The gene for sex-linked imperfect albinism (S*ALS) has been associated with reduced early growth and slow utilization of the yolk sac contents. Neonatal growth was studied using albino and nonalbino full siblings that were dissected at 2-d intervals from Day 16 of incubation to 7 d after hatch. Fatty acid composition of the yolk, yolk sac membrane, and liver was determined to study neonatal lipid metabolism. At hatch, albinos had similar BW and lower (P < 0.01) liver weights, suggesting reduced lipid transfer from the yolk sac during late incubation. Nonalbinos started gaining weight at 3 d after hatch, 1 d earlier than albino chicks. Albinos had reduced growth (P < 0.01), larger yolk sacs (P < 0.05), and similar (P > 0.05) yolk uptake from hatch to 7 d after hatch. Albino chicks also had lower body temperatures (P < 0.05) at 2, 4, and 6 d after hatch. Albinos had a slower rate of transfer of yolk lipids to the developing embryo in the last 2 d of incubation. The fatty acid composition of the yolk and yolk sac membrane was similar for both genotypes during the last 3 d of incubation, except for the level of stearic acid, which was higher (P < 0.05) for nonalbinos on Day 18 of incubation for both tissues and at 1 d after hatch for the yolk. The fatty acid composition of the livers of albinos and nonalbinos were similar (P > 0.05) during the neonatal period. For both genotypes, the hepatic level of oleic acid increased to Day 20 of incubation, remained constant to 1 d after hatch, and decreased sharply thereafter. The major difference between the genotypes was a slower rate of transfer of yolk lipids to the developing albino embryo in the last 2 d of incubation.
The feasibility of using the sex-linked gene for imperfect albinism (S*ALS) to sex chicks during incubation by candling was studied. With this technique, the dark eye of nonalbino embryos can be positively identified. Two trials were performed. In a first trial, 66.5 and 89.5% of the 254 nonalbino and 210 albino chicks produced in four hatches were correctly identified by candling at 7 d of incubation. Of 191 eggs predicted to be nonalbinos, 22 were albinos, resulting in an overall accuracy of 88.5% for identification of nonalbino embryos. In a second trial, the accuracy of the technique from 7 to 10 d of incubation was evaluated. Increased age resulted in a tendency for lower accuracy, but candling at 8, 9, or 10 d of incubation allowed identification of a greater (P < 0.05) proportion of the nonalbino population than at 7 d of incubation. Candling at 8 d of incubation allowed identification of nonalbinos and albinos with an accuracy of 81.3 and 84.9%, respectively, suggesting that the ALS gene could be used to sex chicks during incubation when used in a sex-linked cross. This technique may prove advantageous to the laying industry because of savings of incubator and hatcher space. The males of commercial layer lines are normally killed at hatch. Reducing the number that hatch by eliminating them before 10 d of incubation could diminish animal welfare concerns.
The sex-linked gene for imperfect albinism (S*ALS) has been associated with slow early growth in some trials but not in others. Albino (59) and nonalbino (73) chicks were raised to 3 d of age to study early growth. At 3 d of age, plasma beta-hydroxybutyrate (beta-HBA) levels were measured and the chicks were euthanatized and dissected to measure liver, gall bladder, and yolk sac weights. Fatty acids of the liver and the yolk sac were also analyzed. On average, albino chicks lost weight between hatch and 3 d of age and nonalbinos gained weight (-2.41 vs 0.74 g/d, P < 0.01). At 3 d of age, livers from albinos contained higher (P < 0.01) levels of docosahexaenoic acid than those of nonalbinos, likely reflecting the dependence on yolk sac nutrients of albinos and on dietary lipids of nonalbinos at this time. Albinos had lower body temperatures (P < 0.01), liver weights (P < 0.01) and gall bladder weights (P < 0.05), and heavier yolk sacs (P < 0.01) than did nonalbinos. Plasma levels of beta-HBA were higher (P < 0.01) for albinos than for nonalbinos. At similar body weights, chicks of both genotypes had similar body temperatures, gall bladder weights, and plasma beta-HBA levels. Linear regressions indicated that in albinos weight loss is associated with larger yolk sacs, smaller livers, larger gall bladders, lower body temperatures, and higher levels of beta-HBA. Yolk sac utilization seemed to be correlated with activation of the digestive system. The inability of starving chicks to use the yolk sac nutrients while lipolysis is taking place suggests that yolk sac absorption does not respond to lipolytic hormones. Because under certain conditions a large proportion of albinos (90% in this experiment) show the symptoms of the starve-out syndrome, the S*ALS gene could serve as a model for the study of this syndrome.
This study aimed to evaluate the development of suckling piglets using morphometric parameters. Different models were created to predict the probability to occur any of the three weight classes (light, medium, and heavy) based on the piglets weaning weight. The variables in this research were birth weight (PWB), lactation length (Lac), and morphometric parameters, body length (BL), heart girth (HG), body mass index (BMI), ponderal index (PI), surface-mass ratio (SM), and birth order (BO). An adjustment of the ordinal regression was proposed to predict the weight classifications. The model with a significant effect of the Lac variables was selected. The light and heavy piglets, regardless of their morphometry, have a high chance of staying in the same weight class at weaning. However, this does not occur in medium piglets with diverse morphometry.
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