Effect of hen production age on egg composition and embryo development in commercial Pekin ducks

At 26, 31, 36, and 42 wk of age, eggs were collected from the same duck breeder flock to study the effects of hen production age on egg composition and embryo development. At each hen age, yolk and albumen measurements were made on a random subsample of unincubated eggs. Embryo and yolk sac measurements were made at 20, 22, 24, 26, 27, and 28 d of incubation. Egg weight was significantly affected by hen production age, but most of the observed age effects occurred between 26 and 31 wk with minimal age differences thereafter due to a quantitative feed restriction for egg weight. Yolk weight increased significantly with hen production age, with the largest increase, 6.6 g, also occurring between 26 and 31 wk of age. Yolk-free duckling weight increased with hen production age at 27 d of incubation. The yolk sacs of embryos from the 31-, 36-, and 42-wk-old hens were heavier at 20 and 22 d, before the differentiation in embryo weight. Differences in yolk sac weight were not consistently affected by hen production age between 26 and 28 d of incubation. The eggs from the 42-wk-old hens weighed 3.3 g less than those from the 31-wk-old hens, but yolk-free duckling weight at 27 d was 2.9 g heavier from the 42-wk-old hens.     

Effect of selenium and mercury on survival of chick embryos

Factorial experiments were arranged in a completely randomized or randomized block design. The factors included: selenium and day of injection; mercury and day of injection; selenium and mercury; and selenium, mercury and day of injection. Each treatment factor consisted of several levels, selenium ranged from 0.00 p.p.m. to 0.05 p.p.m., mercury from 0.00 p.p.m. to 0.30 p.p.m. and injection was performed on day-3, 9, and 15 of incubation. Babcock-300, and White Leghorn x New Hampshire cross eggs were obtained from 13-15 month old hens. Mercury was injected into the air cell at 4 or 24 hours after selenium injection. Analysis of variance on arcsine transformed data showed that selenium significantly decreased survival at all 3 injection times (P less than 0.01). Survival was significantly greater with increasing age at injection (P less than 0.01). Survival of embryos significantly decreased (P less than 0.01) with increasing levels of mercury from 0.00 p.p.m. to 0.20 p.p.m. injected into eggs on day-3 of incubation. Survival of embryos injected at later stages was less than that of controls but not significantly less. Injection of low levels of selenium, 0.01 p.p.m. or 0.02 p.p.m., to mercury treated eggs tended to improve the survival of embryos as compared to treatment with mercury alone, although individual differences were not significant. At higher levels, selenium accentuated the toxicity of mercury.     

Effects of 3,3',4,4'-tetrachlorobiphenyl, 2,3,3',4,4'-pentachlorobiphenyl, and 3,3',4,4',5-pentachlorobiphenyl on the developing chicken embryo when injected prior to incubation

Great Lakes waterbird populations have experienced less-than-expected hatchability of eggs and a greater-than-expected incidence of developmental abnormalities. Such deleterious effects have been attributed to polyhalogenated hydrocarbons such as polychlorinated biphenyls (PCBs). PCBs are of primary concern since they are present in significant quantities in the environment. Specific PCB congeners, 3,3',4,4',5-pentachlorobiphenyl (IUPAC number 126), 3,3',4,4'-tetrachlorobiphenyl (IUPAC number 77), and 2,3,3',4,4'-pentachlorobiphenyl (IUPAC number 105), were injected (singly or in combination) into the yolks of White Leghorn chicken (Gallus domesticus) eggs prior to incubation. Teratogenicity was assessed in dead embryos and in hatchlings. Hatchlings were raised for 3 wk to assess body weight gain and mortality. At the end of the 3-wk period, chicks were subjected to necropsy and the brain, bursa, heart, liver, spleen, and testes were removed and weighed. All 3 congeners caused increased embryo mortality, with approximately 50% mortality occurring at 0.6, 8.8, and 5592 micrograms/kg egg for congeners 126, 77, and 105, respectively. All three congeners also produced significantly more abnormalities than the vehicle. Chicks from PCB-injected eggs had lower body weights at wk 2 and 3 of age. Congener 126 caused lower relative bursa weights, congener 77 caused greater relative spleen weights and lower relative liver weights, and all three congeners caused relative heart weights to be greater when compared to control.     

Incidence of childhood cancer in Thailand 1988-1991

1. The ostrich industry in South Africa (and elsewhere) experiences a high rate of embryo mortality during artificial incubation of eggs. Most of this mortality takes place in the last l0-l4 d of incubation. 2. We carried out post-mortem examinations on 111 embryos that died within this period to assess the causes of this mortality. 3. Malpositioning and severe oedema were the predominant symptoms of dead-in shell embryos with 55% being malpositioned and 41% showing severe oedema. Of these, 22 embryos (24%) showed both symptoms. Malpositioning generally results from incorrect setting of the eggs or inadequate turning and oedema was significantly correlated with the amount of water lost from the eggs which in turn was correlated with egg size. 4. Myopathy, gross lesions of internal organs, haemorrhage, bacterial infections and congenital deformities were found in less than 10% of chicks examined for these symptoms.     

Congenital complete atrioventricular block

A new system, the Toxorhynchites-fluorescent antibody (TFA) test in which the larvae of Toxorhynchites splendens mosquitoes were used for the detection of bluetongue virus (BTV) from Culicoides midges, was developed. Twenty-seven pools of Culicoides midges were collected from bluetongue-prone areas of Tamil Nadu by use of the light-trap and suction-trap methods. A suspension of each pool was injected intrathoracically into T. splendens IV instar larvae and inoculated onto Vero cell monolayers. An indirect fluorescent antibody technique and an immunoperoxidase test were used to detect BTV antigen in smears of crushed midges, crushed larval head smears after incubation for 7 d at 28 degrees and cell monolayers showing cytopathic effects 48 h post inoculation. The suspensions were also injected intravenously into embryonated chicken eggs, and the characteristic BTV-induced lesion(s), viz. cherry-red appearance of embryos, were observed after 48 h. Virus was confirmed by a qualitative neutralization test conducted simultaneously in embryonated chicken eggs. A total of seven out of 27 samples (26%) were positive for the presence of BTV antigen in all the diagnostic systems used. Since BTV propagates readily in experimentally infected T. splendens larvae and the BTV antigen can be detected by the fluorescent antibody technique with a sensitivity comparable to that for virus propagated in tissue culture and embryonated eggs, the TFA system can be adopted as a new method for the isolation of BTV from vectors. The advantages of the TFA system are discussed.     

Ce在雏鸡各组织器官中的分布、积累以及对鸡胚生物效应影响的研究

以海兰种蛋作为实验材料,把C e的EDTA盐注入种蛋后孵化。探讨了C e对鸡胚的影响和C e的EDTA盐进入胚胎的情况,并分析了C e在雏鸡各组织中的分布。结果发现C e对鸡胚有一定的影响,既影响小鸡的出壳时间又影响其体重,当剂量达到一定值时,会使出壳小鸡致畸。鸡胚在发育过程中,可以部分吸收C e,在胚胎发育过程中吸收后的C e可在各组织中转移。     

The use of the chicken embryo screening test and brine shrimp (Artemia salina) bioassays to assess the toxicity of fumonisin B1 mycotoxin

Chicken embryos and brine shrimp naulpii were utilized in short-term toxicity bioassays to assess their sensitivity to the mycotoxin fumonisin B1 (FB1). Fertile chicken eggs (Cobb x) were dosed with FB1 on day 2 of incubation by the injection of 100 microliters of aqueous solution into the air space of each egg. Eggs were incubated with mechanical rotation until hatch, at which time mortality was assessed. Probit transformation of the mortality data produced a linear line of best fit (P < 0.05), from which an LD50 of 52 micrograms FB1/egg, equivalent to a concentration of 1.3 microns hatched in artificial seawater and exposed to FB1 in an optimized 96-well plate assay with a 48 hr mortality endpoint. Probit transformation of the mortality data resulted in an LC50 of 1.7 microns FB1, or 1.2 micrograms FB1/ml. Thus, at the cellular level, both bioassays appeared sensitive to FB1; however, from the standpoint of use as a screening assay, the chicken embryo bioassay is limited by the relatively high dose of FB1 required per egg. It is anticipated that the design and simplicity of the brine shrimp bioassay will accommodate screening for FB1 toxicity in contaminated samples.     

Functional regulation of tyrosinase and LAMP gene family of melanogenesis and cell death in immortal murine melanocytes after repeated exposure to ultraviolet B

The aim of the present study was to evaluate the effect of human follicle stimulating hormone (hFSH) on cellular proliferation in the chick embryo ovary. Chick embryos (Babcock B300) were injected on chorioallantoic membrane with a single dose of hFSH (2.0 IU/ embryo) at Days 7, 9, or 13 of incubation or with hCG (2.0 IU/embryo) at Day 13 of incubation. At 17 days of incubation and within 24 h after hatching, left ovaries were dissected and completely dissociated. Cells from the whole ovary were classified into germ cells (primary oocytes), typical steroidogenic cells, and poorly differentiated somatic cells and counted with the aid of a hemocytometer. Aliquots of the cell suspension from the whole left ovary were analyzed by flow cytometry, in order to determine the percentage of cells at each phase of the cell cycle. In addition, samples of the suspension (1.0 x 10(6 )cells) were incubated for 2 h in basal and stimulated conditions measuring 17beta-estradiol secretion in the medium. The ovarian cell number at 17 days of incubation showed that hFSH treatment at Day 7 did not modify the cell number in any of the subpopulations evaluated; treatment at Day 9 resulted in an increase in poorly differentiated somatic cell number, without changes in steroidogenic and germ cells, whereas hFSH treatment at Day 13 augmented the number of poorly differentiated, steroidogenic, and germ cells. The percentage of cells in S-phase was increased 12 and 15 h after hFSH treatment (Day 13). Secretion of 17beta-estradiol was increased in the hFSH-treated group (Day 13) measured at 17 days of incubation. The increase in cell number of the three subpopulations was still observed in the left ovary of the newly hatched chicken. Treatment with hCG at Day 13 of incubation did not change the number of poorly differentiated, steroidogenic, and germ cells in the left ovary, neither in the 17-day-old chick embryo nor in the newly hatched chicken. The 17beta-estradiol secretion in hCG-treated embryos was similar to controls. The present study is the first evidence of an effect of FSH on somatic and germ cell number, together with an increase in 17beta-estradiol production during chick embryo ovary development.     

A randomized study of the efficacy of the PROPATH Program for patients with Parkinson disease

By polymerase chain reaction (PCR) using a pair of primers specific for Salmonella phoE gene a 365-bp specific gene fragment could be amplified from yolk of infertile eggs and dead-in-shell chicken embryos, and from environmental samples. Out of 45 dead-in-shell embryo samples, 20 (44.4%) were found positive for Salmonella DNA by PCR compared to 11 (24.4%) by bacteria isolation. Salmonella DNA could also be detected from infertile eggs, chicken faeces, floor litter and chick fluff, which incidence was higher than that by bacteria isolation.     

Duration of fertility in ad libitum and feed-restricted caged broiler breeders

It has been shown in previous studies that fertility can be reduced in overweight broiler breeder (BB) flocks. In an effort to determine the effect of ad libitum feeding on the duration of fertility in BB hens, 60 52-wk-old Shaver Starbro hens were randomly assigned to one of two treatments, ad libitum feeding (F) or restricted feeding (R) to maintain breeder target weights. All hens were reared to 52 wk under conditions of feed restriction. All birds were weighed individually on a weekly basis. At the beginning of each of two 4-wk study periods (56 to 60 wk and 60 wk to 64 wk), all birds were inseminated on 2 consecutive d with 0.05 mL pooled BB semen. All eggs were weighed and placed in a forced air incubator the same day that they were laid. After 7 to 10 d of incubation, the eggs were broken out and scored macroscopically as fertile with live embryo, fertile with dead embryo (early embryonic death), or clear (assumed infertile). The duration of fertility was defined as the number of days from the day after the second insemination to the last fertile egg before two consecutive interfile eggs. Hen BW were significantly different between treatments within each of the two 4-wk studies. The mean BW of the F hens was 4,261 g in Study 1 and 4,448 g in Study 2. The BW of the R hens were 3,459 g in Study 1 and 3,565 g in Study 2. Egg production levels and average egg weight was not different between treatments in either study. In Study 1, the duration of fertility for the F hens (12.7 d) and the R hens (12.7 d) were not different. In Study 2, the durations of fertility were significantly higher (P < 0.05) in the R hens (12.7 d) than in the F hens (10.0 d). These results support the theory that overweight BB have a reduced duration of fertility that may contribute to a reduced fertility in artificially inseminated and naturally mated flocks.     

Effects of dietary fat and eggshell cuticle removal on egg water loss and embryo growth in broiler hatching eggs

The effects of dietary fat and eggshell cuticle removal on egg water loss, embryo growth, and hatchability were determined in eggs from broiler breeder hens at different ages. Hens were fed isocaloric diets containing one of three different types and levels of added fat. In addition, eggs were either left intact or washed to remove the eggshell cuticle prior to set. Cuticle removal increased egg water loss between 43 and 62 wk. Cuticle removal increased relative wet embryo weight at Week 52 and relative dry embryo weight at 52 and 62 wk. Furthermore, at 62 wk, diet and day of incubation interacted to affect wet embryo weight, and diet variably affected dry embryo weight. No treatment differences were observed for cumulative hatchability, rate of hatch, and relative yolk sac weight at Day 19 of incubation. It was concluded that cuticle removal and the addition of fat to breeder diets may influence embryonic growth without having any subsequent effects on hatchability.     

The role of antibiotics in the management of elective and post-traumatic hand surgery

Stunting syndrome (SS) is a viral enteric disease of turkey poults. The etiologic agent (stunting syndrome agent [SSA]) of this disease has been reported recently. The objective of this study was to develop a method for in vitro propagation of SSA. Primary cells, various continuous cell lines, and embryonated eggs were evaluated. Turkey embryos that were inoculated via the amniotic cavity at 24-25 days of incubation were susceptible to SSA infection. The jejunal maltase activity of SSA-inoculated turkey embryos was significantly (P < or = 0.001) lower than that of control embryos. D-xylose absorption was also altered in SSA-infected turkey embryos. The extent of reduction of D-xylose absorption and maltase activity in the infected embryos was nearly identical to that observed when day-old poults were infected with SSA. The intestines from the infected turkey embryos were pale, thin walled, and distended with fluid. Electron microscopic examination of the intestinal fluid and epithelial cell lysate of infected embryos revealed pleomorphic membraned SSA viral particles. SSA that had been serially passaged in turkey embryos retained its ability to induce SS in day-old poults. All the primary and continuous cells that were evaluated did not support the replication of SSA on the basis of cytopathic effects, electron microscopy, and turkey embryo inoculation. Inoculation of chicken embryos by various routes failed to support SSA. All routes of inoculation, other than the amniotic route at 24-25 days, failed to support SSA in turkey embryos. The results of the this study indicate that the SSA was successfully propagated in turkey embryos that exhibited alterations in embryo intestinal absorption and digestive enzyme activity similar to poults with SS. Successful propagation of SSA in turkey embryos should prove beneficial for future studies including characterization of SSA, prevention and control strategies, and enteric disease modeling.     

Alterations in colonic mucosal vessels in patients with cirrhosis and noncirrhotic portal hypertension

The purification, biochemical characterization and functional features of a novel extracellular matrix protein are described. This protein is a component of the basal lamina found in embryos from the sea urchin species Paracentrotus lividus and Hemicentrotus pulcherrimus. The protein has been named Pl-200K or Hp-200K, respectively, because of the species from which it was isolated and its apparent molecular weight in SDS-PAGE under reducing conditions. It has been purified from unfertilized eggs where it is found packed within cytoplasmic granules, and has different binding affinities to type I collagen and heparin, as assessed by affinity chromatography columns. By indirect immunofluorescence experiments it was shown that, upon fertilization, the protein becomes extracellular, polarized at the basal surface of ectoderm cells, and on the surface of primary mesenchyme cells at the blastula and gastrula stages. The protein serves as an adhesive substrate, as shown by an in vitro binding assay where cells dissociated from blastula embryos were settled on 200K protein-coated substrates. To examine the involvement of the protein in morphogenesis of sea urchin embryo, early blastula embryos were microinjected with anti-200K Fab fragments and further development was followed. When control embryos reached the pluteus stage, microinjected embryos showed severe abnormalities in arms and skeleton elongation and patterning. On the basis of current results, it was proposed that 200K protein is involved in the regulation of sea urchin embryo skeletogenesis.     

Preparation of lipid-free protein extracts of egg yolk

1-Butanol extraction of chicken egg yolk homogenates containing 1 M NaCl yields lipid-free aqueous solutions of egg yolk proteins. These solutions, after dialysis, can be applied to a variety of chromatographic media without clogging. Although some proteins are denatured by this procedure, most of the water-soluble proteins remain in solution, including biotin-binding protein and riboflavin-binding protein.     

IS-RT-PCR assay detection of MT-MMP in a human breast cancer cell line

The effect of the host system on the pathogenicity, immunogenicity, and antigenicity of infectious bursal disease virus (IBDV) was investigated. One classic (SAL) and one variant strain (IN) of IBDV were passaged separately six times in three host systems, namely BGM-70 continuous cell line, primary chicken embryo fibroblast (CEF) cells, or embryonating chicken eggs (embryos) or one time in the bursa of Fabricius (BF) of specific-pathogen-free (SPF) chickens. Passage in BGM-70 cells or CEF cells resulted in loss of pathogenicity, but viruses passaged in embryos or BF maintained their pathogenicity. For the immunogenicity study, the viruses described above were used to prepare live and inactivated vaccines, containing 10(3) mean embryo infectious doses (EID50s) and 10(5) EID50s respectively. These vaccines induced different levels of protection. It was concluded that the antigen titration methodology employing embryonating chicken eggs was not suitable for titration of viruses propagated in other host systems because of varying degrees of adaptation and/or pathogenicity of the viruses resulting in variability in antigen mass of the tested vaccines. To test this assumption, an antigen-capture enzyme-linked immunosorbent assay was used as a titration system to compare the antigenicity of viruses propagated in BGM-70 cells or BF. Preparations containing similar antigen masses were inactivated then inoculated into two age groups of SPF chickens and antibody titers were monitored. During the experimental period, the geometric mean virus-neutralizing (VN) antibody titers of the vaccinated groups did not differ significantly (P > 0.05).     

稀土对鸡胚胎生物效应的影响

选用鸡胚作为实验对象,La、Eu、Y作稀土实验代表元素,对不同孵化期进行了跟踪性实验。结果发现不同稀土在各孵化期对胚胎平均体重的影响有较大差别,且孵化期与减重无线性关系,其中以Eu减重最多,La最少。稀土在胚胎中的含量,随孵化时间增加而增加,但不同稀土元素其屏障作用差别较大。     

Avian paramyxovirus type 1 from pigeons: isolate characterization and pathogenicity after chicken or embryo passage of selected isolates

Nine pigeon paramyxovirus type 1 isolates from the United States and Canada were characterized and three of the isolates were pathotyped before and after passage in chickens and serial passage in chicken embryos. One isolate previously passaged in Madin Darby bovine kidney cells was also pathotyped after chicken and embryo passage. Hemagglutination (HA) titers of all isolates were low when tested by microtiter procedures and all were negative by rapid-plate HA. The HA titers were increased by a factor of 8 to 32 by Tween-ether treatment, and treated antigen had the same reactivity as untreated antigen in hemagglutination-inhibition (HI) tests. All isolates had a slow elution rate and an HA thermostability equal to or greater than 60 minutes. Mean death times in embryos were 99 hours or greater, except for one isolate with a mean death time of 81 hours, and intracerebral pathogenicity indices of all isolates were greater than 1. Antigenic differences among the pigeon isolates were identified by three different binding patterns in HI tests against a battery of five Newcastle disease virus (NDV) monoclonal antibodies. Pathogenicity enhancement by bird, embryo, or cell passage was limited to an intravenous pathogenicity index increase for one of three viruses passaged in embryonated eggs. Cloacal samples collected during chicken passage contained higher virus titers than did oral samples. The pigeon isolates reported here, like those of earlier reports, have properties that prevent characterization within a single NDV pathotype. Finally, there was no evidence that any of these isolates was highly virulent for chickens.     

No Mycobacterium paratuberculosis detected in intestinal tissue, including Peyer''s patches and lymph follicles, of Crohn''s disease

1. The present study evaluated developmental characteristics in the chick embryo throughout incubation following cell removal from the freshly laid egg. 2. Between 10 and a few hundred cells of the blastoderm were removed for sex diagnosis. Incubation of the treated embryos was then continued in an open egg shell culture system. 3. Cell recovery from different regions within the blastoderm was performed. 4. The experiments presented here demonstrate the persistence of the developmental potential of chicken embryos in an in ovo culture system after removal of different numbers of cells from the germinal disc prior to incubation. 5. No deviations in developmental characteristics were recorded when compared to untreated control cultures. 6. No detrimental effects of double cell biopsies could be observed. 7. A similar number of chicks developed to hatch regardless of the location of manipulation within the blastoderm.