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Asian-Australas J Anim Sci > Volume 29(2); 2016 > Article
Wang, Song, Wu, Xue, Zhong, and Zhang: Effects of Graded Levels of Isomaltooligosaccharides on the Performance, Immune Function and Intestinal Status of Weaned Pigs

Abstract

The objective of this study was to investigate the effects of graded levels of isomaltooligosaccharides (IMO) on the performance, immune function and intestinal microflora and intestinal mucosal morphology of weaned pigs. In a 28-day experiment, one hundred eighty, twenty eight-day-old, crossbred (Duroc×Large White×Landrace), weaned pigs, with an initial body weight of 8.19±1.45 kg, were fed either an unsupplemented corn-soybean meal based diet or similar diets supplemented with 0.2%, 0.4%, 0.6%, or 0.8% IMO added at the expense of corn. Each treatment was replicated six times with six pigs (three barrows and three gilts) per pen. From day 0 to 14, weight gain was linearly increased (p<0.05), while gain:feed (p<0.05) was linearly improved and diarrhea rate (p = 0.05) linearly declined as the IMO level increased. On d 14, the level of the immunoglobulins IgA, IgM, and IgG in the serum of pigs were linearly increased (p<0.05) with increasing IMO supplementation. Interleukin-6 (IL-6) was linearly (p<0.05) and quadratically (p<0.05) decreased as IMO intake increased. From day 15 to 28, there was a trend for weight gain to be linearly increased, and IL-2 was linearly (p<0.05) increased as IMO supplementation increased on d 28. Over the entire experiment, weight gain was linearly increased (p<0.05), while gain:feed (p<0.05) was linearly improved and diarrhea rate (p<0.05) was linearly decreased as the IMO level increased. Supplementation with IMO had no effect on the intestinal microflora of pigs in the ileum and cecum of pigs, as well as the villus height and crypt depth in the ileum and jejunum (p>0.05). These results indicate that dietary inclusion of IMO increases weight gain, gain:feed and enhanced the immune status of pigs, and could be a valuable feed additive for use in weaned pigs, particularly during the period immediately after weaning.

INTRODUCTION

Isomaltooligosaccharides (IMO) have an α 1→6 glucosidic linkage in their molecular structure (Kohmoto et al., 1992), and are mainly derived from starch by an enzymatic transgalactosylation reaction (Hayashi et al., 1994; Vetere et al., 2000). Their composition is complex and the degree of polymerization ranges from di- to hexasaccharides (Kaneko et al., 1995b). They typically contain isomaltose, panose, isomaltotriose, and several other branched oligosaccharides made up of four or five glucose residues (Kaneko et al., 1995a).
Isomaltooligosaccharides are widely used in the food industry (Goffin et al., 2011), and have a wide spectrum of biological activities, such as improving the intestinal function in humans and animals (Chen et al., 2001; Ketabi et al., 2011; Yen et al., 2011). Furthermore, IMO are known for their potential to activate the immune system, thereby enhancing resistance to diseases and improving lipid metabolism (Wang et al., 2001; Mizubuchi et al., 2005; Li et al., 2009b).
Isomaltooligosaccharides have already been shown to have beneficial effects in a number of animal species including broilers (Zhang et al., 2003; Thitaram et al., 2005; Rehman et al., 2009), pigs (Li et al., 2009b; Li et al., 2010), shrimp (Li et al., 2009a; Zhang et al., 2011) and rats (Watanabe et al., 2002; Sung et al., 2004; Mizubuchi et al., 2005). In pigs, the beneficial effects appear to be mediated through enhancement of cell-mediated and humoral immunity of piglets (Li et al., 2010). However, the levels of IMO providing benefits for piglets have been inconsistent, so the optimum level of IMO for weaned pigs needs further research. The effects of supplementation with IMO in diets on intestinal microflora of weaned pigs and any potential risks in response to increasing inclusion dosages also needs to be studied. Therefore, the objective of the current experiment was to investigate the effects of graded levels of IMO in commercial diets on the performance, immune function, intestinal microflora and intestinal mucosal morphology in weaned pigs.

MATERIALS AND METHODS

The Institutional Animal Care and Use Committee of China Agricultural University (Beijing, China) approved the procedures used in this experiment. The IMO used in this study was provided by the Baolingbao Biology Company (Shandong, China) and its content of isomaltose, panose and isomaltotriose exceeded 45% (manufacturer’s specifications).

Diets and experimental design

One hundred and eighty, twenty eight-day-old, crossbred (Duroc×Large White×Landrace) weaned pigs, with an initial body weight (BW) of 8.19±1.45 kg, were blocked by weight, sex, and ancestry and allotted to 1 of 5 dietary treatments in a 28-d experiment. The dietary treatments consisted of a corn-soybean meal based diet or similar diets (including roxarsone and olaquindox) supplemented with 0.2%, 0.4%, 0.6%, or 0.8% IMO added at the expense of corn (based on results of a preliminary experiment). During the first 14 days of this experiment, 2,000 ppm zinc oxide was added to all diets. The diets (Table 1) were formulated to meet or exceed nutrient requirements as suggested by the National Research Council (1998).
All pigs were housed indoors in 1.2 m×2.0 m concrete-floored pens with half of the pen area solid concrete and the remainder plastic slats. The pigs were provided ad libitum access to feed and water throughout the experimental period. The room temperature was maintained at 25°C to 27°C. Each treatment was replicated six times with six pigs (three barrows and three gilts) per pen.
The pigs were individually weighed on d 0, 14, and 28 of the experiment and feed consumption was measured per pen at the same time. These values were used to calculate weight gain, feed intake and gain:feed. All piglets were observed for evidence of scouring daily and the diarrhea rate was calculated. Fecal scores were monitored and quantified using a scale ranging from 0 to 3 as described by Marquardt et al. (1999), with 0 = normally shaped feces, 1 = soft feces, 2 = mild diarrhea, and 3 = severe diarrhea. A piglet with a score greater than 1 was regarded as having diarrhea. The diarrhea rate is expressed as the ratio between the number of pigs with diarrhea each day and the total number of pigs in each group (Zhao et al., 2015). On d 14 and 28, one pig was randomly chosen from each pen (3 males and 3 females for each treatment) and blood samples were collected from the vena cava cranialis using tubes without anticoagulant. Serum samples were separated by centrifugation at 1,342×g at 4°C for 10 min, and stored at −20°C until needed for analysis.
On d 28, the pigs which were blood sampled were slaughtered. The pigs were stunned by electric shock and then killed by exsanguination. The abdominal cavity was quickly opened to ensure a sterile operation and the ileum and cecum of each pig was isolated, and digesta samples were collected and stored at −20°C until analysis for intestinal microflora. Meanwhile, jejunum and ileum samples were flushed with normal saline to remove the digesta and fixed by 10% formalin buffer for 48 h.

Chemical analysis

Calcium and total phosphorus in the diets were analyzed according to the methods of the Association of Official Analytical Chemists (2000), while crude protein was measured by the method of Thiex et al. (2002). For dietary lysine determination, feed samples were hydrolyzed with 6 N HCl for 24 h (AOAC, 2000). Ash was determined after ignition in a muffle furnace (Nabertherm, Bremen, Germany) at 500°C for 4 h. Crude fiber was determined according to the intermediate filtration method (ISO 6865:2000). Amino acids were chromatographically separated and quantified using a Model L-8900 Amino Acid Analyzer (Hitachi, Tokyo, Japan).
Samples were analyzed for serum immunoglobulins, including immunoglobulin A (IgA, which is an antibody that plays a critical role in mucosal immunity), immunoglobulin M (IgM, which is a basic antibody that is produced by B cells) and immunoglobulin G (IgG, which is synthesized and secreted by plasma B cells) and interleukins (ILs), including IL-2 (which is a cytokine signaling molecule in the immune system), IL-6 (which acts as an anti-inflammatory myokine) and IL-8 (which is a chemokine produced by macrophages and other cell types). All kits used in this trial were validated for pig serum (Kit numbers H0003, H0007, H0008, N0048, N0049 and N0050, Sino-uk Institute of Biological Technology, Beijing, China) following the standard procedures described by the manufacturer. Analyses were conducted using a Hitachi Auto-Analyzer (Hitachi 7020) and R-911 Automatic Radioimmunoassay Counter (China University of Technology Industrial Co., Hefei, China).

Microbiological analysis

Total aerobic bacteria, total anaerobic bacteria, Escherichia coli and Lactobacillus were analyzed by the Tablet Coated Colony Counting Method with three replicates. About 1 g of ileal and cecal digesta was diluted (1:10) in 9 mL aliquots of maximum recovery diluents (MRD, Oxoid, Basingstoke, UK), and 0.1 mL was chosen to spread onto selective agars. The medium for Lactobacillus was de Man, Rogosa and Sharp Agar (Oxoid), and incubation was carried out at 37°C overnight (18 to 24 h) in an atmosphere filled with 5% CO2. The medium for E. coli and total aerobic bacteria were MacConkey and Brian Heart Infusion Agars (Oxoid), respectively and incubation was carried out at 37°C. The total anaerobic bacteria were isolated on Wilkins-Chalgren Anaerobe Agar (Oxoid) with 5% defibrinated sheep blood, and incubated 18 to 24 h at 37°C in an anaerobic tank (Mitsubishi Gas Chemical Co., Tokyo, Japan). Bacterial counts are expressed as colony-forming unit/g, and presented as log10-transformed data.

Intestinal histological analysis

Jejunum and ileum samples were dehydrated, paraffin sectioned and hematoxylin-eosin stained, then observed under the microscope to measure villus height and crypt depth with three sections examined for each of three replicates. Histological slices were examined with an Olympus BX51 microscope coupled with an Integrated Digital Imaging Analysis System (Olympus Co., Tokyo, Japan). Images were viewed (4×) to observe morphometric parameters of intestinal architecture. Villus height and crypt depths were measured manually. The villus height was denoted by the vertical distance from the crypt opening to the tip of the villus. The crypt depth was represented from the base of the crypt to the level of the crypt opening (Kik et al., 1990).

Statistical analysis

Analysis of variance was performed using pen means. Differences among treatments were examined using a one-way analysis of variance analysis version 8.0 (SAS Institute Inc., Cary, NC, USA). The linear and quadratic effects of IMO levels were assessed using orthogonal polynomial contrasts. A p-value of less than 0.05 was considered statistically significant, and less than 0.10 was considered a trend.

RESULTS

Performance

The effects of different levels of IMO on the performance of weaned pigs are presented in Table 2. From day 0 to 14, the daily gain (p<0.05) of pigs was linearly increased as the level of IMO supplementation increased, while gain: feed (p<0.05) was linearly improved. Diarrhea rate showed both a linear (p = 0.05) and quadratic (p = 0.05) decrease with increasing IMO supplementation. From day 15 to 28, there was a trend (p = 0.07) for increasing weight gain with IMO supplementation increased, but no effect on gain:feed or diarrhea rate of pigs. From day 0 to 28, weight gain was linearly increased (p<0.05), while gain:feed (p<0.05) was linearly improved and diarrhea rate (p<0.05) was linearly decreased as the IMO level increased.

Immune function

Table 3 presents the results of the analysis for serum immunoglobulins and ILs of pigs supplemented with different levels of IMO. On d 14, the level of the IgA, IgM and IgG in the serum of weaned pigs were linearly increased (p<0.05) with increasing IMO supplementation. IL-6 was linearly (p<0.05) and quadratically (p<0.05) decreased as IMO intake increased. On d 28, the level of IL-2 was linearly (p<0.05) increased as IMO supplementation increased.

Intestinal microflora and intestinal mucosal morphology

The number of total aerobic bacteria, total anaerobic bacteria, E. coli and Lactobacillus in the ileum and cecum contents were unaffected by dietary treatments (Table 4). In addition, no significant difference was found in villus height and crypt depth in the ileum and jejunum, regardless of the dietary level of IMO (Table 5).

DISCUSSION

Isomaltooligosaccharides are oligosaccharides with interesting nutritional properties, and have been given considerable attention in the scientific field. Li et al. (2009b) indicated that dietary IMO (0, 25, 50, and 75 g/kg) fed to eight Large White castrated male pigs with an initial bodyweight of 25.6±1.1 kg for 8 days did not influence the total tract apparent digestibility of organic matter, crude protein and total ash, so that IMO had limited influence on the performance of growing pigs. However, the results of the present study showed that supplementation with 0.6% and 0.8% IMO significantly increased weight gain and gain:feed of weaned piglets. The main reason for this discrepancy might be that, the immune system is still developing in weaned pigs and therefore there is more likely to be a response to IMO in younger pigs than older pigs.
Studies concerning for effects of IMO supplementation for weaning piglets are scarce. Zhang et al. (2003) reported that supplementation with IMO enhanced performance only during the initial 3 wk, and the final BW of broilers consuming a diet with 0.3% IMO was somewhat greater at the end of 7 wk. However Thitaram et al. (2005) found that no differences existed in feed intake and feed conversion, although the weight of broilers fed 1% IMO showed a significant reduction.
Immunoglobulins, also known as antibodies, are large Y-shape proteins that mainly exist in the plasma and are used to identify and neutralize bacteria and viruses (Litman et al., 1993). ILs are a group of cytokines that were first found to be expressed by white blood cells and play an important role in the immune system (Brocker et al., 2010). They could activate and regulate immune cells, including mediating T and B cell activation, proliferation and differentiation and play an important role in the inflammatory response. The improvement in pig performance observed in the present experiment is most likely mediated by increases in IgA, IgM and IgG, since the increases of IgA, IgM and IgG indicate the activation of an immune reaction which might lead an improvement in immune status. Wang et al. (2012) reported that IMO had a positive effect on humoral and cell-mediated immunity for host animals. Mizubuchi et al. (2005) reported that the level of IgA in feces was increased when mice were fed a diet supplemented with 20% IMO (commercially available IMO, which contained 25.6% IMOs in the dry substance). This is in contrast to a study carried out previously which indicated that level of plasma IgA was not significantly affected in IMO treated rats (Sung et al., 2004).
In general, the main function of antibiotics is correlated with their capacity to eliminate a microorganism. However, toxins are released during the destruction of bacteria, which may, at least temporarily, deteriorate the condition of the microcirculation (AI-Banna et al., 2013). Thus, in this trial, antibiotics (including roxarsone and olaquindox) were added to the diets to enhance disease resistance, the function of IMO were not able to be completely expressed.
Mizubuchi et al. (2005) reported that IL-12 production was increased when mice were fed 20% IMO. However, there is little literature about IL changes when IMO are fed to pigs. The present study found that IL-6 was decreased in the earlier stage while IL-2 was increased in the later period with an increase in IMO supplementation. This is mainly because IL-6 is a factor involved in inflammation, while IL-2 is a kind of chemokine which could induce immune function.
Oligosaccharides (e.g. IMO) could inhibit enzymic reactions taking place in the upper part of the gastrointestinal tract, so that intestinal bacterial species might convert oligosaccharides into short-chain fatty acids by expressing specific hydrolases and gas by fermentation in the lower part (Ketabi et al., 2011). They could also promote some specific bacterial species (such as Lactobacilli and Bifidobacteria) selectively in the intestine, thus equilibrating the intestinal microflora (Delzenne, 2003). In the present study, the quantities of total aerobic bacteria, total anaerobic bacteria, E. coli and Lactobacillus in the ileum and cecum contents were unaffected by dietary treatment. This is similar to the finding that the total aerobes, Lactobacillius, and E. coli in the crop and cecum in broilers were not affected by the inclusion of IMO (Zhang et al., 2003). Wang et al. (2012) reported that increases in fecal Lactobacilli were observed when fermented milk supplemented with two probiotic strains and IMO were fed to mice.
Otherwise, IMO products differ substantially in composition, including the proportion of maltose and glucose, or the degree of polymerization, and such differences probably affect their functions on the intestinal microflora. In addition, the villus height and crypt depth of ileum and jejunum were not affected by the addition of IMO in this trial. The main reason might be that in the interaction of gut microflora and animal digestive enzymes (especially isomaltase), IMO were broken down and lost their expected stimulation on the substrate of the gut microflora. In conclusion, under these experimental conditions, a weaned piglet diet supplemented with 0.6% and 0.8% of isomaltooligosaccharide significantly improved piglet weight gain and gain:feed. Adding 0.2% to 0.8% IMO reduced the diarrhea rate of weaning piglets aged 0 to 14 days, and enhanced the immune status of pigs after weaning. However, the microflora in the ileum and cecum contents, and jejunum or ileum intestinal mucosa morphology were not affected by IMO addition.

ACKNOWLEDGMENTS

This study was supported by the Ministry of Agriculture (Beijing, China), and we acknowledge the Baolingbao Biology Company for donation of the isomaltooligosaccharides used in this study.

Notes

CONFLICT OF INTEREST

We certify that there is no conflict of interest with any financial organization regarding the material discussed in the manuscript.

Table 1
Ingredient composition and nutrient content of basal diet (% as fed)1,2
Variable %
Ingredient (%)
 Corn 58.52
 Dehulled soybean meal3 16.50
 Fish meal 4.00
 Extruded soybean 10.00
 Whey 4.00
 Wheat bran 1.50
 Soybean oil 1.50
 Dicalcium phosphate 1.60
 Limestone 0.60
 DL-methionine (99%) 0.04
 L-Lysine·HCl (78%) 0.34
 Sodium chloride 0.35
 Vitamin-mineral premix4 1.00
 Mold inhibitor 0.05
Nutrient content5
 Metabolizable energy (MJ/kg) 14.08
 Crude protein 19.21
 Crude fiber 2.88
 Ash 6.14
 Calcium 0.82
 Total phosphorus 0.65
 Lysine 1.32

1 Isomaltooligosaccharides were simply added to the control diet at concentrations of 0.2%, 0.4%, 0.6%, and 0.8% at the expense of corn.

2 2,000 ppm zinc oxide was added to the diets from day 0 to 14.

3 Crude protein concentration of dehulled soybean meal is 47.60%.

4 Provided per kg diet: vitamin A, 9,000 IU; vitamin D3, 3,000 IU; vitamin E, 20 IU; vitamin K3, 3.0 mg; thiamine, 1.5 mg; riboflavin, 4.0 mg; pyridoxine, 3.0 mg; cobalamin, 0.2 mg; biotin, 0.1 mg; pantothenic acid, 30 mg; nicotinic acid, 15 mg; folic acid, 0.75 mg; iron (from FeSO4•H2O), 75 mg; copper (from CuSO4), 150 mg; zinc (from ZnSO4), 75 mg; manganese (from MnSO4), 60 mg; iodine (from KI), 0.35 mg; selenium (from Na2SeO3), 0.3 mg; roxarsone, 25 mg; olaquindox, 50 mg.

5 All nutrient levels except metabolizable energy were chemically analyzed and the results are the means of duplicate determinations.

Table 2
Performance of 28-day old weaned pigs fed diets containing graded levels of isomaltooligosaccharides (d 0 to 28)
Item Level of isomaltooligosaccharides (%) SEM p-value


0.0 0.2 0.4 0.6 0.8 Linear Quadratic
0 to 14 d
 Daily gain (kg) 0.36 0.36 0.39 0.43 0.45 0.01 <0.01 0.45
 Daily feed intake (kg) 0.57 0.62 0.64 0.61 0.66 0.02 0.31 0.79
 Gain:feed 0.64 0.58 0.60 0.71 0.69 0.05 0.01 0.14
 Diarrhea (%)1 8.93 2.50 2.86 4.28 2.14 1.53 0.05 0.05
15 to 28 d
 Daily gain (kg) 0.45 0.47 0.49 0.56 0.56 0.02 0.07 0.92
 Daily feed intake (kg) 0.88 0.93 0.92 0.96 0.99 0.06 0.26 0.98
 Gain:feed 0.51 0.51 0.53 0.60 0.57 0.11 0.11 0.99
 Diarrhea (%) 3.21 4.64 3.57 1.78 1.43 1.50 0.21 0.48
0 to 28 d
 Daily gain (kg) 0.40 0.42 0.44 0.49 0.51 0.01 0.01 0.78
 Daily feed intake (kg) 0.73 0.78 0.78 0.79 0.82 0.04 0.26 0.92
 Gain:feed 0.56 0.54 0.56 0.64 0.62 0.06 0.02 0.55
 Diarrhea (%) 6.07 3.57 3.21 3.04 1.79 1.13 0.02 0.56

SEM, standard error of the mean.

Values are the means of six replicates.

1 Diarrhea, the ratio between the number of pigs with diarrhea each day and the total number of pigs in each group.

Table 3
Serum biochemical measures of weaned pigs fed diets containing graded levels of isomaltooligosaccharides
Item Level of isomaltooligosaccharides (%) SEM p-value


0.0 0.2 0.4 0.6 0.8 Linear Quadratic
d 14
 Immunoglobulin A (g/L) 0.95 1.11 1.27 1.26 1.31 0.08 <0.01 0.21
 Immunoglobulin M (g/L) 0.71 0.84 0.93 0.87 0.94 0.04 <0.01 0.13
 Immunoglobulin G (g/L) 6.92 8.05 8.58 8.69 8.12 0.26 0.01 <0.01
 Interleukin-2 (ng/mL) 4.87 5.10 5.58 5.44 4.67 0.37 0.96 0.11
 Interleukin-6 (pg/mL) 216.77 162.64 169.11 148.68 156.17 9.96 <0.01 0.03
 Interleukin-8 (ng/mL) 0.70 0.67 0.63 0.61 0.66 0.05 0.39 0.34
d 28
 Immunoglobulin A (g/L) 1.19 1.10 0.92 1.10 1.07 0.09 0.46 0.20
 Immunoglobulin M (g/L) 0.90 0.90 0.98 0.83 0.83 0.05 0.29 0.28
 Immunoglobulin G (g/L) 8.36 8.22 8.64 8.40 8.40 0.25 0.76 0.72
 Interleukin-2 (ng/mL) 3.63 3.57 4.17 5.69 5.67 0.34 <0.01 0.51
 Interleukin-6 (pg/mL) 143.39 136.56 141.66 158.06 147.24 11.84 0.47 0.94
 Interleukin-8 (ng/mL) 0.38 0.34 0.34 0.53 0.33 0.03 0.51 0.49

SEM, standard error of the mean.

Values are the means of six replicates.

Table 4
Intestinal microflora (log10 CFU/g) of weaned pigs fed diets containing graded levels of isomaltooligosaccharides (d 28)
Item Level of isomaltooligosaccharides (%) SEM p-value


0.0 0.2 0.4 0.6 0.8 Linear Quadratic
Ileum
 Total aerobic bacteria 7.34 7.15 7.39 7.20 8.31 0.34 0.20 0.23
 Total anaerobic bacteria 7.90 7.30 7.75 6.93 7.35 0.33 0.31 0.66
Lactobacillus 7.07 6.42 6.43 6.95 7.08 0.38 0.73 0.29
Escherichia coli 5.19 4.12 5.16 3.34 3.84 0.58 0.19 0.94
Cecum
 Total aerobic bacteria 7.67 7.44 7.54 7.26 6.62 0.34 0.12 0.49
 Total anaerobic bacteria 7.77 7.95 8.26 7.75 6.66 0.41 0.20 0.12
Lactobacillus 7.73 7.83 8.17 7.76 7.47 0.21 0.54 0.17
Escherichia coli 3.96 3.87 3.96 3.86 3.60 0.58 0.75 0.85

SEM, standard error of the mean.

Values are the means of six replicates.

Table 5
Intestinal mucosal morphology of weaned pigs fed diets containing graded levels of isomaltooligosaccharides (d 28)
Item Level of isomaltooligosaccharides (%) SEM p-value


0.0 0.2 0.4 0.6 0.8 Linear Quadratic
Jejunum (μm)
 Villus height 280 294 308 306 290 10.41 0.41 0.20
 Crypt depth 313 310 286 343 314 14.08 0.62 0.90
Ileum (μm)
 Villus height 341 315 371 347 316 16.28 0.98 0.39
 Crypt depth 361 400 336 363 351 14.09 0.51 0.82

SEM, standard error of the mean.

Values are the means of six replicates.

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