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Poultry Science logoLink to Poultry Science
. 2020 Sep 12;99(12):6705–6714. doi: 10.1016/j.psj.2020.09.009

Effect of feed form, soybean meal protein content, and Rovabio Advance on poult live performance to 3 wk of age

KR Flores 1, AC Fahrenholz 1, JL Grimes 1,1
PMCID: PMC7704967  PMID: 33248586

Abstract

Based on research reports, feed characteristics can increase poult growth via several factors. Two rearing experiments (EXP) were conducted to test the effects of feed form and ingredient quality in turkey poults. Bird performance and the duodenum, jejunum, ileum, and cecum morphology were observed in both EXP. Poults were reared in battery cages (48 cages in EXP 1 and 72 cages in EXP 2). Four dietary treatments with differing feed form and function factors were evaluated in EXP 1. A completely randomized block design with a 2 × 2 × 2 factorial arrangement of treatments consisting of 2 levels of fines, 2 soybean meal (SBM) sources, and 2 levels of an enzyme cocktail (Rovabio Advance) was tested in EXP 2. Poult BW, BW gain (BWG), feed intake (FI), and feed conversion ratio (FCR) were determined in both EXP. Apparent metabolizable energy corrected for nitrogen (AMEn) was determined in EXP 2. Differences were considered to be statistically significant at P ≤ 0.05. Feeding increased feed crumble particle size with fewer fines in the starter feed resulted in an increased BWG accompanied by an increased FI. Reduced feed fines reduced AMEn when the dietary enzyme cocktail was not present. The feed formulation with 60% CP SBM resulted in a lower FI and an improved FCR. The enzyme cocktail interacted synergistically with screening and fed SBM source factors on the AMEn and FCR. It was concluded that both the feed form and quality, as used in this study, affect poult performance.

Key words: feed form, feed quality, particle size, enzyme, soybean meal

Introduction

Increasing market demand for birds reared without the use of antibiotic growth promoters (AGP) such as “antibiotic-free programs” or “no antibiotics ever” is creating concerns and opportunities for the poultry industry (Gould, 2017; Rubin, 2014; Olenjnik, 2016). Consumers have stated preferences for reduced purchases of meat produced with antibiotics (Dibner and Richards, 2005; Polansek, 2014; Huffstutterand and Baertlein, 2015; Calderone, 2017). Therefore, new goals are being developed to reduce the rearing of poultry, such as turkeys and broilers, using less antibiotics (Butterball, 2018; Perdue, 2018). Eliminating dietary inclusion of AGP can adversely affect digestibility by allowing the proliferation of enteric fermentative organisms (Montagne et al., 2003). Fermentative organisms proliferate in the small intestine because of the increased digesta retention time when nonstarch polysaccharides (NSP) are present in the feed (Choct et al., 1996; Choct, 1997). Feed NSP values are especially crucial during the starter phase when young birds have an immature microbiota and their dietary level NSP from soybean meal (SBM) can be higher than for older birds (Choct et al., 2010). Thus, controlling the antinutritional effects of NSP in starter diets could have a significantly positive impact on AGP, antibiotic-free programs, and no-antibiotics-ever production systems.

An increased feed intake (FI) and reduced feed wastage in young birds can be encouraged by reducing the abundance of fines in the starter crumble feed at placement. An early FI is an essential factor affecting the poult performance and gut health (Noy et al., 2001), and the initial FI is also critical in the transition from a yolk-based diet to a feed-based diet (Uni and Ferket, 2004). Although there is an established understanding of the nutritional requirements for the starter phase, the evaluation of the abundance of fines fed to poults must be further examined. Corn and SBM-based diets contain high amounts of NSP, which are classified as antinutritional and can be detrimental to growth performance and health (Choct, 1997; Montagne et al., 2003). Although SBM contains a high amount of protein, it also includes a significant amount (35%) of indigestible carbohydrates (Choct et al., 2010). Less than 1% of SBM carbohydrates are considered starch; the rest are deemed free sugars and NSP (Choct et al., 2010). Consequently, grain and plant protein by-product NSP contents have a significant effect on the feed quality, enzyme efficiency, and poult growth performance. New varieties of SBM with high CP levels could be associated with reduced NSP content and thus result in better growth performance for turkey poults consuming high-protein starter feed. Moreover, this new variety of high-protein SBM should be tested with supplemental enzymes that are already used to reduce the adverse effects of dietary NSP.

The use of a high-CP SBM in the starter feed may enhance the growth performance characteristics, increase feed digestibility, and affect the duodenum, jejunum, and cecum morphology during the starter feed phase of turkeys. Crumble quality in this work is defined as the percentage of fines in the crumbles offered to the bird. Birds will prehend feed particles according to their beak size and mechanoreceptors in the beak (Moran, 1982). However, beak conditioning is a common practice in turkeys at the hatchery, resulting in a shortened upper beak with an effect to reduce injuries to birds by reducing bird-to-bird pecking. Beak conditioning may lead to consumption issues and feed wastage when excessive fines are present. Minipelleting or micropelleting the starter feed phase could reduce the abundance of fines and increase the particle size in comparison to crumbles. Alternatively, feed milling procedures to increase the particle size of crumbles with reduced fine content could be an option to consider.

The objective of this work was to determine the effects of the feed particle size, feed enzymes, and increased relative CP content of SBM on turkey poult performance, feed digestibility, and effects on the poult duodenum, jejunum, and cecum morphology.

Materials and methods

Treatments and Experimental Design

For the first experiment (EXP), treatment 1 (control) was an all-vegetable–based crumble feed. Treatment 2 (medicated three-way) was as treatment 1 but with the inclusion of 3 medications: amprolium (113.5 g per ton of feed), bacitracin (125 g per ton of feed), and penicillin (125 g per ton of feed). The United States Food and Drug Administration approval for the use of medications combined with penicillin was withdrawn in June 2015. However, this three-way feed treatment was used as an example of past industry practices for improving poult performance. The control and three-way feed were formulated based on breeder recommendations using typical commercial turkey industry corn-SBM–based diets. AlphaStart is a commercial proprietary feed with a combination of phytogenic, probiotic, and prebiotic feed additives (Devenish Nutrition LLC, Fairmont, MN).Nutrient composition is provided in Table 1, Table 2, Table 3. Treatment 3 (AlphaStart Crumble) was a mash AlphaStart turkey starter pelleted and crumbled at North Carolina State University (NCSU). Treatment 4 (AlphaStart Mini) was an outsourced AlphaStart 2-mm minipellet turkey starter. Treatments 3 and 4 were from the same basal mix, and test ingredients were hand-added. The hand-adds were checked against batch records. Although the manufacturer shared no specific nutritional or ingredient information, these diets were formulated to be isonitrogenous and isocaloric to treatments 1 and 2. The basal feed was minipelleted, achieving a 2,000-μm pellet size at the Devenish feed mill in Maquoketa, IA. The control crumbles and three-way medicated feeds were formulated to be isocaloric and isonitrogenous with AlphaStart diets (Table 1). Treatment diets were randomly assigned to one of 48 cages of poults (7 poults/cage), with 12 replicate cages of poults per treatment. AlphaStart minipellet, AlphaStart crumble, and medicated three-way were fed from 0 to 14 d of age and then all pens of birds were fed treatment 1 (control crumble) from 14 to 21 d.

Table 1.

Diet composition in experiments 1 and 2.

Ingredient (%) Starter experiment one1
Starter experiment 22
Control Three-way
Medicated2
Low-CP SBM3 High-CP SBM4
Corn 35.00 34.90 44.87 47.50
Wheat 10.00 9.97 2.50 3.00
Wheat middlings 0.00 0.00 1.00 6.00
Soybean meal 43.00 42.88 42.00 34.00
Soybean oil 5.00 4.99 2.00 2.03
Calcium carbonate 2.20 2.19 2.30 2.30
Monocalcium phosphate 2.55 2.54 3.30 3.30
Salt 0.25 0.25 0.23 0.23
Mineral mix5,6 0.15 0.15 0.20 0.20
Vitamin mix7 0.15 0.15 0.15 0.15
Selenium mix 0.05 0.05 0.05 0.05
Choline chloride 0.20 0.20 0.20 0.20
Lysine8 0.61 0.61 0.54 0.40
Methionine9 0.50 0.50 0.32 0.30
Sodium bicarbonate 0.20 0.20 0.25 0.25
Threonine8 0.15 0.15 0.10 0.10
Quantum Blue 5G 0.01 0.01 - -
Amprolium1 - 0.05 - -
Penicillin1 - 0.104 - -
BMD 601;10 - 0.104 - -
Ingredient total 100 100 100 100

Abbreviation: SBM, soybean meal.

1

AlphaStart ingredient composition information was not provided.

2

Two basal feeds were formulated with the 2 different sources of soybean meal, one with 48% CP and the other one with 60% CP.

3

High-CP soybean meal, 60% CP.

4

Low-CP soybean meal, 48% CP.

5

In experiment 1, the mineral premix provided the following per kg of diet: manganese, 90 mg; zinc, 90 mg; iron, 60 mg; copper, 7.5 mg; iodine, 1.9 mg; cobalt, 0.75 mg.

6

In experiment 2, the mineral premix provided the following per kg of diet: manganese, 120 mg; zinc, 120 mg; iron, 80 mg; copper, 10 mg; iodine, 2.5 mg; cobalt, 1 mg.

7

Donated by DSM Nutritional Products; vitamin premix provided the following per kg of diet: vitamin A, 19,841 IU; vitamin D3, 5952 IU; vitamin E, 99 IU; vitamin B12, 0.06 mg; biotin, 0.38 mg; menadione, 6 mg; thiamine, 6 mg; riboflavin, 20 mg; pantothenic acid, 33 mg; vitamin B6, 12 mg; niacin, 165 mg; folic acid, 3 mg.

8

Ajinomoto North America.

9

Evonik North America.

10

Bacitracin Methylene Disalicylate (BMD) 60 g per pound of feed.

Table 2.

Estimated NSP1 composition (%) for ingredients in experiment 2.

Antinutritional Factor Corn2 Wheat2 Wheat middlings1,4 SBM Total
Feed formulated with 48% CP SBM2,5
Soluble NSP 1.12 0.05 0.01 4.73 5.91
Insoluble NSP 1.70 0.16 0.23 2.42 4.50
Cellulose 0.76 0.03 0.07 3.36 4.22
Total NSP 3.63 0.24 0.31 10.50 14.68
Feed formulated with 60% CP SBM3,6
Soluble NSP 1.19 0.06 0.07 0.69 2.01
Insoluble NSP 1.81 0.19 1.36 0.35 3.71
Cellulose 0.81 0.04 0.40 0.49 1.74
Total NSP 3.85 0.29 1.84 1.54 7.51

Abbreviation: NSP, nonstarch polysaccharides.

1

Values estimated using feed formulation and estimated ingredient nonstarch polysaccharides.

2

Values adapted and estimated from Jaworski et al. (2015).

3

Values adapted and estimated from Choct et al. (2010).

4

Values adapted from Choct et al. (2010) corrected with analyzed values.

5

Soybean meal source with 48% CP.

6

Soybean meal source with 60% CP.

Table 3.

Calculated nutrient contents (%) for diets in experiments 1 and 2.

Nutrient Starter experiment one1
Starter experiment 22
Control Three-way medicated Low-CP SBM3 High-CP SBM4
CP 26.60 26.53 25.86 25.79
ME (kcal/kg) 2,983.00 2,975.00 2,820.00 2,836.00
Crude fat 7.14 7.12 4.39 4.48
Lysine 1.82 1.81 1.74 1.74
Methionine 0.82 0.82 0.65 0.64
Methionine + cysteine 1.18 1.18 1.01 1.01
Tryptophan 0.32 0.32 0.32 0.31
Threonine 1.08 1.08 1.03 1.01
Arginine 1.65 1.65 1.64 1.71
Valine 1.19 1.19 1.18 1.26
Calcium 1.45 1.45 1.52 1.51
Available phosphorus 0.72 0.72 0.75 0.76
Sodium 0.19 0.19 0.19 0.19
Chloride 0.21 0.21 0.19 0.20
1

AlphaStart ingredient composition information was not provided.

2

Two basal feeds were formulated with the 2 different sources of soybean meal, one with 48% CP and the other one with 60% CP.

3

Low-CP soybean meal, 48% CP.

4

High-CP soybean meal, 60% CP.

For EXP 2, a completely randomized block design with a 2 × 2 × 2 factorial arrangement of treatments was used. In EXP 2, 2 sources of SBM was used: a feed formulated with high CP SBM (60% CP SBM) and a feed formulated with a standard CP SBM (48% CP SBM). The second factor was the reduction of fines in the diet: reduced feed fines (RFF) and increased feed fines (IFF). The third factor was the presence (200 mL/mt) or absence of an enzyme cocktail containing arabinofuranosidases and xylanases (Rovabio Advance, Adisseo France S.A.S, Antony, France). Treatments diets were randomly assigned to one of 72 cages of poults (7 poults/cage), with 9 replicate cages of poults per treatment.

Housing and Management

In both EXP, Petersime battery cages (Petersime Incubator Co., Gettysburg, OH) were used. The cages had wire floors, and each was equipped with a trough drinker and feeder and a thermostatically controlled cage heater. The ambient temperature was gradually decreased from 95°F at placement to 85°F at 21 d of age. Humidity was approximately 55%. Twenty-three hours of light per day was provided.

Poult Origin and Management

Experiment 1 was conducted with 336 male Nicholas Select poults (Aviagen Turkeys, Lewisburg, WV) placed on the day of hatch. Poults were weighed individually at placement and on days 7, 14, and 21. Experiment 2 was conducted with 504 Nicholas Select female poults (Aviagen Turkeys) placed on the day of hatch. Poults were weighed individually at placement and on days 7, 14, and 21. The weight of each cage of birds plus culls and mortalities was used to determine the feed conversion ratio (FCR). Poults consumed feed and water ad libitum throughout the EXP. Birds were checked a minimum of 4 times per day. All bird handling procedures were approved by the NCSU Institutional Animal Care and Use Committee.

Feed Manufacturing

For EXP 1, both the control and the three-way medicated starter feeds were manufactured at the NCSU Feed Mill Education Unit. Corn was milled with a hammer mill using 6/8 screens (model 1522, Roskamp Champion, Waterloo, IA) generating corn with a particle size of 300 μm. The basal diets for these 2 feeds were batched and blended in a counterpoise ribbon mixer (model TRDB126060, Hayes & Stolz, Fort Worth, TX) for 3 min of a dry mix followed by 90 s of a wet mix. The AlphaStart (in the mash form and already blended), the control, and the three-way medicated starters were then conditioned for 30 s at 175°F in a single pass conditioner (model C18LL4/F6, California Pellet Mill, Crawfordsville, IN). The feeds then were pelleted by a 30-HP pellet mill (model PM1112-2, California Pellet Mill, Crawfordsville, IN), using an 11/64” × 1 3/8″ pellet mill die. The pellets of each feed were cooled in a counterflow cooler (model VK09X09KL, Geelen Counterflow USA, Inc., Orlando, FL), and then crumbled (model 624s, Roskamp Champion). The treatment 4 diet, the AlphaStart minipellet, was provided by Devenish Nutrition (Devenish Nutrition LLC, Fairmont, MN).

For EXP 2, all feed were manufactured at the NCSU Feed Mill Educational Unit. Two basal feed formulations were used to create the 8 total combinations of feed treatments. One basal feed was manufactured with a 48% CP SBM and the other with 60% CP SBM. All treatment feeds were formulated to the same CP and amino acid levels. Celite (Celite, Millipore Sigma, Darmstadt, Germany) was added at 2% to both basal feeds as an indigestible marker to determine AMEn. Each basal feed was mixed in a counterpoise ribbon mixer (model TRDB126060, Hayes & Stolz), conditioned in a single pass conditioner (model C18LL4/F6), and pelleted in a 30-HP pellet mill (model PM1112-2), using an 11/64” × 1 3/8″ pellet mill die. The pellets of each feed were cooled in a counterflow cooler (model VK09X09KL, Geelen Counterflow USA, Inc.), crumbled (model 624S, Roskamp Champion), and split into 4 batches for further processing. The first 2 batches were sent to a double-ribbon mixer (model SRM304, Scott equipment, New Prague, MN); the first was mixed for 1.5 min with no additions, whereas the second had the enzyme (Rovabio Advance, 200 mL/metric ton in 1 L water) added before mixing. The other 2 batches were sent to a pellet shaker (model 2 × 4 two-decker general Roto-shaker, Andritz Sprout-Bauer, Inc, Muncy, PA) with U.S. Tyler 6 and 10 screens to reduce the abundance of feed fines. The screened diets were then sent to a mixer, and the enzyme was added to one batch. This entire process was completed for both SBM types, thus achieving 8 feed treatments.

Feeding Program

One starter feed phase, by treatment, was provided to day 14 ad libitum to the poults in EXP 1. All feed allocations were weighed to the nearest gram. The weight of feed remaining in feeders at the end of each data collection period was recorded. All feeders were dumped at 14 d. All poults were then fed the treatment 1 control crumble feed from 14 to 21 d of age. Feed allocation and feed weigh backs were used to determine poult feed consumption. The FCR was calculated using all birds, including weights of mortalities and culled birds.

In EXP 2, each starter feed treatment was fed ad libitum to all birds from placement to 20 d of age. The weight of feed issued was recorded when added to feeders and at 7, 14, and 20 d of age to calculate the bird FI and FCR.

Feed Analysis

For both EXP, proximate analysis (250 g) was outsourced for DM, CP, crude fat, minerals, and total lysine for samples of each dietary treatment feed (Carolina Analytical Services, Bear Creek, NC). For EXP 2, ingredient NSP calculations were based on analysis and published reviews (Choct et al., 2010; Jaworski et al., 2015). The estimated NSP content for the 60% CP SBM was calculated with laboratory analysis and completed with minerals and NSP ratios assumptions by Choct et al. (2010). The total estimated NSP content was calculated using the percentage of corn, wheat, wheat middlings, and SBM present in the formulation and each ingredient's estimated NSP content (Table 2). No analyses for test ingredients in any treatment were performed; however, all were hand-added directly to the mixer and confirmed against batch records.

Particle Size Determination

For both EXP, the particle size and variation calculations were determined using the American Society of Agricultural and Biological Engineers standard 319.4 methodologies. Treatment composite samples were collected from each feed bag. Three subsamples were collected from each composite sample after being homogenized. From each subsample, 100 g of feed and 0.5 g of sieve aid were weighed for sieve analysis. The sieves used were U.S. sieves 4, 6, 8, 12, 16, 20, 30, 40, 50, 70, 100, 140, 200, 270, and a collection pan. The group of sieves was shaken in a sieve shaker (Ro-Tap Model RX-29, W.S. Tyler Industrial Group, Mentor, OH) for 15 min. The feed present on each sieve was weighed in grams and analyzed per formulas described in the American Society of Agricultural and Biological Engineers standard 319.4 methodologies for the log-normal mean particle size and SD. Pellets were defined as the feed retained on U.S. sieve number 4, crumbles were defined as the feed retained on U.S. sieve numbers 6 and 12, and fines were defined as all feed passing through U.S. sieve number 12.

AMEn Sampling and Analysis

The AMEn analysis was performed only in EXP 2. Fecal samples (100 g) were collected from cage pans on 13, 14, and 15 d of age from every cage. On the third day of sampling, the 3 d of samples were mixed in a single bag for each pen of birds. The samples were then dried in a Blue M drying oven (General Signal, Blue Island, IL) for 48 h at 60°C. The dried samples were ground and analyzed in duplicate for gross energy, protein, and insoluble ash (Celite, Millipore Sigma, Darmstadt, Germany) content to calculate the AMEn. The gross energy was determined using a plain jacket bomb calorimeter (model 1341, Parr Instrument Company, Moline, IL) using the Parr instrument procedure. The protein content was estimated by multiplying the nitrogen content of the samples by 6.25. The nitrogen content in the samples was analyzed by the LECO Truespec N analyzer (Leco Corporation, St. Joseph, MI) using the Dumas method. Insoluble ash content was determined (Vogtmann et al., 1975).

Duodenum, Jejunum, Ileum, and Cecum Morphology

In EXP 2, one poult per cage was chosen randomly and sampled at 14 and 21 d of age for the duodenum, midgut, and cecum. Samples were prepared for histology and analyzed by Veterinary Diagnostics Pathology, LLC, at Fort Valley, VA.

In EXP 2, small intestine and cecum samples were collected from one bird per cage on 20 d of age. Samples were taken from the duodenal loop, jejunum, and ceca and then submerged in neutral buffered formalin. Samples were trimmed and tinted in slides at NCSU College of Veterinary Medicine. Slides were observed under a microscope and photographed and then measured with AmScope software (version 3.7, AmScope, Irvine, CA) corrected with a 4× magnification. Measurements were for the villus height, crypt depth, and muscular thickness. Up to 10 subsamples were taken per measurement per slide.

Statistical Analysis

Both EXP 1 and EXP 2 had a completely randomized block design. The effect of feed treatment on performance parameters and intestinal tissue observations was determined using the GLM procedure of JMP Pro 12 (SAS Institute, Cary, NC) for ANOVA for EXP 1. Data for EXP 2 were analyzed using the PROC MIXED procedure from SAS, version 9.4. (SAS Institute, Cary, NC). For both EXP, the pen was the experimental unit for comparisons of performance, whereas for intestinal comparisons, the experimental unit was the bird. The intestinal subsamples and the person taking the measurements of the subsamples were nested in the bird using a Proc mixed model. For both EXP, significant differences in main effects were separated using the Tukey HSD test. A P ≤ 0.05 was used to set a significant difference between the primary and interaction effects of the parameters analyzed.

Results

Feed Analysis

Calculated nutrient content for NCSU-manufactured feed is presented in Table 3. Results for the nutrient analysis of all 4 feeds are presented in Table 4 and are reflective of the calculated nutrient content.

Table 4.

Feed nutrient analysis1 (%) and feed physical characteristics for diets in experiments 1 and 2.

Nutrient Experiment 1
Experiment 2
NCSU
Control
Three-way
Medicated
Alpha Crum2 Alpha
Mini2
High-CP SBM3
Low-CP SBM4
IFF5
RFF6
IFF5
RFF6
NEnz7 WEnz8 NEnz7 WEnz8 NEnz7 WEnz8 NEnz7 WEnz8
Moist 13.57 13.59 13.07 13.03 13.51 14.56 14.12 14.15 14.01 14.16 13.49 13.62
Fat 6.16 5.80 4.03 4.77 3.43 3.55 3.33 3.50 3.73 3.70 4.17 3.63
Protein 26.69 26.57 26.73 25.55 25.73 27.39 29.66 29.35 28.30 27.00 27.76 29.03
Ash 7.18 7.08 7.06 6.96 8.39 8.50 8.69 8.80 8.69 9.00 8.54 8.21
P 0.79 0.93 0.84 0.84 0.85 0.8 0.92 0.89 1.03 1.00 0.95 0.79
Ca 1.39 1.45 1.27 1.30 1.49 1.58 1.46 1.40 1.67 1.77 1.47 1.56
Na 0.19 0.17 0.13 0.15 0.16 0.14 0.16 0.17 0.17 0.17 0.14 0.16
Lysine 1.95 1.98 1.92 1.93 - - - - - - - -
Dwg9 919 930 1,102 2,440 1,655 1,188 1,508 1,666 1,337 1,420 1,702 1,436
Swg10 2.44 2.44 2.51 1.73 2.83 3.23 2.77 2.3 3.033 3.13 2.47 2.4
Crums11 71 69 71 - 57 44 70 72 50 56 78 61
Fines12 29 31 29 - 38 52 30 28 47 40 22 39
1

Feed analysis was performed by Carolina Analytical Services (17570 NC Highway 902, Bear Creek, NC 27207).

2

The AlphaStart Crumble and minipellet feeds were provided by Devenish Nutrition and came from the same batch.

3

High-CP soybean meal, 60% CP.

4

Low-CP soybean meal, 48% CP.

5

Increased feed fine feed not screened by U.S. sieves 6 and 12.

6

Reduced feed fine feed screened and retained by U.S. sieves 6 and 12.

7

No enzyme cocktail added.

8

200 ml/mt enzyme cocktail added, (Rovabio Advance, Adisseo France S.A.S, Antony, France).

9

Geometric mean diameters of the particle by mass.

10

The geometric SD of the particle diameter by mass.

11

Crumbles determined as feed under U.S. sieve number 12.

12

Fines determined in crumbles as feed over U.S. sieve number 12.

Treatment Particle Size

In EXP 1, the particle size of the minipellets was twice that of the crumble feeds. The abundance of fines in the crumbled feeds was determined to be approximately 30%. The minipellet feed was not measured for fines, as few to none were observed (Table 4).

In EXP 2, RFF feed had a larger feed particle size (1,504 μm compared with 1,474 μm) and a lower SD for its sample distribution than the IFF feed (Table 4). The IFF feed had a higher abundance of fines present in the feed. The RFF feed had a mean percentage of 30% fines and 70% crumbles, while IFF consisted of 44% fines, 52% crumbles, and 4% pellets.

Performance Parameters

In EXP 1, no differences due to treatment were observed for the BW of the bird at placement (59 ± 0.5 g) or in any performance parameter at 7 d of age. The poults fed the AlphaStart minipellet had higher cumulative BW gain (BWG) at 14 d, followed by the birds fed the AlphaStart crumble (Table 5). It appears that there was possibly both a form and function advantage to the AlphaStart minipellet as compared with the control crumble, or the three-way medicated feeds. Although the pattern of the treatment means comparison for the BWG appear to be similar at 21 and 14 d, the means for treatments at 21 d were not as easily separated statistically as the means for treatments at 14 d. This may be potentially due to the substantial increase in the SEM at 21 d compared with the SEM at 7, 7 to 14, and 0 to 14 d. At 14 d, the birds fed the medicated diet had a lower FI, and the birds fed the control diet had a higher FCR than birds fed the other diets. As the EXP proceeded by only feeding the control feed from 14 to 21 d, birds previously fed the AlphaStart minipellet treatment consumed more feed and had a higher BW and a similar FCR than those fed the medicated diet (Table 5).

Table 5.

Effect of feed treatment on poult performance (g) in experiment 1.

Treatment1 Age (day)
0–7 7–14 14–21 0–14 0–21
BWG2
Control crumble 116 250b 417 365c 773b
Medicated three-way crumble 115 261a,b 498 376b,c 773b
AlphaStart crumble 119 270a 392 389a,b 781a,b
AlphaStart minipellet 122 276a 414 398a 812a
SEM3 2.99 4.11 9.05 4.63 9.5
P-value 0.36 0.0004 0.17 0.0001 0.02
Feed intake
Control crumble 125 285b 594 410b 1004a,b
Medicated three-way crumble 125 281b 558 404b 964b
AlphaStart crumble 125 299a,b 570 424a,b 996a,b
AlphaStart minipellet 127 309b 598 435a 1034a
SEM3 1.94 5.0 13.9 6.0 16.00
P-value 0.91 0.001 0.14 0.004 0.02
Feed conversion ratio (feed:gain)
Control crumble 1.055 1.517a 1.775 1.112a 1.258a
Medicated three-way NCSU crumble 1.094 1.425b 1.764 1.079b 1.224b
AlphaStart crumble 1.059 1.410b 1.778 1.085b 1.251a,b
AlphaStart minipellet 1.035 1.432b 1.767 1.089b 1.252a,b
SEM3 0.025 0.020 0.037 0.007 0.009
P-value 0.43 0.003 0.99 0.001 0.05

a-cMeans within a column lacking a common superscript differ (P ≤ 0.05).

Abbreviation: NCSU, North Carolina State University.

1

Treatments were fed to birds until 14 d; from 14 to 21 d all, birds received the control feed.

2

The BW at placement was not significantly different (59 ± 0.5 g).

3

The SEM for n = 12 cages of 7 birds each per treatment.

In EXP 2, no differences due to treatment were observed for the BW at placement (57 ± 0.26 g). Birds fed RFF had a significantly higher BWG than those fed IFF (Tables 6 and 7). The FI was significantly higher for birds fed the RFF and low CP SBM feed treatment diets than those fed the IFF and feed formulated with a high CP SBM treatment throughout the EXP (Tables 6 and 7). The poult FCR was significantly improved at 7 and 14 d for birds fed feed formulated with the high CP SBM. At 20 d, feed with low and high SBM sources interacted with the dietary enzyme. Birds fed feed formulated with a low CP SBM had a significantly lower FCR when the enzyme was present compared with when the enzyme was not present. Birds fed a feed formulated with a high CP SBM had a lower FCR than when fed the low CP SBM regardless of the enzyme. Birds fed RFF had a lower FCR at 7 d than those fed IFF. At 14 and 20 d, the feed screening process interacted with the dietary enzyme. Birds fed RFF with the enzyme had a significantly lower FCR than when fed RFF without the enzyme, and IFF with or without the enzyme (Tables 6 and 7).

Table 6.

Treatment effects on AMEn1 at 14 d (kcal/kg) and poult performance (g) in experiment 2.

SBM2 Fines3 ENZ4 AMEn1
BWG
Feed intake
FCR5
14 d 0–7 d 0–14 d 0–20 d 0–7 d 0–14 d 0–20 d 0–7 d 0–14 d 0–20 d
HSBM 2,978 93 289 552 111b 367b 750b 1.201 1.275b 1.350b
LSBM 2,955 93 294 558 116a 391a 797a 1.249 1.307a 1.395a
SEM6 39 2 4 7 2 4 8 0.014 0.005 0.009
P-value 0.14 0.97 0.33 0.50 0.03 <0.0001 0.004 0.064 <0.0001 0.001
IFF 2994a 90a 284b 541b 113 373b 761b 1.253a 1.313a 1.387s
RFF 2939b 95b 300a 569a 113 384a 786a 1.187b 1.270b 1.359b
SEM6 39 2 4 7 2 4 8 0.014 0.005 0.009
P-value 0.001 0.04 0 0 0.82 0.03 0.03 0.001 <0.0001 0.021
WENZ 2986a 95 292 560 113 378 778 1.185b 1.284 1.368
NENZ 2947b 91 291 551 113 379 770 1.255a 1.299 1.376
SEM6 39 2 4 7 2 4 8 0.012 0.005 0.009
P-value 0.02 0.1 0.85 0.30 0.78 0.86 0.49 <0.0001 0.051 0.510

a,bMeans within a column lacking a common superscript differ (P ≤ 0.05).

1

Apparent metabolized energy corrected for protein.

2

Feed soybean meal factors, high-CP soybean meal 60% (HSBM), and low-CP soybean meal 48% (LSBM).

3

Feed fine abundance factors, increased feed fines (IFF), and reduced feed fines (RFF).

4

The enzyme in diet factors, 200 ml/mt enzyme cocktail added, Rovabio Advance, Adisseo France S.A.S, Antony, France (WENZ), and no enzyme added (NENZ).

5

Feed conversion ratio corrected for mortality using BWG as the numerator.

6

The SEM n = 36 cages with 7 birds per factor.

Table 7.

Treatment first-order interactions1 on AMEn2 at 14 d (kcal/kg) and poult performance(g) in experiment 2.

SBM3 Fines4 ENZ5 AMEn2
BWG
Feed intake
FCR6
14 d 0–7 d 0–14 d 0–20 d 0–7 d 0–14 d 0–20 d 0–7 d 0–14 d 0–20 d
HSBM IFF 2976a 91 282 541 111 365 740 1.229 1.297 1.365
HSBM RFF 3012a 94 295 556 109 369 756 1.169 1.251 1.336
LSBM IFF 2995a 89 285 541 116 382 771 1.284 1.328 1.401
LSBM RFF 2882b 97 308 582 116 400 817 1.205 1.289 1.377
SEM7 41 2.52 4.82 9.97 2.24 5.54 13.15 0.013 0.007 0.009
P-Value <0.0001 0.29 0.32 0.18 0.55 0.21 0.25 0.610 0.631 0.782
HSBM WENZ 288 96 291 554 112 369 759 1.164 1.271 1.358b
HSBM NENZ 2,968 89 286 543 109 365 737 1.234 1.277 1.343b
LSBM WENZ 2,983 94 297 565 115 388 785 1.213 1.296 1.371a,b
LSBM NENZ 2,926 93 296 558 118 394 802 1.276 1.320 1.408a
SEM7 41 2.52 4.97 9.97 2.24 5.54 13.15 0.013 0.007 0.009
P-Value 0.24 0.18 0.74 0.87 0.16 0.31 0.14 0.859 0.238 0.007
IFF WENZ 2,995 91 283 543 113 372 762 1.231 1.315a 1.389a
IFF NENZ 2,961 89 284 539 114 375 749 1.282 1.310a 1.378a,b
RFF WENZ 2,993 98 305 576 113 385 783 1.146 1.252b 1.341b
RFF NENZ 2,917 92 298 562 113 384 790 1.228 1.287a 1.373a,b
SEM7 41 2.52 4.97 9.97 2.24 5.54 13.15 0.013 0.007 0.009
P-Value 0.19 0.48 0.44 0.62 0.91 0.80 0.44 0.411 0.011 0.026

a,bMeans within a column lacking a common superscript differ (P ≤ 0.05).

1

No significant interaction was found between Fines∗SBM∗ENZ.

2

Apparent metabolized energy corrected for protein.

3

Feed soybean meal factors, high-CP soybean meal 60% (HSBM), and low-CP soybean meal 48% (LSBM).

4

Feed fines abundance factors, increased feed fines (IFF), and reduced feed fines (RFF).

5

The enzyme in diet factors, 200 ml/mt enzyme cocktail added, Rovabio Advance, Adisseo France S.A.S, Antony, France (WENZ), and no enzyme added (NENZ).

6

The feed conversion ratio corrected for mortality using the BWG as the numerator.

7

The SEM n = 18 birds per interaction.

Apparent Metabolizable Energy Corrected for Nitrogen

In EXP 2, birds fed feed formulated with either SBM source had a similar AMEn at 14 d. The feed screening process and enzyme factors had a first-order interaction with AMEn at 14 d. The RFF treatment resulted in a similar AMEn compared with the IFF treatment when the enzyme was present. Not having the enzyme lowered the AMEn at 14 d for birds fed RFF than for birds fed IFF (Tables 6 and 7).

Duodenum, Jejunum, Ileum, and Cecum Morphology

In EXP 1, statistical differences were observed among the treatments at 14 d; however, they did not persist to 21 d (Table 8). Data were not consistent throughout EXP 1. Statistical differences were observed only in the jejunum crypt depth and villus height–to–crypt depth ratio at 20 d in EXP 2. Feed formulated with a high CP SBM resulted in a significantly shallower crypt depth (93 vs. 104 ± 4 μm, P = 0.02) and a higher villus height–to–crypt depth ratio (12 vs. 10 ± 0.5, P = 0.003). These data indicate a change in the number of enterocytes developed between feed SBM sources.

Table 8.

Treatment effects on the small intestine morphology at 14 d (μm) in experiment 1.

Treatment 14 d
21 d
Villus height Crypt depth V:C1 Muscularis thickness Villus height Crypt depth V:C1 Muscularis thickness
Duodenum
Control crumble 1,711 136a 13 1,847 2,217 147 15.7 2,363
Medicated three-way crumble 1,655 106b 15 1,785 2,162 142 13.6 2,305
AlphaStart crumble 1,671 113a,b 16 1,784 2,116 139 15.6 2,255
AlphaStart minipellet 1,750 135a 14 1,886 2,110 147 14.7 2,257
SEM2 74 7 1 77 58 7 0.66 60
P-value 0.8 0.05 0.22 0.73 0.55 0.8 0.66 0.55
Jejunum
Control crumble 696a 126a 5.6 822a 877 142 6.3 1,019
Medicated three-way crumble 427b 91b 4.8 518b 827 129 6.5 955
AlphaStart crumble 481b 96b 5.2 576b 855 140 6.3 996
AlphaStart minipellet 552a,b 116a,b 4.8 668a,b 888 137 6.7 1,025
SEM2 45 8 0.3 50 65 9 0.4 71
P-value 0.001 0.009 0.16 0.001 0.91 0.76 0.87 0.9
Ileum
Control crumble 367 99 3.7 466 699 139 5.3 875a
Medicated three-way crumble 311 90 3.5 401 640 133 4.9 806a
AlphaStart crumble 381 101 3.8 482 730 150 4.9 879a
AlphaStart minipellet 373 108 3.7 481 565 125 4.6 688b
SEM2 28 6.5 0.3 32 52 9.5 0.3 59
P-value 0.33 0.31 0.85 0.28 0.13 0.33 0.53 0.05

a,bMeans within a column lacking a common superscript differ (P ≤ 0.05).

1

Villus height–to–crypt debt ratio.

2

The SEM n = 36 cages with birds per factor.

Discussion

Experiment 1 was considered a preliminary EXP. The treatments that can be compared directly are the NCSU control with the three-way medicated and the AlphaStart crumbles with the AlphaStart minipellet; however, there were similarities in the nutritional content. Therefore, statistical analysis was conducted across all treatments, and inferences were made which were used to determine the experimental design used in EXP 2.

The efficiency of feed prehension by the bird will determine the amount of energy and nutrients used related to the energy and nutrients gained by eating. Mash feeds are more difficult for the bird to prehend, possibly resulting in the bird expending more energy for eating and wasting more feed than when eating pelleted feeds (Jensen et al., 1962; Calet, 1965). Birds select the feed particle size depending on the size of the beak (Moran, 1982), and as the beak grows, the preferred particle size increases (Portella et al., 1988). The particle size is also referred to as the feed form by some authors. Inferior feed form (i.e., decreased pellet quality) can be a significant limiting factor for performance (Quentin et al., 2004). The first feed is an essential factor in early gut health and poult performance (Noy et al., 2001). This first feed is also part of a critical transition from a yolk-based diet to a solid-based diet (Uni and Ferket, 2004). The starter phase is where the crumble form and quality might be the most important. Favero et al. (2009) concluded that minipellets could be used after the second week of placement.

In the first EXP herein, birds fed the minipellet as the starter feed were observed to have a higher BWG due potentially to an increased FI and also having an improved FCR compared with birds consuming the control crumble feed. It is also possible that difference in feed ingredients in the AlphaStart contributed to differences in bird performance. However, given that the birds fed the AlphaStart crumble were intermediate in performance between the AlphaStart minipellet and the control crumble, the inferences made concerning the feed form seem at least potentially valid for EXP 1. Therefore, minipellets in EXP 1 were concluded to be an option to affect the feed form by increasing the feed particle size resulting in higher quality starter feed pellets. One potential disadvantage of the minipellet may be the cost of production. In most feed mills, minipelleting would require new equipment fitted to the feed mill. In addition, feed production may not be as energy or time efficient as standard crumble production. However, minipelleting cost determination and production efficiency were not conducted in this study.

Screened crumbled feeds, RFF (1.5 mm), were selected as an alternative to a minipelleted feed for the second EXP. Similar results were observed in advantages for the bird BWG and FI, and also for an improved FCR. Therefore, an RFF crumble starter diet might be comparable in effects to minipelleted starter diets. Minipellet and RFF crumbles share similar characteristics with pelleted feed. Pelleted feed results in lower feed wastage, is heat-treated, and has a lower abundance of fines, all of which have been shown to result in an increased FI, increased BWG, and improved FCR compared with feeding a mash feed (Calet, 1965; Nir et al., 1995; Amerah et al., 2007a; Amerah et al., 2007b; Zang et al., 2009; Dozier et al., 2010; Selle et al., 2010; Serrano et al., 2012; Serrano et al., 2013; Lanson and Smyth, 1955).

Ingredient quality is as, or more, important than feed form. The quality of ingredients received by the feed mill will dictate the quality of the produced feed. Cereals and SBM contain NSP and are widely used as the base for animal feeds. The presence of NSP in poultry diets increases the viscosity of the unstirred water layer of the gut mucosa and changes the morphology in the gut. Therefore, NSP can be detrimental to bird nutrient efficiency (Choct, 1997). A higher bird FI and an improved FCR for the feed formulated with a high CP SBM source could be due to the changes in the amount of NSP that the birds consumed. The effect may be further explained by the interaction of feed formulated with low CP SBM and the enzyme at 20 d in EXP 2. The enzyme cocktail used herein has arabinofuranosidases and xylanases, which act on components of the cell wall of the grain, thereby increasing the amount of available and digestible nutrients by reducing the amount of NSP and cell wall components. This enzyme was designed to be used in corn and SBM formulations. Thus, a low CP SBM source increases the enzyme efficiency by increasing the enzyme-substrate ratio when corn and SBM are present in the formulation. The feed source of SBM used in this EXP did not affect the AMEn. However, when a feed formulated with a low CP SBM was fed to the birds, it may have increased the number of fermentative organisms.

The presence of NSP in the diet is detrimental to poultry because it increases the digest time and the number of fermentative organisms in the small intestine (Choct et al., 1996; Choct, 1997). Birds fed RFF feed had a reduced AMEn value, which may have been caused by a reduction in the transit time of the digesta. Nutrient digestibility depends on the digesta retention time. In broilers fed wheat-based diets, AMEn increased linearly by increasing the whole tract transit time (Hughes, 2008). Transit time through the small intestine is reduced for diets with whole wheat when compared with ground wheat (Svihus et al., 2002).

Similarly, increasing the feed particle size by pelleting the feed reduces the transit time of the digesta (Sundu, 2008). Adding the enzyme to the RFF increased feed digestibility and led to similar AMEn values as IFF with or without the enzyme. Feed formulated with a high CP SBM reduced the enlargement of the birds' crypts and increased the villus height–to–crypt depth ratio. The difference in the birds' crypt depths at the jejunum could be explained by the lower amount of soluble NSP in the feed formulated with high CP SBM. Soluble NSP increases the viscosity of the intestinal contents, thereby reducing the nutrient absorption efficiency of poultry (Choct et al., 1996, 2010; Choct, 1997; Montagne et al., 2003; Hetland et al., 2004; Hughes, 2008). The NSP may not only prevent the bird from absorbing nutrients but also may have changed the gut physiology (Choct et al., 2010). Dietary fiber increases the crypt-cell proliferation and reduces the villus height–to–crypt ratio (Montagne et al., 2003). A decrease in the villus height–to–crypt depth ratio is considered to be detrimental to digestion and absorption (Montagne et al., 2003).

In both EXP, the poult FI and BWG were improved because of an increased feed particle size and RFF during the starter phase. An increase in the feed particle size increased the FI and, therefore, increased nutrient intake, consequently increasing the BWG of the bird. The feed formulation containing a high CP SBM source could be used to improve poult FI, BW, and FCR by decreasing the percentage of NSP in the feed. Functional factors in the mini-pellet and dietary enzyme may have improved the digestibility of feed formulated with a low protein CP SBM and RFF by reducing the adverse effects of NSP in the intestinal tract. Therefore, improved feed form and ingredient quality improved poult performance during the starter period.

Acknowledgments

Funding sources had no role in any aspect of the preparation of this article.

Conflict of Interest Statement: The authors did not provide a conflict of interest statement.

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