Chicken egg yolk antibodies (IgY) for detecting circulating antigens of Schistosoma japonicum

BackgroundIgY isolated from egg yolk has been widely used in immunodiagnostic tests, including tests to detect circulating antigen (soluble egg antigen or SEA) of Schistosoma japonicum.ResultsA sandwich ELISA was established using a combination of anti-S. japonicum SEA-IgY polyclonal antibodies and IgM monoclonal antibodies. To explore sensitivity and specificity of the sandwich ELISA, serum samples from 43 patients infected with S. japonicum were tested. All acute cases and 91.3% of the chronic cases showed a positive reaction. Only 5% of the control sera from healthy persons gave a positive response. Cross-reactions with antibodies to nine other parasites were rare.ConclusionThe developed immunoassay is reasonably sensitive and specific. It could be used for field research and treatment efficacy assessments.     

Schistosoma japonicum: Immediate hypersensitivity reactions to egg antigen in humans and rodents

Immediate hypersensitivity reactions in schistosoma japonicum infections were examined in both man and experimental animals. In man higher reaction to soluble egg antigen than to adult worm antigen was detected by the use of the radioallergosorbent test (RAST). Blood-collecting filter paper can be used in RAST for seroepidemiological study in place of a skin test. Reaginic antibody formation against egg antigen was detected at the approximate time of egg deposition in strains of mice, Mongolian gerbils, cotton rats, and laboratory rats by the use of passive cutaneous anaphylaxis or Prausnitz-Küstner-type skin tests. At the same time circumoval precipitin tests were positive. Results with athymic nude mice suggest that these reactions are T-cell dependent. No detectable reagin synthesis against adult worm antigen was found in the animals so far examined, confirming stronger allergenic reaction to egg antigen than to that of adult worms in S. japonicum infections in man and animals.     

Diclidophora merlangi and Entobdella soleae: egg production and oxygen consumption at different oxygen partial pressures

The rates of respiration and of egg production of the monogenean trematodes Diclidophora merlangi and Entobdella soleae were compared at different oxygen partial pressures. In D. merlangi the respiratory rate declined sharply as the oxygen pressure in the water fell and egg production almost ceased at pO₂s little below air saturation. Diclidophora lives on the gills of a pelagic fish and the likelihood that the parasite normally has air saturated water passing over it is discussed. Both respiratory rate and egg production in E. soleae were almost independent of ambient pO₂. Entobdella lives on the undersurface of a flat fish, which spends part of its time buried in sandy mud.     

Intracellular calcium release at fertilization in the sea urchin egg.

Fertilization or ionophore activation of Lytechinus pictus eggs can be monitored after injection with the Ca-sensitive photoprotein aequorin to estimate calcium release during activation. We estimate the peak calcium transient to reach concentrations of 2.5–4.5 μM free calcium 45–60 sec after activation and to last 2$\text{3}\text{?}$ min, assuming equal Ca²⁺ release throughout the cytoplasm. Calcium is released from an intracellular store, since similar responses are obtained during fertilization at a wide range of external calcium concentrations or in zerocalcium seawater in ionophore activations. In another effort to estimate free calcium at fertilization, we isolated egg cortices, added back calcium quantitatively, and fixed for observation with a scanning electron microscope. In this way, we determined that the threshold for discharge of the cortical granules is between 9 and 18 μM Ca²⁺. Therefore, the threshold for the in vitro cortical reaction is about five times the amount of free calcium, assuming equal distribution in the egg. This result suggests that transient calcium release is confined to the inner subsurface of the egg.     

Measles immunisation in children with allergy to egg.

OBJECTIVE--To examine the occurrence of adverse reactions to measles vaccine given as a single dose to children with egg allergy, and to determine if the administration of single dose to children with a positive result in an intradermal skin prick test with the vaccine is associated with adverse reactions. DESIGN--Review of results of immunisation and prospective study of 96 consecutively presenting children given intradermal skin testing with the vaccine. SETTING--Children''s allergy centre. SUBJECTS--410 children sensitive to egg referred to the allergy unit for advice about measles immunisation. MAIN OUTCOME MEASURES--Nature and severity of reactions associated with the administration of measles vaccine. RESULTS--All children had a positive result in a skin prick test with egg white, and five had a positive result in a skin prick test with vaccine. Of 96 consecutive children, 46 had a positive result in an intradermal test with vaccine. After immunisation with a full dose (0.5 ml) of vaccine adverse reactions were associated with a mild reaction in four children, none of whom required treatment. Only one of the 46 children with a positive result in an intradermal vaccine skin test had a reaction associated with vaccine administration. None of the children with a positive result in a skin prick test with measles vaccine reacted to the vaccine. The rate of minor reactions to the vaccine not requiring treatment was 0.98% (95% confidence interval 0.27% to 2.48%) and serious reactions requiring treatment was 0% (0% to 0.9%). CONCLUSION--Children with IgE mediated allergic reactions to egg protein should be investigated and managed by practitioners with special knowledge in this subject. Measles immunisation should be performed in a setting where any adverse reactions can be dealt with appropriately. Skin tests and measles vaccine and desensitisation are not necessary.     

The metabolic control of schistosome egg production

Schistosomiasis is a neglected tropical disease caused by infection with trematode parasites of the genus Schistosoma. Despite ongoing treatment programmes, the prevalence of schistosomiasis has failed to decline and the disease remains a cause of severe morbidity in millions of people. Understanding the biology of egg production by schistosomes is critical since eggs allow transmission of the infection, and when trapped in host tissues induce the immune responses that are responsible for the pathologic changes that underlie disease development. Unusually among trematodes, adult schistosomes exhibit sexual dimorphism and display a fascinating codependency in that the female is dependent on the male to grow and sexually mature. Thus, virgin females are developmentally stunted compared with females from mixed‐sex infections and are unable to lay eggs. Moreover, fecund female schistosomes rapidly lose the ability to produce eggs when placed in tissue culture. Here we discuss the metabolic regulation of egg production in schistosomes, and in particular the critical role played by fatty acid oxidation in this process.     

Mode of Parasitism of Meloidogyne and Other Nemaiode Eggs by Dactylella oviparasitica

Hyphae of Dactylella oviparasitica proliferated rapidly through MeIoidogyne egg masses, and appressoria formed when they contacted eggs. The fungus probably penetrated egg shells mechanically, although chitinase production detected in culture suggested that enzymatic penetration was also possible. In soil, D. oviparasitica invaded egg masses soon after they were deposited on the root surface and eventually parasitized most of the first eggs laid. Occasionally the fungus grew into Meloidogyne females, halting egg production prematurely. The fungus parasitized eggs in the gelatinous matrix or eggs freed from the matrix and placed on agar or in soil. Specificity in nematode egg parasitism was not displayed, for D. oviparasitica parasitized eggs of four Meloidogyne spp., Acrobeloides sp., Heterodera schachtii, and Tylenchulus semipenetrans. In tests in a growth chamber, parasitism by D. oviparasitica suppressed galling on M. incognita-infected tomato plants.     

Trophic modification of food quality by heterotrophic protists: species-specific effects on copepod egg production and egg hatching

Recent literature suggests that heterotrophic protists could improve the biochemical constituents of poor quality algae for subsequent use by higher trophic levels, a phenomenon dubbed “trophic upgrading”. We conducted experiments to test trophic upgrading effects on the omnivorous calanoid copepod Acartia tonsa. Two heterotrophic protists, Oxyrrhis marina and Gymnodinium dominans, were grown on three algal species of different nutritional qualities: Dunaliella tertiolecta, Isochrysis galbana and Rhodomonas salina. In parallel incubations, the copepods were fed the heterotrophic protists or the algae that the protists grew on. We measured the ingestion rate, egg production rate and egg hatching success of the copepods in each treatment. Comparison of the egg production efficiency (EPE; egg carbon production/carbon ingestion×100%) between parallel diet treatments allowed us to calculate the trophic upgrading index (TUI; ratio of EPE-heterotrophic protist to EPE-alga). The copepods ingested similar amount, or 20-30% more algae than heterotrophic protists. Daily rations ranged 50-122% of body C per day. Copepods feeding on O. marina that grew on D. tertiolecta had higher egg production rate and egg hatching success than copepods feeding on D. tertiolecta directly, and the resultant TUI between the two treatments was 19.7. Similarly, the copepod egg production was improved by G. dominans that grew on D. tertiolecta and the resultant TUI was 23.3. TUI was near 1 between I. galbana treatment and the parallel heterotrophic protist treatments, indicating no or little trophic upgrading effects on the copepod's egg production. However, egg hatching success was significantly lower with G. dominans growing on I. galbana. O. marina that grew on R. salina induced a lower EPE relative to the alga itself, yielding a TUI of less than 1. Biochemical data showed that the heterotrophic protists contained eicosapentanoic acid (EPA) and docosahexanoic acid (DHA) even when they fed on alga that lacked these essential fatty acids, which may explain some of the observed trophic upgrading effects and species-specific differences in our experiments. However, our data also suggested that dietary EPA and DHA could not be the sole factors regulating the copepod's reproductive output, and that egg production and egg hatching appeared to have different nutritional requirements and respond differently to the copepod's diets.     

Rhipicephalus sanguineus: amino acid composition of egg shell

Acid hydrolysis of the protein fraction of a batch of egg shells of Rhipicephalus sanguineus was followed by determination of the amino acids in the hydrolysate. Using thin layer chromatography, the amino acids—lysine, arginine, aspartic acid, serine, glycine, glutamic acid, alanine, threonine, valine, tyrosine, isoleucine, and leucine were identified. Alkaline hydrolysis of the fraction followed by TLC revealed the presence of tryptophane. Chitin was revealed utilizing a chitosan test.     

Host selection by Homalodisca vitripennis: the interplay between feeding, egg maturation, egg load, and oviposition

For some phytophagous insects, egg maturation may be dependent on adult feeding. Accordingly, rates of egg maturation may be dependent on the quality and quantity of available food sources. In turn, oviposition behavior could be affected by diet quality via changes in egg load (number of mature eggs carried by a female). Experiments were conducted to determine whether adult feeding may affect oviposition behavior of the glassy-winged sharpshooter, Homalodisca vitripennis. No-choice tests demonstrated that eggs accumulated in glassy-winged sharpshooter abdomens as time since last oviposition increased largely as a function of feeding plant species. In choice tests, glassy-winged sharpshooter females were observed most frequently on the plant species that imparted the greatest egg maturation rate in no-choice tests. Direct tests of the effects of egg load on glassy-winged sharpshooter oviposition behavior found that females were more likely to deposit eggs as egg load increased. Similarly, acceptance of a low-ranked oviposition plant species by female glassy-winged sharpshooters increased with egg load and time since last oviposition. The results indicate that adult feeding affected glassy-winged sharpshooter egg maturation, plant species varied in quality for providing nutrients for egg maturation, and egg load affected oviposition behavior. Thus, the quantity and quality of available feeding plant species may affect glassy-winged sharpshooter egg maturation rates, which in turn may affect the plant species female glassy-winged sharpshooters select for oviposition.     

Toxicity,tissue accumulation and residue in egg and excreta of copper in laying hens

To study the effects of a high dietary copper dosage on the performance, liver function, and copper residues in the liver, egg and excreta of the laying hen, seventy-five 28-week-old layers were selected and randomly allocated to five dietary treatments with three replications of five birds each for each treatment. The feeding period was 4 weeks followed by a 1 week withdrawal period. The experimental diets were supplemented with 0, 200, 400, 600 or 800 mg kg⁻¹ copper. The response to copper in the diet in terms of feed intake and egg production fitted a quadratic model (P < 0.05), with 200 mg kg⁻¹ giving a positive response and levels of 400 mg kg⁻¹ and above giving a progressively negative response. Enzyme activities, i.e. aspartate aminotransferase (AST), lactate dehydrogenase (LDH), and creatine kinase (CK) in the serum were significantly (P < 0.05) increased with 600 mg of dietary copper inclusion. Histological examination of livers revealed damage by high dosages (over 600 mg) of dietary copper. Copper residues in the liver and excreta were significantly (P < 0.05) increased as dietary copper increased. The copper content of egg reached a maximum at 400 mg kg⁻¹ dietary copper. Serum enzyme activities of AST, LDH and CK returned to normal after the 1 week withdrawal period. Copper residues in the liver, egg and excreta also declined significantly (P < 0.05) during the withdrawal period.     

Vesicle involvement in the egg cortical reaction of the horseshoe crab,Limulus polyphemus L

Ultrastructural observations (TEM) of the cortical reaction in Limulus polyphemus have been difficult to obtain due to the relative impermeability of the transparent egg envelope to standard fixatives. With the application of trialdehyde fixation techniques [Kalt, M. R., and Tandler, B. (1971). J. Ultrastruct. Res.36, 633–645], the cortical reaction has now been examined and the role of cortical vesicles has been determined. The size of these vesicles in uninseminated eggs is heterogeneous, with small vesicles (0.5 μm) being apposed to the plasmalemma and with large vesicles (4 μm) located in a lower layer of the egg cortex. The contents of the small vesicles are translucent under the electron beam. With the onset of egg activation these vesicles fuse with the overlying plasmalemma. The contents of the large vesicles appear electron dense and exhibit distinctly different morphologies. Shortly after insemination these large vesicles begin to enlarge by fusing together. By 9 min after insemination some enlarged vesicles fuse with the plasmalemma to form pits on the egg surface. The remaining enlarged vesicles continue to fuse with the plasmalemma until approximately 60 min after insemination when few vesicles are remaining.     

Immobilization of lipase using egg shell and alginate as carriers: optimization of reaction conditions

The use of egg shell and alginate as carriers for lipase were studied and the kinetic parameters K _m and V _max were found out. These values were compared with those obtained for free lipase. The reaction conditions were optimized at a pH of 6.0–6.5, temperature at 40?°C and the time of reaction for 40 minutes. 600?μl of free enzyme, 30 numbers of alginate beads with lipase and 2.5?mg of egg shell loaded with lipase. The critical reaction velocity in case of free lipase, lipase adsorbed on egg shell and entrapped in alginate was found to be 53.779 I.U., 37.450 I.U., 31.543 I.U. respectively. It was found that the egg shell loaded with lipase could be reused for 8 times while the alginate beads only for 4 times. It was finally concluded that egg shell was an efficient carrier as far as lipase was concerned, especially in presence of an insoluble substrate.     

Lysozyme in egg whites of tortoises and turtle. Purification and properties of egg white lysozyme of Trionyx gangeticus Cuvier.

Egg white proteins of three species of tortoises and turtle and of hen have been compared by electrophoretic and immunochemical methods. The proteins lacked similarity in electrophoresis, but tortoise and turtle egg white proteins which did not crossreact with those of the hen showed some cross-reaction among themselves. The occurrence of lysozyme as two allelic variants which were distinguishable in electrophoresis was noted only in the egg white of one of the species of tortoise, namely, Trionyx gangeticus Cuvier. Tortoise lysozyme which showed strong lytic activity toward cell walls of Micrococcus lysodeikticus did not exhibit any cross-reaction with hen lysoyzme. It was purified, crystallized, and found to be homogeneous in sodium dodecyl sulfatepolyacrylamide gel electrophoresis, immunochemical tests, and sedimentation. The physicochemical and enzymatic properties of tortoise lysozyme were found to be strikingly similar to those of hen lysozyme with minor differences which could be due to differences in their primary structure. Its average molecular weight of 15,400 was determined from sedimentation and diffusion coefficient values, Archibald experiment, and amino acid composition. The molecule appeared to undergo pH-dependent expansion at pH 2 and dimerization above pH 5.7. In enzymatic properties, tortoise lysozyme showed a specific activity of 29,000–31,000 units and gave a pH optimum at pH 7.5 and an apparent K_a value of 250 mg· liter^?1. Like hen lysozyme, its activity showed strong ionic strength dependence, weak chitinase activity, susceptibility to inhibition by N-acetyl-glucosamine, and stability toward heat.     

Net genetic and temporary epistatic or maternal environmental responses to selection for egg production in chickens

The difference between progeny from selected and unselected parents (T) was experimentally partitioned into net genetic change (G_A), temporary favorable epistatic combinations (G_EP) and egg-transmitted maternal environment (M) in two strains of Leghorns selected over 14 years for early pure-strain egg production. Differences among progeny from selected sires and dams, selected sires only, selected dams only, unselected sires and dams and the parental generation were equated to expected G_A, G_EP and M responses for each trait. Total response was 3.3% for early egg number, 3.7% for total egg number, 0.5% for egg weight, 3.8% for early egg mass and 4.2% for total egg mass. Among progeny that survived the test period and were judged to be normal, total response was 2.6% for total number of eggs, 3.0% for early egg mass and 3.1% for total egg mass. The percentage of T attributed to G_A was 9% for early egg number, 24% for total egg number, 43% for early egg mass and 47% for total egg mass; but 52% for total egg number, 98% for early egg mass and 71% for total egg mass of normal survivors. Temporary maternal selection responses (M) were (1) positive for number of eggs and egg masses, (2) greater for all progeny than for normal survivors, and (3) increased with progeny age. The results suggest that M was caused by reduced egg-transmitted disease. Epistatic selection response was positive for earlier sexual maturity and for number of eggs, but negative for egg weight and thus was small for egg masses. Temporary epistatic and maternal responses can explain overestimation of additive genetic response from offspring-parent regression or from replicated single-generation selection and apparent superiority of mass selection over family or combined selection.     

CHANGES IN NUCLEAR HISTONES DURING FERTILIZATION, AND EARLY EMBRYONIC DEVELOPMENT IN THE PULMONATE SNAIL, Helix aspersa

Calf thymus histories comprising two fractions, one rich in lysine, the other having roughly equal amounts of lysine and arginine, Loligo testes histones rich in arginine, and salmine, are compared with respect to their amino acid compositions, and their staining properties when the proteins are fixed on filter paper. The three types of basic proteins; somatic, arginine-rich spermatid histones, and protamine can be distinguished on the following basis. Somatic and testicular histones stain with fast green or bromphenol blue under the same conditions used for specific staining of histones in tissue preparations. The former histones lose most or all of their stainability after deamination or acetylation. Staining of the arginine-rich testicular histones remains relatively unaffected by this treatment. Protamines do not stain with fast green after treatment with hot trichloracetic acid, but are stained by bromphenol blue or eosin after treatment with picric acid. These methods provide a means for the characterization of nuclear basic proteins in situ. Their application to the early developmental stages of Helix aspersa show the following: After fertilization the protamine of the sperm is lost, and is replaced by faintly basic histones which differ from adult histones in their inability to bind fast green, and from protamines, by both their inability to bind eosin, and their weakly positive reaction with bromphenol blue. These "cleavage" histones are found in the male and female pronuclei, the early polar body chromosomes, and the nuclei of the cleaving egg and morula stages. During gastrulation, the histone complement reverts to a type as yet indistinguishable from that of adult somatic cells.     

Integration of sperm and egg plasma membrane components at fertilization

Studies examining the integration of the sperm and egg plasma membranes, subsequent to gamete fusion in the surf clam, Spisula solidissima, were carried out employing the concanavalin A-horseradish peroxidase-diaminobenzidine procedure (Con A-HRP-DAB). When unfertilized Spisula eggs were incubated in Con A, either prior to or after aldehyde fixation and reacted with HRP-DAB, enzymatic precipitate was found associated with the vitelline layer and plasmalemma. The plasma membranes of sperm treated in a similar manner failed to stain. The plasma membranes of fertilized eggs reacted with Con A-HRP-DAB and examined by 1 min postinsemination were associated uniformly with enzymatic precipitate except at sites of sperm incorporation. These portions of unstained plasma membrane were derived from the spermatozoon and delimited the contents of the fertilization cone. From 2 to 4 min postinsemination, HRP-DAB reaction product became associated with the plasma membrane delimiting the fertilization cone. By 4 min postinsemination no difference in staining of the plasma membranes derived from the egg or the sperm (plasmalemma delimiting the fertilization cone) was detected. Evidence is presented suggesting that the acquisition of HRP-DAB reaction product by the former sperm plasmalemma is due to the movement of Con A binding sites from the egg plasma membrane.     

Lectin Binding to Radopholus citrophilus and R. similis Proteins

Lectin-binding glycoproteins in seven populations of two burrowing nematode sibling species were probed with five different biotinylated lectins on Western blots, and differences were correlated with nematode ability to parasitize citrus and to overcome citrus rootstock resistance. Banding patterns of molecular weight standards were fit best by an exponential decay function, and a predictive equation was used to estimate molecular weights (r² = 0.999). A band (131 kDa) that labeled with the lectin Concanavalin A (Con A) occurred in extracts from cuticles and egg shells of populations of Radopholus citrophilus that parasitize citrus. Wheat germ agglutin labeled a band (58 kDa) in aqueous homogenates of populations that reproduce in roots of citrus rootstock normally resistant to burrowing nematodes. The two sibling species R. citrophilus and R. similis were distinguished by a high molecular weight Con A-labeled band (608 kDa) from cuticle and egg shells. Probing blots with the lectin Limulus polyphemus agglutinin indicated that each population contained a band (12-16 kDa) specifically inhibited by the addition of 25 mM neuraminic acid, suggesting that glycoproteins with sialic acid moieties are present in burrowing nematodes.     

Digenetic trematodes: quinone tanning system in eggshells

Three species of digenetic trematodes with colorless and transparent eggshells, Philophthalmus megalurus, Gorgoderina attenuata, and Megalodiscus temperatus, were compared by histochemical tests with Haematoloechus medioplexus, which has an identifiable quinone tanning system. Precursors for tanning including basic and tyrosine-rich proteins were identified histochemically in all species. Autoradiograms indicated that tyrosine was taken up after in vitro exposure of adult worms by vitelline tissue of G. attenuata and M. temperatus, but at a slower rate in the latter species. Protein synthesis inhibitor studies utilizing cycloheximide showed a reduction of tyrosine incorporation in the vitelline tissue of G. attenuata suggesting that tyrosine is incorporated into protein. Inhibition in M. temperatus was negligible, but evidence from other studies indicated absorption of cycloheximide by the adult may be minimal. Phenolase could not be found in G. attenuata and M. temperatus but was identified in P. megalurus. However, the enzyme system in the latter species seemed to be a partial one capable of oxidizing dihydroxyphenols but not monohydroxyphenols. Histochemical and solubility tests for keratin-type protein in the eggshells were inconclusive. It is suggested that positive identification of keratin as a structural protein of trematode eggshells be withheld until more reliable techniques can be employed. Possible evolutionary implications of the tanned eggshell in the Digenea are discussed.     

Structural studies of the hen's egg lipovitellins. NMR and fluorescence investigations

The pH dependent reversible association-dissociation reaction of α- and β-lipovitellins from egg yolk has been studied by ¹H NMR and fluorescence probe methods. Increased mobility of the choline methyl groups has been demonstrated on dissociation. The lipid methylene resonance of β-lipovitellin shows clear doublet character suggesting that the fatty acid chains exist in distinct environments. The high field component increases with temperature but is suppressed on treatment with pronase, suggesting a significant role for proteins in maintaining the differences in lipid environments. 1-Anilino-8-naphthalene sulfonate has been shown to bind less effectively to the monomeric lipovitellins. This is in agreement with earlier results suggesting that dissociation may be accompanied by increased hydration and conformational changes.