RESEARCH ARTICLE
Spanish Journal of Agricultural Research
20 (3), e0605, 12 pages (2022)
eISSN: 2171-9292
https://doi.org/10.5424/sjar/2022203-18804
INIA-CSIC
OPEN ACCESS

Replacing soybean meal with micronized soybeans in starter piglet diets and their residual effects during growing and finishing phases

Letícia B. Ferracioli

Institute of Animal Science and Pastures, Secretariat of Agriculture and Supplies of São Paulo State, Nova Odessa, 13380-011, São Paulo, Brazil.

http://orcid.org/0000-0001-8157-461X

Larissa C. Carvalho

Institute of Animal Science and Pastures, Secretariat of Agriculture and Supplies of São Paulo State, Nova Odessa, 13380-011, São Paulo, Brazil.

http://orcid.org/0000-0003-3733-1594

Camila M. S. Chaves

Institute of Animal Science and Pastures, Secretariat of Agriculture and Supplies of São Paulo State, Nova Odessa, 13380-011, São Paulo, Brazil.

http://orcid.org/0000-0003-4451-7506

Simone R. Oliveira

Institute of Animal Science and Pastures, Secretariat of Agriculture and Supplies of São Paulo State, Nova Odessa, 13380-011, São Paulo, Brazil.

http://orcid.org/0000-0001-8895-9045

José E. Moraes

Institute of Animal Science and Pastures, Secretariat of Agriculture and Supplies of São Paulo State, Nova Odessa, 13380-011, São Paulo, Brazil.

https://orcid.org/0000-0003-3405-5360

Carla C. Pizzolante

Institute of Animal Science and Pastures, Secretariat of Agriculture and Supplies of São Paulo State, Nova Odessa, 13380-011, São Paulo, Brazil.

http://orcid.org/0000-0002-4992-5982

Fábio E. L. Budiño

Institute of Animal Science and Pastures, Secretariat of Agriculture and Supplies of São Paulo State, Nova Odessa, 13380-011, São Paulo, Brazil.

http://orcid.org/0000-0002-4129-6763

Abstract

Aim of study: To assess the effects of replacing soybean meal (SBM) with micronized soybean (MS) on the digestibility (Experiment I) and performance (Experiment II) of piglets in the starter phase and its residual effects on the growing/finishing phases and carcass and meat quality traits.

Area of study: São Paulo, Brazil.

Material and methods: The treatments consisted of different levels of dietary replacement of SBM with MS at intervals of 25%, totaling five inclusions (0%, 25%, 50%, 75%, and 100%).

Main results: In Exp. I, the administration of the pre-starter I diet resulted in a positive linear effect (p<0.05) on the apparent digestibility coefficient (ADC) of crude protein and a quadratic effect (p<0.01) on the ADCs of dry matter and crude fat. For the pre-starter II diet, there was a quadratic effect on the ADCs of dry matter and crude fat (p<0.05). For the starter diet, a negative linear effect on the ADC of dry matter was observed (p<0.01). In Exp. II, the feed intake and weight gain decreased linearly throughout the starter phase (p<0.01), while no significant difference (p>0.05) in feed conversion was observed with increasing inclusion level of MS.

Research highlights: Replacing SBM with MS in the starter diet did not influence performance during the growing and finishing phases. Meat quality was not affected but a lower retail cut weight were observed in animals fed a starter diet with higher levels of MS.

Additional key words: carcass meat quality; digestible energy; protein solubility; soybean replacement; urease activity.

Abbreviations used: ADC (apparent digestibility coefficient); ADFI (average daily feed intake); ADWG (average daily weight gain); ANF (antinutritional factors); CF (crude fat); CP (crude protein); DE (digestible energy); DFD (dark, firm, dry); DM (dry matter); FC (feed conversion); GE (gross energy); LL (Longissimus lumborum); ME (metabolizable energy); MS (micronized soybean); PSE (pale, soft, exudative); SBM (soybean meal); SM (Semimembranosus).

Citation: Ferracioli, LB; Carvalho, LC; Chaves, CMS; Oliveira, SR; Moraes, JE; Pizzolante, CC; Budiño, FEL (2022). Replacing soybean meal with micronized soybeans in starter piglet diets and their residual effects during growing and finishing phases. Spanish Journal of Agricultural Research, Volume 20, Issue 3, e0605.
https://doi.org/10.5424/sjar/2022203-18804

Supplementary material: (Table S1) accompanies the paper on SJAR’s website.

Received: 08 Aug 2021. Accepted: 15 Jul 2022.

 

Funding agencies/institutions Project / Grant
São Paulo Research Foundation (FAPESP) 2014/12191-8
Coordination for the Improvement of Higher Education Personnel (CAPES) Scholarships to LBF, LCC, and CMSC

Competing interests:The authors have declared that no competing interests exist.

Correspondence should be addressed to Maria A. M. dos Reis: mralbertinars@gmail.com

CONTENT

INTRODUCTION

 

Soybeans are the most used protein source in animal feed because of their attractive nutritional characteristics. Pig farming and experimental studies have investigated different soy products and by-products in order to reduce feed costs. It is known that the use of raw grains in the diet of non-ruminant animals can compromise nutrient digestion and absorption due to the presence of antinutritional factors (ANF). These factors can be inactivated by heat treatment, rendering the ingredient adequate for the mechanism in the gastrointestinal tract of these animals. The micronization process is used to reduce the particle size in order to improve solubility and to maintain the lipid content of the grain. The product generated is called “micronized soybean” (MS), which contains about 39% crude protein and 21.5% fat (Rostagno et al., 2011).

The higher energy content of MS when compared to soybean meal is interesting for the formulation of diets destined for animals that require maximum energy intake per amount of diet ingested, such as weaned piglets. Immediately after weaning, feed intake by piglets is reduced and diets must be able to provide the energy necessary for proper maintenance and growth (Berrocoso et al., 2014).

Knowledge of the nutritional value and digestibility of products destined for animal feed is essential for the formulation of balanced diets. However, most experiments only compare ingredients and few tests the levels of inclusion. Considering the nutritional importance of soybeans for the feeding of non-ruminants animals and the lack of information about the best inclusion level of this product (micronized soybean) in the diet of weaned piglets, the present study evaluated the effects of increasing levels of dietary replacement of soybean meal with MS on diet digestibility and growth performance of piglets in the starter phase, as well as its residual effects on the growing/finishing phases and carcass, and meat quality traits.

MATERIAL AND METHODS

 

The experimental protocol was developed in accordance with the ethical guidelines on animal experimentation determined by the Ethics Committee on Animal Experimentation of the Institute of Animal Science and Pastures (APTA/SAA), Nova Odessa, SP, Brazil (Protocol No.: 216/2015-CEUA).

The experiments were conducted in Nova Odessa, state of São Paulo, Brazil (22º46’39”S, 47º17’45”W, altitude of 570 m).

Chemical-bromatological composition

 

Urease activity and protein solubility of the test ingredients were determined according to Sindirações (2013). In addition, particle size, dry matter at 105°C, crude protein, ether extract and mineral matter were analyzed (AOAC, 2006).

Digestibility trial

 

A total of 25 barrows with an average initial body weight of 7.38 ± 0.73 kg were used. The animals were housed in metabolic cages similar to those described by Pekas (1968) and allocated in a randomized complete block design consisting of five treatments and five replications, with one animal per experimental unit.

The treatments consisted of different levels of dietary replacement of soybean meal (SBM) with MS at intervals of 25%, totaling five inclusions (MS0, MS25, MS50, MS75, and MS100). The diets were formulated to meet the minimum nutritional requirements of piglets from 21 to 63 days of age (Table S1 [suppl]), according to NRC (2012). Three diets were tested: pre-starter I, pre-starter II, and starter.

The experimental period lasted 25 days, with 10 days for adaptation to the facilities and determination of feed intake, which was defined as the maximum intake during the period analyzed. After the adaptation period, the samples were collected within 5 days for each test diet (pre-starter I, pre-starter II, and starter).

The animals were fed daily at 8:00 and 17:00 h. The feed was weighed and supplied reducing the amount defined as maximum intake (established during the adaptation period) by 10% in order to avoid leftovers. The total fecal and urine collection method was used. Feces were collected once a day, weighed and stored in a freezer (-20ºC). Urine was collected once a day into plastic buckets containing 10 mL of sulfuric acid solution (1:1) to prevent nitrogen losses and the proliferation of microorganisms. The urine volume produced was measured in a 20% aliquot that was stored in a freezer (-20ºC). Ferric oxide (Fe2O3) was used at 1% as a fecal marker to determine the beginning and end of the collection period between test diets. At the end of the experiment, the feces of each animal were homogenized and a representative sample was removed to determine the first dry matter (55ºC/72 h). The sample was then ground in a knife mill with a 1-mm screen.

The following parameters were analyzed in the collected material according to the AOAC (2006): dry matter (DM; residue obtained by drying the sample in an oven at 105°C); mineral matter (residue obtained by incinerating the sample in a muffle at 550°C); nitrogen (N; combustion of the sample by the method of Dumas); gross energy (GE; combustion of the sample by bomb calorimetric), and crude fat (CF; residue of petroleum ether-soluble substances). The apparent digestibility coefficients were then calculated using the formulae of Adeola & Cowieson (2001).

Growth performance evaluation, pre-slaughter and slaughter handling

 

A total of 70 crossbred weaned piglets (35 females and 35 barrows) with an initial age of 21 days and average initial body weight of 5.52 ± 1.0 kg were used. The animals were housed in experimental pens (2 m² each) equipped with a nipple-type drinking fountains and semiautomatic feeder and were allocated in a randomized complete block design consisting of five treatments and seven replications, with one couple per experimental unit. The weight and gender of the animals were used as criteria for formation of the blocks.

The diets were the same as those formulated for the digestibility assay (Table S1 [suppl]) and were supplied during the following phases: pre-starter I (21 to 35 days of age); pre-starter II (36 to 50 days of age) and starter (51 to 63 days of age).

After the nursery phase, the animals were transferred to growing/finishing facilities where they were kept in individual pens (1.0 × 2.0 m) with smooth concrete floor and metal divisions, equipped with a trough type feeder and nipple-type drinking fountains. The animals were allocated in a completely randomized design consisting of five residual treatments and 14 replications per treatment. During this period, the animals received the same corn and soybean diet formulated according to the nutritional requirements (NRC, 2012) of each phase: growing I – from 64 to 91 days of age; growing II – from 91 to 119 days of age; finishing – from 119 to 140 days of age.

Average daily weight gain (ADWG) was determined by weighing the animals at the beginning and end of each phase. Average daily feed intake (ADFI) and feed conversion (FC) were determined by weighing the feed at the beginning and end of each phase, subtracting leftovers. The total experimental period was 42 days during the nursery phase and 76 days during the growing/finishing phase.

At the end of the growing/finishing phase (140 days of age), the animals were slaughtered in a commercial slaughter house. Feed was withheld for 4 h before the animals (n = 70) were weighed and transported to a packing plant in Piracicaba, SP, Brazil (22º43’31” S; 47º38’57” W; altitude of 547 m). The animals were kept in pens for 6 h before being electrically stunned, exsanguinated from major blood vessels near the heart, and processed according to industry-accepted procedures.

Evaluation of carcass traits

 

After slaughter, the hot carcass of the 70 animals was weighed. Then, the carcasses were chilled in a cold storage room for 24 h at 2ºC and weighed again for the determination of cold carcass weight. The pH of the left half-carcass was measured 45 min and 24 h post mortem in the center of the Semimembranosus (SM) muscle with a portable digital pH meter (DM-2 Digimed©). The 24-h pH was also measured in the Longissimus lumborum (LL) muscle.

Backfat thickness was measured with a caliper at three specific points: near the first thoracic vertebra (P1), near the last thoracic vertebra (P2), and near the last lumbar vertebra (P3). The arithmetic average of the three measurements was used for analysis. The loin eye area was obtained by delimiting the contour of the LL muscle between the last and penultimate rib and the area was calculated using a planimeter.

After the establishment of rigor mortis (24 h after slaughter), the LL muscle of the left half-carcass was exposed for 30 min to allow the occurrence of blooming. Three color measurements per animal were then obtained using a Konica Minolta CM-600d spectrophotometer, which uses the CIELAB color scale with the following coordinates: L* (lightness), a* (redness), and b* (yellowness).

For the determination of retail cut weight, the following cuts were obtained from left half-carcass: ham, pork chops, shoulder, ribs, sirloin, and belly. After weighing the cuts, the shoulder and sirloin were deboned to determine the boneless cut weight.

Pork meat quality

 

Drip loss was determined as described by Costa et al. (2018). Briefly, approximately 100 g of an LL sample collected between the 6th and 7th rib was cut into cubes, placed in a nylon net, and subjected to its own weight for 72 h in a cold chamber (4ºC). The result is reported as the difference between the initial and final weight divided by the initial weight and multiplied by 100.

Samples of LL muscle (approximately 130 g) were collected 24 h after slaughter. The samples were vacuum packed and stored frozen (-20°C). Next, the samples were thawed in a refrigerator at 4oC for 24 h. After this period, the samples were weighed and cooked in a water bath (80ºC) until their core temperature reached 72ºC. The samples were cooled at room temperature and weighed again for the calculation of cooking losses. For the determination of meat tenderness (shear force), four cubes per sample were removed and placed with the muscle fibers perpendicular to the blades of a TAXT-plus Texture Analyzer 2i equipped with Warner-Bratzler shear force (WBSF) with a 25-kg load cell and crosshead speed of 200 mm/min.

Statistical analyses

 

All data were submitted to analysis of variance using the GLM (General Linear Models) procedure of the SAS 9.0 program (SAS Inst., Cary, NC, USA). Means were considered significantly different at the 5% level of probability (p<0.05) by the Tukey test. Regression analyses were performed for the treatments and linear and quadratic effects were evaluated. Regression equations are demonstrated in the table footers when significant.

RESULTS

 

Chemical-bromatological composition

 

Table 1 shows the chemical-bromatological composition, protein solubility, and urease activity of the test ingredients.

Table 1.  Chemical-bromatological composition, protein solubility, and urease activity of the test ingredients.
Description analysed Soybean meal Micronized soybean
Dry matter, % [1] 87.56 91.37
Crude protein, % [1] 45.72 38.68
Ether extract, % [1] 1.85 22.21
Mineral matter, % [1] 5.99 4.77
Particle size, µm [2] 122.0 453.0
Protein solubility in KOH, % [3] 74.43 78.80
Urease activity, Δ pH [3] 0.09 0.03

Digestibility trial

 

For the pre-starter I diet, the nitrogen retention coefficient and the apparent digestibility coefficient of crude protein (ADCCP) increased linearly with increasing replacement of SBM with MS (p<0.05), while a quadratic effect was observed for the apparent digestibility coefficients of dry matter (ADCDM), crude fat (ADCCF) and gross energy (ADCGE), digestible energy (DE), and metabolizable energy (ME). For the pre-starter II diet, only ADCDM and ADCCF differed (p<0.01), while there was no effect of treatment on the other variables analyzed. The starter diet resulted in a significant difference only for ADCDM (p<0.01), which decreased linearly with increasing level of replacement of SBM with MS (Table 2).

Table 2.  Coefficient of nitrogen retention (CNR), apparent digestibility coefficients of dry matter (ADCDM), crude protein (ADCCP), crude fat (ADCCF), gross energy (ADCGE), digestible energy (DE), and metabolizable energy (ME) obtained for the pre-starter I, pre-starter II and starter diets.
Variable Treatment, % Reg CV%
MS0 MS25 MS50 MS75 MS100
Pre-starter I
CNR, % 66.83 68.85 70.88 72.91 74.94 L** 3.4
ADCDM, % 79.97 82.07 82.76 82.05 79.92 Q** 1.7
ADCCP, % 81.45 82.10 82.76 83.42 84.07 L* 2.2
ADCCF, % 76.52 83.44 84.01 83.77 82.86 Q** 3.0
ADCGE, % 83.95 85.92 86.98 87.14 86.40 Q** 1.4
DE, Mcal/kg 3.77 3.93 4.01 4.00 3.90 Q** 1.4
ME, Mcal/kg 3.72 3.87 3.95 3.94 3.85 Q** 1.4
Pre-starter II
CNR, % 67.05 64.69 64.28 65.81 69.28 NS 4.0
ADCDM, % 80.90 82.76 83.57 83.34 82.05 Q** 1.4
ADCCP, % 79.76 76.84 79.99 76.17 79.59 NS 3.1
ADCCF, % 76.26 72.77 72.51 75.47 81.66 Q* 3.5
ADCGE, % 85.90 86.22 89.23 86.26 86.69 NS 1.8
DE, Mcal/kg 3.82 3.98 4.04 4.01 3.88 NS 1.8
ME, Mcal/kg 3.78 3.94 4.00 3.97 3.83 NS 1.9
Starter
CNR, % 71.35 70.41 64.16 69.08 66.29 NS 5.8
ADCDM, % 83.37 82.82 82.27 81.72 81.17 L** 1.5
ADCCP, % 81.04 80.04 79.04 78.05 77.05 NS 3.2
ADCCF, % 70.57 76.17 73.19 75.37 76.52 NS 2.9
ADCGE, % 87.31 86.88 86.46 86.03 85.61 NS 1.6
DE, Mcal/kg 3.72 3.68 3.64 3.60 3.56 NS 1.6
ME, Mcal/kg 3.68 3.64 3.60 3.56 3.51 NS 1.7

Growth performance during the starter, growing and finishing phases

 

There was a linear decrease in ADWG and ADFI with increasing level of replacement of SBM with MS throughout all periods of the starter phase (p<0.05), while FC increased linearly (p<0.01) in the first and second periods analyzed (Table 3). The animals entered the growing phase with the following mean body weights: MS0: 25.07 kg, MS25: 23.57 kg, MS50: 22.02 kg, MS75: 21.33 kg, and MS100: 19.62 kg.

Table 3.  Average daily feed intake (ADFI), average daily weight gain (ADWG) and feed conversion (FC) of piglets from 21 to 63 days of age according to treatment.
Treatment, % Reg CV%
MS0 MS25 MS50 MS75 MS100
21 to 35 days
ADFI, kg 0.33 0.31 0.29 0.26 0.24 L* 31.22
ADWG, kg 0.25 0.23 0.20 0.18 0.15 L** 34.85
FC 1.32 1.39 1.45 1.52 1.59 L** 12.92
21 to 50 days
ADFI, kg 0.52 0.48 0.45 0.41 0.38 L** 21.59
ADWG, kg 0.35 0.32 0.29 0.26 0.24 L** 21.76
FC 1.48 1.50 1.53 1.56 1.58 L** 4.77
21 to 63 days
ADFI, kg 0.76 0.72 0.68 0.64 0.60 L** 18.11
ADWG, kg 0.46 0.43 0.40 0.37 0.34 L** 17.50
FC 1.67 1.65 1.66 1.70 1.78 NS 4.25

Piglets fed different levels of MS as substitute of SBM during the starter phase had lower ADFI during the grower I phase (Table 4), with the observation of a negative linear effect (p<0.05), i.e., the higher the inclusion level of MS during the starter phase, the lower the feed intake of the animals between 64 and 91 days of age. However, piglets receiving different dietary levels of MS during the post weaning phase had better feed efficiency during the grower I phase (p<0.05). The higher the inclusion level of MS, the better FC. Consequently, there was no difference in ADWG between treatment during the grower I phase (p>0.05) (Table 4).

Table 4.  Residual effect of replacing soybean meal with micronized soybean during the starter phase on average daily feed intake (ADFI), average daily weight gain (ADWG) and feed conversion (FC) of pigs during the grower I and II and finisher phases.
Variable Gender Treatment, % Reg CV%
MS0 MS25 MS50 MS75 MS100 Average
64 to 91 days of age
ADFI, kg Male 1.93 1.94 1.89 1.80 1.86 1.88 A
Female 1.93 1.94 1.89 1.80 1.86 1.88 A
Mean 1.94 1.86 1.88 1.84 1.77 L* 11.79
ADWG, kg Male 0.86 0.86 0.87 0.88 0.86 0.87 A
Female 0.90 0.81 0.85 0.87 0.80 0.84 A
Mean 0.88 0.83 0.86 0.88 0.83 NS 10.25
FC Male 2.24 2.25 2.18 2.03 2.17 2.17 A
Female 2.18 2.20 2.20 2.16 2.13 2.17 A
Mean 2.21 2.22 2.19 2.10 2.15 L* 7.25
64 to 119 days of age
ADFI, kg Male 2.32 2.32 2.30 2.20 2.21 2.27 A
Female 2.27 2.09 2.13 2.19 2.04 2.15 B
Mean 2.30 2.20 2.21 2.19 2.12 NS 9.69
ADWG, kg Male 0.97 1.00 1.02 0.96 0.98 0.99 A
Female 0.97 0.88 0.90 0.94 0.88 0.91 B
Mean 0.97 0.94 0.96 0.95 0.93 NS 7.82
FC Male 2.38 2.33 2.24 2.27 2.25 2.29 A
Female 2.34 2.36 2.37 2.33 2.33 2.35 A
Mean 2.36 2.35 2.30 2.30 2.29 NS 5.17
64 to 140 days of age
ADFI, kg Male 2.51 2.50 2.49 2.38 2.40 2.46 A
Female 2.41 2.19 2.23 2.31 2.18 2.27 B
Mean 2.46 2.35 2.36 2.35 2.29 NS 9.51
ADWG, kg Male 0.99 1.01 1.03 0.96 0.99 1.00 A
Female 0.98 0.88 0.89 0.96 0.88 0.92 B
Mean 0.98 0.94 0.96 0.96 0.94 NS 7.85
FC Male 2.54 2.48 2.40 2.46 2.41 2.46 A
Female 2.47 2.50 2.50 2.40 2.46 2.47 A
Mean 2.50 2.49 2.45 2.43 2.44 NS 5.26

Analysis of the grower I and II phases (64 to 119 days of age) and of the grower I, II and finisher phases (64 to 140 days of age) showed no difference in any of the zootechnical parameters evaluated when the diet factor was analyzed (p>0.05). However, barrows had higher ADFI and ADWG than females (p>0.05).

Carcass and meat traits

 

There was a difference in body weight (p<0.05) before slaughter, with the weight of the animals being higher the lower the inclusion of MS during the starter phase. This fact was confirmed after slaughter of the pigs, with the cold and hot carcass weight, being lower in animals fed starter diets with higher levels of MS (Table 5).

Table 5.  Residual effect of replacing soybean meal with micronized soybean during the starter phase on carcass and meat quality traits of pigs at 140 days of age.
Variable Gender Treatment, % Reg CV%
MS0 MS25 MS50 MS75 MS100 Average
pH SM, 45 min[1] Male 6.02 B 6.19 A 6.25 A 6.06 A 6.05 B 6.11 Q#
Female 6.29A 6.26A 6.05A 6.18A 6.27A 6.21 Q#
Mean 6.16 6.22 6.15 6.12 6.16 NS 3.14
pH SM, 24 h[1] Male 5.64 5.75 5.66 5.61 5.80 5.69A
Female 5.82 5.70 5.60 5.50 5.86 5.70A
Mean 5.73 5.72 5.63 5.56 5.83 NS 3.32
pH LL, 24 h[2] Male 5.43 5.47 5.50 5.51 5.55 5.49A
Female 5.61 5.56 5.53 5.39 5.73 5.56A
Mean 5.52 5.51 5.51 5.45 5.64 NS 3.03
BW 140d, kg Male 99.16 99.60 101.29 93.20 97.47 98.14A
Female 102.39 92.76 91.43 97.93 87.83 94.46A
Mean 100.77 96.18 96.36 95.56 92.65
HCW, kg Male 79.43 80.06 81.28 74.47 77.35 78.52A
Female 82.94 74.23 74.68 78.81 70.57 76.25A
Mean 81.18 77.14 77.98 76.64 73.96 L# 8.97
CCW, kg Male 77.93 78.31 79.54 73.03 75.85 76.93A
Female 81.07 72.77 72.76 76.96 69.33 74.58A
Mean 79.50 75.54 76.15 74.99 72.59 L# 8.94
CY, % Male 80.08 80.37 80.22 79.88 79.36 79.98B
Female 81.01 80.02 81.73 80.42 80.35 80.71A
Mean 80.55 80.19 80.97 80.15 79.86 NS 1.73
BT, mm Male 25.89 25.38 26.03 23.95 24.57 25.17A
Female 24.79 20.04 22.75 24.85 23.27 23.14B
Mean 25.35 22.71 24.4 24.4 23.92 NS 11.28
LEA, cm2 Male 43.03 42.11 42.57 40.17 42.06 41.99A
Female 41.54 43.87 45.54 42.42 45.19 43.71A
Mean 42.29 42.99 44.06 41.29 43.62 NS 14.24
DL, % Male 7.08 5.60 5.84 7.01 4.92 6.09A
Female 5.31 5.70 5.44 7.83 4.91 5.84A
Mean 6.19 5.65 5.64 7.42 4.91 NS 16.21#
CL, % Male 27.15 24.42 24.93 24.69 21.97 24.63A
Female 27.58 28.52 27.35 28.68 23.83 27.20A
Mean 27.36 26.47 26.14 26.69 22.90 NS 23.96
SF, kgf Male 2.51 2.64 2.93 2.98 2.31 2.68A
Female 2.55 2.88 2.67 2.57 2.32 2.60A
Mean 2.53 2.76 2.80 2.78 2.31 NS 26.35
Color
L* Male 53.54A 51.35A 50.81A 50.70A 48.41A 50.96 L#
Female 48.06B 47.53B 48.64A 53.42A 48.64A 49.26
Mean 50.80 49.44 49.72 52.06 48.52 NS 6.72
a* Male 2.24 2.45 1.96 2.51 2.04 2.24A
Female 2.10 1.72 1.60 1.96 2.34 1.94A
Mean 2.17 2.08 1.78 2.24 2.19 NS 17.98
b* Male 11.54 11.25 10.01 10.82 9.99 10.72A
Female 10.03 8.95 9.48 10.60 9.53 9.72B
Mean 10.79 10.10 9.75 10.71 9.76 NS 11.38

Backfat thickness was not influenced by the addition of MS (p>0.05). In addition, carcass yield and loin eye area, which were used to predict the amount of lean meat in the carcass, did also not differ between treatments when the diet factor was analyzed (p>0.05). The 24-h post mortem pH of the SM muscle was not influenced by diet or gender (p>0.05). However, when the gender factor was analyzed, females had higher carcass yield (p<0.05) and males exhibited greater backfat thickness (p<0.05). In addition, a difference in 45-min post mortem pH values of the SM muscle were observed for the gender-diet interaction. The 24-h post mortem pH of the SM and LL muscles was not influenced by diet or gender (p>0.05).

There were no differences in the technological quality of the LL samples (drip loss, cooking loss, and shear force) between treatments (p>0.05) for the diet or gender factor (Table 5).

A negative linear effect (p<0.05) was observed on the L* value, which corresponds to the degree of meat lightness, with an interaction between gender and diet. Males fed higher inclusion levels of SBM during the starter phase had meat with higher lightness values, while those receiving the starter diet with higher inclusion of MS had meat with lower lightness values (Table 5). In addition, there was a difference (p<0.05) in lightness (L*) between males fed the MS0 and MS25 diets during the nursery phase and females of the same groups, with higher lightness values in the former (53.54 and 51.35 for males vs. 48.06 and 47.53 for females, respectively). Redness values (a*) did not differ between treatments for the diet or gender factor (p>0.05). However, b* values (yellowness) were higher (p<0.05) in males compared to females (10.72 and 9.72, respectively) (Table 5).

There was a linear decreasing effect (p<0.05) on the retail cuts shoulder, boneless shoulder, boneless sirloin, and ribs, i.e., the higher the inclusion level of MS in the starter diet of pigs, the lower the yield of these cuts. The remaining cuts evaluated, including nobles cuts such as ham and pork chops, were not influenced by the diet (Table 6). However, males had higher shoulder yield and higher rib weight than females (p<0.05). In addition, there was an interaction between diet and gender for sirloin weight (p<0.05). A decrease in the weight of this cut was observed in females fed increasing levels of MS during the starter phase (Table 6).

Table 6.  Residual effect of replacing soybean meal with micronized soybean during the starter phase on the retail cut weight of finished pigs.
Variable Gender Treatment, % Reg CV%
MS0 MS25 MS50 MS75 MS100 Average
Ham, kg Male 10.70 10.54 10.93 9.70 10.31 10.44A
Female 11.22 9.30 10.16 10.89 9.78 10.27A
Mean 10.96 9.92 10.55 10.29 10.04 NS 12.52
Pork chops, kg Male 7.08 7.20 7.08 6.91 7.09 7.07A
Female 7.54 6.98 6.66 7.26 6.37 6.97A
Mean 7.31 7.09 6.87 7.09 6.73 NS 11.83
Shoulder, kg Male 5.90 5.87 5.63 5.24 5.64 5.66A
Female 5.76 5.22 5.20 5.48 4.93 5.32B
Mean 5.83 5.54 5.42 5.36 5.29 L* 9.97
Boneless shoulder, kg Male 3.89 3.94 3.69 3.50 3.66 3.72A
Female 3.90 3.55 3.54 3.76 3.31 3.61A
Mean 3.85 3.75 3.62 3.63 3.48 L* 11.54
Sirloin, kg Male 2.68 2.94 3.10 2.57 2.72 2.80 A
Female 3.11 2.79 2.61 2.71 2.32 2.71 A L*
Mean 2.89 2.87 2.86 2.64 2.52 NS 14.76
Boneless sirloin, kg Male 1.74 1.91 1.99 1.68 1.74 1.81A
Female 2.02 1.81 1.72 1.90 1.41 1.77A
Mean 1.88 1.86 1.85 1.79 1.57 L* 16.99
Ribs, kg Male 4.29 4.46 4.64 4.09 4.23A 4.34A
Female 4.46 3.94 3.99 3.92 3.81B 4.03B
Mean 4.38 4.20 4.31 4.01 4.02 L* 13.55
Belly, kg Male 2.86 2.77 2.93 2.72 2.70 2.80A
Female 3.12 2.78 2.64 2.99 2.65 2.84A
Mean 2.99 2.78 2.78 2.85 2.68 NS 13.77

DISCUSSION

 

Chemical-bromatological composition

 

The chemical-bromatological composition found in the present study (39.14% CP and 21.50% CF for MS and 45.22% CP and 1.69% CF for SBM) (Table 1) is similar to that reported in the tables of Rostagno et al. (2011). The urease activity values for MS and SBM were within the reference range indicated by Sindirações (2013) (Table 1). Szmigielski et al. (2010) demonstrated that micronization is effective in reducing urease activity levels (from 2.0 to 0.10 ΔpH) without compromising protein content. The protein solubility values obtained for SBM were lower than the minimum of 75% recommended by Sindirações (2013). Excessive heating of the ingredient is known to denature proteins, which reduces protein solubility (Woyengo et al., 2017). In the present study, the lower protein solubility of SBM compared to MS may have been responsible for the lower digestibility of the diets containing a higher level of SBM.

Digestibility trial

 

The digestibility results obtained for the pre-starter I diet differ from those reported by Valencia et al. (2008) who studied the influence of particle size of SBM and full-fat soybean on the digestibility of diets for piglets at 23 days of age. The lower digestibility of diets with a higher SBM percentage can be attributed to the greater crude fiber content of this ingredient compared to MS (5.3 vs. 1.36% according to Rostagno et al., 2011). The presence of fiber can negatively affect protein digestion because of the effect of the association with lignocellulose, which reduces protein availability (De Coca-Sinova et al., 2008). On the other hand, the quadratic effect observed for ADCDM, ADCGE, ADCCF, DE and ME might be related to the increase in dietary CF content with increasing replacement level of SBM with MS. Azain (2001) suggested that dietary fat reduces the rate of food passage through the gastrointestinal tract and consequently increases nutrient digestibility because of the longer exposure to digestive enzymes. This higher amount of fat may have exceeded the enzymatic capacity of the gastrointestinal tract of piglets at this age.

The lack of significant differences between variables (except ADCDM and ADCCF for the pre-starter II diet and ADCDM for the starter diet) agrees with the results reported by Berrocoso et al. (2014), who found no benefit of micronization of common SBM or high protein content. According to these authors, the effects of micronization appear to be clearer in studies on cereals compared to soybeans. Agunbiade et al. (1992) observed a higher digestibility coefficient of diets containing SBM and soybean oil compared to diets with full-fat soybean. The authors suggested that how this ingredient is present in the diet seems to be an important factor for the utilization of soybean products. Thus, the integral oil present in the plant cell may not be fully available for enzymatic digestion even after micronization.

The effects of micronization on nutrient digestibility have not been fully elucidated. Although improving diet digestibility, the reduction in the particle size of the food may also affect gastrointestinal motility and function and health of the piglet (Berrocoso et al., 2014). Thus, the two effects may oppose each other and the magnitude of the responses observed can vary among experiments and phases studied. Furthermore, the differences found in the nutrient and energy digestibility coefficients of the diets compared to those reported in the literature suggest lower digestibility in weaned piglets compared to older animals whose gastrointestinal tract is more developed (Latorre et al., 2004).

Growth performance during the starter, growing and finishing phases

 

With respect to the starter phase (Table 3), the results corroborate those reported by Trindade Neto et al. (2002) who demonstrated superiority of SBM compared to other protein sources, assuming that this soy by-product triggers less damage to the piglet’s digestive process and gastrointestinal system in the early stages of development. However, our findings differ from Berrocoso et al. (2014) who observed better FC in animals fed diets with micronized SBM compared to common SBM in the first week of the assay. Although soybean micronization is able to improve nutrient digestibility by improving the mixing with digestive enzymes, this process may also negatively affect gastrointestinal motility and function, as well as the “healthy” status of the piglet, compromising growth performance of the animal.

In general, feed intake was considered low during the starter phase (especially for the treatments containing a higher percentage of MS), which may have caused poor growth performance. According to Jha & Berrocoso (2015), newly weaned piglets do not consume the adequate amount of energy to meet their energy requirements for body weight gain, particularly during the first days after weaning, and may recruit fat reserves only to sustain their body weight. Another factor that may have affected feed intake during the starter phase is the fact that no flavoring was used in the diet. Diet intake by adult pigs is generally regulated so that energy needs can be met (Costa et al., 2018), but the ability to adapt feed intake according to the energy content of the diet is variable in piglets. According to Valencia et al. (2008), palatability of the food is the factor that most influences the feed intake level during this stage of the piglet’s life. It is possible that the palatability of MS was not acceptable, but scientific studies on this topic are scarce.

The texture of the diets with higher inclusion levels of MS may have also influenced feed intake. The processing and physical form of the diet directly influence the diet preference of newly weaned piglets. Completing this reasoning, after weaning, feed intake is basically controlled by palatability, which mainly includes flavor, but can also be estimated by the texture and physical properties of the dietary ingredients (Lee et al., 2019). As reported by Solà-Oriol et al. (2009) and also observed in studies on infants and children, they reject foods that are difficult to move around in the mouth and that take longer to be swallowed. It is possible that foods that require fewer chewing movements are also preferred by newly-weaned piglets. These authors also emphasized that, for piglets, particle size seems to be less important than the texture of the foods. In view of these considerations, the higher fat content of the diets containing MS may have altered their texture, with a subsequently negative influence on feed intake.

Although the urease activity and protein solubility values obtained were within the acceptable range (Table 1), other ANF that were not analyzed could have affected food utilization by the animal because they possess heat resistance features and consequently the growth performance of piglets in this study, in addition the amount of ANF consumed daily is more important than their concentration in the ingredient or diet (Woyengo et al., 2017).

The high fat content of the diets, especially in the early stages, may have influenced the results of the present study. Trindade Neto et al. (2002) attributed the poor growth performance of piglets fed diets with ground full-fat soybeans to their high fat content, which would exceed the piglet’s digestive capacity at this stage of life. According to Adeola & Cowieson (2011), the total fat digestive capacity is not reached until 40 kg of body weight. In addition, a marked reduction in the activity of different digestive enzymes such as lipase is observed immediately after weaning.

Regarding the subsequent phases (growing/finishing), animals fed diets with higher inclusion of MS entered the grower phase with a lower body weight. Thus, the lower feed intake observed from 64 to 90 days of age in animals previously fed increasing levels of MS would be due to lower body weight (lower gastric capacity) and the better feed efficiency would be related to the higher rate of protein deposition, which is more intense in smaller animals and requires twice less energy than that needed for the deposition of adipose tissue (Pierozan et al., 2016).

Latorre et al. (2004) reported higher feed intake and weight gain of male pigs during the growing and finishing phases compared to females of the same age. This fact might be explained by the greater intake capacity and lower maintenance requirements of males.

Good growth performance of piglets in the early stages of growth depends on many factors, including weight upon entry to the nursery, existence of some nutrient restriction, feed intake, health status of the animals, diet composition and digestibility, and the presence of ANF (Jha & Berrocoso, 2015; Woyengo et al., 2017). Thus, considering the same sanitary standards, homogeneous weight at the beginning of the treatments and formulation of diets that were approximately isoproteic and isoenergetic and that met the nutritional requirements of this phase, the factors that could have compromised the animals’ growth performance during the previous phase would be the low feed intake, digestibility of MS, or ANF.

Carcass and meat quality traits

 

The pH measured 45 min and 24 h after slaughter is one of the parameters most used in slaughterhouses to predict meat quality because of its reliability and easy application. In addition, studies have demonstrated an association between pH values at 45 min and 24 h and the results of technological meat evaluations, such as water retention capacity, color, and drip loss. Quality standard pork is defined when the pH 45 min is between 6.0 and 6.5 and the pH 24 h between 5.5 and 5.8 (Costa et al., 2018). Hence, despite the significant difference in pH at 45 min, with an interaction between gender and diet, these values were within the reference range. These findings show that the inclusion of MS in the starter diet for piglets did not influence the conversion of muscle to meat. The measurement of meat color is essential to ensure attractiveness by consumers. In addition, color measurement assists in the diagnosis of PSE (pale, soft, exudative) and DFD meat (dark, firm, dry). AMSA (2012) established normal L* values for pork meat between 49 and 60. However, other authors defined a L* value between 43 and 49 as normal meat (Bridi et al., 2008; Garbossa et al., 2013). Thus, considering the latter reference, male pigs fed SBM had a L* value outside the expected range, while the L* values were within the range for quality pork meat according to the first reference.

With respect to lightness, males of the MS0 treatment had meat with greater lightness, i.e., paler meat. In addition, males fed the MS0 and MS25 diets in the early stages had meat with greater lightness when compared to females of the same group. Genetic factors, production system, feeding, age, and the final pH of meat can exert important effects on the L*, a* and b* values. These values also tend to change with increasing slaughter weight due to the greater muscularity of the animal (Costa et al., 2018). With development of the muscle, the amount of myoglobin increases, fat deposition becomes more evident, and the amount of water in the muscle decreases, consequently reducing lightness. This fact was not observed in the present study since feeding males higher levels of SBM during the starter phase benefitted their growth performance, resulting in larger pigs with more intense muscle activity, which would favor myoglobin accumulation and fat deposition and consequently result in meat with lower lightness (Garbossa et al., 2013).

The drip loss values found for animals fed diets with higher SBM levels during the starter phase were above those proposed by Bridi et al. (2008) for fresh pork meat, who recommend a drip loss of up to 6%. However, other authors define a drip loss of about 9.8% for normal pork meat and of about 12.9% for PSE meat (Latorre et al., 2004).

Taken together, the pH 24 h, L* value and drip loss of animals fed higher inclusions of SBM during the starter phase suggest the occurrence of PSE meat, which would explain the presence of meat with greater lightness. However, considering the literature, the lack of a sudden pH drop within the first 45 min post mortem and the fact that pH values at 24 h post mortem were close to those recommended by more rigorous references and that the cooking loss was within the quality standard, we conclude that no PSE meat occurred. Similarly, the DFD classification cannot be applied to the present study since the meat derived from the treatments evaluated had a L* value>42, drip loss ≥ 5%, and final pH<6.0 (Bridi et al., 2008).

Analysis of the carcass traits of animals fed the MS100 diet showed that the lower final body weight of these animals resulted in a reduction of 8.22% in rib weight, of 9.26% in shoulder weight, of 9.6% in boneless shoulder weight, and of 16.48% in boneless sirloin weight. In addition, females fed the diet with MS inclusion exhibited a linear reduction in the weight of the sirloin, with the observation of a 25.4% decrease in treatment MS0 compared to MS100.

With respect to gender, the quality of carcasses from barrows was lower than that of female carcasses because of the higher amount of fat and lower carcass yield (about 0.9% lower) in the former. According to Bridi et al. (2008), castrated male pigs fed similar diets as females will exhibit a poorer carcass quality (lower carcass yield and greater fat deposition) at the same slaughter age. This fact was also observed in the present study in which backfat thickness in males was 8.77% higher than in females. Higher fat thickness values in males have also been reported by other authors (Peinado et al., 2008). Studies suggest that fat deposition is favored in males compared to females because of higher feed intake (Costa et al., 2018) and the lack of production of testicular steroids.

Rib and shoulder weights also differed (p<0.05) between genders, with the observation of a higher weight of these cuts in barrows. Taken together, the results show that animals fed the MS0 diet had a higher weight of some cuts and females exhibited better carcass traits. However, it is important to note that carcass yield and ham and pork chops weight, which are considered noble cuts with a high added value, were not influenced by the diets tested.

In the present study, the lower weight upon entry to the growing phase demonstrates poor growth performance of animals receiving increasing levels of MS during the starter phase. Literature data (Trindade Neto et al., 2002) and those obtained in this study show that the growth performance of animals during the starter phase influences subsequent phases. In this respect, the poor growth performance of animals fed increasing levels of MS in the early stages of growth, despite their better FC in the grower I phase, did not influence the other phases and did therefore not compensate for the losses observed at the beginning of their productive life, resulting in lower slaughter weight, cold and hot carcass weight, and lower retail cut weights.

AUTHOR'S CONTRIBUTIONS

 

Conceptualization: F.E.L. Budiño

Data curation: F.E.L. Budiño, L.B. Ferracioli, L.C. Carvalho, S.R. Oliveira, J.E. Moraes

Formal analysis: C.C. Pizzolante

Funding acquisition: F.E.L. Budiño

Investigation: F.E.L. Budiño, S.R. Oliveira, C.M.S. Chaves, C.C. Pizzolante, J.E. Moraes

Methodology: F.E.L. Budiño

Project administration:F.E.L. Budiño

Resources: L.B. Ferracioli, L.C. Carvalho, C.M.S. Chaves, S.R. Oliveira

Software: C.C. Pizzolante

Supervision: F.E.L. Budiño, J.E. Moraes

Validation:: F.E.L. Budiño

Visualization: F.E.L. Budiño

Writing – original draft:L.B. Ferracioli, L.C. Carvalho, F.E.L. Budiño

Writing – review & editing: F.E.L. Budiño

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