IgG and IgM antibody responses to fluke cysteine proteinases in Paragonimus ohirai- and Fasciola sp.-infected rats were followed by means of cystatin capture ELISA using fluke excretory-secretory products for 10 weeks after infection. The specific IgG antibodies were detectable at week 2 postinfection in all P. ohirai-infected and some Fasciola-infected rats. Levels of specific IgG antibodies increased rapidly between week 2 and 6, and slightly thereafter, in both infected groups. From week 3, specific IgG antibody levels were higher in Fasciola-infected than P. ohirai-infected rats. Sera from infected rats did not react with heterologous cysteine proteinases throughout the infection periods. In both infected groups, the kinetic patterns of specific IgM antibody responses were similar to those of specific IgG antibody responses although the ELISA levels of the IgM antibody responses were much lower. In abnormal infections with P. ohirai metacercariae x-irradiated at 2 krad, the specific IgG antibodies were detectable at week 2 postinfection with similar ELISA values to normal P. ohirai infection, but thereafter increased little. In infections with P. westermani, for which the rat is not a suitable host, even stunted worms induced a comparable specific IgG antibody response, although the response was lower than in normal infections with P. ohirai. These results indicate that cystatin capture ELISA can distinguish clearly between Paragonimus and Fasciola infections which show immunodiagnostic cross-reactivity and is useful even in the early stages of the infection and in the infection of unsuitable hosts.

Morphometric and chaetotactic studies were carried out on the body and cephalic regions of the rediae of Fasciola hepatica (Trematoda: Fasciolidae) in order to precisely identify the different redial generations of this trematode in Lymnaea truncatula under experimental infection. At day 49 post-exposure at 20°C, the length of the redia was significantly higher in the first group of the first generation (R1a) compared with successive generations, R1b, R2a and R2b/R3a. The width of the body was similar in the R1a, R1b, and R2a rediae, but was significantly lower in the R2b/R3a groups. The intrapharyngeal cavity of R1a rediae was significantly wider compared with the R1b, R2a, and R2b/R3a groups, whereas the pharyngeal wall was significantly thicker in the R2b/R3a rediae compared with the R1b and R2a groups. Four other measurements, namely the maximum length and width of the pharynx, diameter of the mouth, and width of intestine, also showed significant variations in relation to pharyngeal morphology and age of infection. Discriminant analysis based on these measurements demonstrated that 98% of the rediae were readily categorized into the four groups identified. The number of perioral sensillae ranged from 126 to 160 but a significant difference was only noted between the mean values of the first generation and those of the group R2b/R3a. From these parameters, the maximum width of the pharyngeal lumen was found to be the best characteristic in the identification of the redial generations.

The structuring process of the macroparasite community of caged Cichlasoma urophthalmus was studied over time using sentinel fish. Three thousand uninfected cichlids were stocked in floating cages introduced into a quarry in which a wild population of the same species was present. Caged and wild cichlids were sampled monthly over 6 and 7 months, respectively. Seventeen macroparasite species were found in the wild C. urophthalmus population, ten of which were detected in the caged population after 6 months. Early infections were by those species that were more frequent and abundant in the wild population, while helminths with a low prevalence and abundance in the wild appeared later in the caged fish population. The results suggested that the structuring process of the macroparasite community of caged C. urophthalmus followed a predictable pattern, in which those species that were most frequent and abundant in the wild were the first to establish in sentinel fish.

In an in vitro trial, the trapping ability of Arthrobotrys robusta and Monacrosporium gephyropagum against Strongyloides papillosus infective larvae on corn meal agar plates, was evaluated after seven days of interaction at 25°C. Monacrosporium gephyropagum trapped 93.1% of the larvae whereas A. robusta trapped only 32.3%. Variability in the capture of S. papillosus infective larvae by both trapping fungi is discussed.

Centrocestus armatus (Trematoda: Heterophyidae) develops rapidly and produces eggs at 3 days postinfection in albino rats. Excysted metacercariae are pear-shaped and concave ventrally, with 42–44 peg-like circumoral spines. The entire body surface is densely covered with scale-like serrated spines. On juveniles, serration of the tegumental spines is greatest in the middle of the ventral and dorsal surfaces, and decreases anteriorly and posteriorly. Ciliated sensory papillae are concentrated around the oral sucker. Several nonciliated sensory papillae (type II papillae) occur equidistantly on the acetabulum and are arranged in a linear symmetry on the dorsal surface. On adults, the serration of the tegumental spines decreases to 14–17 tips on the ventrolateral surface. The high density of tegumental spines on posterior half of the body and the distribution of type II papillae on dorsal surface are considered to be characteristic of C. armatus.

Specimens of 12 helminth species were collected from carcasses of eight Lynx pardinus (Temminck, 1827), a carnivore endemic to the Iberian Peninsula. These species included: Brachylaima sp. (12.5%) (Trematoda); Taenia pisiformis (12.5%), T. polyacantha (25%), T. taeniaeformis (25%) and Mesocestoides litteratus (37.5%) (Cestoda); Eucoleus aerophilus (12.5%), Ancylostoma tubaeforme (12.5%), Toxocara cati (37.5%), Toxascaris leonina (62.5%), Vigisospirura potekhina potekhina (12.5%), Mastophorus muris (12.5%) and Physaloptera praeputialis (12.5%) (Nematoda). The helminth fauna in Iberian lynx is compared with that of L. canadensis and L. rufus in America, and for L. lynx in Eurasia. The potential relationships between the parasitological data and some geographical, historical and dietary factors are discussed.

An erratic parasitism was observed in the lungs of sheep experimentally infected with Fasciola gigantica at autopsy 14 weeks after inoculation. Macro-scopically, several hyperaemia of 7.5–12.5 mm in diameter were found on the surface of the lungs. Juvenile flukes detected in the lungs were much smaller than those in the liver of the same sheep. A slight inflammatory reaction was observed in the lungs and it is likely that the flukes had migrated in the pleural cavity for some time. Occasionally, a mixed thrombus with many eosinophils was found in the blood vessels adjacent to the bronchia, although no cough was observed clinically. This suggests that diagnosis of juvenile fluke is difficult not only by parasitological but also serological methods.

During studies on the ecology of fish helminths, the tapeworm Proteocephalus torulosus (Batsch, 1786) was frequently found in the intestine of the blue bream (Abramis ballerus) from the Oder River (Germany/Poland). In total, 633 fish, ranging between two and 16 years old, were sampled at monthly intervals over a two year period during 1993–1995. Statistically significant differences in the seasonal occurrence of the parasite in its fish host were observed. In 1993, the prevalence remained at a high level, ranging between 61.9 and 100%. During the summer of 1994, this value decreased to 5.5% and remained low for the rest of the year. The pattern of mean intensity of infection was similar to that of the prevalence. In 1993, the mean intensity varied between 8.4 and 31.8 worms per infected fish, with a continual loss of worms being observed in the summer of 1994. Changes in the amount of suspended particulate matter in water have been identified as the main cause of these observed differences in the course of infection of blue bream.

The study describes methods developed for using video-imaging technology to record and measure the velocity of Schistosoma mansoni miracidia. The efficacy of the classical bioassay procedure (a qualitative behavioural assay) was compared with that of the new quantitative protocol, for assessing the sub-lethal impact of a larvicidal dichloromethane extract of the seeds of Millettia thonningii on miracidia. The new technique confirmed the efficacy of the classical bioassay for rapid determination of the lethal and sub-lethal impact of larvicides but also provided quantitative information on sub-lethal impacts on miracidial velocity and shape.

The structure of the digestive tract of Euclinostomum multicaecum (Digenea: Euclinostomatidae) is unusual, comprising several main lateral caeca which extend posteriorly and further divide, giving rise to numerous smaller branches which are widely distributed throughout the fluke. These multicaeca presumably promote nutrient absorption during rapid and prolonged feeding directly following excystment. The caecal wall consists of a syncytial gastrodermal epithelium, bearing loop-like lamellae which extend into the lumen and enclose spherical inclusion bodies and presumably also, increase the absorptive surface area. There was no evidence of endo- or exocytosis, nor were lysosomes, phagosomes or residual bodies observed. The gut caeca are supported by a fibrous basal lamina and an underlying layer of muscle fibres, while parenchymal cells occupy much of the extracellular space. The protonephridial system resembles that observed in other digeneans consisting of flame cells and collecting ducts which join to form a bladder that opens externally through a single excretory pore. The syncytial epithelium of the collecting ducts is elevated by numerous lamellae while the basal lamina is highly infolded. The luminal contents of these ducts comprise bar-shaped crystalline structures, lipid droplets and electron-dense inclusion bodies. The excretory system is supported by a network of muscle fibres and parenchymal cells.

Metacercariae of Plagiorchis muris, obtained from naturally infected dragonflies, Sympetrum eroticum, successfully established in 4-week-old albino rats up to 14 days post-infection (p.i.) but by day 28 p.i. the recovery rate had significantly decreased. The genital primordia in excysted metacercariae were differentiated into those of metraterm, Mehlis' gland, ovary and cirrus pouch, with the primordial testes appearing on day 1 p.i. The vitellaria and eggs in the uterus were present in flukes on days 2 and 4 p.i., respectively. Mature flukes were established in the lower part of the small intestine on day 5 p.i., with the peak of egg production occurring on day 14 p.i. Growth of the flukes continued up to day 28 p.i.

The ultrastructure of the cuticle of infective juveniles (IJs) of Steinernema carpocapsae (newly emerged and 80-day-old) and newly emerged IJs of S. riobravis, S. feltiae and S. glaseri was examined using transmission electron microscopy. The thickness of four distinctive layers of the cuticle was measured: epicuticle, cortical and median layer, striated layer and fibrous mat. The thickness of the cuticle was correlated with the size of the IJ. In the case of newly emerged IJs, the smallest species, S. carpocapsae, had a cuticle thickness of c. 270 nm compared with c. 460 nm for S. glaseri, the largest of the four species. The overall thickness of the cuticle or the thickness of the cuticle layers was not correlated with the ability of the IJs of the four species to survive desiccation per se. The major difference between newly emerged IJs of the four species was that S. carpocapsae had a proportionately thicker striated layer compared with the other three species. The significance of this is not known but it may be an adaptation involving the nictation behaviour of this species. A substantial change was observed in the cuticle of aged (80-day-old) IJs of S. carpocapsae, whereby the thickness of the cortical and median layer increased by more than 100% and the overall thickness of the cuticle increased by about 50%. Two possible explanations for this increase are: (i) new material was synthesized; or (ii) the fluid content of this layer increased due to an increase in the permeability of the outer layers of the cuticle. The ultrastructure of the sheaths of S. feltiae and S. glaseri was also examined and, apart from S. glaseri having a thicker sheath, the structure of the sheath in both species was similar, with the epicuticle and striated layer still visible.

A data set comprising individual host/parasite lists from 100 Lacerta viridis (Reptilia: Lacertidae) belonging to four isolated populations in Bulgaria was studied. A total of seven helminth species was recovered (Leptophallus nigrovenosus, Plagiorchis molini, Oswaldocruzia filiformis, Spauligodon extenuatus, Skrjabinelazia hoffmanni, Physaloptera clausa and Mesocestoides sp.). Lacerta viridis is a new host record for the first five of these species. Communities of intestinal helminths of L. viridis consist of a few species which resulted in a low species richness, abundance and diversity of infracommunities, which exhibit substantial homogeneity among the four samples. A similar pattern of dominance of two nematode species leading to a relatively high community similarity at both infra- and component community levels was observed. While intestinal helminth communities in lizards from ‘marginal’ habitats were dominated by the host generalist, O. filiformis, those in hosts from ‘typical’ habitats were dominated by the lizard specialist S. extenuatus. The results indicate that the characteristics of the host's habitat are important in determining the composition rather than structure of intestinal helminth communities in L. viridis.

A comparative study of eosinophil chemotactic factors was carried out using cysticercoids and oncospheres of Hymenolepis nana. Cysticercoids showed twice the chemotactic activity for eosinophils than the oncospheres. Eosinophilia induced by oncospheres and cysticercoids observed in secondary and primary infections, respectively, were discussed from the view point of the immunobiology of this parasite.

Vol. 71, Page 321, Col. 1, Line 10. For ‘bovine-GST’ read ‘Schistosoma japonicum-GST’

Vol. 71, Page 321, Col. 2, Line 22. For ‘anti-bovine-GST’ read ‘anti-Schistosoma japonicum-GST’