Twelve enzymes (encoded by 14 loci) in liver flukes of Fasciola species originating from Japan (parthenogenetic triploids), Korea (parthenogenetic diploids), the United States of America (USA) and Australia (all sexual diploids) were analysed using starch gel electrophoresis. Variation in electrophoretic patterns between samples was detected at five enzyme loci (Ak, Got, Gpi, 6-Pgd and Pgm-2). Japanese worms (31, of which six were established as uniparental laboratory strains), which reproduce by parthenogenesis, exhibited three different isozyme patterns. This indicates that triploidy has arisen more than once in Japanese flukes. Japanese Fasciola sp. can be separated into three types on morphological grounds. For the six laboratory strains of Japanese worms, the parental morphological type was known. Each of the three isozyme patterns observed was restricted to one morphological type. Most alleles detected in the Japanese triploids were also found in diploid worms from the other countries: the only alleles not represented elsewhere were four at the Got locus and two at the Pgm locus. Flukes from a laboratory strain derived from a single Korean diploid worm resembled the Japanese worms in genotype more closely than did American (seven uniparental laboratory strains) or Australian (30 worms) specimens. Worms from the last two countries were closely related.

Levels of intestinal nematode infections were assessed six months after a two year trial of ivermectin for efficacy against onchocerciasis had ended. In the trial the inhabitants of six villages in Sierra Leone were offered treatment with ivermectin or placebo at six monthly intervals for four rounds in total. Quantitative faecal egg counts were carried out on stool samples provided by 202 subjects, all of whom had received all four rounds of treatment, in two of the villages (Dodo and Mogibisi). These data were analysed by a novel procedure in which a 3-way ANOVA with negative binomial errors enabled village and host gender influences on the outcome of treatment to be identified. Necator americanus was the most common species showing an overall prevalence of 90% but a higher intensity in Mogibisi relative to Dodo, particularly among male subjects. Neither prevalence nor intensity of infection were altered in ivermectin-treated compared with placebo-treated subjects. Trichuris trichiura was the least common species with a prevalence of 15%. It was concluded that there was no significant protection from infection with this species among the ivermectin relative to the placebo-treated subjects. Ascaris lumbricoides, with an overall prevalence of 39%, was more common among female (50%) compared with male (27%) villagers. Prevalence was not significantly affected by ivermectin but the intensity of infection declined by 91.3% in Dodo whilst in Mogibisi intensity was only reduced by 14.6%. The results indicate that the long-term benefits of treatment of necatoriasis and trichuriasis with ivermectin are likely to be minimal whilst those of ascariasis will depend on the individual characteristics of local communities and may differ quite markedly within a limited geographical area. Possible explanations for the discrepancy in efficacy between villages are considered.

The relationship between different climatic factors (temperature, relative humidity and rainfall) and the pattern of lungworm larval excretion was studied in sheep under a continuous grazing pattern in North-west Spain, where the climate is intermediate between sub-humid Mediterranean with an Atlantic tendency and European Atlantic. Over a period of one year, 44 animals were sampled once a month at random from a flock of 80 Galician breed sheep, all over 4 years old. Faeces were taken directly from the rectum and the number of first stage larvae per gram of faeces was determined for each animal, and the species of Protostrongylidae (Nematoda) identified. Larval excretion was irregular during the study. The prevalence and intensity of infection were greater in the colder months (40.9%; x=12.3 ± 40.4) and less in the warmer months The species of Protostrongylidae identified and prevalences (%) were Neostrongylus linearis (71.5), Muellerius capillaris (18.8) and Cystocaulus ocreatus (9.7). Between November and March, with low temperatures, the prevalence and intensity of parasitism with N. linearis and M. capillaris were greater than in the months with high temperatures (May to September). Multiple linear regression analysis showed statistical correlation between temperature, relative humidity and rainfall considered together and the number of N. linearis larvae per gram of faeces. Linear regression showed a correlation between the temperature and the percentage of sheep that passed M. capillaris. In general, the prevalence and intensity of infection of the sheep with N. linearis, M. capillaris and C. ocreatus larvae decrease when the temperature increases and increase when the relative humidity and rainfall increases.

Female ICR mice, 6–8 weeks old, were exposed to 6 (group A) or 25 (group B) metacercarial cysts/host of Echinostoma caproni to determine the effects of these cyst dosages on infectivity, growth, distribution and fecundity of worms in the small intestines. All 30 mice exposed (15 in group A and 15 in group B) were infected and there was no significant difference in the percentage of worm recovery between group A and B at 2, 4 and 8 weeks postinfection (PI). Growth was rapid in both groups with worm body areas increasing from about 3mm2 at 2 weeks PI to about 7 mm2 at 8 weeks PI. More worms from group B were in the anterior sections of the small intestines at 2 and 4 weeks PI than those from group A. However, at 8 weeks PI more worms from Group A were in the anterior sections of the small intestines than those from group B. There were marked differences in our findings on infectivity, growth and distribution of E. caproni in ICR mice using 6 and 25 cyst inocula compared to a previous study using the same echinostome and cyst inocula in NMRI mice, presumably related to the mouse strain. Fecundity studies were somewhat comparable in both studies showing an approximate three to four times increase in the average number of eggs/gram of faeces in mice receiving 25 versus 6 cyst inocula.

Development of Neostrongylus linearis larvae was studied in the snail intermediate hosts Oestophora (Oestophora) barbula, Oestophorella buvinieri, Cepaea nemoralis and Helix (Cryptomphalus) aspersa. The molluscs of each species, all adults, were divided into groups of 40 for infection purposes. The infection doses for the first two snail species were 90 and 50 first stage larvae (L1) of N. linearis, respectively. For C. nemoralis two batches were tested: one with 200 L1 kept at 19°C and the other with 250 L1 at a temperature of 21°C. The same was done with Helix (C.) aspersa with 200 L1 at a temperature of 21°C, on the one hand and 300 L1 at 24°C on the other. One or two molluscs of each species were killed in series from the 6th day post-infection (p.i.) until the 44th. Percentage values for total larvae (1, 2 and 3) and L3 were higher with the lower dose for C. nemoralis, whilst the same was true with the higher dose in Helix (C.) aspersa. In both cases, the higher temperature appeared to contribute to cycle acceleration. Using one way analysis of variance, statistically significant differences were detected between the species of molluscs tested concerning percentages of L1 which penetrated, total larvae and L3. According to our results, the decreasing order of susceptibility of these species of molluscs as experimental intermediate hosts of N. linearis is: O. buvinieri, Oestophora (O.) barbula, C. nemoralis and Helix (C.) aspersa. It is the first time that Oestophora (O.) barbula and Oestophorella buvinieri have been named as experimental intermediate hosts of N. linearis.

The tegument of juvenile Paramphistomum epiclitum and Fischoederius elongatus (Paramphistomidae: Digenea) resembles those of other digeneans. Seven types of papillae were observed, mostly on the oral and acetabular surfaces, and increase in number during migration. Also evident are two types of secretory body (T1 and T2) which are synthesized separately in tegumental cytons underlying the syncytium. Exocytosis of T2 bodies occurs at the apical membrane and appears to contribute to a fibrous glycocalyx. The tegumental syncytium lining the pharynx and acetabulum is thinner and has a higher capacity for vacuolation than the general tegument. These may represent important sites for osmoregulation. The absence of mitochondria from the tegument in migrating juveniles suggests limited involvement in energy demanding processes. Pigmentation of the subtegument is first evident in mature cercariae and is progressively eliminated during migration.

The trapping capability of Arthrobotrys oligospora and A. conoides (Hyphomycetales) against third stage larvae (L3) of Haemonchus contortus (Trichostrongylidae) was evaluated in an in vitro trial. Arthrobotrys oligospora showed a 35.87% and 25.71% trapping effectiveness against H. contortus infective larvae at 18 and 25°C, respectively; whereas the trapping capability of A. conoides was 92.17% and 90.40% at the same temperatures, respectively. Microscopic examination demonstrated that A. conoides spontaneously developed a large quantity of three-dimensional loops before the nematodes were added. Neither of the two species studied developed three-dimensional adhesive loops at 30°C, consequently no trapped nematode was observed. In a second trial, the trapping capability of A. conoides against H. contortus (L3) and second stage larvae (J2) of Nacobbus aberrans (Pratylenchidae), was evaluated at 25°C. The trapping capability shown by A. conoides was higher than 90% for both kinds of nematode. The possible use of A. conoides to control ovine haemonchosis is discussed.

This paper reports the development of the canid filarial worm, Dipetalonema dracunculoides, in the brown dog tick, Rhipicephalus sanguineus by determining whether development is similar within larval, nymphal and adult stages of infected ticks. This study demonstrates that only infected nymphal ticks can support the complete development of the filarial worm. Infected larval ticks are not suitable intermediate hosts, nor are infected adults. Development depends on some stage-specific property of the vector, and the maturation to the infective stage is stimulated during the course of the nymphal-adult moult.

A total of nine playground sites in Dublin city and county were surveyed from which 228 samples were removed. Of these samples, 15% were positive for Toxocara canis ova and a mean egg density of 1.4 ova/100 g was calculated. Two types of playground sites were identified and that the level of toxocaral contamination was found to be greater in ‘neighbourhood playgrounds’ than in ‘adventure playgrounds’. There was no significant difference in the number of positive samples taken from sites both inside and outside these playgrounds. No evidence of Toxocara cati ova was found. Only one sample was positive for Toxascaris leonina ova. Over 50% of the T. canis ova identified were infective. The findings in this study suggest that the sample's moisture content contributes to the long term survival of infective Toxocara ova in the environment. A recovery rate of 69.8% was achieved with a modified version of the flotation method.

Blood samples from 50 dogs with episodic weakness and 50 clinically normal dogs, all belonging to hunting breeds, were examined for microfilariae using the modified Knott's method. The prevalence of microfilaraemia in dogs belonging to the episodic weakness group was 10% for Dirofilaria immitis, 30% for Dirolfilaria repens and 8% for Acanthocheilonema reconditum. In the clinically normal group, the figures were 14% for Dirofilaria repens and 4% for Acanthocheilonema reconditum. The overall percentage of dogs with microfilaraemia in the episodic weakness group was 44 and that of the clinically normal group 16, with a statistically significant difference (P<0.01). The prevalence of microfilaraemia due to the nonpathogenic filarial species (Dirofilaria repens, Acanthocheilonema reconditum) was 34% and 16% for the episodic weakness group and the clinically normal dogs, respectively, with no significant difference.

One hundred and six of 109 common shrews (Sorex araneus) and 62 of 72 pygmy shrews (S. minutus), obtained by Longworth trapping in Southeast England, were infected with cestodes. Ten species were recovered: Choanotaenia hepatica and Hymenolepis prolifer (found in S. araneus); Choanotaenia crassiscolex, Hymenolepis furcata, H. jacutensis, H. schaldybini, H. scutigera, H. singularis, H. diaphana and H. infirma (in both hosts). The morphology, taxonomy and ecology of these species are discussed and the findings of the present study are discussed with reference to previous studies of the helminth fauna of British shrews. Cysticercoids of C. crassiscolex were found in the snail, Vitrina pellucida, and cysticercoids of H. schaldybini in the staphylinid beetle, Anthobium unicolor.

The ultrastructure of various regions of the male reproductive tract and the prostate gland of Cotylophoron cotylophorum (Trematoda: Digenea) is described. The internal lining of the entire male duct system is syncytial in nature, and regional variation is quite evident. The syncytial epithelium of the vas deferens and seminal vesicle is very thin, flat and lamellate and the lumen is packed with spermatozoa. In the pars musculosa (PM) the syncytium is also flat but lamellae are sparsely distributed and anastomosed at places to form loops. The syncytium of the PM is invested by several layers of circular and longitudinal muscle. The pars prostatica (PP) is lined by an uneven but moderately thick syncytial epithelium with nuclei projecting into the lumen. The syncytium bears numerous very long lamellae. The ejaculatory duct epithelium is devoid of lamellae. It is even and moderately thick throughout. The prostate gland cells are uneven in outline and bear long ducts which open into the lumen of the PP. They show an ultrastructural organization suggestive of protein secretion.

The complete gene encoding an immunodominant antigen of Dirofilaria immitis was isolated from a Charomid 9–36 genomic DNA library. This genomic DNA clone termed ‘Dg2’ was characterized by restriction mapping, DNA sequencing of the 5′ flanking region, the exon/intron boundaries and the polyadenylation addition site. The Dg2 with 4872 bp in length consisted of five exons interspersed with four introns. These exons reveal a single open reading frame followed by a long 3′ non-coding region of 1383 bp. The open reading frame of 969 bp encodes a polypeptide of 322 amino acids with a molecular weight of 34,400. The ATG translation initiation codon starts 22 nucleotides downstream from the 5′ end of the first exon. The polyadenylation signal sequence, AATAAA, is located at the 3′ end of the last exon. The transcription initiation site was determined by primer extension technique. S1 nuclease mapping analysis demonstrated that the primary transcript derived from Dg2 is synthesized in microfilariae but not in male or female adult worms. The result suggests that the stage-specific expression of Dg2 is regulated at the level of primary transcript.

The present study was designed to determine the susceptibility of domestic animals to an isolate of Taenia solium from Hainan Province, People's Republic of China. A total of 162 cysticerci were recovered from two pigs and 21 from two dogs after experimental inoculation. Cats, goats and a calf were not susceptible to T. solium. Cysticerci were recovered mainly from muscles of the pigs and all were alive. The remainder were in the liver and only one was alive. In the dog, all cysticerci were recovered from the muscles and all were alive.

Antibody responses against crude antigens and the two (Em18 and Em16) epitopes of Echinococcus mulfilocularis were analysed by Western blotting using sera from the wild vole, Clethrionomys rufocanus bedfordiae (Crb), which were captured in Hokkaido, Japan and found to have been naturally infected with eggs, and compared with those in patients of AHD and mice experimentally infected with protoscoleces of this parasite. Antibody responses in the wild vole were demonstrated most clearly with anti-Crb-IgG antiserum but more faintly with anti-rat-IgG antiserum and poorly with anti-mouse-IgG or anti-human-IgG antisera or Protein G. Although only two serum samples of the wild vole found naturally infected were analysed, antibody responses against Em18 and Em16 in these voles appeared to be similar to those in AHD patients but differed from those in mice.

In order to establish a simple means of handling eggs of taeniid cestodes under non-biohazardous conditions, gravid segments of Taenia taeniaeformis were fixed in ethanol or formalin or were frozen. In vitro hatching of oncospheres was carried out by the 0.5% sodium hypochlorite method using eggs isolated from the nonviable and viable segments. No oncospheres hatched from formalized eggs, whereas almost all oncospheres hatched from all other eggs but the number of oncospheres recovered was highly variable. Oncospheres hatched from eggs isolated from frozen segments were highly fragile. The highest figures for in vitro hatching of oncospheres were recorded when eggs isolated either from segments fixed in 70% ethanol or from viable segments were used.