Different energy evaluating systems have been used to formulate poultry diets including digestible energy, total digestible nutrients, true metabolizable energy, apparent metabolizable energy ( AME ), and effective energy. The AME values of raw materials are most commonly used to formulate poultry diets. The net energy ( NE ) system is currently used for pig and cattle diet formulation and there is interest for its application in poultry formulation. Each energy evaluating system has some limitations. The AME system, for example, is dependent on age, species, and feed intake level. The NE system takes AME a step further and incorporates the energy lost as heat when calculating the available energy for the production of meat and eggs. The NE system is, therefore, the most accurate representation of energy available for productive purposes. The NE prediction requires the accurate measurement of the AME value of feed and also an accurate measurement of total and fasting heat production using nutritionally balanced diets. At present, there is limited information on NE values of various ingredients for poultry feed formulation. The aim of this review is to examine poultry feed energy systems with the focus on the NE system and its development for chickens.
Three experiments were conducted to determine the effect of different dietary net energy ( NE ) and AMEn ratios ( NE:AMEn ) on performance, egg quality, and heat production ( HP ) in laying hens. In experiment 1, 62 Hy-Line Brown hens were fed 2 treatments with 31 replicates from 44 to 54 wk of age. In experiment 2, 600 hens of the same strain were fed 3 treatments from 22 to 42 wk of age with 10 replicates. Both used a completely randomized design. Diets were based on corn, wheat, wheat bran, barley, soybean meal, canola meal, meat and bone meal, and canola oil. In both experiments, the NE:AMEn ratio of diets was increased with higher oil inclusion compared with T1 controls. The AMEn (kcal/kg), NE (kcal/kg), ether extract (g/kg), and CP (g/kg), respectively, on a DM basis in experiment 1 was T1: 3,011, 2,288, 42, 202 and T2: 3,023, 2,374, 81, 203; and in experiment 2, T1: 3,026, 2,324, 25, 187; T2: 2,949, 2,315, 61, 185; and T3: 3,026, 2,397, 73, 181. Increasing the ratio of NE:AMEn decreased feed intake ( P < 0.001) and increased egg mass ( P < 0.05) in experiment 2 and increased egg weight ( P < 0.01), decreased feed conversion ratio ( P < 0.01), increased egg albumen % ( P < 0.001), and decreased yolk % ( P < 0.05) and shell % ( P < 0.05) compared with T1 controls in both experiments. Haugh units and yolk color scores were increased with high NE:AMEn in both experiments ( P < 0.001; P < 0.01). Experiment 3 was conducted in calorimetry chambers to measure HP in birds fed experiment 2 diets. Increasing the NE:AMEn increased total retained energy ( RE ), RE as fat, and RE in the body (kcal/kg BW 0.75 /D) and NE:AME. The results indicate that using oil to increase the NE:AMEn results in improved performance and egg quality and more efficient energy utilization.
Ascaridia galli is one of the most abundant nematode parasites in poultry. A. galli infections can significantly impact the profitability of egg farms and have negative implications for bird health and welfare. The main objectives of this study were to determine whether A. galli specific antibodies in egg yolks can be used to detect prior or current exposure to A. galli in laying hens, and to distinguish between eggs obtained from caged and free-range hens. Twenty-two laying hen flocks from different production systems (10 free-range, 2 barn-housed, and 9 caged flocks) were enrolled in the study. An in-house enzyme-linked immunosorbent assay was used to analyze levels of A. galli specific antibodies in yolk. The numbers of A. galli eggs in hen excreta were also determined in a subset of farms. Free-range flocks had higher and also more variable levels of anti-A. galli antibodies in the egg yolk compared to those of the cage flocks (0.50 ± 0.39 vs. 0.16 ± 0.13 OD units) (P < 0.001). Results also confirmed that excreta from free-range and barn-housed flocks contained higher numbers of A. galli eggs than did excreta from caged flocks in which no A. galli eggs were detected. In conclusion, analysis of anti-A. galli antibodies in the egg yolk can be used to detect worm exposure in commercial layer flocks. However, the method used in this study cannot be used in isolation to distinguish between eggs from cage and free-range production systems as anti-A galli antibodies were detected in egg yolk samples from all production systems, and the range of antibody levels overlapped between production systems.
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