Phytase supplementation improved growth performance and bone characteristics in broilers fed varying levels of dietary calcium.

An experiment was conducted to investigate the effect of dietary Ca level on the efficacy of phytase. A total of 288 male Ross × Ross 708 broilers with initial and final BW of 37 and 705 g, respectively, were used in brooder batteries from 0 to 21 d posthatch. Each treatment had 8 replications with 6 broilers/replicate pen. All diets were corn-soybean meal based and formulated to contain 1.26% total Lys. The treatments were positive control with 0.45% nonphytate P and 1% Ca and a negative control with 0.20% nonphytate P with 0.67, 1.00, or 1.33% Ca fed with or without 500 phytase units of Optiphos (Escherichia coli-derived phytase; JBS United Inc., Sheridan, IN). Increasing Ca from 0.67 to 1.33% linearly decreased (P ≤ 0.003) ADG, ADFI, bone breaking strength, bone weight, tibia ash weight, and percentage tibia ash; however, quadratic effects were found for ADFI, G:F, percentage tibia ash, and mortality (P ≤ 0.09). Phytase supplementation increased (P < 0.001) ADG, ADFI, bone breaking strength, bone weight, ash weight, and percentage tibia ash and decreased (P = 0.054) mortality. The increase in ADG, ADFI, bone weight, ash weight, and percentage tibia ash (P ≤ 0.026) and decrease in mortality (phytase × Ca linear; P = 0.058) from phytase supplementation was greater in broilers fed the higher levels of Ca. Calcium utilization was linearly decreased (P < 0.002) with increasing Ca. Phosphorus digestibility and utilization were increased with increasing levels of Ca (P ≤ 0.002); however, P utilization decreased at 1% Ca and increased at 1.33% (quadratic; P < 0.070). Phytase supplementation increased Ca utilization (P < 0.024), P digestibility (P < 0.001), and P utilization (P < 0.029). However, the increase in P digestibility (phytase × Ca; P < 0.021) was greater at the lower levels of Ca whereas P utilization (phytase × Ca; P < 0.001) was greater at 1.33% Ca with phytase supplementation. The results of this research indicate that dietary Ca level, within the ranges used in this experiment, does not negatively affect the efficacy of phytase.

Effects of glycine supplementation at varying levels of methionine and cystine on the growth performance of broilers fed reduced crude protein diets.

Two experiments were conducted to investigate Gly addition to reduced crude protein corn-soybean meal (C-SBM) diets with varying levels of TSAA achieved by varying Met and Cys. The experiments were conducted with female Ross 708 broilers in brooder batteries from 0 to 18 d posthatching. Treatments had 6 replicates with 6 broilers/pen. Diets in all experiments were fed without or with Gly supplementation to contain 2.32% total Gly + Ser. All diets were C-SBM based and formulated to contained 1.27% standardized ileal digestible Lys supplemented with 0.20% Lys (0.394% Lys·SO(4)) and to meet or exceed the requirement of all nutrients except Met and Cys where appropriate. Experiment 1 consisted of 8 dietary treatments. Three ratios of Met to Cys (60:40, 50:50, and 40:60) were used on a mole for mole basis to achieve 0.063 mol of TSAA/kg of feed and a positive control with Met:Cys of 50:50 at 0.76 TSAA:Lys. Glycine supplementation did not affect ADG or ADFI; however, G:F was increased (P = 0.003) with Gly supplementation. An increase in Cys and a decrease in Met resulted in a decrease (P = 0.028) in ADG but had no effect on ADFI or G:F. In experiment 2, Met was kept constant at a marginal level of 0.45% and Cys was increased in 0.05% increments from 0.35 to 0.50%. Glycine supplementation had no main effect on ADG, ADFI, or G:F; however, Gly increased G:F at the lower levels of Cys but not at the higher levels (Gly × Cys, P = 0.031). A linear decrease (P = 0.071) was found in ADFI with increasing Cys supplementation. These data indicate that Gly increased G:F in female broilers fed suboptimal levels of Met and Cys but not at Cys levels at or above the requirement. This implies that the synthesis of Cys accounts for a portion of the increased G:F observed from Gly supplementation in female broilers fed reduced CP C-SBM diets.

Uric acid, urea, and ammonia concentrations in serum and uric acid concentration in excreta as indicators of amino acid utilization in diets for broilers.

Five experiments were conducted to determine if serum uric acid, serum urea N (SUN), serum ammonia, and the uric acid content of the excreta (UAE) could be used to determine the efficacy of amino acid (AA) utilization in diets for broilers. All experiments were conducted with Ross x Ross 308 or 708 broilers from 0 to 14 or 0 to 18 d posthatching in brooder batteries. Treatments had 6 or 7 replications with at least 6 broilers per replicate pen. All diets were corn and soybean meal-based and formulated to contain 1.0% Ca and 0.45% nonphytate P and to meet or exceed the requirements of all nutrient requirements except total Lys, Met, and Thr (experiment 1) or Met (experiments 2 to 5). Experiment 1 consisted of 2 dietary treatments. Diet 1 was formulated to be deficient in Lys, Thr, and Met and diet 2 was formulated to be adequate in all nutrients. Broilers fed the AA-adequate diet had increased (P<0.01 to 0.03) ADG, ADFI, and G:F compared with broilers fed the AA-deficient diet. Serum uric acid, SUN, serum ammonia, and UAE were not affected (P=0.34 to 0.70) by dietary treatment. In experiments 2 to 5, diets contained 1.35% total Lys, 2 levels of Met (0.50 or 0.76 TSAA:Lys), and without or with Gly supplementation up to 2.32% Gly+Ser. Broilers fed diets containing supplemental Met in experiments 2 to 5 had increased (P=0.01 to 0.03) ADG, ADFI, and G:F. Gain:feed was increased (P=0.01 to 0.07) in broilers fed supplemental Gly. Serum uric acid and SUN were decreased (P<0.01) after a 2-h fast in broilers fed supplemental Met and Gly. Serum uric acid and SUN also were decreased at other times after fasting, but the 2-h fast gave the most consistent response. Uric acid content of the excreta was decreased (P<0.01) in broilers fed supplemental Met. Serum ammonia was decreased (P<0.01 to 0.02) in experiments 2, 3, and 4 at varying times postfeeding but was not affected by diet in experiment 5. The results of this research indicate that serum uric acid, SUN, and UAE concentrations can be used as an indicator of AA utilization in broilers fed AA-adequate and AA-deficient diets.

Contribution of exogenous dietary carbohydrases to the metabolizable energy value of corn distillers grains for broiler chickens.

The objectives of this study were to determine the ileal digestible energy (IDE), ME, and ME(n) contents of corn distillers grains (CDG) for broiler chickens and to quantify these energy utilization responses to carbohydrase supplementation by the regression method. The CDG sample used in the current experiment contained (by analysis) 936 g/kg of DM, 4,894 kcal/kg of gross energy, 315.1 g/kg of CP, 94.6 g/kg of crude fat, 94.8 g/kg of crude fiber, 495.6 g/kg of neutral detergent fiber, 179.1 g/kg of acid detergent fiber, 0.19 g/kg of Ca, and 4.8 g/kg of P. The studies were conducted at 2 locations (Purdue or Louisiana State University) and CDG were incorporated into a practical corn-soybean meal diet at 3 levels (0, 300, or 600 g/kg) without or with added carbohydrase in a 2 x 3 x 2 factorial arrangement. The carbohydrase premix was added to supply 2,000 U of xylanase + 1,800 U of amylase/kg of feed. The diets were fed to 288 broiler chickens from d 15 to 22 posthatch with 6 birds per cage and 8 replicate cages per diet in a randomized complete block design at each of 2 locations. The broiler chicks were fed a standard broiler starter diet from d 1 to 15 posthatch. The IDE of diets decreased both linearly (P < 0.01) and quadratically (P < 0.05) as CDG increased from 0 to 600 g/kg regardless of carbohydrase supplementation. There was a linear (P < 0.01) decrease in ME of diet from 3,239 to 2,510 kcal/kg as CDG increased from 0 to 600 g/kg in the diets without added carbohydrase, whereas for birds fed the carbohydrase-supplemented diets, there were both linear (P < 0.01) and quadratic (P < 0.01) decreases from 3,398 to 2,613 kcal/kg as CDG increased from 0 to 600 g/kg. Dietary ME(n) linearly decreased (P < 0.01) regardless of carbohydrase supplementation as CDG increased from 0 to 600 g/kg. Supplementation with carbohydrase improved (P < 0.01) IDE, ME, and ME(n). Regressions of CDG-associated IDE, ME, or ME(n) intake in kilocalories against kilograms of CDG intake without added carbohydrase generated the following: IDE = 44 + 2,340X, r(2) = 0.953; ME = 10 + 2,315X, r(2) = 0.993; and ME(n) = 10 + 2,132X, r(2) = 0.991. Corresponding regressions when carbohydrase was added were as follows: IDE = -17 + 2,622X, r(2) = 0.985; ME = -25 + 2,448X, r(2) = 0.979; and ME(n) = -22 + 2,264X, r(2) = 0.978. These data indicate that the respective IDE, ME, and ME(n) values (kcal/kg of DM) of the CDG sample evaluated were 2,340, 2,315, and 2,132 when carbohydrase was not added and 2,622, 2,448, and 2,264 when carbohydrase was added. Comparison using ANOVA procedures indicated that the slope when carbohydrase was added was greater (P < 0.05) than when carbohydrase was not added. This response implies that carbohydrase supplementation improved (P < 0.05) the IDE, ME, and ME(n) of CDG in practical corn-soybean meal-based diets used in this current study by 12, 5.7, and 6.2%, respectively.

The interactive effects of glycine, total sulfur amino acids, and lysine supplementation to corn-soybean meal diets on growth performance and serum uric acid and urea concentrations in broilers.

Four experiments were conducted to determine the interactive effects of Gly, TSAA, and Lys in corn-soybean meal diets on growth performance of broilers. All experiments were conducted with female Ross x Ross 308 or 708 broilers in brooder batteries from 0 to 18 d posthatching. Treatments had 5 to 8 replications with 5 or 6 broilers per replicate pen. Diets in all experiments were fed without or with Gly (2.32% total Gly + Ser). All diets contained 0.25% l-Lys.HCl except in experiment 1, where no crystalline Lys was added. In experiment 1, the total dietary Lys level was 1.26% with TSAA:Lys of 0.72 and 0.76. Increasing TSAA:Lys increased (P < 0.07) G:F. The main effect of Gly was not significant for ADG, ADFI, or G:F; however, G:F was increased by Gly in broilers fed 0.72 but not in those fed 0.76 TSAA:Lys (Gly x TSAA:Lys, P < 0.03). In experiment 2, the total dietary Lys level was 1.26% with TSAA:Lys of 0.51, 0.68, 0.72, and 0.76. Glycine addition did not affect ADG, ADFI, or G:F; however, increasing TSAA:Lys linearly increased (P < 0.01) ADG, ADFI, and G:F and the response was quadratic for ADG and G:F. Experiment 3 was similar to experiment 2 except the total dietary Lys level was 1.35%. Glycine addition increased (P < 0.03) G:F and decreased (P < 0.04) serum uric acid (SUA) and serum urea N concentrations. Also, increasing TSAA:Lys linearly and quadratically (P < 0.02) increased ADG, ADFI, and G:F. In experiment 4, broilers were fed 2 levels of total dietary Lys (1.26 and 1.35%), 3 levels of TSAA:Lys (0.72, 0.76, and 0.80), and without or with Gly supplementation up to a total of 2.32% Gly + Ser. Glycine addition increased ADG (P < 0.02) and G:F (P < 0.01). The increase in G:F with Gly was not the same for all TSAA:Lys (Gly x TSAA:Lys, P < 0.07). Increasing Lys increased (P < 0.01 to 0.10) ADG, ADFI, and G:F. Glycine addition increased ADG and ADFI more in broilers fed 1.35% Lys than in those fed 1.26% Lys (Lys x Gly, P < 0.09). Glycine addition increased SUA in broilers fed 1.26% Lys but decreased SUA in broilers fed 1.35% Lys (P < 0.01). Glycine addition decreased SUA in broilers fed the TSAA:Lys of 0.80 but not at the other TSAA:Lys (P < 0.08). These data indicate that Gly increased G:F and decreased SUA in diets with 1.35% Lys and excess TSAA.

Effect of incremental levels of L-lysine and determination of the limiting amino acids in low crude protein corn-soybean meal diets for broilers.

Research was conducted to determine the level of l-Lys that can be included in corn-soybean meal (C-SBM) diets for broilers before an amino acid (AA) beyond Met, Lys, Thr, or Gly becoming limiting and to determine the order of limiting AA in low CP C-SBM diets. All experiments were conducted with Ross 708 broilers (0 to 18 d of age) in brooder batteries. Treatments contained 7 or 8 replicates with 6 birds per replicate. In all experiments, a control C-SBM diet containing no l-Lys.HCl and a similar diet [positive control (PC) + Gly] with supplemental Gly to provide 2.32% total dietary Gly + Ser were fed. All diets were formulated to contain 1.26% total Lys. All diets with added l-Lys.HCl contained supplemental Gly to provide 2.32% total dietary Gly + Ser. In experiment 1, l-Lys.HCl was added to the diets at 0.02% increments from 0.15 to 0.27%. Compared with the PC + Gly diet, there were no negative effects (P > 0.10) of supplemental Lys on ADG, ADFI, or G:F. In experiment 2, l-Lys.HCl was added to the diets at 0.05% increments from 0.25 to 0.60%. Compared with the PC + Gly diet, ADG and G:F were decreased (P < 0.03) in broilers fed diets containing greater than 0.30% l-Lys.HCl but not (P > 0.10) in the 0.25% l-Lys.HCl diet. In experiment 3, l-Lys.HCl was added to the diets at 0.05% increments from 0.20 to 0.30%. Daily gain was decreased (P < 0.03) in broilers fed 0.30% l-Lys.HCl but not in those fed 0.20 or 0.25% l-Lys.HCl. In experiment 4, the order of limiting AA was determined in a C-SBM diet containing 0.45% L-Lys.HCl. In addition to the PC and PC + Gly diets, diets consisted of a negative control (NC) diet with 0.45% l-Lys.HCl, NC + 0.247% Ile, NC + 0.484% l-Arg.HCl, NC + 0.249% Val, and all possible 2- and l-way combinations of all 3 AA. Compared with the NC diet, addition of Arg and the combination of Arg and the other AA increased ADG and ADFI, indicating that Arg was the limiting AA in this diet. Experiment 5 was conducted in an identical manner to experiment 4 except the diets with the added AA contained the same ratio of corn to soybean meal that is present in a diet with 0.25% l-Lys.HCl. The results of experiment 5 suggest that Arg and Val are equaling limiting in a diet with 0.25% l-Lys.HCl. In summary, 0.25% l-Lys.HCl can be added to C-SBM diets supplemented with Met, Thr, and Gly with no negative effects on growth performance, and Arg and Val are equaling limiting (after Met, Thr, Lys, and Gly) in diets containing 0.25% l-Lys.HCl.

The effect of dietary phosphorus level and phytase supplementation on growth performance, bone-breaking strength, and litter phosphorus concentration in broilers.

This research was conducted to determine the effects of feeding different P levels with and without phytase supplementation on broiler growth performance, bone-breaking strength (BBS), and litter P concentration. An experiment with 4 trials was conducted with 7,840 Ross x Ross straight-run broilers. For each trial, 1,960 broilers were allotted on d 0 to treatments, with 7 replications each and with 70 broilers per replication. The broilers were fed a 4-period feeding program consisting of starter (0 to 14 d), grower (14 to 32 d), finisher (32 to 41 d), and withdrawal (41 to 50 d) periods. For each trial, the same pen was used continuously for each treatment-replication combination, and the litter was not removed between trials. Broilers were fed a control diet [0.43, 0.40, 0.36, or 0.32% nonphytate P (nPP)] in the starter, grower, finisher, and withdrawal periods, respectively, a low Ca and P (LCaP) diet with a 0.05% reduction in nPP in each period, and these 2 diets supplemented with phytase at 600 phytase units/kg (nPP and Ca were reduced by 0.094% in diets with phytase). Diet did not affect (P > 0.10) broiler performance in the starter or withdrawal periods. Generally, both phytase addition and the LCaP diet decreased some aspects of growth performance during the grower and finisher periods. There was no main effect of phytase on BBS, but BBS was decreased in the broilers fed the LCaP diet with phytase addition (nPP x phytase, P < 0.01) in the grower period, and BBS was decreased in the finisher (P < 0.02) and withdrawal (P < 0.01) periods for broilers fed the LCaP diet. Total P, soluble P (SP), and reactive soluble P (RSP) were decreased (P < 0.04) in the litter of broilers fed the LCaP diets. Total P, SP, and RSP were decreased (P < 0.01) in the litter of broilers fed phytase. These data indicate that phytase supplementation at 600 phytase units/kg reduces growth in some periods, has no effect on BBS, and reduces total P, SP, and RSP in the litter.

The effect of carrier for vitamin E on liver concentrations of vitamin E and vitamin E excretion in broilers.

Two experiments were conducted to determine the effect of 2 carrier sources of vitamin E on growth performance and excreta and liver vitamin E concentrations of broilers. Chicks were pretested from d 0 to 7 posthatching on a corn-soybean meal diet without vitamin E supplementation, and the experiments lasted from d 7 to 19 posthatching. Each treatment in both experiments was replicated with 6 pens with 5 chicks each. Initial and final BW were 155 and 684 g in experiment 1 and 155 and 691 g in experiment 2. In experiment 1, the dietary treatments were the corn-soybean meal diet with varying concentrations (0, 30, 100, or 300 IU/kg) of supplemental vitamin E either absorbed to verxite (VE) or adsorbed to silica (SE). In experiment 2, the dietary treatments were the 0 and 30 IU/kg of vitamin E as VE or SE. In experiment 1, feed intake decreased and gain:feed increased as concentration of VE increased, but feed intake increased and gain:feed decreased as concentration of SE increased (source x concentration, P < 0.03). Gain, feed intake, and gain:feed were not affected (P > 0.10) by the vitamin E carrier source in experiment 2. The mean excreta vitamin E concentration at d 7 posthatching was 17.2 IU/kg (DM basis). The percentages of vitamin E excreted were based on analyzed vitamin E concentrations in the diet. At 100 and 300 IU/kg of supplemental vitamin E, an average of 94 and 44% of vitamin E intake from broilers fed vitamin E from VE and SE, respectively, was excreted (vitamin E source, P < 0.01; source x concentration, P < 0.08), but at 30 IU/kg of vitamin E, 49 and 45% of vitamin E intake from broilers fed vitamin E from VE and SE was excreted. In experiment 2, 52 and 43% of vitamin E intake from VE and SE was excreted (source, P < 0.02). Liver alpha-tocopherol concentration was not different (P > 0.10) between the sources of vitamin E in either experiment. Increased concentrations of vitamin E increased liver alpha-tocopherol concentrations (P < 0.01). On the basis of the results of excreted vitamin E, vitamin E adsorbed to SE was more available than vitamin E absorbed to VE, but on the basis of liver vitamin E concentration, their availabilities were similar.

Effects of methionine and lysine on fermentation in vitro and in vivo, nutrient flow to the intestine, and milk production.

Three experiments were conducted to investigate the feasibility of using crystalline methionine and lysine as protein supplements for lactating Holstein cows. In the first experiment, Met (dl-methionine) and Lys (l-lysine-HCl) were added to diets used in continuous culture bioreactors to estimate optimal concentrations for use in subsequent in vivo experiments. The second experiment measured ruminal fermentation and nutrient flow to the small intestine when Met and Lys were top-dressed on diets fed to nonlactating cows. The third experiment measured lactation performance when Met and Lys were added to diets fed to late-lactation cows. Providing 0.29 and 2.27% of dry matter as Met and Lys, respectively, provided the largest improvement in fermentation in vitro and these concentrations were used in subsequent experiments. When Met and Lys were top-dressed on diets fed to nonlactating cows, no changes in total tract N digestion were observed. No changes in microbial protein production or ruminal fermentation were observed. Adding Met and Lys did not change production or efficiency of production of milk or milk components by late lactation cows. These data indicate that providing supplemental Met and Lys during late lactation does not significantly improve the protein status of the cow and therefore may not improve milk production.

Glycine supplementation to low protein, amino acid-supplemented diets supports optimal performance of broiler chicks.

Six experiments were conducted to determine the effects of low CP in diets for broilers and to evaluate limiting essential and nonessential amino acids (AA) in these diets. All experiments were conducted with Ross x Ross broilers in brooder batteries from 0 to 17 or 18 d posthatch. Treatments were replicated with 6 pens of either 5 or 6 broilers each. In Experiment (Exp.) 1, corn-soybean meal diets were formulated to 16.18, 17.68, 19.18, 20.68, or 22.18% CP. The 22.18% CP diet provided 1.23% Lys and 0.89% TSAA, met or exceeded all nutrient requirements of young broilers, and served as the positive control (PC) diet in all experiments. Increasing dietary CP linearly increased final BW, daily gain (ADG), and gain:feed (G:F) (P < 0.005). In Exp. 2, additions of crystalline essential (EAA) or nonessential AA (NEAA) were added to the low CP diet to simulate the AA profile of the PC. Daily gain, final BW, and G:F were decreased (P < 0.01) when CP was reduced, but the addition of the NEAA increased final BW, ADG, and G:F (P < 0.07) to the level of broilers fed the PC. Addition of EAA alone was without effect. In Exp. 3, chicks fed diets with supplemental Glu, Ala, Asp, or Pro had reduced daily feed intake (ADFI), ADG, and final BW (P < 0.05) compared with the PC diet. Addition of Gly or the combination of Gly, Glu, Asp, Ala, and Pro to the low CP diet increased G:F (P < 0.01) compared with chicks fed PC, and ADG was not different from that of broilers fed the PC diet. In Exp. 4, chicks were fed either the PC diet, the low CP diet with Gly + Ser concentrations of 1.23, 1.35, 1.47, 1.59, 1.71, 1.83, 1.95, or 2.07%, or a 10th diet that contained 1.23% Gly + Ser and with Glu to equal the N concentration of the 2.07% Gly + Ser diet. Final BW, ADG, and G:F were increased linearly (P < 0.001) as the concentration of dietary Gly + Ser was increased. Chicks fed the low CP diet with 2.07% Gly + Ser had growth performance that was not different from that of chicks fed the PC. The addition of Glu to the low CP diet was without effect. In Exp. 5, chicks were fed the PC with additions of 0, 0.15, or 0.30% Gly or the low CP diet containing 1.60, 1.72, 1.84, 1.96, 2.08, 2.20, or 2.32% Gly + Ser. Glycine addition to the PC had no effect, but Gly addition to the low CP diet increased G:F linearly (P < 0.001). Growth performance of chicks fed the low CP diet with 2.32% Gly + Ser was equal to that of chicks fed the PC diet. In Exp. 6, chicks were fed the PC or the low CP diet containing 1.80, 1.95, 2.10, 2.25, 2.40, 2.55, 2.70, 2.85, or 3.00% Gly + Ser. Glycine addition to the low CP diet increased G:F linearly (P < 0.001). In summary, low CP diets result in optimal growth of broilers with Gly + Ser levels of 2.44%.

The effects of phytase on growth performance and intestinal transit time of broilers fed nutritionally adequate diets and diets deficient in calcium and phosphorus.

Five experiments (Exp.) were conducted to determine the effects of phytase on growth performance and intestinal transit time in chicks fed nutritionally adequate diets and diets deficient in Ca and nonphytate P (nPP). In Exp. 1 and 2, chicks were fed a nutritionally adequate diet from 0 to 6 d or from 0 to 4 d posthatching; assay periods were 8 or 10 d; average initial BW were 98 or 79 g; and average final BW were 371 or 369 g, respectively. Treatments were replicated with 12 pens of 5 chicks each. Corn-soybean meal (C-SBM) diets were adequate in all nutrients except Ca and nPP where appropriate. The treatments were 1) C-SBM, 1.0% Ca, and 0.45% nPP; 2) C-SBM, 0.80% Ca, and 0.25% nPP; 3) Diet 1 + 600 phytase units/kg of diet; 4) Diet 2 + 600 phytase units/kg of diet. Experiments 3, 4, and 5 were conducted to determine the effects of phytase on intestinal transit time in broilers. Broilers were fed the same nutritionally adequate diet from 0 to 18, 27, or 23 d posthatching, and the assay periods were 7 d. Treatments were replicated with 18 individually penned broilers. Average initial BW were 768, 1,108, or 838 g, and average final BW were 1,299, 1,704, or 1,392 g in Exp. 3 to 5, respectively. Transit time data were collected on d 1 and 7 of the Exp. Diets were 1) C-SBM, 0.9% Ca, and 0.35% nPP; 2) C-SBM, 0.80% Ca, and 0.25% nPP + 600 phytase units/kg of diet. Transit time was calculated as the difference between the time feed was first ingested and the time of first appearance of solid feces. In Exp. 1 and 2, the reduction in dietary Ca and nPP reduced (P < 0.01) average daily gain (ADG), average daily feed intake (ADFI), and gain:feed. Phytase addition increased (P < 0.02) ADG and ADFI in diets deficient in Ca and nPP and in the nutritionally adequate diets. In Exp. 2, the reduction in Ca and nPP reduced (P < 0.01) toe and tibia ash percentage, but phytase addition increased (P < 0.01) toe and tibia ash percentage. The increase in toe ash percentage was greater in chicks fed the Ca and nPP deficient diet than in chicks fed the nutritionally adequate diet (Ca and nPP x phytase, P < 0.01). In Exp. 3, 4, and 5, transit time on d 1 was faster (P < 0.03) in chicks fed phytase. On d 7, transit time tended to be faster in chicks fed phytase, but the effect was not significant (P = 0.15). These data indicate that phytase increases ADG and ADFI in diets deficient in Ca and nPP and in diets formulated to be adequate (or excess) in all nutrients for broiler chicks. The increase in ADG and ADFI in chicks fed the nutritionally adequate diet may be due to a faster transit time of feed through the digestive tract, resulting in a greater feed intake and gain.

Early primary biliary cholangitis is characterised by brain abnormalities on cerebral magnetic resonance imaging.

BACKGROUND: Brain change can occur in primary biliary cholangitis (PBC), potentially as a result of cholestatic and/or inflammatory processes. This change is linked to systemic symptoms of fatigue and cognitive impairment. AIM: To identify whether brain change occurs early in PBC. If the change develops early and is progressive, it may explain the difficulty in treating these symptoms. METHODS: Early disease brain change was explored in 13 patients with newly diagnosed biopsy-proven precirrhotic PBC using magnetisation transfer, diffusion-weighted imaging and 1 H magnetic resonance spectroscopy. Results were compared to 17 healthy volunteers. RESULTS: Cerebral magnetisation transfer ratios were reduced in early PBC, compared to healthy volunteers, in the thalamus, putamen and head of caudate with no greater reduction in patients with greater symptom severity. Mean apparent diffusion coefficients were increased in the thalamus only. No 1 H magnetic resonance spectroscopy abnormalities were seen. Serum manganese levels were elevated in all PBC patients, but no relationship was seen with imaging or symptom parameters. There were no correlations between neuroimaging data, laboratory data, symptom severity scores or age. CONCLUSIONS: This is the first study to be performed in this precirrhotic patient population, and we have highlighted that neuroimaging changes are present at a much earlier stage than previously demonstrated. The neuroimaging abnormalities suggest that the brain changes seen in PBC occur early in the pathological process, even before significant liver damage has occurred. If such changes are linked to symptom pathogenesis, this could have important implications for the timing of second-line-therapy use.

Comparison of inorganic and organic selenium sources for broilers.

An experiment was conducted to compare the effects of organic and inorganic sources of Se on growth performance, carcass traits, breast and plasma Se concentrations, and plasma glutathione peroxidase (pGPX3) activity in broilers. Broiler chicks were sexed on d 0 and within sex, randomly allotted to dietary treatment. Average initial and final BW of the broilers were 47 and 2,684 g, and the experiment lasted 49 d. A 3-phase feeding program similar to industry recommendations was used, and the basal diets for each phase were corn-soybean meal based. For each growth phase, the basal diet was supplemented with 0 (control) or 0.30 ppm Se from sodium selenite (SS) or Se-enriched yeast (SY). Each treatment was replicated 7 times (4 pens of males and 3 pens of females) with 50 male or 55 female broilers per replicate. Daily gain, feed intake, gain:feed, eviscerated and chill weights, carcass yield, breast weight, and moisture loss from the breast were not affected (P > 0.05) by Se supplementation. Dietary supplementation with SY increased (P < 0.05) muscle and plasma Se concentrations compared with broilers fed the control diet or the diet with SS. Plasma GPX3 activity was not affected (P > 0.05) by Se source or concentration. The results from this experiment indicate that organic Se increases tissue Se concentration, but it does not affect growth performance, carcass traits, or pGPX3 activity compared with inorganic Se.

Changes in glutathione peroxidase and tissue selenium concentrations of broilers after consuming a diet adequate in selenium.

Three experiments (EXP) were conducted with commercial broilers to develop a low-Se diet for comparing plasma glutathione peroxidase (pGPX3) concentrations and then to compare pGPX3 and plasma and tissue Se concentrations in broilers fed this low-Se diet after being supplemented with sodium selenite (SS) or Se-enriched yeast (SY). With the exception of Se, all diets were nutritionally adequate. The EXP lasted from 0 to 20 or 22 d posthatching, and treatments were replicated with 6 to 8 pens of 6 to 15 chicks per pen. The results of EXP 1 and 2 indicated that a cornstarch-dextrose diet containing 10% torula yeast and 31% soybean meal (SBM) resulted in similar gain as a corn-SBM (C-SBM) diet, but the cornstarch-dextrose-torula yeast-SBM diet with no added Se reduced pGPX3 activity 6-fold. In EXP 3, the treatments were a C-SBM diet with 0 or 0.30 ppm added Se from SS or SY. These diets were fed from 0 to 10 d posthatching. Beginning on d 10, all broilers were fed the cornstarch-dextrose-torula yeast-SBM, low-Se diet. On d 10, 13, 16, 19, and 22, three broilers per replicate were randomly selected for plasma and tissue collection. Treatment differences were significant at P < 0.05. Daily gain, daily feed intake, and gain:feed were not affected by diet during the 0-to-10-d or 0-to-22-d periods. Plasma GPX3 activity and plasma, liver, and breast Se concentrations were greater in broilers previously fed the diets with added Se, regardless of source, than in those fed the C-SBM diet, except for liver Se concentration on d 19 of broilers previously fed the SS diet. The pGPX3 concentrations were not different in broilers previously fed either Se diet on d 10 and 13 but were greater in broilers previously fed the SY diet on d 16, 19, and 22. Plasma Se concentrations were not different in broilers previously fed diets with SS or SY on d 10 and 22 but were greater in broilers previously fed the SY diet on d 13, 16, and 19. Breast Se concentrations were greater in broilers previously fed the SY diet than in those fed the SS diet on each day. Liver Se concentrations were not different in broilers previously fed SS or SY diets on d 19 and 22 but were greater in those previously fed the SY diet on d 10, 13, and 16. These results indicated that SY supplementation in broiler diets resulted in greater tissue Se concentrations than SS and that pGPX3 and tissue Se concentrations remained greater in birds previously fed a diet with SY than in those fed SS after being fed a low-Se diet.

The effect of virginiamycin in diets with adequate or reduced dietary calcium or nonphytate phosphorus for broilers.

Four experiments (EXP) were conducted to evaluate the effects of virginiamycin (Vm) in diets adequate or reduced in Ca or nonphytate P (nPP) levels on growth performance and bone response variables in chicks. All diets were corn-soybean meal (C-SBM) based, and all treatments were replicated 6 or 8 times with 5 or 6 chicks each. In EXP 1 and 2, the dietary treatments were 1) C-SBM with 1.00% Ca and 0.45% nPP (positive control; PC); 2) C-SBM with 0.80% Ca and 0.45% nPP (0.80Ca); 3) C-SBM with 1.00% Ca and 0.35% nPP (0.35nPP); and 4 to 6) Diets 1 to 3 with 11 (EXP 1) or 22 (EXP 2) ppm of Vm. In EXP 1, daily gain (ADG), feed intake (ADFI), bone breaking strength (BBS), milligrams of ash per gram of Ca intake (ASH/Ca), and BBS per gram of Ca (BBS/Ca) or nPP (BBS/nPP) intake were increased in chicks fed Vm (P < 0.04 to 0.07). Chicks fed the 0.35nPP diet with Vm had increased ADG, ADFI, BBS, milligrams of tibia ash (ASH), BBS/Ca, and BBS/nPP (nPP x Vm, P < 0.03 to 0.10). Chicks fed the 0.80Ca diet with Vm had increased ASH, milligrams of ASH per gram of nPP intake (ASH/ nPP), and ASH/Ca (P < 0.01 to 0.09). Tibia ash, BBS, gain:feed (G:F), BBS/nPP, and ASH/nPP were decreased in chicks fed the 0.80Ca diet (P < 0.01 to 0.07). Bone ash percentage (BAP), BBS, BBS/Ca, ASH, and ASH/Ca were decreased in chicks fed the 0.35nPP diets (P < 0.01); ASH/ nPP was increased (P < 0.01). In EXP 2, BAP, ASH, ASH/ Ca, and ASH/nPP were increased in chicks fed Vm (P < 0.02 to 0.07). Chicks fed the 0.80Ca diet had a decreased ASH/nPP (P < 0.04) but an increased BBS/Ca and ASH/ Ca (P < 0.01 to 0.02). Chicks fed the 0.35nPP diet had decreased ADG, ADFI, G:F, BBS, BAP, ASH, ASH/Ca, and BBS/Ca (P < 0.01 to 0.04), but BBS/nPP and ASH/ nPP were increased (P < 0.01 to 0.04). In EXP 3, the dietary treatments were 1) PC; 2) C-SBM with 0.70% Ca and 0.45% nPP (0.70Ca); 3) C-SBM with 1.00% Ca and 0.25% nPP (0.25nPP); 4 to 6) Diets 1 to 3 with 9 ppm of Vm. The addition of Vm to the 0.25nPP diet decreased BBS (nPP x Vm, P < 0.06), but Vm increased BBS in the 0.70Ca and PC diets (P < 0.02). Chicks fed the 0.25nPP diet had decreased ADG, ADFI, and BBS (P < 0.01), and chicks fed the 0.70Ca diets had reduced ADFI, BBS, and G:F (P < 0.03 to 0.10). In EXP 4, 4 levels of nPP (0.15, 0.25, 0.35, or 0.45%) and 3 levels of Vm supplementation (0, 11, or 22 ppm) in a 4 x 3 factorial arrangement were used. The addition of Vm increased ADG, BBS, ASH, ASH/Ca, and ASH/nPP only in chicks fed diets with 0.35 or 0.45% nPP (nPP x Vm, P < 0.05). Daily gain, ADFI, G:F, BBS, BAP, BBS/Ca, and ASH were increased as nPP levels were increased (P < 0.01), but BBS/nPP and ASH/nPP were decreased (P < 0.01) as nPP levels were increased. The results obtained from these EXP indicate that Vm, regardless of supplementation level, can partially overcome an nPP deficiency when nPP levels are = 0.35%.

Effect of inorganic versus organic selenium on hen production and egg selenium concentration.

A 28-d experiment using 288 Hy-Line W-36 laying hens was conducted to compare sodium selenite (SS) with Se-enriched yeast (SY). The Se from SS or SY was supplemented into a corn-soybean meal basal diet at 0, 0.15, 0.30, 0.60, or 3.00 ppm, and the basal diet was formulated to provide 0.82% lysine and 2,950 kcal/kg of ME. Each treatment was replicated 4 times with 2 cages of 4 hens per cage in each replicate. Hen production was assessed daily, and 2 eggs per replicate were collected every 4 d for whole-egg Se analysis. Albumen quality was assessed at 2 egg storage temperatures (7.2 vs. 22.2 degrees C) with the eggs collected on d 24 and 28, respectively. The percentage of dirty and cracked eggs was greater (P < 0.04) in hens fed SY than in those fed SS. Percentage hen-day production was not affected (P > 0.05) by diet. Albumen quality of eggs stored at 22.2 degrees C was improved (P < 0.04) in eggs from hens fed SS, but there was no difference (P > 0.05) in albumen quality of eggs stored at 7.2 degrees C. Egg weight was linearly increased (P < 0.01) by SY. Whole-egg Se levels were linearly increased (P < 0.01) as dietary Se level increased for both sources of Se, but eggs from hens fed SY had higher (P < 0.01) Se concentrations than those fed SS. The results from this experiment indicate that percentage hen-day production is not affected by Se source, and that SY increases egg Se concentrations more than SS.

A comparison of two sources of phytase in liquid and dry forms in broilers.

Research with corn-soybean meal diets was conducted to compare phytase sources in commercial broilers. A Ca to nonphytate P (nPP) ratio of 2.5:1 was maintained in all diets. Experiments 1 and 2 were conducted from d 4 to 13 (experiment 1) or d 9 to 23 post-hatching (experiment 2) in batteries. The 10 treatments used in both experiment were: Diets 1 to 4 = 0.20, 0.25, 0.30, or 0.35% nPP; Diets 5 to 7 = diet 1 plus 100, 200, or 300 phytase units/kg of diet from Natuphos (NAT); and Diets 8 to 10 = diet 1 plus 100, 200, or 300 phytase units/ kg of diet from Ronozyme (RON). As nPP levels increased, daily gain (ADG), feed intake (ADFI), gain:feed, and toe and tibia ash percentage were linearly increased (P < 0.06) in experiments 1 and 2. Incremental addition of phytase, regardless of source, linearly increased (P < 0.07) ADG and ADFI in experiment 1. Broilers fed NAT had higher (P < 0.07) toe ash percentage in experiment 1 and 2, and higher (P < 0.02) ADG and ADFI in experiment 2 than those fed RON. In experiment 3, 3,360 broilers were used to test 2 dry phytase products from 0 to 41 d posthatching in a 3-phase feeding program. The treatments were: Diet 1) adequate Ca and nPP; Diet 2) nPP reduced by 0.20%; Diets 3 to 5 = diet 2 plus 300, 500, or 750 phytase units/kg of diet from NAT; and Diets 6 to 8 = Diet 2 plus 300, 500, or 750 phytase units/kg of diet from RON. Broilers fed the adequate Ca and nPP diet had improved ADG and ADFI overall, and tibia ash weight and percentage in all growth phases (P < 0.03) compared with those fed the reduced Ca and nPP diets. Overall, ADG and ADFI were linearly increased (P < 0.05) by incremental phytase addition in experiment 3. Both NAT and RON produce similar growth and bone ash traits in commercial broilers.

The interactive effects of Eimeria acervulina infection and phytase for broiler chicks.

An experiment was conducted to determine the interactive effects of Eimeria acervulina infection and phytase in male broiler chicks. Chicks were standardized from 0 to 4 d posthatching, and the assay period was 5 to 15 d. Treatments were replicated with 6 pens of 5 chicks each. The initial and final BW were 67 and 363 g. A corn-soybean meal diet formulated to provide 1.26% total Lys and 3,200 kcal of ME/kg was used, and it was adequate in all other nutrients except Ca and nonphytate P (NPP) when appropriate. The treatments were in a 2 x 2 x 2 factorial arrangement: adequate Ca and NPP (1.0% Ca and 0.45% NPP) or inadequate Ca and NPP (0.80% Ca and 0.25% NPP), 0 or 600 phytase units/kg of diet, and uninfected or infected with 400,000 E. acervulina oocysts on d 0, 3, and 6 of the experiment. Daily gain, average daily feed intake, and gain:feed (GF) were reduced (P < 0.01) by the coccidial infection and the reduction in Ca and NPP. Phytase addition increased (P < 0.02) average daily gain and average daily feed intake, regardless of the Ca and NPP contents of the diet or the presence of coccidiosis. The GF was increased by phytase but only in uninfected chicks (phytase x coccidiosis, P < 0.02). Toe and tibia ash percentages were decreased (P < 0.01) in chicks fed diets deficient in Ca and NPP, but tibia ash was decreased more by Ca and NPP in healthy chicks than in infected chicks (coccidiosis x Ca and NPP, P < 0.02). Phytase increased (P < 0.02) toe and tibia ash but only in diets deficient in Ca and NPP (phytase x Ca and NPP, P < 0.01). Phytase increased toe ash percentage of healthy chicks fed diets deficient in Ca and NPP, but it had less of an effect in infected chicks fed diets deficient in Ca and NPP (coccidiosis x Ca and NPP x phytase, P < 0.08). Also, phytase was less effective in increasing tibia ash percentage in coccidiosis-infected chicks than in uninfected chicks (phytase x coccidiosis, P < 0.02). These data indicate that phytase is effective in the presence of a coccidial infection, but based on GF and tibia ash percentage, it may not be as effective as in uninfected chicks. Also, phytase increased average daily gain and average daily feed intake in uninfected chicks fed diets formulated to be adequate (or in excess) in all nutrients for male broiler chicks.

Effect of protein and energy sources and bulk density of diets on growth performance of chicks.

Four completely randomized designed experiments (EXP) were conducted to determine the effect of energy, amino acid (AA) levels, and bulk density of diets on growth performance of chicks fed diets containing corn (C) or cornstarch:dextrose (CD) as energy sources and soybean meal (SBM) or soy protein isolate (SPI) as protein sources. The chicks were fed C-SBM diets 6 to 8 d posthatching before allotment to treatment, and the assay periods ranged from 7 to 14 d. Initial weights were 86, 93, 94, and 71 g in EXP 1 to 4, respectively. Treatments were replicated 6 to 8 times with 4, 5, or 6 chicks per replicate. In EXP 1, the treatments were 1) C-SBM (1.26% Lys and 3,200 kcal of ME/kg); 2) CD-SPI (1.26% Lys and 3,460 kcal of ME/kg); 3) CD-SPI (1.36% Lys and 3,460 kcal of ME/kg); and 4) CD-SPI (1.26% Lys and 3,200 kcal of ME/kg). The AA in all diets were increased in proportion to Lys. In EXP 2, chicks were fed C or CD as the energy source and SBM or SPI as the protein source in a 2 x 2 factorial arrangement. In EXP 3, the treatments were 1) C-SBM (1.26% Lys and 3,200 kcal of ME/kg); 2) CD-SPI (1.26% Lys and 3,200 kcal of ME/kg); 3) Diet 1 limit-fed to chicks consuming 90% of Diet 2; 4) Diet 2 limit-fed to chicks consuming 90% of Diet 2. In EXP 4, Diets 1 and 2 were the same as Diets 1 and 2 in EXP 3, but fed in mash or pelleted form. In all EXP, chicks with access ad libitum to diets with SPI had decreased (P < 0.02) average daily gain (ADG) and feed intake (ADFI) compared with those with access ad libitum to diets with SBM. In EXP 2, feeding C- or CD-dextrose as the energy source had no effect (P > 0.05) on ADG, ADFI, or gain:feed. In EXP 3, ADG was decreased in chicks fed the diets with SPI relative to those fed diets with SBM, but the decrease was much greater in chicks that had access ad libitum to feed (protein source x feed intake, P < 0.01) than in those limit-fed to the same feed intake. In EXP 4, ADG, ADFI, and gain:feed were decreased (P < 0.01) in chicks fed diets with SPI as the protein source. Pelleting increased (P < 0.01) ADG, ADFI, and gain:feed regardless of protein source, but the increase was much greater in chicks fed the diets with SPI (protein source x feed form, P < 0.01). Results from these EXP indicate that diets with SPI compared with SBM do not result in maximum growth performance in commercial broilers, and the problem may be due somewhat to nutrient deficiency but more to the physical form of the diet.

Glutaraldehyde-induced cross-links: a study of model compounds and commercial bioprosthetic valves.

BACKGROUND AND AIM OF THE STUDY: The treatment of bioprosthetic tissue routinely involves the use of glutaraldehyde, although the specific chemistry of glutaraldehyde fixation is not fully understood. Descriptions of definitive work on this reaction using model compounds are limited. The aim of the present study was to increase our understanding of the chemistry involved in the treatment of collagen-rich tissue with glutaraldehyde. Initially, 6-aminohexanoic acid (6-AHA) was used to model the lysine/hydroxylysine molecules in collagen before studying the more complex chemistry of the tissue. METHODS: The reaction between 0.6% glutaraldehyde and 6-AHA was studied by positive ion electrospray-mass spectroscopy. Untreated, locally treated and commercially produced explanted and non-implanted tissue were hydrolyzed under various conditions and analyzed both directly and after derivatization with 4-chlorophenylhydrazine, 4-bromophenacyl bromide and dansyl chloride by reverse-phase-high performance liquid chromatography-mass spectrometry. RESULTS: The mass spectral data obtained from the reaction of glutaraldehyde with 6-AHA showed the presence of alpha,beta unsaturated aldehydes and their further condensation products involving Michael reactions of glutaraldehyde, Schiff base cross-links and various cyclization products incorporating pyridinium and dihydropyridine ring structures. The only stable cross-link detected was an 'anabilysine'-like compound. Similar structures were present in the tissue, and anabilysine was identified by tandem mass spectrometry. CONCLUSION: The results from the reaction of glutaraldehyde with 6-AHA agree with those published previously. The only detectable stable cross-link definitively identified in treated bioprosthetic tissue was anabilysine. No long-chain polymers of glutaraldehyde were detected.