Rohdella siamensis, a new genus and species of aspidogastrean, is described from freshwater fishes in Thailand. A new subfamily, the Rohdellinae, is erected to accommodate this worm on the grounds that it differs from all known aspidogastreans in that the male and female ducts unite to form an hermaphroditic duct, with the result that the intromittent organ is a sinus-organ and not a cirrus. A new classification of the subclass Aspidogastrea is presented. Two orders are recognized: the Aspidogastrida, containing a single family, the Aspidogastridae, which in turn contains 3 subfamilies, the Aspidogastrinae, the Cotylaspidinae and the Rohdellinae subfam.nov.; and the Stychocotylida ord.nov., containing 3 families, the Stichocotylidae, the Multicalycidae fam.nov. and the Rugogastridae. The systematic position of the Stichocotylida, and especially the Rugogastridae, is commented upon.

Fed adult Argas (Persicargas) arboreus produce a fecundity-reducing pheromone which affects all or most females in crowded conditions. Unfed adults and unfed and fed nymphs do not produce this pheromone. The effect of this pheromone is probably additive, increasing with additional crowding of adults. Mechanical disturbance is excluded as the cause of fecundity reduction. Fed females separated by a perforated barrier from crowded adults also exhibit very low fecundity. Adult excretory materials used 31 days post-feeding do not contain the fecundity-reducing pheromone. Preliminary experiments suggest that this pheromone is spatially limited in action, does not affect gonadotropic hormone synthesis and/or release, and does not induce oviposition deterrence behaviour. This may be considered to be a primer pheromone, causing alteration in normal vitellogenin synthesis and/or uptake and deposition in oocytes. The source and chemical nature of this pheromone should be investigated.

Borrelia crocidurae infection rates in different organs of adult Ornithodoros (Pavlovskyella) erraticus and O. (Ornithodoros) savignyi were studied at intervals during a 60-day period following an infective meal. The spirochaetes persisted in tick guts for 1 month, were first observed in other organs 1–7 days post-feeding, and persisted for 20–60 days in different organs. The ovaries, Gene's organ, testes and male accessory glands of only O. erraticus were infected. The infection rates in adult and immature O. erraticus and O. savignyi post-feeding on infected hamsters were 26·7–60·0% and 26·7–80·0%, respectively. Spirochaete trans-stadial transfer from originally infected larval O. erraticus to first-instar nymphs (N1) was 33·3%; to subsequent N2–N5 it was 40·0–60·0%. Infection rates in the resulting adults were 26·7% (males) and 46·7% (females). In O. savignyi, trans-stadial transfer from originally infected N1 to N2 was 26·7% and to subsequent N3–N7 13·3–33·3%; of the resulting males and females, 20·0% were infected. Transovarial transmission from female O. erraticus infected as adults occurred after the second gonotrophic cycle to 33·3–53·3% of the F1 larvae, and to 26·7 and 46·7% of the F1 males and females, respectively. All infected F1 females transmitted the spirochaetes to 26·7–73·3% of the F2 larval progeny after the first gonotrophic cycle. Transovarial transmission was not observed in O. savignyi.

The behaviour of mice exposed to graded doses of Trichinella pseudospiralis larvae was monitored in an open-field situation. Ambulatory activity declined briefly during the acute phase of the infection (day 11) but regained pre-infection levels 1 week later. Animals receiving heavy doses of T. pseudospiralis exhibited a mild increase in the level of ambulatory activity during the chronic phase of the infection. The infections did not affect the level of exploratory activity. The effects of the T. pseudospiralis infections on the behaviour of the mouse host were much less pronounced than those induced by T. spiralis. It is suggested that these differences may be associated with the small size of T. pseudospiralis and the lack of capsule formation.

The effects of the direction of gut flow, of injections of glucose and saline into different regions of the small intestine and of surgical re-routing or ligature of gastric, biliary and pancreatic secretions into the small intestine have been correlated with changes in the migratory response of the rat tapeworm Hymenolepis diminuta. Reversing the normal anterior to distal flow of luminal contents in the small intestine did not affect worm migration following feeding. Injections of a glucose-saline solution into the duodenum did not initiate a migratory response; similar injections into the mid- and posterior regions of the small intestine resulted in migrational responses similar to those following intragastric glucose feeding. Re-routing gastric secretions to the distal duodenum inhibited anterior migration of the worms beyond the new point of entry of gastric juices. Results following re-routing and ligation of the biliary and pancreatic secretions suggest that there is a potent cue to anteriad migration in the pancreatic secretions. Biliary secretions also appear to contain an additional migratory cue to worm migration. In order of importance the factors stimulating/inhibiting worm migration are pancreatic > gastric > biliary > glucose. The results support the hypothesis that the factors affecting worm distribution in the small intestine are interactive and synergistic, involve other luminal factors, such as 5- hydroxytryptamine and the physico-chemical gradients, and are of a regional nature such that the migratory response of a particular worm is directly related to its position in the small intestine when the cues to relocation are received.

Conventional mice and congenitally athymic, nude mice were infected with 20 metacercariae of the intestinal trematode Echinostoma revolutum. The sequential events in the pathological changes in the intestine were studied at different intervals post-infection. By day 11 onwards the conventional mice displayed dilatation of the region of the intestine which harboured the parasites. The mucosa in the dilated region showed marked crypt hyperplasia, villous atrophy and subepithelial fibrosis as the most conspicuous features which, together with a hypertrophy of the muscular layers, made the wall of the gut in the dilated region thicker than normal. The changes were thymus-independent as they were found to be as severe in the athymic, nude mice as in the conventional mice. The main histological features observed in the mice are discussed in relation to other conditions with similar changes, such as coeliac disease, nippostrongyliasis and trichinellosis. It is concluded that the present results support the view that there may be more than one effector mechanism of the change.

The tegumental mitochondria from the anterior, mid-ventral and mid-dorsal regions of the body surface of Corrigia vitta have been analysed using stereological and statistical methods. Mitochondria from the ventral tegument were more numerous and contained a greater density of cristae than either the anterior or dorsal tegumental mitochondria. A close association between the size and numbers of mitochondria in the anterior regions of tegument appears to be important in maintaining a relatively constant mitochondrial volume fraction. Results are discussed with respect to worm surface function in the intact host-parasite system.

Populations of Fasciola hepatica infecting sheep are regulated by at least 3 density-dependent processes. Parasite deaths due to parasite-induced primary host mortality, fluke fecundity and asexual multiplication in the intermediate snail host, Lymnaea truncatula, vary according to the intensity of infection. Empirical and theoretical evidence is used to assess the extent to which each of these processes in turn affects parasite population numbers.

The pattern of DNA synthesis in male and female Schistosoma mansoni from mixed and single-sex infections in mice has been determined biochemically and autoradiographically using the incorporation of [3H]-thymidine as a specific marker of DNA synthesis. During early development (up to 35 days post-infection (p.i.)) adult males and females from mixed infections had a comparable specific activity of DNA. In males, from 35 days p.i. onwards, the specific activity of DNA decreased rapidly to become significantly different from that observed in females. In single-sex infections DNA synthesis in females was depressed compared to that observed in males from single-sex infections and was also significantly different (P ≼ 0·01) from DNA synthesis in females from mixed infections. There was no significant difference in DNA synthesis between males from single or mixed infections. DNA synthesis in both sexes was found to be sensitive to hydroxyurea treatment, the inhibition in sexually mature females being approximately 75% and in males approximately 45%. Autoradiography using both light microscope and electron microscope techniques revealed that the testes and ovary had labelled cells. In male schistosomes the only other labelled cells were small undifferentiated cells found scattered through the tissues. In females the vitelline gland had large numbers of densely labelled nuclei within Stage 1 vitelline cells, as well as numerous small undifferentiated cells.

Volume conducted potentials were recorded from schistosomula of Schistosoma mansoni transformed mechanically (MS) and by skin penetration (SS). The spontaneous electrical activity recorded consisted of bi and triphasic transients ranging from 20 to 200 μV in amplitude and 10 to 300 msec in duration. Low amplitude potentials occurred at a much greater frequency than large amplitude potentials, which appeared to correlate with peristaltic-like contractions of the schistosomulum's musculature. Electrical activity in the schistosomulum was highly sensitive to a number of agents believed to affect metabolic pathways, the neuromuscular system or the host/parasite interface of adult schistosomes. Among the most reactive substances were potassium antimony tartrate, eserine, poly-L-arginine and potassium cyanide. Over a wide range of experimental treatments, electrophysiological responses in schistosomula transformed from cercariae by mechanical decaudation and skin penetration were remarkably similar, supporting the notion that MS are suitable material for in vitro immunochemical, biochemical and physiological study. Some treatments, however, were more or less effective in altering electrophysiological activity and motility in the schistosomulum than in adult S. mansoni. This suggests that significant physiological alterations may occur during development from skin stage to adult parasites concomitant with immunochemical and morphological changes already known to occur.

Purified eosinophil and neutrophil cationic proteins isolated from the lysosomal secretion granules of human leucocytes have been tested for cytotoxic capacity against lung-stage schistosomula of Schistosoma mansoni in vitro. Eosinophil cationic protein (ECP) caused paralysis but not death at high concentration; this effect was reversible and involved no gross pathological manifestations. Eosinophil protein X (EPX) and neutrophil cationic protein (NCP) were highly toxic at concentrations of 10−5 mol/1, and induced paralysis at sublethal concentrations. These two proteins exerted their cidal effect principally against the subtegumental musculature and internal tissues of the parasite rather than against the surface syncytium and tegumental outer membrane. ECP and NCP were shown to bind to lung worms at paralysing concentrations, but this binding occurred independently of the charge of the parasite surface. Of several control proteins tested, only protamine was capable of destroying lung-stage parasites; the manifestations of damage were different, however, from those induced by the granulocyte-derived proteins. Parallel assays demonstrated that EPX also possessed cytotoxic capacity against newly transformed schistosomula, but it was less efficient than ECP in this respect. The data are discussed in relation to potential post-skin mechanisms of challenge attrition in the immunized host.

Using groups of 4 baboons (Papio anubis), 21·0% of a trickle exposure of 480 Schistosoma mansoni cercariae/baboon (10/week for 48 weeks) were recovered as adult worms (Group A) compared with 72·6% from a single massive exposure of 2500 cercariae/baboon (Group C). Group B, exposed first to the trickle and then to the massive exposure simultaneously with Groups A and C, yielded a worm recovery of 54% which was slightly but significantly less than Group C. The trickle infection apparently induced a substantial resistance to light re-exposure, but only a partial, although significant, resistance to a massive re-exposure. In Group B, however, there was a marked reduction in the degree of gross pathology, despite high tissue egg production by the mature challenge worms. The parasitological results, in terms of resistance to reinfection by and development of pathology to a trickle infection, are not materially different from those obtained in studies using conventional heavy primary and challenge exposures with S. mansoni. The significance of these findings is discussed in relation to the epidemiology of human schistosomiasis mansoni in which heavy exposures are believed to be the exception rather than the rule.

A method is described for the reproducible purification of greater than 1·0 × 108 sporozoites of Eimeria spp. by centrifugation on metrizamide density-gradients. The mean contamination of the purified sporozoite fraction by sporocysts and sporocyst debris was less than 6% and the recovered sporozoites were fully viable, infective and ultrastructurally intact.

The initial infection and first-generation development of Eimeria tenella was quantified using a cloned MDBK (Madin-Darby Bovine Kidney) cell line, irradiated with gamma radiation prior to infection, as the host cell. Irradiated cell cultures were found to be more susceptible to infection and had a greater capacity to support parasite development than non-irradiated cultures. It was suggested that the larger proportion of cells in the G2 phase of the cell cycle, the larger individual cell size and the inhibition of cell division in the irradiated cultures were all factors contributing to the increased susceptibility to infection and capacity to support parasite growth and development. The application of this technique (host cell irradiation) to the cultivation of other intracellular, protozoan parasites is discussed.

DNA contents of individual stages of Isospora (Toxoplasma) gondii and other Eucoccida were measured after Feulgen-pararosaniline (SO2) staining either by direct microfluorometry or by scanning of microphotographic negatives. Frequency distributions were analysed using a computer program based on a mathematical model describing cell division. All stages of I. (T.) gondii, except fertilized macrogametes (2c), contained a haploid amount of DNA (1c), indicating that meiosis in I. (T.) gondii occurs during sporogony. Microgametes possessed 3·3% DNA in excess, presumably mitochondrial DNA. Nuclei of M2-and M3-merozoites differed in two characteristics: a small but distinct nucleolus was observed in almost 50% of the M2-merozoites but in none of the M3-merozoites; all M2 merozoites were strictly haploid, while all M3-merozoites were synthesizing DNA (17% above the haploid value). It may be concluded that all M2- and M3-merozoites are already sexually differentiated, i.e. are macro- and microgamontoblasts, respectively. DNA synthesis necessary for the development of the microgamont starts already in the microgamontoblast stage (M3-merozoite). M2-merozoites macrogametes, synthesize 11% extra DNA before fertilization, (after fertilization an extra amount of 12% of the diploid value was found), probably by amplification of genes for proteins which are needed for rapid maturation and later sporogony. Essentially parallel results have been found in Eimeria tenella and in crescent cystozoites of Sarcocystis cruzi. Absolute DNA values in representatives of the Eucoccida have been estimated as follows (10−15 g): I. (T.) gondii, 96; E. tenella and E. acervulina, both 75; S. cruzi, 216; Plasmodium berghei, 27. The value of the estimation of total haploid amounts as a tool in taxonomy of Eucoccida is discussed.