A combination of yeast beta-glucan and milk hydrolysate is a suitable alternative to zinc oxide in the race to alleviate post-weaning diarrhoea in piglets
A combination of yeast beta-glucan and milk hydrolysate is a suitable alternative to zinc oxide in the race to alleviate post-weaning diarrhoea in piglets
Zinc oxide (ZnO) is currently used as a dietary supplement to support gut homeostasis during the standard 'abrupt' weaning practices in commercial pig production. However, a replacement is urgently required as a ban on ZnO usage is imminent. The objective of this study was to explore the potential of a bovine casein hydrolysate (5kDaR) and yeast β-glucan, and their combination, as an alternative to ZnO. Eighty 21d old male piglets received a basal diet or supplemented with 5kDaR and yeast β-glucan alone or in combination, or ZnO from the day of weaning and were monitored for 10 days (n=8/group; dietary groups: control diet; control diet+5kDaR; control diet+yeast β-glucan; control diet+5kDaR+yeast β-glucan; control diet+ZnO). Individually, supplement yeast β-glucan or 5kDaR did not improve gut health. In contrast, the yeast β-glucan+5kDaR combination supplement supported a healthy gut, indicated by healthy faecal scores and improved growth parameters; similar to ZnO inclusion (P>0.05). There was no negative efect on the gut microbiota with yeast β-glucan+5kDaR supplementation; while ZnO negatively afected the Bifdobacterium spp. abundance (P<0.05). The infammatory NFκB pathway was suppressed by yeast β-glucan+5kDaR supplementation, similar to ZnO (P>0.05). In conclusion, the dietary supplement yeast β-glucan+5kDaR restored homeostasis of the newly weaned piglet gut similar to the widely used ZnO, and can potentially replace ZnO.
Weaning is typically initiated between 14–28 days afer birth and is a critical period in commercial pig production systems. During this period, piglets are vulnerable to a variety of physiological and environmental stressors, as reviewed by Lallès et al.1. The 'abrupt weaning' that occurs in commercial pig production can result in reduced feed intake, with consequent efects on weight gain and both transitory and long-lasting modifcations to the absorptive, secretory and barrier properties of the intestine2. There are also changes to the microbiota, characterised by a marked decrease in biodiversity3; which increases the risk of pathogenic bacteria such as enterotoxigenic Escherichia coli (ETEC) gaining a niche in the gastrointestinal tract (GIT). This ofen leads to post-weaning diarrhoea in the piglets4,5. Traditionally, the dietary inclusion of antibiotic growth promoters (AGP) and/or high concentrations of zinc oxide (ZnO) have been used to overcome the anticipated gastrointestinal disturbances at this vulnerable time6–10. Both the EU ban on AGPs and environmental concerns over the use of heavy metals have been highlighted by Sales9; driving eforts to identify natural bioactives with growth promoting and/or immunomodulatory properties which could be used to overcome these post-weaning complications11–13.
The process of identifying natural sustainable sources of bioactives that could support a healthy gastrointestinal system in both animals and humans include preliminary screening and testing of the compounds in-vitro. Milk hydrolysates, based on their source and chemical composition have wide ranging bioactive properties including anti-microbial and anti-infammatory properties14. Yeast β-glucan15 also has bioactive properties across a range of diferent contexts. Beta-glucans are complex polysaccharides derived from a range of sources including plants, yeast and fungi with a variety of in-vitro bioactivities including anti-cancer, anti-infammatory and immune-modulating properties, reviewed by Zhu et al.16. While the in-vitro screening approach is cost efective and non-invasive relative to in-vivo studies, many compounds reported to have bioactive properties in-vitro have reduced bioavailability in in-vivo; this is in part attributable to the exposure of the bioactive ingredient to digestive enzymes and alterations in gastric pH that subsequently alters the bioavailability of the compound17. In a previous study, a 5 kDa retentate (5kDaR), derived from moderate degree of hydrolysis (11–16%) of bovine milk casein, demonstrated potent anti-infammatory activity both in-vitro and ex-vivo colonic models18. However, the anti-infammatory activity of this 5kDaR protein hydrolysate was no longer evident when it was used as a feed supplement in an experimental weaning piglet model19.
Protecting the bioactive properties of any natural compound in-vivo is a growing area of interest20. Natural encapsulating and delivery agents like β-glucan, can be used to protect the digestion of bioactive compounds in the stomach21,22. Yeast β-glucans are of interest, as apart from serving as a natural delivery agent, they also elicit immunomodulatory efects, both in-vitro and in-vivo15,23. Hence, the objectives of this experiment were frstly to compare the efects of a milk protein hydrolysate (5kDaR), a yeast β-glucan and a combination of the 5kDaR+yeast β-glucan on growth performance and gut health in the newly weaned pig. Secondly, to determine if any of these supplements are comparable to ZnO. The hypothesis of this study was that a combination of yeast β-glucan and milk hydrolysate will support growth and gut health parameters similar to ZnO in a post-weaned pig diet.
Materials and Methods
All procedures described in this experiment were conducted under the experimental license from the Irish Department of Health (License number: AREC-P-12-54-Sweeney; License holder: Prof. Torres Sweeney), in accordance with the Cruelty to Animals Act 1876 and the European Communities (amendments of the Cruelty to Animals Act 1876) regulations, 1994.
Experimental Design and Dietary Treatments. This study was designed as a complete randomised design comprising of 5 dietary treatments. The dietary treatments were as follows: 1) control diet, 2) control diet+ 5kDaR, 3) control diet+ yeast β-glucan, 4) control diet+ 5kDaR + yeast β-glucan and 5) control diet+ZnO (3.2 g/kg feed, pharmacological dose). The generation of 5kDaR, used in this study, from bovine milk derived sodium caseinate, has been reported previously18. The optimum concentrations of 5kDaR and yeast β-glucan were established from previous studies19,23. The diets were formulated to contain similar concentrations of digestible energy (DE) (14.5 MJ/kg) and standardized ileal digestible (SID) lysine (12.5 g/kg) contents. All amino acid requirements were met relative to SID lysine24. All diets were milled on site and fed in meal form for 10 days post-weaning. The ingredient composition and compositional analysis of the experimental diets are presented in Table 1.
Animals and Management. Eighty male weaned piglets, twenty one days old, [progeny of Landrace boars x (Large White x Landrace) sows] were weighed and blocked on the basis of initial live weight (7.3±0.2 kg) and assigned to one of the fve dietary treatment groups and housed in pairs on fully slatted foors (1.68×1.22 m) (n=8). Piglets were weighed individually at the beginning of the experiment (day 0=day of weaning) and subsequently on days 5 and 10. The ambient environmental temperature within the house was thermostatically controlled at 30 °C and humidity was maintained at 65%. All feed and water was available ad libitum. Feed, in meal form, was available up to the fnal weighing and all remaining feed was re-weighed for the purposes of calculating average daily feed intake (ADFI) and gain to feed ratio (G:F).
Faecal scoring. One measure of gut health in a live animal is the faecal score, which is performed by scoring the consistency of the faeces, as described previously25. From day 0 until day 10, faecal scores were assessed twice daily for each individual pen to indicate the presence and severity of diarrhoea. The following scoring system was used to assign faecal scores: 1=hard, 2=slightly sof, 3=sof, partially formed, 4=loose, semi-liquid, 5=watery, mucous-like.
Animal sacrifce and sample collection. On day 10, piglets were sacrifced following a lethal injection of Euthatal -pentobarbitone sodium BP- (Merial Animal Ltd, Sandringham House, Essex, UK) at a rate of 1mL/1·4 kg live body weight. Following this, the digestive tract was surgically removed and tissue samples from duodenum, ileum and colon were collected in sterile phosphate bufer saline (PBS) (Oxoid, Basingstoke, UK). Digesta samples were then recovered aseptically from the caecum and colon and transported on ice for storage at −20 °C.
Extraction of microbial DNA from caecal and colonic digesta. Samples of digesta (approximately 10 g) were recovered from the caecum and colon and stored in sterile 50 ml tubes (Sarstaedt, Wexford, Ireland) at −20 °C and transported to the laboratory within 2h. Bacterial genomic DNA was extracted from digesta samples using the QIAamp DNA stool kit (Qiagen, West Sussex, UK) following manufacturer's instructions. The quantity and quality of DNA was assessed using the Nanodrop spectrophotometer (Nanodrop, ND1000; Termo Scientifc, Wilmington, DE) and the purifed DNA stored at −20 °C.
Microbial quantifcation using quantitative real time polymerase chain reaction (qPCR). Standard curve preparation: A pooled aliquot of bacterial DNA derived from all animals was used to prepare standard curves for qPCR. Phylum, family, genus and strain specifc primers were used to amplify the 16s rRNA gene (Table 2). Standard curves were subsequently generated by carrying out qPCR on serial dilutions of amplicons using the same genus and species-specifc primers to permit absolute quantifcation, based on gene copy number26.
Table 1. Ingredient and compositional analysis of the diets. *Calculated for tabulated nutritional composition51 Provided (mg/kg complete diet): Cu, 100; Fe, 140; Mn, 47; Zn, 120; I, 0·6; Se, 0·3; retinol, 1·8; cholecalciferol, 0·025; α-tocopherol, 67; phytylmenaquinone, 4; cyanocobalamin, 0·01; ribofavin, 2; nicotinic acid, 12; pantothenic acid, 10; choline chloride, 250; thiamin, 2; pyridoxine, 0·015. Celite included at 300mg/kg complete diet.
Table 2. Oligonucleotide sequence of forward and reverse primers used for qPCR of bacterial 16s rRNA.
Estimation of selected bacterial groups in the caecal and colonic digesta: Estimation of selected bacterial groups in the caecal and colonic digesta: All reactions were performed on the ABI 7500 Fast PCR System (Applied Biosystems Ltd., Warrington, UK). For bacterial groups, qPCR was performed in a fnal reaction volume of 20μL containing 1μL template DNA, 1μL of forward and reverse primers (25 pM), 10μL Fast SYBR Green Master Mix (Applied Biosystems) and 8μL nuclease-free water. The cycling conditions included a denaturation step of 95 °C for 10min followed by 40 cycles of 95 °C for 15 s and 65 °C for 1min. All reactions were performed in triplicate.
Dissociation curves were generated to confrm the specifcity of the resulting PCR products. The dry matter (DM) of the digesta was determined afer drying overnight at 103°C. Estimates of gene copy numbers for select bacteria were log transformed and are presented as gene copy numbers per gram of DM of digesta.
Gene expression profling using qPCR. RNA extraction: Tissue samples were collected from the duodenum, ileum and colon, rinsed with ice-cold sterile PBS (Oxoid, Basingstoke, UK) and then the overlying smooth muscle was stripped of. The samples were then cut into 1 cm2 sections using a sterile scalpel and stored in 5ml of RNAlater™ (Applied Biosystems, Foster City, CA, USA) overnight, followed by storage at −20 °C prior to RNA extraction. Approximately 50mg of tissue was used for RNA extraction, using the GenElute™ Mammalian Total RNA Miniprep Kit (Sigma–Aldrich Ireland Ltd., Co. Wicklow, Ireland), following the manufacturer's instructions. Quantifcation of the total RNA was performed using 1.5μL of total RNA on a NanoDrop™ Spectrophotometer ND1000 (Termo Scientifc, Wilmington, DE, USA) and samples with 260:280 ratio ≥2.0 were considered suitable for omplementary DNA (cDNA) synthesis. Total RNA integrity (i.e. quality and quantity) was assessed by analysing 1 μl of total RNA using the Agilent 2100 Bioanalyser™ version A.02.12 (Agilent Technologies, Santa Clara, CA, USA) using RNA Nano LabChips® (Caliper Technologies Corporation, Mountain View, CA, USA).
cDNA synthesis: Total RNA (1 µg) was used for the synthesis of First Strand cDNA using the First Strand cDNA Synthesis Kit (Qiagen Ltd. Crawley, UK) using oligo dT primers following the manufactures instructions. Afer the cDNA synthesis, the fnal volume was adjusted to 120 µL with nuclease free water.
Quantitative Real-Time PCR: qPCR was performed on a select panel of cytokines including; IL1A, IL1B, IL4, IL6, IL8, IL10, IL17, IL21, Interferon (INFG), Tumor Necrosis Factor (TNF), transforming growth factor (TGFB), Forkhead box P3 (FOXP3), nutrient transporters including, Fatty acid binding protein (FABP), Glucose transporter 2 (GLUT2), Peptide transporter 1 (PEPT1) and tight junction protein Occludin (OCLN). All primers were designed using Primer Express™ sofware and were synthesised by MWG Biotech (Milton Keynes, UK) and are presented in Table 3, all assays had efciencies in the range of 90–110%. Dissociation analysis confrmed the specifcity of the resulting PCR products. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH), β2 microglobulin (B2M), Beta-actin (ACTB), Peptidylprolyl isomerase A (PPIA) and 14-3-3 protein zeta/delta (YWHAZ) were used as endogenous controls. Quantitative PCR was carried out using 96 well fast optical plates on a 7500HT ABI Prism Sequence Detection System (Applied Biosystems, Foster City, CA) using Fast SYBR Green PCR Master Mix (Applied Biosystems). All reactions were performed in triplicate in a total volume of 20 µL containing 10 µL Fast SyBr PCR Master mix, 1 µL forward and reverse primer (5 µM) and 8 µL water and 1 µL of template cDNA. The thermal cycling conditions were as follows, 95 °C for 10min, 40 cycles of 95 °C for 15 s and 65 °C for 1 min.
Normalization of data: Mean Ct values were converted to relative quantities using the formula, Relative quantity=2−ΔCt, where ΔCt is the change in the Ct values of the sample relative to the highest expression (minimum Ct value). Relative quantities for the endogenous controls were imported into geNorm27 and a normalization factor was derived. B2M and ACTB had the lowest M value of all the reference genes tested and were therefore chosen for subsequent normalization. The relative quantities for the target genes were then divided by the normalization factor to give the fnal normalized relative quantity for each target gene in each sample.
Laboratory analysis of feed. The feed samples were milled through a 1mm screen (Christy and Norris hammer mill, Ipswich, UK). The dry matter (DM) of the feed was determined after drying at 103 °C for a minimum of 16 h. Ash was determined afer ignition of a known weight of concentrate in a mufe furnace (Nabertherm, Bremen, Germany) at 500 °C for 4h. The crude protein (CP) content was determined as Kjeldahl N × 6.25 using the LECO FP 528 instrument. The neutral detergent fbre (NDF) content was determined according to Van Soest et al.28.
Statistical analysis. The data were initially checked for normality using the UNIVARIATE procedure of SAS. The growth performance and faecal scores were analysed by repeated measures analysis using PROC MIXED procedure of SAS29. The model included the fxed efects of yeast β-glucan, 5kDaR, time and the associated two and three way interactions while the random efect was pen. Initial body weight was used as a covariate for growth performance data. The data on microbial population and gene expression were analysed using PROC MIXED procedure of SAS. The model included yeast β-glucan, 5kDaR and the associated two way interaction and the random efect was pen. Contrast statements were used to compare (1) T1 and T3 vs. T2 and T4 – non-5kDaR-supplemented vs. 5kDaR-supplemented pigs (5kDaR efect), (2) T1 and T2 vs. T3 and T4 – non-yeast-supplemented vs. yeast-supplemented pigs (yeast β-glucan efect), (3) the interaction between the 5kDaR efect and yeast β-glucan efect. Additionally contrast statements were used to compare ZnO (T5) with the control diet (T1) (Contrast 4) and with the combination of yeast β-glucan+5kDaR inclusion (T4) (Contrast 5). The individual pen served as the experimental unit for all variables measured. Least square means were computed, and P-values were adjusted for multiple comparisons using the Tukey-Kramer adjustment. The mean values were considered to be signifcantly diferent when P<0.05 and considered a numerical tendency when P<0.10. Least square means are reported with pooled standard errors.
Faecal score. The efects of dietary treatments on faecal scores are presented in Fig. 1. A healthy gut is associated with faecal scores between 2.0 to 2.5 whereas faecal scores of 3.0 to 4.0 represent diarrhoea scores and 4.5 to 5.0 represent severe diarrhoea that requires antibiotic intervention. While there was no yeast β-glucan x 5kDaR x time interaction on faecal scores (P>0.05); a time efect on faecal scores was evident. There was an interaction between yeast β-glucan x 5kDaR on faecal scores (P<0.05; Contrast 3); the inclusion of 5kDaR alone or yeast β-glucan alone had no efect on faecal scores compared to the control diet, while the combination of 5kDaR+yeast β-glucan decreased faecal scores compared to the individual supplements. The inclusion of ZnO decreased faecal scores relative to the control treatment (P<0.05; Contrast 4) while faecal scores were similar between ZnO and the combination of 5kDaR+yeast β-glucan (P>0.05; Contrast 5) throughout the experimental period.
Table 3. Oligonucleotide sequence of forward and reverse primers used in all qPCR assays.
Growth parameters. The efects of dietary supplements on body weight (at d 10), average daily gain (ADG), average daily feed intake (ADFI) and gain to feed ratio (G:F) are presented in Table 4. There was no yeast β-glucan x 5kDaR x time interaction on body weight, ADG, ADFI or G:F. There was a signifcant time efect on ADG (P<0.05) and ADFI (P<0.001). There was an interaction between yeast β-glucan x 5kDaR on body weight and ADG (P<0.05; Contrast 3); the inclusion of 5kDaR alone or yeast β-glucan alone had no efect on body weight or ADG compared to the control diet, while the combination of 5kDaR+yeast β-glucan increased bodyweight and ADG compared to the individual supplements. The inclusion of ZnO increased body weight (P < 0.05), ADG (P<0.01) and ADFI (P<0.05) compared to the control group (Contrast 4) while these parameters were similar between the piglets ofered ZnO and the combination of 5kDaR+yeast β-glucan (P>0.05; Contrast 5).
Figure 1. Efect of dietary treatments on faecal scores from 0 d up to 10 d post-weaning. Values are LS means, with their standard errors represented by vertical bars. Scale from 1 to 5: (1) hard, frm faeces; (2) slightly sof faeces; (3) sof, partially formed faeces; (4) loose, semi-liquid faeces; and (5) watery, mucous-like faeces (Pierce et al., 2007). The dietary treatments are represented as: (-♦-) control diet, (-■-) 5kDaR diet, (--▲--) yeast β-glucan diet, (-Ο-) 5kDaR+yeast β-glucan diet and (-□-) ZnO diet. The contrast statement used and statistical signifcance values achieved are as follows: Contrast 1, the efect of 5kDaR vs. non 5kDaR diet (P<0.001); Contrast 2, the efect of yeast β-glucan vs. non yeast β-glucan diet (P>0.05); Contrast 3: the interaction between 5kDaR and yeast β-glucan (P<0.05); Contrast 4, the efect of ZnO vs control diet (P<0.01); and Contrast 5: the ZnO vs. 5kDaR and yeast β-glucan (P>0.05).
Table 4. Efect of feed supplements on body weight, average daily gain (ADG), average daily feed intake (ADFI) and gain to feed ratio (G:F) in weaning pigs (LSM ± SEM). aContrast 1: the efect of 5kDaR vs. non 5kDaR diet. bContrast 2: the efect of yeast β-glucan vs. non yeast β-glucan diet. cContrast 3: the interaction between 5kDaR and yeast β-glucan. dContrast 4: the efect of ZnO vs. control diet. eContrast 5: the ZnO vs 5kDaR and yeast β-glucan.
Caecal digesta. There was a yeast β-glucan x 5kDaR interaction observed on the abundance of Bifdobacterium spp. and Attaching and Efacing Escherichia coli (AEEC) strains (P<0.05; Contrast 3). The inclusion of yeast β-glucan increased the abundance of AEEC strains and decreased the abundance of Bifdobacterium spp. compared to the control diet, however the abundance of AEEC strains and Bifdobacterium spp. were not altered when yeast was added to the 5kDaR diet. The piglets ofered diets supplemented with 5kDaR had increased Bacteroidetes (12.498 vs. 11.607±0.255, P<0.05) compared to the diets without 5kDaR inclusion (Contrast 1). The inclusion of ZnO in the diet increased the Bacteroidetes abundance and decreased the abundance of Bifdobacterium spp. (P<0.05) compared to the control (Contrast 4) and the combination of 5kDaR+yeast β-glucan diets (P<0.05; Contrast 5).
Colonic digesta. There was no interaction between yeast β-glucan x 5kDaR on the selected microbial populations (Contrast 3). Similar to the caecum, dietary inclusion of yeast β-glucan decreased the abundance of Bifdobacterium spp. compared to non yeast β-glucan diets (8.911 vs. 9.302±0.127, P<0.05). The inclusion of ZnO in the diet decreased the abundance of Bifdobacterium spp. compared to the control diet (P<0.05).
Table 5. Efect of feed additives on log transformed gene copy number/g dry matter of digesta of a panel of selected bacterial groups present in caecal and colonic digesta (LSM ± SEM). aContrast 1: the efect of 5kDaR vs. non 5kDaR diet. bContrast 2: the efect of yeast β-glucan vs. non yeast β-glucan diet. cContrast 3: the interaction between 5kDaR and yeast β-glucan. dContrast 4: the efect of ZnO vs. control diet. eContrast 5: the ZnO vs 5kDaR and yeast β-glucan.
Gene expression analysis of duodenum, ileum and colon. The efect of dietary supplements on the normalized relative expression of a selected panel of genes expressing cytokines (IL1A, IL1B, IL4, IL6, IL8, 1L10, IL17. INFG, TNF, TGFB), nutrient transporters (FABP, PEPT1, GLUT2) and tight junction proteins (OCLN) in the duodenum and ileum are presented in Table 6.
Duodenum. There was no interaction between yeast β-glucan x 5kDaR on the selected panel of genes examined in the duodenal tissue (Contrast 3). Inclusion of 5kDaR in the diet suppressed the expression of IL1A (0.827 vs. 1.257±0.085, P<0.01), IL8 (0.827 vs. 1.190±0.080, P<0.05) and a tendency to suppress IL1B (0.939 vs. 1.313±0.121, P<0.06) and INFG (0.993 vs. 1.046±0.121, P<0.07) compared to the diets without 5kDaR supplementation (Contrast 1). The inclusion of yeast β-glucan had no efect (P>0.05) on the selected panel of genes examined in the duodenum.
The inclusion of ZnO in diet suppressed the expression of IL8, IL17, INFG and TGFB (P<0.05) compared to control diet (Contrast 4). The expression levels of the selected panel of genes were similar between the ZnO diet and yeast β-glucan+5kDaR diet, except for TGFB, which was decreased in the ZnO diet (P<0.05).
Ileum. There were no interactions observed between yeast β-glucan x 5kDaR on the selected panel of genes (Contrast 3). The inclusion of 5kDaR in the diet increased the expression of GLUT2 compared to diets without 5kDaR supplementation (1.012 vs. 0.707±0.101, P<0.05). The yeast β-glucan inclusion suppressed the expression of IL10 (0.933 vs. 1.242±0.0899, P<0.05) compared to diets without yeast β-glucan supplementation. Zinc oxide suppressed the expression of IL1A, IL1B, IL8 and IL10 and increased the expression of PEPT1 and GLUT2 (P<0.05) compared to the control diet. The expression levels of the selected panel of genes were similar between the ZnO diet and yeast β-glucan+5kDaR diet, other than a numerical increase in PEPT1 (P<0.06) in the ZnO diet.
Colon. There was no yeast β-glucan x 5kDaR interactions observed on the selected panel of genes in the colonic tissues. The inclusion of 5kDaR in diet suppressed the expression of IL8 (0.952 vs. 2.298±0.2914; P<0.01) and INFG (0.743 vs. 1.719±0.1852; P<0.01) and numerically decreased TNF (0.823 vs. 1.495 ±0.240; P<0.06) compared to non-5kDaR diets. The inclusion of yeast β-glucan increased the expression of IL8 (2.083 vs. 1.167; P<0.01) and decreased the expression of INFG (0.798 vs. 1.664±0.1830; P<0.05) and TGFB (0.986 vs. 1.662±0.2130; P<0.01) compared to non-yeast β-glucan diets. The inclusion of ZnO suppressed the expression of INFG (P<0.01) compared to the control diet. The expression levels of the selected panel of genes were similar between the ZnO diet and yeast β-glucan+5kDaR diet.
This study examined the potential health benefts of dietary inclusion of a sodium caseinate derived milk hydrolysate (5kDaR) and a yeast β-glucan, individually or in combination, in piglets following early and abrupt separation from the sow. These dietary supplements were compared to the recommended pharmacological dose of zinc oxide (ZnO) and evaluated on parameters including faecal scores, growth performance and the re-establishment of gut homeostasis (microbial composition and mucosal infammation). While numerous studies have explored the potential benefts of diferent feed supplements following abrupt weaning, no single compound has been able to replace ZnO. There is, however, imminent pressure to eliminate the use of heavy metals in pig diets13. In the current study, the individual inclusion of either 5kDaR or yeast β-glucan did not support the re-establishment of gut homeostasis during the post-weaning challenge period. However, supplementing the piglet diet with a combination of yeast β-glucan+5kDaR suppressed post-weaning diarrhoea, improved faecal scores, growth parameters and suppressed the expression of infammatory gene markers in duodenal and ileal tissues – efects comparable to those observed in piglets supplemented with the pharmacological dose of ZnO.
Table 6. Efect of dietary treatments on relative quantity (RQ) of a panel of selected cytokine and nutrient transporter gene expression in porcine colonic tissues (LSM ± SEM). The targets IL4, IL6, IL21, FABP, FOXP3 and OCLN expression were undetectable in all the analysed tissue samples. PEPT1 and GLUT2 expression were undetectable in colonic tissues. aContrast 1: the efect of 5kDaR vs. non 5kDaR diets. bContrast 2: the efect of yeast β-glucan vs. non yeast β-glucan diets. cContrast 3: the interaction between 5kDaR and yeast β-glucan. dContrast 4: the efect of ZnO vs. control diet. eContrast 5: the ZnO vs 5kDaR and yeast β-glucan.
Post-weaning diarrhoea is a consequence of decreased digestive and absorptive capacity of the small intestine that leads to an increase in pathogenic bacterial numbers in the large intestine30. An established method of evaluating gut health of a newly weaned piglet is by scoring their faeces based on consistency25. This is also accepted as a criterion for claims on maintenance of normal gut function for humans by the European Food Safety Authority31. In this study, piglets supplemented with pharmacological doses of ZnO maintained healthy faecal scores of approximately 2.0 to 2.5 throughout the experimental period. In contrast, the pigs receiving the basal diet or individual inclusion of 5kDaR or yeast β-glucan showed signs of diarrhoea (faecal score range 3.0 to 4.0) from day 2–3 until day 9–10 post-weaning. In contrast, the combination of yeast β-glucan+5kDaR restored healthy functioning of the gut during the post-weaning period similar to ZnO supplementation.
In the current study, piglets receiving the basal diet had higher numbers of Enterobacteriaceae and AEEC strains in caecal and colonic digesta along with diarrhoea/raised faecal scores. A plausible explanation for this might be the high crude protein concentration in the diet, a high soybean meal inclusion level and a low level of lactose32, which can disrupt gut homeostasis in the weaned piglet. In a previous study, the high level of dietary crude protein predisposed the piglet to post-weaning colibacillosis33. In contrast, supplementation of the basal diet with the combination of yeast β-glucan+5kDaR maintained healthy faecal scores with lower abundance of pathogenic bacteria in the digesta.
The maintenance of a healthy gut, by supplementation with yeast β-glucan+5kDaR combination and ZnO, was not only evident through improved faecal scores, but these piglets also had improved growth parameters (ADG, ADFI and body weights on d 10). In contrast, the individual inclusion of 5kDaR or yeast β-glucan had no efect on the measured growth parameters. Dong & Pluske34 clearly identifed the necessity to improve feed intake immediately post-weaning, as low feed intake, which is synonymous with commercial weaning practices, leads to disrupted gut morphology, poor growth rate and higher risk of disease. In the current study, both yeast β-glucan+5kDaR and ZnO supplemented pigs had higher ADFI than the pigs fed the basal diet. While commercial weaning negatively impacts the absorptive capacity of the small intestine30; the ZnO and yeast β-glucan+5kDaR supplemented piglets had increased expression of GLUT2 and PEPT1 in the ileum. Glucose transporter 2 is widely known to facilitate the absorption of glucose in the small intestine35, and was recently associated with maintenance of gut homeostasis in rats36. The intestinal absorption of hydrolysed proteins is facilitated by PEPT1; in fact PEPT1 also has a role in gut homeostasis37. The increased expression of GLUT2 and PEPT1 is most likely related to a higher availability of glucose and amino acids in the small intestine as well as increased villus surface area, as a consequence of the higher ADFI in both the yeast β-glucan+5kDaR and ZnO groups.
The gut microbiota plays an important role in maintaining gut homeostasis in both humans and animals38,39. Four important phyla in the caecum and colon of healthy pigs are Bacteroidetes, Firmicutes, Actinobacteria and Proteobacteria40–42. The main role of Bacteroidetes and Firmicutes is to ferment the undigested fbre in the distal part of the gastrointestinal tract. The phylum Bacteroidetes is further associated with gastrointestinal tract development, activation of T cell mediated immune response and limiting the colonization of the gut with pathogenic bacteria43. In this study, the inclusion of both ZnO and 5kDaR was associated with an increase in Bacteroidetes in the caecal digesta. An important member of the Actinobacteria phylum is the Bifdobacterium spp., because of its probiotic potential44. This species was decreased with the inclusion of ZnO and yeast β-glucan. Interestingly, the yeast β-glucan+5kDaR combination did not negatively infuence the abundance of the analyzed gut bacteria and was associated with higher abundance of the Bifdobacterium spp. A more indepth metagenomic analysis of the gut microbiome would be benefcial to confrm that the combination diet does indeed have an enhanced benefcial microbial efect over ZnO.
Within the Proteobacteria phylum, the abundance of Enterobacteriaceae family and AEEC strains were measured in this study. The inclusion of yeast β-glucan in the newly weaned piglet was associated with a signifcant increase in the pathogenic AEEC strains in the large intestine, which may explain the diarrhoeal faecal scores, the lower performance and increased infammation of the gut in the piglets. This appears contradictory to a previous study that identifed that the abundance of Enterobacteriaceae was decreased following dietary inclusion of similar yeast β-glucan in mature healthy 19kg pigs23. This variation in response to β-glucans may refect the diference in the status of the piglet immune system at these diferent stages of development. Abrupt commercial weaning normally occurs during a time period where the piglet is partially dependent on maternal imunoglobulins, via the milk, and does not yet have a fully developed adaptive immune system. In contrast to a more mature pig, yeast β-glucan may not have a benefcial efect during this time-period as it elicits its response against pathogens by activating immune cells such as granulocytes, monocytes and macrophages45. This suggests that consideration must be given to the stage of development of the pig while exploring the options of dietary supplementation.
Homeostasis of the gut is dependent on the orchestration of a signaling network that exists between the intestinal epithelial cells, gut microbiota and the local immune cells. Disruption of this regulatory mechanism can lead to chronic intestinal infammation, as observed in pigs12 and humans43. The plausible role of ZnO in maintaining gut homeostasis during abrupt weaning in the pig, by suppressing the infammatory nuclear factor κB (NFκB) pathway46, is clear in this experiment. The inclusion of both ZnO and the combination of yeast β-glucan+5kDaR was associated with a decrease in the pro-infammatory cytokines IL1A, IL1B, IL8, IL17 and INFG expression in both duodenal and ileal tissues. Similar efects of ZnO on the NFκB pathway were shown previously by Bouwhuis et al.47. This suggests that the combination of yeast β-glucan+5kDaR also suppresses of the NFκB pathway. The inclusion of 5kDaR suppressed the expression of pro-infammatory IL1A and IL8 genes in the duodenal tissue; however this suppression was no longer evident in the ileum and only evident for IL8 in the colon, indicating a gradual breakdown of the bioactive molecules during transit through the small intestine. In contrast, the inclusion of yeast β-glucan alone in the diet had no efect on the immune gene expression profle in the duodenal or ileal tissues, with increased IL8 expression in the colon.
An interesting fnding from this study was the synergistic interaction observed between the yeast β-glucan and the 5kDaR. While it was not within the scope of this study to explore the biochemical nature of this interaction, one possibility is that the β-glucan acted as a microencapsulating agent for the milk hydrolysate, thus preserving its bioactivity in-vivo. Beta-glucans, from a range of sources including yeast48,49, oats50 and barley22 have properties that make them suitable encapsulation agents. More in-depth studies are warranted to identify how the current combination of supplements exerts this protective function in the gastric environment.
The combination of 5kDaR+yeast β-glucan supplementation in the weaning pig diet was associated with an improvement in overall performance and gut health parameters (faecal consistency, microbiota and infammation) that are, at least, omparable to ZnO. This study also suggests that yeast β-glucan may have a protective function for proteins in the gastric environment worthy of further exploration.
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Article made possible through the contribution of T. Sweeney et al. and University College Dublin