The histochemical localization of acid phosphatase in an adult filaria, Setaria sp. obtained from the peritoneal cavity of a cow was closely examined and compared with that of adult nematodes parasitic in the host alimentary canal; special attention was paid to the intestine and body wall of the parasites. Setaria sp. was found to show high acid phosphatase activity in the interchordal hypodermis of the body wall and uterine microfilariae, and similar activity is suspected to occur in the cuticle. The intestine of this nematode exhibited very low, if any, activity. In contrast, nematodes parasitic on the alimentary canal, such as Toxocara cati, T. canis, Physaloptera sp. and Ancylostoma caninum, showed no activity in the body wall and very high activity in the luminal surface of their intestine. The possible function of the abundant acid phosphatase in the body wall of this filaria is discussed.

The surface morphology of fixed ovarian balls from female Moniliformis dubius, aged 12, 18, 26, 28, 42, 77, 105 and 118 days, has been examined by means of scanning electron microscopy. The appearance of the surface has been found to be variable between ovarian balls from worms of the same and different ages. Some parts of the surface are seen to possess micro-projections, cavities and ridges while other parts have the appearance of an irregular meshwork of fibres. Various protruding features have been observed to extend from the surfaces of the ovarian balls taken from the inseminated female worms. In most cases, the surfaces of the protruding features differ in appearance from the surrounding surfaces of the ovarian balls. Some of these features have been assumed to represent growing zygotes and developing eggs covered by the supporting syncytium of the ovarian ball. Single or several thread-like structures have been observed in association with the surfaces of ovarian balls taken from the inseminated female worms. At present, the thread-like structures are believed to be portions of spermatozoa. By means of light microscopy, preliminary observations have been made on what is considered to be the division process of ovarian balls taken from uninseminated and inseminated worms varying in age from 7 to 98 days.

In this study two aspects of the biology of the cercaria of Himasthla militaris were examined. Firstly, the cercarial emergence from the first intermediate host, Hydrobia stagnorum, was studied. On a 9 h light (9L)/15 h dark (15D) schedule cercariae of Himasthla militaris emerged from naturally infected Hydrobia stagnorum predominantly during darkness. Inversion of the photo-period resulted in an immediate reversal of the emergence pattern. A comparison between the cercarial release patterns under natural conditions and in a constant light/temperature environment showed that an endogenous as well as an exogenous factor is controlling this process. Secondly, the penetration of the cercaria in Nereis diversicolor and the site-finding of the larva within this second intermediate host was investigated. After a short external migration on the body of N. diversicolor the cercaria enters the polychaete via the anus opening, perforates the gut-wall and moves through the coelom to the anterior segments to encyst in the muscle tissue. This internal migration results in a specific distribution pattern of the metacercariae, with more than 50% of the cysts localized in the first 12 segments and a maximum in segment number 9 (13·8%).

A novel tetrahydroquinolinyl ester, quinfamide, administered orally in multiple doses for 3 days had an ED50, of 0·25 mg/kg/day (total dose 0·75 mg/kg) for eradicating Entamoeba criceti in hamsters in several tests. It was significantly more active by direct comparison than 3 commercially available amoebicides and at least as active as 2 other esters of the parent compound, 1-(dichloroacetyl)-1,2,3,4-tetrahydro-6-quinonnol. After administration of a single dose, ED50, calculations for quinfamide averaged 0·9 mg/kg. Quinfamide was considerably more active than the other tetrahydroquinolinols, diloxanide furoate and teclozan, and it was approximately 1·5 times more active than etofamide; a statistical significance between the latter 2 drugs could be demonstrated in one of 4 tests. Administered prophylactically, quinfamide was shown to protect hamsters from re-infection with E. criceti. It also inhibited propagation of E. histolytica in vitro at a concentration of 20 /tg/ml. No adverse effects were noted in rodents after a single dose as high as 10 g/kg. Daily administration to monkeys of doses up to 500 mg/kg for as long as 37 days produced no pharmacological aberrations during or after medication; haematological studies and urine analyses were normal and no gross or microscopical tissue changes attributable to quinfamide were observed. No toxicity was revealed following acute (2 g/kg) and chronic (500 mg/kg/day × 31 days) administration of the drug to dogs and rats, respectively.

By means of light and electron microscopical techniques, the organization of the reproductive tract of female Moniliformis dubius is described. The tract consists of an efferent duct system associated with 2 ligament sacs present in the body cavity. The efferent duct system consists of uterine bell, uterus and vagina. The uterine bell contains a complex system of routes and is associated with the ligament sacs in a way that facilitates egg sorting. The dorsal and ventral ligament sacs exist with separate cavities at the posterior end, where they are attached to the efferent duct, but merge into a single sac at the anterior of the trunk.

The transmission of parasites often involves a high mortality of free-living stages in the environment outside the host. This may be offset by a high biotic potential. In addition, adaptations of nematode eggs and larvae that ensure their survival or increase their chances of infecting a host will reduce the potential wastage rate. Increasing transmission will have an effect equivalent to increasing the fecundity of the parasite and, energetically, may be the more favourable strategy.

Biological control is understood here in the classical sense, which is precisely defined by De Bach (1964) as ‘the action of parasites, predators or pathogens in maintaining another organism's population density at a lower average than would occur in their absence’. This account consists of a survey of the principal causes of disease in nematodes, with a summary of the efforts made to use certain pathogens in practise and a discussion of nematode pathology with reference to destruction of plant pathogenic nematodes.

A morphological study of the fine structure of the spores of Minchinia chitonis, a haplosporidian parasite of the chiton, Lepidochitona cinereus, is described. The spores contained a single nucleus, mitochondria, haplosporosomes, smooth endoplasmic reticulum, ribosomes and a large spherule (presumed Golgi apparatus). The spore wall was discontinuous at the spherule end, forming an opening covered by a lid which rested on a circumscribed flange. The flange of the spore wall and the lid were continuous in only one area which served as a hinge. The entire spore was encapsulated by epispore cytoplasm bounded by a strengthened membrane and extended to form 2 long projections, one at either end.

Studies were performed to identify specific parasite proteins synthesized within Plasmodium knowlesi-infected rhesus erythrocytes. Sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) of whole parasites freed from the host erythrocyte by immune lysis, of membranous and cytoplasmic parasite fractions, and of isolated merozoites, detected several parasite-specific components after Coomassie Blue staining of the separated proteins. However, significant contamination with host erythrocyte material generally occurred, particularly in the whole parasite and parasite membrane preparations. Improved identification of plasmodial proteins was subsequently afforded by a radioisotope labelling technique in which parasitized erythrocytes were cultivated in vitro with [3H] isoleucine prior to electrophoretic analysis. Of 11 principal labelled peaks ranging in molecular weight from approximately 17000 to 145000 which were detected upon electrophoresis of whole parasites harvested from culture, all were observed in the cytoplasmic fraction while at least 5 were also associated with the membranous cell fraction. Analysis of different developmental stages of the intra-erythrocytic parasite revealed no significant stage-specific qualitative variations in the electrophoretic profiles. Quantitatively, however, the middle to late trophozoites incorporated more [3H] isoleucine into protein than the other intra-erythrocytic stages. Analysis of merozoites purified from labelled schizonts showed a protein pattern similar to the other stages. This confirmed that host components did not contribute to the labelling pattern and that none of the labelled proteins were specific to the residual cytoplasm remaining after merozoite formation.

Labelled antigens sharing determinants with both membrane and cytoplasmic fractions of Plasmodium knowlesi were detected in culture medium after in vitro incubation of schizont-stage parasites previously pulse-labelled with [3H]isoleucine. Release of antigens occurred only during schizont rupture and merozoite re-invasion. Antigenic material accounted for up to a third of the total trichloroacetic acid-insoluble radioactivity released by the cells. Absorption experiments indicated that approximately two-thirds of this antibody-precipitable material shared determinants with parasite membrane antigens, with a similar quantity sharing determinants with cytoplasmic proteins. Using antisera derived against 2 different antigenic variants of P. knowlesi, no evidence for the release of variant-specific antigens was obtained. Centrifugal analysis revealed that the majority of the radio-isotope labelled antigens were particulate in nature; however, some appeared to exist in true solution.

The expression of the virulence character in the virulent line (YM) of Plasmodium yoelii yoelii was investigated. The level of virulence was measured by counting the parasitaemia of the mature red blood cells. Several sub-clones were isolated from the virulent line YM and each was tested for its level of virulence. Out of 10 sub-clones 1 showed a marked decrease in virulence. However, transmission of this sub-clone through mosquitoes fully restored its virulence. A clone isolated from the progeny of a cross between mild and virulent parents had an intermediate level of virulence. A sub-clone isolated from this intermediate virulent line exhibited greatly reduced virulence. Mosquito transmission of this sub-clone also restored its virulence to a level comparable with the virulent line YM.

There is a need for more applied and experimental research to determine more precisely the relationships between nutrition, particularly childhood malnutrition, and intestinal parasitic infections, particularly Ascaris infection. Nevertheless, it is clear that in certain communities Ascaris infection is associated with poor growth in malnourished children and that deworming improves growth. Periodic deworming of children using a mass treatment approach may be needed to control soil-transmitted helminths in areas where parasites and protein energy malnutrition are highly prevalent. The main aims of treatment should be to reduce parasite loads below the level of clinical significance for the individual child and to reduce future environmental contamination with infective faeces for the sake of the community.