Astragalus and Ginseng Polysaccharides Improve Developmental, Intestinal Morphological, and Immune Functional Characters of Weaned Piglets

Antibiotic resistance is a major issue in animal industries and antibiotic-free alternatives are needed to treat infectious diseases and improve performance of pigs. Plant extracts have been suggested as a potential solution. The present study was conducted to investigate the effects of Astragalus polysaccharides (Aps) and ginseng polysaccharide (Gps) on growth performance, intestinal morphology, immune function, volatile fatty acids (VFAs), and microfloral community in weaned piglets. A total of 180 weaned piglets were randomly divided into three treatment groups during a 28-days feeding experiment, including a basal diet (Con), basal diet supplemented with 800 mg/kg Aps (Aps), and basal diet supplemented with 800 mg/kg Gps (Gps). Results showed that both Aps and Gps increased body weight, average daily gain and feed conversion rate, and reduced the rate of diarrhea. Gps also decreased aspartate aminotransferase compared to the Con piglets after 14 days. No significant effects on alanine aminotransferase were observed. Both Aps and Gps piglets exhibited higher serum immunoglobulin M levels after 14 and 28 days, and also decreased jejunal crypt depth, increased jejunal villus length and villus height/crypt depth ratio, and increased expression of toll-like receptor 4, myeloid differentiation primary response 88, nuclear factor-kappa B proteins in the jejunum. Aps and Gps piglets also had higher concentrations of acetic acid, isobutyric acid, and butyrate in their colon. Data of high-throughput sequencing revealed that Aps and Gps affected bacterial quantity and diversity in the colon. Species richness and evenness were higher in both Aps and Gps piglets than the control piglets. Aps and Gps piglets also had a higher relative abundance of Lachnospiraceae and Anaerostipes, and the Aps piglets had a higher relative abundance of Lactobacillus gasseri and L. amylovorus. Therefore, dietary supplementation with Aps and Gps could be beneficial for optimizing the performance of industry pigs and reducing dependence on antibiotics. Furthermore, Plant polysaccharides play a great role in promoting the sustainable development of animal husbandry.


INTRODUCTION
Early weaning is a stressor, and sometimes exhibit intestinal development, digestive, or immune dysfunction in weaned piglets, which leads to diarrhea and growth inhibition (Hampson, 1986;Wu et al., 1996). Antibiotics are usually used to control the incidence of infectious diseases and improve growth in weaned piglets (Tang et al., 2005;Kong et al., 2007;Niekamp et al., 2007). However, antibiotic resistance has become a major issue in recent years. Hence, effective antibiotic substitutes are urgently required to reduce antibiotic dependence in the animal industry.
Plant polysaccharides have great potential as an antibiotic substitute owing to their natural characteristics (Leon et al., 2008). Reports have shown that Astragalus polysaccharides (Aps) extracted from Astragalus membranaceus, act as mild immunomodulators, restoring intestinal morphology and alleviating intestinal inflammation in acetic acid-induced colitis rats (Li et al., 2011;Zhao et al., 2014). Xu et al. (2019) reported that Aps decreased cytotoxicity and enhanced splenic lymphocyte proliferation in mice. Ginseng polysaccharides (Gps) has been shown to rescue intestinal epithelial cell viability from rotavirus infection dose-dependently (Baek et al., 2010). Kim et al. (2017) revealed that Gps exerted an anti-immunosenescent effect by suppressing thymic involution, reduced serum levels of IL-2, and modulated several types of immune cells in mice. Li et al. (2019) also showed that Gps altered the composition and diversity of gut microbiota in mice with antibiotic-associated diarrhea, restored gut microbiota, balanced metabolic processes, and promoted the recovery of mucosa.
Although the anti-inflammatory and immunomodulatory effects of plant polysaccharides have been recognized, more previous studies have focused on the immune function in vitro and in mice, while less on the effects of plant polysaccharides on gut volatile fatty acids (VFAs) and microbiota in weaned piglets. The present experiment was conducted to assess the effects of Aps and Gps on the growth performance, serum index, intestinal morphology, immune function, volatile fatty acid content, and colonic microbial community composition in weaned piglets. The aim was to provide valuable insights into antibiotic-free alternatives for improving weaned piglet performance.

Animals and Treatments
A total of 180 weaned piglets (Duroc × Landrace × Yorkshire), which weaned at day 28, were randomly assigned to three treatment groups, each group contained 6 pens per treatment, and 10 animals per pen. The experiment lasted for 29 days. The control group (Con) received a basal diet; the Aps group received the basal diet with 800 mg/kg Aps; the Gps group received the basal diet with 800 mg/kg Gps. The basal diet was formulated to meet the nutrient requirements suggested by NRC (1998) and contained no antibiotics ( Table 1). Water and feed were provided ad libitum. All pigs were housed in a room with the temperature controlled between 26 • C and 28 • C. This study was carried out in accordance with the recommendations of the care and use of laboratory animals, Institutional Animal Care and Use Committee of Zhejiang Agricultural and Forestry University. The protocol was approved by the Ethics Committee of Zhejiang Agricultural and Forestry University, Hangzhou, China (SYXKzhe 2016-087).

Preparation of Aps and Gps
The polysaccharide product had a purity of 80% and a molecular weight of 20,000-60,000. Aps was composed of hexanoic acid, glucose, fructose, rhamnose, arabinose, and galacturonan. Gps was composed of rhamnolipid, xylose, glucose, and galactose. Aps and Gps were provided by Vegamax Biotechnology Co., Ltd. (Anji, China).

Growth Performance
Piglets were weighed individually at the beginning and end of experiment. Feed intake was recorded each day. Average daily feed intake (ADFI), average daily gain (ADG), and feed to gain (F:G) for each pen were calculated. The amount of diarrhea was observed daily and recorded for calculating the rate of diarrhea.

Sample Collection
On day 14 and 28, six piglets per treatment (one piglet per pen) were randomly selected for sample collection. Blood samples were taken from the front cavity vein and centrifuged (3,000 × g, 10 min) at 4 • C, and then the serum was separated and promptly stored at −20 • C for further analysis. At 28 days, one pig per pen were slaughtered and sampled at a local commercial slaughterhouse. About 1 cm jejunal segment was immediately collected after slaughtering, and colon contents were collected and promptly stored at −80 • C for the detection of VFAs and high throughput sequencing.

Morphological and Immunohistochemical Analysis of Jejunum
The jejunum was fixed with 10% formaldehyde solution, routinely sampled, dehydrated, paraffin-embedded, sliced (4 µm thick), stained with hematoxylin-eosin, observed under an optical microscope for description (200 × ) with the main descriptive parts being photographed (Microscope: Nikon Eclipse ci; imaging system: Nikon digital sight DS-FI2). The villus height and crypt depth were measured at 10 visual fields from each intestinal sample and villus height/crypt depth ratio (VCR) values were calculated for each treatment group. Pathological changes were also observed in the same field of vision. Immunohistochemical TLR4, MyD88, and NF-κB were performed on each sample, which antibodies were anti-TLR4 (ab8376), anti-MyD88 (ab119048) and anti-NF-kB (ab86299). Three 400-fold visual fields were randomly selected for one photography. Image-Pro Plus 6.0 software was used to select the same brown-yellow color in the blue circle as a unified criterion for judging all positive photographs. The accumulated optical density of each positive circle was obtained by analyzing the three circles of each photograph, and the average value was calculated.
VFAs Analysis VFA levels were tested by Headspace Sampler Gas Chromatography (Agilent Technologies, United States) using the method of Thanh et al. (2009). The commercial standards of acetic acid, butyrate, propionic acid, isovalerate, isobutyric acid, and valerate treated as external standards, were purchased from China Sinopharm Chemical Reagents Co., Ltd. (Beijing, China). Metaphosphoric acid were acquired from Shanghai Aladdin Biotech Inc. (Shanghai, China). A mixture of 1 g colon content with 6% phosphorous acid (m/v, 1:3) was injected into an Agilent Technologies GC7890 Network System (Agilent Technologies, United States) equipped with a 30 m × 0.25 mm × 0.25 µm column (HP-FFAP, Agilent Technologies) for flame ionization (Yang et al., 2018).

Colonic Microflora Content by 16S rRNA Sequencing
Colonic content samples from each pig were used for the microbial community analysis. The V4 region of the 16S rRNA gene was detected using the Illumina-HiSeq platform (Novogene Bioinformatics Technology Co., Ltd., Beijing, China). The analysis was carried out following the method of Wang et al. (2007). The specific primer sequences 515F (5 -GTGCCAGCMGCCGCGGTAA-3 ) and 806R (5 -GGACTACHVGGGTWTCTAAT-3 ), were used for the analysis of V4 region of 16S rRNA gene. Briefly, through "quantitative insights into microbial ecology" (QIIME) and UPARSE software, we allocated 97% similarity between taxonomy and ribosomal database project (RDP) classifiers. Operational taxonomic units (OTUs) were clustered and species classified based on valid data. According to OTU clustering results, species annotations were made for each OTU sequence to obtain the corresponding species information and speciesbased abundance distribution. The alpha diversity calculations and Venn diagrams were analyzed to obtain species richness and evenness counts and information on the common and specific OTUs among different groups. Furthermore, OTUs were subjected multiple sequence alignment and a phylogenetic tree was constructed. A principal component analysis (PCA) and unweighted pair-group method with arithmetic mean (UPGMA) cluster tree displayed the differences in community structure among different groups, and results were explored in MetaStat.

Statistical Analysis
SPSS Statistics 21.0 (SPSS Inc., United States) and GraphPad Prism 7 (GraphPad Software Inc., United States) were used for the statistical analysis. The growth performance, serum parameters, jejunal morphology, concentration of VFAs in colon contents and relative abundance of fecal microbial communities were compared and analyzed by one-way ANOVA, and results were deemed significant if P < 0.05.

Effects of Aps and Gps on the Growth Performance
Piglets fed Aps or Gps had higher final body weight (P < 0.05) and ADG compared to the Con group ( Table 2). A reduced F:G (P < 0.01) and diarrhea rate (P < 0.01) were observed in Aps and Gps piglets.

Effects of Aps and Gps on Liver Function Indexes
The effect of Aps or Gps on liver function indices in serum are shown in Figure 1. Gps decreased the concentration of serum AST compared to the control piglets (P < 0.01) at 14 days. There were no significant effects observed on the levels of ALT.

Effects of Aps and Gps on Immunoglobulins in Serum
The effect of diet supplementation with Aps or Gps on serum immunoglobulins are shown in Figure 2. Compared to the control piglets, Aps piglets showed a higher concentration of IgA (P < 0.05) by 14 days, and IgM (P < 0.05) by 14 and 28 days. Furthermore, Gps piglets showed higher serum levels of IgM (P < 0.05) after 14 days. In the same row, values with different letter superscripts mean significant difference (P < 0.05). 1 Con, Aps and Gps represents the piglets supplemented with basal diet, piglets supplemented with the astragalus polysaccharides and piglets supplemented with ginseng polysaccharide, respectively. 2 Pooled SEM; n = 6 per treatment.

Effects of Aps and Gps on the Jejunal Morphology
The effect of diet supplementation with Aps or Gps on jejunal morphology are shown in Figure 3. Compared to control group piglets, Aps or Gps decreased jejunal crypt depth (P < 0.01), and increased jejunal villus length (P < 0.01) and VCR (P < 0.01). In addition, there was no obvious difference regarding the jejunal villus structure between the control group and the piglets supplemented with plant polysaccharides (Supplementary Figure S1).

Effects of Aps and Gps on Protein Expression Regarding TLR4 Signaling Pathways in Jejunal Mucosa
Expression of proteins involved in the TLR4 signaling pathway in the jejunal mucosa is shown in Figure 4. Relative to the control piglets, both Aps and Gps increased (P < 0.05) the expression of jejunal TLR4, MyD88, and NF-κB proteins. This means that the plant polysaccharides promoted the expression of proteins involved in the TLR4 signaling pathway. Furthermore, the levels of proteins involved in the TLR4 signaling pathways in the Gps piglets was higher than those in the Aps piglets.

Effects of Aps and Gps on VFAs in Colon Contents
The levels of VFAs in colon contents are shown in Figure 5.
The concentrations of acetic acid, isobutyric acid, and butyrate in Aps and Gps piglets were higher (P < 0.01) than those in the control piglets. Propionic acid was higher in Aps (P < 0.01) than it was in the control piglets. No significant differences in isovalerate and valerate concentrations were observed among all the different treatments.

Effects of Aps and Gps on Colonic Microbial Community Composition
The abundance and diversity of colonic microorganisms were described by 16S-rRNA high-throughput sequencing. The colonic microbiota composition is shown in the Venn diagram in Figure 6A. A total of 1133 OTUs were shared between the three treatment groups. The Con piglets had 66 unique OTUs, Aps piglets had 46 unique OTUs, and the Gps piglets had 41 unique OTUs. The UPGMA cluster tree and PCA both indicated that the microflora of both plant polysaccharide groups were more similar (Figures 6B,C). The alpha diversity (Shannon) was higher in both the Aps and Gps piglets than in the control group ( Figure 6D). A taxonomic classification of the microbial composition of colonic contents in piglets revealed that Firmicutes, Bacteroidetes, Proteobacteria, Tenericutes and Euryarchaeota were the dominant bacterial phyla (Figures 6E,F). The relative abundance of Firmicutes and Negativicutes in the Aps group was significantly higher (P < 0.05) than that in the control group (Figure 6G). At the family level, we observed that Clostridiales, Ruminococcaceae, Lachnospiraceae, Prevotellaceae, and Muribaculaceae were the dominant strains (Figures 6H,I).
The abundance of Melainabacteria in the control group tended to be lower than that in the Aps and Gps groups FIGURE 1 | Effect of Aps and Gps on the serum liver function indexes in weaned piglets. Con represents the control piglets on d 14 and 28, respectively; Aps represents the piglets supplemented with the astragalus polysaccharide on d 14 and 28, respectively; Gps represents the piglets supplemented with ginseng polysaccharide on d 14 and 28, respectively. * * Means significant difference (P < 0.01). Values means n = 6 for the analysis of serum liver function indexes.
Frontiers in Physiology | www.frontiersin.org FIGURE 2 | Effect of the Aps and Gps on the serum immunoglobulins in weaned piglets. Con represents the control piglets on d 14 and 28, respectively; Aps represents the piglets supplemented with the astragalus polysaccharide on d 14 and 28, respectively; Gps represents the piglets supplemented with ginseng polysaccharide on d 14 and 28, respectively. * Means significant different (P < 0.05), * * Means significant difference (P < 0.01). Values means n = 6 for the analysis of serum immunoglobulins.
FIGURE 3 | Effect of the Aps and Gps on jejunum villus of weaned piglets. A represents the villus length in the jejunum of weaned piglets. B represents the crypt depth in the jejunum of weaned piglets. C represents the ratio of the villus length and crypt depth. Con represents the control piglets; Aps represents the piglets supplemented with the astragalus polysaccharide; Gps represents the piglets supplemented with ginseng polysaccharide. * * Means significant difference (P < 0.01). Values means n = 10 for the analysis of the jejunum form. (Figure 6J). At the genus level, the results showed that Clostridiales, Subdoligranulum, Faecalibacterium, Prevotellaceae, and Lactobacillus were the dominant genera in all samples (Figures 6K,L). The relative abundance of Lachnospiraceae and Anaerostipes in the Aps groups was significantly higher (P < 0.01) than that in control group (Figure 6M). At the species level, we found that Ruminococcus sp., Alloprevotella sp., Clostridium butyricum, Lactobacillus gasseri, and L. amylovorus were the dominant species in all samples. L. gasseri and L. amylovorus were higher in the Aps group (P < 0.01) than they were in the Con group (Figures 6N-P).

DISCUSSION
In recent decades, the polysaccharides from medicinal plants have attracted much attention due to their significant bioactivities, such as increasing growth performance, antioxidant FIGURE 4 | Effect of the Aps and Gps on the protein expression about TLR4 signaling pathways in jejunum of weaned piglets. A represents Immunohistochemical results of TLR4; B represents Immunohistochemical results of MyD88; C represents Immunohistochemical results of NF-κB. Con represents the control piglets; Aps represents the piglets supplemented with the astragalus polysaccharide; Gps represents the piglets supplemented with ginseng polysaccharide. Shooting multiples: 400×. * * Means significant difference (P < 0.01). Values means n = 6 for the analysis of jejunal mucosa. activity, anti-viral activity, and immunomodulatory activities, which make them suitable as antibiotic replacements (Xie et al., 2015). Yuan et al. (2006) reported that dietary Aps increased the average daily gain of weaned piglets. The optimal Aps supplemental level was found to be between 381 mg/kg and 568 mg/kg. Han et al. (2014) reported adding 0.1% ginseng or Acanthopanax senticosus polysaccharides improved the growth performance and feed utilization rate in weaned piglets. Supplementation with Atractylodes macrocephala polysaccharides led to lower diarrheal incidence in early weaned piglets (Li et al., 2011). A study of (Li et al., 2018) showed that the supplementation of Gps modulated the intestinal microflora in rats. Current results showed that two plant polysaccharides increased growth performance, feed conversion ratio, and decreased the incidence of diarrhea in weaned piglets, especially those fed with Aps.
Plant polysaccharides have been confirmed to act as mild immunomodulators by previous studies (Yan et al., 2009;Jiao et al., 2016). Pu et al. (2015) reported that Aps decreased the activities of AST, ALT, and malondialdehyde and enhanced the activity of superoxide dismutase in carbon tetrachloride-treated mice. Liu et al. (2014) reported that 100 mg/kg of Aps not only restored the activity of serum transaminase, but also recovered intestinal pathology and ultrastructure of mice stimulated by docetaxel. Furthermore, Hu et al. (2017) reported that black ginseng significantly decreased the levels of serum ALT and AST in mice stimulated by acetaminophen. These effects were partly due to the antioxidant properties of Aps and Gps, which can scavenge free radicals, improve oxidative stress, and inhibit lipid peroxidation. Similarly, our results showed that ginseng polysaccharide reduced the levels of AST in serum on day 14.
Animal immune response to infection is closely related to immunoglobulin levels. Li et al. (2018) found that Aps alleviated a decreased serum IgG concentration in broilers treated with cyclophosphamide. Similarly, administration of Aps significantly increased the values of immune organ indices and serum IgM and IgG in mice and rats (Li et al., 2009;Meng et al., 2017). Tan et al. (2017) found that dietary supplementation with Aps significantly enhanced the presence of IgG and IgM in sow blood. Lan et al. (2016) indicated that pigs fed with A. membranaceus had higher IgG and IgA concentrations than those fed the control diet. The Aps injection increased the content of IgG, IgM, and IgA in weaned piglets (Xie et al., 2015). In addition, research found that the Gps increased the number of NK cells in the blood of immunosuppressed mice and promoted the expression of perforin and granzyme (Sun et al., 2016). We found that adding Aps could increase IgA and IgM levels in piglets after 14 and 28 days compared with control piglets. The results indicated that Aps and Gps could enhance immune function in piglets. Wang et al. (2015) evaluated the immunomodulating activities of Aps in chicks. Aps was found to increase jejunal villus height at 8 mg/kg body weight. In rat, Aps in the range of 50-200 µg/ml FIGURE 5 | Effect of the Aps and Gps on the VFAs in colon content of weaned piglets. Con represents the control piglets; Aps represents the piglets supplemented with the astragalus polysaccharide; Gps represents the piglets supplemented with ginseng polysaccharide. * * Means significant difference (P < 0.01). Values means n = 6 for the analysis of VFAs.
significantly increased the number of intestinal epithelial cells (IEC-6), remarkably increased cell migration rate at the wound site and accelerated the recovery of tissue calluses . Lv et al. (2017) indicated that the addition of 200 µg/ml Aps significantly increased the density of intestinal cells and the regular distribution of intestinal microvilli by increasing the transcription and expression of cytokeratin (CK18, ZO-2, etc.). Cui et al. (2018) found that A. membranaceus decoction restored villus height and V/C of duodenum, jejunum, and ileum under lipopolysaccharides stimulation in mice. We found that both dietary Aps and Gps enhanced the intestinal healthy development of weaned piglets by decreasing crypt depth and increasing villus height and intestinal gland ratio in weaned piglets.
TLR4 to nuclear factor-kappa B (TLR4-NF-κB) pathway is involved in pathogen identification and infection defense in mammals . Aps enhanced immune response including anti-tumor activities (Li et al., 2018). Wang et al. (2017) reported that Aps-mediated immunomodulatory activities in macrophages are involved in TLR4/NF-κB signaling pathways. Zhou et al. (2017) found that Aps stimulated the key nodes in the TLR4-MyD88-dependent signaling pathway, including TLR4, MyD88, TRAF-6, and NF-κB, both in vitro and in mice. Wang et al. (2018) confirmed that the NF-κB mRNA and protein levels were significantly increased in macrophages treated with Aps. These findings were similar to ours, in that both Aps and Gps increased expression of jejunal TLR4, MyD88, and NF-κB proteins, which means that the plant polysaccharides promoted the expression of proteins involved in the TLR4 signaling pathway. Wei et al. (2016) revealed that Aps enhanced the production of the tumor necrosis factor (TNF-α) that is blocked by the inhibitor of TLR4. The above results demonstrated that plant polysaccharides may regulate host immune functioning by activating the TLR4-mediated MyD88-dependent signaling pathway.
Generally, cecal and colonic VFAs were indicators of intestinal health and microbial activity (Bindelle et al., 2009). The cecal and colonic microorganisms ferment polysaccharides to produce VFAs such as acetic acid, propionic acid, and butyric acid. Che et al. (2018) indicated that supplementation with A. membranaceus significantly increased intestinal acetic acid, isobutyric acid, butyrate, and total VFAs in piglets. While, no trials have been conducted to investigate the effects of Gps on the colonic VFAs in weaned piglets. In the present study, piglets supplemented with Aps or Gps tended to have markedly higher concentrations of acetic acid, isobutyric acid, and butyrate.
The colon is the main habitat for microorganisms that affect host growth, development, and health (Pajarillo et al., 2014;Kim et al., 2015). Che et al. (2018) established that supplementation with 2.5-5% of A. membranaceus fiber decreased intestinal pH and increased intestinal levels of VFAs and gut microbial population and diversity, which enhances the health and wellbeing of piglets. In our case, Firmicutes and Bacteroidetes were the advantage bacterial phyla. Lamendella et al. (2011) pointed out that Firmicutes and Bacteroides were the dominant (G,J,M,P) Represent a species with significant differences between groups (level phylum, family, genus, species). Con represents the control piglets; Aps represents the piglets supplemented with the astragalus polysaccharide; Gps represents the piglets supplemented with ginseng polysaccharide. OTU, operational taxonomic unit. Piglets were regarded as the experimental units, each treatment with n = 6. * Means different (P < 0.05), * * means significant difference (P < 0.01).
Frontiers in Physiology | www.frontiersin.org bacteria in pig feces, which was supported by our data. Moreover, supplementation with Aps and Gps significantly increased the levels of Firmicutes and Negativicutes, which may improve unsaturated fatty acid synthesis in geese . Furthermore, Aps and Gps increased the relative abundance of Melainabacteria and Selenomonas in the colon. Also, Melainabacteria was found to be beneficial to the host because it fermented plant fibers in the gut and synthesized vitamin B and vitamin K (Di et al., 2013;Soo et al., 2014).
At the genus level, we observed that the levels of Lanchnospiraceae and Anaerostipes in the Aps piglets were significantly higher than those in the control group. Anaerostipes was shown to increase the level of acetic acid, propionic, and isobutyric acid in human feces (Bier et al., 2018). At the species level, our sequencing results indicated that L. gasseri and L. amylovorus were the dominant bacterial species in Aps piglets. Lactobacillus are recognized probiotics. Oh et al. (2016Oh et al. ( , 2018 reported that L. gasseri showed greater inhibition of nitric oxide production, considerably higher antioxidant activity and inhibition of α-glucosidase activity than other strains, which led to improved immune health of cows by fermenting lactic acid, propionic acid, and modulating pro-inflammatory cytokines. Similar findings were reported by Nobutani et al. (2017), who explained that L. gasseri significantly improved intestinal irritable bowel syndrome severity. L. amylovorus has also been found to modulate the negative regulators Tollip, interleukin-1 receptorassociated kinase, and extracellular heat shock proteins (Hsp72 and Hsp90) to achieve anti-inflammatory effects (Finamore et al., 2014). Furthermore more, Martinez et al. (2013) reported that L. amylovorus promoted short chain fatty acids and ammonia in feces of humans and piglets. In the present study, piglets supplemented with Aps or Gps enhanced the concentration of VFAs by increasing the microbial population and diversity in the colon of piglets. The present results suggest that growth performance was increased by modulating the microbial populations and increasing colonic microflora, which may be relative to the improvement of VFAs and intestinal morphology.

CONCLUSION
In conclusion, dietary supplementation with Aps or Gps could improve the growth performance, liver function, and intestinal villus morphology, and may regulate host immune functioning by activating the TLR4-mediated MyD88-dependent signaling pathway, and also enhance the concentration of VFAs in the colon and increase the colonic microbial population and diversity in weaned piglets. Plant polysaccharides may regulate the final fermentation products and the number and diversity of bacteria in the colon to promote the healthy growth of piglets.

DATA AVAILABILITY
The raw data supporting the conclusions of this manuscript will be made available by the authors, without undue reservation, to any qualified researcher.

ETHICS STATEMENT
This study was carried out in accordance with the recommendations of the care and use of laboratory animals, Institutional Animal Care and Use Committee of Zhejiang Agricultural and Forestry University. The protocol was approved by the Ethics Committee of Zhejiang Agricultural and Forestry University, Hangzhou, China (SYXKzhe 2016-087).

AUTHOR CONTRIBUTIONS
CY, QH, and GC designed the trials, performed the experiments, and edited the manuscript. KW and YX performed the samples detection. YX, KW, and JL analyzed the data. QH wrote the manuscript, which was edited by CY and GC. All authors read and approved the final manuscript.