Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Lymnaea”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 271 records · Page 15Linked to original sources

Alterations in the internal defence system of the pond snail Lymnaea stagnalis induced by infection with the schistosome Trichobilharzia ocellata.

In order to investigate whether the schistosome Trichobilharzia ocellata interferes with defence activities in its snail intermediate host Lymnaea stagnalis, aspects of the immune system of infected snails and of non-infected controls were compared. The elimination of injected live Staphylococcus saprophyticus bacteria starts at a lower rate in infected snails 1 and 5 weeks after exposure to the parasite, but then proceeds faster than in control snails. During the first 3 weeks of infection, when only mother sporocysts are present, the haemocytes of the infected snails have an increased capacity to phagocytose rabbit red blood cells in vitro. From 5 weeks onwards, when mother and daughter sporocysts are present but cercariae are not yet mature, the phagocytic activity decreases to below control level. The number of circulating haemocytes is also higher in infected snails than in controls at this time. Moreover, the cells are larger, have more inclusions and an increased surface area with many long, branched, spiked pseudopods. The development of the parasite is retarded in a subpopulation of snails in which the haemolymph plasma agglutinates erythrocytes with high titres, compared to a subpopulation with low haemagglutinating activity. The haemagglutinating activity in infected snails of the first decreases significantly from 6 weeks onwards.

Animals↗

Schistosomin: a pronase-sensitive agent in the hemolymph of Trichobilharzia ocellata-infected Lymnaea stagnalis inhibits the activity of albumen glands in vitro.

The schistosome parasite, Trichobilharzia ocellata, nearly completely inhibits the reproductive activity of its intermediate host, Lymnaea stagnalis. The synthetic activity of albumen glands of infected snails at day 35 postinfection (p.i.) is only 1% of the control value. The parasite acts by humoral means. We tested the hypothesis that (a) specific humoral agent(s) is (are) involved and refer to this (these) agent(s) as schistosomin. The presence of schistosomin in the hemolymph of infected snails was investigated by using galactogen synthesis in albumen glands as an in vitro bioassay. The synthetic activity of albumen glands of noninfected snails decreased by about 50% during a 1-h incubation in the hemolymph of infected snails. This inhibition is attributed to schistosomin. Based on these results, with the present bioassay schistosomin appears in the hemolymph between days 28-36 p.i. onwards. Schistosomin is heat-stable (100 degrees C) and pronase-sensitive, and therefore it might have a peptide nature. Schistosomin suppresses the stimulating action of the female, gonadotrophic dorsal body hormone at relatively low doses, which suggests that it may compete with this hormone for the same receptors. The development of two other bioassays for schistosomin in our laboratory is discussed.

Animals↗

The isolation of a cDNA encoding a neuropeptide prohormone from the light yellow cells of Lymnaea stagnalis.

1. The central nervous system (CNS) of the freshwater snail Lymnaea stagnalis contains several clusters of neuroendocrine cells, which synthesize neuropeptides that act as neurotransmitters, neurohormones, and/or neuromodulators, controlling a broad range of physiological processes. Using a protein chemical approach, we have previously characterized a peptide [named LYCP-A (Hoek et al., 1992], which is produced by the neuroendocrine light yellow cells (LYC), which are present as two clusters of endogenously bursting neurons in the visceral and right parietal ganglion, respectively. 2. A differential screening technique was used to isolate the cDNA that encodes the prohormone of LYCP-A. The prohormone appeared to contain three or four putative neuropeptides, one of which is LYCP-A. The organization of the identified prohormone resembles that of the histidine-rich basic peptide precursor previously identified in the R3-14 neurons of the marine snail Aplysia californica (Campanelli and Scheller, 1987). 3. In situ hybridization analysis indicates that the gene encoding the LYC prohormone is expressed in a subset of the LYC. The LYC release their peptides into the hemolymph from a neurohemal area, which is located around the CNS. In addition, the peptides are released from axonal branches in the aorta of the heart, suggesting a role in the regulation of cardiovascular functions.

Amino Acid Sequence↗

Alternative splicing generates diversity of VD1/RPD2 alpha peptides in the central nervous system of Lymnaea stagnalis.

1. Two giant peptidergic neurons, VD1 and RPD2, of the visceral ganglion and right parietal ganglion of Lymnaea stagnalis, respectively, play an important role in the modulation of complex physiological and behavioral adjustments that occur as a result of changes in O2 availability. 2. By cDNA cloning, we have identified two types of VD1/RPD2 transcripts expressed in VD1 and RPD2. In addition, these transcripts are also expressed in other neurons. 3. Both transcripts encode distinct yet related VD1/RPD2 preprohormones that may be cleaved to yield distinct but overlapping sets of neuropeptides. 4. Using the polymerase chain reaction technique, we could show the existence of additional splice variants. 5. Analysis of the organization of the VD1/RPD2 gene indicates that the alpha peptide coding region is interrupted by a number of introns. 6. We concluded that the mRNA segment encoding the alpha peptide domain of the VD1/RPD2 preprohormones is alternatively spliced, thus generating different alpha peptides.

Amino Acid Sequence↗

The parasitic castration and gigantism of Lymnaea truncatula infected with the larval stages of Fasciola hepatica.

The shells of Lymnaea truncatula infected with the larval stages of Fasciola hepatica were significantly longer than those of comparable uninfected controls. The dry mass (tissue, shell + parasite) of the same infected snails, 56 days after infection, was approximately twice that of the controls (tissue + shell). The increased mass of infected snails was not due to a disproportionate increase in shell weight relative to tissues. Infected snails maintained at 20 degrees C had virtually ceased egg production by 21 days post-infection whereas control snails continued to lay eggs steadily for the duration of the experiment. The dry mass of snail tissue plus the cumulative dry weight of eggs produced was taken as an indication of the ability of control snails to generate biomass. Similarly the tissue mass plus cumulative egg weight and parasite weight was taken as an indication of the ability of the infected snails to generate biomass. The control and infected snails were not significantly different in this respect indicating that the gigantism of infected snails could be the result of a switch in nutrient supply from reproduction to somatic tissue growth and parasite growth. Castration was brought about 17-21 days after infection as a result of the direct consumption of the ovotestis by a proportion of the redial population. In a separate experiment it was demonstrated that a population of infected snails maintained at 20 degrees C survived as long as a similar group of control snails. The findings with this host-parasite system are discussed in relation to possible mechanisms causing castration and gigantism in other digene-snail interactions, and in relation to parasitic castration in other groups. It is concluded that the observed gigantism of infected snails is more likely to have a nutritional rather than endocrine origin.

Animals↗

[Description and characteristics of an amebocytic reaction in Lymnaea truncatula Müller infested by Fasciola hepatica L. (author's transl)].

The development of an amebocytic reaction is described in tissues of Lymnaea truncatula infested by Fasciola hepatica. When the snails are bred at 20 degrees C (uniform temperature), this reaction is maximum after five to seven weeks of infestation; afterwards the intensity of the reaction decreases until 10 weeks of infestation. This reaction also develops in snails bred at different temperatures (uniform temperatures of 25 degrees C or 16 degrees C, daily fluctuations from 4 degrees C to 18 degrees C). The maximum intensity of this reaction is chronologically delayed as the temperature goes down. The young snails infested after hatching do not show amebocytic reaction. When the infested snails fast for seven days the number of amebocytes rapidly decreases; these cells disappear from tissues from a snail fasting 14-35 days (depending on the snail organ). The significance of this amebocytic reaction is discussed.

Animals↗

Search for shared antigens in the schistosome-snail combination Trichobilharzia ocellata-Lymnaea stagnalis.

Mother and daughter sporocysts of Tricholbilharzia ocellata, developing in the snail host Lymnaea stagnalis, were searched for substances with antigenic similarities to the snail's haemolymph. Antisera to cell-free snail haemolymph and fractions thereof were used in three different immunocytochemical staining methods, applied on sections of parasitized snails. Snail tissue was consistently stained; cercariae were stained, indicating that the applied methods were successful. Most sections through mother and daughter sporocysts were completely unstained. It is concluded that neither mother nor daughter sporocysts are masked by the antigens studied or substances mimicking these. The relevance of the present observations is discussed.

Animals↗

The development of the amoebocyte-producing organ in Lymnaea truncatula Müller infected by Fasciola hepatica L.

The amoebocyte-producing organ in Lymnaea truncatula is located between the pericardium and the kidney. In control snails bred at 20 degrees C, the organ only has fibroblast-like cells and type I amoebocytes; its growth is associated with a decrease in cellular density. The organ in infected snails bred at 20 degrees enlarges from day 1 to day 21 after exposure (phase 1) with a rapid increase in the number of type I amoebocytes. Then a gradual cellular rarefaction occurs in this organ from day 21 to day 70 after exposure (phase 2) with a fall in the number of type I amoebocytes and a correlated increase in the number of type II amoebocytes. The connective septae become "fibrous" with thickening from day 42 to day 70 after exposure. The breeding temperature only affects the timing and the dates when the different developmental phases begin in this organ. At a given temperature, the body volume of the snail affects only the cellular density. The amoebocytic rarefaction in the organ is uninterrupted if the snail begins its fast on day 49 after exposure (phase 2, 20 degrees C); the organ becomes "fibrous" if the fast begins on day 14 after exposure (phase 1, 20 degrees C). The significance of these observations is discussed.

Animals↗

Development of Trichobilharzia ocellata in Lymnaea stagnalis and the effects of infection on the reproductive system of the host.

Juvenile specimens of Lymnaea stagnalis were exposed to 0 or 4 miracidia of Trichobilharzia ocellata. Highly productive infections developed in all infected snails. Qualitative and/or quantitative light microscopic observations were performed at various intervals between day 0 and 83 post exposure (p.e.). Gonadal maturation started between day 4 and 7 p.e. in all snails, but in infected animals gonadal growth was retarded considerably after day 7 and was blocked from day 19 onwards. This resulted in very small gonads (10% of the volumes of those of controls on day 83 p.e.) in infected snails, in which however, gametogenesis was initially normal. Due to the small gonad volume gamete production was highly reduced. From day 33 onwards spermatogenesis appeared to be inhibited and around day 83 oocyte maturation seemed to be impaired. The accessory sex organs (ASO) of infected snails showed a similar reduced growth. The cellular differentiation and production of secretory granules in these small ASO was normal albeit delayed in both the male and female organs. The severe reduction in growth of the gonad and the ASO started in the presence of immature primary sporocysts, the later effects on gametogenesis were simultaneous with the production of massive numbers of cercariae. These results are discussed in view of the available data on the endocrine control or reproduction in L. stagnalis. It is suggested that either the secretion of gonadotrophic hormones or the response of their targets is reduced by humoral effects of the parasites.

Animals↗

The relationship between miracidial dose, production of cercariae, and reproductive activity of the host in the combination Trichobilharzia ocellata and Lymnaea stagnalis.

The effects of exposure of juvenile Lymnaea stagnalis to one, two or, four miracidia of Trichobilharzia ocellata on the following parameters were studied: infection rate, length of prepatent period, production of cercariae, growth and ovipository activity of the snails, and the weights of their accessory sex organs. An infection rate of 100% was established with all miracidial doses. Morality of the snails was low in all experimental groups. In cercarial production high-(HP) and low-productive (LP) infections could be distinguished. An increase in miracidial dose at exposure results in an increase in the number of snails with HP-infections and decreases the length of the prepatent period of these infections. Snails with HP-infections grow faster than controls after day 14 post-exposure and show giant growth, while the accessory sex organs remain very small. The snails show hardly any ovipository activity. In all snails with HP-infections these effects are observed independent of the miracidial dose at exposure. Snails with LP-infections demonstrate no signs of gigantism, their accessory sex organs are almost identical to those of controls, and the snails show ovipository activity. It is concluded that the occurrence of HP- and LP-infections indicates differences in reproductive capacity of the parasite. HP-infections can only develop when the parasites can adjust the host to their requirements at an early stage of the infection.

Animals↗

Hemocyte production in trematode-infected Lymnaea truncatula.

In trematode-infected Lymnaea truncatula, as in other lymnaeids, hemocytes are formed in the connective tissue. Mitoses are found singly in blood vessels or connective tissue or occur in hemocyte nodules, developing along the mantle epithelium or associated with blood sinuses. The so-called hemocyte-producing organ in L. truncatula is not equivalent to that in Biomphalaria glabrata, but rather involves the proximal part of the kidney sac. It has a dual structure: the main part, containing podocytes and broad hemal spaces, is adapted for hemolymph filtration; the apical portion, adhering to the mantle and pericardial epithelia, has a thicker connective-tissue frame in which hemocyte nodules may develop. The role of this region of the kidney in hemocyte formation is discussed.

Animals↗

Increased activity of the female gonadotropic hormone producing dorsal bodies in Lymnaea stagnalis infected with Trichobilharzia ocellata.

Juvenile specimens of Lymnaea stagnalis were exposed to 0 or 4 miracidia of Trichobilharzia ocellata. Dissection followed at day 22 post exposure. The effects of infection on the activity of the female gonadotropic hormone producing Dorsal Bodies (DB) were studied by phase-contrast and electron microscopy. Morphometry shows that the relative volume of DB cells of infected snails is 1.6 times as high as in controls. This is mainly due to a 45% higher cytoplasmic volume. The number of profiles of the Golgi apparatus increases by nearly 90% and the Golgi volume by 40% as a result of infection. Numerous omega-shaped indentations of the plasma membrane of the DB cell processes indicate the release of the contents of the DB hormone containing elementary granules. It is concluded that parasitic infection causes a clear increase in the synthetic activity of the DB. Most probably, the parasites exert the inhibiting effects on reproductive activity at the level of the targets of the reproductive hormones.

Animals↗

Comparative studies on the productivity of Fasciola gigantica and F. hepatica sporocysts in Lymnaea tomentosa that died after a cercarial shedding or without emission.

A histology study was performed on Fasciola gigantica- or F. hepatica-infected Lymnaea tomentosa that died after a cercarial shedding or without emission to compare the parasite productivity of each trematode. Degenerated rediae increased in number throughout the experiment. Their number rose rapidly after day 79 in snails that died after shedding in the F. gigantica group; they increased more slowly in snails that died without shedding. In the F. hepatica group the number rose after day 63 in the former snails and after day 79 in the latter. The contents of normal rediae evolved inversely. The number of morulae, for example, dropped rapidly after day 79 in the F. gigantica group. In the F. hepatica group it dropped after day 63 in snails that died after shedding and decreased after day 79 in the other dead snails. Free and degenerated cercariae were more numerous in snails that died without emission than in those that died at shedding. They rapidly increased in number after day 77. The numbers of rediae of F. gigantica were substantially greater than those of F. hepatica. In each group considered separately, it was likewise higher in snails that died without shedding than in those that died after the shedding of cercariae.

Animals↗

Structural and cytochemical study of the hemocytes in normal and trematode-infected Lymnaea truncatula.

The ultrastructural study of adult Lymnaea truncatula hemocytes reveals a preponderance of spreading cells at different stages of differentiation. A few round cells may represent a distinct population of hemocytes. As in L. stagnalis, spreading cells are remarkable in that they synthesize peroxidase that is stored in secretory granules, but in L. truncatula hemocytes, endogenous peroxidase activity is also localized in multivesicular bodies. The ultrastructure and peroxidase content of hemocytes do not seem to be affected in snails with established parasites. Evidence that parasites interfere with normal hemocyte functions is that in the few capsules that occurred in parasitized snails the hemocytes did not spread normally and their peroxidase granules were resorbed into multivesicular bodies.

Acid Phosphatase↗

Possible role of reactive forms of oxygen in in vitro killing of Schistosoma mansoni sporocysts by hemocytes of Lymnaea stagnalis.

The interactions between sporocysts of Schistosoma mansoni and hemocytes of the pond snail Lymnaea stagnalis were studied in an in vitro system. All sporocysts were encapsulated and killed in the hemolymph of juvenile or adult snails within 24 h; the killing patterns of both age groups were not very different. The separation of hemolymph into hemocytes and plasma and subsequent incubation of sporocysts showed that the cells, not the plasma, were responsible for parasite killing. The possible involvement of reactive oxygen intermediates and the enzyme peroxidase in the cytotoxic mechanism was studied. Chemiluminescence (CL) could not be detected during the hemocyte-parasite encounter. Histochemical staining with nitroblue tetrazolium (indicative for superoxide) and diaminobenzidine (indicative for hydrogen peroxide) showed that oxygen intermediates were produced by snail hemocytes that encapsulated sporocysts. Histochemistry also suggested the presence of peroxidase activity at the hemocyte-sporocyst interface. The cytotoxic mechanism underlying parasite killing by hemocytes and the role of reactive forms of oxygen and peroxidase are discussed.

3,3'-Diaminobenzidine↗

Identification of a GDP-Fuc:Gal beta 1-3GalNAc-R (Fuc to Gal) alpha 1-2 fucosyltransferase and a GDP-Fuc:Gal beta 1-4GlcNAc (Fuc to GlcNAc) alpha 1-3 fucosyltransferase in connective tissue of the snail Lymnaea stagnalis.

Connective tissue of the freshwater pulmonate Lymnaea stagnalis was shown to contain fucosyltransferase activity capable of transferring fucose from GDP-Fuc in alpha 1 -2 linkage to terminal Gal of type 3 (Gal beta 1-3GalNAc) acceptors, and in alpha 1-3 linkage to GlcNAc ot type 2 (Gal beta 1-4GlcNAc) acceptors. The alpha 1-2 fucosyltransferase was active with Gal beta 1-3GalNAc beta 1-OCH2CH=CH2 (Km = 12mM, V(max) = 1.3 mUml-1) and Gal beta 1-3GalNAc (km =20 mM, V(max) = 2.1 mUml-1), whereas the alpha 1-3 fucosyltransferase was active with Gal beta 1-4GlcNAc (Km = 23 mM, V(max) = 1.1 mUml-1). The products formed from from Gal beta 1-3GalNAc beta 1-OCH2CH=CH2 and Gal beta 1-4GlcNAc were purified by high performance liquid chromatography, and identified by 500 MHz 1H-NMR spectroscopy and methylation analysis to be Fucalpha1-2Gal beta 1-3GalNAc beta 1-OCH2CH=CH2 and Gal beta 1-4(Fucalpha1-3)GlcNAc, respectively. Competition experiments suggest that the two fucosyltransferase activities are due to two distinct enzymes.

Animals↗

Ultrastructural neuropathologic effects of Taxol on neurons of the freshwater snail Lymnaea stagnalis.

Cerebral ganglia of the freshwater snail Lymnaea stagnalis were incubated in vitro in 10 microM Taxol for 8 and 24 h. Cremophor EL (0.1%) was used as a diluant. The tissue was processed for electron microscopy. Various ultrastructural parameters were assessed quantitatively. Cremophor EL appeared to seriously affect the cell somata of the multipeptidergic caudodorsal cells. In the Cremophor-controls the mean area of Golgi zones, the percentage dense material (neuropeptides) in these zones, the number of large electron dense granules (these are involved in neuropeptide processing) and the mean nuclear heterochromatin clump size, were significantly smaller than in the Ringer-controls, whereas the number of lipid droplets was higher. All these parameters, except for the lipid droplets, were not different in the Cremophor-controls and the Taxol-treated specimens. After 24 h treatment, but not after 8 h, Cremophor EL furthermore induced an increase in the number of axonal microtubules. It is argued that the results might signify activation of the neurons by Cremophor EL. Taxol induced a significant increase in the number of microtubules in axons and cell somata. Furthermore an increase in the number of Golgi zones was observed, suggesting activated neuropeptide synthesis. In all groups immunostaining with antibodies to neuropeptides produced by the caudodorsal cells was normal. Release of neuropeptide (exocytosis) from axon endings was elevated after Taxol treatment, and exceptionally high in specimens cotreated with Taxol and Org 2766 (incubation time 22 h). The effect of Org 2766 and Taxol on the number of microtubules was cumulative.(ABSTRACT TRUNCATED AT 250 WORDS)

Adrenocorticotropic Hormone↗

Comparative toxicokinetics of 2,2'- and 4,4'-dichlorobiphenyls in the pond snail Lymnaea stagnalis (L.).

Pond snails (Lymnaea stagnalis (L.)) were treated with 2,2'-dichlorobiphenyl (DCB) or 4,4'-DCB, to examine the toxicokinetic profile of these compounds. Snails were treated orally with 210 micrograms 4,4'-DCB (impregnated on food) for 14 hr, or snails were injected with 50 micrograms of 2,2'-DCB or 4,4'-DCB in the foot. At different times after starting feeding or injection, tissues (albumen gland, digestive gland and digestive tube, central nervous system, remainder parts), hemolymph and faeces were analyzed for unchanged 2,2'- or 4,4'-DCB. The results showed that in case of oral administration of 4,4'-DCB after 144 hr, 97.5% of the dose was excreted unchanged in the faeces. During the first 48 hr 4,4'-DCB was found in all tissues. Thereafter, an exponential elimination was found (the rate constant of elimination (kel) varied from 0.010-0.021 per hr, t1/2 from 33-60 hr and the apparent clearance from 0.02-0.3 g/hr for the different tissues). After injection, the compounds were found in all the above mentioned tissues, especially in the digestive gland. There was a clear difference between snails injected with 2,2'- and 4,4'-DCB. Firstly, kel for 2,2'-DCB was higher (0.028 per hr vs 4,4'-DCB: 0.001 per hr). Secondly, 2,2'-DCB was lethal; 63% of the animals died after 72 hr.

Animals↗