Infection with Plasmodium vivax was established in splenectomized Callithrix jacchus marmosets by inoculation of parasitized blood from Aotus trivirgatus carrying the Vietnam Palo-Alto line of P. vivax. Subsequent blood passage through intact marmosets resulted in higher peak parasitaemias (about 1% of red cells infected) and the loss of stainable Schüffner's dots in infected cells. Primary infections with the adapted line were patent for 74 days or more, and induced both a substantial antibody response, as determined by indirect fluorescence, and some lymphocytosis, but no marked anaemia. Marmosets which had recovered from their primary infection (or in which it was drug-cured) suffered abbreviated patency with low-grade parasitaemia on re-infection.

The proportion of blood meals taken on humans which are infectious to mosquitoes in the Madang area, Papua New Guinea was estimated by two methods. In the first, laboratory reared Anopheles farauti were fed on individuals of all ages at village surveys. The results showed that 3·8% of people were infectious and that the mean percentage of mosquitoes which became infected by feeding on these people was 37·9%. From the average proportion of mosquitoes infected, the probability that a mosquito feeding on a human would pick up infection was 0·013±0·005. In the second approach mosquitoes were fed on identified Plasmodium falciparum, P. vivax and P. malariae gametocyte carriers. The results indicated that 46% of gametocyte carriers were infectious and that the mean probability of a mosquito becoming infected after feeding on a gametocyte carrier was 0·151±0·029. Gametocyte prevalence rates in all ages measured over 18 months in three villages averaged 3·3% P. falciparum, 4·0% P. vivax and 0·7% P. malariae, totalling 8·0±0·7%. Combining gametocyte prevalence rates with the probability of a mosquito becoming infected from a gametocyte carrier, the probability of a mosquito becoming infected following a blood meal on a member of the human population was estimated to be 0·012±0·003.

A new method of computing the infectivity index of microfilariae (mf) for the mosquito population is proposed using the estimated mf density distribution in the human population. The observed density distribution is considered a compound of the Poisson and the gamma distributions. The former distribution describes the probability of a specimen containing a specified number of mf and the latter describes the density distribution of mf in the host population. The mf infectivity index is the probability that a blood meal will include at least 1 mf, conditional on the population-density distribution of mf as specified by the gamma distribution. Actual data indicate that this population-density-based infectivity index can be considerably different from the conventional index based on the survey-density distribution. The level of the carrier rate of mf in a survey is greatly influenced, apart from the sample variation, by the average volume of blood taken from each person. The rate computed on the estimated population-density distribution of mf is convertible to any base amount of blood.

A monoclonal antibody against the circumsporozoite proteins of the Plasmodium berghei sporozoite was used to trace the synthesis and expression of these proteins, via the Lowicryl immunogold technique, within the developing oocyst. The proteins were detected on the endoplasmic reticulum of the oocyst and were present in the sporozoite membranes at the point of their formation.

Two strains of Eimeria tenella with different decoquinate sensitivity and different glucose phosphate isomerase (GPI) isozymes were used in genetic recombination experiments: a line derived from a laboratory strain (NIAH) was decoquinate-resistant (DR) and had the isozyme GPI-9, while a field isolate (Iwate strain) was decoquinate-sensitive (DS) and had GPI-1. Coccidia-free chickens were orally inoculated with mixed oocysts of the two strains and parasites of the F1 generation were recovered. The F1 progeny showed both forms of the isozyme. Next, oocysts of the F1 progeny were passaged through chickens given the decoquinate-containing diet. The F2 progeny also had GPI-1 and GPI-9, indicating crossfertilization between the two strains. Six single oocysts were isolated from F2 progeny; 1 showed both phenotypes of GPI, 1 had GPI-1 and the remaining 4 lines had GPI-9. Analysis of the amount of GPI in recombinant oocysts suggested that the proliferation rate of the DR strain was slower than that of the DS strain. We concluded that GPI isozymes in E. tenella can serve as useful markers in experiments on chicken coccidia.

L-amino acid esters such as leucine methyl ester (Leu-OMe) destroy Leishmania mexicana amazonensis amastigotes by a mechanism which may involve hydrolysis of the compounds by parasite enzymes. Moreover, several esters (e.g. Ile-OMe) prevent the killing of parasites by Leu-OMe, perhaps by inhibition of the hydrolytic enzymes. We show here that certain amino acid amides are also leishmanicidal. Killing of Leishmania within macrophages was assessed microscopically, and that of isolated amastigotes was measured by reduction of the tetrazolium MTT. Amino acid amides were generally less active than the methyl esters and several were more toxic to the macrophages, as determined by inspection of Giemsa-stained preparations. Ranks of activity of the amides on isolated amastigotes were Trp > Leu > Phe > Met > Tyr. The amides of Ala, Gly, Val, Ile, His and D-Leu were inactive. This pattern of activity is similar to that of amino acid methyl esters. Ile-NH2 and a few other amides protected intracellular as well as isolated parasites from killing by Leu-OMe. Conversely, Ile-OMe reduced the toxicity of Leu-NH2 for isolated amastigotes. None of the esters or amides assayed prevented the destruction of Leishmania by Trp-NH2. The results are compatible with the view that amino acid esters and amides may be recognized by the same or similar parasite enzymes.

Female DBA/2 mice were found to be highly resistant to Leishmania mexicana and rarely developed lesions even when inoculated subcutaneously with high numbers (5 × 106) of amastigotes. Male DBA/2 mice, on the other hand, were much more susceptible to this parasite and often developed non-healing lesions even when inoculated subcutaneously with comparatively few (5 × 104) amastigotes. Conversely, although both male and female DBA/2 mice developed ulcerating lesions when inoculated subcutaneously with L. major amastigotes, lesions invariably healed in males but did not heal in females. Male DBA/2 mice recovered from L. major infection subsequently were found to be resistant to subcutaneous challenge with L. mexicana. Conversely female DBA/2 mice that had failed to develop lesions when infected with L. mexicana developed lesions which healed following subcutaneous challenge with L. major. Thus there is bilateral cross-immunity between L. mexicana and L. major in DBA/2 mice which overrides differences in sex-determined susceptibility to both organisms.

Experimental work has established that a sexual process can occur in African trypanosomes (Jenni, Marti, Schweizer, Betschart, Le Page, Wells, Tait, Paindavoine, Pays & Steinert, 1986; Paindavoine, Zampetti-Bosseler, Pays, Schweizer, Guyaux, Jenni & Steinert, 1986; Tait, personal communication). However, the role of the process in natural populations of trypanosomes is poorly understood. This paper considers what information can be gained from analyses of isoenzyme polymorphism. A cladistic approach is used to help determine whether trypanosome diversity could have been produced by mutation alone. When applied to three East African populations of Trypanosoma brucei it provides evidence that some diversity has arisen through a sexual process; this explains the variation observed within a locality and can account for the evolution of differences between localities. However, the extent to which genetic exchange currently operates is less clear. Analysis of genotype frequencies indicates that agreements with Hardy-Weinberg expectations can be obtained even if genetic exchange exerted no influence over genotype frequencies. Moreover, analysis of joint locus frequencies reveals disequilibrium between loci and that trypanosome populations may be lacking several genotype combinations. Thus, genetic exchange may not occur sufficiently frequently, or in such a way as to break up associations between loci. The relevance of these observations to the evolution of strain differences within T. brucei is discussed.

Praziquantel (500 mg/kg) administered orally to BALB/c mice with secondary equine E. granulosus daily for 21, 30 or 30 + 30 days without the drug resulted in the majority of cysts, using bench criteria of turgidity and eosin exclusion, being assessed as ‘alive’. Ultrastructural examination of 54 of these ‘alive’ cysts did not support this conclusion. They all showed increased vesiculation of the germinal layer leading, in many, to the loss of its integrity. Increased mitochondrial numbers occurred frequently. The longer drug treatments appeared to have greater effects on the germinal layer of ‘alive’ cysts and there was no detectable re-establishment of structural organization within 30 days after drug withdrawal. Subjectively, there was no substantial difference between cysts from 4-month and 9-month infections or between affected peritoneal and hepatic cysts. Tissue from collapsed cysts was necrotic. Peak serum levels of praziquantel (6430–6136 μg/l) occurred 5–10 min after drug administration (500 mg/kg) and dropped rapidly to less than 10 μg/l at 3 h. In an in vitro study at praziquantel concentrations of 1000 and 5000 μg/l over a 10-day period, most cysts were judged ‘alive’ by bench criteria but showed ultrastructurally a time- and concentration-dependent loss of integrity identical to that seen in vivo. Turgidity and eosin exclusion therefore underestimate the effect of praziquantel and the results indicate that in vitro experiments can fulfil a legitimate preliminary role in a hydatid chemotherapy programme.

The plerocercoid of Callitetrarhynchus gracilis was found in the body cavity of 14 species of fishes from Bermuda. The scolex, having completed its development, continues to grow within the blastocyst. The two mobile bothridia possess lateral grooves containing backwardly directed spines. Rapid evagination of the proboscides is effected by two layers of contra-rotating spiral muscles in the walls of the proboscis bulbs. The proboscis retractor is protected from constriction, during contraction of the bulbs, by a rigid ring at the junction of bulb and sheath. Nine series of extrinsic muscles anchor the proboscis sheaths to the body wall and a ladder-like series of dorsal, ventral and lateral muscles anchors the bulbs to one another. The bulbar nerves arise from the lateral nerve cords and are joined by a series of central ring commissures along the length of the bulbs. Uniciliate sensilla occur on the scolex and glandular cells in the peduncle.

Blatticola monandros Zervos lives in the hind gut of the endemic New Zealand cockroach Parellipsidion pachycercum Johns. A field survey showed that infection prevalence was high (54 %) in small nymphs and increased further with cockroach size to a maximum (92 %) in penultimate nymphs. Variance to mean ratios and the Chi-square test for goodness of fit of a Poisson distribution provide strong evidence that the distribution of the nematode was not clumped (over-dispersed) or Poisson (random) but under-dispersed in most host size classes. The modal infrapopulation type consisted of 1 adult male and 1 adult female. Other infrapopulations were transitional to this type. Monogamous infrapopulations increased in prevalence with increased host size. Juvenile males were uncommon and probably develop faster into adults than juvenile females. Infrapopulations with 2 juvenile males were very rare and no cockroach contained 2 adult males, although some contained 2 adult females. Seasonal variations in prevalence and infrapopulation structure were slight over a 3 year period, except during one unusually dry summer. During the drought, prevalence of monogamous infrapopulations and of transitional infrapopulations were lowest, while prevalence of single-worm and single-sex infrapopulations were greatest. It is evident that competition between females reduces fecundity. When only 1 adult female nematode is present in an adult cockroach, more eggs are produced than the total produced if 2 adult females are present. Eggs were produced cyclically with short periods of high egg production interspersed with several days of very low or no egg production. Most eggs produced on any one day were attached to the outer surface of only 1 of the up-to-6 faecal pellets produced by the host/day. Mechanisms which may regulate infrapopulations and control reproductive competition and cyclical egg production are discussed. It is suggested that B. monandros regulates its own infrapopulation.

Experimental infection of adult Drymaplaneta variegata Shelford, 1909 (Blattodea) with known numbers of eggs of Protrellus dixoni Zervos, 1987 (Nematoda: Thelastomatidae) showed that each infrapopulation was regulated by a density-dependent and sex-dependent reduction in infection intensity with infrapopulation age. This reduction was not equal in initial speed or intensity between the sexes (reduction in number of males was faster) and led to infrapopulations with never more than a single adult male, 1–8 (usually 1–3) adult females and 0–28 juvenile females. In structure, these laboratory-produced infrapopulations resembled those in field-collected hosts. Parasite-mediated chemical interference competition is suggested as the cause of infrapopulation regulation. Per capita egg production was greater in uncrowded worms which suggests that self-regulation benefits those nematodes that survive competition. Unmated females produced male offspring only (probably by arrhenotokous parthenogenesis). Only females that occurred with a male produced females although some also produced males; such females may avoid insemination or prevent fertilization of some or all eggs. Female offspring probably result from amphimixis.

The availability of restriction fragment length polymorphisms (RFLPs) would be useful for studying the extent of diversity among morphologically indistinguishable populations of filarial parasites. Such polymorphisms may be useful in correlating various physiological and clinical differences with parasite heterogeneity. In order to identify such RFLPs, we isolated DNA from microfilaria of 6 filarial species (Acanthocheilonema viteae, Brugia malayi, Brugia pahangi, Dirofilaria immitis, Litomosoides carinii and Setaria digitatum), digested the DNA with several restriction endonucleases, prepared Southern blots and probed with 32P-labelled DNA probes. The patterns of fragments generated using two restriction endonucleases, Mbo I and Tag I, in combination with two probes, rDNA from the free-living soil nematode Cenorhabditis elegans, and pBM103, an anonymous DNA probe from B. malayi, unequivocally distinguish between all 6 of the species. To ensure that the differences we observed between the species represent true interspecies variation rather than fortuitous individual variations we analysed DNA from several individual B. malayi and B. pahangi worms. The individual B. malayi worms demonstrated restriction profiles that were invariant, as did the individual B. pahangi worms, demonstrating that the differences we observed were true interspecies variations.

A Theileria parva lawrencei isolate in the form of a sporozoite stabilate, derived by feeding clean Rhipicephalus appendiculatus nymphal ticks on an African buffalo (Syncerus caffer) captured in the Laikipia District, Kenya, was inoculated into groups of cattle at dilutions between 100 and 10-3. Groups of 3 cattle infected with 1 ml inocula at 100, 10-1 and 10-2 dilutions were treated with 2·5 mg/kg body weight of buparvaquone on day 0 and similar groups were left untreated to act as controls. An additional group, given 100 dilution of the stabilate, was treated with buparvaquone on day 8 post-inoculation. It was found that all control cattle inoculated with the stabilate at dilutions between 100 and 10-2 became infected, but only 2 out of 3 cattle developed patent infections at 10-3 dilution. All 3 control cattle receiving 100 dilution died of theileriosis, 2 at 10-1 and 10-2 dilutions, and 1 at 10-3 dilution died. Buparvaquone treatment on day 0 at 100 dilution resulted in the survival of 2 of 3 cattle and all the cattle at 10-1 and 10-2 dilutions. All the surviving cattle eventually developed a significant serological response against T. parva in the indirect fluorescent antibody test, except 1 in the 10-3 dilution group, and were immune to homologous challenge when tested 3 months later with a lethal inoculum of stabilate, except 2 cattle in the 10-3 dilution group. As a result of a theileriosis problem at about day 60 after inoculation in 2 cattle given 10-2 dilution of stabilate and buparvaquone treatment on day 0, an additional 5 cattle were given 10-2 dilution of stabilate and developed a good immunity after buparvaquone treatment. None was shown to develop the carrier state. Treatment with buparvaquone on day 8 after infection with 100 dilution of stabilate was not successful since 2 died. The stabilate used was shown to produce reproducible infection in cattle at different dilutions.

The problems caused by tick and tick-borne diseases for livestock particularly cattle on the African continent are described and discussed. The control of ticks and tick-borne diseases must receive high priority in Africa with regard to both research and control application because of their widespread distribution in areas of high livestock potential and productivity. The conventional methods of tick and tick-borne disease control are discussed and are found to be inadequate in the conditions prevailing in Africa. Methods of integrated control are suggested and discussed in light of recent development in control methods and those still under development. Any one of these methods may not be adequate to control the problem on its own but when several of the methods are combined an economic and robust integrated control is likely to result. Encouragement is given to attempt this approach in Africa to solve what must be the largest animal health problem of livestock remaining in the world.