Min Song,Fenglin Zhang,Yiming Fu,Xin Yi,Shengchun Feng,Zhichang Liu,Dun Deng,Qiang Yang,Miao Yu,Canjun Zhu,Xiaotong Zhu,Lina Wang,Ping Gao,Gang Shu,Xianyong Ma,3,Qingyan Jiang*and Songbo Wang*

Abstract Background: Tauroursodeoxycholic acid (TUDCA),a hydrophilic bile acid,is the main medicinal component of bear bile and is commonly used to treat a variety of hepatobiliary diseases.Meanwhile,TUDCA has been shown to modulate the intestinal barrier function and alleviate DSS-induced colitis in mice.However,the effect of TUDCA on the intestinal barrier of weaned piglets remains largely unclear.Methods:The weaned piglets and porcine IPEC-J2 intestinal epithelial cells were used to investigate the effects of TUDCA on intestinal barrier function in weaned piglets and explore the possible underlying mechanisms.In vivo,72 healthy weaned piglets were randomly allocated into 2 groups according to their gender and body weight,and piglets were fed the basal diet with 0(control,CON) and 200 mg/kg TUDCA for 30 d,respectively.Three female and three male piglets reflecting the average bodyweight were slaughtered in each group and samples were collected.In vitro,IPEC-J2 cells were subjected to 100 μmol/L TUDCA to explore the possible underlying mechanisms.Results:Our results demonstrated that dietary TUDCA supplementation significantly reduced the diarrhea incidence of weaned piglets,possibly attributing to the TUDCA-enhanced intestinal barrier function and immunity.In addition,TUDCA supplementation altered serum metabolites and the relative abundance of certain gut bacteria,which might contribute to the improved intestinal barrier function.Furthermore,the in-vitro results showed that TUDCA improved the E.coli-induced epithelial barrier impairment of IPEC-J2 cells and increased Takeda G-coupled protein receptor 5 (TGR5) protein expression.However,knockdown of TGR5 and inhibition of myosin light chain kinase (MLCK) pathway abolished the TUDCA-improved epithelial barrier impairment in E.coli-treated IPEC-J2 cells,indicating the involvement of TGR5-MLCK in this process.Conclusions:These findings showed that TUDCA improved intestinal barrier function associated with TGR5-MLCK pathway and the alteration of serum metabolites and gut bacteria in weaned piglets,suggesting the potential application of TUDCA in improving gut health in piglet production.

Keywords: Gut bacteria,Intestinal barrier function,Serum metabolites,Tauroursodeoxycholic acid (TUDCA),TGR5-MLCK pathway,Weaned piglets

Introduction

In the modern pig breeding industry,weaning is the key stage of pig breeding process.Sudden changes in diet and living environment during weaning often cause weaning stress of piglets,which leads to atrophy of intestinal villi,crypt hyperplasia,reduction of gastrointestinal volume and appetite [1,2].In addition,the gastrointestinal tract is immature when piglets are weaned,and the secretion of bile and endogenous digestive enzymes such as lipase is insufficient.Thus,lipids in the feed are difficult to be digested and absorbed,leading to diarrhea,decreased immunity,slow growth and even death of weaned piglets.

Bile acids (BAs),derived from cholesterol in the liver,are amphiphilic molecules composed of hydrophilic and hydrophobic groups,and are known for promoting lipid digestion.In addition,more and more evidence has demonstrated that BAs also act as signal molecules to participate in the regulation of bile acid synthesis,glycolipid metabolism,immunity and energy homeostasis by activating bile acid receptors such as farnesoid X receptor (FXR) and Takeda G-coupled protein receptor 5(TGR5) [3–6].

It has been well characterized that gut microbiota plays a very important role in bile acid metabolism.The bile acids synthesized by the liver are defined as primary bile acids,including chenodeoxycholic acid (CDCA) and cholic acid (CA).The primary bile acids are first conjugated to taurine or glycine,and then they are secreted into the digestive tract after eating [7].After reaching the ileum,primary bile acids are transformed to secondary bile acids under the action of gut microbiota via deconjugation,dehydrogenation,and dehydroxylation [8,9].The secondary bile acids produced include lithocholic acid (LCA),deoxycholic acid (DCA),ursodeoxycholic acid (UDCA),hyodeoxycholic acid (HDCA) and their conjugated forms and isomeride.In addition,accumulating evidence have suggested a crosstalk between the gut microbiota and serum metabolites [7,9].Changes in the gut microbiome are often accompanied by alterations in the host’s serum metabolome,and thus have a profound effect on the overall host health [10].

TUDCA,a taurine-conjugated derivative of UDCA,is the main medicinal component of bear bile and is approved by the Food and Drug Administration (FDA) for the treatment of primary biliary cholangitis due to its protective effects on hepatocytes [11].UDCA is a secondary bile acid,which is produced by gut microbiota through the epimerization of hydroxyl groups of CDCA[12,13].The generated UDCA directly enters the liver through the hepato-intestinal circulation,and then conjugated with taurine to form TUDCA [14].UDCA and TUDCA have similar physiological functions,but TUDCA is more soluble and less toxic than UDCA.Recently,the effects of TUDCA have been shown to extend beyond hepatobiliary disorders.TUDCA is also recognized as a chemical chaperone to enhance protein folding and protect cells from endoplasmic reticulum (ER)stress,and is widely used in clinical and experimental research for the treatment of obesity,liver disease and neurodegenerative diseases [15,16].In addition,it has been shown that TUDCA is an agonist of TGR5 and plays an anti-inflammatory role by activating TGR5.Furthermore,it has been reported that TUDCA alleviates the weight loss,colon shortening and increasing inflammatory factors expression in DSS-induced colitis mice[17].In term of mechanism,TUDCA alleviates mouse colitis by reducing ER stress of intestinal epithelial cells and inhibiting early intestinal epithelial cell apoptosis[18,19].However,the effect of TUDCA on the intestinal barrier of weaned piglets has rarely been reported.Based on previous studies and the properties as a bile acid,we hypothesized that: i) TUDCA might improve intestinal barrier function in piglets,thereby improving growth performance and intestinal health of weaned piglets;ii)TUDCA amelioratesE.coli-induced impairment of epithelial barrier function in IPEC-J2 cells through TGR5-MLCK signaling pathway.The IPEC-J2,originally derived from neonatal piglet jejunum,is a noncancerous and nontransformed cell line.IPEC-J2 has similar characteristics to the porcine intestinal epithelium cells and is often used as an experimental model of porcine intestinal epithelial cells in vitro.

Therefore,the objective of this study is to investigate the effects of TUDCA on intestinal barrier function using in vivo and in vitro models.An in vivo study was carried out to determine the effects of TUDCA on intestinal epithelial barrier function,serum metabolic profiles and gut microbiota in piglets.In vitro,E.coli-induced epithelial barrier impairment model of IPEC-J2 cells was used to identify the role of TGR5-MLCK pathway in TUDCA improving intestinal barrier function.Our findings show that TUDCA improves intestinal barrier function associated with TGR5-MLCK pathway and the alteration of serum metabolites and gut bacteria in weaned piglets.

Materials and methods

Animals management and experimental design

The animal protocol for this study was conducted with the permission number of SYXK (Guangdong) 2019–0136,and the animal care procedures for this study were performed in accordance with the guidelines of The Animal Ethics Committee of South China Agricultural University.

Seventy-two crossbred healthy weaned piglets (Duroc× Landrace × Yorkshire) were weaned at 21±2 days of age.After 7-day adaptation,piglets (initial body weight of 7.02±0.08 kg) were raised on a local commercial farm(Guangdong Huahong Farming and Husbandry Group Co.,Ltd.,Yangjiang,Guangdong Province,China).All weaned piglets had free access to the basal diet during the 7-day adaptation period.The based diet (Table 1)was formulated to meet all nutrient requirementsrecommended by National Research Council (NRC,2012) [20].At 28±2 days of the age,piglets were randomly assigned into two groups according to the gender and body weight.Each group had 4 replications (pens)of 9 piglets per replicate (male:female=4:5).The piglets in the control group (CON) were fed with a basal diet,while the piglets in the TUDCA group were fed with the basal diet supplemented with 200 mg/kg TUDCA(Hangzhou Baoji Biotechnology Co.Ltd.,Hangzhou,China.The dosage of TUDCA in piglets diet is based on our previous piglets experimental results [21] and the recommended dosage of similar bile acid products).In addition,the basal diet also included 50 mg/kg of quinocetone and 75 mg/kg of chlortetracycline.The experiment lasted 30 d.The piglets were fed three times daily at approximately 08:00 h,13:00 h and 18:00 h.All piglets had free access to food and water throughout the experimental period.

Table 1 Composition and nutrient levels of the basal diet for weaned piglets

Growth performance

Piglets were weighed individually at the beginning and end of the experiment and feed intake of piglets in each pen was recorded daily.Average daily gain (ADG),average daily feed intake (ADFI) and feed/gain ratio (F/G)were calculated for the piglets in each pen.Additionally,during the entire experiment,piglets (from 28 to 57 days of age) were monitored for diarrhea symptoms twice a day at 8:00 h and 18:00 h.The severity of diarrhea was assessed by fecal consistency: solid 0,semi-solid 1,semiliquid 2,liquid 3.Excreting level 2 or 3 feces for two consecutive days was defined as diarrhea [22].Diarrhea incidence was calculated according to the followed formula:

Sample treatment and collection

On day 30 of the experiment,3 female and 3 male piglets reflecting the average body weight (BW)were selected for sample collection from each group.Meanwhile,we ensured that at least one piglet was selected for sample collection per replicate.Blood samples were collected after 12-h fasting by jugular venipuncture before euthanasia.After incubation at room temperature for 30 min,the blood was centrifuged at 3000 r/min for 15 min,then the serum was separated and stored at ?20°C for further analysis.The middle sections of jejunum and the ileum were collected and then divided into 2 segments.One segment was fixed in a 4% neutral-buffered formalin solution for intestinal morphological analysis and the other segment was stored at ?80°C until the extraction of total RNA and protein.The pancreas samples were also collected,and then stored at ?80°C prior to mRNA analysis.In addition,fecal samples were collected from the rectum near the anus of the slaughtered piglets and then stored at?80°C until 16S rRNA gene sequences.

Intestinal histomorphology analysis

The fixed intestinal segments were dehydrated and then embedded in low-melting paraffin wax.Cross sections of intestinal segments were cut into 5-μm thick histological sections and stained with haematoxylin and eosin (H& E)as previously described [23].Histological section were examined using a light microscopy.

At least 10 microscopic fields per sample were randomly selected to measure villus height (V) and crypt depth (C) of the small intestine by using Program Image-pro Plus 6.0 (Media Cybernetics Bethesda,MD,USA),and the V/C ratio was calculated.Goblet cells in jejunum and ileum were identified using periodic acidschiff (PAS) stain described previously [24].

Measurement of serum lipopolysaccharide (LPS),diamine oxidase (DAO) and immune indices

Serum LPS,DAO and IgG levels and ileal mucosal secretory immunoglobulin A (sIgA) level were detected by porcine LPS,DAO,IgG and sIgA ELISA kit (Nanjing Jiancheng Bioengineering Institute,Nanjing,China) according to the manufacturer’s instructions.The ileal mucosal contents of IL-1β,NF-κB,IL-6,IL-4 and IL-10 were detected by porcine ELISA kit (Shanghai Enzymelinked Biotechnology Co.,Ltd.,Shanghai,China) according to the manufacturer’s instructions.

Western blot (WB) analysis

Expression of tight junction (TJ) proteins in jejunum was determined by WB analysis which was conducted as previously described [25].Proteins were detected by primary antibodies: anti-Tubulin antibodies (1:5000,Bioss,China),anti-Occludin (OCC) (1:500,Bioss,China),anti-ZO-1 (1:2000,Santa Cruz,USA) and anti-Claudin-1 (1:500,Bioss,China),and then incubated with the secondary antibodies (1:2000,Bioss,China).Finally,chemiluminescence detection was performed with western ECL reagent and band densities were quantified using a FluorChem M Fluorescent Imaging System (ProteinSimple,Santa Clara,CA,USA).The intensity of bands was analyzed and quantified by Image J Sofware (NIH,Bethesda,MD,USA).

Serum metabolic profiles

Untargeted metabolic profiling of serum samples by liquid chromatography tandem mass spectrometry (LC-MS/MS)was performed to analyze serum metabolic profiles.Serum sample preparation and LC-MS/MS method were performed according to the method described previously[26].Use the database of Kyoto Encyclopedia of Genes and Genomes (KEGG) to perform functional annotations on the identified metabolites,and then map the annotated metabolites to the KEGG pathway database.

DNA extraction and 16S rRNA gene sequencing

The total DNA was extracted and purified from fecal samples using an E.Z.N.A.? stool DNA Kit (Omega) following the manufacturer’s instructions.DNA quality was confirmed by agarose gel electrophoresis.The V3–V4 regions of 16S rRNA genes were amplified by PCR using primers 341F (5′-CTCCTACGGGAGGCAGCAGT-3′)and 806R (5′-GGACTACHVGGGTWTCTAAT-3′).Mix the purified products in equal proportions for sequencing using the Illumina Hiseq 2500 platform.The sequencing protocol was performed according to a previous method [27].Raw sequencing data were processed with QIIME software package.The 16S rRNA gene sequences were selected to compare the relative abundance of bacterial groups.Operational taxonomic units(OTUs) clustering was performed by Uparse software and delimited at a threshold of 97% sequence similarity using USEARCH v.10.The alpha and beta diversity of microflora was determined.In our present study,the alpha diversity was analyzed using Chao1 index and Shannon’s index,while the beta diversity was analyzed by principal component analysis (PCoA).Bacterial species differences between the TUDCA and the CON groups were compared using metastat analysis.

Finally,the bacterial functions were predicted by PICRUSt based on the obtained data,and the differential functions and metabolic pathways between the TUDCA and the CON groups were obtained.In addition,the Spearman correlation was used to analyze the correlation between intestinal differential OTUs and serum differential metabolites.

Bacterial preparation

TheE.coli K88strain,purchasing from the China Veterinary Culture Collection Center,was grown in Luria-Bertani (LB) broth.After incubation at 37°C with shaking overnight,bacteria were 1:100 diluted in fresh LB and grown for 2 h.Bacteria were harvested by centrifugation at 3000×g for 10 min at 4°C,washed twice with phosphate buffer solution (PBS) and resuspended in RPMI-1640 medium free of antibiotics.The bacterial concentration (colony-forming units,CFU) was determined by serial dilution method.

Cell culture conditions and treatments

IPEC-J2 cells were cultured in RPMI-1640 medium supplemented with 10% of fetal bovine serum (FBS),1% of penicillin (100 U/mL),and streptomycin (100 U/mL) in humidified atmosphere with 5% CO2at 37°C.The medium was changed every 2 days.TUDCA was dissolved in dimethyl sulfoxide (DMSO) for in vitro experiments.

For experiment,IPEC-J2 cells were inoculated into 6-well plates with a density of 3×105cells/cm2.After reaching 70% to 80% confluence,cells were cultured with RPMI-1640 medium supplemented with 100 μmol/L TUDCA (Preliminary results showed that 100 μmol/L TUDCA could significantly increase TGR5 protein expression of IPEC-J2 cells,with no significant effect on IPEC-J2 cell viability.At the same time,100 μmol/L TUDCA has a significant anti-inflammatory effect on LPS-induced macrophages.Thus,100 μmol/L TUDCA were finally selected in our experiments) or PBS or 10 μmol/L ML-7 for 12 h.Afterward,cells were stimulated withE.coli K88(1×103CFU/well) for 6 h.

To silenceTGR5gene,siRNAs (small interfering RNAs) targeted againstTGR5were transfected into IPEC-J2 cells for 6 h according to the manufacturer’s instructions.The empty plasmid vector was used as a negative control (CON).Subsequently,the medium was replaced with complete medium and the cells were treated with TUDCA andE.coli K88.The efficiency of gene silencing was determined by WB after the treatments.

Measurement of lactate dehydrogenase(LDH) in cell culture supernatant

The LDH activity of cell culture supernatant was detected by LDH Assay Kit (Nanjing Jiancheng Bioengineering Institute,Nanjing,China) according to the protocol of kit.

Statistical analysis

Data were statistically analyzed using Sigmaplot 14.0(Systat Software,Inc.,San Jose,CA) and the statistical significance of differences was evaluated by two-tailed Student’st-test.A confidence level ofP<0.05 was considered to be statistically significant.All data were expressed as mean value ± standard error of the mean(SEM).Moreover,Variable Importance in Projection(VIP)≥1,and the fold change ≥2 or fold change ≤0.5 were used as indicators to screen the serum differential metabolites between the CON group and the TUDCA group.Spearman correlation was used to analyze the correlation between intestinal differential OTUs and serum differential metabolites.

Results

TUDCA supplementation reduced the diarrhea incidence of weaned piglets

As shown in Table 2,compared with the CON group,TUDCA supplementation had no significant effect on the final BW,ADG,ADFI and F/G of weaned piglets.However,TUDCA significantly reduced the diarrhea incidence of weaned piglets.

Table 2 Growth performance and diarrhea incidence of weaned piglets

TUDCA supplementation enhanced intestinal barrier function of weaned piglets

Compared with the CON group,TUDCA supplementation improved the intestinal morphology by increasing the V/C ratios in jejunum and ileum (P<0.05) (Fig.1A,B).In addition,PAS staining results showed that TUDCA supplementation increased the number of goblet cells secreting mucopolysaccharides in jejunum and ileum (P<0.05,Fig.1C and D).Furthermore,the expression of TJ proteins,such as OCC and Claudin-1,was higher in jejunum of piglets supplemented with TUDCA(P<0.05,Fig.2A,B).Accordingly,the intestinal permeability was reduced,which was manifested by the decreased serum LPS and DAO levels (P<0.05,Fig.2C,D).These above results suggested that dietary supplementation of TUDCA enhanced intestinal barrier function of weaned piglets.

TUDCA supplementation improved the immunity of weaned piglets

Compared with the CON group,TUDCA supplementation increased the IgG level in serum and the sIgA level in ileum mucosa of weaned piglets (Fig.3A and B).In addition,TUDCA supplementation reduced the contents of IL-1β and NF-κB and increased the contents of IL-4 and IL-10 in the ileal mucosa of weaned piglets (Fig.3C).These above results revealed that dietary supplementation of TUDCA reduced intestinal inflammation and improved intestinal immunity of weaned piglets.

TUDCA supplementation changed the serum metabolic profiles of weaned piglets

Fig.1 Effects of TUDCA supplementation on the intestinal morphology and mucosa mucopolysaccharide of weaned piglets(n=6).A The intestinal morphology of the jejunum and ileum with H& E staining(scale bar,1000 μm). B Statistical diagram of the villus height-to-crypt depth ratio in the jejunum and ileum.C The intestinal mucosa mucopolysaccharide of jejunum and ileum stained with periodic acid-schiff(PAS)(scale bar,200 μm).D Statistical diagram of the number of PAS positive cells in each villus.*P<0.05,versus the CON group

In this study,an untargeted UPLC-MS/MS approach was used to comprehensively analyze serum metabolic profiles of weaned piglets.The orthogonal partial least squares-discriminant analysis (OPLS-DA) scores plot showed that there was a clear separation between the CON and TUDCA groups (Fig.4A),indicating that the serum metabolic profiles of TUDCA group was significantly different from that of CON group.The 14 serum metabolites with the largest change were screened out as shown in Fig.4B.Among the 14 serum metabolites,the up-regulated serum metabolites included 3-(Methylthio)-1-propanol,theobromine,N′-formylkynurenine,indole-3-acetic acid,triethyl phosphate,tryptamine,citramalic acid and (+)-borneol,and the downregulated serum metabolites included uric acid,15-deoxy-δ-12,14-PGJ2,hexanoyl glycine,isoquinoline,N-(3-indolylacetyl)-L-alanine and trimethoprim.In addition,the influences of TUDCA on the metabolic pathways of weaned piglets were explored by using KEGG pathway analysis.As shown in Fig.4C,TUDCA supplementation altered 15 metabolic pathways,and the predominantly involved metabolic pathways were tryptophan metabolism,microbial metabolism in diverse environments and metabolic pathways.

TUDCA supplementation altered gut bacteria of weaned piglets at the genus level

Fig.2 TUDCA supplementation enhanced intestinal barrier function in weaned piglets.A and B Effects of TUDCA supplementation on expression of tight junction proteins ZO-1,OCC and Claudin-1 in jejunum of weaned piglets.Tubulin was used as the loading control(n=4).C and D Serum levels of LPS and DAO(n=6).*P<0.05 versus the CON group

To investigate the effects of TUDCA supplementation on the gut microbiota of weaned piglets,16S rRNA gene sequencing was used to evaluate the fecal microbiota composition.As shown in Fig.5A and B,the parameters of the alpha diversity of gut microbiota,including Chao1 value and Shannon index,showed no difference between Control and TUDCA treatment.Moreover,PCoA result demonstrated that there was no clear separation of bacterial communities structure between the CON and TUDCA groups,which meant no significant differences in microbiota beta diversity between the 2 groups (Fig.5C).These above results indicated that TUDCA supplementation had no significant effect on diversity of gut microbiota of weaned piglets.In addition,the analysis of relative abundance of bacteria at the phylum level indicated that Firmicutes and Bacteroidetes were the dominant phylums (Fig.5D).Although TUDCA supplementation did not altered the relative abundance of gut microbiota at the phylum level,it increased the relative abundance ofParabacteroidesandMucispirillumand decreases the relative abundance ofStreptococcusandTreponema 2at the genus level(P<0.05,Fig.5E and F).

Correlations between the differential gut bacteria and serum metabolites

To explore the relationship between gut microbiota and serum metabolites,Spearman correlation analysis between the serum differential metabolites and the 71 differential OTUs was performed.As shown in Fig.6,red represented positive correlation and blue represented negative correlation.In the figure,we can find that the color of up-regulated metabolites is clearly distinguished from the color of down-regulated serum metabolites,indicating that the correlation between differential OTUs and up-regulated metabolites was just the opposite to the correlation between the differential OTUs and down-regulated serum metabolites.Moreover,each differential metabolite was significantly correlated with multiple differential OTUs.The above results indicated that these differential gut bacteria were closely related to and might contribute to the alterations of serum metabolic profiles in response to TUDCA treatment.

Fig.3 TUDCA supplementation improved the immunity of weaned piglets(n=6).The serum IgG level(A) and ileal mucosal sIgA(B) were detected by ELISA.C The relative content of inflammatory factors IL-1β,IL-6,NF-κb,IL-4 and IL-10.*P<0.05 versus the CON group

Fig.4 TUDCA supplementation changed serum metabolic profiles of weaned piglets(n=6).A The scores plots of serum metabolites of CON group and TUDCA group were obtained by orthogonal partial least squares discriminant analysis(OPLS-DA). B The main up-regulated(redmarked)and down-regulated(green-marked)serum differential metabolites.C Kyoto Encyclopedia of Genes and Genomes(KEGG)enrichment of serum differential metabolites.The color of the point and the size of the spot represented P-value and the number of different metabolites enriched,respectively

TUDCA improved E.coli-induced epithelial barrier impairment and enhanced TGR5 expression in IPEC-J2 cells

An epithelial barrier impairment model of IPEC-J2 cells induced byE.coliwas used to study the mechanism of TUDCA in protecting intestinal barrier function at the cellular level.The IPEC-J2 cells were treated with 100 μmol/L TUDCA according to the pre-test results.As shown in Fig.7A and B,E.colisignificantly reduced the expression of TJ proteins,such as ZO-1,Claudin-1 and OCC in IPEC-J2 cells,while 100 μmol/L TUDCA significantly reversed the decrease in TJ proteins expression induced byE.coli.Meanwhile,TUDCA also alleviatedE.coli-induced increase in LDH activity in cell supernatant(Fig.7C),implying that TUDCA attenuated theE.coli-induced increase in cell permeability.In addition,100 μmol/L TUDCA could significantly increase the protein expression of TGR5 in IPEC-J2 cells,with no significant effect on that of FXR (Fig.7A and B).The above results implied that the effect of TUDCA on improving epithelial barrier impairment of IPEC-J2 cells induced byE.colimight be related to the activation of the bile acid receptor TGR5.

Fig.5 TUDCA supplementation altered gut microbiota of weaned piglets(n=6).A and B Chao1 value(A) and Shannon index(B) of gut microbiota, C Principal component analysis(PCoA)scores plot for gut microbiota of the CON and TUDCA groups.D The relative gut microbiota abundance at the phylum level in the CON and TUDCA groups.E and F Gut bacteria with significant differences in the genus level after TUDCA supplementation.*P<0.05 versus the CON group

Knockdown of TGR5 abolished the TUDCA-improved epithelial barrier impairment in E.coli-treated IPEC-J2 cells

To further confirm whether TGR5 was involved in TUDCA-improved epithelial barrier impairment induced byE.coliin IPEC-J2 cells,the specific TGR5 siRNA was used to knock down the expression of TGR5 in IPEC-J2 cells.As shown in Fig.8A and B,the protein expression of TGR5 decreased significantly after TGR5 siRNA interference.The results showed that after interference with TGR5,TUDCA failed to improve theE.coli-induced decrease of protein expression of ZO-1 OCC and Claudin-1 in IPEC-J2 cells (Fig.8A-D).In agreement,the TUDCA-induced increase in the intracellular cAMP concentration was blocked in the presence of TGR5 siRNA (Fig.8E).These results provided evidence that TGR5 was responsible for the TUDCA-improved epithelial barrier impairment of IPEC-J2 cells induced byE.coli.

TGR5-MLCK signaling pathway was involved in the TUDCA-improved epithelial barrier impairment in E.colitreated IPEC-J2 cells

To further determine whether the MLCK signaling pathway is involved in TUDCA-improved epithelial barrier impairment induced byE.coliin IPEC-J2 cells,as well as its relation with TGR5,we examined activation of the MLCK signaling pathway in the presence of TUDCA and/orE.coliand/or TGR5 siRNA.As shown in the Fig.9A-C,the MLCK signaling pathway was activated byE.coli,with increased MLCK expression and an elevated p-MLC/MLC ratio.However,theE.coli-induced the MLCK signaling pathway activation was abolished by TUDCA treatment.After interference with TGR5,TUDCA was no longer able to suppress theE.coli-induced activation of the MLCK signaling pathway,with no difference in MLCK expression and p-MLC/MLC ratio betweenE.coliandE.coli+TUDCA groups.These results indicated that the effect of TUDCA on blockingE.coliinduced the activation of MLCK signaling pathway was TGR5-dependent.

In addition,inhibition of MLCK with the inhibitor ML-7 significantly blocked theE.coli-activated MLCK signaling pathway,which was similar to the effects of TUDCA (Fig.9D,E).Furthermore,ML-7 also reversed the decreased expression of ZO-1,OCC and claudin-1 induced byE.coli.These results revealed that TUDCA improvedE.coli-induced impairment of IPEC-J2 cell barrier function through the TGR5-MLCK signaling pathway.

Fig.6 Correlations between serum main differential metabolites and differential operational taxonomic units(OTU)of weaned piglets(n=6).Blue and red cells represent negative and positive correlations,respectively.The significant correlations are indicated by“+”and “*”(+P<0.05 and*P<0.01)

Discussion

Fig.7 TUDCA improved E.coli-induced epithelial barrier impairment and enhanced TGR5 expression in IPEC-J2 cells.A Western blot analysis of ZO-1,OCC,Claudin-1,FXR and TGR5 in IPEC-J2 cells.Tubulin was used as the loading control.B Mean±SEM of immunoblotting bands of ZO-1,OCC,Claudin-1,FXR and TGR5(n=4).C LDH activity in the supernatant of IPEC-J2 cells,expressed as fold of control.*P <0.05 and***P<0.001 versus the control(CON)group,#P<0.05 and ##P<0.01versus the E.coli group

Fig.8 Knockdown of TGR5 abolished the TUDCA-improved epithelial barrier impairment in E.coli-treated IPEC-J2 cells.A-D Western blotting measurements of the protein levels of ZO-1,OCC and Claudin-1 in IPEC-J2 cells after treatment with TUDCA and/or E.coli and/or TGR5 siRNA.Tubulin was used as the loading control(n=4).E The intracellular cAMP level in IPEC-J2 cells(n=6).?P<0.05.NS=not significant

Fig.9 TGR5-MLCK signaling pathway was involved in TUDCA-improved epithelial barrier impairment in E.coli-treated IPEC-J2 cells. A-C Western blotting measurements of the protein levels of MLCK,p-MLC and MLC in IPEC-J2 cells after treatment with TUDCA and/or E.coli and/or TGR5 siRNA.Tubulin was used as the loading control(n=4)?P<0.05 and ??P<0.01.NS=not significant.D and E Western blotting measurements of the protein levels of MLCK,p-MLC/MLC,ZO-1,OCC and Claudin-1 in the presence of E.coli and/or ML-7.Tubulin was used as the loading control(n=4).?P<0.05 versus the control group.#P<0.05 versus the E.coli group

In this study,we provided evidence that TUDCA improved intestinal barrier function associated with TGR5-MLCK pathway and the alteration of serum metabolites and gut microbiota in weaned piglets.Although having no significant effect on the growth performance of weaned piglets (such as the final BW,ADG,ADFI and F/G),TUDCA supplementation significantly reduced the diarrhea incidence of weaned piglets.To investigate the underlying mechanism by which TUDCA alleviates post-weaning diarrhea,we determined the effect of TUDCA on gut barrier integrity and function.Studies have shown that weaning stress could cause intestinal damage,which is manifested as destroyed the intestinal morphology,increase in intestinal permeability [28].Our study showed that TUDCA supplementation improved the intestinal morphology,increased the secretion of mucopolysaccharides and expressions of tight junction proteins and reduce intestinal permeability.The intestinal tight junctions,include occludin,claudins,and scaffolding proteins like zona occludens (ZO),are the most important structure of the epithelial barrier and play an important role in maintaining the stability of intestinal epithelial barrier and permeability [29].Intestinal mucosal permeability indicators,including DAO and LPS,are the main basis to evaluate the intestinal barrier function[30,31].Collectively,our results indicated that TUDCA supplementation contributed to the reconstruction of intestinal morphology and enhanced intestinal barrier function and thereby reduced the diarrhea incidence of of weaned piglets.

Inflammatory cytokines not only play a crucial role in inflammatory and immune responses,but also regulate the integrity of the intestinal barrier,which is closely related to the occurrence of diarrhea [32].In the current study,our results showed that TUDCA supplementation reduced intestinal inflammation and promoted immunity function in weaned piglets.Consistent with our findings,it was also reported that TUDCA had antiinflammatory effects and could alleviate increasing inflammatory cytokines expression in DSS-induced colitis mice [17].Some researchers have studied the antiinflammatory mechanism of TUDCA and found that TUDCA alleviates acute and chronic colon inflammation by reducing ER stress [18,19].Another study has shown that TUDCA induces cellular apoptosis by inhibition of NF-κB-regulated anti-apoptotic genes [33].In addition,our study also found that the protein expression of TGR5 in the intestine was elevated.It was reported that TGR5 is a mediator of the immunosuppressive effects of bile acids and plays an anti-inflammatory effect by inhibiting the proinflammatory NF-κB and cytokines production by macrophages [34,35].Our findings suggested that TUDCA may exert an anti-inflammatory effect through TGR5,but its specific mechanism remains to be further studied.

The OPLS-DA scores plot results showed that the serum metabolic profile of weaned piglets in the TUDCA group was significantly different from that in the CON group.Among the 14 serum differential metabolites identified,we noticed two upregulated serum differential metabolites after TUDCA supplementation,indole-3-acetic acid and N′-formylkynurenine,are microbiota-derived tryptophan metabolites.Interestingly,KEGG pathway analysis also showed that TUDCA supplementation affected tryptophan metabolism of weaned piglets.Tryptophan and bile acids are two important gut microbial metabolites.It has been found that certain gut bacteria,such asBififidobacteriumandBlautiaspecies,are closely associated with both tryptophan and bile acids metabolism [36],so alterations in bile acid metabolic,including bile acid intake,are often accompanied by changes in tryptophan metabolites.Metabolites produced by the intestinal flora metabolizing tryptophan,especially indole derivatives,play a key role in maintaining the integrity of the intestinal barrier and protecting the mucosa from inflammation,which is beneficial to intestinal health [37–39].In addition,theobromine has been reported to inhibit the growth of harmful bacteria in rats,includingEscherichia coli,Streptococcusspp.,andClostridium histolyticum-C[40].These results indicated that TUDCA-improved intestinal barrier function of weaned piglets might be mediated,at least in part,by alteration of serum metabolic profiles.

The composition of intestinal flora is also an important factor affecting intestinal barrier function [41].In the present study,we found thatParabacteroidesandMucispirillumat the genus level were markedly increased in response to TUDCA.Parabacteroideswas reported to be negatively correlated with body weight gain and hepatic triglyceride content [42].The increase relative abundance ofParabacteroidesmight be one of the reasons why TUDCA supplementation did not improve the growth performance of weaned piglets.Mucispirillumhas been observed to be positively correlated with intestinal proliferation and differentiation [43].Moreover,Mucispirillumis closely related to the production and secretion of T cell-dependent IgA,which is the main component of mucosal immune barrier and mediate intestinal mucosal immunity [44].Therefore,the increased relative abundance ofMucispirillumindicated the enhancement of intestinal proliferation,differentiation and mucosal immunity,and the decrease of diarrhea rate and the enhancement of intestinal barrier functions of weaned piglets in the TUDCA group might be related to the increased relative abundance ofMucispirillumin the intestine.In addition,TUDCA supplementation reduced the relative abundance of harmful intestinal bacteria,StreptococcusandTreponema 2at the genus level.Streptococcusis a common and harmful bacterium that can cause meningitis,septicaemia,pneumonia and arthritis in pigs,causing significant economic losses to the pig industry [45].Therefore,changes in the relative abundance of these intestinal bacteria of weaned piglets might be closely related to the improvement of intestinal barrier function after TUDCA supplementation.

A correlation analysis between serum differential metabolites and intestinal differential OTUs was carried out.Our study found that the correlation between the increased serum differential metabolites and the differential OTUs was just opposite to the correlation between the decreased serum differential metabolites and the differential OTUs.Moreover,most of the serum differential OTUs were positively or negatively correlated with each serum differential metabolites,and many of them were significantly correlated,indicating that the changes in certain intestinal bacteria was contribute to the alteration of serum metabolites.

The results of the weaned piglet feeding experiment showed that TUDCA improved intestinal barrier function and reduced the relative abundance of intestinal harmful bacteria of weaned piglets.To further investigate the underlying mechanism of TUDCA improving the intestinal barrier function of weaned piglets,E.coliinduced IPEC-J2 cells were used as a model system.Our results showed thatE.coli-induced intestinal barrier function impairment in IPEC-J2 cells was abolished by TUDCA pretreatment.Numerous studies have shown that TUDCA is an agonist of TGR5 and can act by activating TGR5 and its downstream signaling pathways [46,47].Consistent with these studies,we found that TUDCA treatment increased TGR5 expression in IPECJ2 cells.Then the TGR5-knockdown experiment was conducted for further verify that TGR5 was involved in the process of TUDCA improvingE.coli-induced intestinal barrier function impairment in IPEC-J2 cells.In line with our result,a previous study has reported that TGR5 is involved in regulating the integrity of intestinal barrier and its absence manifests by an increased intestinal permeability,while its activation attenuates colon inflammation in rodent models of colitis [48].

It has been reported that epithelial MLCK signaling pathway is crucial to tight junction barrier regulation[49,50].MLCK has been demonstrated to be closely associated with the LPS-induced impairment of the intestinal epithelial barrier [21,51].Similarly,in our present study,we observed that the MLCK pathway was involved in theE.coli-induced impairment of intestinal epithelial barrier.However,theE.coli-induced activation of the MLCK signaling pathway was abolished by TUDCA,presenting similar effects to that of MLCK inhibitor,ML-7.In addition,our findings showed that TUDCA blockedE.coli-induced activation of the MLCK signaling pathway in a TGR5-dependent manner.Collectively,we concluded that TUDCA alleviatedE.coli-induced impairment of the intestinal epithelial barrier in IPEC-J2 cells through the TGR5-MLCK signaling pathway.

Conclusions

In conclusion,these findings showed that TUDCA improved intestinal barrier function associated with TGR5-MLCK pathway and the alteration of serum metabolites and gut bacteria in weaned piglets.These data provided new evidence into the regulation of bile acids on the intestinal barrier function and suggested the potential application of TUDCA in improving intestinal health in piglet production.

Abbreviations

ADFI: Average daily feed intake;ADG: Average daily gain;BAs: Bile acids;BW: Body weight;CA: Cholic acid;CDCA: Chenodeoxycholic acid;CFU: Colony-forming units;CON:Control;DAO: Diamine oxidase;DCA: Deoxycholic acid;DMSO: Dimethyl sulfoxide;ER: Endoplasmic reticulum;FDA: Food and Drug Administration;F/G: Feed/gain ratio;FXR:Farnesoid X receptor;HDCA:Hyodeoxycholic acid;H& E: Haematoxylin and eosin;KEGG: Kyoto Encyclopedia of Genes and Genomes;LB: Luria-Bertani;LCA: Lithocholic acid;LC-MS/MS: Liquid chromatography tandem mass spectrometry;LDH: Lactate dehydrogenase;LPS: Lipopolysaccharide;MLCK: Myosin light chain kinase;OCC: Occludin;OPLS-DA: Orthogonal partial least squares-discriminant analysis;OTU: Operational taxonomic unit;PBS: Phosphate buffer solution;PAS: Periodic acid-schiff;PCoA: Principal component analysis;SEM: Standard error of the mean;sIgA: Secretory immunoglobulin A;TGR5: Takeda G-coupled protein receptor 5;TJ: Tight junction;TUDCA: Tauroursodeoxycholic acid;UDCA: Ursodeoxycholic acid

Acknowledgments

We would like to thank Guangdong Huahong Farming and Husbandry Group Co.,Ltd.for providing us good piglets feeding condition.

I did what I could to console her, but she looked so tired and pale that I persuaded her to go to her room and rest, promising19 to return the next day

Authors’contributions

MS and FLZ was the principal investigator of the study.MS drafted the manuscript,carried out the animal trials,sample analysis,data collection,and statistical analysis.YMF,XY,SCF,ZCL,DD,QY,MY,CJZ carried out the animal trials and contributed to data collection during the animal experiments.XTZ,LNW,PG,GS,XYM provided a guarantee for the smooth running ofthe entire trial.QYJ and SBW designed and supervised the study and revised the manuscript.All authors contributed to the article and approved the submitted version.

Funding

This work was supported by the National Natural Science Foundation of China (31972636,31672508,31790411 and 31802103),the National Key Research and Development Program of China (2017YFD0500501),the Guangdong Key Areas Research and Development Project (2019B020218001),and the Provincial Agricultural Science and Technology Innovation Promotion and Agricultural Resources and Ecological Environmental Protection Construction Project(2021KJ266).

Availability of data and materials

All data generated or analyzed during this article are available from the corresponding author upon reasonable request.

Declarations

Ethics approval and consent to participate

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Author details

1Guangdong Provincial Key Laboratory of Animal Nutrition Control,ALLT ECH-SCAU Animal Nutrition Control Research Alliance,and National Engineering Research Center for Breeding Swine Industry,College of Animal Science,South China Agricultural University,Guangzhou 510642,P.R.China.2Institute of Animal Science,Guangdong Academy of Agricultural Sciences,State Key Laboratory of Livestock and Poultry Breeding,Key Laboratory of Animal Nutrition and Feed Science in South China,Ministry of Agriculture and Rural Affairs,Guangdong Key Laboratory of Animal Breeding and Nutrition,Guangdong Engineering Technology Research Center of Animal Meat Quality and Safety Control and Evaluation,Guangzhou 510640,P.R.China.3Maoming Branch,Guangdong Laboratory for Lingnan Modern Agricultural Science and Technology,Maoming 525000,P.R.China.

Received:26 November 2021Accepted:1 April 2022