©2014 Poultry Science Association, Inc. Copper and lysine amino acid density responses in commercial broilers H. Wang,* C. Zhang,* Y. Mi,*1 and M. T. Kidd† *Department of Veterinary Medicine, College of Animal Science, Zhejiang University, Hangzhou 310058, China; and †Center of Excellence for Poultry Science, Division of Agriculture, University of Arkansas, Fayetteville 72701 Primary Audience: Nutritionists, Feed Mill Managers SUMMARY Nutritional modulation of live performance and meat yield must be continuously tested as broiler strains become more efficient every year. This study evaluates both copper- and lysinederived amino acid balance. In experiment 1, amino acid balance (high, moderate, and low) and copper (5 and 200 ppm) were investigated in a factorial array of treatments (6 treatments with 8 replications; 1,536 Cobb 500 male broilers across 48 floor pens from 1–40 d of age; 32 birds per pen). In experiment 2, amino acid density (high and low) was assessed in 2 broiler strains (a multipurpose and a high-yield strain) obtained from the field in a factorial array of treatments (4 treatments with 21 replications; 1,344 multipurpose and 1,344 high-yield broilers across 84 floor pens from 1–42 d of age; 32 birds per pen). Amino acid density treatments were created by altering digestible lysine and other essentials amino acids at a fixed ratio. Copper and amino acid density did not interact, but supplementing broilers with 200 ppm of copper in the form of tribasic copper chloride improved growth rate. Lysine-derived amino acid density improved performance and yields, but should be assessed as strains are improved for efficiency to ensure digestible lysine adequacy in the nutrient formulation matrix. Although both copper and lysine influence growth rate, interactive effects were not assessed in this study. Key words: tri-basic copper chloride, lysine, processing attribute 2014 J. Appl. Poult. Res. 23:470–477 http://dx.doi.org/10.3382/japr.2014-00959 DESCRIPTION OF PROBLEM The essentiality of copper for poultry has been well documented [1]. Moreover, copper is typically an essential supplement in poultry diets for growth promotion and antimicrobial effects. Dietary concentrations to support the former are higher than that established by the NRC [2]. Feeding either 125 or 250 mg/kg of copper improved growth and feed conversion rate in broilers, but supplementation of 375 mg/kg of 1 Corresponding author: [email protected] copper was of no further benefit [3]. The inorganic copper sources used in poultry diets are typically copper sulfate pentahydrate (CuSO4 × 5H2O) or tribasic copper chloride [TBCC; Cu2 (OH)3 Cl]. Because of the lower hygroscopicity and solubility in water, TBCC is considered to be a less reactive and destructive form of copper compared with CuSO4. Also, TBCC is a more concentrated form of copper relative to CuSO4 (58 vs. 25%). Spears et al. [4] reported that the copper in TBCC is more bioavailable compared Wang et al.: COPPER AND AMINO ACID DENSITY with CuSO4. Studies with chicks have shown that the copper from TBCC has the same availability and safety as that in feed-grade CuSO4 [4]. Miles et al. [5] demonstrated that the oxidation in TBCC diets is lower than oxidation in diets supplemented with CuSO4. Furthermore, research has established that dietary supplementation of copper has a positive effect on intestinal microbiota profiles and decreases the growth of pathogenic bacteria in birds [6]. Because copper has growth-promoting and intestinal health effects, it was hypothesized that copper might alter the efficacy of amino acid balance. Lysine is the second-limiting amino acid for broilers fed diets based on corn and soybean meal [2] and is the reference amino acid in the ideal protein concept [7]. Moreover, lysine is known to exhibit strain-specific improvements in breast muscle yield [8–10]. Corzo et al. [11] conducted amino acid density research in highyield and multipurpose strains and observed live performance, processing, and economic improvements with increasing amino acid density. Dietary limitation of lysine, especially early in the birds’ life, decreases skeletal muscle synthesis from a reduction in protein synthesis and RNA content [12]. Because dietary Cu modifies intestinal bacteria and amino acid density dictates bird performance and meat yields, the current study was conducted to investigate possible synergies between copper and amino acid density on broiler performance and carcass characteristics, and to further assess amino acid density effects on modern commercial broiler strains. MATERIALS AND METHODS Bird Husbandry In experiment 1, Cobb 500 male chicks (byproduct off-sex males) were sourced from a commercial hatchery, transferred to the university hatchery, and provided a triple dose of coccidiosis vaccination [13] at d 1 by spray cabinet to create early a mild enteric stress. Chicks were vaccinated for Marek’s disease, Newcastle disease, and infectious bronchitis in the commercial hatchery. Chicks were weighed in groups of 32 and allocated to each of 48 floor pens measuring 5 × 5 ft (0.78 ft2/bird or 0.07 m2/ bird). The facility was a solid side-walled house with radiant tube heating and negative pressure 471 ventilation for air exchange and cooling. Each pen was equipped with 1 supplemental heater for brooding, 1 tube feeder (32-lb capacity), 1 nipple drinker line, and used built-up shavings. The light procedure followed the primary breeder recommendation for Cobb 500 broilers [14]. Feed and water were provided ad libitum. Mortality was obtained daily and the weights were recorded to calculate adjusted feed conversion. One bird per pen was evaluated for lesion scores at d 7 but lesions were not detectable, verifying that any enteric stress was mild. In experiment 2, eggs from a multipurpose broiler strain (strain A; 1,800 eggs; rapidly growing broiler strain with good performance and meat yield) and a high-yield strain (strain B; 1,800 eggs; slow-growing broiler strain with good performance and high meat yield) were obtained from commercial broiler breeder farms and set in hatchers at the university hatchery. Chicks from both strains hatched simultaneously and were sexed. All chicks were vaccinated for coccidiosis via coarse spray at d 1 at a rate of 3 times the commercial recommended dose, as in experiment 1 [13], and were vaccinated against Marek’s disease, Newcastle disease, and infectious bronchitis at the university hatchery. A total of 1,344 broilers from each strain were placed into 84 floor pens (16 male and 16 female broilers per pen). Housing conditions were identical to experiment 1, except birds were reared in pens that measured 2.5 × 10 ft (0.78 ft2/bird or 0.07 m2/bird). Also, litter was built-up from previous research and downtime between flocks was 1 d. In both experiments, all bird procedures were approved by the University of Arkansas Institutional Animal Care and Use Committee. Experimental Design, Methods, and Statistical Analysis In experiment 1, the corn-soybean meal diet (Table 1) was formulated to have 3 levels of digestible lysine (1.0, 1.1, and 1.2% in the 1- to 18-d starter period; 0.8, 0.9, and 1.0% in the 18to 40-d finisher period) and 2 levels of copper (5 and 200 ppm) from TBCC (6 treatments with 8 replications per treatment randomized across 48 pens). The experimental period was from d 1 to 40. In experiment 2, the test diets were formulated to contain low- or high-amino acid density. JAPR: Research Report 472 Table 1. Test diets and calculated and analyzed contents fed from 1 to 40 d of age (experiment 1)1 Starter diet (1–18 d) Item Finisher diet (18–40 d) 5 ppm of 200 ppm of 5 ppm of 200 ppm of Cu, Cu, Cu, Cu, low Lys low Lys high Lys high Lys Ingredient, % Corn 67.05 Soybean meal 23.91 Proplus 542 5.00 Poultry fat 0.50 Dicalcium P 1.39 Limestone 1.08 Salt 0.40 0.23 dl-Met l-Lys HCl 0.22 l-Thr 0.09 Mineral3 0.08 Vitamin4 0.03 TBCC5 0.00 Phytase6 0.02 Content ME, kcal/kg 3,031 CP, % 18.59 Digestible Lys, % 1.00 Digestible TSAA, % 0.74 Digestible Thr, % 0.69 Digestible Ile, % 0.67 Digestible Val, % 0.77 Cu, ppm 5 Analyzed Lys,7 % 1.20 Analyzed Cu,8 ppm 13 5 ppm of 200 ppm of 5 ppm of Cu, Cu, Cu, low Lys low Lys high Lys 67.01 23.92 5.00 0.50 1.39 1.08 0.40 0.23 0.22 0.09 0.08 0.03 0.03 0.02 57.68 32.12 5.00 1.64 1.31 1.06 0.40 0.31 0.23 0.12 0.08 0.03 0.00 0.02 57.41 32.13 5.00 1.66 1.31 1.06 0.40 0.31 0.23 0.12 0.08 0.03 0.03 0.02 75.46 17.05 4.00 0.59 1.04 0.99 0.36 0.16 0.19 0.05 0.06 0.03 0.00 0.02 75.40 17.06 4.00 0.61 1.04 0.99 0.36 0.16 0.19 0.05 0.06 0.03 0.03 0.02 3,040 18.59 1.00 0.74 0.69 0.67 0.77 200 1.19 160 3,031 21.71 1.20 0.89 0.83 0.80 0.90 5 1.39 13 3,031 21.71 1.20 0.89 0.83 0.80 0.90 200 1.42 150 3,131 15.46 0.80 0.60 0.54 0.54 0.64 5 0.99 NA9 3,131 15.46 0.80 0.60 0.54 0.54 0.64 200 0.88 NA 65.74 25.41 4.00 1.95 0.96 0.97 0.35 0.24 0.19 0.08 0.06 0.03 0.00 0.02 200 ppm of Cu, high Lys 65.69 25.41 4.00 1.97 0.96 0.97 0.35 0.24 0.19 0.08 0.06 0.03 0.03 0.02 3,131 3,131 18.61 18.61 1.00 1.00 0.75 0.75 0.68 0.68 0.68 0.68 0.77 0.77 5 200 1.18 1.13 NA NA 1 Test diets consisted of low-amino acid density ratios to Lys and high-amino acid density ratios to Lys. The medium amino acid density was achieved by blending the 2 diets. The 15-ppm Cu diets represent no TBCC and 15 ppm of Cu from copper sulfate contained in the mineral premix. The 215-ppm Cu diets were achieved by restricting the minimum and maximum inclusion of TBCC resulting in a 200 ppm of Cu addition. 2 Proplus 54, H. J. Baker, Little Rock, AR. 3 Mineral premix contained per kilogram of diet: Mn, 150 mg; Zn, 150 mg; Fe, 75 mg; Cu, 15 mg; I, 1.5 mg; and Se, 0.1 mg. The finisher mineral levels were reduced accordingly. 4 Vitamin premix contained per kilogram of diet: vitamin A, 9,259.4 IU; vitamin D3, 6,613.9 IU; vitamin E, 19.84 IU; vitamin B12, 0.016 mg; menadione, 1.80 mg; riboflavin, 7.94 mg; d-pantothenic acid, 11.90 mg; niacin, 46.3 mg; folic acid, 1.06 mg; pyridoxine, 3.31 mg; thiamine, 1.85 mg; and biotin, 0.08 mg. 5 TBCC = tribasic copper chloride [Cu2 (OH)3 Cl]. 6 Phytase used was Phyzyme 2500 (Danisco Animal Nutrition, St. Louis, MO), providing 500 FTU/kg. 7 Analyzed total Lys for the medium (blended) starter diets in the 15- and 215-ppm Cu diets were 1.29 and 1.29%, respectively. Analyzed total Lys for the medium (blended) finisher diets in the 15- and 215-ppm Cu diets were 1.00 and 1.04%, respectively. 8 Analyzed Cu for the 15- and 215-ppm treatments in the medium (blended) Lys starter diets was 12 and 180 ppm, respectively. 9 NA = not analyzed. As in experiment 1, diets were formulated to digestible lysine (1 to 14 d, 1.0 vs. 1.2%; 14 to 28 d, 0.9 vs. 1.1%; and 28 to 42 d 0.8 vs. 1.0%) to derive 2 amino acid density treatments by 2 commercial strains (4 treatments with 21 replications per treatment; Table 2). All feed was pelleted and the starter feeds (1 to 18 d in experiment 1 and 1 to 14 d in ex- periment 2) were crumbled. The mash low- and high-lysine diets were blended to derive the moderate-lysine diet in both the starter and finisher feeds in experiment 1 before pelleting. Essential amino acids were maintained at a ratio to lysine mimicking industry standards (Tables 1 and 2); therefore, as lysine was changed diet amino acid density was proportionately altered. Wang et al.: COPPER AND AMINO ACID DENSITY 473 Table 2. Test diets and calculated and analyzed contents fed from 1 to 42 d of age (experiment 2)1 Starter (1 to 14 d diets) Item Ingredient, % Corn Soybean meal Proplus 542 Poultry fat Dicalcium P Limestone Salt dl-Met l-Lys HCl Choline Cl 60 l-Thr Mineral3 Vitamin4 Phytase5 Content ME, kcal/kg CP, % Digestible Lys, % Digestible TSAA, % Digestible Thr, % Digestible Ile, % Digestible Val, % Analyzed CP, % High Low Grower (14 to 28 d diets) High Low Finisher (28 to 42 d diets) High Low 53.96 35.40 5.00 2.17 1.36 1.02 0.40 0.28 0.13 0.09 0.06 0.08 0.03 0.02 65.71 25.22 5.00 0.50 1.46 1.03 0.40 0.22 0.18 0.09 0.06 0.08 0.03 0.02 60.25 29.96 4.50 2.05 1.16 0.99 0.38 0.27 0.18 0.08 0.08 0.06 0.02 0.02 70.93 20.77 4.50 0.55 1.25 1.00 0.38 0.19 0.19 0.08 0.06 0.06 0.02 0.02 64.88 26.02 4.00 2.19 0.96 0.95 0.35 0.24 0.18 0.07 0.07 0.05 0.02 0.02 74.74 17.55 4.00 0.82 1.04 0.96 0.36 0.16 0.17 0.07 0.04 0.05 0.02 0.02 3,031 22.80 1.20 0.89 0.82 0.86 0.96 25.24 3,031 19.04 1.00 0.74 0.68 0.69 0.79 20.93 3,086 20.56 1.10 0.83 0.75 0.76 0.86 21.66 3,086 17.13 0.90 0.68 0.61 0.61 0.71 18.13 3,142 18.82 1.00 0.76 0.68 0.69 0.78 20.83 3,142 15.63 0.80 0.61 0.54 0.55 0.65 17.60 1 Test diets consisted of low-amino acid density ratios to Lys and high-amino acid density ratios to Lys. Proplus 54, H. J. Baker, Little Rock, AR. 3 Mineral premix contained per kilogram of diet: Mn, 150 mg; Zn, 150 mg; Fe, 75 mg; Cu, 15 mg; I, 1.5 mg; and Se, 0.1 mg. The grower and finisher mineral levels were reduced accordingly. 4 Vitamin premix contained per kilogram of diet: vitamin A, 9,259.4 IU; vitamin D3, 6,613.9 IU; vitamin E, 19.84 IU; vitamin B12, 0.016 mg; menadione, 1.80 mg; riboflavin, 7.94 mg; d-pantothenic acid, 11.90 mg; niacin, 46.3 mg; folic acid, 1.06 mg; pyridoxine, 3.31 mg; thiamine, 1.85 mg; and biotin, 0.08 mg. Subsequent diets (grower and finisher) were reduced accordingly. 5 Phytase used was Phyzyme 2500 (Danisco Animal Nutrition, St. Louis, MO), providing 500 FTU/kg. 2 Hence, the lysine amino acid treatment represents dietary amino acid density in both experiments. Complete diets were collected after mixing for analyses. For mixing verification, starter feed from experiment 1 was analyzed for copper, starter and finisher feed in experiment 1 were analyzed for CP, and all feed in experiment 2 was analyzed for lysine [15]. In experiment 1, pen weights of birds and feed disappearance were obtained at d 1 and 40. At d 40, after pen weights for live performance and 6 h after feed withdrawal time, 6 broilers per pen were randomly selected for processing and weighed. In experiment 2, pen weights and feed disappearance were measured on d 1 and 42. Two male and 2 female broilers per pen were randomly selected for processing at d 42 after pen weights were obtained, marked for processing with paint, weighed, and processed after a 6-h feed withdrawal period. In both experiments, processing was conducted in a pilot processing plant. After birds exited the feather picker, all subsequent processing (e. g., hock removal, evisceration, and lung removal) was done manually. After a 3-h chill, carcasses were placed on cones for manual cutting. In both experiments, the factorial arrangement of treatments [16] was analyzed by the General Linear Models procedure of SAS [17]. RESULTS AND DISCUSSION Experiment 1 The dietary addition of TBCC was calculated to be an increase of 195 ppm of elemental cop- JAPR: Research Report 474 per. The starter diets were verified for treatment additions and averaged 142 ppm higher than the control diets (Table 1). Copper additions were not analyzed in the finisher diets because the additions were large enough to verify at the feed mill. However, we expect the lower estimated level of copper verified in the starter diets was due to sampling too tight a range of feed from the pellet mill. All diets were analyzed for total lysine. Calculated digestive lysine versus total analyzed lysine, respectively, for all diets presented from starter to finisher in Table 1 was 1.00 versus 1.20%; 1.00 versus 1.19%; 1.20 versus 1.39%; 1.20 versus 1.42%; 0.80 versus 0.99%; 0.80 versus 0.88%; 1.00 versus 1.18%; and 1.00 versus 1.13%. The digestible coefficient used for lysine was 90%. On average, our total lysine was analyzed 3.4% higher than calculated lysine, which we attribute to the source of the soybean meal. However, all analyses validated proper diet-mixing procedures. Copper has not only been shown to have antimicrobial activity [6], but to improve growth and FE in broilers when it is added above that considered adequate [2] (i.e., 125–250 ppm [3]). Pesti and Bakalli [3] conducted 4 studies evaluating copper responses and 2 of the experiments were dose responses. Broiler BW gain was improved in 1 experiment by increasing copper from 125 to 250 ppm and in another experiment by increasing copper from 65 to 125 ppm [3]. In our work, increasing copper from 5 to 200 ppm improved BW gain, but our primary objective was to assess interactions with amino acid density, which approached significance (P = 0.08) for BW gain (Table 3). Improvements to broiler live weight occurred with copper, but our work demonstrated its efficacy was independent of amino acid density. Future work should be conducted to assess potential copper × amino acid density responses in diets differing in stress models than those used in the current study (coccidiosis vaccination and built-up litter). Increasing amino density from low to moderate in broilers improved (P < 0.05) overall BW gain and feed conversion, as well as 40-d carcass yield (Table 3). Further improvements (P < 0.05) from increasing amino acid density from moderate to high occurred with breast meat yield (21.83 vs. 22.58%; boneless and skinless pectoralis major and minor). Both abdominal fat and thigh (bone-in and skin-on) yields were decreased (P < 0.05) as amino acid density was increased from moderate to high. Because our Table 3. Cobb male broiler performance and carcass traits (1–40 d) when fed diets varying in dietary Lys density1 and Cu level2 Live performance3 Dietary variable Cu 5 200 SEM P-value Cu Lys Cu × Lys a–c Lys L M H SEM Processing attribute4 BW gain, kg/bird FCR, kg/kg Livability, % Carcass, % Fat, % Breast, Wing, Thigh, Drumstick, % % % % 2.58 2.64 0.016 2.52b 2.64a 2.66a 0.043 1.726 1.717 0.0122 1.794a 1.705b 1.665b 0.0149 98.18 98.05 0.419 98.83 97.46 98.05 0.513 71.47 71.76 0.157 70.97b 71.80a 72.07a 0.192 1.06 0.98 0.033 1.23a 1.02b 0.81c 0.040 21.61 21.86 0.139 20.79c 21.83b 22.58a 0.170 0.010 0.001 0.081 0.633 0.001 0.151 0.827 0.180 0.138 0.194 0.001 0.841 0.084 0.001 0.100 7.76 7.74 0.029 7.71 7.72 7.82 0.035 12.97 12.96 0.060 13.07a 13.04a 12.79b 0.073 9.75 9.69 0.060 9.78 9.69 9.69 0.073 0.233 0.633 0.001 0.052 0.286 0.066 0.913 0.016 0.856 0.432 0.609 0.900 Means within a column for Cu or Lys with uncommon superscripts differ (P ≤ 0.05). Dietary Lys density represents low (L), medium (M), and high (H) levels for dietary Lys of 1.0, 1.1, and 1.2% digestible Lys, respectively, fed from 1 to 18 d of age and 0.8, 0.9, and 1.0% digestible Lys, respectively, fed from 19 to 40 d. Essential amino acid ratios were maintained for adequacy in all diets. 2 Dietary Cu represents diets containing 5 or 200 ppm of Cu provided from tri-basic CuCl. 3 n = 32 birds per pen averaged in each experimental unit; FCR represents feed conversion corrected for the weight of mortality. 4 Processing attributes are expressed relative to live weight of birds selected for processing; n = 6 birds per pen averaged in each experimental unit. 1 Wang et al.: COPPER AND AMINO ACID DENSITY amino acid density treatments fed from 1 to 40 d were continuous, amino acid density needs by phase cannot be referenced. Amino acid density research in the early 2000s was initiated to evaluate industry feeding practices for performance and carcass yields. Our work agrees with an initial report in that moderate amino acid density diets can support good feed conversion, but not optimal breast meat yield [18]. Experiment 2 Dietary high- and low-amino acid density treatments were validated by CP analyses. In all 3 phases, CP was decreased on average by 17%. Analysis of CP verified a 16% decrease in amino acid density when comparing CP reductions between high and low. Hence, although analyzed CP was 5 to 10% higher than calculated levels, treatment differences represented a valid comparison. Dietary lysine density and strain effects are presented in Table 4. However, interactions (P < 0.05) between strain and amino acid density occurred for BW gain and livability (Table 5). For BW gain, decreasing amino acid density in the high-yield, but not the multipurpose strain, reduced BW gain indicating the sensitivity of the high-yield strain to amino acids. Livability was reduced in the multipurpose, but not the 475 high-yield strain, in the low-amino acid density treatment. It is important to point out that birds received coccidiosis vaccination at a 3-fold higher need than normal and were raised on built-up litter with less than 1 wk of down time. Our work points to strain-dependent amino acid needs for health. Indeed, specific amino acids (e.g., methionine and arginine [19]) have profound effects on bird immunity, but immune response and disease-resistant work with broilers fed diets differing in amino acid density has not been carried out. No interaction between broiler strain and amino acid density was noted for feed conversion. Hence, both strains lost between 8 and 9 points of feed conversion by decreasing lysine by 15 to 20% from d 1 to 42. The high-yield strain weighed less (P < 0.05) but had similar (P = 0.55) feed conversion as the multipurpose strain. However, the high-yield strain had less (P < 0.05) percentage fat and higher (P < 0.05) carcass and total breast yields than the multipurpose strain. Further, feeding broilers high-amino acid density diets from 1 to 42 d improved (P < 0.05) all live performance and carcass traits. Again, it is interesting to note the improvement in livability (92.0 to 94.3%; P = 0.01) from feeding birds higher amino acid density diets. Corzo et al. [11] fed varying amino acid density diets to 2 multipurpose broiler strains and 1 high-yield broiler strain from 1 Table 4. Multipurpose (A) and high-yield (B) broiler strain performance and carcass traits (1 to 40 d) when fed diets varying in dietary Lys density1 Dietary variable Lys H L SEM P-value Strain Lys Strain × Lys 1 Strain A B SEM Live performance2 Processing attribute3 BW gain, kg/bird FCR, kg/kg Livability Carcass, % Fat, % Major, Minor, Breast, Wing, % % % % 2.368 2.318 0.0143 2.393 2.293 0.0142 1.788 1.784 0.0047 1.742 1.829 0.0047 92.13 94.10 0.609 94.25 91.98 0.614 73.13 73.63 0.144 73.91 72.85 0.144 1.59 1.43 0.027 1.23 1.79 0.027 18.57 19.38 0.127 19.79 18.16 0.127 0.015 0.001 0.009 0.549 0.001 0.200 0.025 0.010 0.028 0.015 0.001 0.146 0.001 0.001 0.674 Leg, % 4.20 4.24 0.032 4.40 4.04 0.032 22.77 23.62 0.135 24.20 22.19 0.139 7.86 7.85 0.035 7.91 7.79 0.035 21.91 22.11 0.081 21.83 22.18 0.0841 0.001 0.443 0.001 0.001 0.082 0.238 0.001 0.001 0.061 0.875 0.014 0.077 0.100 0.003 0.743 Dietary Lys density represents low (L) and high (H) levels for dietary Lys of 1.0 and 1.2% digestible from d 0 to 14, 0.90 and 1.10% digestible from 14 to 28 d, and 0.80 and 1.0% digestible from 28 to 42 d, respectively. Essential amino acid ratios were maintained for adequacy in all diets. 2 n = 32 birds per pen averaged in each experimental unit; FCR represents feed conversion corrected for the weight of mortality. 3 Processing attributes are expressed relative to live BW of birds selected for processing; n = 4 birds per pen averaged in each experimental unit. JAPR: Research Report 476 Table 5. Multipurpose (A) and high-yield (B) broiler strain interactions for BW gain and livability (1–40 d) when fed diets varying in dietary Lys density1 Dietary Lys density Strain,2 % BW gain, kg/bird A B Livability, % A B H 2.391a 2.395a 94.23a 94.27a L 2.345a 2.241b 90.02b 93.93a SEM P-value 0.0200 0.009 0.861 0.028 a,b Body weight gain and liveability means with uncommon superscripts differ (P ≤ 0.05). Dietary Lys density represents low (L) and high (H) levels for dietary Lys of 1.0 and 1.2% digestible from d 0 to 14, 0.90 and 1.10% digestible from d 14 to 28, and 0.80 and 1.0% digestible from d 28 to 42, respectively. Essential amino acid ratios were maintained for adequacy in all diets; n = 32 birds per pen averaged in each experimental unit. 2 Significant dietary lysine density by strain interaction. 1 to 56 d. At 42 d, amino acid density by strain interactions occurred for breast meat yield, indicating the sensitivity of skeletal muscle accretion in the high-yield strain compared with the multipurpose strain; other diet by strain interactions at d 42 did not occur, however [11]. Also, no amino acid density effects were noted for mortality [11]. The differences in our strain by amino acid density results compared with previous work [11] may be attributable to the wide degree of dietary amino acid density, the strains used, and the coccidiosis vaccination procedure used on all birds at d 1. CONCLUSIONS AND APPLICATIONS 1. Increasing copper from 5 to 200 ppm in the form of TBCC improved growth promotion, but did not interact with amino acid density. 2. The high-yield strain, but not the multipurpose strain, had depressed BW gain when fed low-amino acid density. REFERENCES AND NOTES 1. Davis, G. K., and W. Mertz. 1987. Copper. Pages 301–364 in Trace Elements in Human and Animal Nutrition, 5th ed., Vol. 1. W. Mertz, ed. Academic Press, New York, NY. 2. NRC. 1994. Nutrient Requirements of Poultry, 9th rev. ed. Natl. Acad. Press, Washington, DC. 3. Pesti, G. M., and R. I. Bakalli. 1996. Studies on the feeding of cupric sulfate pentahydrate and cupric citrate to broiler chickens. Poult. Sci. 75:1086–1091. 4. Spears, J. W., E. B. Kegley, L. A. Mullis, and T. A. Wise. 1997. Bioavailability of copper chloride in cattle. J. Anim. Sci. 75(Suppl. 1):265 (Abstr.). 5. Miles, R. D., S. F. O’keefe, P. R. Henry, C. B. Ammerman, and X. G. Luo. 1998. The effect of dietary supplementation with copper sulfate or tribasic copper chloride on broiler performance, relative copper bioavailability and dietary prooxidant activity. Poult. Sci. 77:416–425. 6. Xia, M. S., C. H. Hu, and Z. R. Xu. 2004. Effects of copper-bearing montmorillonite on growth performance, digestive enzyme activities, and intestinal microflora and morphology of male broilers. Poult. Sci. 83:1868–1875. 7. Fuller, M. 1991. Present knowledge of amino acid requirements for maintenance and production. Pages 116–126 in Protein Metabolism and Nutrition. EAAP Publication No. 59. Herning, Denmark. 8. Moran, E. T., and S. F. Bilgili. 1990. Processing losses, carcass quality and meat yields of broiler chickens receiving diets marginally deficient to adequate in lysine prior to marketing. Poult. Sci. 69:702–710. 9. Kidd, M. T., B. J. Kerr, K. M. Halpin, G. W. McWard, and C. L. Quarles. 1998. Lysine levels in starter and growerfinisher diets affect broiler performance and carcass traits. J. Appl. Poult. Res. 7:351–358. 10.Kerr, B. J., M. T. Kidd, K. M. Halpin, G. W. McWard, and C. L. Quarles. 1999. Lysine level increases live performance and breast yield in male broilers. J. Appl. Poult. Res. 8:381–390. 11.Corzo, A., M. T. Kidd, D. J. Burnham, E. R. Miller, S. L. Branton, and R. Gonzalez-Esquerra. 2005. Dietary amino acid density effects on growth and carcass of broilers differing in strain cross and sex. J. Appl. Poult. Res. 14:1–9. 12.Tesseraud, S., N. Maaa, R. Peresson, and A. M. Chagneau. 1996. Relative responses of protein turnover in three different skeletal muscles to dietary lysine deficiency in chicks. Br. Poult. Sci. 37:641–650. 13.Coccivac-D, which contained live oocysts of Eimeria acervulina, Eimeria mivati, Eimeria maxima, Eimeria tenella, Eimeria necatrix, Eimeria praecox, Eimeria brunetti, and Eimeria hagani; Merck, Whitehouse Station, NJ. 14.Cobb-Vantress. 2010. Cobb broiler management guide. Cobb-Vantress Inc., Siloam Springs, AR. Wang et al.: COPPER AND AMINO ACID DENSITY 15.AOAC. 1990. Official Methods of Analysis, 15th ed. Assoc. Off. Anal. Chem., Arlington, VA. 16.In experiment 1, the 6 treatments of the factorial arrangement of 2 copper by 3 amino acid density treatments were analyzed by the following model: Yijk = µ + Cui + AAj + CuAAij + eijk, where µ is the common mean; Cui is the effect of the ith copper; where AAj is the effect of the jth amino acid density; CuAAij is the effect of the interaction of the ith copper with the jth amino acid density; and eijk is random error. Experiment 2 was analyzed in an identical matter to assess main effects and interactions of the factorial arrangement of 2 strains by 2 amino acid density diets. Pen was the experimental unit for all analyses. Both experiments were blocked from tunnel inlet to exhaust fan outlet. When significant differences (P < 0.05) were obtained, as taken from type III sums of squares from the ANOVA generated via the general linear models procedure of SAS [17], means were separated with repeated t test. 477 17.SAS Institute. 2004. SAS User’s Guide. Statistics. Ver. 9.1 ed. SAS Institute Inc., Cary, NC. 18.Kidd, M. T., C. D. McDaniel, S. L. Branton, E. R. Miller, B. B. Boren, and B. I. Fancher. 2004. Increasing amino acid density improves live performance and carcass yields of commercial broilers. J. Appl. Poult. Res. 13:593– 604. 19.Kidd, M. T. 2004. Nutritional modulation of immune function in broilers. Poult. Sci. 83:650–657. Acknowledgments The authors gratefully acknowledge James Usry of Micronutrients (Indianapolis, IN) for supporting this research, diet formulation, and experimental design input.
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