The effect of various concentrations of praziquantel at different time intervals post-treatment on the ultrastructure of Schistosoma margrebowiei using scanning and transmission electron microscopy has been examined. The major changes involved blebbing of the entire surface tegument of both sexes (although more marked in males) together with vacuolation of the basal membrane accompanied by the development of membraneous whorls. These effects were progressively more marked with increased concentration and time of exposure resulting in severe erosion of the tubercles and collapse of the sensory organelles. Exposure of the underlying tegumental tissue resulted and paralysis and contraction of the suckers and neck region was apparent. Disruption of the subtegumental musculature and the appearance of vacuolation and membraneous whorl formation were seen. The gastrodermis was similarly affected and the S4 cells of the vitelline gland showed protein disruption of the vitelline droplets. Host cells were seen adhering to the surface of the worms following drug treatment and the synergism between PZQ and the action of the hosts immune system has been discussed.

The existence of adult Schistosoma haematobium worm proteins (Sh31/32) homologous to the diagnostic Sm31/32 of S. mansoni is shown. Sm31/32 and Sh31/32, adsorbed on nitrocellulose and kept dry on the bench before immunoblot analysis, were antigenically stable for at least 4 years including storage for 17 months in tropical climates. The antigens react with patient sera in the absence of defined buffers under rather simple conditions (“humid chamber blot”). The results add to the use of these antigens for serodiagnosis of schistosomiasis in endemic areas.

Frequent reports of haematuria among resettlers at Ibaro and Abule-titun located close to a newly constructed reservoir. 20 km north-west of Abeokuta. Ogun State, Nigeria. prompted a pre-control survey to assess age and sex distribution of urinary schistosomiasis in the communities. 210 persons were examined at Ibaro and 145 at Abule-titun between April 1988 and February 1989. Overall prevalence was about 80% in both villages, and all age and sex groups examined were affected. The pattern of infection in both villages was similar, prevalence being high in all age and sex groups and, unlike most endemic communities, the rate of infection was not significantly higher among the 5–14 year age groups. Intensity of infection was also high in all age and sex groups with mean range egg output of between 73±73 and 2016±3875 ova/10ml urine at Ibaro and between 231±122 and 1340±1786 ova/10ml urine at Abule-titun. This is attributed to an occupation-related high rate of human water contact in both villages.

An acid phosphatase activity (APA; EC 3.1.3.2) was demonstrated in homogenates of adult Hymenolepis diminuta. The APA was soluble based on the observation that it did not sediment at 130 000 g. APA was partially purified using a combination of differential centrifugation, ammonium sulphate precipitation, chloroform extraction, and gel and fast-protein-liquid-chromatography. This combination of techniques resulted in a preparation with a specific activity approximately 500 times greater than the crude enzyme preparation. The temperature and pH optima of the partially purified APA were 44°C and pH 5·0. The enzyme appeared to be a monomer with a molecular weight of approximately 62 000. APA had a higher affinity for a greater activity towards aromatic than aliphatic phosphoesters and phosphoryl transferase activity was demonstrable using 1-butanol and ethylene glycol as acceptors. APA was inhibited significantly by sodium dodecyl sulphate, fluoride, molybdate and tartrate, but CuSO4 and Fast Garnet GBC were poor inhibitors. The precise cellular localization and function of this enzyme remains unknown since it possesses characteristics of both cytoplasmic and lysosomal APA's of other organisms.

The cyst wall of Microphallus madrasensis resisted 6 N and 11·3 N hydrochloric acids (HCL) 36 N concentrated sulphuric acid (H2S04) and 0·35 M sodium hypochlorite. It was partially dissolved in 0·6 M sodium azide and completely dissolved in 16 N nitric acid (HNO3). An HCl hydrolysate of the cyst wall contained 10 amino acids viz. alanine, leucine, aspartic acid, glutamic acid, lysine, histidine. phenylalanine. tyrosine. cystine and proline. Polyacrylamide gel electrophoresis revealed the presence of a fast moving fraction which stained with periodic acid-Schiffs (PAS) reagent and toluidine blue was noticed in tris-glycine buffer soluble and methanol water soluble substances present in the cyst wall. Triton X-100 soluble substances present in the cyst wall revealed the presence of two slow-moving fractions stained only with PAS, and also a fast-moving fraction stained only with toluidine blue. Sodium dodecyl sulphate (SDS) soluble substances in the cyst wall revealed the presence of two fast-moving fractions which stained with PAS and toluidine blue. The slow-moving fractions are protein-bound carbohydrates. The fast-moving fractions obtained after fractionation with SDS are acid mucopolysaccharides or nucleoproteins whereas the single fraction (Triton X-100 soluble substances) which stained with toluidine blue appears to be a carbohydrate-free protein. The cyst wall of M. madrasensis also consisted of phospholipids and neutral lipids.

The influence of nonspecific immunomodulation on the course of experimental infection was examined in larval cestodosis (Mesocestoides corti) and ascaridosis (Ascaris suum) in mice. Immunosuppressive treatment (with azathioprine or hydrocortisone) resulted in a decrease of resistance in both models. The subsequent administration of T-activin to immunosuppressed mice led to the restoration of resistance to a level equal to that of untreated control mice. The administration of different immunomodulators partially protected mice against M. corti (T-activin. thymomodulin) or A. suum (T-activin. thymomodulin. thymosin fr.5. bursa-activin) infection. The protective effect of different treatments did not correlate with the level of specific antibody in the sera of infected mice. These results, which confirmed the decisive role of T-cell immunity in the resistance to the helminth infections, raise the possibility of the use of immunomodulators (thymic preparations) in the immunoprophylaxis of helminthoses.

The effects of larval stages of Ascaris lumbricoides on human blood clotting was studied in vitro. Extracts and excretory/secretory products of third-stage larvae (L3) and late third-stage larvae (LL3) cultured from ova obtained from infected patients were analysed for anti-coagulant activity. Prothrombin time (PT) was prolonged by the addition of either whole extract of L3/LL3 or ES products of L3/LL3 as compared to controls. Partial thromboplastin time with kaolin (PTTK) was also prolonged on the addition of either extracts of ES products of L3/LL3. The prolongation of PTTK was significantly higher with extracts/ES products of L3 when compared to the extracts/ES products of LL3 (p<0.005). Thrombin time (TT) was prolonged by extracts of L3/LL3 and their ES products.

Fifty children aged 6 to 13 years and infected with Ascaris lumbricoides were selected for the study. The number of eggs laid daily by a female Ascaris increased with increase in its length, weight and diameter. Female worms became mature and started laying eggs when they reached a length of 118 mm. Adult female worms measuring 3·7 mm or more in diameter were found to be mature. The minimum weight of a worm producing eggs was 1·1 g. On average the number of eggs produced by the female decreased with increase in the worm load.

An immunodominant antigen of Dirofilaria immitis was studied using recombinant DNA techniques. The mRNA from D. immitis adult female worms was translated in vitro and a major 34 k Da antigenic polypeptide product was demonstrated by immunoprecipitation. cDNA was synthesized from mRNA and a λ gt11 expression library was constructed and immunoscreened with dirofilariasis positive serum. A positive clone containing a nearly full length cDNA was isolated. The cDNA was 2415 bp in length and consider of a single open reading frame followed by a long 3' non-coding region of 1446 bp. The open reading frame of 969 bp encoded a polypeptide of 322 amino acids with a molecular weight of 34 400. A cDNA fusion protein synthesized by bacteria (Escherichia coli JM109) using the expression vector pGEMEX-1 was identified as an immunodominant antigen by absorption experiments and had no cross-reactivity with sera from patients with other filarial species.