During my third year as an undergraduate reading Zoology at Cambridge, I found a relatively large parasite inside one of the Asellus aquaticus that had been allocated to me for the afternoon's practical work. After we had failed to identify even the group of animals to which it belonged, someone suggested that I should take my find to The Molteno Institute on the Downing Site. There I was ushered into Room 3 where I first met Dr Tate. After listening to my account he looked at my specimen and said, ‘Now just one second …’ in his rich Irish accent. As I later came to know, so much of his teaching or advice began with that highly characteristic phrase. He told me that I had found an acanthocephalan worm in its intermediate host, and when I returned some days later to tell him the results of my search of the literature, he suggested that I should work on the Acanthocephala under his supervision for the Ph.D. Degree after my graduation. I never regretted for one moment my decision to take up his offer. He maintained close contact with me, as he did with all his former research students, and the last letter I received from him was dated 16 September 1985, written just a few weeks before his death on 7 November 1985 in hospital in Cork. During the 24 years of our association I was never on Christian-name terms with him. He was always ‘Dr Tate’ or, when talking with equally close mutual associates like Donald Lee, David Molyneux, John Barrett, Vaughan Southgate or Roger Tatchell, we referred to him as ‘P.T.’. He had great integrity and fairness in all that he did and an ability of seeming to know exactly what you were thinking. These attributes, coupled with his extraordinarily wide parasitological knowledge, generated our respect. He also had a delightful sense of fun and even his sarcasm was kind and gentle. Our children loved him and his steady supply of sweets for those who visited him in Room 3 and the book tokens that came without fail every Christmas were expressions of his kindness.

Changes in the response of black mollies Poecilia latipinna to infection with Ichthyophthirius multifiliis subsequent to single I. multifiliis infections were examined experimentally. Incomplete resistance to infection was established, the degree of which did not depend on the intensity of the initial infection. Resistance was maintained for longer periods, however, by those fish with higher initial levels of infection. Previous experience of infection by their hosts had a significant, though small, effect on the time for which trophozoites remained on the fish. The influence of these results on the population dynamics of the Ichthyophthirius-fish interaction is examined with the aid of simple mathematical models.

An automated suspension culture system for the cultivation of Plasmodium falciparum is described which retains a degree of flexibility which is absent in other automated culture apparatuses. Not only does this system of cultivation promote rapid multiplication of asexual parasites but also permits the development and maturation of gametocytes. Using a combination of gelatin flotation and N-acetyl glucosamine treatment synchronous development of gametocytes was achieved. The total time for gametocyte maturation in vitro under the conditions provided was 7 days. Stages II and V required 48 h for development whilst I, III and IV needed 24 h each. Mature microgametocytes were relatively long lived in comparison with macrogametocytes. Electron microscopic study of the synchronized stages confirmed the observations of Sinden (1982) but, in addition, we noted the presence of Garnham bodies, a cytostome in all stages and dense spherules in stages I–III similar to the fenestrated buttons in sporozoites and exoerythrocytic forms. The relationship between the number of osmiophilic bodies in the mature gametocytes and their ability to escape from the red cell is reaffirmed.

The uptake of radioactive pyrimethamine by a sensitive and a resistant strain of Plasmodium falciparum, the metabolic fate of pyrimethamine inside these parasites and the kinetic properties of dihydrofolate reductase (DHFR) from both strains have been studied. Uptake of the drug was identical in both strains and no metabolite of pyrimethamine was found in either strain. DHFR from the resistant strain was 300 times less sensitive to inhibition by pyrimethamine than the enzyme from the sensitive strain, while the Michaelis constant for dihydrofolate remained unchanged and inhibition was competitive in both cases. Altered properties of plasmodial DHFR are apparently the only mechanism responsible for pyrimethamine resistance in the strain of Plasmodium falciparum studied.

Four common blood parasites belonging to the genera Babesia, Hepatozoon, Trypanosoma and Grahamella were detected in sympatric populations of Clethrionomys glareolus and Apodemus sylvaticus. Seasonal changes in the abundance of hosts and parasites were monitored in a longitudinal field survey for 18 months. All parasites in both hosts showed similar seasonal patterns with most transmission occurring in summer and autumn and ceasing in winter. Amongst aged subsets of each host population, Hepatozoon and Grahamella spp. were primarily parasites of young animals whereas Babesia and Trypanosoma spp. generally infected older hosts. Data from the aged subsets were also used to estimate values for the basic reproductive rate, R0, for each parasite. In C. glareolus, R0 = 2·0 for B. microti, 2·6 for H. erhardovae, 1·7 for T. evotomys and 2·8 for Grahamella sp. In A. sylvaticusR0 = 2·2 for Grahamella sp. These estimates are probably representative only for summer and autumn of each year.

Genetic proximity between two karyotypic groups of Trypanosoma congolense was investigated using as hybridization probes: (i) total genomic DNA, (ii) a 35 nucleotide long synthetic oligonucleotide, and (iii) non-variant antigen type (non-VAT) specific complementary DNAs. The phylogenetic relationship between Trypanosoma brucei and T. evansi, both of which are accepted species in the subgenus Trypanozoon, was used as a reference to assess the phylogenetic proximity of the two groups of T. congolense. Results indicate that some morphologically indistinguishable T. congolense populations differ in a variety of molecular and genetic properties: molecular karyotypes, majority of the DNA sequences, and the restriction enzyme sites in the genomic environments of various conserved genes. The implications of these findings for trypanosome evolution and T. congolense epidemiology are discussed.

The cutaneous cellular reactions associated with aquisition of resistance by cattle to Hyalomma anatolicum anatolicum feeding were investigated by comparing the nature and sequence of cellular events at H.a. anatolicum feeding sites following primary and tertiary infestations. Cattle acquired resistance to H.a. anatolicum feedings after a single infestation. The resistance was manifested by a significant reduction in the mean weight of engorged females and mean weight of egg mass produced, failure to lay eggs and sometimes death of ticks in situ. The acquisition of resistance corresponded with pronounced epidermal vesiculation and a significant change in the nature of the cellular infiltrate at tick feeding sites indicating the development of cutaneous hypersensitivity. On primary infestation the cellular infiltrate was dominated by neutrophils (43–71%) followed by mononuclear cells (25–35%). Basophil and eosinophil infiltration in small numbers was noticed for the first time at 72 and 144 h, respectively, post-primary infestation. Unlike primary infestation, the dermal infiltrate on tertiary infestation, 24 h after attachment, was characterized by infiltration of basophils (6%) and eosinophils (3%) and a marked degranulation of mast cells and basophils. Basophils showed a consistent increase in absolute as well as relative numbers as the feeding advanced. They were the second most abundant cell types after neutrophils (48–68%) at 72 h (16%), and 144 h (23%). Eosinophils (3–9%) and mononuclear cells also showed a significant increase in their mean numbers as compared with primary infestation. There was a progressive decrease in the number of detectable mast cells following tick infestation and they were significantly lower post-tertiary infestation, compared to primary infestation. These results suggest that the pharmacological mediators released by degranulation of mast cells and basophils are perhaps the major effectors of resistance in cattle to H.a. anatolicum.

Excretions and secretions (E–S) were collected from a series of developmental stages of Litomosoides carinii maintained in vitro. Measurement of the protein content of E–S obtained from each stage indicates that the rate of production of E–S varies enormously during development of the worm. E–S was iodinated using both Iodogen and the Bolton and Hunter Reagent and was also biosynthetically labelled by incubating worms in the presence of [35S]methionine and [3H]leucine. Attempts to biosynthetically label E–S of mature worms and microfilariae with [3H]glucose were unsuccessful. Examination of radio-isotope labelled E–S by SDS–PAGE revealed that some components were sex specific and that the differences in total E–S production during development were due to the existence of both stage-specific components and components whose rate of release varied during parasite maturation. Antigenic characterization of E–S, carried out by immunoprecipitation in combination with SDS–PAGE, indicated that E–S consists of immunogenic components, a molecule which is probably a non-immunogenic parasite product, and host albumin. The implications of these findings for the construction of diagnostic tests to detect products of human filarial parasites are discussed.

Experiments to investigate the linked metabolism of L-serine and L-alanine by Moniliformis moniliformis in vitro were carried out by incubating adult worms aerobically for 3 h at 37 °C in Tyrode’s solution containing L-[U-14C]alanine and other amino acids. When present in the medium alone, alanine was totally removed by the worms and metabolized almost entirely to ethanol and a compound identified as carbon dioxide. When present in the medium with serine and no other amino acids, alanine was largely metabolized as before but additional alanine, believed to originate from serine, was excreted. The same results were obtained with serine and 16 other amino acids in the incubation medium.

An instrument for measuring the motility of larval and adult nematodes is described along with an analysis of its use as a tool to analyse drug action on these parasites. Motility was detected from larval parasites of Nippostrongylus brasiliensis and Ascaris suum in the absence and presence of various anti-nematodal drugs. These agents produced, within 48 h, a significant decrease in larval parasite motility. The instrument was also capable of detecting the motility of Caenorhabditis elegans, adult female Brugia pahangi and their response to anti-nematodal drugs. The design of the instrument allows us to accurately measure motility in a single sample within 60 sec.

Protoscoleces of Echinococcus granulosus were incubated in a 10 μm solution of monensin and their viability and the ultrastructure of their tegument were monitored over a 36 h period. The earliest effects of the lonophore, apparent within 15 min, involved a degree of cisternal swelling of the tegumentary Golgi complexes. Swelling became more pronounced with time and cytons eventually contained numerous large electron-lucent vesicles. Residual bodies indicative of autophagy were observed in the cytons and distal cytoplasm from 1 h onwards. All movement of protoscoleces ceased after 1 h and the surface of the soma subsequently became folded, possibly suggesting spastic paralysis. Later, vacuoles and large cytoplasmic blebs were observed in the distal cytoplasm and viability dropped rapidly after 12 h. All protoscoleces were dead at 36 h. The potential of monensin as an in vivo protoscolicidal agent is discussed.

A comparative study has been made of the progress in the control of ovine echinococcosis caused by Echinococcus granulosus and the ovine cysticercoses caused by Taenia hydatigena and T. ovis in New Zealand. The methods of control included an educational and a dog-dosing programme. In the Styx field trial, the Otago/Southland Surveillance Programme and the national control programme, E. granulosus declined towards extinction. In contrast, this same control effort transformed the cysticercoses from hyper-endemic to endemic status with focal epidemics. In this unstable state, the density-dependent constraint was negligible and superinfection occurred.

The life-cycle of Haemonchus contortus, a pathogenic stomach nematode of sheep, is typical of those of the other members of the superfamily Trichostrongyloides, all of which require a period of development outside the definitive host. Classically, gravid H. contortus, known as strictly oviparous, releases her eggs into the abomasal lumen. The eggs are passed out in the faeces in which they hatch into the 1st-stage larvae and then develop into the infective 3rd-stage larvae. We have developed a method to study the fate of eggs within gravid worms. Using this procedure, we have shown that H. contortus may also exhibit viviparity with apparently normal development from the egg to the 4th larval stage taking place within the gravid female maintained in vitro. On the basis of these observations we speculate that viviparity might occur in vivo with consequent autoinfections; if so, this might explain some puzzling clinical and epidemiological features of haemonchosis, as well as the incomplete efficacy of current control measures.

The genetic structure of Anisakis physeteris from the Mediterranean Sea has been analysed electrophoretically at 22 enzyme loci. The samples studied, although differing in the life-stage (larvae and adults), and in the host (the fishes Micromesistius poutassou and Trachurus trachurus, and the sperm whale Physeter macrocephalus) were genetically homogeneous. Of these loci 11 (Ldh, Sod, Np, Adk-2, Pgm-1, Est-1, Est-2, Acph-1, Acph-2, Lap-2 and Ca) were found to be monomorphic, while the other 11 (Sdh, Mdh, ldh, 6-Pgdh, G3pdh, Got, Adk-1, Pgm-2, Lap-1, Mpi and Gpi) showed from 2 to 7 alleles. The following values of genetic variability were estimated: He = 0·ll, P = 0·50, A = 1·95. Distinct alleles were found between A. physeteris and the A. simplex complex at 19 out of the 22 loci studied, and only few rare alleles were shared at the remaining 3 loci. The genetic divergence between A. physeteris and A. simplex A and B is therefore very high, the values of Nei’s index D being 7·384 and 6·443 respectively (I = 0·001 and 0·002). The assignation of A. physeteris and the A. simplex complex to two distinct subgenera, Skrjabinisakis and Anisakis, as proposed by Mosgovoy on a morphological basis, appears to be fully justified according to our genetic data.

Onchocerca volvulus proteins labelled with 125I were immunoprecipitated with onchocerciasis and lymphatic filariasis human serum pools in order to differentiate between cross-reacting and non-cross-reacting antigens. Analysis of the immunoprecipitates by two-dimensional gel electrophoresis revealed that all high molecular weight (Mr) O. volvulus antigens cross-reacted with the lymphatic filariasis serum pools. We observed, however, that at least 8 0. volvulus antigens were specifically immunoprecipitated only by the onchocerciasis serum pools, with Mr ranging from 20000 up to 43000 Daltons. These results suggest that the lower MrO. volvulus antigens are more species specific than the other antigens. The significance of these findings for the immunodiagnosis of onchocerciasis is discussed.

Praziquantel is a broad-spectrum anthelmintic active against schistosome species which are major parasites of man. Two major effects on Schistosoma mansoni have been demonstrated; (i) spastic paralysis of the parasite musculature, possibly arising as a consequence of an influx of Ca2+ into the worm (Pax, Bennett & Fetterer, 1978; Coles, 1979) and (ii) vacuolation and degeneration of the worm tegument (Becker, Mehlhorn, Andrews, Thomas & Eckert, 1980). These events may contribute to the elimination of schistosomes in vivo, but this elimination may partly be dependent on the host immune response as infected T-cell-deprived mice are less able than immunologically intact animals to reduce their worm burdens following drug treatment (Doenhoff, Harrison, Sabah, Murare, Dunne & Hassounah, 1982). This latter observation raises the possibility that praziquantel may lower the ability of the parasite to evade host immunity by increasing the exposure of parasite antigens capable of acting as targets for host antibody, or antibody-armed cells at the worm surface. Consistent with this idea is the observation that adult schistosomes in praziquantel-treated mice are invaded a few hours after treatment by host granulocytes (Mehlhorn, Becker, Andrews, Thomas & Frenkel, 1981).