T cell populations and IL-3 mRNA expression were analysed in mesenteric lymph node cells and intestinal intraepithelial lymphocytes (IEL) in Strongyloides ratti- infected mice. On days 7 and 12 post-infection, 2.6 times as many mesenteric lymph node cells were present in S. ratti- infected mice compared with uninfected mice. Although the percentages of CD3+, CD4+ and CD8+ cells decreased during infection, the absolute numbers of these cell types increased on day 7 due to an overall increase in the mesenteric lymph node cell number. The CD4/CD8 ratio in IEL was increased on day 5, whereas no significant change in the CD4/CD8 ratio was observed in the mesenteric lymph node cells. Expression of IL-3 mRNA, which is an important cytokine for the induction of murine mucosal mastocytosis and S. ratti- expulsion, was examined in mesenteric lymph nodes and IEL of uninfected and infected mice. IL-3 mRNA was detected in mesenteric lymph nodes of S. ratti-infected mice but not detected in the lymph nodes of uninfected mice. IL-3 mRNA was detected in IEL from both infected and uninfected mice with an 20-fold increase in expression in IEL of infected mice. Overall, IL-3 mRNA levels were higher in IEL than in mesenteric lymph nodes following S. ratti- infection. Expression of IL-4, IL-10, stem cell factor (SCF or c-kit ligand) and IFN-γ mRNA was also examined in these two tissues. IL-10 mRNA was not detected in any tissue examined and IFN-γ mRNA levels were unaltered as a result of an S. ratti- infection. Elevated expression of mRNA for SCF (5-fold) and IL-4 (20-fold) was observed in the mesenteric lymph nodes of infected mice. In contrast, SCF mRNA levels were similar in IEL of uninfected and infected animals and only a modest increase in IL-4 mRNA was observed in IEL of infected mice.

Rainbow trout were experimentally infected with the ectoparasitic monogenean Gyrodactylus derjavini at three temperatures, 5.5°C, 11.6°C and 18.7°C. Subsequently, the infection level was monitored during the following 6 weeks. The population growth was positively correlated with temperature in the initial part of the investigation. At 18.7°C growth of the parasite population was fast reaching a peak abundance within 3 weeks, whereafter the infection level decreased significantly. Peak abundance was recorded in week 5 at 11.6°C. A very slow but steady parasite reproduction was noted at 5.5°C, but no peak abundance was reached within 6 weeks. The decline in parasite population after reaching peak levels is likely to be caused by a host response. The host response is also indicated by the parasites' active selection of particular microhabitats. This anti-monogenean response developed fastest at 18.7°C, more slowly at 11.6°C and was not recorded within 6 weeks at 5.5°C.

A herd of goats naturally infected with lungworm and gastrointestinal nematodes was divided into three groups and treated with either morantel tartrate or fenbendazole at strategic periods, i.e. in June (at pre-mating), in November (at pre-kidding) and in January (at early lactation) or left untreated. Morantel tartrate treatment (8mg kg−1) was efficient in reducing the gastrointestinal nematode egg output and fenbendazole treatment (15 mg kg−1) was efficient in reducing the gastrointestinal nematode egg and small lungworm larvae faecal output. Reductions in mortality of adult goats and their progeny and improvement of rearing percentages were recorded in both treated groups, with fenbendazole showing a greater response than morantel tartrate. A relative risk analysis showed that mortality in goats and kids was significantly reduced in treated kids and goats. Reduction of 6.6% in kidding rates, 0.21 in prolificacy, and an increase of 1.3 in abortion rates, 8.3% in kid and 2.2% in goat mortalities, could be attributable to the small lungworm infection. Small lungworm infections seem therefore to be one of the main causes of indirect kid mortality and inadequate breeding performance of goats in the semi-arid Middle Atlas region of Morocco.

Two sets of dung-derived organisms from soil routinely fertilized with manure (MA) and soil chemically fertilized (CH) were cultured separately in the laboratory. Baermannized organisms from these cultures were added to 20 g of faeces from strongyle-infected horses to form three treatment groups: (i) no soil organisms; (ii) low inoculum of soil organisms containing all organisms present in a suspension of approximately 100 adult female free-living nematodes; and (iii) high inoculum containing those soil organisms present with approximately 1000 adult female free-living nematodes. Three studies were conducted using MA cultures and faeces containing 50 strongyle epg, CH cultures and faeces containing 1500 strongyle epg, and a mixture of soil organisms from the two cultures (MC) and faeces containing 600 strongyle epg. Within each study, five control cultures and 15 each of low and high inoculum cultures were prepared and incubated at 24°C and 95% humidity in a climate chamber for 15 days. Parasitic and free-living nematodes were then recovered by the Baermann technique and counted. The numbers of third stage larvae were significantly lower in the high inoculum group compared to controls. The percent reductions in the number of third stage larvae for the low and high inoculum groups were 63.6% and 90.9%, 85.1% and 97.1%, 84.5% and 98.4% for MA, CH, and MC studies, respectively, indicating that mortality increased with the number of soil organisms added to cultures. Examination of the source cultures detected the presence of two species of nematophagous fungi and three genera of free-living nematodes reported to be predacious.

In an abattoir study, 514 camels, slaughtered for meat production in different areas of northern Libya were examined for the presence of cystic echinococcosis (CE). In addition, 367 sheep and 184 goats were examined. The overall prevalence of infection with CE was 48% in camels, 15.8% in sheep and 3.8% in goats. The infection rate, number and size of cysts were significantly higher in older camels. In six city abattoirs across northern Libya, i.e. Zawia, Tripoli, ElKhumes, Mesurata, Sirt and Benghazi, the prevalence rate of infection in camels ranged from 38.7% to 55.2%, in comparison with sheep and goat rates which were between 0% and 37.9% and 0% and 8.2%, respectively. In camels, the lungs were the most frequently infected organs (85.4%) with liver cysts occurring at a significantly lower rate (33%). In contrast, the liver was the predominant infected site with prevalence values of 86% and 100% in sheep and goats, respectively. More than 90% of camel hydatid cysts were fertile. The possible role of camels in the transmission of CE in Libya is discussed.

The histopathological response of carp to Sanguinicola inermis was investigated by serial sectioning laboratory infected fish up to 90 days post infection (d p.i.). Juvenile flukes and adults caused mechanical damage to tissues during invasion and migration up to 28 d p.i. Adults partially occluded blood vessels and may have reduced blood circulation. In the initial phase of egg production (28–42 d p.i.), eggs and emigrating miracidia in gill tissue caused breakdown of vascular integrity, necrosis, hyperplasia, haemorrhage and eosinophilic infiltration of epithelial tissue. After 42 d p.i. the host granulomatous inflammatory response encapsulated eggs lodged in the gills, visceral sites and connective tissue displacing normal tissue. Encapsulation and subsequent degradation of eggs and miracidia within granulomata was highly developed by 90 d p.i. Laboratory infections of S. inermis can induce respiratory distress and therefore impair respiration of fish. The parasite also caused pathological changes in osmoregulatory, excretory and haemopoietic tissue and may impair function in these organ systems.

The influence of soil texture (silt, sand and laterite) and flotation solutions (saturated NaCl, sucrose, NaNO3 and ZnSO4) upon the recovery of Toxocara ova from seeded soil samples with the centrifugal flotation technique was investigated. Soil samples of different texture were artificially seeded with Toxocara spp. ova and subjected to a centrifugal flotation technique which used various flotation solutions. The results showed significant (P<0.001) interactions between the soil types and the flotation solutions. The highest percentage of ova recovery was obtained with silty soil (34.9−100.8%) with saturated NaC1 as the flotation solution (45.3−100.8%). A combination of washing of soil samples with 0.1% Tween 80, and flotation using saturated NaCl and a 30 min coverslip recovery period was used to study the prevalence of contamination of soil samples. Forty-six soil samples were collected from up to 24 public parks/playgrounds in urban areas of Petaling Jaya and suburban areas of Serdang. The prevalence of Toxocara species in the urban and suburban areas was 54.5% and 45.8% respectively.

Calves and lambs heavily infected with Strongijloides papillosus develop cardiac arrest by ventricular fibrillation which is preceded by continuous sinus tachycardia and prolongation of the PQ interval during the patent infection. In the present study, cardiac rhythms following anthelmintic treatment were investigated in lambs infected with S. papillosus to ascertain whether cardiac disorders due to the infection are based on a reversible and curable change. Eight lambs were given a lethal dose of S. papillosus. Five of the animals were injected with ivermectin when they developed continuous sinus tachycardia and prolongation of the PQ interval. The other three animals served as untreated controls. In the treated animals, elevated heart rates and PQ intervals began to decrease between 10 and 21 h, then continuous sinus tachycardia and prolongation of PQ interval disappeared within 39 h of treatment. No arrhythmias were detected after the disappearance of sinus tachycardia. Faecal egg counts became negative within 61 h of treatment. Only a few worms were collected from the small intestine at necropsy. The control animals developed ventricular fibrillation by 349 h after infection, having high faecal egg counts and intestinal worm burdens. These results indicate that cardiac disorders generated by S. papillosus infection are reversible and curable following worm elimination.

Three hundred and twenty seven European lynx (Lynx lynx) were examined forTrichinella sp. larvae using the muscle digestion method. The animals were of both sexes, various ages, and collected between 1989 and 1994 in different locations in Finland. Forty percent of them (132) were found to be infected. Infection was overdispersed, so that the majority of infected lynx only harboured small amounts of larvae, while a minority had higher densities of infection, but never significantly exceeding 40 larvae per gram of muscle (lpg). The median density of infection was 1.04 lpg. To find factors statistically associated with the risk of infection, multivariate logistic regression analysis was performed. Male sex, increasing age, and the density of raccoon dog population in the area were all significantly associated with infection. However, the association with age was not linear and prevalence did not increase after middle age. The mean density of infection decreased slightly with age. The association with the density of the raccoon dog population leads to a tentative hypothesis that the raccoon dog might be an important reservoir of sylvatic trichinellosis in Finland.

The strobila of an adult tapeworm represents a continual gradient of developmental stages from immature to gravid proglottids. The purpose of this study was to determine if organogenesis (as measured by the develop mental gradient) in tapeworms within a single host and among different hosts occurred at the same rates. Rats were infected with Hymenolepis diminuta and the tapeworms were recovered 20 days post-infection. The total number of proglottids in each worm was determined, and five “benchmarks” of organogenesis were quantified. The data demonstrated that organogenesis in worms from a single host occurred at a relatively constant rate, but that rates in tapeworms from different hosts were different.

Experimental infection of larval Echinococcus multilocularis in the rodent brain was attempted to establish a murine model for cerebral alveolar echinococcosis. Balb/c mice and jirds were injected intracranially with 10% of a homogenated hydatid cyst mass. Small cystic larvae were observed macroscopically in the cranial cavity 1, 2 and 5 months post-infection in both mice and jirds. Some larval cysts from both rodents contained mature or immature protoscoleces. In mice, the laminated layer was found in the lateral ventricle 2 months post-infection but without protoscoleces. At five months post-infection, larger larval cysts were found in the cranial cavity of a mouse, which also demonstrated partial palsy of the legs. A laminated layer with mature protoscoleces was observed in the third ventricle and the mouse also harboured, in the left lung, a larval cyst containing protoscoleces surrounded by lymphocytes. Jirds were also found to be infected with metacestodes in the cranial cavity, but neither unusual behaviour nor establishment of cysts inside the brain was observed in jirds during the course of infection.

Taxonomic characters of the male posterior end and the body cuticle of Euchordodes nigromaculatus (Nematomorpha) were described by scanning electron microscopy (SEM) and compared with the original description by Poinar (1991a) and with other Euchordodes species. Intraspecific variation was found in the body length, the distance between the cloacal opening and the posterior end and especially in the form of the male posterior end. The latter either possesses two short lobelike structures and a ventral groove or lacks these structures. The importance of SEM investigations and observations of intraspecific variation is stressed for the taxonomy of nematomorph species.

Most carcinogens and xenobiotics are metabolized primarily by the mixed function oxidase system which includes cytochrome P450, cytochrome b5, NADPH-cytochrome c reductase and aryl hydrocarbon [benzo(a)pyrene] hydroxylase. The present study investigates the influence of infection with different levels of Schistosorna mansoni cercariae on the hepatic levels of reduced glutathione, glutathione S-transferase and glutathione reductase in addition to the enzymes of mixed function oxidase. Cercariae infection levels of 60, 120, 180, 300 and 600 per mouse increased: (i) the hepatic content of cytochrome P450 by 27%, 38%, 72%, 57%, 48% respectively; (ii) the aryl hydrocarbon hydroxylase activity by 44%, 64%, 76%, 90%, 51% respectively; and (iii) the hepatic level of reduced glutathione by 67%, 83%, 103%, 60%, 38% respectively. The cytochrome b5 content did not change at the lowest level of infection but increased at the other four levels by 45%, 76%, 49% and 38% respectively. The activity of glutathione S-transferase increased at the first three levels by 42%, 40%, 27% respectively and decreased at the last two levels by 28% and 52% respectively. On the other hand, the activity of glutathione reductase did not change at any level, whereas, NADPH-cytochrome c reductase activity decreased at the last two levels by 44% and 54%. The alterations in the activities of phase I & II of drug-metabolizing enzymes as a result of infection with different levels of S. mansoni may thus change the liver's capacity to detoxify many endogenous compounds and may also potentiate the deleterious effects of aromatic hydrocarbons, e.g. benzo(a)pyrene, upon the liver and probably other organs. Such alterations may also change the therapeutic actions of drugs that are primarily metabolized by the P450 system, when administered to patients with schistosomiasis.

Malacological samplings were made from January 1994 to December 1996 in the Albufera Natural Park (Valencia, Spain) to trace the dynamics of molluscan populations and the prevalence and intensity of infection by larval trematodes. A total of 10,533 freshwater gastropods belonging to seven species (Lymnaea auricularia, L. truncatula, L. palustris, L. peregra, Bithynia tentaculata, Physa acuta and Gyraulus chinensis) was examined, and 110 (1.04%) were found to harbour some of the nine distinguishable types of cercariae, namely four echinostome cercariae (Hypoderaeum conoideum, Echinoparyphium recurvatum, Euparyphium albuferensis, and Echinostoma sp.), four furcocercous cercariae, and one xiphidiocercous cercaria. This study shows that the composition of the snail and trematode communities may be determined by the particular environmental conditions present and the human intervention in the area.

Histochemical glycogen and neutral lipid studies were conducted on Echinostorna trivolvis cercariae maintained in artificial spring water (ASW) at 24–25°C for up to 24 h after emergence from host snails. Treatment of whole cercariae by the periodic acid Schiff (PAS) reagent with or without 1% malt diastase showed that cercariae depleted glycogen mainly from the tail by 6 to 24 h postemergence. The posterior tip of the tail remained PAS positive and diastase fast suggesting the presence of mucopolysaccharides there. Fresh cercariae or those stained up to 24 h postemergence with Oil Red 0 showed the presence of neutral lipid droplets in the excretory system. There was no discernible difference in the size, abundance, or distribution of these droplets in fresh or aged cercariae. Cercariae maintained in ASW plus 1% glucose for 12 or 23 h showed no evidence of resynthesizing glycogen. Nevertheless, cercariae survived longer in 1% glucose than in either 0.0, 0.1 or 0.5% glucose; but only at 23 h were any differences statistically greater (one way ANOVA, P <0.05).

The intestines of 20 grey Peruvian foxes (Pseudalopex culpaeus) were examined for the presence of Echinococcus granulosus and other intestinal parasites. Echinococcus granulosus was not found in foxes but Taenia hydatigena and T. multiceps were found in 7 and 4 animals respectively. The grey fox may not be a suitable definitive host for E. granulosus. However, it may act as a sylvatic reservoir of T. hydatigena and T. multiceps in the central Peruvian Andes.

Helisoma trivolvis (Pennsylvania strain) snails naturally infected with Echinostoma trivolvis larvae were maintained for 10 months (300 days) at 4°C in artificial spring water to determine the effects of storage on parasite survival. Three of 20 snails were alive at 10 months and when isolated in spring water at 22−24°C released active cercariae. The mean number of cercariae released in 2 h from each stored snail was significantly less than that from freshly collected snails. Infectivity of cercariae from stored hosts to experimentally infected, laboratory-raised Helisoma trivolvis (Colorado strain) snails was significantly less than that of cercariae from fresh hosts based on cyst recoveries in the Colorado strain of H. trivolvis within 24 h p.i. There was no significant difference in the redial number or the number of cercariae per redia in stored versus fresh snails. In conclusion, some reduction in cercarial emergence and decrease in cercarial infectivity to a second intermediate snail host occurred following storage of H. trivolvis naturally infected with E. trivolvis in ASW at 4°C for 10 months.