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Control of snail hosts of bilharziasis in Egypt. 3. Effect of the organophosphorous insecticide, dursban, on carbohydrate metabolism of the snails Biomphalaria alexandria and Bulinus truncatus.

The effects of the organophosphorous insecticide, Dursban, on aerobic oxidation, glycolysis, glucose utilization and gluconeogenesis in snails tissues were determined. Dursban had a biphasic effect on the aerobic oxidation of succinate, glutamate + malate and TMPD + ascorbate while it had only an inhibitory action on pyruvate oxidation. The compound significantly inhibited glycolysis, glucose utilization and gluconeogenesis when used at high concentrations (ten times higher than its LC50). However, it had a slight effect on thepreviously mentioned process when its concentration was equal to or approximated its LC50. The relationship between the metabolic effect of Dursban and its molluscicidal activity is discussed.

Animals

Uptake of the mosquito larvicide Temefos by the salt marsh snail, New Jersey--1973-1974.

Uptake of the mosquito larvicide temefos (Abate) by the salt march snail (Melampus bidentatus Say) in New Jersey was measured by gas-chromatographic analysis. Measurable quantities of temefos were found in the snails within 1 day after the first treatment with a 2% granular formulation but 3 weeks elapsed before uptake occurred following treatment with a temefos emulsion. Residues in the snails exposed to the granular formulation were generally more than 10 times higher than those in snails exposed to the emulsion although application rates of the granular formulation were only about three times higher than those of the emulsion. Residues in snails exposed to the emulsion fell below detectable levels less than 3 weeks after cessation of treatments although measurable amounts were found in snails exposed to the granular formulation for more than 5 weeks after the last treatment. The persistence of temefos in M. bidentatus suggests the potential for its movement through food webs exposed to the granular formulation.

Animals

Cost of snail control.

In the last 10 years, there has been general agreement that niclosamide (bayluscide) is the preferred molluscicide for control of the snails transmitting Schistosoma mansoni and Schistosoma haematobium. This chemical has been widely tested in pilot projects and is in use in expanded control projects in Brazil, Puerto Rico, Egypt, Iran, and other countries. A comparison of the results from six pilot projects in these countries was analyzed with particular attention to the costs of the programs, since the benefits were fairly similar in terms of rapid snail control. It was shown that costs were generally related to simple geographic parameters such as volume of snail habitat and distance between habitats. The annual costs in 1972 prices ranged from a minimum of US $1 per 100 m3 of snail habitat treated for dry regions with large irrigation systems, to a maximum of US $40 per 100 m3 treated in areas of high rainfall with only a few scattered, natural waterbodies. Use of the reported data for estimating the cost of current programs was demonstrated by projecting costs for Puerto Rico and the Sudan in 1978 prices.

Animals

Glycogen metabolism in the snail, Biomphalaria glabrata.

1. The distribution of glycogen in different tissues of the snail, Biomphalaria glabrata was determined; the cephalopedal region contained 15-17 mg, the mantle region 23-29 mg, the hepatopancreas 31-45 mg, and the ovotestis 50 mg of glycogen/g wet wt. 2. There was a significant decrease in the glycogen content in the cephalopedal region after incubating the snails with 5-hydroxytryptamine (4 x 10(-5) M) in vivo. 3. Enzymatic degradation of glycogen from different tissues revealed that the degree of branching was 9% of the total glucosyl residues, and the length of outer branches was about 40% of the total glucosyl residues. 4. There was an active form of glycogen phosphorylase in the cephalopedal region and the mantle region. Phosphorylase in the hepatopancreas was generally inactive, but could be activated by an endogenous phosphorylase kinase. 5. Glycogen synthetase of the snail tissues required glucose-6-phosphate to be active.

Animals

[The disulfide bridges of the trypsin-kallikrein inhibitor K from snails (Helix pomatia). Thermal inactivation and proteolysis by thermolysin (author's transl)].

Isoinhibitor K is the main component of the complex mixture of isoinhibitors of broad specificity secreted into the mucus by the Roman snail (Helix pomatia). The disulfide pairing was determined after the amino acid sequence had been elucidated. Two cystine-containing peptides with the disulfide bridges Cys32-Cys53 and Cys32-Cys53 plus Cys7-Cys57 were obtained after thermolytic hydrolysis of the native inhibitor at 80 degrees C and chromatographic separation of the peptides using SE-Sephadex. The Cys16-Cys40 disulfide bridge could be reduced selectively by sodium borohydride with no loss in biological activity. This property and the covalent structure correspond to that of the intracellular inhibitor from bovine organs, which is largely homologous in its amino acid sequence to the secretory inhibitor from the snail. The complete covalent structure of isoinhibitor K will be presented. The snail inhibitor is less stable against proteolytic inactivation by thermolysin and against thermal denaturation at pH 8.0 than the inhibitor from bovine organs (Kunitz inhibitor).

Amino Acid Sequence

Enzyme analyses of Bulinus africanus group snails (Mollusca: Planorbidae) from Tanzania.

38 population samples of snails of the Bulinus africanus group, collected from three separate areas of Tanzania, have been examined. Enzymes in crude digestive gland extracts of individual snails have been analysed by isoelectric focusing in polyacrylamide gels. The enzymes studied were: malate dehydrogenase (MDH); phosphoglucomutase (PGM); glucosephosphate isomerase (GPI); acid phosphatase (AcP) and hydroxybutyrate dehydrogenase (HBDH). Samples of B. nasutus were clearly differentiated from other species and enzyme differences were apparent between samples from the lake and coastal areas. Similarly, although clear distinctions could not always be made, samples of B. africanus, B. globosus and B. ugandae were characterized by their enzyme types. Individual variation was detected within populations and the significance of enzyme polymorphisms in relation to identification has been considered. No correlation was found between snail enzyme type and susceptibility to Schistosoma haematobium or S. bovis.

Acid Phosphatase

The chemical ecology of Biomphalaria glabrata: the effects of ammonia on the growth rate of juvenile snails.

When juvenile specimens of Biomphalaria glabrata were subjected to concentrations of ammonia ranging from 1-100 mug/ml in various media the following effects were observed: the addition of ammonia to borate buffered media caused mortality. Both borate and tris-buffered media caused a decrease in the growth rate of snails when compared with controls in SSW. The growth rates of the snails could be enhanced by increasing the concentration of ammonia to critical thresholds, but further increases beyond these thresholds resulted in growth inhibition. The toxicity of ammonia in ambient water was augmented by an an increase in pH. The possible causation and ecological significance of these effects are discussed. There are indications that the snails are physiologically well-adapted to utilize ammonia when required and also to control its excretion and uptake from the medium.

Ammonia

Snail immunity to schistosomes: insights from omics studies.

Schistosomiasis is a serious public health concern, with transmission facilitated by a small number of freshwater snail intermediate host species. Infection outcomes vary greatly across the primary vector genera, Biomphalaria (for Schistosoma mansoni), Bulinus (for S. haematobium), and Oncomelania (for S. japonicum), even within species, ranging from full resistance to high compatibility. Omics methods have altered this field by correlating host genotype, baseline immunological status, and time-resolved responses to whether invading miracidia are eliminated or develop sporocysts. Evidence from genomes, transcriptomics, proteomics, and epigenomics suggests that resistance is frequently primed prior to exposure. However, the clearest divergence between resistant and susceptible trajectories occurs during a small early window (<12-48&#x202f;h) after penetration. During this time, recognition, hemocyte recruitment, and soluble effector deployment either come together quickly or are delayed and guided by parasite-derived modulators. Established infections cause the host to adapt to chronic conditions through immune regulation, metabolic reprogramming, tissue and neuroendocrine remodeling, microbiome modification, and parasite castration. Comparative genomics reveals that each vector genus has evolved its own immunogenomic profile, which includes lineage-specific expansions of recognition and effector gene families. Together, these findings can help with field surveillance and intervention by providing molecular compatibility markers, functional tools for testing candidate genes, and tactics that target parasite-derived immune modulators. Integrated multi-omics approaches are a top priority, yet they are still limited in snail vectors compared to other disease vector systems.

Animals

The beta-glucosidase in the gut contents of the snail Achatina achatina.

1. The enzyme beta-glucosidase (beta-D-glucoside glucohydrolase, EC 3.2.1.21) from the gut contents of active Achatina achatina exists in two molecular forms, beta-glucosidase C (mol.wt. about 82000) and D (mol.wt. about 41000). 2. Only the lower-molecular-weight species was found in the gut contents of aestivating snails or in extracts from their digestive glands and washed gut walls. 3. On re-activation of some aestivating snails, betion of ATP and Mg2+ to the isolated gut contents or to extracts from washed gut walls led to the formation of higher-molecular-weight forms of the enzyme, beta-glucosidase A (mol.wt. about 329000) and beta-glucosidase B (mol.wt. about 165000). 5. All these forms of the enzyme have similar pH optimum (pH 5.0-5.6). 6. The Michaelis constants (Km) and heat stability of the enzyme increased with increasing molecular complexity.

Adenosine Triphosphate

Genome Report: De novo genome assembly of the greater Bermuda land snail, Poecilozonites bermudensis (Mollusca: Gastropoda), confirms ancestral genome duplication.

Poecilozonites bermudensis, the greater Bermuda land snail, is a critically endangered species and one of only two extant members in its genus. These snails are one of Bermuda's few endemic animal clades and their rich fossil record was the basis for the punctuated equilibria model of speciation. Once thought extinct, recent conservation efforts have focused on the recovery of the species, yet no genomic information or other molecular sequences have been available to inform these initiatives. We present a high-quality, annotated genome for P. bermudensis generated using PacBio long read and Omni-C short read sequencing. The resulting assembly is approximately 1.36 Gb with a scaffold N50 of 44.t Mb and 31 chromosome-length scaffolds. Nearly 43 percent of the genome was identified as repeat content. This assembly will serve as a resource for the conservation and study of P. bermudensis, and its only close extant and also critically endangered relative, P. circumfirmatus. Additionally, this genome adds to the growing body of data needed for a more complete understanding of gastropod evolution and for evolutionary processes in general.

Annotation

Complexity of schistosome vector bulinine snails in Kenya: Insights from nuclear genome size variation, complete mitochondrial genome sequence, and morphometric analysis.

Investigations of nuclear genome size, complete mitochondrial genome (mitogenome) sequence, and morphometrics were conducted on specimens of Bulinus snails (Gastropoda: Planorbidae) collected from 14 locations across the east coast, central Kenya, and western Kenya around the Lake Victoria region (November 2013 and January 2024). Flow cytometry measurements of DNA content (C-value) revealed unexpected variation in nuclear genome size, with diploid Bulinus africanus and B. forskalii species groups showing C-values ranging from 0.76 to 1.98 pg, while tetraploid B. truncatus had a C-value of 1.82 pg. Additionally, C-values for six B. globosus specimens from different localities ranged from 1.43 to 1.98 pg. These findings suggest that bulinine snails, particularly the B. africanus species group, have undergone genome expansion, whole genome duplication (polyploidization), or both, which have not been previously recognized. Next-generation sequencing was performed to determine and annotate 14 complete mitogenome sequences. Despite the well-conserved arrangement of protein-coding genes, two versions of mtDNA genome structure, distinguished by the tRNA-D (Asp) location, were found, designated as DCF (Asp-Cys-Phe) type (in the B. forskalii group and the B. truncatus/tropicus complex) and CF (Cys-Phe) type (in the B. africanus group). Phylogenetic analyses based on complete mtDNA sequences of bulinines from Kenya, along with cytochrome c oxidase subunit I (COX1) sequences from various localities across Africa, contributed to resolving species identities and provided further support for the presence of multiple or cryptic species in the taxon B. globosus. A landmark-based morphometric analysis was ineffective in distinguishing these species. This study reveals unexpected nuclear genome size variation, provides new mitogenome sequences, and highlights the limitations of morphological analysis. It offers valuable insights into the cytogenetics, polyploidy, genomics, taxonomy, and evolution of bulinines, which serve as intermediate hosts for schistosomes responsible for human urogenital schistosomiasis and intestinal schistosomiasis in domestic and wild mammals.

Animals

Histochemical studies on mucosubstances in the prostate gland of the pulmonate snail Semperula maculata in the annual breeding-aestivation cycle.

Prostate gland of the pulmonate (terrestrial) snail Semperula maculata was studied histochemically for the presence of polysaccharides. PAS technique and differential staining methods employing Alcian blue, aldehyde fuchsin and Azure A at different pH values and combined with enzyme digestion test and lipid extraction were used. Two histochemically different cell types were found in the prostate gland: the type 1 cells which elaborate neutral mucosubstances and supposedly also phospholipoproteins, and type 2 cells producing glycogen. Both these cell types show seasonal fluctuations of the stores of materials secreted by them. Thus in type 1 cells the weakest histochemical reactivity indicating the lowest concentration of their secretion appears just after cessation of the snails' breeding activity (September) and persists throughout the post-breeding and early pre-breeding seasons which both together constitute the aestivation period. During the rest of the pre-breeding season a strong reactivity gradually develops and culminates in May i.e. immediately before the onset of the breeding activities which in turn initiate a decline of the reactivity. The type 2 cells become most reactive in the middle of the pre-breeding season (May) and decrease their reactivity after cessation of the breeding season. The number of both types of cells parallels the reactivity changes.

Adaptation, Physiological

Intraspecific variations in the hemolymph of Biomphalaria glabrata, a snail host of Schistosoma mansoni.

An attempt was made to characterize the hemolymph of Biomphalaria glabrata with reference to "normal" intra-specific variation, i.e., both inter- and intra-strain differences. Total protein concentration, per cent hemoglobin, pH, and osmolarity were studied. Seven geographic strains of B, glabrata were examined. In addition, observations were made on the hemolymph of Biomphalaria straminea, several strains of Helisoma caribaeum, and on B. glabrata subjected to infection with Schistosoma mansoni or to periods of starvation. Intra-strain differences in total protein concentration and total hemoglobin concentration in B. glabrata appeared to be more closely related with snail size than with absolute age. Inter-strain variation in B. glabrata was also noted, but the differences were of the same magnitude as those from intra-strain samples. Significant differences in total protein concentration were observed, however, between the means of similar size B. glabrata, B. straminea and H. caribaeum. The osmolatity of the hemolymph from different size B. glabrata was similar as were the osmolalities of the hemolymph from similar size snails of different strains. However, all B. glabrata strains exhibited hemolymph osmolalities lower than observed in strains of H. caribaeum. Infection with S. mansoni reduced the protein concentration of B. glabrata hemolymph. Differences were noted as early as 1.5-24 hr post-infection, with significant alterations occurring at about 11 days post-infection. To a lesser extent, starvation also depleted the protein content of the hemolymph.

Animals

The mobilization of calcium and bicarbonate by raised concentrations of potassium in the haemolymph of the snail, Helix pomatia.

1. After the concentration of potassium in the haemolymph of Helix pomatia has been raised by the infusion of KCl, it falls approximately exponentially for a time and then tends to rise. The accompanying rise and fall of calcium concentration can be fitted to a simple mathematical model. 2. The mobilization of calcium is accompanied by the generation of bicarbonate in equivalent amounts, without much change in pH or Pco2. 3. There is probably an increased production or retention of carbon dioxide at this time, but the main cause of the changes in calcium and bicarbonate is not respiratory acidosis. 4. The concentration of potassium rises in snalis that have been infused with CaCl2. 5. The adverse responses visible in snails infused with KCl are largely prevented when CaCl2 is infused at the same time. 6. Homeostasis seems to involve the maintenance of a proper balance of calcium and potassium concentrations.

Animals

Chromosome-associated paracrystalline nuclear inclusions in the spermatocytes of a pulmonate snail, Planorbarius corneus L.

Chromosome-associated paracrystalloids are regularly found in the spermatocytes of snails which were reared in the laboratory. They seem to be largely specific for the male gametocytes as they have been observed only in few cases in the oocytes. It is likely that paracrystalloids are formed during pachytene at the site of large heterochromatic knobs which originate by fusion of heterochromatic terminal segments of some bivalents. During diplotene they are always connected with the telomeres of three or four bivalents, thus forming a large trefoil-like structure. During metaphase I paracrystalloids are shed off from the chromosomes and transferred to the cytoplasm. In early spermatids they are found again in the nuclei, where they "fade away" during spermiogenesis. Histochemically they consist of basic proteins, which are probably crystallized in the cubic system. Radioactive labeling of the structure could not be achieved, neither by 3H-uridine or thymidine, nor by amino acids. The functional significance of this peculiar structure in unknown. Certain features justify a comparison with synaptonemal polycomplexes.

Animals

Regulation of neuronal properties by afferent connections. I. Functional changes in snail neurons following section of presysnaptic nerve fibers.

The left cerebral connective of snail ganglia containing afferent inputs to a particular neuron was sectioned. One week after the operation synaptic potentials were not obtained when the connective was stimulated, and they had not reappeared after 60 days. The current-voltage relationship of denervated cells showed a rectification in the hyperpolarizing direction, whereas that of control cells had an ohmic behavior. Depolarization or conductance changes produced by ACh or carbachol showed a supersensitivity in denervated cells, evidenced by a shift to the left of the dose-response curve and an increase of the maximal responses obtained. The reversal potential of ACh shifted from--22 mV in the control to--8 mV in denervated cells. Depolarization produced by serotonin was similar in control and denervated cells.

Acetylcholine

Comparison of the mechanisms controlling intracellular pH and sodium in snail neurones.

Ion-sensitive microelectrodes were used to record intracellular pH, Na+ and Cl- in snail neurones. NaCl or HCl was injected iontophoretically to compare the Na pump with the pHi regulating system. The Na pump was inhibited by ouabain, carbonyl cyanide m-chlorophenyl hydrazone and increasing the membrane potential, whereas the pHi regulating system was relatively unaffected. Activation of the Na pump had no effect on pHi whereas activation of the pHi recovery process increased internal Na+. Activation of the pHi recovery process by CO2 application increased internal Na+ and also decreased internal Cl-. The results show that there is no direct connexion between the Na pump and the pHi recovery process, and that the pHi recovery process is electroneutral, and appears not to require metabolic energy. The results also confirm that the pHi recovery process involves the influx of Na+ ions and the efflux of Cl- ions.

Acid-Base Equilibrium