Influence of egg storage length and orientation on hatching traits and spread of hatch in Transylvanian naked neck chickens.

Effects of egg storage length and orientation on hatching traits and spread of hatch were determined in Transylvanian naked neck chickens. Eggs (n = 640) stored in a cold room (16 ± 1.5°C, 75 ± 1.5% RH) in batches of 160 eggs each, for 1, 3, 5 or 7 days were used. Half of each batch was stored with a broad end up (BEU) and the other in a narrow end up (NEU). Eggs were incubated in a two-stage incubator (37.5°C, 64% RH). Storage length caused a significant increase in egg weight loss (EWL; p < 0.001). Egg fertility (FERT) was significantly lower in 7 days than in 1, 3 and 5 days stored eggs (p < 0001). Dead in shell (DIS) was lower (p < 0.001) in 1-day storage than in other lengths (p < 0.001). Hatchability of total (HSE) and fertile eggs (HFE) decreased (p > 0.001) gradually from 1 to 7 days, though 3 and 5 days were found to be similar. Hatching commenced earlier (p = 0.055) in 5 days than 1-day storage. Incubation time at 100% hatch, hatch window and spread of hatch were not (p > 0.05) affected by storage length. At the end of the hatch, longer storage than 1 day caused 45, 45 and 15 min/day delay in hatching for 3, 5 and 7 days storage respectively. The chicks from 3 days storage (17.3 cm) were longer (p = 0.05) than those from 5 (17.1 cm) and 7 days groups (17.1 cm). Higher DIG and DIS but lower HSE and HFE (p < 0.05) were recorded in BEU than in NEU orientation. Earlier commencement of hatch (CH) was recorded in BEU than in NEU eggs. There were significant (p < 0.05) interactions between storage length and orientation in FERT, DIG, HSE, HFE, CH and hatch windows. To achieve HFE up to 70%, eggs could be stored for up to 7 days in NUE orientation but should not exceed 3 days in BEU orientation.

Association of insulin-like growth factor 1 (IGF1) gene polymorphism with the reproductive performance of three dual-purpose chicken breeds.

The study was designed to investigate the association of Insulin-like growth factor 1 (IGF1) gene polymorphism with the reproductive performance of FUNAAB-Alpha, Sasso, and Kuroiler dual-purpose chicken breeds. To achieve this, a total of 250 healthy hens were selected at 12 wk of age and were intensively managed in cages for 52 wk. Blood sample was taken from each chicken at the 34th week and genomic DNA was extracted using Qiagentm DNA extraction kit, PCR was used to amplify the DNA fragments, and the PCR products were electrophoresed. Amplicons obtained were digested with restriction enzyme hinf1, and were further electrophoresed on 1.5% agarose gel. Data obtained were analyzed using the General linear model of SAS (2002) version 9.0 to determine the effect of IGF1 gene polymorphism and the distribution of alleles within the breeds. Results show polymorphism of the IGF1 gene and the restriction analysis indicated two alleles; A 58% and C 42% with the identification of genotypes AA, AC, and CC, and genotypic frequency of 22%, 43%, and 35%, respectively. Significant associations were observed between the polymorphism of the IGF1 gene, age of the bird at first lay, and weight of the hen at first lay. Chickens with haplotype CC came earlier into lay compared to those with the other two haplotypes (AA and AC). Therefore, the study suggests that haplotype CC could be used as a genetic marker to select for an improved laying performance in chickens.

Effect of storage duration on egg quality, embryo mortality and hatchability in FUNAAB-ɑ chickens.

Effect of extended storage on egg quality, embryo mortality and hatchability in FUNAAB-ɑ chickens was determined. Hatchable eggs (n = 288; weighing 53.2 ± 4.67 g) collected from a flock of FUNAAB-ɑ layer breeder hens aged 32 weeks were stored in egg tray with broad end up under 16 ± 1.5°C for either 0, 4, 8, 12, 16 or 20 d. Before incubation, eight eggs from each group were evaluated for internal and external quality traits. Remaining eggs were set in an incubator and transferred into hatcher on embryonic day 18. Data collected were subjected to one-way analysis of variance. Egg weight loss (EWL; p < .001), surface area (p < .001), yolk diameter (p < .001), inner and outer blastoderm diameters (p < .05) and dead in germ (DIG; p < .001) increased with storage duration while yolk height (p < .001), yolk index (p < .001), albumen weight (p < .05), albumen height (p < .05), albumen index (p < .01), Haugh's unit (HU; p < .05), fertility (p < .001), hatchability of set (HATCHS; p < .001) and fertile eggs (p < .05) decreased. Weight losses of 0, 1.2, 2.2, 3.4, 4.6 and 6.1% were recorded in egg stored for 0, 4, 8, 12, 16 and 20 days respectively. Eggs stored beyond 8 days exhibited higher DIG and lower HATCHS. Shell percentage in 4 days storage (11.4%) was lower (p < .05) than in 16 days storage (13.4%). Shell thickness was similar in eggs stored for 0 to 12 days, but 8 days storage (0.60 mm) had thinner (p < .01) shell than day 16 (0.71 mm) and day 20 (0.73 mm) storage. Internal quality unit (IQU) was higher (p < .05) in fresh eggs (180.4) than in 12 days (167.8) and 20 days (167.8) stored eggs. Extended storage of FUNAAB-ɑ eggs caused EWL, surface area shrinkage, lowered HU and IQU, loss of yolk and albumen quality, increased blastoderm diameters and DIG, and decreased egg fertility and HATCHS from day 8 forward. Storing FUNAAB-ɑ eggs beyond 8 days reduced quality parameters; therefore, other mitigating factors are recommended when storing beyond 8 days.