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. 2019 Apr 17;98(10):4868–4877. doi: 10.3382/ps/pez229

Effect of low protein diets supplemented with free amino acids on growth performance, slaughter yield, litter quality, and footpad lesions of male broilers

J van Harn 1,, M A Dijkslag 2, M M van Krimpen 1
PMCID: PMC6748714  PMID: 30995304

ABSTRACT

A study with 884 Ross 308 male broilers, housed in 68 floor pens (0.75 m2) from 0 to 35 days of age was conducted to evaluate the effects of low crude protein (CP) diets, with partial replacement of soybean meal by free amino acids (AA), on performance, slaughter yields, litter quality and footpad lesions. During the first 11 d, all broilers received the same control starter diet (216 g/kg CP, 11.5 g/kg apparent fecal digestible (AFD) lysine, and 2900 kcal/kg AMEn). Thereafter, four experimental feeding programs with different levels of dietary CP (control and control with 1% (CP-1%), 2% (CP-2%) and 3% (CP-3%) less CP units) were provided in both the grower and finisher phase. In the control grower and finisher diet, the CP content was 208 and 198 g/kg, respectively. All diets were formulated to meet or exceed the recommendations concerning AFD AA, and to be iso-caloric within each feeding phase. Feed and water were provided for ad libitum intake during the entire experimental period.

None of the low CP feeding programs affected body weight gain, feed intake or mortality from 0 to 35 d. However, CP conversion was improved with the reduction of CP content of the diet. Broilers fed the CP-2% or CP-3% feeding program had an improved feed conversion ratio. Broilers fed the low CP protein feeding programs had a better litter quality and less footpad lesions, compared to broilers fed the control feeding program. Broilers fed the CP-3% feeding program had a lower breast meat yield than broilers fed the control feeding program. Slaughter yields of broilers fed CP-1% or CP-2% feeding program did not differ from the control feeding program. This study demonstrated that the CP content of grower and finisher diets can be reduced by 2.2–2.3% units without adverse effects on growth performance of broilers, while CP reduction seems promising to reduce nitrogen excretion from broiler houses, improve bird welfare, and reduces dependence on vegetable protein sources.

Keywords: Broiler, low protein, growth performance, litter quality, footpad lesion

INTRODUCTION

World population is expected to grow from 7.7 billion in 2018 to almost 10 billion in 2050. This trend and the expected increase in prosperity, implies that the market demand for animal derived food will continue to grow (FAO, 2009; FAO, 2017). It is expected that the demand for poultry meat will increase rapidly worldwide. As a result, the demand for vegetable proteins, e.g., soybean meal, for use in animal feed will increase (Alexandratos and Bruinsma, 2012). In Europe, the rate of self-sufficiency for soybean meal is only 5% (EU, 2017). This strong dependency for this important protein source in poultry diets on other areas, mainly South America makes the EU livestock sector vulnerable to price volatility and trade distortions, causing feed price to rise, thereby, increasing farmers’ production costs and reducing the sectors’ profitability (Euractiv, 2011). On the other hand, there is concern about the deforestation of tropical rain forest which is done to fulfil the need for arable land for soybean cultivation (WNF, 2011; Van Gelder and Kuepper, 2012).

Reduction of the CP of broiler diets can contribute to reduce the import and use of soybeans in Europe as well. However, reducing the CP content of broiler diets will pose a risk for reduced growth performance, when (semi-) essential AA become limiting. When the CP content is reduced, glycine and serine levels among other nonessential AA decrease as well (Dean et al., 2006). Therefore, it is possible that marginal levels of dietary glycine and serine cause a decrease in performance of broilers when feeding low CP diets, even if these are supplemented with essential AA up to bird's requirement (e.g., Ferguson et al., 1998a, b; Bregendahl et al., 2002; Veldkamp et al., 2017). Several studies showed that glycine supplementation prevented the adverse effects of low CP diets on broiler performance (Dean et al. 2006; Ospina-Rojas et al., 2012; Ospina-Rojas et al., 2013; Ospina Rojas et al., 2014).

A large part of the dietary nitrogen intake is not retained by the animal, but excreted into the environment. Lowering the CP content of the diet could therefore be a tool to reduce the nitrogen excretion and ammonia emission from broiler houses (Elwinger and Svensson, 1996; Kidd et al., 1996; Van Harn and Van Middelkoop, 1996; Ferguson et al., 1998a; Nahm, 2002; Khajali and Moghaddam, 2006; Namroud, et al., 2008; Hernandez et al., 2013). A reduced CP content in broiler diets can also reduce water intake, because there is a reduced need to excrete the surplus of nitrogen (Elwinger and Svensson, 1996; Alleman and Leclercq, 1997; Bailey, 1999). A lower water intake might reduce the risk of wet litter, and thus the risk of impaired welfare, since wet litter is the main reason for skin dermatitis such as footpad lesions, hock burns and breast blisters (Martland, 1985). Wet litter could also lead to more rejections at the slaughter house (Shepherd and Fairchild, 2010), because there is a high probability of broilers in permanent contact with wet and sticky litter developing contact dermatitis caused by humidity (water), non-identified irritants in the fecal materials and by ammonia (Allain et al., 2009). Moreover, field experiences show that low CP levels in broiler diets can reduce the risk of digestion problems and necrotic enteritis.

In summary, reduction of the dietary protein content has a number of potential benefits on EU protein self-sufficiency, environmental pollution and broiler health and welfare, provided that the growth performance and slaughter yield are not compromised. The objective of this study was to evaluate the effects of a reduction of 1, 2 or 3% units in dietary CP content in the grower (11–28 d) and finisher phase (28– 35 days), with a partial replacement of soybean meal by free AA (including glycine), on growth performance, slaughter yields, litter quality and footpad lesions of broilers.

MATERIALS AND METHODS

This experiment was performed in accordance with the Dutch rules and regulations and approved by the Ethics Committee of Wageningen University and Research, the Netherlands.

Diets and Diet Analysis

The experimental diets were formulated and produced by ForFarmers, Heijen, The Netherlands. A three-phase feeding program was applied. Starter, grower and finisher diets were provided from 0 to 11, 11 to 28 and 28 to 35 days of age, respectively. During the starter phase, all animals received the same control diet with a CP content of 216 g/kg and 11.5 g/kg digestible Lys. Thereafter, four experimental feeding programs differing in CP levels (control and with 1% (CP-1%), 2% (CP-2%) and 3% (CP-3%) lower dietary CP content in each phase) were provided. The control diets had a CP content in the grower and finisher phase of 208 and 198 g/kg, respectively. The diets were formulated to meet or exceed the recommendations for apparent fecal digestible AA (lysine, methionine, threonine, tryptophan, isoleucine, valine, arginine) according to CVB recommendations (CVB, 2012), and to be iso-energetic within each phase. Because of the importance of glycine + serine in low protein diets, it was decided in the present study to add free glycine to the low protein diets to the apparent fecal digestible glycine + serine in the control diet, to maintain the production results of broilers. Free glycine was not approved to be used as a feed additive in The Netherlands. Therefore, permission (BD 15.290/FV/MS) from the Veterinary Medicinal Products Unit was obtained to carry out this study. All diets of each phase were prepared with the same batch of ingredients. Dietary soybean meal content in the grower diets was reduced from 27.3% (control) to 17.3% (CP-3%), while soybean meal content in the finisher diets was reduced from 25.0% (control) to 14.6% (CP-3%). The ingredient and calculated nutrient compositions of the diets are given in Table 1.

Table 1.

Ingredient and calculated nutritional composition of the starter (0 to 11 d), grower (11 to 28 d) and finisher diets (28 to 35 d) to determine the effect of a reduction of 1 to 3%-units of crude protein (CP) in grower and finisher diets.

Grower diets Finisher diets
Starter diet Control CP CP-1% CP-2% CP-3% Control CP CP-1% CP-2% CP-3%
Raw materials
Wheat % 30.87 37.29 30.00 30.00 30.00 39.64 30.00 30.00 30.29
Corn % 25.00 18.80 29.04 32.75 36.51 20.56 33.02 36.49 40.00
Soybean meal 48% % 30.47 27.34 24.84 21.07 17.30 24.99 22.55 18.41 14.62
Rapeseed meal 00 % 3.00 5.00 4.96 5.00 5.00 4.28 4.40 5.00 5.00
Oat hulls % 2.00 2.00 2.00 2.00 2.00 2.00 2.00 2.00 2.00
Palm oil % 1.54 2.71 2.45 2.19 1.51 2.51 2.25 1.68 1.01
Soya lecithin % 1.00 1.00 1.00 1.00 1.00 1.00 1.00 1.00 1.00
Soya oil % 0.92 1.51 0.87 0.50 0.50 1.22 0.50 0.50 0.50
Lauric fatty acids % 0.50 0.50 0.50 0.50 0.50 0.50 0.50 0.50 0.50
Mono calcium phosphate % 0.99 0.66 0.69 0.76 0.82 0.15 0.19 0.22 0.26
Limestone % 0.25 0.25 0.25 0.25 0.26
Sodium bicarbonate % 0.28 0.21 0.25 0.31 0.39 0.24 0.28 0.34 0.41
Sodium chloride % 0.11 0.13 0.10 0.06 0.12 0.09 0.05
L-Lysine HCl % 0.22 0.16 0.24 0.36 0.48 0.16 0.24 0.36 0.47
DL-Methionine % 0.28 0.23 0.25 0.29 0.32 0.21 0.24 0.27 0.31
L-Threonine % 0.09 0.05 0.09 0.14 0.19 0.05 0.08 0.14 0.19
L-Valine % 0.07 0.02 0.07 0.14 0.21 0.02 0.07 0.14 0.20
L-Arginine % 0.08 0.19 0.30 0.08 0.19 0.30
L-Isoleucine % 0.04 0.11 0.18 0.04 0.11 0.18
Glycine % 0.09 0.21 0.34 0.09 0.22 0.34
L-Tryptophan % 0.02 0.04 0.06 0.02 0.04 0.06
Premix A1 % 2.00 2.00 2.00 2.00 2.00
Premix B2 % 2.00 2.00 2.00 2.00
Maxiban G160 (anti-coccidial)3 % 0.30 0.30 0.30 0.30 0.30
Xylanase 6.25% (Endo-1,4-beta-xylanase)4 % 0.10 0.10 0.10 0.10 0.10 0.10 0.10 0.10 0.10
Phyzyme® XP 5000 L (phytase enzyme)5 % 0.01 0.01 0.01 0.01 0.01 0.01 0.01 0.01 0.01
Calculated nutrient composition
AMEn broiler kcal/kg 2900 3000 3000 3000 3000 3025 3025 3025 3025
Crude protein g/kg 216 208 198 188 178 198 188 178 168
Crude fat g/kg 67 83 76 70 64 79 71 66 60
Crude fiber g/kg 35 37 36 35 34 35 35 34 34
Crude ash g/kg 54 48 47 46 44 43 42 40 39
Starch g/kg 353 351 373 397 421 376 399 421 445
Calcium g/kg 8.0 6.5 6.5 6.5 6.5 5.5 5.5 5.5 5.5
Phosphorus g/kg 6.2 5.5 5.5 5.5 5.5 4.2 4.2 4.2 4.1
Sodium g/kg 1.4 1.3 1.3 1.3 1.3 1.3 1.3 1.3 1.3
Potassium g/kg 9.7 9.3 8.7 8.0 7.2 8.7 8.2 7.5 6.7
Chloride g/kg 1.5 1.5 1.5 1.5 1.4 1.5 1.5 1.5 1.5
dEB6 meq 260 245 232 213 196 236 223 203 185
6-Phytase E4a1640 FYT/kg 500 500 500 500 500 500 500 500 500
AFD7 lysine g/kg 11.5 10.5 10.5 10.5 10.5 9.9 9.9 9.9 9.9
AFD methionine g/kg 5.6 5.0 5.1 5.3 5.5 4.7 4.9 5.1 5.2
AFD Met+Cys g/kg 8.5 7.9 7.9 7.9 7.9 7.5 7.5 7.5 7.5
AFD threonine g/kg 7.5 6.8 6.8 6.8 6.8 6.4 6.4 6.4 6.4
AFD tryptophan g/kg 2.37 2.30 2.30 2.30 2.30 2.17 2.17 2.17 2.17
AFD isoleucine g/kg 7.8 7.4 7.4 7.4 7.4 7.0 7.0 7.0 7.0
AFD valine g/kg 9.2 8.4 8.4 8.4 8.4 7.9 7.9 7.9 7.9
AFD arginine g/kg 12.5 12.0 12.0 12.0 12.0 11.3 11.3 11.3 11.3
AFD glycine + serine g/kg 16.3 15.7 15.7 15.7 15.7 14.9 14.9 14.9 14.9
AFD P broiler g/kg 4.4 3.8 3.8 3.9 3.9 2.8 2.8 2.8 2.8

1Premix provided per kg of diet: 10,000 IU vitamin A (retinylacetate), 3500 IU vitamin D3 (cholecalciferol), 0.025 mg 25-hydroxycholecalciferol, 100 IU vitamin E (all-rac alpha tocopheryl acetate), 4 mg vitamin K3 (menadione nicotinamide bisulfite), 4 mg vitamin B1 (thiamine mononitrate), 9 mg vitamin B2 (riboflavin), 21.7 mg d-pantothenic acid, 70 mg niacin amide, 250 μg biotin, 30 μg vitamin B12 (cyanocobalamin), 1.5 mg folic acid, 6 mg vitamin B6 (pyridoxine hydrochloride), 150 mg betaine, 30 mg L-carnitine, 50 mg Fe (as FeSO4•H2O), 10 mg Cu (as CuSO4•5H2O), 4 mg Cu (as Cu chelate), 70 mg Zn (as ZnSO4•H2O), 30 mg Zn (as Zn chelate), 40 mg Mn (as MnSO4•H2O), 15 mg Mn (as Mn chelate), 2.0 mg I (as CaI2), 0.1 mg Se (as Na2SeO3•5H2O), 0.2 mg selenomethionine, 2 mg E310 (propyl gallate), 1 mg E320 (butylated hydroxyanisole, BHA) and 1.3 mg E321 (butylated hydroxytoluene, BHT).

2Premix provided per kg of diet: 10,000 IU vitamin A (retinylacetate), 3000 IU vitamin D3 (cholecalciferol), 45 IU vitamin E (all-rac alpha tocopheryl acetate), 3 mg vitamin K3 (menadione nicotinamide bisulfite), 2 mg vitamin B1 (thiamine mononitrate), 7 mg vitamin B2 (riboflavin), 16.3 mg d-pantothenic acid, 60 mg niacin amide, 200 μg biotin, 25 μg vitamin B12 (cyanocobalamin), 1 mg folic acid, 5 mg vitamin B6 (pyridoxine hydrochloride), 100 mg betaine, 30 mg L-carnitine, 30 mg Fe (as FeSO4•H2O), 10 mg Cu (as CuSO4•5H2O), 80 mg Zn (as ZnSO4•H2O), 20 mg Zn (as Zn chelate), 40 mg Mn (as MnSO4•H2O), 2.0 mg I (as CaI2), 0.1 mg Se (as Na2SeO3•5H2O), 0.1 mg selenomethionine, 2 mg E310 (propyl gallate), 1 mg E320 (butylated hydroxyanisole, BHA) and 1 mg E321 (butylated hydroxytoluene, BHT).

3Maxiban G160, Trouw Nutrition Nederland B.V., The Netherlands

4Xylanase 6.25% (EC Registration Number: 4a11, EC 3.2.1.8), Trouw Nutrition Nederland B.V., The Netherlands

5Phyzyme® XP 5000 L (EC Registration Number: 4a1640, EC 3.1.3.26), Danisco, Malborough, United Kingdom

6dEB = dietary electrolyte balance ( = Na++K+-Cl−)

7AFD = Apparent Fecal Digestibility CVB Feed Table (2007)

All diets were pelleted (starter diets as 2.5 mm diameter pellets, grower and finisher diets both as 3.2 mm diameter pellets). All diets were analyzed for dry matter, ash, crude protein, crude fat, crude fiber, starch and AA (except tryptophan and tyrosine). All proximate analyses were performed at the laboratory of ForFarmers, Lochem, The Netherlands. The amino acid analyses were performed at Evonik Nutrition & Care GmbH, Hanau-Wolfgang, Germany.

Dry matter content was determined gravimetrically after 4 h at 103°C (ISO, 1998). The content of ash was determined gravimetrically after ashing at 550°C (ISO, 2002). Nitrogen content was determined by the Kjeldahl method (ISO, 1997). Crude fat was performed with a gravimetrical method based on EC 3–9-1998; nr. L 257/23–25. For crude fiber a method with intermediate filtration was used (ISO, 2000). Starch content was determined enzymatically according to NEN-EN-ISO 15914 (2005). The AA were assayed by ion exchange chromatography in an Amino Acid Analyzer (Evonik, 2010).

Birds and Management

A total number of 936 day-old male broilers Ross 308 were obtained from a commercial hatchery (Probroed & Sloot, Groenlo, The Netherlands), and equally distributed to 72 floor pens (floor space: 0.75 m2) bedded with wood shavings (2 kg/m2). In each pen, 13 broilers were placed. The floor pens were located in a naturally ventilated poultry house. Sixty-eight of these 72 pens were used for this trial. In the remaining four pens, spare animals were housed, which were used to maintain the number of animals in the experimental pens in case of mortality during the starter phase (0 to 11 d).

The birds were visually observed twice a day to check animal health. All broilers were vaccinated against New Castle Disease (Nobilis® ND Clone 30, MSD Animal Health, spray vaccination) at 15 days of age at the experimental facility. Water and feed were provided ad libitum during the entire experimental period (0–35 days of age). Feed was supplied via feeding bins (0.75 m feeding space/pen). Water was supplied by one drinking cup (Impex, Barneveld, the Netherlands) per pen. The temperature at placement of the broilers was 34°C and it was gradually decreased to 20°C at 34 days of age. During the first two days light was nearly continuously switched on (23L:1D), from 3–35 days of age a day/night schedule of 18 h light and 6 h dark (18L:6D) was given per 24 h. Light intensity was 20 lux at bird level during the entire experimental period.

Growth Performance

Body weight (BW) of the birds was determined per pen at 0, 11, 28 and 35 days of age. Feed intake per pen was determined at 11, 28 and 35 days of age as provided feed minus remaining feed in each feeding phase. Body weight gain (BWG, g), average daily gain (ADG, g/d), feed conversion ratio (FCR, g/g), feed intake (FI, g), and average daily feed intake (ADFI, g/d) were calculated on a pen basis from these data for the following periods: 0–11d, 11–28d, 28–35d, 11–35d and 0–35d. BWG = BW end period—BW start period; ADG = BWG/length period; FCR = (Total FI/(Total BW end period—total BW start period + total BW of dead or culled birds)); FI = FCR × BWG; ADFI = FI/length period. The crude protein conversion (CPC) was calculated over the above mentioned periods as CPC = FI (kg) × CP content diet (g/kg)/BWG (g). Culling, mortality and health (including probable causes of any culling, illness or deaths) were recorded daily. EPEF (European Production Efficiency Factor) was calculated per pen at 35 days as (mean daily body weight gain (g) × (100–% mortality)/(FCR × 10).

Slaughter Yields

Slaughter yields of 10 randomly selected birds per pen were determined at 35 days of age. Selected birds were removed, individually marked, weighed and transported to a commercial slaughter house. At the slaughter house, the broilers were manually dissected by trained personnel to determine carcass, wing, leg (thigh and drums), back and breast meat weight and yield. All yields were expressed as percentage of carcass weight, except carcass yield which is expressed as percentage of the live body weight. All measurements were performed by Plukon, Wezep, The Netherlands.

Litter Quality Assessment and Litter Composition

Litter quality was visually scored at 35 days of age by an experienced assessor, who scored the friability and wetness of the litter in each pen on a 1 to 10 point scale. The scores and the description of each score are presented in Table 2.

Table 2.

Description of scoreyes for friability and wetness of the litter.

Score Friability description Wetness description
1 Complete caked litter Wet litter, by pressure on the litter water is appearing in the total area
2 80–90% of the area is caked Wet litter, by pressure on the litter water is appearing beneath the drinking line
3 70–80% of the area is caked Wet litter, by pressure on the litter no water is appearing beneath the drinking line
4 60–70% of the area is caked Wet litter, dark colored, litter can be pressed ball-shaped
5 50–60% of the area is caked Wet litter, dark colored, ridges beneath drinking line
6 40% of the area is caked Almost dry litter, small ridges beneath drinking line. Litter between drinking line and feeders is still friable
7 30% of the area is caked Almost dry litter, dark colored beneath drinking line and in other areas light colored, ridge formation beneath drinking lines just started
8 10% of the area is caked Almost dry litter, light colored, no ridges beneath drinking line
9 Friable litter, some litter particles are caked Dry litter, light colored
10 Friable litter, no caked litter particles Very dry litter

At the end of the study, representative samples of the litter were taken from all pens. These samples were analyzed for dry matter, total N, ammoniacal N and pH. These analyses were performed by the service lab of Wageningen Livestock Research, Wageningen, the Netherlands. Dry matter and total N were measured according to NEN 7432 (1998) and NEN 7434 (1998), respectively. Ammoniacal N was determined according to NEN 7438 (1997). For the pH determination, 50 grams of litter material was added to 200 mL demi-water, thoroughly mixed and after 16 hours the pH was measured with a pH electrode (XS-instruments pH 8).

Footpad Lesions

Occurrence and severity of footpad lesions (scale 0, 1, 2) was determined at 34 days of age by an experienced assessor. All broilers in a pen were used for these assessments. Footpad lesions were scored per broiler for both feet according to Berg (1998), i.e., score 0: no lesions or very small discoloration; score 1: discoloration but no deep lesion; score 2: deep lesion with ulcers or scabs, bumble foot. The severity of footpad lesions was expressed as footpad score (FPS) per pen. This score was calculated as: 100% × ((0.5 × the total number of birds with score 1) + (2 × the total number of birds with score 2))/the total number of scored birds. The FPS can range from 0 (all birds having no lesions) to 200 (all birds having score 2).

Statistical Analysis

Raw data were analyzed for statistical outliers. An outlier was defined as an observation deviating more than 2.5 standard deviations from the mean. No outliers, however, were detected, meaning that all data were included in the statistical analysis. Pen was served as the experimental unit and statistical analyses were carried out using Genstat (18th edition, VSN International LTD, Hemel Hempstead, UK). All data were analyzed using ANOVA with groups of four consecutive pens included as a blocking factor and diet as fixed factor (explanatory variable). Differences between treatments were analyzed using Fisher's Least Significant Difference (LSD) in case the treatment effect was significant (P ≤ 0.05).

RESULTS

Diet Composition

The analyzed nutrient contents of the experimental diets were consistent with the expected values (Table 3), except for the CP content of the control grower and finisher diets, which were 8 and 7 g/kg lower than calculated values, respectively. The absolute difference in analyzed crude protein content between control and CP-3% was 2.2% and 2.3% for the grower and finisher diet, respectively, instead of the calculated difference of 3%. In general, the analyzed AA contents met the calculated contents, except for the glycine level of the glycine supplemented diets which was on average 10% higher than calculated (Table 4).

Table 3.

Calculated and analyzed nutrient composition (g/kg) of the grower and finisher diets fed to broilers to determine the effect of a reduction of 1 to 3%-units of crude protein (CP).

Grower diets Finisher diets
Nutrient Control CP CP-1% CP-2% CP-3% Control CP CP-1% CP-2% CP-3%
Calculated
Crude protein g/kg 208 198 188 178 198 188 178 168
Crude fat g/kg 83 76 70 64 79 71 66 60
Crude fiber g/kg 37 36 35 34 35 35 34 34
Crude ash g/kg 48 47 46 44 43 42 40 39
Starch g/kg 351 373 397 421 376 399 421 445
Analyzed
Crude protein g/kg 200 194 186 178 191 184 176 168
Crude fat g/kg 81 76 70 66 75 71 66 61
Crude fiber g/kg 37 37 35 36 37 38 38 34
Crude ash g/kg 47 46 45 42 42 40 39 36
Starch g/kg 350 364 385 404 359 379 407 432

Table 4.

Calculated and analyzed amino acid contents of the grower and finisher diets fed to broilers to determine the effect of a reduction of 1 to 3%-units of crude protein (CP).

Grower diets Finisher diets
Control CP ( = 208 g/kg CP) CP-1% CP-2% CP-3% Control CP ( = 198 g/kg CP) CP-1% CP-2% CP-3%
Calculated
Lysine g/kg 11.8 11.7 11.6 11.5 11.1 11.1 11.1 10.8
Methionine g/kg 5.4 5.5 5.6 5.8 5.1 5.2 5.4 5.5
Cysteine g/kg 3.5 3.4 3.2 2.9 3.4 3.3 3.1 2.8
Threonine g/kg 8.1 8.0 7.9 7.8 7.6 7.6 7.5 7.4
Tryptophan g/kg 2.6 2.4 2.2 2.1 2.4 2.2 2.0 2.0
Isoleucine g/kg 8.4 8.3 8.2 8.1 7.9 7.8 7.8 7.7
Arginine g/kg 13.2 12.8 12.7 12.6 12.4 12.1 12.0 11.9
Valine g/kg 9.7 9.7 9.6 9.5 9.2 9.2 9.1 9.0
Phenylalanine g/kg 9.8 9.2 8.4 7.8 9.3 8.7 7.9 7.3
Histidine g/kg 5.3 5.0 4.6 4.2 5.0 4.7 4.3 4.0
Leucine g/kg 15.7 15 13.9 13 15.2 14.3 13.3 12.3
Tyrosine g/kg 6.6 6.2 5.6 5.1 6.2 5.8 5.3 4.8
Alanine g/kg 9.1 8.7 8.1 7.6 8.8 8.4 7.8 7.2
Aspartic acid g/kg 19.3 17.9 16.1 14.6 18.1 16.6 14.7 13.5
Glutamic acid g/kg 39.7 37.6 34.9 32.3 38 35.8 33.1 30.6
Proline g/kg 12.6 12.2 11.5 10.8 12.3 11.8 11.1 10.3
Glycine g/kg 8.6 8.2 8.7 9.2 8.2 7.7 8.1 8.5
Serine g/kg 9.8 9.2 8.5 7.8 9.3 8.7 7.9 7.3
Gly+Ser g/kg 18.4 17.4 17.2 17.7 17.5 16.4 16.0 15.8
Analyzed
Lysine g/kg 11.5 11.6 11.5 11.3 10.7 10.8 10.7 10.7
Methionine g/kg 5.1 5.2 5.4 5.5 4.9 5.0 5.1 5.3
Cysteine g/kg 3.3 3.2 3.1 2.9 3.3 3.2 3.0 2.8
Threonine g/kg 8.0 8.1 7.8 7.7 7.4 7.4 7.3 7.3
Tryptophan g/kg Not determined
Isoleucine g/kg 8.6 8.5 8.4 8.0 8.0 8.0 7.8 7.8
Arginine g/kg 13.2 13.2 13.0 12.7 12.3 12.2 12.0 12.0
Valine g/kg 9.9 9.9 9.5 9.3 9.4 9.2 9.0 8.9
Phenylalanine g/kg 10.0 9.6 8.7 8.0 9.4 9.0 8.1 7.5
Histidine g/kg 5.1 5.0 4.5 4.1 4.7 4.6 4.2 3.8
Leucine g/kg 15.6 15.4 14.2 13.1 14.7 14.6 13.3 12.6
Tyrosine g/kg Not determined
Alanine g/kg 9.1 9.0 8.3 7.8 8.5 8.6 7.9 7.4
Aspartic acid g/kg 19.3 18.3 16.2 14.5 17.7 16.9 14.8 13.3
Glutamic acid g/kg 39.6 37.5 34.2 31.5 37.6 35.1 32.0 29.9
Proline g/kg 12.6 12.3 11.4 10.8 12.1 11.6 10.8 10.3
Glycine g/kg 8.7 9.0 9.5 9.9 8.0 8.5 9.0 9.5
Serine g/kg 9.8 9.4 8.5 8.0 9.2 8.8 7.9 7.4
Gly+Ser g/kg 18.4 18.4 18.0 17.9 17.2 17.3 16.9 16.9

Growth Performance

In the grower phase (12–28 d), finisher phase (29–35 d) and over the entire experimental period (0–35 d), no adverse effects of the reduction in dietary CP content on BW, BWG, mortality and FI were observed (Table 5). In the finisher phase (P<0.01) and in the entire period (P = 0.002), the reduction in dietary CP content decreased the FCR of the birds with the lowest FCR in birds of the 2 and 3% reduced CP content. In all feeding phases and overall, the protein efficiency increased with each reduction of the dietary CP content as indicated by the decrease (P<0.001) of the CP conversion (CP intake per g of body gain, CPC). Broilers fed the CP-2% feeding program had the highest (P = 0.035) EPEF. The EPEF of the broilers receiving the CP-1% or CP-3% feeding program did not differ from the control.

Table 5.

Influence of a 1 to 3%-units crude protein (CP) reduction in grower and finisher diets on growth performance of male broilers from 11–28 d (grower phase), 28–35 d (finisher phase) and 0–35 d of age (entire experimental period).

Control CP CP-1% CP-2% CP-3% P-value LSD
Calculated CP content grower phase (in g/kg) 208 198 188 178
Calculated CP content finisher phase (in g/kg) 198 188 178 168
11–28 days
Body weight d11 324 323 323 321 0.656 4.3
Body weight d28 (g) 1752 1751 1752 1739 0.759 29.1
Body weight gain (g/d) 84.0 84.0 84.1 83.4 0.811 1.63
Mortality (%) 3.2 3.6 2.0 3.6 0.834 3.39
Feed conversion ratio (g/g) 1.456 1.468 1.443 1.458 0.553 0.0340
Crude protein conversion (CPC)1 0.3029a 0.2906b 0.2713c 0.2595d <.001 0.0064
Feed intake (g/d) 122.3 123.2 121.3 121.5 0.566 2.92
28–35 days
Body weight gain (g/d) 95.2 97.9 99.6 101.1 0.143 5.29
Mortality (%) 2.6 1.5 0.5 1.0 0.458 2.69
Feed conversion ratio (g/g) 1.954a 1.886ab 1.801bc 1.772c <.001 0.0806
Crude protein conversion (CPC)1 0.3868a 0.3546b 0.3206c 0.2977d <.001 0.0154
Feed intake (g/d) 184.2 183.8 179.0 179.1 0.175 6.25
0–35 days
Body weight d35 (g) 2416 2431 2447 2448 0.595 53.4
Body weight gain (g/d) 68.0 68.4 68.8 68.9 0.595 1.53
Mortality (%) 6.0 5.8 2.5 6.3 0.324 4.72
Feed conversion ratio (g/g) 1.549a 1.542ab 1.505c 1.510bc 0.002 0.0265
Crude protein conversion (CPC)1 0.3178a 0.3023b 0.2814c 0.2685d <.001 0.0051
Feed intake (g/d) 105.2 105.4 103.6 103.9 0.147 1.93
European Production Efficiency Factor (EPEF) 2 413b 417b 447a 428ab 0.035 24.5
Footpad score (FPS) 3 143a 110b 79c 39d <.001 28.1

a–dValues without a common superscript per row differ significantly (P < 0.05).

1CPC = FI (kg) × analyzed CP content diet (g/kg)/BWG (g)

2EPEF = (daily body weight gain (g) × (100–% mortality)/FCR × 10)

3FPS = 100% × ((0.5 × n birds with score 1) + (2 × n birds with score 2))/n total birds.

Broilers fed the control feeding program had the highest incidence and the most severe footpad lesions as indicated by the highest FPS (P < .001). The footpad score decreased with each reduction of the CP content of the diet.

Slaughter Yields

In Table 6, the slaughter yields per treatment on 35 days of age are given. Providing broilers with low CP diets had no significant effect on live weight, carcass weight, and carcass yield. Relative to the carcass weight, broilers fed the CP-3% diets program had a lower wing and breast meat yield (P < .001), but a higher leg (P < 0.028) and back yield (P < 0.028) compared to the control group. Absolute weights of the wing, back and breast meat did not differ between the control group and the CP-3% group. Broilers fed the CP-3% feeding program had a higher leg weight compared to broilers that received the control feeding program (P < 0.035). No differences in slaughter yields were found between broilers fed the control, CP-1% or CP-2% diets.

Table 6.

Influence of a 1 to 3%-units crude protein (CP) reduction in grower and finisher diets on the slaughter yields of male broilers on 35 d of age. Slaughter yields were based on 10 randomly selected birds per pen.

Control CP CP-1% CP-2% CP-3% F-prob. LSD
Calculated CP content grower phase (in g/kg) 208 198 188 178
Calculated CP content finisher phase (in g/kg) 198 188 178 168
Live weight (LW, g) 2446 2481 2488 2495 0.250 51.4
Carcass weight (CW, g) 1615 1645 1648 1647 0.145 33.1
Carcass yield (% of LW) 66.0 66.3 66.2 66.0 0.402 0.46
Wing (g) 166 169 168 167 0.270 3.3
Wing (% of CW) 10.3a 10.3a 10.2ab 10.1b 0.027 0.12
Leg (g) 547b 555ab 557ab 564a 0.035 11.3
Leg (% of CW) 33.9b 33.8b 33.8b 34.3a 0.028 0.33
Back (g) 243 246 251 253 0.051 7.3
Back (% of CW) 15.1b 15.0b 15.2ab 15.3a 0.028 0.27
Breast meat (g) 520ab 532b 526ab 513a 0.046 13.5
Breast meat (% of CW) 32.1ab 32.3a 31.9b 31.2c <.001 0.39

a–cValues without a common superscript per row differ significantly (P < 0.05).

Litter Quality Assessment and Litter Composition

Table 7 presents the visual litter quality (friability and wetness) and the litter composition at 35 days of age. Visual litter quality linearly improved, indicating more friable and dryer litter, with decreasing CP content of the diet (P < .001). The results of the visual litter quality corresponded reasonably well with the dry matter (DM) contents of the litter. Dry matter content of the litter of broilers fed with the CP-3% feeding program was higher compared with the litter DM-content of the control fed broilers, where the litter DM-contents of the CP-1% and CP-2% groups were in between (P < 0.033).

Table 7.

Influence of a 1 to 3%-units crude protein (CP) reduction in grower and finisher diets on the visual quality (friability and wetness) and dry matter, total nitrogen, ammoniacal nitrogen and pH content of the litter on 35 days of age.

Control CP CP-1% CP-2% CP-3% F-prob. LSD
Calculated CP content grower phase (in g/kg) 208 198 188 178
Calculated CP content finisher phase (in g/kg) 198 188 178 168
Friability1 3.3c 4.2b 4.7b 6.1a <.001 0.79
Wetness2 2.7c 3.7b 4.4b 5.8a <.001 0.82
Dry matter (g/kg) 387b 401ab 404ab 436a 0.033 32.7
Total-N (g/kg DM) 43.7a 42.6a 40.8ab 38.2b 0.002 2.78
Ammoniacal N (g/kg DM) 11.3ab 13.3a 12.7ab 11.1b 0.026 1.65
pH 6.5 6.8 7.1 7.0 0.122 0.53

a–cValues without a common superscript per row differ significantly (P < 0.05).

11–10: 1 completely caked–10: completely friable; 21 -10: 1 very wet–10 dry

Total nitrogen (N) of the litter of the control and the CP-1% fed birds was significantly higher than the litter total-N of the CP-3% fed group (P < 0.002). The litter total-N of the CP-2% fed animals was in between and did not differ from either the control or the CP-3% group. Litter ammoniacal N content of broilers fed the CP-3% was significantly lower than of broilers fed the CP-1% diets, but it did not significantly differ from the control and CP-2% fed groups (P < 0.026). Dietary treatment had no effect on the pH of the litter.

DISCUSSION

This study demonstrated that growth performance of broilers fed low protein diets was unaffected or increased when decreasing dietary CP in the grower (11 to 28 d) and finisher phase (28 to 35 d) with 1 to 3% units (10 to 30 grams per kg of diet), when such diets were supplemented with essential AA including glycine up to the same level of the control. Providing broilers with low CP diets, even when supplemented with free AA, often resulted in deteriorated growth performance (e.g., Ferguson et al., 1998a, b; Bregendahl et al., 2002). In the present study, no difference in BWG was found between the control fed birds and the broilers who received the AA supplemented low CP diets. Feed conversion ratio of the broilers receiving the CP-2% and CP-3% diets was improved compared to the control fed birds. It might be that the decreased growth performance results of broilers fed the control diet could be explained by the deteriorated litter quality (Greene et al., 1985; Martland, 1985). The deteriorated litter quality (more caked and wetter) in the control group may also have led to some thermal discomfort of the birds, which may also have affected their growth performance results (especially FCR) negatively (De Jong et al., 2014).

Another reason for the deteriorated FCR of the control fed birds could be a poorer intestinal health. It is well known that high protein diets might have negative effects on gut health and performance (Qaisrani et al., 2015; Apajalahti and Vienola, 2016). Protein that was not digested up to the end of the small intestine can potentially be fermented by putrefactive bacteria in the caecum. Putrefaction produces many harmful and toxic compounds like amines, indoles, phenols, cresol and ammonia, which in high concentrations may have adverse effects on chicken growth and performance (Apajalahti and Vienola, 2016). Reduction of the protein bypassing the small intestine, by reducing the dietary CP content, might reduce the production of toxic protein fermentation metabolites in the caeca.

Moreover, the inclusion of free glycine in the low CP diets in the present study, whereby the glycine and serine recommendation (CVB, 2018) of the animal is covered, could be a reason for the similar (CP-1% and CP-3% feeding program) or even better (CP-2% feeding program) growth performance results in the low protein groups. According to Ospina-Rojas et al. (2013), supplemental glycine may be necessary to support maximum performance for broiler chickens when they are fed diets based on vegetable ingredients and with low protein levels.

The incidence of footpad lesions in the present study decreased linearly with the reduction of the dietary CP content. It is well known that the most important factor causing footpad lesions is considered to be wet litter (Shepherd and Fairchild, 2010). In the present study, the observed differences in litter quality are in good agreement with the determined footpad scores. Broilers fed the control feeding program had the lowest scores for litter quality and the highest footpad scores. The share of soybean meal decreased with the decrease in the protein content of the diets. As a result, the potassium content and the electrolyte balance (dEB) also decreased with the protein content of the diets. It is well known that water intake increases with the increase of both dEB and potassium (Mushtaq et al., 2013) and that this is the most likely reason for the deteriorated litter quality and the higher footpad score of the broilers fed the control diet. In addition to potassium, soybean meal contains also other components that can be responsible for a higher water excretion, such as fiber with high water retention capacity and fermentable sugars (Francesch and Brufau, 2004).

Reducing dietary CP resulted in a decrease of the litter moisture and nitrogen content. These results were in agreement with the findings of Ferguson et al. (1998a), Kamran et al. (2010) and Belloir et al. (2017), but not completely in line with Moran et al. (1992), Elwinger and Svensson (1996), Ferguson et al. (1998b), Khajali and Moghaddam (2006) and Ospina-Rojas et al. (2012), who also reported a decrease in the nitrogen content, but no change in the moisture content of the litter. Several studies have shown a reduction in nitrogen excretion by about 10% for each 1 percentage point reduction in the dietary CP content in broilers (Ferguson et al. (1998a); Aletor et al. 2000; Bregendahl et al., 2002). The measured reduction in total nitrogen in the present study, however, was only 3 to 4% per percentage point lower dietary CP. In this study, none of the low protein groups had a significantly lower ammoniacal N compared with the control group. This might be caused by the fact that the process of uric acid conversion to ammoniacal N is depending on a lot more factors than ammoniacal N content only. The conversion of uric acid is also influenced by temperature, pH, oxygen and moisture content (Groot Koerkamp, 1994).

In previous experiments, feeding low protein diets did not always affect litter moisture content (Elwinger and Svensson, 1996; Ferguson et al., 1998b; Hernandez et al., 2013; and Ospina-Rojas et al., 2014). Differences in season, diet composition, raw material composition, housing, animal health, equipment (e.g., drinking system) and management (in particular stocking density, ventilation and heating) could explain absence of effects on litter moisture content in the present study (Dunlop et al., 2016).

In the present study, no effects of the dietary CP content on the acidity or pH of the litter were observed, which is in agreement with previous studies (Elwinger and Svensson, 1996; Ferguson et al., 1998b; Hernandez et al., 2013 and Ospina-Rojas et al., 2014). In contrast to our study, Ferguson et al. (1998a) reported a decrease in the pH of the litter with diets with a reduction in dietary CP content. The pH of the litter is influenced by many factors that could cause these different findings, e.g., diet composition, type of bedding material, uric-acid conversion rate.

Broilers fed the CP-3% feeding program had a lower wing and breast meat yield but a higher leg and back yield compared to the control group. However, due to the higher BW at slaughter, the absolute weight of the different parts did not differ from the control fed broilers. Feeding AA supplemented diets with up to two percent lower CP did not affect the slaughter yields. These results are in line with Ospina-Rojas et al. (2014), who also found no differences in slaughter yields in diets with a 3% units reduction in crude protein AA supplemented diets. According to Ospina-Rojas et al. (2014), it is important that glycine and arginine are added to low protein diets, accompanied by the supplementation of valine and isoleucine, besides lysine, methionine and threonine, to maintain slaughter yields. In the present study, the contents of essential AA, including glycine, of the low protein diets met CVB recommendations (CVB, 2018). The results of this study regarding breast meat yield were in agreement with the study of Aletor et al. (2000), who observed no effects on slaughter yields when CP content of the diet was reduced from 225 to 153 g/kg. Belloir et al. (2017) found no effects on breast meat yield up to 3% point reduction of the CP content of the diet.

CONCLUSIONS

The present study in growing broilers showed that a 2.2–2.3% units (22–23 g/kg) reduction of the CP content of grower and finisher diets, with adequate supplementation of essential amino acids, including lysine, methionine, threonine, arginine, isoleucine, valine and glycine, did not result in adverse effects on growth performance and slaughter yields. Moreover, the CP reduction reduced nitrogen and moisture content of litter and occurrence and severity of footpad lesions. Thus, reducing dietary CP seems to be a promising approach to reduce nitrogen excretion from broiler houses and to reduce the amount of vegetable protein in broiler diets, while simultaneously improving broiler welfare.

Acknowledgements

This research was conducted within the framework of the public private partnership “Feed4Foodure”, and partially funded by “Vereniging Diervoederonderzoek Nederland” (VDN), and partially funded by the Ministry of Agriculture, Nature and Food Quality.

REFERENCES

  1. Aletor V. A., Hamid I. I., Nieß E., Pfeffer E.. 2000. Low-protein amino acid supplemented diets in broilers chickens: effects on performance, carcass characteristics, whole-body composition and efficiencies of nutrient utilization. Poult. Sci. 80:243–253. [Google Scholar]
  2. Alexandratos N., Bruinsma J.. 2012. World Agriculture Towards 2030/2050: the 2012 Revision. ESA Working paper No. 12-03; Rome, FAO. [Google Scholar]
  3. Allain V., Mirabito L., Arnould C., Colas M., Le Bouquin S., Lupo C., Michel V.. 2009. Skin lesions in broiler chickens measured at the slaughterhouse: Relationships between lesions and between their prevalence and rearing factors. Br. Poult. Sci. 50:407–417. [DOI] [PubMed] [Google Scholar]
  4. Alleman F., Leclercq B.. 1997. Effect of dietary protein and environmental temperature on growth performance and water consumption of male broiler chickens. Br. Poult. Sci. 38:607–610. [DOI] [PubMed] [Google Scholar]
  5. Apajalahti J., Vienola K.. 2016. Interaction between chicken intestinal microbiota and protein digestion. Anim. Feed Sci. Technol. 221:323–330. [Google Scholar]
  6. Bailey M. 1999. The water requirements of poultry. In: Recent developments in poultry nutrition 2 Wiseman (J, Garnsworthy PC, eds). Nottingham Univ. Press, UK.pp: 321–335. [Google Scholar]
  7. Belloir P., Méda B., Lambert W., Corrent E., Juin H., Lessire M., Tesseraud S.. 2017. Reducing the CP content in broiler feeds: impact on animal performance, meat quality and nitrogen utilization. Animal. 11:11, pp: 1881–1889. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Berg C. 1998. Footpad dermatitis in broilers and turkeys. Doctoral diss. Dept. of Animal Environment and Health, SLU. Acta Universitatis Agriculturae Sueciae, Sweden. [Google Scholar]
  9. Bregendahl K., Sell J. L., Zimmerman D. R.. 2002. Effect of low-protein diets on growth performance and body composition of broiler chicks. Poult. Sci. 81:1156–1167. [DOI] [PubMed] [Google Scholar]
  10. CVB 2012. Livestock Feed Table (Tabellenboek Veevoeding); Tables Values Poultry Nutrition. 2012. Centraal Veevoederbureau, Lelystad, the Netherlands. [Google Scholar]
  11. CVB 2018. Tabellenboek Veevoeding 2018. Voedernormen Pluimvee en voederwaarden voedermiddelen voor Pluimvee [Livestock feed table 2018. Tables values poultry nutrition and feed values raw materials for Poultry]. CVB-reeks nr. 60. Juli 2018. [Google Scholar]
  12. Dean D. W., Bidner T. D., Southern L. L.. 2006. Glycine supplementation to low protein, amino acid-supplemented diets supports optimal performance of broiler chicks. Poult. Sci. 85:288–296. [DOI] [PubMed] [Google Scholar]
  13. De Jong I. C., Gunnink H., van Harn J.. 2014. Wet litter not only induces footpad dermatitis but also reduces overall welfare, technical performance, and carcass yield in broiler chickens. J. Appl. Poult. Res. 23:51–58. [Google Scholar]
  14. Dunlop M. W., Moss A. F., Groves P. J., Wilkinson S. J., Stuetz R. M., Selle P. H.. 2016. The multidimensional causal factors of ‘wet litter’ in chicken-meat production. Sci. Total Environ. 562:766–776. [DOI] [PubMed] [Google Scholar]
  15. Elwinger K., Svensson L.. 1996. Effect of dietary protein content, litter and drinker type on ammonia emission from broiler houses. J. Agric. Eng. Res. 64:197–208. [Google Scholar]
  16. EU , 2017. https://ec.europa.eu/agriculture/market-observatory/crops/oilseeds-protein-crops/balance-sheets_en. [Google Scholar]
  17. Euractiv 2011. MEPs want to end ‘protein deficit’ for EU livestock. https://www.euractiv.com/section/agriculture-food/news/meps-want-to-end-protein-deficit-for-eu-livestock/. [Google Scholar]
  18. Evonik 2010. Total Amino Acid Contents in Feed – Method Oxidation and Hydrolysis. AMINODat 4.0. Evonik Industries, Evonik Degussa GmbH, Hanau-Wolfgang, Germany. [Google Scholar]
  19. FAO 2009. Global agriculture towards 2050. High Level Expert Forum - How to Feed the World in 2050. Rome, 12–13 October 2009. [Google Scholar]
  20. FAO 2017. The future of food and agriculture – Trends and challenges. Rome. [Google Scholar]
  21. Ferguson N. S., Gates R. S., Taraba J. L., Cantor A. H., Pescatore A. J., Ford M. J., Burnham D. J.. 1998a. The effect of dietary crude protein on growth, ammonia concentration, and litter composition in broilers. Poult. Sci. 77:1481–1487. [DOI] [PubMed] [Google Scholar]
  22. Ferguson N. S., Gates R. S., Taraba J. L., Cantor A. H., Pescatore A. J., Straw M. L., Ford M. J., Burnham D. J.. 1998b. The effect of dietary protein and phosphorus on ammonia concentration and litter composition in broilers. Poult. Sci. 77:1085–1093. [DOI] [PubMed] [Google Scholar]
  23. Francesch M., Brufau J.. 2004. Nutritional factors affecting excreta/litter moisture and quality. World's Poult. Sci. J. 60:64–75. [Google Scholar]
  24. Greene J. A., McCracken R. M., Evans R. T.. 1985. A contact dermatitis of broilers – Clinical and pathological findings. Avian Pathol. 14:23–38. [DOI] [PubMed] [Google Scholar]
  25. Groot Koerkamp P. W. G. 1994. Review on emissions of ammonia from housing systems for laying hens in relation to sources, processes, building design and manure handling. J. Agricultural Engineering. 59:73–87. [Google Scholar]
  26. Hernandez F., Megias M. D., Orengo J., Martinez S., Lopez M. J., Madrid J.. 2013. Effect of dietary protein level on retention of nutrients, growth performance, litter composition and NH3 emission using a multi-phase feeding programme in broilers. Span. J. Agric. Res. 11:736–746. [Google Scholar]
  27. International Organization for Standardization 1997. Animal feeding stuffs. Determination of nitrogen content and calculation of crude protein content. Kjeldahl method. ISO 5983. Int. Organ. Standardization, Geneva, Switzerland. [Google Scholar]
  28. International Organization for Standardization 1998. Animal feeding stuffs. Determination of moisture and other volatile matter content. ISO 6496. Int. Organ. Standardization, Geneva, Switzerland. [Google Scholar]
  29. International Organization for Standardization 2000. Animal feeding stuffs. Determination of crude fibre content. Method with intermediate filtration. ISO 6865. Int. Organ. Standardization, Geneva, Switzerland. [Google Scholar]
  30. International Organization for Standardization 2002. Animal feeding stuffs. Determination of crude ash. ISO 5984. Int. Organ. Standardization, Geneva, Switzerland. [Google Scholar]
  31. Kamran Z., Sarwar M., Nisa M. U., Nadeem M. A., Mahmood S.. 2010. Effect of low levels of dietary crude protein with constant metabolizable energy on nitrogen excretion, litter composition and blood parameters of broilers. Int. J. Agric. Biol. 12:401–405. [Google Scholar]
  32. Khajali F., Moghaddam H. N.. 2006. Methionine of low protein broiler diets: Influence upon growth performance and efficiency of protein utilization. Int. J. Poult. Sci. 5:569–573. [Google Scholar]
  33. Kidd M. T., Kerr B. J., Firman J. D., Boling S. D.. 1996. Growth and carcass characteristics of broilers fed low-protein, threonine-supplemented diets. J. Appl. Poult. Res. 5:180–190. [Google Scholar]
  34. Martland M. F. 1985. Ulcerative dermatitis in broiler chickens – The effect of wet litter. Avian Pathol. 14:353–364. [DOI] [PubMed] [Google Scholar]
  35. Moran E. T. Jr., Bushong R. D., Bilgili S. F.. 1992. Reducing dietary crude protein for broilers, while satisfying amino acids requirements by least cost formulations: Live performance, litter composition and yield of fast food carcass cuts at six weeks. Poult. Sci. 71:1687–1694. [Google Scholar]
  36. Mushtaq M., Pasha T., Mushtaq T., Parvin R.. 2013. Electrolytes, dietary electrolyte balance and salts in broilers: An updated review on growth performance, water intake and litter quality. World's Poult. Sci. J. 69:789–802. [Google Scholar]
  37. Nahm K. H. 2002. Efficient feed nutrient utilization to reduce pollutants in poultry and swine manure. Critical Rev. Environ. Sci. Tech. 32:1–16. [Google Scholar]
  38. Namroud N. F., Shivazad M., Zaghari M.. 2008. Effects of fortifying low crude protein diet with crystalline amino acids on performance, blood ammonia level, and excreta characteristics of broiler chicks. Poult. Sci. 87:2250–2258. [DOI] [PubMed] [Google Scholar]
  39. NEN 7432 1998 Manure and derivatives - Determination of the contents of dry matter and organic matter - Gravimetric method. [Google Scholar]
  40. NEN 7434 1998 Manure and derivatives - Determination of the nitrogen content in digests. [Google Scholar]
  41. NEN 7438 1997 Manure and derivatives - Determination of the ammoniacal nitrogen content - Titrimetric method. [Google Scholar]
  42. NEN-EN-ISO 15914 2005Animal feeding stuffs - Enzymatic determination of total starch content. [Google Scholar]
  43. Ospina-Rojas I. C., Murakami A. E., Eyng C., Nunes R. V., Duarte C. R., Vargas M. D.. 2012. Commercially available amino acid supplementation of low-protein diets for broiler chickens with different ratios of digestible glycine+serine:lysine. Poult. Sci. 91:3148–3155. [DOI] [PubMed] [Google Scholar]
  44. Ospina-Rojas I. C., Murakami A. E., Oliveira C. A., Guerra A. F. Q. G.. 2013. Supplemental glycine and threonine effects on performance, intestinal mucosa development, and nutrient utilization of growing broiler chickens. Poult. Sci. 92:2724–2731. [DOI] [PubMed] [Google Scholar]
  45. Ospina-Rojas I. C., Murakami A. E., Duarte C. R. A., Eyng C., Oliveira C. A. L., Janeiro V.. 2014. Valine, isoleucine, arginine and glycine supplementation of low-protein diets for broiler chickens during the starter and grower phases. Br. Poult. Sci. 55:766–773. [DOI] [PubMed] [Google Scholar]
  46. Qaisrani S. N., van Krimpen M. M., Kwakkel R. P., Verstegen M. W. A., Hendriks W. H.. 2015. Dietary factors affecting hindgut protein fermentation in broilers: A review. Worlds Poult. Sci. J. 71:139–160. [Google Scholar]
  47. Shepherd E. M., Fairchild B. D.. 2010. Footpad dermatitis in poultry. Poult. Sci. 89:2043–2051. [DOI] [PubMed] [Google Scholar]
  48. Van Gelder J. W., Kuepper B.. 2012. Verdeling van de economische waarde van de mondiale sojateelt. Edited by Profundo. Amsterdam. [Google Scholar]
  49. Van Harn J., van Middelkoop J. H.. 1996. Invloed van eiwitverlaging in voer op resultaten en stikstofuitscheiding bij vleeskuikens. Praktijkonderzoek 96/2. [Google Scholar]
  50. Veldkamp T., Dekker R., Smit-Heinsbroek A., van der Lee A., Jansman A. J. M.. 2017. Effect of isoenergetic exchange of dietary fat and starch on growth performance and body composition of broilers – Experiment 2. Wageningen, Wageningen Livestock Research, Livestock Research Report 1062. [Google Scholar]
  51. WNF 2011. Http://www.Wnf.Nl/nl/wat_wnf_doet/thema_s/bossen/ontbossing/sojateelt/. [Google Scholar]

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