The parasite reaction phenotype of 80 lambs was determined with natural infection on pasture. These lambs were then assigned to outcome groups and randomized into treatment groups. Developing some simple but unusual analytical techniques it was possible to demonstrate that mixed natural infections of trichostrongyles with the chief biomass component Haemonchus contortus cayugensis protected against superinfections with 35000 infective larvae but protected against superinfections with 1000 infective larvae per day only within the limits characteristic of the enclosing barn ecosystem. The limits of the barn ecosystem were less constraining on more diathetic sheep than the natural pasture infection. Internal evidence from the experiment suggests that the interaction of sheep × pasture × infective trichostrongylid larvae constrains the parasite biomass in the host in more diathetic animals at significantly lower levels. Anaphylactoid ‘self-cure’ did not occur in this experiment but something like premunition certainly did.

A new haemogregarine, Schellackia landauae sp.nov., is described in the Brazilian lizard Polychrus marmoratus (Linn) from Pará State, north Brazil. Sporozoites are found principally in the red blood cells (84%) in the peripheral blood but also occur in lymphocytes and monocytes. Experimental transmission to three uninfected P. marmoratus was achieved after feeding them with laboratory-bred Culex pipiens fatigans which had engorged on an infected lizard 14 days previously. The cycle of development in the small intestine of P. marmoratus takes approximately 30 days: schizogony, gametogony and fertilization of the macrogametocytes is in the epithelial cells of the gut, with zygotes penetrating the lamina propria, where the mature oocysts develop. Living oocysts average 14·3 × 13·3 μm, and are approximately 10·0 μm as seen in histological sections. During the period of intestinal development, the parasite also undergoes asexual multiplication within cells of the spleen and liver by a process which appears to be endodyogeny. The exact time required before the first invasion of the peripheral blood by the sporozoites remains to be ascertained, but is some time within 30–45 days after the lizard ingests the infected mosquitoes. Morphology of the sporozoite in the vertebrate host is variable and depends on the host cell occupied; there may be 1 or 2 refractile bodies. Reduction or fusion of these to a single refractile body in those sporozoites within the gut cells of the infected mosquito suggests that the bodies may represent some form of energy source that is used up during this latent phase in the insect vector. Accumulation of sporozoites takes place in the reticulo-endothelial cells of the viscera, in particular the pigmentladen cells of the liver and lung. Attempts to infect other species of lizards, Tropidurus torquatus (Iguanidae) and Ameiva ameiva (Teiidae) failed.

In snails maintained at 20 °C rediae of Fasciola hepatica emerge from sporocysts from 11 days after infection onwards. The number of mother rediae rises steadily thereafter until at least 40 days after infection. Daughter rediae are seldom observed in mother rediae dissected from snails maintained at 20 °C. Their production can, however, be stimulated by subjecting the snail host to starvation, to low, and to high temperature shocks. The parasite is susceptible to stress from immediately after infection for about 16 days, when maintained at 20 °C. In general, the more extreme the shock, the greater is daughter redial production. Increasing the length of the period of stress from 12 h up to 9 days does not increase the production of daughter rediae, nor does repeated on/off cold shocks or continuous maintenance at 10 °C. Daughter rediae develop more rapidly than cercariae and leave the mother rediae several days earlier. There is no evidence that presence of daughter rediae coincides with the suppression of cercarial production. The findings are discussed with reference to possible mechanisms by which parasite development might be controlled.

A prominent filamentous and granular cell coat is associated with the plasma membraneof haptomonads of Crithidia fasciculata attached to the cuticular lining of the hindgut of Anopheles gambiae. This surface material is completely absent from morphologically identical haptomonads from the mosquito foregut and from rosettes in culture. On the basis of these observations, it is suggested that cell coat formation is dependent on suitable environmental conditions. A cytochemical staining technique indicates the presence of carbohydrates in (a) the cell coat, (b) the outer leaflet of the plasma membrane of haptomonads from all locations and (c) small cytoplasmic vesicles and multivesicular bodies in all haptomonads. It is suggested that these cytoplasmic organelles represent stages in the intracellular pathway for material ingested by pinocytosis rather than elements involved in surface coat formation.

Larvae of Taenia pisiformis were cultured in vitro in medium containing 2·5, 5 or 20% (v/v) of normal rabbit serum (NRS). Greatest development occurred in 20% NRS, and the potency of antigens collected in medium from each culture tested by intradermal (i/d) skin tests in infected rabbits paralleled the in vitro growth rate of larvae. ‘Culture’ antigens from 5% NRS stimulated good immunity in rabbits to a challenge infection with T. pisiformis eggs, although they were poorly reactive in skin tests.

T. pisiformis larvae were also cultured in 10% (v/v) of nitrates of serum reduced to one-half of its volume by passage through 300 000 MW cut oif (XM300F) or 100000 MW cut off (XM100F) ultrafiltration membranes. Larvae cultured using XM300F had growth rates comparable with those cultured in 20% NRS, and the antigens released into the culture medium had equal potency in i/d tests and in stimulating protective immunity in rabbits. Larvae did not develop in XM100F orproduce skin-reactive or protective antigens.

Crude ‘culture’ antigen from cultures in 20% NRS was separated into 4 fractions by nitration on Sephadex G200. All of these fractions gave i/d skin reactions in infected rabbits. Fraction 3 (F3) was the most active, but was shown by acrylamide gel electrophoresis and immunoelectrophoresis to be highly contaminated with rabbit serum proteins. F3 was separated into fractions on DEAE-Sephadex A50, and the third fraction from this was as active as the original culture medium in i/d skin tests, but had only 5% of the original protein concentration. Electrophoresis demonstrated few serum contaminants, and 2 indistinct protein bands that were not present in a similar fraction of NRS.

Neither Sephadex G200 F3 nor DEAE-Sephadex F3 stimulated protective immunity in rabbits, suggesting that antigens stimulating immunity against the establishment of T. pisiformis in rabbits and those provoking cell-mediated immune reactions may be different.

The biological parameters which generate seasonal fluctuations in the size of populations of Caryophyllaeus laticeps are examined in detail. A mathematical model is formulated to describe the dynamics of the adult parasite within the fish host Abramis brama, and the predictions of the model are compared with observed population data.

The seasonality of parasite population size is shown to be caused by the combined effects of a temperature dependent mortality rate and fluctuations in host feeding activity, which controls the immigration rate of larval parasites. The observed overdispersed distribution of adult parasite numbers within the host population is shown to be generated by variability in feeding habits between individual members of the fish population.

The theoretical population model is used as a framework for the investigation of, among other factors, the comparative influences of the immigration and death rates on the dynamics of the adult parasite, the future behaviour of the system under altered environmental conditions and the importance of chance effects in the dynamics of individual parasite populations within a single host.

The stability of the dynamics of the complete life-cycle of C. laticeps is discussed in relation to the inherent biological complexity of host/helminth parasite interactions.

Immunity to the adult stage of Trichinella spiralis, assessed by an acceleration of worm expulsion, was transferred to recipient mice with mesenteric lymph node cells (MLNC) or serum taken from infected donors. Immunity was transferred most effectively by MLNC taken from donors infected for 8 days, i.e. donors actively responding to infection. Transfer of both MLNC and serum brought about a marked acceleration of worm expulsion in all cases, even where MLNC or serum given separately failed to transfer a significant degree of immunity.

Groups of mice were infected with 1,5 or 10 cysticercoids of Hymenolepis microstoma. Infections were terminated with the anthelmintic ‘Zanil’ after 5, 15 or 30 days and the mice challenged with 6 cysticercoids. The growth of the worms in the secondary infections decreased as either the intensity (number of cysticercoids administered) or duration of the primary infections increased. It is postulated that the results have an immunological basis.

The effects of complement and/or specific antibodies on the larval and adult stages of Echinococcus granulosus were studied in vitro. Lysis and death of both protoscoleces and adult E. granulosus occurred within 10 min to 24 h in 50% fresh normal sera used as a source of complement, without the presence of specific antibodies. The lytic and lethal reaction was marked in fresh sera from guinea-pigs, calves, dogs, man and sheep, but only slight in fresh sera from English rabbits and horses. Guinea-pig sera were shown to be complement deficient after reacting with worms and all reactions were abolished after sera had been heated to 56 °C for 30 min. Fluorescent antibody studies failed to detect host antibodies at the parasite tegument. It is suggested that activation of the complement system occurs via the alternate pathway, that it acts independently of the immune system and that it is lethal to a wide range of cestode parasites.

In contrast, marked agglutination/precipitation reactions with protoscoleces and precipitation reactions with adult E. granulosus were observed after incubation in heat inactivated 50% canine antisera, but not in normal sera. The antigen-antibody nature of these reactions was established by fluorescent antibody studies and the areas of antibody attack pinpointed. In spite of these reactions, worms remained healthy and active over a period of 8 days.

Sporulation rates of normal oocysts and oocysts isolated from lambs infected with coccidia and fed Aureo-S-700R for 25 days were studied at different temperatures. The viability and infectivity of the latter were also investigated.

Temperatures of 5 and 10 °C inhibited sporulation of oocysts, but when the same oocysts were subsequently incubated at 25 °C, they sporulated. At 35 and 40 °C, sporulation was initially fast, but death and degeneration of oocysts occurred at these temperatures after 3 days.

Normal oocysts sporulated faster and in greater numbers than oocysts isolated from medicated lambs; both kinds of oocysts sporulated best between 20 and 25 °C.

Lambs inoculated with oocysts from medicated lambs passed fewer oocysts for a shorter period of time than lambs inoculated with normal oocysts. The former lambs gained more weight, passed better formed faeces, ate better and had higher PCV and haemoglobin values than the latter.

Oocysts of the Weybridge and Houghton strains of Eimeria maxima and a fresh field isolate were similar and measured on average 30·9 × 22·4 μm. The Weybridge strain and the field isolate produced similar pathogenic effects in 6-week-old chickens, high doses causing 50–80% mortality and severe weight loss. The Houghton strain was slightly less pathogenic and few birds died but more oocysts were produced. With each strain, a single dose gave complete immunity to a light challenge with the homologous strain. Two or 3 immunizing doses gave complete immunity to a heavy homologous challenge but were not sufficient to protect against heterologous challenge.

The numbers of mature worms which developed in young rats after their mothers were injected with 4000 L3 late in lactation were 1% (Nippostrongylus brasiliensis) and 24% (Strongyloides ratti) of the dose administered. The low value for N. brasiliensis validates the conclusion that milk is a real and important vehicle for infection in S. ratti since possible errors from skin invasion of the young would have been common to both species.

The level of mature S. ratti infection in lactating mothers in this experiment was negligible, 97–99% of the adult worms appearing in the offspring.

These results may indicate that the milk route is possible with N. brasiliensis even though it is quantitatively insignificant.