This study was carried out to compare potential methods of transplanting adult Oesophagostomum dentatum from experimentally infected donor pigs to helminth naive recipient pigs. The following methods were each tested in five pigs: A. Transfer of worms by stomach tube to the gastric ventricle of pigs per os pretreated with 0.5 mg/kg cisapride to increase gastrointestinal peristalsis; B. Transfer by stomach tube to the gastric ventricle of pigs per os pre-treated with cisapride (0.5 mg/kg) and omeprazol 20 mg which blocks hydrochloric acid secretion; C. Surgical transfer of worms to caecum of pigs. Worms for transplantation to pigs were obtained after slaughter of experimentally infected donor pigs and following isolation from the contents of the large intestine, using an agar gel migration technique. A mean of 1054 nematodes were transferred into each recipient pig within 2 hours. Procedures A and B resulted in establishment rates corresponding to only 0.5% and 7.6% of the transferred worms. In contrast, surgical transfer allowed 74.2% of the transplanted worms to be established. In all groups the transplanted worms migrated to the normal predilection site, i.e. the middle part` of the large intestine. More female than male worms established in all groups. It was concluded from this study that surgical transfer was the most reliable of the methods tested for experimental establishment of adult O. dentatum in helminth naive pigs.

The metacercaria of the heterophyid digenean Cryptocotyle concavum (Creplin, 1825) Lühe 1899, as seen by light and transmission electron microscopy, from the common goby (Pomatoschistus microps) is enclosed within a rigid cyst wall composed of four layers of parasite origin surrounded by a host-derived capsule. The encysted parasite contains anterior glands with secretion-filled ducts opening at the anterior extremity of the ‘head’. Excystment in vitro occurred most readily at 40–42°C on treatment with alkaline bile salts following pretreatment with acid pepsin. After 1 min in pepsin, the metacercaria became intermittently active, periods of rotation lasting 1–3 sec alternating with quiescent periods of 20–40 sec. Metacercariae excysted, some in less than 1 min, after transfer to bile salts. The metacercaria emerged through a hole, which appeared in the cyst wall at the site of application of the ‘head’ of the parasite. Some of the anterior gland ducts of excysted metacercariae were empty, indicating that their secretions are involved in penetrating the cyst wall. Following pretreatment in acid pepsin, no excystment occurred in EBSS (Earle's balanced salt solution) ranging in pH from 2.0 to 4.0, but above pH 4.0, excystment increased, reaching a maximum between pH 7.5 and 8.5. Pepsin and bile salts were not essential for excystment and metacercariae emerged, although less readily, in alkaline EBSS with or without acid EBSS pretreatment. Some emerged in distilled water with no pretreatment. Although no excystment occurred in acid pepsin or in EBSS at pH 2.0 and already-excysted metacercariae were rapidly killed by acid (pH 2.0), acid pepsin pretreatment enhanced excystment in alkaline bile salts.

In order to clarify the taxonomic status of the Taenia saginata-like tapeworm in East Asia, the morphological characteristics of the adult and cysticercus of classical T. saginata (American, Swiss and Poland strains) and the Taiwan Taenia were compared in the present study. The morphologic characteristics of these two parasites are very similar. The protoscolex of cysticercus of the Taiwan Taenia has a sunken rostellum while that of classical T. saginata has only an apical pit. In addition, the rostellum of the Taiwan Taenia cysticercus is usually surrounded by two rows of rudimentary hooklets. However, this structure is rarely found in classical T. saginata. Based on the results of molecular studies and morphological characteristics, the T. saginata-like tapeworm in East Asia represents a subspecies of T. saginata, named T. saginata asiatica

Nematodes identified as Spirura rytipleurites seurati are described and illustrated by light and scanning electron microscopy from specimens collected from the stomach of hedgehogs (Erinaceus europaeus) in Sicily. They differ from S. auriti, a stomach parasite of Hemiechinus auritus, in the length of body, the position of the second pair of post-cloacal papillae in the male and the structure of the spicules. The nematodes are classified as S. rytipleurites seurati, a stomach parasite of Erinaceus algirus, but they differ slightly from it in the dimensions of the eggs, that we measured in the uterus, and in the shape of the amphids. This appears to be the first report of S. rytipleurites seurati from Italy and from E. europaeus.

Steinernema feltiae is the most effective nematode for controlling sciarid species but S. carpocapsae does exert some control. S. feltiae is less effective at 30°C than at 22°C. S. anomali, S. riobravis and two Heterorhabditis spp. gave better control at the higher temperature. All six sciarid species tested were susceptible to S. feltiae but there was some variation in the level of infection. UK isolates of S. feltiae were more effective against UK sciarids than the nematode isolates from other European countries which were tested. Adult sciarids are infected by S. feltiae and can disperse nematodes to nematode-free compost.

To investigate antigenic differences between the developmental stages of Anisakis simplex, somatic, excretion–secretion and detergent-solubilized surface antigen preparations of third- and fourth-stage A. simplex larvae, and a somatic antigen preparation of adults, were characterized by SDS–PAGE and immunoblotting using mouse immune serum containing antibodies against the two larval stages. Excretion–secretion and surface antigen preparations from thirdstage larvae behaved very differently from those of fourth-stage larvae, in both SDS-PAGE and immunoblotting; this suggests that certain excretion–secretion and surface antigens are highly stage-specific. By contrast, somatic components of third- and fourth-stage larvae were found to have very similar banding patterns, suggesting conservation of these components during the development of the parasite in mice. The SDS-PAGE and immunoblotting results for adult somatic components seem to support this hypothesis

Studies were carried out to determine the predilection sites of Trichinella nativa muscle larvae in arctic foxes (Alopex lagopus) caught in Greenland. The highest number of larvae per gram of tissue was found in the muscles of the eyes and the legs. With regard to predilection sites no significant differences were demonstrated either between age groups or between foxes with high and low total parasite burdens. Predilection sites were comparable with those recorded earlier in experimentally infected caged foxes and in other carnivorous species. Hypotheses on predilection sites of Trichinella muscle larvae are discussed.

Protective immunity against Brugia pahangi was examined after adoptive transfer of immune spleen cells. Spleen cells obtained from gerbils at 8 weeks post-infection (p.i.) with 100 infective larvae (L3) of B. pahangi were transferred into naive recipients, and then 24 h later, they were infected with 100 L3 of B. pahangi. The recipients given normal spleen cells and infected by the same manner served as controls. Microfilarial counts in the circulation were monitored at designated times after infection and worm burden and the size of individual female worm were determined at 16 weeks p.i. to evaluate the effects of adoptive immunization. In addition, eosinophil responses and serum antibody titres were examined during the course of infection. In the control group, microfilariae first appeared in circulation at 9 weeks p.i. and continuously increased in number throughout the course examined. In contrast, microfilaraemia was almost completely suppressed in the group given immune spleen cells. Although worm burden was comparable between the two groups, the average size of female adult worms recovered from the adoptively immunized group was significantlysmaller than that from the control group. Eosinophil response was hastened and enhanced by adoptive transfer of immune spleen cells in the early stage of infection. Parasite- specific antibody response was also hastened by adoptive immunization. These results suggest that immune spleen cells could confer protective immunity mainly directed against adult B. pahangi.

The effect of temperature on infection, development and reproduction of five Heterorhabditis isolates was examined in Galleria mellonella larvae. Infectivity was examined at six temperatures (5,10, 15,20,25 and 30°C). The proportion of Galleria infected remained relatively constant, only dropping at extremes of the temperature range tested. However, the mean number of nematodes per host produced a different trend, with each isolate displaying optimal infectivity at 25°C. The temperature range over which the juveniles could infect differed between the isolates. This is thought to be related to the geographic origins of the species. Development and reproduction occurred over a slightly narrower temperature range than that allowing infection to occur. Differences between the isolates at which development and reproduction occurred were noted. There were also differences in the mean number of juveniles produced per cadaver following either infection in sand (10 nematodes/larva) or the injection of one juvenile per larva, suggesting that reproduction is tightly regulated by density-dependent constraints.

Karyometrical analysis of conventional Giemsa-stained mitotic chromosomes of parthenitae of Sphaerostomum bramae (Trematoda: Opecoelidae) was carried out. The karyotype displays a typical ‘plagiorchiid’ pattern with 22 chromosomes in a diploid set including a first pair of large metacentric elements. Chromosomes with medially or submedially located centromeres prevail in the karyotype; only chromosomes 7 and 9 are subtelocentric. With the data now available, close karyological affinity was noted between S. bramae, the representative of the family Opecoelidae, and other karyologically studied species of some families in the order Plagiorchiiformes: Troglotrematidae, Plagiorchiidae, Prosthogonimidae, Lecithodendriidae and Telorchiidae.

The structure of the female reproductive tract, and the patterns of oogenesis, fertilization and embryogenesis were examined from two adult female Loa loa (Nematoda: Filarioidea) from Gabon. They were found to be indistinguishable in the two specimens, and almost indistinguishable from the pattern previously described from Dirofilaria immitis, except in chromosome number. Loa loa has 2n=10+X0.

Isolates from eight gastrointestinal nematode species parasitic in sheep, cattle and deer were maintained in sheep, to provide eggs in similar faecal environments and to compare temperature and moisture requirements for their development. Faecal cultures were processed at different temperatures (for four species) and moisture contents (for eight species). At 60% of faecal moisture content (FMC), maximal rates of development (expressed as L3/100 hatchable eggs estimated by an extraction technique from the faeves) were observed at 20, 23 and 28°C respectively for Ostertagia leptospicularis, O. ostertagi, Teladorsagia circumcinctaand Trichostrongylus colunriformis. For the eight species, the curves of development rates as functions of FMC were Gaussian, without modification between 18 and 28°C. Optimal developments were when the FMC ranged from 57 to 68%; low development of 1L3/100eggs were observed when the FMC ranged from 85 to 95% and from 25 to 55%. The main differences between species were in the ability of the eggs of Teladorsagia circumcincta, Trichostrongylus colubriformis, T. vitrinusand Chabertia ovina to develop at lower FMC than Haemonchus contortus, O. ostertagi, O. legptospicularis and Cooperia oncophora.

The life history of Grysoma indica n.sp., a psilostome trematode, obtained experimentally in ducklings, after feeding with metacercariae occurring in the snail Thiara tuberculata, is elucidated. Natural infections with cercariae were found in T. tuberculata, collected from a freshwater stream at Visakhapatnam, India. Metacercarial cysts were found in the same and other species of snails in the locality. The new species differs from other species of the genus in the sucker proportions, position of the testes and distribution of the vitelline follicles.

The infectivity of the eggs of Asian Taenia sp. for humans is not known. Using baboons (Papio hamadryas) as a model to extrapolate the findings, three animals were exposed per os with 1000, 10,000 and 50,000 infective eggs of theAsian Taenia sp. The serological, biochemical, haematological and parasitological (based on necropsy) results show that baboons are refractory to the infection. It is concluded that the Asian taeniid eggs may fail to develop in man.

The assay system for antibody responses against Em2, the most specific antigen for serodiagnosis of alveolar echinococcosis (AE), has been established by enzyme-linked immunosorbent assay (ELISA) but not by Western blot assay, since Em2 antigen is not protein but carbohydrate in nature. Recently we reported that previously undescribed protein epitopes, designated Em18 and Em16 due to their molecular weights, were good serologic markers for AE by Western blot analysis. It has been shown that Em18 and Em16 are the only two epitopes recognized by commercially available weak positive (cut off) sera for the Em2plus-ELISA.

Female ICR mice, 5 to 6 weeks old, were exposed by stomach tube to 25 metacercarial cysts of Echinostoma caproni per mouse. At 14 days post-exposure, mice were fed by stomach tube clorsulon (1000 mg/kg, 25 mg/kg, 500 mg/kg and 100 mg/kg) or rafoxanide (50 mg/kg, 25 mg/kg and 5 mg/kg) dissolved in dimethy lsulphoxide (DMSO) carrier and mebendazole (1000mg/kg and 500 mg/kg) or arprinocid (100 mg/kg and 50 mg/kg) suspended in a2:1 polyethylene glycol (PEG)/DMSO carrier. All drugs were obtained from Meerck In. (Rahway, New Jersey, USA) and only single dose regimes were used. Experimentally infected mice that served as controls received either DMSO or 2:1 PEG/DMSO carriers or were not given the carrier. Mice were necropsied 15v, 16, 18 and 20 days post-exposure to worms. Doses of 100 mg/kg of clorsulon and 50 mg/kg of rafoxanide were 100% effective in eliminating the echinostomes on day 1 post-administration of the anthelmintics. Mebendazole and arprinocid were ineffection in eliminating worms at 1 or 2 days post drug daministration.