On three occasions, antibody positive blood from wild red deer produced overt infections with Babesia when inoculated into splenecto-mized red deer. One of the deer also became infected with Eperythrozoon sp. Babesia divergens, B. capreoli and the Babesia of red deer are morphologically similar and the marginal position of the parasites in the host cell is characteristic. Babesia were not seen and no antibody was formed in five out of six splenectomized bovine calves which were injected with parasitaemic red deer blood. Two of these calves when challenged with B. divergens were fully susceptible. A transient infection with the deer Babesia may have occurred in the sixth calf since antibody was detected and the animal resisted challenge with B. divergens.In indirect fluorescent antibody tests there was little or no difference in the titre of sera from naturally or experimentally infected cattle and deer when reacted with B. divergens or the red deer Babesia antigens. Despite their similarities, specific status for B. divergens and the red deer Babesia is probably justified; at present there is insufficient evidence to justify separation of the red deer Babesia from B. capreoli.

The ultrastructural changes accompanying oocyte differentiation in the ovaries of the monogeneans, Diclidophora merlangi, Diplozoon paradoxum and Calicotyle kröyeri have been described. In each case, oogenesis in the ovary proceeds as far as meiotic prophase in the primary oocyte. A three-stage sequence of development based on oocyte morphology is proposed: (1) Oogonia and early, immature primary oocytes are typically undifferentiated, with chromatin-laden nuclei occupying most of the cell volume. The cytoplasm contains small clumps of mitochrondria and unattached ribosomal aggregates. There is evidence of mitosis and, in later stages, meiotic prophase is indicated by the appearance of nuclear synaptonemal complexes. (2) Maturing primary oocytes are characterized by increased nucleolar volume associated with the production of RNA for export to the cytoplasm. An organized GER and Golgi apparatus are established and involved in the synthesis and packaging of membrane-limited cortical granules. Annulate lamellae and nucleolus-like bodies appear in the cytoplasm and, with development, the cells increase in size and, peripherally, become interdigitated. (3) Mature primary oocytes represent a resting phase when cellular activity is minimal. Golgi disappear and the ER fragments or becomes reduced in dimensions. Mitochondria and free ribo-somes are numerous and cortical granules move to the cell periphery. The cells separate and, when mature, are released from the ovary. There are minor species differences in oocyte ultrastructure and development.

An attempt was made to determine the relative importance of the different life-cycle stages of Eimeria maxima in the induction of immunity and also those stages most affected by the immune response of the host. In one experiment the life-cycle was controlled by chemotherapy but in all other experiments partial life-cycles were induced by transfers of infected mucosa between hosts.

The results indicated that the second generation schizont stage is probably that most concerned in the induction of protective immunity and that sexual stages are most susceptible to immune inhibition. After initial inhibition in the immune host the earlier asexual stages were able to resume development when transferred to a susceptible host. The longer the period of exposure to the immune environment, the less able was the parasite to recover.

Young, previously uninfected white mice became infected with Hymenolepis nana when exposed in small cages to parasite eggs which had been sprinkled in suspension onto the floor of their cage, or to faeces from mice with patent infections. The mean daily probabilities of infection for individual eggs under these two conditions were 2·9 × 10−6 and 5·4 × 10−6 respectively. If the mice were starved for 24 h prior to exposure to faeces, then the mean daily probability of infection increased to 2·6 × 10−4. These differences in transmission are interpreted as being due to differences in the extent of coprophagy; they are not due to any effect of starvation on the hatchability of eggs.

A primary infection with Schistosoma mansoni, of 5 or more weeks duration, stimulated a high level of resistance to a challenge infection in the WO outbred strain of golden hamster. In sharp contrast, the LGN strain showed no statistically significant immunity to reinfection in most experiments and where detected the level of resistance was only about half that observed in the WO strain. Immunity to reinfection was assayed with the lung recovery method which assesses resistance a few days after challenge and with the conventional perfusion assay which measures immunity 6 weeks after challenge. Wide differences in the immune response to S. mansoni in different strains of the same host species have not been reported previously.

Hamsters (WO strain) with a primary infection of Schistosoma mansoni or S. haematobium rapidly developed immunity to homologous challenge judged by the lung recovery assay. Immunity was detected at 4–5 weeks and reached a plateau 6 weeks after infection.

Using this information, hamsters with an 8-week primary infection with S. mansoni or S. haematobium were tested for resistance to homologous reinfection and resistance to a challenge with the other species of schistosome. Primary infection with S. mansoni or S. haematobium conferred a high level of immunity to reinfection with either species of schistosome judged by the perfusion assay, involving recovery of adult worms 6–10 weeks following challenge. Estimation of the level of immunity with the lung recovery assay, 5 days after challenge, indicated that immunity due to a primary infection with S.mansoni acted at or before migration of the challenge through the lungs but immunity stimulated by a primary S. haematobium infection was only partially effective at the lung stage and substantial destruction of challenging organisms occurred at a later stage of development.

Antibodies in immune sera of hamsters with a primary S. mansoni or S. haematobium infection were shown to bind to common antigens on the surface of young schistosomula of either species by u.v. microscopy using as detecting agent a fluorescein-labelled rabbit antiserum directed against hamster globulins.

By means of conventional light microscopical and counting procedures, estimations have been made of the average number and size of ovarian balls from unfertilized and fertilized female Moniliformis dubius. The observations were made on worms recovered from experimental primary infections lasting 1, 2, 3, 4, 5, 8, 11, 14, 17 and 20 weeks in male rats. The number of ovarian balls rises to about 6300 per worm, with the maximum being attained more rapidly in unfertilized than in fertilized females. On average more ovarian balls were present in unfertilized than in fertilized females, but a marked decline in number occurred in both groups of worms towards the end of the experimental period. Similarly, on the basis of the area within the elliptical profiles of fixed ovarian balls, it appeared that those from unfertilized females were generally larger on average than those from fertilized worms.

Almost 100% of 7- to 10-day-old Hymenolepis diminuta became established when surgically transplanted from donor mice into the duodenum of naive recipient mice. Transplanted tapeworms survived 8–12 days, by which time they had survived much longer in total than they would have done in the donor. Mice previously immunized by a primary infection rejected transplants within 4 days. Sub-lethal irradiation (550 rad) delayed rejection by immune mice but such mice still rejected worms much more quickly than did naive mice.

Surgery was shown to delay by 2–3 days the rejection of worms by naive mice, and the importance of circumventing surgery by administering the worms per os is emphasized.

Prospects for reconstituting irradiated immune mice are considered vis-à-vis work with nematodes, and the differences which, on present knowledge, appear to exist between nematode and cestode rejection are briefly discussed.

A particulate polysaccharide was isolated by differential centrifugation and alkali extraction from homogenates of the cestode Moniezia expansa. The polysaccharide had the structure of a glycogen. Its chemical properties, infra-red spectrum and optical rotation showed that it consisted of α-1, 4- and α-1, 6-linked glucopyranose units. Examination of the complex with iodine and the precipitate with concanavalin-A showed that the structure was highly branched. Oxidation with periodate and hydrolysis with α- and β-amylase were used to measure mean chain lengths. For the particulate preparation the average chain length was 12·9 glucose units and the exterior and interior chain lengths were 9·0 and 2·9 units respectively. The particulate preparation had a very high sedimentation constant (s20, w = 910) with a smaller component at about s20, w = 600, but the alkali extracted material had an s20, w = 61 similar to that shown by alkali degradation of the particulate preparation. The morphology of the particulate material was similar to that of rat liver glycoge, α, β- and possible γ-particles being identified by electron microscopy. The α-particles were relatively stable under acidic conditions remaining intact down to pH 2·5. At pH 1·7 the α-particles dissociated into their constituent β-particles with a consequent decrease in the opalescence of the solution. The nitrogen content of 0·9% was high for a glycogen.

Larvae of Hymenolepis diminuta develop in the haemocoele of the beetles Tribolium and Tenebrio, and of the locust Schistocerca gregaria, without being encapsulated by haemocytes. The mechanism of this evasion of the haemocytic defence reaction has been examined using various techniques. Larvae grown in culture and injected into S. gregaria have few or no haemocytes adherent even after 8 h, although latex beads injected at the same time have been thickly encapsulated. This, and results of transplanting cysticercoids and host tissue between different insect species, suggests that the surface of the larvae may bear an inherent similarity to the surface of host tissues and thus escape recognition as ‘not-self’ by the host’s haemocytes.

The initial process in the hatching mechanism of Ascaris eggs is the sudden onset of permeability in the previously impermeable ascaroside membrane. During this change the ascaroside membrane remains intact and no chemical changes can be detected. Using the molecular probe 1-anilino-8-naphthalene sulphonic acid no conformational changes were detected in the ascaroside membrane during the induction of permeability. It is suggested that either the permeability change is due to a very localized chemical or conformational change, not detectable by conventional analytical techniques, or the change is due to mechanical damage of the ascaroside membrane, brought about by the activity of the infective larva.

Growth and behaviour of Boophilus microplus larvae on British breed cattle, with different resistance levels to the tick, were studied to elucidate the nature of resistance. On highly resistant animals, larval growth rate was slower for the first 3 days, but by day 4 they had attained the normal weight and the majority were subsequently able to moult.

Using phosphorus-32 labelled larvae, it was found that attachment times were shorter and more time was spent wandering on highly resistant animals during the first 16 h. On the second day, attachments had stabilized, but more detachments were still made from highly resistant animals. This was considered to impose an additional stress as the cattle skin environment can rapidly desiccate larvae. However, the larvae were able to compensate by uptake of fluid from the host.

Loss by repulsion of live larvae from the host or drowning in serous exudate were also not considered of major importance. The nature of rejection is discussed in a further paper.

The distribution of larvae after 24 h suggests that their early behaviour largely determines the areas favoured by adults. Movement to, and accumulation in, favoured areas is discussed.