschizonts were morphologically distinct from those of other Theileria species described from East Africa.In tick-induced infections, the piroplasm parasitaemia increased rapidly and there was evidence of restored pathogenicity of the parasite since high piroplasm parasitaemias were associated with a marked anaemia.

Life-cycle of Isospora ohioensis in dogs.

Abstract: The life-cycle of Isospora ohioensis in dogs is described. Eight dogs were killed 6, 16, 24, 48, 72, 96, 114 and 120 h after feeding 106I. ohioensis sporocysts to each. First divisional stages occurred in the jejunum at 48 h post-inoculation (p.i.). At 48 h, zoites occurred in pairs in parasitophorous vacuoles of surface epithelial cells of the jejunum. The parasitophorous vacuoles were 7–9 × 6 μm and the zoites were 7–9 × 2·5 μm in sections. At 72 h, uninucleated zoites, multinucleated zoites and meronts containing fully formed merozoites occurred in surface epithelial cells of the jejunum. At 96, 114 and 120 h asexual multiplication occurred throughout the small and large intestine, mostly in the ileum. The number of asexual generations was not determined. At least 2 structurally distinct meronts were identified at 96–120 h p.i. Type I meronts contained larger merozoites (11 × 3 μm) than those (7·5 × 1·5 μm) in Type II meronts. Meronts were merozoite-shaped and contained up to 8 nuclei. Uninucleated, binucleated and multinucleated zoites occurred within the same parasitophorous vacuole. Gamonts occurred in surface epithelial cells of the small intestine, caecum and colon, but predominantly in the ileum, 96–120 h p.i. Macrogamonts were 13–17 × 11–12 (14·5 × 12·8) μm in sections and 21–26 × 17–25 (21·7 × 17·6) μm in smears. Microgamonts were 13–17 × 8–15 (15·3 × 11·4) μm in sections and 24–30 × 15–24 (27 × 19) μm in smears and contained up to 50 microgametes. The cycle was also studied in 6 dogs killed 6, 12, 24, 48, 96 and 120 h after feeding tissues of laboratory mice that had been infected with I. ohioensis oocysts 17 days earlier. Stages were not seen in the dogs killed at 6 and 12 h p.i. Asexual and sexual stages were structurally similar in size and location to the oocyst-induced cycle but their development was faster by 24 h in the mouse-induced cycle. Extra-intestinal stages were not found in sections of mesenteric lymph nodes, spleen, lung, liver, heart, skeletal muscle and brain. However, biological evidence indicated that I. ohioensis invaded the spleens and mesenteric lymph nodes of dogs fed oocysts.

Schistosoma mansoni : evidence for a role of serum factors in protecting artificially transformed schistosomula against antibody-mediated killing in vitro

Abstract: Artificially transformed schistosomula of Schistosoma mansoni develop a consistent but small protection against the lethal effects of antibody plus complement when cultured for 24 h in a chemically defined medium. In contrast, they become rapidly resistant to antibody plus complement, when cultured in the presence of a complex medium consisting of equal parts of heat-inactivated rabbit serum and Earle's/lactalbumin or in defined medium supplemented with small amounts of heat-inactivated rabbit serum. Sephadex G-200 gel filtration revealed that the protective factor in rabbit serum is a macromolecule with a molecular weight between 7 and 19 S. Parasites cultured at 10 degrees C or in the presence of 200 microgram of puromycin show less serum-induced protection against the lethal effects of antibody plus complement than do controls.

Trichostrongylus colubriformis infection of guinea pigs: genetic basis for variation in susceptibility to infection among outbred animals.

Abstract: Two lines of guinea-pigs, whose susceptibilities to infection with the parasitic nematode Trichostrongylus colubriformis differ significantly, have been established. This difference is probably based on genetically determined differences between the ability of members of each line to bring about immune expulsion. of the parasite.

Oviposition, hatching and the oncomiracidium of Eupolystoma anterorchis (Monogenoidea)

Abstract: Eupolystoma anterorchis Tinsley, 1978, infects the urinary bladder of Bufo pardalis at the Cape, South Africa. Reproduction occurs throughout the year but the eggs are not deposited continuously: up to 300 are retained in the long uterus of the parasite and may develop to the point of hatching. The eggs are deposited intermittently en masse. The stimulus for deposition appeared to be osmotic, since worms transferred from the host's bladder into freshwater released their stored eggs. However, in simple experiments where hosts were transferred from dry land to water such egg deposition did not follow and the stimulus requires further investigation. Once discharged from the uterus the oncomiracidia hatch rapidly both in water and in host urine. Those eggs immediately expelled from the bladder at urination release larvae which can infect the same or other host individuals via the cloaca. But when eggs are deposited in the bladder between successive host urinations larvae can emerge and attach themselves directly to the bladder wall. These larvae develop to maturity alongside their parents, and this internal re-infection can give rise to massive levels of infestation. The distributions of the tegumental ciliated cells and sensillae of the oncomiracidium have been determined with silver impregnation. There are 55 ciliated cells whose pattern corresponds with that of Polystoma species except for the orientation of three dorsal cephalic cells. The distributions of their tegumental sensillae show greater divergence and the Eupolystoma larva lacks the hamulus primordia typical of Polystoma.

The energy metabolism of adult Haemonchus contortus, in vitro

Abstract: A comparison was made of the major excretory products when adult Haemonchus contortus worms were incubated with D-[U- 14 C]glucose under aerobic and anaerobic conditions. Catabolites measured were propan-1-ol, acetate, n -propionate and CO 2 and the only major difference was that nearly twice as much CO 2 both in terms of quantity and radioactivity was excreted under aerobic than anaerobic conditions. The worms were also much more physically active under aerobic conditions. When worms were incubated under aerobic conditions with increasing amounts of fluoroacetate their CO 2 production was progressively reduced to the anaerobic level. Their movement and their ability to clump together was also progressively reduced. After aerobic incubation with fluoroacetate and D-[U- 14 C]g1ucose the quantity and radioactivity of citrate within worms increased greatly. When worms were similarly incubated anaerobically no increase in citrate occurred, no radioactivity was associated with the citrate and the worms appeared physically unaffected. When worms were incubated aerobically with fluoro[1- 14 C]acetate they produced radioactive fluorocitrate.

A scanning electron microscope study of the effect of an ovicidal fungus on the eggs of Ascaris lumbricoides.

Abstract: Aspects of the ovicidal activity of the fungus Verticillium chlamydosporium Goddard on the eggs of Ascaris lumbricoides were observed in the laboratory using a scanning electron microscope. The hyphae of the fungus form structures which are considered to be penetration organs. The hyphae also form a network over the surface of the eggs. After penetration of the eggs, the hypha or hyphae ramify and the embryos are destroyed.

The metabolic profile of adult Fasciola hepatica obtained from rafoxanide-treated sheep.

Abstract: Sheep infected with adult Fasciola hepatica were drenched with rafoxanide. At 4, 8, 16 and 24 h after drenching the sheep were killed and the flukes removed, washed and rapidly frozen in liquid nitrogen. The content of key metabolites in the fermentation pathway were determined and compared with those in control F. hepatica, whose hosts were not treated with rafoxanide. Rafoxanide decreased glycogen, malate, NADH and ATP levels. The level of other metabolites in the pathway increased for the first 8-16 h after rafoxanide treatment. The marked decrease in ATP and glycogen, and the increase in total [NAD+]/[NADH] and [oxaloacetate]/[malate], together with the changed content of other metabolites, led to the conclusion that the mode of action of rafoxanide against F. hepatica in vivo is by uncoupling oxidative phosphorylation.

The effect of variations in host and parasite density on the level of parasitization of Lymnaea truncatula by Fasciola hepatica.

Abstract: Groups of the snail Lymnaea truncatula, maintained at a range of spatial densities, were exposed to different densities of miracidia of Fasiola hepatica. The resulting degree of parasitization was measured 3--4 weeks after infection. The relationship between parasite densities and parasitization appeared to be curvilinear. The lower than expected parasitization at high parasite densities could be explained by the multiple infection of some snails by two or more miracidia. The level of parasitization was not related exponentially to the temperature at which infection was carried out. This was thought to be due to the inverse relationship between miracidial longevity and swimming speed, with respect to temperature. A depth of free water overlying a mud surface was an absolute requirement for miracidia to successfully infect snails.

Host-parasite relationships of Zygocotyle lunata (Trematoda) in the domestic chick.

Abstract: Domestic chicks were infected with Zygocotyle lunata to determine gross and histopathological effects on the caecal tissues, to observe the method of feeding by worms and to examine the effects of crowding on the growth and development of the worm. Caecal weights and dimensions were significantly reduced in infected chicks. Caecal debris, abundant in control chicks, stained positive for proteins, polysaccharides, acid mucopolysaccharides and neutral fats. Caecal debris was rarely seen in infected chicks. The lumen of the intestinal caeca of the worms contained acellular material which showed protease activity and stained positive for proteins, polysaccharides and acid mucopolysaccharides. Histopathological effects of the infection showed a disruption of the architecture of host caecal mucosa, worm to worm attachment, tissue plugs in the worm acetabulum, and an engorgement of host mucosal tissue with erythrocytes. Stunting due to worm crowding was very evident and by 2 weeks post-infection, worms from single-worm infections were sexually mature and more than twice the length of immature flukes obtained from chicks infected with 100-500 cysts.

A suggested terminology for populations of coccidia (Eimeriorina), particularly of the genus Eimeria (Protozoa: Apicomplexa).

Abstract: A short list of terms has been compiled which provides for the discussion of variation of coccidia of the genus Eimeria at infrasubspecific levels Based upon this list, guidelines are given for the designation of strains and lines