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Superinfection of Biomphalaria glabrata with Schistosoma mansoni.

Biomphalaria glabrata 2 to 12 mm in diameter were exposed to 1 miracidium of Schistosoma mansoni and after 15, 30, or 60 days were reexposed to the homologous strain. The criterion of superinfection was the subsequent escape of cercariae of both sexes. Opposite sex superinfection was acquired by 45 of 106 snails of various sizes, all of which were in the group reexposed at 30 days. The observations confirm those of Kagan and Geiger and suggest that in the schistosomes a maximizing of the number of intermediate hosts with larval populations of both sexes may be an adaptation having a high species survival value.

Animals↗

Bioactivity of Anagallis arvensis and Calendula micrantha plants, treated with ammonium nitrate, superphosphate and potassium sulphate fertilizers, on Biomphalaria alexandrina.

The survival rate of B. alexandrina snails maintained in aqueous solutions of the two tested plants (Calendula micrantha and Anagallis arvensis) decreased gradually with time until the 9th week and 10th week where the survival rate was zero in the high concentration of A. arvensis and C. micrantha, respectively, meanwhile, the survival rate of the control was 20%. Also, the two plants caused reduction in hatchability of snails egg masses. Thus, the percent of hatching in A. arvensis (82 ppm) was 46% and in C. micrantha was 72% compared with control (97.29%). Both plants reduced the infection rate of Biomphalaria alexandrina snails with Schistosoma mansoni miracidia to 41.17% and 61.9%, respectively, compared with control (90%). C. micrantha caused much higher reduction in snail infection rate than A. arvensis. The prepatent period was significantly prolonged in snails maintained at higher concentration of both plants. The cercarial output (expressed as mean number/snail) revealed that, A. arevensis caused a significant reduction in cercarial production than control. While, high concentration (120 ppm) of C. micrantha caused a significant elevation in the mean number of cercariae/snail. However, the total number of cercariae produced by all snails in each group showed a reverse relation with the tested concentrations in both plants.

Animals↗

In vivo, attenuation of schistosome cercarial development and disturbance of egg laying capacity in Biomphalaria alexandrina using sublethal concentrations of plant molluscicides.

The dry powdered of Sinapis arvensis, Thymelaea hirsuta, Callistemon lanceolatus and Peganum harmala showed molluscicidal activity against Biomphalaria alexandrina, specific intermediate hosts to Schistosoma mansoni. Effect of LC25 of dry powdered plant molluscicides on hexokinase (HK), glucose phosphate isomerase (GPI), AMP deaminase, adenosine deaminase and phenol oxidase (PO) of B. alexandrina was traced. C. lanceolatus showed the highest molluscicidal activity as it has the lowest LC50 compared to S. arvensis, T. hirsuta, and P. harmala. LC25 of the latter three plants resulted in more significant inhibition of HK, GPI, AMP-deaminase and PO than C. lanceolatus. Treatment of snails with LC10 of these plants markedly affected compatibility of B. alexandrina to S. mansoni infection. Significant decrease in cercarial production recorded in snails treated with sublethal concentrations of S. arvensis, T. hirsuta, and P. harmala. Remarkable impairment of the egg laying capacity of molluscicide-treated snails was also recorded. Correlation between activity levels of HK, GPI and AMP deaminase and compatibility to parasitic infection and role of PO in the egglaying capacity of these snail species were discussed.

Animals↗

Laboratory assessment of the molluscicidal activity of Commiphora molmol (Myrrh) on Biomphalaria alexandrina, Bulinus truncatus and Lymnaea cailliaudi.

The molluscicidal properties of the oil extract of Commiphora molmol (Myrrh) were tested against Egyptian snail species: Biomphalaria alexandrina, Bulinus truncatus and Limnaea cailliaudi. The impact of the extract on the egg cluches of B. alexandrina and L. cailliaudi was also evaluated. Snails and their eggs were exposed for 24 and 48 hr at 22-26 degrees C to various concentrations of the extract. The results showed different susceptibilities B. alexandrina showed higher LD50 and LD90 (155, 195 ppm) than B. truncatus (50, 95 ppm) and L. cailliaudi (50, 85 ppm) after 24 hr exposure. 100% mortality was obtained for the egg cluches of B. alexandrina and L. cailliaudi at concentrations of 100 ppm and 75 ppm respectively. Lower concentrations were needed to obtain the same results after 48 hr. The present laboratory studies demonstrated that Myrrh has a molluscicidal effect on the snail intermediate hosts, particularly on their eggs. Field studies are recommended.

Animals↗

Potential effect of Allium cepa and Allium sativum on haemolymph of Biomphalaria alexandrina, the intermediate host of Schistosoma mansoni.

Biomphalaria alexandrina were fed on either Allium cepa or A. sativum to study their effects on some biochemical parameters such as total proteins, free amino acids and liver enzymes (ALT, ALP and AST) on egg laying activity of the snails. The results revealed that ALP was highly significantly reduced in haemolymph of snails that fed on either Allium cepa or A. sativum. Also, ALT and AST were highly significantly reduced in haemolymph of snails that were fed on A. cepa while those fed on A. sativum showed no change in ALT activity and a high significant increase in AST activity. Total proteins were significantly decreased in haemolymph of all treated snails whereas variations in free amino acids contents were also observed. The reproductive activity of snails fed on either Allium cepa or A. sativum was highly affected. In addition, growth rate of newly hatched snails fed on either A. cepa or A. sativum was affected. Exposure of snails to water containing either A. cepa or A. sativum caused snail toxicity which may result from alterations in the snails' habitat.

Amino Acids↗

Cellular response to Schistosoma mansoni infection in Biomphalaria alexandrina strains selected for susceptibility and resistance.

Exposure of juvenile and adult Biomphalaria alexandrina to Schistosoma mansoni miracidia resulted, typically, in three susceptibility patterns: a) non-infected snails; b) normal infections, and c) retarded infections. Under laboratory conditions, a vigorous resistant-type cellular response to invading miracidia was seen in the histological sections of non-susceptible snails. Accordingly, they were classified as resistant snails. Data pertaining to the influence of host size on suceptibility to S. mansoni indicates that adult snails (i.e. 10-20 mm shell diameter) were significantly less likely to harbour sporocysts than juvenile ones (i.e. 5-10 mm shell diameter). Cellular reaction to the infection varied with sporocysts location and length of infection. At 2 days post-exposure (DPE), most sporocysts were viable. Approximately 8-12% of the sporocysts had elongated shaped transverse constriction and were categorized "normal", while those showing no elongation were categorized "retarded". All remaining sporocysts at 4 DPE were categorized "dead", while at 30 DPE, most sporocysts were "amorphous" with eosinophilic masses. Although encapsulation of sporocysts never occurred in susceptible snails, haemocyte aggregations could sometimes be observed in the proximity of well developed sporocysts. In resistant snails, this cellular response continued to increase and resulted in the encapsulation of the sporocysts. In susceptible snails, the nucleus of secretory cells of the albumen cytoplasm were different in susceptible and resistant snails.

Animals↗

Fasciola immature stages sought in Lymnaea species and Biomphalaria species in the water bodies of Dakahlia Governorate.

Examination of the five different water bodies in Dakahlia governorate, revealed four species of Lymnaea. These were L. natalensis (68.4%). L. truncatula (16%), L. stagnalis (12.2%) and L. columella (3.4%). Also, two species of Biomphalaria were recovered. These were B. alexandrina (54.7%) and B. glabrata (45.3%). Examination of all these snails showed natural infection with immature stages of Fasciola sp. in 5.5% of L. natalensis (= cailliaudi), 3.1% in L. truncatula and 0.67% in B. alexandrina. The importance of these snails in dissemination and spreading of fascioliasis was discussed.

Animals↗

Effect of sublethal concentrations of Atriplex halimus (Chenopediaceae) on Biomphalaria alexandrina, the snail-vector of Schistosoma mansoni in Egypt.

Effect of sublethal concentrations of Atriplex halimus on the mortality rate, longevity, egg production of Biomphalaria alexandrina and hatchability of their eggs were studied. The sublethal concentrations of Atriplex caused reduction in survival rates, longevity and egg production of B. alexandrina. Hatchability of snail eggs exposed to tested plant was decreased by increasing its concentrations.

Animals↗

The molluscicidal efficacy of three products against Biomphalaria alexandrina and Lymnaea natalensis.

Toxicity of three local formulated products, Sol E.C (mineral oil), Sisi-6 (surfactant) and Castor bean oil E.C (plant oil) were tested against Biomphalaria alexandrina and Lymnaea natalensis, in two water sources. Results indicated that in dechlorinated water after 24 hr exposure, castor bean oil was the most toxic product against the snails, followed by Sisi-6 and sol (E.C) with LC90 of 250 ppm and 8 ppm against B. alexandrina and L. natalensis, respectively. When Nile water was used after 6 hr. exposure, a high concentration of castor bean oil (4 LC90) did not achieve 100% mortality of the snails. A 100% mortality was achieved by 2 LC90 of Sisi-6 with Nile water. On the other hand, caster bean oil was more fatal to eggs of the snails (LC90=660 ppm) than the other two products. In general, L. natalensis was more susceptible to the experimental products than B. alexandrina.

Animals↗

[Isolation and partial study of an anti-hemoglobine precipitine in "Biomphalaria glabrata" (author's transl)].

A protein (PaHb) with a precipiting capacity with regard to normal and pathological human hemoglobin as well as horse and hen hemoglobin has been separated on immunoadsorbent from hemolymph of Biomphalaria glabrata. The joining of PaHb and hemoglobin takes place at the level of the polypeptidic chain. A reconnaissance of the spatial structure of the globin seems to exist. The absence of heme does not lead to a decrease in the intensity of the reaction. The coefficient of the sedimentation of PaHb is of 2.74 S and its molecular weight has been estimated at 47,000 per chromatography in thin layer. The divalent cation MgCl2 strengthens the intensity of the reaction, as for CaCl2 no change is observed, and in the presence of sodium citrate one observes a clear decrease in the reaction. The intensifying of the reaction when in presence of divalent cation MgCl2 could be the result of a stabilization or an activation of the natural structure of PaHb when in presence of Mg. PaHb shows no fonctional impairment after exposure at 65 degrees C during 45 min. The localization of PaHb in the total antigenic structure of the hemolymph is situated around the level of the 5th precipitine line. The functional role of the protein seems to carry the hemoprotein of the hemolymph.

Animals↗

Esterification of cholesterol by the hepatopancreas of the mollusc Biomphalaria glabrata.

Homogenates of the hepatopancreas of the mollusc Biomphalaria glabrata, previously called Australorbis glabratus Say, 1818 (Pressoa, 1969), were incubated with cholesterol-4-C14 (dispersed on celite) at 37 degrees C for 24 hr. The lipids were extracted, separated into classes by thin-layer chromatography and the radioactivity associated with the different classes determined. Net esterfication of cholesterol was then obtained by calculating the percent of the total cholesterol radioactivity incorporated into the esterified cholesterol. The esterified cholesterol was also fractionated by thin layer chromatography, and the relative distribution of radioactivity associated with the different cholesterol ester groups was determined. The results showed the presence of cholesterol esterifying activity in the hepatopancreas with a percent esterification of 20.6%. It was found that the accumulation of radioactivity was higher in the polyunsaturated esters and lower in the monounsaturated esters.

Animals↗

Embryonic development of the freshwater snail Biomphalaria glabrata under microgravity conditions (STS-89 mission).

The embryonic development of the fresh-water snail Biomphalaria glabrata was examined under microgravity-conditions and compared with the ground control and standard embryos, putting special emphasis on the shell formation. The process of shell formation may be particularly sensitive to the change of gravitational forces. The project aimed at determining whether the processes of mineralization during the formation of the exoskeleton in the growing snail embryo take place normally under microgravity conditions. Twenty-four adult individuals of the tropical freshwater snail B. glabrata were maintained 9 days in the Closed Equilibrated Biological Aquatic System (CEBAS Minimodule) on Space Shuttle flight STS-89. The animals produced spawning packs throughout the duration of the mission so that embryos of all developmental stages were achieved. The embryos developed slightly slower in the CEBAS than under standard conditions, and in older embryos a decreased mineralization of the shell was detected. These phenomena, however, were observed in the flight module as well as in the ground control specimens and was not an effect caused by the microgravity conditions. Embryos of B. glabrata showed a correct morphogenesis under microgravity, no teratological effects were noticed, and the shell formation proceeded normally.

Animals↗

The influence of hydrocortisone on cellular defence mechanisms of Biomphalaria glabrata.

Since the internal defense system of mollusks consists of cellular and humoral mechanisms, we examined the role of hydrocortisone in mollusks defense cells and the influence of this steroid on the development of Schistosoma mansoni in its intermediary host. Hydrocortisone had an immunosuppressive action in Biomphalaria glabrata, as reflected in the reduced number of defense cells and the altered cell physiology. Histopathological analysis showed that hydrocortisone facilitated the intramolluscan development of S. mansoni, by reducing the extent of the inflammatory response, seen as a greater number of viable sporocysts with no surrounding hemocytes.

Animals↗

Carbohydrate inhibition of Biomphalaria glabrata embryonic (Bge) cell adhesion to primary sporocysts of Schistosoma mansoni.

Due to shared characteristics with snail haemocytes, the Biomphalaria glabrata embryonic (Bge) cell line has been used as a model in vitro system for the study of snail-trematode interactions. In this study, Bge cells were used to characterize the adherence of snail host cells to schistosome primary sporocysts, and to test the effect of carbohydrates as inhibitors of this behaviour. Bge cells bound to the surface of >90% of Schistosoma mansoni sporocysts and, based on a semi-quantitative cell adhesion scale of 1-4, exhibited a cell adhesion index (CAI) of 2.45. This cellular adhesion was significantly inhibited in the presence of selected carbohydrate-containing substances. Fucoidan was the most potent inhibitor, reducing Bge cell-binding prevalence to approximately 50% and the CAI to 1.6. Other inhibitory compounds included mannose-6-phosphate, heparin, dextran sulfate, and various forms of the polysaccharide carrageenan. Fluoresceinated-fucoidan was found to attach to Bge cells confirming their ability to associate with sugar moieties. These results were further supported by the specific binding of surface biotinylated Bge cell proteins to sporocyst tegumental glycoproteins ranging from 40 to 120 kDa. N-linked tegumental carbohydrates appeared to represent ligands for Bge cell proteins since N-glycosidase treatment of blotted tegumental glycoproteins completely abolished biotinylated Bge protein binding. We hypothesize that the involvement of lectins as potential host cellular receptors in snail cell-sporocyst interactions, and suggest that negatively charged (mainly sulfated) carbohydrate moieties may represent the schistosome surface ligand(s).

Animals↗

Studies on resistance in snails. 3. Tissue reactions to Echinostoma lindoense sporocysts in sensitized and resensitized Biomphalaria glabrata.

The resistance of Biomphalaria glabrata snails that have been sensitized by various levels of irradiated or nonirradiated Echinostoma lindoense miracidia increased after a second challenge infection with nonirradiated miracidia of the same species. This was demonstrated by increased suppression of migrating capacity of invading sporocysts, an accelerated host tissue reaction, and a greater tendency of snail amebocytes to flatten while attacking the parasite. Three methods of elimination of invading sporocysts were observed: (1) encapsulation by amebocytes followed by destruction of the sporocysts; (2) expulsion of the sporocyst through the host epithelium after its encapsulation in the subepithelial tissues; (3) blockade of the parasite's entry into subepithelial tissues by a localized amebocyte aggregation. The basic mechanism of host snail response to a single or a repeated challenge infection appears to be similar, though an anamnestic reaction is evident in the accelerated response following a second challenge exposure.

Animals↗

Oral immunization of mice against Schistosoma mansoni using drinking water from trays containing Biomphalaria alexandrina infected with Schistosoma mansoni.

Water collected from trays containing Biomphalaria alexandrina infected with Schistosoma mansoni at the time of cercariae shedding (SmISW) and trays containing clean, non-infected, B. alexandrina (NISW) and underground water (UW), were filtered used as a drinking water for 3 groups of albino mice males. After two months, blood samples were collected from the 3 groups and serum was tested for anti-cercarial IgG, then mice were infected with 150 S. mansoni cercariae. Eight weeks after infection, mice were perfused and adult S. mansoni worms were counted. Anti-cercarial IgG was positive in 23 (82.1%) out of the 28 samples collected from mice drinking SmISW and only in 2 (9.5%) out of the 21 samples collected from mice drinking NISW, while all samples collected from mice drinking UW were negative for anti-cercarial IgG (X2=45.897; P<0.001). Worm load was significantly lower in the group of mice drinking SmISW than mice drinking NISW (P=0.032) and mice drinking UW (P=0.02). In mice drinking SmISW, adult worm count showed significant negative correlation with anti-cercarial IgG concentration (Kendall's taub =-0.325 and P=0.018). The results indicate that antigens present in drinking water stimulate a level of immunity against schistosomiasis, (inhabitants of endemic areas) resulting in a lower intensity and severity of infection. Also, it may reduce the specificity of serological tests used for diagnosis of Schistosoma infection, based on antibody determination.

Administration, Oral↗

Population-level responses to long-term cadmium exposure in two strains of the freshwater gastropod Biomphalaria glabrata: results from a life-table response experiment.

A life-table response experiment was conducted to ascertain the demographic effects of low-level cadmium exposure on two strains, BS90 and NMRI, of the freshwater gastropod Biomphalaria glabrata. Snails were exposed to cadmium continuously from the embryonic stage through adulthood. Results indicated that cadmium significantly affected a number of individual-based parameters, including %hatch, juvenile survival, and adult survival in both strains. Also, fecundity and time to maturity were significantly affected in the NMRI strain. A stage-based, deterministic, population model indicated that population growth rate (lambda) was significantly affected by cadmium. Elasticity analysis indicated that juvenile survival, in general, had the greatest contribution to lambda. Decomposition analysis indicated that the effects of cadmium on the juvenile stage in BS90 and the embryonic stage in NMRI contributed most to cadmium-induced changes in lambda. The BS90 strain was more sensitive to cadmium toxicity than NMRI. Moreover, the two strains differed in pattern of response with different aspects of their respective life histories contributing to cadmium-induced changes in lambda. Comparisons were also made between the main model, based on a Z transformation of the life-cycle graph, and more commonly used matrix models.

Animals↗

Studies on resistance in snails. 4. Induction of ventricular capsules and changes in the amebocyte-producing organ during sensitization of Biomphalaria glabrata snails.

Formation of an amebocyte aggregate in the ventricular cavity of Biomphalaria glabrata can be induced 30 hr or more after a single infection by irradiated or (less frequently) by normal Echinostoma lindoense miracidia. The resulting amebocyte mass frequently encapsulated and destroyed the developing E. lindoense sporocysts within the ventricle. The constituent amebocytes of the capsule correspond in vitro and by staining characteristics to circulating amebocytes of uninfected snails, but with additional inclusion bodies, increased mucopolysaccharide, acid phosphatases, and lipid-positive staining reactions. Mitotic activity, rapid growth, and later regression of the amebocyte-producing organ (located between the posterior mantle epithelium and anterior pericardial endothelium) follow the growth and regression sequence of the ventricular capsule. Though peripheral foci of secondary amebocyte production have been found and were previously known, the amebocyte-producing organ appears to be the primary amebocyte source responsible for the snails' rapid intraventricular sporocyst encapsulation.

Animals↗