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Teratogenic effects of sinusoidal extremely low frequency electromagnetic fields on morphology of 24 hr chick embryos.

To examine the potential teratogenicity of electromagnetic fields (EMF; sinusoidal and rectangular) on development of chick embryos (white leghorn), 221 freshly fertilized chicken eggs (55-65 g) were exposed during first 24 hr of postlaying incubation (38 degrees +/- 0.5 degree C) to 24 different EMFs, with 50Hz repetition rate and 8.007-10.143 mT flux density. Following exposure, the exposed fertilized chicken eggs (n = 8-10) and sham-exposed fertilized chicken eggs (n = 15) were incubated simultaneously for 8 more days and unexposed control fertilized chicken eggs (n = 20) for 9 days in absence of EMFs. The embryos were removed from egg shells and studied blind. All 24 EMF exposed-groups (inside the coil with exposure) showed an increase in the percentage of developmental anomalies compared to sham-exposed (inside the coil with no exposure) and control groups (outside the coil). Further, egg's weight was evaluated on day 9. This variable did not show significant difference between control and exposed-groups. The investigation also covered the measurement of body weight, length of crown to rump, length of tip of the beak to occipital bone, heart and liver weight. Statistical comparison between sham-exposed and control values did not show significant differences, but comparison between 8.007, 8.453 and 8.713 mT exposed-groups and control groups showed significant differences; in other exposed-groups, the changes were not significant. These results revealed that 50 Hz electromagnetic fields can induce irreversible developmental alterations in 24 hr chick embryos and confirm that its strength could be a determinant factor for the embryonic response to extremely low frequency electromagnetic fields (window effects).

Animals↗

[Comparative studies on the ultrastructure, homology and analogy of egg envelopes in trematodes and cestodes].

The origin, differentiation and functional ultrastructure of egg envelopes surrounding developing and mature miracidia of Schistosoma mansoni and that of developing and mature coracidia of Bothriocephalus clavibothrium have been examined by means of electron microscopy and cytochemistry. Results obtained on these two species were compared with data from our previous studies on the ultrastructure of egg envelopes in different cyclophyllidean (Hymenolepididae, Taeniidae, Anoplocephalidae, Davaineidae) and proteocephalidean cestodes. In the mature infective egg, the three main egg envelopes (the egg-shell, and the outer and inner envelope) that surround the larvae (miracidia of Digenea, coracidia of Pseudophyllidea, and hexacanths of Cyclophyllidea and Proteocephalidea), show evident similarities in their origin, functional ultrastructure and chemical composition. Conclusions of this comparison, concerning analogy and homology in egg envelopes of trematodes and cestodes, are drawn and discussed.

Animals↗

Association of Salmonella enterica serovar enteritidis yafD with resistance to chicken egg albumen.

Salmonella enterica serovar Enteritidis is a major cause of food-borne diseases in industrialized countries. The incidence of S. enterica serovar Enteritidis infections has increased substantially in recent decades, and S. enterica serovar Enteritidis is now one of the leading serovars of Salmonella in the United States. A unique epidemiological characteristic of S. enterica serovar Enteritidis is its association with chicken shell eggs, since approximately 80% of all human gastrointestinal diseases can be traced to contaminated egg products. Eggs are contaminated when bacteria from reproductive tissues of infected hens are packaged into the eggs and persist inside the hostile egg albumen environment. Therefore, resistance to egg albumen is an important aspect in the transmission of S. enterica serovar Enteritidis. We identified a gene, yafD from S. enterica serovar Enteritidis, whose overexpression conferred upon S. enterica serovar Typhimurium enhanced resistance to egg albumen, while disruption of this gene in S. enterica serovar Enteritidis rendered the organism more susceptible to egg albumen. YafD is homologous to members of an exonuclease-endonuclease-phosphatase family, including some enzymes involved in DNA repair. Furthermore, we discovered that egg albumen has nuclease activities and uses both circular and linear DNA as substrates. We propose that YafD provides a survival advantage to S. enterica serovar Enteritidis in eggs by repairing DNA damage caused by egg albumen and that it may be one of the biologic determinants that contribute to the epidemiological association of S. enterica serovar Enteritidis with egg products.

Albumins↗

The effect of mirex on reproduction of Japanesequail and on characteristics of eggs from Japanese quail and chickens.

Laying White Leghorn chickens were fed mirex at 0, 5, 10, 20, 40, 80, and 160 ppm for 12 weeks, and laying Japanese quail were fed mirex at 0, 5, 40, and 80 ppm for 12weeks. The data suggest that dietary mirex at these levels did not affect egg production, egg weight, shell thickness, shell calcium, the proportion of broken eggs, or the proportion of soft-shelled eggs of either chickens or quail. Statistical significance (P greater than 0.05) associated with dietary mirex was detected in the analysis of eggshell weight for chickens; however, because a dose-response relationship of shell weight vs. level of mirex fed was not evident, this observation was attributed to chance. The data suggest that dietary mirex did not affect eggshell weight, fertility, or hatchability of quail. Mirex accumulation in eggs and carcasses of both species was proportional to dose and was slightly higher in quail than in chickens.

Analysis of Variance↗

Effect of chronic progesterone injection on egg production in Japanese quail.

Young laying turkey hens ceased laying and developed a polycystic ovarian follicle (PCOF) syndrome 3 wk after injections of progesterone (P4) ceased. It was hypothesized that laying Japanese quail chronically injected with progesterone (P4) would respond with reduced or arrested egg production and altered ovarian morphology similar to that seen in turkeys expressing the PCOF syndrome, and could thus serve as a model to study the PCOF syndrome. To test these hypotheses, 6 trials were conducted with young photosensitive Japanese quail photostimulated to induce sexual maturity with either 24L:0D or 14L:10D at 6 or 8 wk of age, and used after 3 to 5 wk of egg production. The quail were injected once daily at dosages of 0, 0.17, 0.33, 0.5, 1.5, 3.0, or 4.5 mg of P4/kg per d, or twice daily at dosages of 0 and 1.5 mg of P4/kg for 8 to 14 d and were then necropsied 1 d after the last injection or after waiting an additional 8 to 14 d. During the injection period, egg production was not different among P4 dosages <1.5 mg of P4/kg per d, but decreased at dosages of 1.5 mg of P4/kg per d or greater. A decrease in egg production was found with twice daily injections of 1.5 mg of P4/kg. The decrease in egg production rate ceased and egg production resumed 5 to 7 d after the last injections of 3.0 and 4.5 mg of P4/kg per d or twice-daily injections of 1.5 mg of P4/kg. Compared with control hens, a high percentage of hens (from 12 to 75%) held a hard-shelled egg in the uterus during single daily injections at dosages of 3.0 and 4.5 mg of P4/kg per d and twice daily injections of 1.5 mg of P4/kg. Ovary and oviductal weights, and number of hierarchical follicles were not changed after chronic P4 injection, but more atretic follicles were found in hens at the end of 8 to 12 d of P4 injection. In conclusion, a decreasing egg production rate was induced by chronic P4 injection, but the decrease ceased and egg production resumed 5 to 7 d after the last injections in laying Japanese quail. Young quail hens, unlike young turkey hens, did not develop a PCOF-like syndrome after P4 injection.

Animals↗

Factors influencing inactivation of Salmonella enteritidis in hard-cooked eggs.

The inside of a hen's egg, once considered sterile, is now known to occasionally harbor Salmonella Enteritidis. At least two recent outbreaks of salmonellosis in which Salmonella Enteritidis PT34 was involved have been associated with hard-cooked eggs. This study was undertaken to compare D56 degrees C values of Salmonella Senftenberg 775W and six strains of Salmonella Enteritidis isolated from outbreaks associated with eggs. D56 degrees C values for Salmonella Enteritidis in liquid egg yolk ranged from 5.14 to 7.39 min; the D56 degrees C value for Salmonella Senftenberg was 19.96 min. The two PT34 strains from outbreaks associated with hard-cooked eggs did not exhibit significantly higher resistance to heat compared with two PT4 strains and one strain each of PT8 and PT13a. A PT4 strain and a PT34 strain of Salmonella Enteritidis were separately inoculated (10(7) to 10(8) CFU) into the yolk of medium and extra large shell eggs at 10 and 21 degrees C, and survival was monitored using two cooking methods: (i) placing eggs in water at 23 degrees C, heating to 100 degrees C, removing from heat, and holding for 15 min (American Egg Board method) and (ii) placing eggs in water at 100 degrees C, then holding for 15 min at this temperature. Within the 15-min holding periods, inactivation was more rapid using the method recommended by the American Egg Board compared with method 2. Within each cooking method, inactivation was most rapid in medium eggs initially at 21 degrees C. The PT4 strain survived in yolk of extra large eggs initially at 10 degrees C when eggs were held in boiling water 9 min using method 2. The final temperature of the yolk in these eggs was 62.3 +/- 2 degrees C. Of the two methods evaluated for hard cooking eggs, the American Egg Board method is clearly most effective in killing Salmonella Enteritidis in the yolk.

Animals↗

The effects of freezing on the viability of Toxocara canis and T. cati embryonated eggs.

Suspensions of embryonated (L2) Toxocara canis and T. cati eggs were maintained under freezing conditions in order to study the impact on their long term viability. The eggs had been removed from the uteri of adult Toxocara spp. worms and the suspended in a 0.4% formalin solution before being frozen in 20 ml plastic tubes in the freezer compartment of a domestic refrigerator. Assessment of embryonated egg viability over a period of 34 days was conducted by microscopic examination under a high light intensity. Embryonated T. cati eggs were found to exhibit a greater resistance to freezing than those of T. canis. A difference in the size, design of the egg shell or the metabolism of the larval form may have accounted for the observed differences in the percentage viabilities over time between the two species of Toxocara.

Animals↗

Comparative development of the ovary and production, fertility and hatchability of eggs from traditional turkeys and a contemporary male-line fed ad libitum or restricted.

1. Ovarian function was assessed at first egg and at 44 and 54 weeks of age in traditional turkeys and in a male-line fed ad libitum or restricted to 0.5 of ad libitum during rearing. Egg production was recorded daily and fertility and hatchability were determined at 2 ages. 2. Age at sexual maturity did not differ between the 3 treatments. 3. The number of follicles at first egg in the male line averaged 16.3 compared with 8.9 in traditional turkeys. Food restriction in the male line decreased the number of yellow follicles to 14.6 at first egg and restricted birds were largely in a non-reproductive state from 44 to 54 weeks of age. 4. The total number of recorded ovipositions to 54 weeks of age in male line fed ad libitum or restricted and traditional turkeys respectively were 40.1, 25.2 and 70.7; comparable productions of normal shelled eggs were 28, 20 and 66.3. 5. There were no differences between treatments in fertility after a single insemination at 2 different ages. Hatch of fertiles after the first inseminations were 71.4, 45.5 and 90.3 respectively for male line fed ad libitum or restricted and traditional turkeys.

Aging↗

Immunohistochemical and ultrastructural localization of Schistosoma mansoni soluble egg antigens processed by the infected host.

The detection of egg-derived antigens in the serum and urine of Schistosoma mansoni-infected individuals and experimental animals would provide an alternative method to assess the tissue egg burden. The detected levels are, however, not only a function of the amounts of antigen produced, but also of the processing or clearance by the host. In the present study the immunolocalization pattern of antigens using 2 recently described monoclonal antibodies to repetitive carbohydrate epitopes of S. mansoni soluble egg antigen (114-5B1-A and 114-4D12-A) in various organs of the host was investigated. In the liver strong immunoreactivity could be detected around the entrapped eggs and in egg-shells, as well as in Kupffer cells accumulating both antigen and schistosomal pigment. In the spleen, immunohistochemistry revealed antigen in the plasma as well as in secondary lysosomes of macrophages. Strong labelling was found in the vesicles of the eosinophilic granulocytes: indirect evidence perhaps for the presence of antigen-antibody complexes. In conclusion, the secreted egg antigens were sequestered in the reticulo-endothelial macrophages of the liver and the spleen as already partly described for worm-derived antigens. The presence of large quantities of antigenic material in the spleen could suggest an important role of this organ in the clearance of antigen and might even provide an additional explanation for the hepatosplenomegaly mainly present in S. mansoni-infected children.

Animals↗

Mannanoligosaccharides and aflatoxin B1 in feed for laying hens: effects on egg quality, aflatoxins B1 and M1 residues in eggs, and aflatoxin B1 levels in liver.

Ninety-six laying hens were allocated to 4 groups and fed diets (control diet (0-0), diet supplemented with 2.5 ppm aflatoxin B1 (0-AF); diet supplemented with 0.11% mannanoligosaccharide (MOS-0); diet supplemented with 0.11% MOS and 2.5 ppm aflatoxin B1 (MOS-AF) for 4 wk to evaluate the effect of aflatoxin B1 (AFB1), mannanoligosaccharide (MOS), or both on egg quality and the in vivo efficacy of MOS to interact with an oral administration of AFB1. After 2 and 3 wk, egg weight decreased (P < 0.05) in the group fed MOS-0 versus groups on 0-0 and 0-AF. Egg shell weight was lower (P < 0.05) in the group fed 0-AF. Aflatoxin influenced color parameters, which were probably related to interference of AFB1 with lipid metabolism and pigmentary substances deposition in yolk. MOS appeared to increase protein percentage in albumen. No AFB1 or aflatoxin M1 (AFM1; a polar metabolite of AFB1) residues were found in eggs of the experimental groups. Livers from groups 0-0 and MOS-0 always tested negative for AFB1 and AFM1. Differences (P < 0.01) were found between AFB1 hepatic levels of group 0-AF (mean +/- SD: 4.13 +/- 1.95 ppb) and group MOS-AF (mean +/- SD: 2.21 +/- 1.37 ppb). The data demonstrated the ability of MOS to adsorb and degrade AFB1, reducing gastrointestinal absorption of AFB1 and its levels in tissues.

Aflatoxin B1↗

Complex study of the physiological role of cadmium. II. Effect of cadmium load on the cadmium content of eggs.

The possibility of "cadmium (Cd) contamination" of eggs and the dynamics of Cd accumulation were studied. A total of 40 (4 x 10) Japanese quails weighing 155-200 g, being at the middle phase of egg production and kept on batteries in a climatized animal house were used. The birds were fed a standard quail layer diet and drank tap-water ad libitum. With the exception of the control group (Cd-0), the diet of the other three groups was supplemented with Cd sulphate homogeneously mixed in the diet so that it contained 75 mg (Cd-75), 150 mg (Cd-150) and 300 mg (Cd-300) per kg. During the 37-day feeding trial the quails' behaviour, health status and daily egg production were monitored and the birds were weighed weekly. The egg production of the experimental groups, particularly of those exposed to a high Cd load, rapidly decreased: at the highest Cd load (300 ppm) egg production completely ceased at days 10-11 of the trial. The total Cd content of the eggs rose already from the 3rd day of the feeding trial and by day 10 it reached a value of 0.777 mg/kg dry matter in the eggs of quails of group Cd-75. This was about five times the value measured in the control quails' eggs (0.165 mg/kg dry matter). The Cd content of the egg-white and egg-yolk (maximum values: 0.212 and 0.107 mg/kg dry matter) also increased to about 2 or 3 times that measured in the control eggs. The Cd content of eggs reached the peak in the 2nd week of the feeding trial, then started to decrease, and in the 3rd and 4th weeks not even the eggs laid by quails exposed to a high Cd load contained more Cd than about twice the concentration measured in the controls' eggs. The elucidation of this hitherto not studied process requires further investigations. The phenomenon may be due to a lack of the protein necessary for Cd transport and to the impairment of Cd absorption and of the excretory activity of the oviduct. The higher Cd concentrations measured in the egg were accompanied by markedly elevated Fe, K and S values. In the egg samples collected in the 4th week a substantial reduction in Ca and P concentration was observed. As regards the mineral elements measured in the egg-shell, a significant negative correlation was established between the concentration of Cd and those of Zn, Mg and Ca.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

Ovarian follicular structure of White Leghorns fed ad libitum and dwarf and normal broiler breeders fed ad libitum or restricted until point of lay.

1. Yellow follicle numbers when the first egg was laid were 6.3, 9.0 and 12.4 for ad libitum reared Leghorns, sex-linked Dwarf (AL Dwarf) and Normal broiler breeders respectively. Multiple ovulation resulted in low egg production and a high proportion of defective egg shells in AL Dwarf and Normal broiler breeders during early lay. 2. Restricting the growth of broiler breeders during rearing by restricting food intake (R Dwarfs) reduced the number of yellow follicles to 6.8 and increased the rate of lay. 3. Atretic yellow follicles were common among broiler breeders but not in Leghorns or R Dwarfs when the first egg was laid. 4. Poor egg production in older broiler breeders was caused by birds with few or no developing yellow follicles, atresia in yellow follicles and the continued occurrence of multiple ovulations. 5. There was no relationship between the number of yellow follicles and the number of white follicles less than 5 mm diameter but atresia in white follicles 2 to less than 5 mm was negatively related to the number of yellow follicles. 7. No relationship was observed between abdominal fat weight and yellow follicle number, though birds which ate more had more yellow follicles. 8. The sex-linked dwarfing gene dw was associated with increased atresia among the white follicles and low numbers of yellow follicles compared with the Normal DW broiler breeder genotype.

Animals↗

Oviductal morphology in relation to hormonal levels in the snapping turtle, Chelydra serpentina.

Microscopic and in situ visual observations were used to relate circulating hormone levels to morphological changes in the oviduct of the snapping turtle Chelydra serpentina throughout the ovarian cycle. Increase in levels of progesterone (P), estradiol (E2) and testosterone (T) levels coincide with an increase in number and growth of endometrial glands, luminal epithelial cells and secretory droplets throughout the oviduct. Testosterone and estradiol levels rose significantly (P < 0.05) after the May-June period and remained high throughout the rest of the summer. Progesterone levels remained stable throughout the summer, with a brief decline in July due to luteolysis. Hormonal values declined significantly (P < 0.001) at the end of the ovarian cycle in the fall. In situ visual observation of fresh oviducts at different stages of gravidity in recently ovulated turtles revealed that proteinaceous like components from the endometrial glands were released into the lumen to form fibers. The morphological features of the oviduct remained active throughout the summer months even though the snapping turtle is a monoclutch species which deposits all the eggs in late-May to mid-June. The high steroid levels correlate with and may be responsible for the secretory activity present throughout the summer and their decline correlates with change to low secretory activity in the fall. Calcium deposition accompanied by morphological changes in luminal cells are suggestive of secretory activity. In the egg-bearing turtles, uterine Ca2+ concentrations measured by flame atomic absorption spectrophotometry revealed significantly higher Ca2+ concentrations (P < 0.001) in eggs with soft shell than eggs without shell. There was a significant increase in calcium granules and proteinaceous fibers in luminal surface of the uterus during the period of eggshelling. This supports the fact that in the snapping turtle like in other reptiles, eggshelling process occurs in the uterus.

Animals↗

Immunopathology of Schistosoma japonicum and S. mansoni infection in B cell depleted mice.

To investigate the role of antibody in the pathogenesis of hepatic granulomas around schistosome eggs, mice were depleted of B cells by treatment from birth with anti-IgM serum and were subsequently infected with Schistosoma japonicum or S. mansoni. Anti-IgM treatment did not affect the development or fecundity of the worms or the larvae within the egg shells. Normal circumoval granulomas were present in the livers of B cell depleted mice 7 or 8 weeks after infection clearly indicating that antibody and immune complexes have no necessary role in the formation of granulomas. Hepatic fibrosis was also similar in B cell depleted and untreated mice at these times. Ten weeks after infection the size of S. japonicum egg granulomas in untreated mice had decreased but no change in the size of granulomas had occurred in B cell depleted mice, and hepatic fibrosis was more marked in treated than in untreated mice. Similar changes were noted in S. mansoni infected mice, assayed at 8 and at 12-13.5 weeks after infection. The effects of B cell depletion in the more chronic infections may be related to the absence of antibody but could also be caused by an influence on B cell-dependent suppressor T cells.

Age Factors↗

Unexpected newcastle disease virus in day old commercial chicks and breeder hen.

Newcastle disease virus (NDV) specific antigen in the gut contents and NDV specific antibody in blood circulation were seen in day old chicks belonging to nine different commercial hatcheries of Tamil Nadu, India. Antigen disappeared by 4th week and antibody by 6th week of age. Fourteen NDV isolates obtained from the gut contents of day old chicks of different commercial hatcheries, one NDV isolate from dead in shell eggs and one NDV isolate from breeder hen were characterized and grouped under velogenic, mesogenic and lentogenic pathotypes. Four isolates were grouped under F and another four isolates were grouped under E based on reaction with monoclonal antibodies (Mabs) but found to be velogenic based on pathogenicity tests. In one particular flock velogenie NDV was isolated from breeder hen, dead in shell embryos and day old chicks and they all belong to Mabs group E. Vertical transmission of velogenic, mesogenic and lentogenic NDVs and role of NDVs in the gut contents have been discussed.

Animals↗

[Simple method for obtaining Toxocara canis antigen for the indirect immunofluorescence technic].

A simple method for the preparation of Toxocara canis antigen for the indirect immunofluorescent test is described: Embryonated Toxocara eggs are treated for 12 hours at room temperature with a 1:1 mixture of 2% NaHO and sodium hypochlorite (NaClO) solution with a concentration of 2% free chlorine in order to remove the outer layers of the egg shells. The larvae which are still enclosed in the lipid membrane are freed by mild ultrasonic treatment. Thereafter, the suspension of larvae is washed and purified in a modified Baermann apparatus. In this way large numbers of larvae in pure suspension were gained and used for the production of frozen sections for the indirect immunofluorescent test. Rabbits and mice experimentally infected with embryonated Toxocara canis eggs showed a positive serological reaction (titers between 1/10 to 1/320) in this test with Toxocara larvae as antigen, while in uninfected control animals no antibodies could be detected. The larval antigen exhibited only a weak cross reaction with sera of animals infected with Ascaris suum eggs.

Animals↗

Effects of feeding tylosin to layers exposed to Mycoplasma gallisepitcum.

Two experiments are reported in which the effect of tylosin upon the development of Mycoplasma gallisepticum (MG) infection in replacement layers was monitored by serological and cultural methods. Concentrations of tylosin tested included 0, 22, 38.5, and 55 ppm. Egg production and feed consumption data were collected for one year. Tylosin slowed the rate of spread of MG infection as measured by serological and cultural methods. The effect of tylosin on the spread of MG infection was dose related. Hen day egg production peaked at 85 to 87% in the mediated groups, while controls peaked at 81 to 84%. The magnitude of tylosin effect on production increased with time to a maximum difference of 10 to 12% at 52 weeks. Feed efficiency was markedly improved by all concentration of tylosin ranging from 5% at peak production to 12 to 18% at 52 weeks. The incidence of shell-less or soft shelled eggs was markedly reduced in the tylosin treated group.

Animal Feed↗

Replacement value of hatchery waste meal for fish meal in layer diets.

An experiment was conducted in which hatchery waste meal (HWM) replaced fish meal (protein for protein) in layer diets at 0%, 33%, 66% and 100% levels. Both feed and protein intake were superior on HWM diets. The highest hen-day production of 73.97% was obtained on diet 2 in which 33% of fish meal was replaced with HWM. Egg weight and egg length were also superior on HWM diets. All birds fed on HWM diets had thicker egg shells (0.33 mm) than did those fed on the control diet, fish meal diet (0.32 mm). Results obtained for yolk weight were statistically different (P < 0.05). Highest values for yolk weight (16.91 g) and albumen weight (40.93 g) were recorded for birds fed with diet 4 in which 100% fish meal was replaced with HWM. HWM can replace fish meal completely in layer diets without adverse effect on egg quality characteristics.

Animal Feed↗