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Distribution patterns and cercarial shedding of Bulinus nasutus and other snails in the Msambweni area, Coast Province, Kenya.

In the Msambweni area of the Kwale District in Kenya, an area endemic for Schistosoma haematobium, potential intermediate-host snails were systematically surveyed in water bodies associated with human contact that were previously surveyed in the 1980s. Bulinus (africanus) nasutus, which accounted for 67% of the snails collected, was the only snail shedding S. haematobium cercariae. Lanistes purpureus was the second most common snail (25%); lower numbers of Bulinus forskalii and Melanoides tuberculata were also recovered. Infection with non-S. haematobium trematodes was found among all snail species. Rainfall was significantly associated with the temporal distribution of all snail species: high numbers of Bulinus nasutus developed after extensive rainfall, followed, in turn, by increased S. haematobium shedding. Spatial distribution of snails was significantly clustered over a range of up to 1 km, with peak clustering observed at a distance of 400 meters. Water lily (Nymphaea spp.) and several aquatic grass species appeared necessary for local colonization by B. nasutus or L. purpureus.

Animals↗

Secretory protein biosynthesis in snail hemocytes: in vitro modulation by larval schistosome excretory-secretory products.

Circulating hemocytes of the snail, Biomphalaria glabrata, synthesize and secrete a variety of polypeptides when maintained in vitro in serum-free medium containing [35S] methionine. SDS-PAGE/fluorographic analysis of supernatants from resistant snail (10-R2-OK strain) hemocyte cultures revealed the presence of numerous labeled polypeptides ranging in Mr from 220 to 14 kDa. Most of these same proteins were also produced by hemocytes of a susceptible B. glabrata strain (M-line), but the overall rate of secretory protein synthesis was reduced from that of resistant snail cells. In addition, excretory-secretory (ES) products contained in supernatants from Schistosoma mansoni miracidial transformation and 1-day primary sporocyst cultures stimulated increases in the synthesis of various polypeptides. Particularly striking was a 3-fold increase in the synthesis of a 66-kDa secretory polypeptide by hemocytes of both snail strains, and a concomitant increase in M-line hemocytes and decrease in 10-R2-OK cells of a 63-kDa polypeptide. Overall, however, the level of ES product-induced secretory protein synthesis was greater in 10-R2-OK snail hemocytes than in those of the M-line strain. Exposure of a nonhemocytic B. glabrata cell line to parasite culture supernatants had no stimulatory/inhibitory effect on labeled protein ouput, suggesting that the observed hemocyte response may be snail cell-type specific. Finally, the larval ES components responsible for modulating hemocyte protein metabolism are mainly concentrated in a heat-stable fraction composed of molecules of greater than 30 kDa. However, the loss of the ability of heated parasite products to stimulate synthesis of certain hemocyte proteins and the presence of minor stimulating activity in a low molecular weight fraction (less than 10 kDa) implies the possible existence of multiple larval components affecting formation of specific hemocyte secretory polypeptides. It is concluded that snail hemocytes are capable of in vitro synthesis and secretion of a variety of methionine-containing polypeptides, and that ES products of early larval schistosomes can modulate (i.e., stimulate or inhibit) this metabolic process. A differential response of susceptible vs. resistant hemocytes to larval products suggests that the degree to which these cells can be metabolically activated may determine their cytotoxic effectiveness.

Animals↗

Electrophoretic studies on the digestive gland esterases of some biomphalarid and lymnaeid snails.

Because of the problems encountered in the classification of snails of medical importance, biochemical methods have been sought to help clarify the situation. Of these, the separation of the enzymes of adult snails by electrophoresis seems the most promising but very few attempts have been made so far to use the results for taxonomic studies. The purpose of the present study was to evaluate the use of the enzyme systems of neotropical planorbid and of lymnaeid snails to elucidate their taxonomy and also snail-schistosome relationships at the species and population levels.The findings show the characteristic electrophoretic patterns of digestive gland esterases of the planorbid and lymnaeid snails used, as well as their variation and the level of such variation among certain populations and the consistency of the patterns among others. The results also show that, in general, the extent of variation between some populations of the same species is greater than the differences between species of the same group. However, at the specific level, there are similarities suggesting close relationships between some populations of Biomphalaria glabrata and B. tenagophila on the one hand, and of certain populations of B. peregrina and of B. obstructa on the other hand.The present study has thrown some light on the question of electrophoretic variation in enzymes, and the ways in which this can be applied to studies of the genetics of snails. A correlation is suggested between certain patterns that indicate biochemical similarities or differences among the planorbid snail populations and the susceptibility of the species or the population to infection with the schistosomes.

Animals↗

Production of heterogeneous carbohydrate-binding proteins by the host snail Biomphalaria glabrata following exposure to Echinostoma paraensei and Schistosoma mansoni.

Hemolymph lectins may play an important role in the internal defense responses of gastropods to parasites. Two groups of known carbohydrate-binding polypeptides, of 150-220 kDa (designated as group 1 molecules, or G1M) and of 75-130 kDa (group 2 molecules, or G2M), were harvested from pooled plasma samples of Biomphalaria glabrata using affinity chromatography and examined using 2-dimensional electrophoresis. Plasma samples were derived from control snails or snails exposed 8 days earlier to the trematodes Echinostoma paraensei or Schistosoma mansoni. Plasma of control and S. mansoni-exposed snails contained little or no G1M, whereas plasma from E. paraensei-infected snails contained G1M covering a broad pI spectrum. G2M resolved as 1-2 isoforms in control plasma and up to 4 relatively faint isoforms in plasma from S. mansoni-exposed snails, and as 5-6 resolvable isoforms in plasma from E. paraensei-infected snails. Plasma from individual snails contained as many as 5 G2M polypeptides following exposure to E. paraensei. Exposure to trematode larvae stimulated production by B. glabrata of increased abundance and diversity of carbohydrate-binding proteins. The 2 trematode species provoked different responses, and 2 B. glabrata strains studied (M line and 13-16-R1 strains) differed from one another in their responses.

Animals↗

Invasion of the Nile Valley in Egypt by a hybrid of Biomphalaria glabrata and Biomphalaria alexandrina, snail vectors of Schistosoma mansoni.

Two years (1996-1997) of systematic survey showed that a hybrid of Biomphalaria glabrata and Biomphalaria alexandrina has invaded the irrigation and drainage systems in the Nile Delta and the Valley nor the of El-Menya. However, the infestation of water courses by and the population density of this snail were variable in various localities. The infestation rate ranged between 7.1% in El-Fayoum Governorate and 52.6% in El-Dakahliya Governorate and the snail density from 2 snails/site to 69.7 snails/site in the same governorates, respectively. Comparing the survey results of the two study years in the sampling sites indicated that the hybrid snail has relatively increased in population density than B. alexandrina. The hybrid snail of B. glabrata and B. alexandrina was found alone in some sites, but was mostly associated with B. alexandrina. The results showed also that both Biomphalaria have almost the same major physicochemical requirements. However, the hybrid snails and B. alexandrina were found differently associated with aquatic snails and plants. The hybrid snail was found naturally infected with S. mansoni thus giving indication that it is presently participating in schistosomiasis mansoni transmission in Egypt.

Animals↗

Schistosomiasis in newly reclaimed areas in Egypt. 1-distribution and population seasonal fluctuation of intermediate host snails.

Two newly reclaimed areas located west & east of Suez Canal, namely El Manayef area and El Morra area, were studied for patterns of distribution and population seasonal fluctuation of Biomphalaria alexandrina and Bulinus truncatus, the intermediate host snails of Schistosoma mansoni and S. haematobium, respectively. In this study Geographic Information System (GIS) techniques were utilized for producing maps and analyzing the results. Habitats of the two vector snail species were categorized into suitability levels depending on the frequency with which snails were collected over a 12 months period. Data obtained from the most suitable habitats were only used for studying the seasonal fluctuation of snail population. The results showed that both study areas were almost similar in major physico-chemical parameters. However, oxygen content in canals was higher than in drains and conductivity was higher in drains than in canals. As regards snail distribution and density, most snails of both considered species were clustering in much fewer numbers of sites, more pronouncedly in the case of Biomphalaria than Bulinus. Population density of snails was significantly higher in El-Manayef area than in El-Morra area and in canals than in drains. Both species exhibited 2 population peaks/year, the peaks of Biomphalaria were in March-April & August in both study areas, while for Bulinus these peaks occurred in March-May and August in El-Manayef area and in May and March, respectively, in El-Morra area.

Animals↗

Thermal susceptibility of Salmonella in the Moroccan food snail, Helix aspersa.

Thirty samples of 10-15 Helix aspersa food snails were examined for Salmonella by a surface rinsing method and by analysis of whole snails rinsed with 70% ethanol. Thirteen samples were positive by the rinsing method and 6 were positive by whole snail analysis, with this difference being significant (P less than 0.01). Although Salmonella contamination in H. aspersa appeared to be predominantly surface, the pathogen was also found within the snail meat. The ability of surface and subsurface Salmonella organisms to survive in cooked snails was determined in 90 samples. Thermocouple readings indicated that an internal temperature of at least 200 degrees F (93 degrees C) was reached within the snail meat during cooking by a typical recipe. This temperature was sufficient to kill both surface and subsurface Salmonella in 29 samples positive for the pathogen prior to heating. A variety of serotypes representing several somatic groups was isolated.

Food Contamination↗

Studies on the snail vectors of bilharziasis mansoni in North-eastern Brazil.

The authors describe the bilharziasis endemic areas in north-eastern Brazil, giving the rainfall and general characteristics of the climate. The life-cycles of the two snail vectors-Australorbis glabratus and Tropicorbis centimetralis-in Pernambuco are described. Considerable attention is given to the effects on the snails of the annual drought, which causes many of the habitats to dry up and seriously affects the snail life-cycles and survival patterns. The snails are able to populate habitats that are dry for 5-7 months every year. They survive during the dry season in the protection of debris, vegetation, etc. A. glabratus is more susceptible to infection with Schistosoma mansoni than is T. centimetralis, but the latter is an effective vector, nevertheless, probably because it often occurs in very large numbers. A. glabratus with mature infections die or lose their infections when removed from the water for 20-30 days. Immature parasites are not killed under the same conditions. Infection with S. mansoni injures the snails and may kill them. It also reduces the reproductive capacity of the vectors, but it does not permanently castrate them. The epidemiological significance of these findings and their meaning in terms of snail control are discussed.

Animals↗

A LARGE-SCALE EXPERIMENT IN THE CONTROL OF AQUATIC SNAILS BY THE USE OF MOLLUSCICIDES ON A SUGAR ESTATE IN THE NORTHERN REGION OF TANGANYIKA.

The author describes a large-scale experiment in which the molluscicide Bayer 73 (Bayluscide) was used in an attempt to eliminate Biomphalaria pfeifferi, the snail host of Schistosoma mansoni, from an irrigation system in Tanganyika. Applied at a concentration of 1 p.p.m., the molluscicide gave a very high kill of snails and much of the treated area remained completely free of vector snails for seven months after treatment. However, there were a few survivors in small pockets associated with a drainage area that became flooded during heavy rains coincident with the application of molluscicide. From these survivors a dramatic resurgence of snails occurred in some of the treated canals. This resurgence may be analogous to similar phenomena observed in some insecticide work. The suggestion is made that removal of parasites and predators, in particular trematode parasites, by a molluscicide might increase the snail's capacity for repopulation. Studies of the seasonal fluctuations of snail population density in an adjacent, but separate, irrigation system suggest that molluscicide applications would be more effective if timed to coincide with the end of the rainy seasons.

Animals↗

Increases in urea synthesis and the ornithine-urea cycle capacity in the giant African snail, Achatina fulica, during fasting or aestivation, or after the injection with ammonium chloride.

The objectives of this study are to determine whether a full complement of ornithine-urea cycle (OUC) enzymes is present in the hepatopancreas of the giant African snail Achatina fulica, and to investigate whether the rate of urea synthesis and the OUC capacity can be up-regulated during 23 days of fasting or aestivation, or 24 hr post-injection with NH(4)Cl (10 micromol g(-1) snail) into the foot muscle. A. fulica is ureotelic and a full complement of OUC enzymes, including carbamoyl phosphate synthetase III (CPS III), was detected from its hepatopancreas. There were significant increases in the excretion of NH(4)(+), NH(3) and urea in fasting A. fulica. Fasting had no significant effect on the tissue ammonia contents, but led to a progressive accumulation of urea, which was associated with an 18-fold increase in the rate of urea synthesis. Because fasting took place in the presence of water and because there was no change in water contents in the foot muscle and hepatopancreas, it can be concluded that the function of urea accumulation in fasting A. fulica was unrelated to water retention. Aestivation in arid conditions led to a non-progressive accumulation of urea in A. fulica. During the first 4 days and the last 3 days of the 23-day aestivation period, experimental snails exhibited significantly greater rates of urea synthesis compared with fasted snails. These increases were associated with significant increases in activities of various OUC enzymes, except CPS III, in the hepatopancreas. However, the overall urea accumulation in snails aestivated and snails fasted for 23 days were comparable. Therefore, the classical hypothesis that urea accumulation occurred to prevent water loss through evaporation during aestivation in terrestrial pulmonates may not be valid. Surprisingly, there were no accumulations of ammonia in the foot muscle and hepatopancreas of A. fulica 12 or 24 hr after NH(4)Cl was injected into the foot muscle. In contrast, the urea content in the foot muscle of A. fulica increased 4.5- and 33-fold at hour 12 and hour 24, respectively, and the respective increases in the hepatopancreas were 4.9- and 32-fold. The exogenous ammonia injected into A. fulica was apparently detoxified completely to urea. The urea synthesis rate increased 148-fold within the 24-hr experimental period, which could be the greatest increase known among animals. Simultaneously, there were significant increases in activities of glutamine synthetase (2.5-fold), CPS III (3.1-fold), ornithine transcarbamoylase (2.3-fold), argininosuccinate synthetase+lyase (13.6-fold) and arginase (3.5-fold) in the hepatopancreas 12 hr after the injection of NH(4)Cl. Taken altogether, our results support the view that the primary function of urea synthesis through the OUC in A. fulica is to defend against ammonia toxicity, but suggest that urea may have more than an excretory role in terrestrial pulmonates capable of aestivation.

Amino Acids↗

Molluscicidal activity of vulgarone B against ram's horn snail (Planorbella trivolvis).

The ram's horn snail (Planorbella trivolvis (Say)) is an intermediate host for a digenetic trematode (Bolbophorus confusus (Krause) Dubois) that has recently been discovered to be a significant problem in commercial channel catfish (Ictalurus punctatus Raf) production ponds in the Mississippi Delta region in the USA. In these catfish ponds, the digenetic life cycle of this parasitic trematode involves two intermediate hosts, the ram's horn snail and the channel catfish, and the final host, the American white pelican (Pelecanus erythrorhynchos Gmelin). One approach to eradicate this problem is to disrupt the life cycle of the parasitic trematodes by eliminating the snails. During our search for natural-product-based molluscicides to control the snails in the catfish ponds, vulgarone B, isolated from the steam distillate of the aerial parts of the plant Artemisia douglasiana Besser (Asteraceae), was found to be active towards the snails with a LC50 of ca 24 microM. Channel catfish toxicity studies indicated a LC50 of ca 207 microM. Vulgarone B may be an environmentally acceptable alternative for snail control in aquaculture.

Animals↗

Toxic effect and bioavailability of malathion spiked in natural sediments from the Ignacio Ramirez Dam on the snail Stagnicola sp.

Malathion (MA) is a widely used insecticide in México. The snail Stagnicola sp is a native species of the Ignacio Ramírez dam (IRD). This work aimed to evaluate the bioavailability and toxicity of MA in sediments of the IRD from the Stagnicola sp snail, taking into account the physicochemical properties of the IRD sediment. The toxic effect of MA on the snail Stagnicola sp was evaluated by biochemical tests of acetylcholinesterase (AchE) activity, protein concentration, lipid peroxidation level (LPL), and lipid content; a toxicokinetic study was also carried out. An increment in all biochemical parameters was observed at the beginning of exposure, while at 48 and 72 h a decrement in AchE activity, LPL, and lipid content was observed. The kinetics study showed gradual uptake and rapid elimination of the insecticide in the test organism. The bioconcentration factor and the absorption and elimination constants led to the conclusion that this compound is not being stored in snails. However, at the end of the experiment, the snails without MA exhibited a lack of recovery in AchE activity, which indicates that there is no correlation between the inhibitory pattern of AchE activity and snail MA concentration.

Acetylcholinesterase↗

Long-term sensitization and environmental conditioning in terrestrial snails.

The hypothesis that a long-term increase of behavioural responses in snails (over a period of days) might be due to environmental conditioning was examined. Training consisted of delivering electric shocks non-contingently with test stimuli twice per day for 5 days to freely moving snails on a ball floating in water. After training, a significant difference in amplitude of a withdrawal reaction to tactile test stimulation appeared between shocked and control snails. Responses were significantly facilitated in shocked animals for up to 12 days after training, but only if the animals were tested in the environment used for training. Testing of the same groups of animals crawling freely on the glass lid of a tank in which they lived between experimental sessions revealed no difference in responses to the same stimuli between shocked and control snails. Injection of the neurotoxin 5,7-dihydroxytryptamine, which selectively impairs serotonergic cells, eliminated the differences between shocked and control animals. Changing the pH of the water in which the ball floated, by addition of citric acid, led to a significant selective increase of responsiveness in snails sensitized in this environment relative to the responsiveness of the same snails with normal water in the tank. The results suggest that the long-term sensitization of withdrawal reactions observed is at least in part a manifestation of an associative process, namely environmental conditioning.

5,7-Dihydroxytryptamine↗

The lipids of slugs and snails: evolution, diet and biosynthesis.

There is a considerable gap in current knowledge of the lipid composition of snails and slugs, both of which belong to the phylum Mollusca. We have therefore analyzed the sterol and fatty acid compositions of three species of slugs and three species of snails. The sterols of slugs included eight different sterols: cholesterol contributed 76-85% of the total sterols, brassicasterol accounted for 4-13%; other sterols we identified were lathosterol, 24-methylene cholesterol, campesterol, stigmasterol, sitosterol and sitostanol. In contrast, snails contained two additional sterols, desmosterol and cholestanol. Of the polyunsaturated fatty acids in slugs, linoleic (18:2n-6) and arachidonic acids (20:4n-6) were the major n-6 fatty acids, while linoleic (18:3n-3) and eicosapentaenoic acids (20:5n-3) were the predominant n-3 fatty acids. Docosahexaenoic acid (22:6n-3), the end product in the n-3 fatty acid synthetic pathway and an important membrane fatty acid of mammals, fish and birds, was absent in both slugs and snails. However, the analogous product of n-6 fatty acid synthesis, 22:5n-6, was found in both snails and slugs. This raises speculation about preference for n-6 fatty acid synthesis in these species. Our data show the unique sterol and fatty acid compositions of slugs and snails, as well as similarities and differences in sterol composition between the two. The results between the two land mollusks are contrasted with those of marine mollusks, such as oysters, clams and scallops.

Animals↗

Integrating nonindigenous aquatic plant control with protection of snail kite nests in Florida.

The endangered snail kite (Rostrhamus sociabilis) feeds primarily on the freshwater apple snail (Pomacea paludosa) in Florida. The nonindigenous, floating water hyacinth (Eichhornia crassipes) and water lettuce (Pistia stratiotes) impede kites from finding snails. Effective control of these aquatic plants in the littoral zone of central and south Florida lakes benefits kites by maintaining open foraging habitat. However, incidental herbicide spraying of nesting substrates result in nest collapse when kites breed in nonwoody, emergent plants [cattail (Typha spp.) and giant bulrush (Scirpus validus)] in the outer littoral zone during lower lake levels. Many endangered species recovery plans and their implementation have experienced problems due to inaction and/or noncooperation by various governmental agencies and their personnel. Herein, we describe the development and implementation of a buffer zone strategy to prevent secondary impacts from an aquatic plant control program to snail kites nesting on lakes in central and south Florida. A strategy was jointly developed by personnel of five state and federal agencies to control herbicide application near kite nesting areas during the normal breeding season. Although requiring various modifications during its implementation, this cooperative effort successfully integrated aquatic plant control objectives with snail kite conservation on Lake Okeechobee during 1988. The program was expanded the following year to lakes Kissimmee and Tohopekaliga. Since the implementation of the snail kite impact preclusion program, no nest loss was attributed to incidental herbicide applications on lakes Okeechobee, Kissimmee, and Tohopekaliga.

Animals↗

Snail3 orthologues in vertebrates: divergent members of the Snail zinc-finger gene family.

Snail genes comprise a family of zinc-finger transcription factor coding genes with multiple roles in early embryonic development of metazoans. The evolutionary history of this family has been studied in detail, revealing an initial duplication in Snail and Scratch genes preceding the protostome/deuterostome split, and posterior independent duplication events in the lineages leading to insects and vertebrates. The distribution of mammalian and teleost Snail genes fits with current models for whole genome duplication events at the base of the vertebrate lineage, plus an extra duplication in teleosts. However, two very divergent Snail genes, one from mammals and the other from teleost fishes, fit poorly into the phylogenetic analysis of the family. By means of database mining and synteny analysis, we provide evidence for these genes being orthologues, and evidence that they originated in an early duplication at the base of the vertebrates resulting in three and not two Snail genes. We further show that all three Snail genes lie in regions of extensive paralogy, revealing their common origin through segmental or chromosomal duplication.

Amino Acid Sequence↗

The presence of uninfected Omphiscola glabra in a breeding of infected Galba truncatula enhanced the characteristics of snail infections with Fasciola hepatica.

Experimental infections of Galba truncatula with Fasciola hepatica were carried out under laboratory conditions to determine if the presence of another lymnaeid, Omphiscola glabra, during snail breeding had an indirect effect on the growth of G. truncatula and to analyse consequences on cercarial production. When the two lymnaeids are raised together, the survival of G. truncatula at day 30 post-exposure (PE), the prevalence of snail infections, and the shell height of cercariae-shedding snails at day 45 PE were significantly higher. By contrast, the other parameters characterizing snail infections only showed insignificant variations. The origin of O. glabra (living in a snail community, or monospecific population) used for the breeding of G. truncatula did not have a significant effect on the values of each parameter. Even if variations in the mean numbers of metacercariae were insignificant, the greater survival of G. truncatula at day 30 PE and the higher numbers of cercariae-shedding snails in the groups living with O. glabra allowed to obtain a higher total number of larvae than in alone-raised groups of G. truncatula.

Animals↗

Inactivation of C/EBP transcription factors specifically affects the synaptic plasticity of a common snail neuron.

Our previous studies showed that the acquisition of nociceptive sensitization in common snails is accompanied by long-term facilitation of synaptic transmission in defensive behavior command neuron LP11, this being dependent on translation and transcription processes. The characteristics of the neurochemical mechanisms of plasticity in the different sensory inputs of this nerve cell were identified. The mechanisms of induction of synaptic facilitation of the responses of neuron LP11 to chemical sensory stimulation of the snail's head involved NMDA glutamate receptors, serotonin receptors, cAMP, and serotonin-modulated transcription-regulating protein SMP-69. The mechanisms of induction of synaptic facilitation of another sensory input of the neuron--from tactile receptors on the head - involved protein kinase C. The present study addresses the involvement of C/EBP transcription factors (CCAAT-enhancer-binding protein) in the processes of synapse-specific plasticity of neuron LP11 during the acquisition of sensitization in snails. C/EBP was inactivated using oligonucleotides specifically binding to these proteins. The results showed that acquisition of sensitization during intracellular administration of oligonucleotides led to the selective suppression of synaptic facilitation in the responses of neuron LP11 to chemical sensory stimulation of the snail's head. Synaptic facilitation in the responses to tactile stimulation of the head or foot developed as in neurons in control sensitized snails. It is suggested that C/EBP transcription factor is selectively involved in the mechanisms of synapse-specific plasticity of the sensory input of neuron LP11 from chemoreceptors on the head during the acquisition of sensitization in snails.

Action Potentials↗