Serological examination and egg production of progeny of fowl experimentally infected with egg drop syndrome 1976 virus

Following EDS'76 virus (BC14 virus) infection of breeder chickens by the conjunctival route, vertical transmission occurred in the first week after infection. In the progeny which had been infected with EDS'76 virus by the vertical route, increasing haemagglutination inhibiting (HI) titres to BC14 virus and increasing numbers of birds with HI titres were observed from 3 weeks to 15 weeks of age. Sixty-one per cent of the hens and 77 per cent of the cocks had 2 log HI BC14 virus titres exceeding 4 at an age of 15 weeks. Some birds which han been serologically negative throughout the rearing period, seroconverted between 25 and 28 weeks of age. This phenomenon occurred in hens as well as in cocks. Simulation of stress twice during the laying period by injection of corticosteroid hormone did not increase the number of birds serologically positive to EDS'76 virus. EDS'76 was observed in the group of hens that was vertically infected, since egg production was significantly depressed between 28 and 34 weeks of age. Probably this was mainly the results of a production drop in the hens showing serconversion at 27 or 28 weeks of age. In this group of fowl vertically infected with EDs'76 virus, serologically positive birds appeared to be protected for the greater part to BC14 virus challenge at 50 weeks of age, while negative birds seemed to be fully susceptible. Chicks hatched from eggs collected in the third and fourth week after infection of the dams had maternal antibodies. Fertility and hatchability of apparently normally shelled eggs seemed not to be affected after BC14 virus infection of the dams. Intensive contact with contaminated faeces is probably an indispensable condition for lateral transmission of the virus.     

Serological examination and egg production of progeny of fowl experimentally infected with Egg Drop Syndrome 1976 virus

Summary

Following EDS'76 virus (BC14 virus) infection of breeder chickens by the conjunctival route, vertical transmission occurred in the first week after infection. In the progeny which had been infected with EDS'76 virus by the vertical route, increasing haemagglutination inhibiting (HI) litres to BC14 virus and increasing numbers of birds with HI litres were observed from 3 weeks to 15 weeks of age. Sixty‐one per cent of the hens and 77 per cent of the cocks had ²log HI BC14 virus litres exceeding 4 at an age of 15 weeks.

Some birds which had been serologically negative throughout the rearing period, seroconverted between 25 and 28 weeks of age. This phenomenon occurred in hens as well as in cocks. Simulation of stress twice during the laying period by injection of corticosteroid hormone did not increase the number of birds serologically positive to EDS'76 virus.

EDS'76 was observed in the group of hens that was vertically infected, since egg production was significantly depressed between 28 and 34 weeks of age. Probably this was mainly the result of a production drop in the hens showing seroconversion at 27 or 28 weeks of age.

In the group of fowl vertically infected with EDS'76 virus, serologically positive birds appeared to be protected for the greater part to BC14 virus challenge at 50 weeks of age, while negative birds seemed to be fully susceptible. Chicks hatched from eggs collected in the third and fourth week after infection of the dams had maternal antibodies. Fertility and hatchability of apparently normally shelled eggs seemed not to be affected after BC14 virus infection of the dams. Intensive contact with contaminated faeces is probably an indispensable condition for lateral transmission of the virus.     

Effects of experimental infection of fowl with EDS'76 virus,infectious bronchitis virus and/or fowl adenovirus on laying performance

Following BCI4 (EDS'76) virus infection of brown layer hens at 33 weeks of age, production of normally shelled eggs dropped from 87 per cent to 49 per cent within 3 weeks. The production of soft shelled and shell‐less eggs attained a maximum of 33 per cent 3 weeks after infection (p.i.). Shell quality recovered completely within 5 weeks p.i.

Egg production problems in White Leghorns infected with BCI4 virus were less severe and of shorter duration than in brown layers.

Both in brown layers and in White Leghorns total egg production, mean weight of normally shelled eggs, and internal egg quality were not affected following BCI 4 virus infection at 33 and 28 weeks of age, respectively. Besides shell abnormalities no clinical disease symptoms were observed. Vaccination with a commercial EDS'76 vaccine (Nobivac EDS'76^®) at 17 weeks of age had no adverse effects on laying performance and provoked adequate immunity against challenge at 33 weeks of age. The same observations were made following BCI4 virus infection at 17 weeks of age.

After infectious bronchitis virus (IBV) (H52 virus) infection of laying fowl the percentage of eggs with shell aberrations (rough, misshapen and/ or soft shells) increased to a maximum of 8 per cent, total egg production was depressed, mean egg weight was reduced I to 2 grams, and up to 10 Per cent of normally shelled eggs showed watery, not ropy thin albumen. This abnormally thin albumen was observed in a considerably higher proportion of eggs with shell defects than in normally shelled eggs. No turbidity of the thick albumen was observed and no symptoms of respiratory disease were noticed.

The severity and duration of adverse effects of IBV infection on laying performance depend very much on the stage of production in which the infection occurs. Following IBV infection at the onset of production a much severer drop in total production and in production of normally shelled eggs, a greater increase in the number of abnormally shelled eggs, and more lasting adverse effects on egg weight and internal egg quality were observed, in comparison with infection after peak production. Compared with single infections, a combined BC14 virus and IBV infection of brown layers at 33 weeks of age resulted in greatly potentiated adverse effects on total egg production, number of eggs with aberrant internal quality, and duration of production problems.

Following a combined BC14 virus and IBV infection, in a great proportion of eggs with shell defects and watery thin albumen, turbidity of the thick albumen was observed also, probably due to combined effects on the uterus of both IBV and BC14 virus.

BC14 virus infection did not reinforce the adverse influence of IBV infection on egg weight.

The same observations as described for the combined BC14 virus and IBV infection were made following BC14 virus infection of fowl previously infected with IBV.

It is concluded that changes of internal egg quality in field cases of EDS'76 are most likely due to subclinical IBV infections.

After infection of brown layers at 33 weeks of age with fowl adenovirus 66 (FA V 66) neither symptoms of clinical disease were observed nor effects on egg production, egg weight, and egg quality. Also, in a combined infection with FA V66, IBV, and BCI4 virus, no pathogenic significance could be attributed to the FAV.     

The Influencing Factor of In Vitro Fertilization and Embryonic Transfer in the Domestic Fowl (Gallus domesticus)

This study was conducted to explore the influencing factors of ova in vitro fertilization (IVF) and transfer of the fertilized ova into the oviduct of recipient hens. The efficiency of fertilization was compared using three aspects: (i) the different time of ova collection and transfer, (ii) egg‐laying period of recipient hen; and (iii) semen volume. The following results are observed: 72%, 40% and 0% of ova were found in ovarian sac in 30～40 min, 50～60 min and more than 90 min post‐oviposition, respectively; 20%, 18%, 14% and 5.8% of ova were fertilized with 0.1, 0.2, 0.5 and 1.0 ml semen, respectively; and 33% and 100% of healthy chickens were hatched from fertile ova with 0.1 and 0.5 ml of semen, respectively. All oocytes obtained from ovary and mid‐oviduct were unfertilized. Embryos were transferred into recipient hens 30 min ± 10 min post‐oviposition, and 70% of shelled eggs were produced. There were no eggs produced in the other transfer times. This demonstrated that live chicken can be obtained by IVF of ova collected shortly after oviposition. It was important that the ovum was transferred into the oviduct infundibulum of recipient hens immediately or shortly after oviposition.     

Experimental infection of laying chickens with egg-drop syndrome 1976 virus

Brown layer hens (BC and HC strains) and white layer hens (WL strain) orally infected with the H-162 strain of the egg-drop syndrome 1976 virus developed few clinical signs except for abnormal egg production. Depressed and/or aberrant-egg production was observed for 3 days or longer in 17 of 18 BC hens, 13 of 15 HC hens, and 10 of 17 WL hens. On the average, abnormal egg production began 8.8, 10.3, and 12.2 days after infection of the BC, HC, and WL hens, respectively. Egg production was depressed in the WL hens, but little depression was observed in the BC and HC hens. Aberrant-egg production was much less frequent in the WL hens than in the BC and HC hens. Aberrant eggs were shell-less, soft-shelled, thin-shelled, and/or discolored. No eggs of abnormal internal quality or shape were observed. The virus spread from infected BC and WL hens to contact hens.     

Colonization of specific regions of the reproductive tract and deposition at different locations inside eggs laid by hens infected with Salmonella enteritidis or Salmonella heidelberg

Internal contamination of eggs by Salmonella Enteritidis has been a significant source of human illness for several decades and is the focus of a recently proposed U.S. Food and Drug Administration regulatory plan. Salmonella Heidelberg has also been identified as an egg-transmitted human pathogen. The deposition of Salmonella strains inside eggs is apparently a consequence of reproductive tissue colonization in infected laying hens, but the relationship between colonization of specific regions of the reproductive tract and deposition in different locations within eggs is not well documented. In the present study, groups of laying hens were experimentally infected with large oral doses of Salmonella Heidelberg, Salmonella Enteritidis phage type 13a, or Salmonella Enteritidis phage type 14b. For all of these isolates, the overall frequency of ovarian colonization (34.0%) was significantly higher than the frequency of recovery from either the upper (22.9%) or lower (18.1%) regions of the oviduct. No significant differences were observed between the frequencies of Salmonella isolation from egg yolk and albumen (4.0% and 3.3%, respectively). Some significant differences between Salmonella isolates were observed in the frequency of recovery from eggs, but not in the frequency or patterns of recovery from reproductive organs. Accordingly, although the ability of these Salmonella isolates to colonize different regions of the reproductive tract in laying hens was reflected in deposition in both yolk and albumen, there was no indication that any specific affinity of individual isolates for particular regions of this tract produced distinctive patterns of deposition in eggs.     

Ultrastructural study of infectious bronchitis virus infection in infundibulum and magnum of commercial laying hens

The infundibulum and magnum of the oviduct were examined in hens in full lay which were infected with two Australian strains of infectious bronchitis virus (IBV). The ultramicroscopic changes in the infundibulum and magnum were compared with control hens which had eggs at different positions in the oviduct. The ciliated and granular cells of the surface epithelia and secretory epithelial cells of the tubular glands were the target cells of IBV. No pathological changes were recorded during 2-8 days post-infection (p.i.). Patchy loss of cilia occurred at 10-14 days p.i. Between 16 and 24 days p.i., there was no cilia loss and lymphoid nodules were observed in the muscularis layer of the infundibulum and magnum of some hens from both infected groups. Virus particles were detected mostly in the rough endoplasmic reticulum (RER) and Golgi complex between 10 and 12 days p.i. Cytopathology was noticed in various cell organelles between the 10th and 14th days p.i. There was an increase in RER deposits in infected cells, irrespective of egg position in the oviduct. The magnum was more affected than the infundibulum. Cellular changes were more severe in the infundibulum and magnum of T-infected hens as compared to N1/88-infected hens. Eggs with watery whites which were laid by infected hens could be attributed to cytopathological changes in the granular epithelial cells and tubular gland epithelial cells of the magnum resulting in reduced synthesis of albumen proteins. IBV can cause pathology in parts of the fully functional oviduct which may persist up to the 30th day p.i. However, both the challenge strains of IBV can cause a small number of hens to cease production. Loss of cilia in both the infundibulum and magnum pose a potential threat of secondary bacterial infection and also may affect fertility in breeder hens.     

Possible causes of subfertility in hens following insemination near the time of oviposition

Spermatozoa incubated in uterine fluid collected 7 or 18 h after ovulation showed no significant differences either in motility or in fecundity, despite wide variations of composition of the uterine fluid itself. The absence of uterine fluid in the oviduct 1 h before oviposition may be partially responsible for spermatozoa being unable to migrate easily to the storage sites after insemination of this time. Females inseminated intravaginally at the presumed time of oviposition showed consistently low fertility, irrespective of whether an egg was present in the uterus or not. Normal fertility rates could be achieved with inseminations intravaginally at or near the time of oviposition if the uterine contractions associated with oviposition were inhibited by treatment with indomethacin. Hens inseminated intravaginally 1 h after oviposition retained lower proportions (0.4 to 0.7%) of the initial dose of spermatozoa (measured 2 h after insemination) in their oviduct that hens inseminated 5 to 6 h after oviposition (4.5 to 23.3%).     

Salmonella enteritidis and other Salmonella in laying hens and eggs from flocks with Salmonella in their environment.

Seven Canadian layer flocks with Salmonella enteritidis in their environment were investigated to determine the numbers of hens infected with S. enteritidis, the localization of S. enteritidis in organs of infected hens and the numbers of S. enteritidis-infected eggs produced by two affected flocks. By a microagglutination test (MAT) using S. pullorum antigens, these flocks had more seropositive hens (mean 51.9 +/- 16.9%) than two Salmonella-free flocks (mean 13.0 +/- 4.2%). Culture of tissues of 580 hens (433 seropositive) from the seven flocks detected 26 (4.5%) S. enteritidis-infected hens from two flocks. In one flock, 2/150 hens were infected with S. enteritidis phage type (PT) 8, which was confined to the ceca, and no Salmonella spp. were isolated from 2520 eggs (one day's lay). In the second flock, where 24/150 hens were infected with S. enteritidis PT13, extraintestinal infection was found in nine hens and involved the ovaries and/or oviduct in two hens. Salmonella enteritidis PT13 was isolated from one sample of egg contents and from one sample of cracked shells from among 14,040 eggs (one day's lay) from this flock. The overall prevalence of S. enteritidis-contaminated eggs from the two flocks with infected hens was less than 0.06%. Other Salmonella spp. isolated were S. heidelberg from 58 hens (10%), and S. hadar, S. mbandaka and S. typhimurium from one hen (0.2%) each. The MAT with antigens of S. pullorum had a sensitivity of 81% and a specificity of 24% for detecting S. enteritidis-infected hens.(ABSTRACT TRUNCATED AT 250 WORDS)     

Features of eggshell formation in guinea fowl: kinetics of shell deposition, uterine protein secretion and uterine histology

1. Rate of calcium carbonate deposition, duration of eggshell formation, organic composition of the uterine fluid, morphology of the egg shells and histochemistry of the uterus were studied in guinea fowl to analyse the origin of such thick, strong egg shells. 2. The egg shell was linearly deposited from 6.4 h to 21.8 h after the oviposition of the previous egg. The rate of egg shell deposition was similar to that in laying hens. However, the duration of linear shell deposition was increased by 2.1 h relative to that in hens. This explained the increased egg shell weight observed in the guinea fowl. 3. Intervals between oviposition of intra-clutch eggs were 24 h throughout the laying period. Ovulation occurred just after oviposition of the previous egg in the guinea fowl, as previously observed in hens but the duration of egg white protein deposition, of plumping and of initiation of shell mineralisation were all 1.5 h shorter than in domestic hen. 4. Uterine fluid can only be collected during the growth and terminal phase of shell formation. The electrophoretic profiles of the uterine fluid differed between phases and were somewhat different from those previously observed in the hen. Ovalbumin and ovocleidin-17 were both present in the uterine fluid and also in egg shell extract. Ovocleidin-17 was predominant during the growth phase. 5. The histology of the uterus differed slightly in guinea fowl compared to hens. Ovocleidin and ovalbumin are both secreted by the tubular glands. 6. Examination of radial ultrathin sections of eggshell showed, above the mammillary layer, intricate interlacing of adjacent exospherite in guinea fowl in contrast to the continuous columnar microstructure in hens. 7. The kinetics of egg shell deposition largely explains the increased egg shell weight of guinea fowl. The organic matrix proteins may be associated with the contrast between the structural organisation of the guinea fowl egg shell and that of the hen egg shell.     

Production of Salmonella enteritidis-contaminated eggs by experimentally infected hens

Laying hens of three different ages were experimentally infected with a strain of Salmonella enteritidis by either oral inoculation or contact transmission. Total egg production was depressed in exposed hens of all three age groups. Persistent intestinal shedding was observed in a small number of hens. Eggs with contents contaminated by S. enteritidis were produced by exposed hens at a high frequency, but only during a fairly short period of time that extended through approximately 1 week postinoculation for older hens and through 2 weeks for younger hens. S. enteritidis was recovered from whole yolks and albumen of these eggs at similar frequencies, but not from the content of yolks. Eggs with contaminated shells were also produced, but at a lower frequency. Contaminated eggs were produced by orally inoculated and contact-exposed hens at similar frequencies. S. enteritidis was not isolated from the contents of eggs laid by hens infected with other S. enteritidis strains.     

Immunohistochemical demonstration of Mycoplasma gallinarum and Mycoplasma gallinaceum in naturally infected hen oviducts

Using indirect immunoperoxidase (IIP), peroxidase anti-peroxidase (PAP) and avidin biotin-peroxidase complex (ABC) immunohistochemical methods, Mycoplasma gallinarum and M gallinaceum antigens were demonstrated in ethanol-fixed paraffin-embedded oviduct sections from hens the eggs from which showed suboptimal hatchability. Specific immunoperoxidase staining was detected at the mucosa in the magnum portion of the oviduct. Optimal staining was achieved by applying the ABC method, though both IIP and PAP methods can also be used for diagnosis. Isolation and identification techniques gave similar results for the species of avian mycoplasmas involved.     

雌性空怀双峰驼生殖道的形态结构

应用组织学方法观察了雌性空怀双峰驼生殖道的形态结构。结果显示，双峰驼生殖道的基本结构与其他哺乳动物相似，但微细结构有差异。双峰驼输卵管粘膜皱襞极其发达，分支多而呈复杂的网状迷路。皱襞基部的迷路酷似固有膜而存在腺体，迷路网格内常见细胞团块。虽然双峰驼怀孕时胎儿位于左侧子宫角，但左、右子宫角以及子宫体的组织结构基本相同。子宫内膜无肉阜，上皮下陷于固有膜内，形成大量长而弯曲的单管状腺。子宫颈固有膜浅层分布有许多小腺体，深层分布有成群的较大腺体。这些腺体为分支管状腺，腺上皮PAS强阳性。阴道粘膜上皮为复层上皮。从输卵管到阴道，粘膜上皮主要为单层柱状上皮，由纤毛细胞和分泌细胞组成，局部可见假复层柱状纤毛上皮。纤毛细胞由前向后逐渐减少，但在子宫颈仍可见到。粘膜上皮和腺上皮内夹有许多淋巴细胞或中性粒细胞，后段局部甚至见到这些免疫细胞浸润于上皮细胞间。固有膜内分布有大量淋巴细胞、中性粒细胞、肥大细胞、浆细胞和巨噬细胞，有时出现淋巴滤泡。     

Influence of hormonal extracts on hens producing eggs with non-calcified or partially calcified shells and factors associated with this condition.

1. Daily injection of hypothalameal extract (HE) and adenohypophyseal extract (AE) into hens aged 56 or 67 weeks for 14 d did not significantly influence the production of shell-less (SL) or ultra-thin-shell (UTS) eggs. 2. The injection of HE significantly increased hard-shell (HS) egg production in the younger hens. 3. Neither AE nor HE affected egg weight, serum calcium, gain in body weight or food consumption. 4. In a third experiment hens selected for poor egg production laid at a rate of 58% of which 36% were SL, 29% UTS and 35% HS eggs. Whereas the production rate of the good layers was 65% of which 1-4% were SL and 1-4% were UTS eggs. 5. Specific gravity of HS eggs, serum calcium, weight of ovary, oviduct, or adenohypophysis did not differ between good and poor layers. 6. Since SL and UTS eggs are easily overlooked the decrease in egg production with age may be as great as indicated by normal production records; the problem may be concerned more with the mechanism of shell formation.     

The relationship between certain blood cations in cows with milk fever and both the state of consciousness and the position of cows when attended

In one study, a comparison was made of the concentrations and ratios of certain blood cations in 2 groups of cows with milk fever, one showing normal consciousness (n = 8) and the other depressed consciousness (n = 24). There were no significant differences in the mean concentrations of serum total calcium, plasma inorganic phosphorus and potassium, erythrocyte sodium and potassium, the serum calcium/serum magnesium ratio or the plasma sodium/erythrocyte sodium ratio. There were significant differences (all P less than 0.05) in the mean (+/- SD) concentrations of serum magnesium and plasma sodium concentrations, and the plasma sodium/serum magnesium ratio of 0.8 +/- 0.28 vs 1.2 +/- 0.37 mmol/l, 155 +/- 3.0 vs 147 +/- 6.4 mmol/l and 180 +/- 40.1 vs 116 +/- 34.1 for normal vs depressed cows, respectively. In a second study, a comparison was made of the concentrations and ratios of the same blood cations in 3 groups of cows in different positions when attended for milk fever, namely standing (n = 6), sternal recumbency (n = 24) and lateral recumbency (n = 31). There were no significant differences between the mean concentrations or ratios of any of the cations.     

Extraneous egg shell calcification as a measure of stress in poultry

The incidence of eggs showing abnormal shell calcification amongst those produced by hens kept in individual battery cages, hens kept in battery cages in groups of 3 and hens kept in battery cages in groups of 4 was studied. There was good agreement between observers in the assessment of abnormal eggs. Hens kept in individual cages laid fewer abnormal eggs than hens kept in groups of 3 or 4. There was no significant difference in the incidence of abnormal eggs between hens kept in groups of 3 or 4. The results of this study support the idea that the incidence of eggs showing abnormal calcification may provide a quick and reliable method of measuring stress in hens which lay brown shelled eggs.     

Relationship between Mucosal Barrier Function of the Oviduct and Intestine in the Productivity of Laying Hens

The mucosa of the intestine and oviduct of hens are susceptible to pathogens. Pathogenic infections in the mucosal tissues of laying hens lead to worsened health of the host animal, decreased egg production, and bacterial contamination of eggs. Therefore, better understanding of the mechanisms underlying mucosal barrier function is needed to prevent infection by pathogens. In addition, pathogen infection in the mucosal tissue generally causes mucosal inflammation. Recently, it has been shown that inflammation in the oviduct and intestinal tissue caused by disruption of the mucosal barrier function, can affect egg production. Therefore, it is vitla to understand the relationship between mucosal barrier function and egg production to improve poultry egg production. This paper reviews the studies on (1) oviductal mucosal immune function and egg production, (2) intestinal inflammation and egg production, and (3) improvement of mucosal immune function by probiotics. The findings introduced in this review will contribute to the understanding of the mucosal barrier function of the intestine and oviduct and improve poultry egg production in laying hens.     

高钙日粮对蛋鸡生产性能及出壳雏体内锌含量的影响

生长期日粮钙>3.11%,可使蛋鸡性成熟期明显延缓,开产日龄推迟;其蛋锌及子代出壳雏血锌和多数组织锌含量明显降低,但胚胎及出壳雏鸡未见畸变.出壳雏血锌含量能反映体内锌状态,可作为其评价指标.产蛋期高钙(6.11%)或低钙(0.83%)日粮均可使产蛋性能及孵化率降低.     

Development of uterine chick embryos after storage at 5 degrees C for 15 hours

Eggs obtained from the uterus of hens by hormonal administration 14 to 10 h before expected oviposition were kept at 5 degrees C for 15 h. Forty-two of these uterine eggs were incubated as whole eggs; in the case of a further 70 eggs the blastoderms were isolated and incubated whilst immersed in liquid egg albumen. Thirty-two of the eggs incubated whole (76%) developed to the primitive streak stage, but only 6 of the incubated blastoderms (9%) reached this stage of development.     

Eggshell conductance,embryonic growth,hatchability and embryonic mortality of broiler breeder eggs dipped into ascorbic acid solution

1. Eggs from a broiler breeder flock between 25 and 29 weeks of age were dipped into solutions of various concentrations of ascorbic acid (AA) for up to 2 min, in order to evaluate its effects on eggshell conductance (EC), amniotic fluid pH, albumen height and pH, embryonic weight and hatchability. 2. Three experiments were conducted and the following treatments were used: control, non-dipped (CND); control, water-dipped (CWD); 10 g AA/l (AA1); 20 g AA/l (AA2) and 30 g AA/l (AA3). Measurements of EC before and after dipping were made in experiments 1 and 2 in eggs from hens at 25 and 27 weeks of age, respectively. Albumen height and pH were measured after dipping the eggs in experiment 2. In experiment 3, egg weight loss, embryonic weight and amniotic fluid pH at 14 d of age, hatchability percentage (HP), and embryonic mortality were measured in eggs from hens at 29 weeks of age. 3. AA treatment of eggs and dipping period of time (1, 1.5 and 2 min) increased EC of eggs from hens at 25 and 27 weeks of age. 4. AA3 treatment for 2 min reduced albumen height and increased albumen pH of eggs when compared with the CND treatment in eggs from hens at 27 weeks of age. 5. HP of AA1-treated eggs from hens at 29 weeks of age was higher than that of the CND treatment. AA2 and AA3 treatments of eggs reduced HP and increased the percentage of non-pips when compared with any of the other treatments. 6. AA2 and AA3 treatments of eggs increased egg weight loss when compared with the control treatments (CND and CWD). Dipping treatment did not influence amniotic fluid pH or embryo weight expressed as a percentage of initial egg weight. 7. It is concluded that dipping hatching eggs into AA solution increased EC of eggs. Dipping eggs into 10 g AA/l for a period of 2 min increased HP in eggs from hens at 29 weeks of age, although this was not associated with a significant increase in egg weight loss.