All of the enzymes involved in the β-oxidation pathway were identified from juvenile and adult postparasites of the mermithid nematode Romanomermis culicivorax. The postparasites readily took up exogenous [14C-U]palmitate and oxidized it to CO2, indicating that the β-oxidation pathway is functional. The extent to which this pathway is utilized during the natural cycle of the nematode is discussed.

The results of control infections from 39 experiments using the ‘exact dose’ technique are analysed and compared with earlier large dose experiments with homogonic S. ratti. A smaller error variance and less added variance between experiments accompany the new method, which therefore provides a more precise experimental system. Using the exact dose technique, it is established that the migratory bahaviour of small numbers of L3 of the homogonic strain in lactating animals is the same as that of large numbers. In previous work the rate of migration of the homogonic strain estimated from conventional large dose experiments (Wilson, Cameron & Scott, 1978b) differed from that deduced from the use of radio-isotope labelled L3 (Wilson, 1979). ‘Exact dose’ data support results with the latter technique. There are significant differences between strains. The heterogonic larvae take longer to migrate in lactating hosts and appear to distribute themselves differently between mother and offspring. The consequences of these findings for theories of pathfinding in hosts are discussed. Experiments are also reported which failed to detect any artifact which might have resulted from ether anaesthesia of rats at injection of larval worms. This observation has implications for other studies in progress in this laboratory.

The syncytium of the scolex and neck regions of Caryophyllaeus laticeps differs from that of the remainder of the body in a number of ways. The microtriches have short shafts and lamellated spines and the surface cytoplasm is characterized by numerous elongated granules, occasional lipid-like bodies and, in the scolex region, is penetrated by ducts from the frontal glands. The elongated granules arise from the tegumentary neck cells and pass into the syncytium via narrow cell processes possessing extensions of the neck cell microtubule system. The granules have a peripheral sub-structure of regularly spaced electron-lucent areas. Evidence suggests that the granular material becomes more diffuse before extrusion. The spherical, lipid-like bodies also arise from the neck cells, but extrusion from the syncytium was not observed. Homology of the neck cells with the tegumentary cells of the rest of the body is discussed. The frontal glands are restricted to the scolex apex and secrete spherical or sub-spherical, homogeneous granules. The cells, with microtubule-lined ducts, open to the surface via pores which possess an electron-dense ring at which point the microtubule system terminates. Sensory bulbs are also present and will be described in a subsequent communication. The inter-relationships of the gland distribution, scolex morphology and host pathology are discussed.

Mice inoculated with 2000 Ascaris suum eggs 7 days before an infection with 2 cysticercoids of Hymenolepis diminuta harboured significantly fewer and/or smaller tapeworms than control mice by day 7 post-infection. When the interval between the infections was increased, the effect on H. diminuta decreased and no effect was found 21 days after the A. suum infection or if the infections were given simultaneously in ńaive or in mice immune to A. suum. Two possible explanations for the rejection and/or stunting of H. diminuta in mice infected 7 days earlier with A. suum are suggested; either a host reaction in the small intestine stimulated by the returning larvae of A. suum after their hepato–pulmonary migration or an indirect effect of decreased food intake of the host caused by this migration. It is concluded that experiments on possible immunodepressive or immunostimulating effects of parasites ought to include studies on living agents and that they should not rely on measurements of immune responses only.

Experiments were carried out to investigate the effects of Ascaris suum infection on the growth, food intake, nitrogen and fat utilization and intestinal function of young pigs receiving diets low in protein. An infection procedure was developed which provided relatively uniform and heavy infections in pigs under study. Ascaris-infected pigs showed statistically significant reduction in growth rate and food intake compared to uninfected controls. The reduction in growth rate was observed after the A. suum were mature and eggs were observed in the faeces of pigs. The degree of growth retardation was significantly correlated with worm burden. Infected pigs showed no consistent reduction in nitrogen and total solids digestibility compared to controls but fat digestion was reduced. The infected pigs showed reduced nitrogen retention compared to uninfected controls. Ascaris-infected pigs had heavier intestinal tracts with increased size of the tunica muscularis. Lactase activity in mucosa from infected pigs was significantly lower than in controls, whereas no consistent effect was observed in mucosal sucrase and maltase activity. When Ascaris-infected pigs were given an oral lactose load, blood glucose levels rose less than in control pigs, suggesting that the infection resulted in impaired lactose tolerance.

The effect of the anthelmintic Mebendazole on Cysticercus cellulosae maintained in culture medium was studied by transmission electron microscopy. In addition to the well-known morphological changes induced by Mebendazole in other cestode and nematode larvae, it also induced the cytoplasmic appearance of paracrystalline bundles in the secretory cells of the bladder wall. These bundles were formed by groups of large parallel tubules arranged in a hexagonal-like pattern. The tubules, which had an external diameter of about 50 nm and a length that might exceed 5 μm, were surrounded by a matrix and a distance between neighbouring tubules of 80–120 nm centre to centre was estimated. The tubules were stable to colchicine and low temperature. The temporary appearance of bundles is described and some alternative explanations on their origin are advanced.

Treatment of cutaneous leishmaniasis by antimonial compounds when administered by various routes to mice infected with Leishmania major or L. mexicana amazonensis is enhanced, relative to the free drug, by entrapment of these compounds within liposomes. The efficacy of the liposome treatment is dependent on the time and route of administration, and upon the phospholipid composition of the liposomes themselves. Drug-loaded liposomes administered intravenously (i.v.) are more effective at reducing the growth of a cutaneous lesion if they are administered after the nodule has begun to develop, rather than at the time of inoculation of the parasites. In contrast to the i.v. route, liposomes administered subcutaneously (s.c.) at the inoculation site are only effective if given at the time of infection.

An in vitro system is described in which over 85% of a population of Leishmania mexicana mexicana amastigotes transforms to promastigotes within 48 h. The differentiation process involves 3 morphologically and biochemically distinct intermediates, including a division stage. Cell division is shown to be necessary for complete development to promastigotes. Foetal calf serum (FCS) has been found to be an essential component of the medium for high percentage transformation to be achieved. One of the important components of the FCS has been identified as non-esterified fatty acids, and these support a relatively high percentage of amastigotes through transformation in the absence of FCS, possibly due to their use as energy substrates. Only small numbers of amastigotes transform to promastigotes if glucose or amino acids are the only energy substrates available. Transformation is inhibited by a number of metabolic inhibitors including anti-leishmanial and other anti-protozoal drugs. The stage at which inhibition is apparent varies with the inhibitor. It is suggested that the system described for the transformation in vitro of L. m. mexicana amastigotes to promastigotes may be the best method available at present for studying the metabolism and drug sensitivity of amastigotes free from possible interference by host macrophage components.

Schistosomula, surface labelled with trinitrophenyl (TNP) target antigens were tested for their susceptibility to killing by humoral- or cell-mediated anti-TNP effector mechanisms in vivo. It was found that mice passively immunized with anti-TNP serum effectively rejected an intravenous (i.v.) challenge infection with TNP-labelled schistosomula. In contrast, mice which demonstrated a strong TNP-specific, delayed hypersensitivity response to the haptenated larvae as evidenced by ear swelling, were unable to eliminate the same challenge infection. Significant passive immunization against TNP-labelled schistosomula was shown to require microlitre quantities of anti-TNP serum and could be conferred with an IgG fraction purified from the serum. The role of cells in the antibody-dependent rejection of TNP-labelled schistosomula was investigated using histopathological methods. In passively immunized mice, haptenated larvae elicited neutrophil-enriched focal reactions in the lungs and showed evidence of degeneration as early as 2 h after injection. These cellular reactions were not observed in recipients which had received prior whole-body irradiation. Nevertheless, by 24 h TNP-labelled larvae were found to have been killed in the lungs of the irradiated mice despite the absence of significant cellular attack. The above observations suggest that the antibody-dependent destruction of haptenated schistosomula results from two overlapping responses, an early response mediated by radio-sensitive cells and a second, radio-resistant response manifesting its effects at later time points. Since mice genetically deficient in the fifth component of complement fail to develop the later response, it probably reflects the effect of the lytic pathway of complement on the parasite.

A passive transfer system, dependent upon hyperimmune rat serum, was used to study in vivo protective humoral immunity to Schistosoma mansoni infection in Fischer rats. Infected recipients of hyperimmune serum exhibited a significant reduction (51%) in the number of recovered adult schistosomes relative to infected recipients of normal rat serum. Furthermore, schistosomula were equally sensitive to the effects of hyperimmune serum injected up to and including 7 days post-infection, a phenomenon which was termed ‘extended sensitivity’. Schistosomula were beginning to lose sensitivity to the effects of hyperimmune serum by the 8th day post-infection and were completely refractile by the 9th day. In addition, it was demonstrated that parasite elimination occurred after the lung stage. Some protection was also observed when hyperimmune rat serum was transferred to mice as late as 5 days post-infection.

Cercaria vaullegeardi develops in daughter sporocysts within the digestive gland of the prosobranch Gibbula umbilicalis. On emergence into the host mantle cavity the cercarial body retracts into the cystophorous tail, the ‘encysted’ cercaria being then shed into the sea. The encysted cercaria is described at the ultrastructural level for the first time and developmental stages are redescribed. The cercarial body has no penetration or cystogenous glands: a single type of sub-tegumental secretory cell produces vesicles containing neutral mucopolysaccharides which pass into the tegument at encystment. The immotile cystophorous tail consists essentially of a fibrous caudal cyst and 8 appendages including a delivery tube. Scanning electron micrographs show the surface of tegumental membranes enveloping the caudal cyst to be covered with a honeycomb pattern of indentations derived from electron-lucent vesicles produced by the caudal gland. The fibrous-walled delivery tube comprises proximal and distal sections and a modified terminal end-piece.

The inoculative mechanism whereby cystophorous cercariae infect the copepod 2nd intermediate host is described for the first time in Cercaria vaullegeardi. Experimental infections of the harpacticoid copepod Tigriopus brevicornis are recorded and the infection process is related to the ultrastructure of the cercaria and to the feeding mechanics of harpacticoids. The cystophorous tail of C. vaullegeardi is shown to be a device whose shape and construction ensure that the cercarial body is neither damaged by copepod mouthparts nor swallowed, but reaches the host haemocoel during the initial stages of feeding. The cystophorous tail consists essentially of a caudal cyst, into which the cercarial body retracts at encystment, and various appendages including a delivery tube. The infection mechanism is triggered when the copepod mandibles bite the narrow posterior caudal cyst beak, when the delivery tube everts into the mouth and penetrates the dorsal mid-gut wall. The cercarial body, lubricated by tegumental secretions, passes simultaneously through the delivery tube and is inoculated into the host haemocoel.

Tsetse flies (Glossina morsitans) were fed on the blood of mice containing any one of 5 variable antigen types (VATs) of Trypanosoma brucei AnTAR 1 serodeme. The VATs of the metacyclic trypanosomes subsequently detected in the flies' saliva probes were investigated using monospecific antisera to AnTAR 1 VATs in indirect immunofluorescence and trypanolysis reactions; these sera included 3 raised against AnTats 1.6, 1.30 and 1.45, previously identified as components of the metacyclic population (M-VATs), and against the 5 VATs originally ingested by the flies. The percentage of metacyclics reacting with a particular M-VAT antiserum remained more or less constant (AnTat 1.6, 6·0–8·3%; AnTat 1.30, 13·7–18·2%; AnTat 1.45, 2·0–8·0%), regardless of the age of the fly or the ingested VAT. As these 3 VATs accounted for no more than 30% of the metacyclic population, the existence of at least one more VAT is envisaged. The ingested VAT could not be detected among the AnTAR 1 metacyclic trypanosomes.

Tsetse flies were infected with 5 different variable antigen types (VATs) or with a mixture of VATs of the AnTAR 1 serodeme of Trypanosoma brucei. Metacyclic forms from the salivary glands of infected flies were used to initiate infections in mice. Immunofluorescence and trypanolysis reactions employing 24 monospecific antisera were used to analyse the VATs present in the mice following cyclical transmission. Regardless of the VAT used to infect tsetse flies, the first VATs detectable in the bloodstream were those previously identified as metacyclic VATs (M-VATs). These were present until at least 5 days after infection, at which time lytic antibodies against at least 2 of the M-VATs were detectable in the blood of infected mice. In mice immunosuppressed by X-irradiation the M-VATs were detectable in the bloodstream for longer periods, but the percentage of the population labelled with anti-metacyclic sera showed a decrease on day 5 as in non-irradiated animals. The VAT ingested by the tsetse was always detectable early during the first parasitaemia following cyclical transmission and was usually the first VAT detected after the M-VATs. Neutralization of selected M-VATs before infecting mice resulted in elimination of the neutralized M-VAT from the first parasitaemia but had no effect on the expression of other VATs in the early infection.

125I-labelled, isolated variable surface glycoproteins (VSGs) of Trypanosoma b. brucei bind both homologous and heterologous anti-VSG sera and binding to heterologous antisera may be blocked by other unlabelled VSGs (Barbet & McGuire, 1978). This paper presents results which suggest that oligosaccharide residues have importance in the antigenic structure of VSG cross-reacting determinants. The ability of VSG to bind heterologous anti-VSG sera was destroyed by periodate oxidation but not by extensive proteolysis. A VSG glycopeptide fragment was isolated from two different VSGs, which blocked by 100 % the binding of VSG to heterologous anti-VSG sera and therefore contained the cross-reacting determinants. The native glycopeptide fragment was resistant to digestion with trypsin, pronase or leucine aminopeptidase and prolidase. We also show that a VSG synthesized in the reticulocyte lysate cell-free system was not immunoprecipitated by heterologous anti-VSG sera in contrast to the same VSG labelled by metabolic incorporation of [35S]methionine in vivo.

Haemonchosis is an acute problem in India. Three species of Haemonchus occur. These are H. contortus (Rudolphi, 1803) which occurs in sheep, goat, cattle, buffalo and other ruminants; H. longistipes Railliet && Henry, 1909 occurring in camels and H. similis Travassos, 1941 in cattle. Seasonal fluctuation of H. contortus occurs, with infection being more frequent in autumn ≻ summer ≻ winter ≻ spring, and infection in sheep and goats has been reported to be 100 %. Various aspects of haemonchosis have been investigated. However, the fundamental and the most challenging areas in Haemonchus research remain almost untouched. In order to forecast the development of haemonchosis, epidemiological studies should be undertaken on the prevalence, distribution and seasonal incidence of the worm to understand the effects of climatological factors like rainfall, humidity and temperature. The sparse and inadequate studies of metabolism need to be extended to other areas of Haemonchus biochemistry to provide additional possibilities for exploration of hostparasite differences. Clinical haemonchosis in sheep, goats and other ruminants should be studied in order to calculate losses caused by mortality and the cost of anthelmintic medication. Most anthelmintics are expensive, and are not easily available to our farming community, therefore a search for many more indigenous anthelmintics (such as Wopell, Krimos, Sonex etc) must be made. Detailed knowledge of the mode of action and route of entry of anthelmintics at the molecular level could also be beneficial, particularly when the strains of H, contortus have been identified as resistant to some anthelmintics. The prospects of producing a vaccine against H. contortus should be explored. Attempts in this field have already been made by overseas workers (see Clegg && Smith, 1978) and in India too, work has been undertaken at Kerala (Sathianesan, personal communication). Therefore, because of its economic importance and wide distribution, H. contortus provides fascinating research material particularly in the warmer regions of the world.