Associations among dietary non-fiber carbohydrate, ruminal microbiota and epithelium G-protein-coupled receptor, and histone deacetylase regulations in goats
© The Author(s). 2017
Received: 15 August 2016
Accepted: 12 September 2017
Published: 19 September 2017
Diet-derived short-chain fatty acids (SCFAs) in the rumen have broad effects on the health and growth of ruminants. The microbe-G-protein-coupled receptor (GPR) and microbe-histone deacetylase (HDAC) axes might be the major pathway mediating these effects. Here, an integrated approach of transcriptome sequencing and 16S rRNA gene sequencing was applied to investigate the synergetic responses of rumen epithelium and rumen microbiota to the increased intake of dietary non-fiber carbohydrate (NFC) from 15 to 30% in the goat model. In addition to the analysis of the microbial composition and identification of the genes and signaling pathways related to the differentially expressed GPRs and HDACs, the combined data including the expression of HDACs and GPRs, the relative abundance of the bacteria, and the molar proportions of the individual SCFAs were used to identify the significant co-variation of the SCFAs, clades, and transcripts.
The major bacterial clades promoted by the 30% NFC diet were related to lactate metabolism and cellulose degradation in the rumen. The predominant functions of the GPR and HDAC regulation network, under the 30% NFC diet, were related to the maintenance of epithelium integrity and the promotion of animal growth. In addition, the molar proportion of butyrate was inversely correlated with the expression of HDAC1, and the relative abundance of the bacteria belonging to Clostridum_IV was positively correlated with the expression of GPR1.
This study revealed that the effects of rumen microbiota-derived SCFA on epithelium growth and metabolism were mediated by the GPR and HDAC regulation network. An understanding of these mechanisms and their relationships to dietary components provides better insights into the modulation of ruminal fermentation and metabolism in the promotion of livestock production.
KeywordsRumen microbiota G-protein-coupled receptors Histone deacetylases Dietary modulation Epithelium physiology Microbe–host interactions
Evidence continues to increase implying that the gastrointestinal (GI) microbiota is the critical contributor to host health and GI homeostasis . The dysbiosis of GI microbiota leads to the pathogenesis of a diverse range of diseases affecting host growth and metabolism. So far, the effects of gut microbiota on the host have been suggested to be achieved, at least in part, through the release of short-chain fatty acids (SCFAs), which are the main bacterial metabolites, followed by the fermentation of dietary carbohydrate in the GI tract .
In ruminants, SCFAs produced in the rumen meet 70–80% of the energy requirement for the rumen epithelia, and 50–70% of the energy requirement for the animal, thereby playing important roles in maintaining the energy homeostasis of the host . In addition, SCFAs have also been established to modulate a variety of physiological functions of the rumen epithelium. For example, global gene expression profiling, in a study of bovine rumen epithelium cell cultures, has shown that exogenous butyrate promotes the expression of genes associated with cell growth, signal transduction, and immune responses . By dietary intervention and ruminal butyrate infusion, our in vivo investigations have demonstrated that SCFAs promote the expression of genes involved in epithelium growth and SCFA transport [5, 6].
The ability of SCFAs to modulate physiological processes of the epithelium is well known to depend on two major mechanisms in monogastric animals. The first involves epigenetic modulation. SCFAs, especially butyrate, acetate, and propionate, have been established as intrinsic inhibitors of histone deacetylases (HDACs), promoting gene expression via the inhibition of the HDAC-induced deacetylation of lysine residues within histones . The second mechanism regarding SCFA effects is signaling through G-protein-coupled receptors (GPRs). In mice, the upregulation of GPR43/FFAR2 expression in colonic cells has been demonstrated to enhance the circulating levels of the anorectic hormones peptide tyrosine tyrosine (PYY) and glucagon-like peptide-1 (GLP-1), both of which play important roles in the modulation of gut motility and SCFA absorption [8, 9]. Our previous study in goats has revealed that the upregulated expressions of GPR4 and GPR41 are associated with the upregulated expression of urea transporter (UT-B) in the rumen epithelium, indicating the existence of GPR regulation in the rumen .
The composition of rumen microbiota has been adequately demonstrated to be correlated with the concentrations of rumen SCFAs in ruminants. For example, the relatively high ratio of Bacteroidetes to Firmicutes is associated with a relatively high SCFA concentration in the rumen [10–12]. Moreover, composition change is an important strategy for rumen microbiota to adapt to external interventions, such as diet, viral infection, and antibiotics. We therefore speculate that the rumen microbiota modulates the physiological processes of the rumen via SCFA-mediated GPR and HDAC mechanisms during dietary modulation. In the present study, we have collected paired epithelial transcriptome and microbial metagenome data from the rumen of goats receiving different concentration diets and have analyzed the correlations among the expression of GPR and HDAC, individual SCFA (acetate, butyrate, propionate, valerate, isobutyrate, and isovalerate) concentrations, and microbiota compositions in the rumen. By the simultaneous measurement of the responses of rumen microbiota and epithelium to dietary modulation, we have gained better insights into the nature of diet–microbiota–host interactions.
Six male goats (Boer × Yangtze River Delta White, aged 4 months, 17.97 ± 0.84 kg) were randomly allocated into two groups and received either a diet of 65% hay plus 35% concentrate (containing 30% NFC, MC group, n = 3) or a diet of 90% hay plus 10% concentrate (containing 15% NFC, LC group, n = 3) (Additional file 1: Table S1). All goats were fed with two equal portions of the designed diet at 0800 and 1700 daily for 28 days. Water was freely available to all of the goats during the experimental period. On day 28, the goats were weighted (the final weights of goats in LC group were 18.93 ± 1.25 kg, and the final weights of goats in MC group were 21.4 ± 1.01 kg) and then sacrificed at a local slaughterhouse. This study was approved by the Animal Care and Use Committee of Nanjing Agricultural University, in compliance with the Regulations for the Administration of Affairs Concerning Experimental Animals .
Sample collection and SCFA determination
On day 28, the ruminal fluid was taken at 0, 2, and 5 h after matinal feeding by using the stomach tube and vacuum pump. The first 40 ml of ruminal content was discarded in the procession of collection to avoid the contamination by the saliva. The following 15 ml of ruminal content was strained through a four-layer cheesecloth and immediately subjected to pH measurement. Subsequently, the ruminal fluid was added by 5% HgCl2 and stored at − 20 °C for the determination of SCFA concentrations. On day 28, all goats were slaughtered at 8 h after matinal feeding. Immediately after slaughter, the ruminal content was collected and strained through a four-layer cheesecloth. An aliquot (15 ml) of ruminal fluid was collected and stored at − 20 °C for the extraction of microbial DNA. The remaining fluid, added by 5% HgCl2, was stored at − 20 °C for the determination of SCFA concentrations. For each goat, around 10 cm2 of rumen tissue from the ventral blind sac was quickly excised and washed repeatedly in ice-cold phosphate-buffered saline (PBS; pH 7.4) until the PBS was clear. The muscle layers were removed, and the epithelium was immediately cut into small pieces (around 0.5 cm2/piece) and added by TRIzol buffer (Thermo Fisher Scientific, Nanjing, China). These samples were transferred into liquid N within 5 min and stored at − 80 °C until RNA extraction.
The ruminal SCFA concentrations were determined by using a chromatograph (HP6890N, Agilent Technologies, Wilmington, DE, USA) as described in Yang et al. . The SCFA concentrations at 0, 2, 5, and 8 h were triplicate measured, respectively.
Microbial DNA extraction and sequencing
The metagenomic DNA of the microbiota was extracted from 15 ml ruminal fluid by using a Bacterial DNA Kit (Omega, Shanghai, China). The DNA concentration was determined by means of a Nanodrop 1000 (Thermo Fisher Scientific, Wilmington, DE, USA) and stored at − 20 °C until further processing. The amplicon library preparation was performed by polymerase chain reaction (PCR) amplification of the V3–V4 region of the 16S rRNA gene. The universal primers 338F (5′-ACTCCTACGGGAGGCAGCAG-3′) and 806R (5′-GGACTACHVGGGTWTCTAAT-3′) , including TruSeq adapter sequences and indices, were used in the PCRs. All libraries were sequenced by using an Illumina MiSeq platform (Illumina, San Diego, CA, USA) at Biomarker Technologies, Beijing, China.
Ruminal microbiota analysis
Paired reads were filtered for quality (Q30) and joined by FLASH version 1.2.11 . Sequences that contained read lengths shorter than 400 bp were removed. The remaining sequences were then classified into taxa by blasting with the ribosomal database project (RDP) database at a 97% similarity threshold. Operational taxonomic units (OTUs), whose counts were more than 3 in at least one of the samples, were retained in the further analysis. The selected OTUs were normalized to the relative abundance for each sample. The diversity of the microbial communities was estimated by using the R program phyloseq package . For a deeper analysis of the diversity of the major evolutional clades in the ruminal microbiota, OTUs were filtered to acquire a relative abundance of at least 1% in at least one sample. Then, MUSCLE version 3.8.31  was used to align the complete 16S rRNA sequences of the corresponding species in the RDP database, and RAxML version 8  and the GTR model were used to construct the maximum likelihood (ML) trees. The R program ape package  was used to plot the tree.
Epithelial RNA extraction and sequencing
Ball mill MM 400 (RETSCH, Germany) was used to homogenize the rumen epithelium before RNA extraction, with the parameters of 25 oscillations/s and 1 min. The homogenized tissue was incubated on ice and immediately used for RNA extraction. Total RNA was extracted by using the RNeasy Mini Kit (Qiagen, Shanghai, China) according to the manufacturer’s instructions. RNA was quantified by using a NanoDrop 1000 spectrophotometer, and its integrity was evaluated by using the RNA 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). High-quality RNA (RNA integrity number > 9.0) was processed by using NEB Next Ultra RNA Library Prep Kit (NEB, USA) following the manufacturer’s instruction. All libraries were sequenced via paired-end chemistry (PE125) on an Illumina HiSeq2500 platform (Illumina, San Diego, CA, USA) at Biomarker Technologies, Beijing, China.
Transcriptome assembling and differentially expressed gene identification
Low-quality reads were first removed by using an in-house perl script (reads including low-quality bases (Q30) of more than 50% and ambiguous bases (N) of more than 10% were removed). Remaining reads were aligned to the NCBI goat genome annotation release version 101 by using TopHat v2.1.0  with standard parameters. Mapped reads were used to estimate the gene expression level of each gene transcript. Gene expression values were then normalized according to the reads per kilobase million (RPKM). In this study, only genes with at least one RPKM in at least one of the samples were considered as expressed. Each SAM output file from the TopHat alignment was used in the Cuffdiff program of the Cufflinks version 2.2.1  as input files to test for differential gene expression.
Sequence conservation of differentially expressed HDACs and GPRs
The mRNA sequences of differentially expressed GPRs and HDACs were blasted to the GenBank nucleotide collection, locally. The matched genes, with e value less than 1E−5, were pulled out and aligned in MUSCLE version 3.8.31. The maximum likelihood trees of each investigated GPR and HDAC were constructed by using the GTR model in RAxML version 8. Visualization of the phylogenetic trees was performed on the ITOL web server .
HDAC and GPR co-expression network
The co-expressed genes were identified by computing the spearman correlation coefficient (SCC) between pair of genes across six samples. Only expressed genes (RPKM > 1 in at least one sample) were used in the correlation analysis. A threshold for the SCC larger than 0.85 and p value less than 0.01 were used to identify significantly co-expressed genes. The expression levels of the first neighbors of investigated HDACs and GPRs on the co-expression network were compared between groups. Only differentially expressed neighbors were further analyzed of Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway on KABAS version 2.0 web server . Finally, cytoscape version 3.4.0  was applied to visualize the gene co-regulation network.
Dimensionality reduction for microbial features and multidata integration
In order to improve power to associate microbial composition with host gene transcriptional activity, we reduced the dimensionality of microbial features through calculating their SCC with the molar proportions of individual SCFAs, since the molar proportions of SCFAs were stable across the time within the group. The OTUs, whose SCC is larger than 0.6 and p value is less than 0.05 with at least one kind of SCFAs, were used in the following analysis. Next, the relationships of the relative abundance of the selected OTUs, the molar proportions of individual SCFAs, and the expressions of the differentially expressed HDACs and GPRs were explored by using the constrained correspondence analysis (CCA) in the R program vegan package . The molar proportions of SCFAs and expression (RPKM) of investigated HDACs and GPRs were used as the environmental factors in the CCA analysis. The R program ggplot2 package  was used to generate the visual interpretation of the gene–SCFA–microbiota relationships. The location of each microbial genus stands for the centroid of corresponding OTUs within investigated genus.
Microbial metabolites in rumen
Structure of bacterial communities
Diversity and richness of microbial communities
Expression profiles of GPRs and HDACs in rumen epithelium
The RNA-Seq method was used to identify the expression profiles of GPRs and HDACs in the rumen of goats. It generated a total of 135 M raw reads (average 22.5 M reads per sample, range 20.9–23.5 M) and 127 M clean reads (average 21.2 M reads per sample, range 19.1–22.5 M). On average, 83% of the clean reads were successfully mapped to the NCBI goat genome annotation release version 101.
The 73 members of the GPR family and the 11 members of the HDAC family were found to be encoded on the goat genome (Additional file 5: Table S3, Additional file 6: Table S4). The transcriptome data showed that 20 members of GPR family and 7 members of HDAC family were expressed in the rumen epithelium (RPKM > 1 in at least one sample). By comparing the gene expressions in the LC group, we found that GPR1, 87, 89A, and 155 were significantly upregulated (p < 0.05), and GPR107, free fatty acid receptor 4 (FFAR4, also known as GPR120), and hydroxycarboxylic acid receptor 2 (HCAR2, also known as GPR109A) were significantly downregulated (p < 0.05) in the MC group. Moreover, HDAC4, HDAC5, HDAC6, and HDAC10 were significantly upregulated (p < 0.05), and HDAC1 was significantly downregulated (p < 0.05) in the MC group. By comparing the gene expressions within the group, we found, in both groups, that the expression of GPR87 was the highest among the GPR members, and HDAC1 was the highest among the HDAC members. Further, GPR87 and HDAC1 are the only members that expressed more than 100 counts (RPKM) in at least one group. In addition, six GPRs (GPR1, 89A, 108, 155, 160, and FFAR4) and four HDACs (HDAC2, 3, 5, and 8) expressed more than 10 counts (RPKM) in at least one group. The previously reported GPRs (GPR4, GPR41/FFAR3, GPR43/FFAR2), whose expressions were detected by quantitative PCRs in rumen epithelium [5, 28], were little expressed in the present study.
Sequence conservation of GPRs and HDACs
To investigate the sequence conservation of differentially expressed GPRs and HDACs during evolution, we constructed ML trees by using all genes found in blast searching, with the threshold of the e value less than 1E−5. According to the trees, all the investigated GPRs and HDACs were highly conserved on both of the division and family levels of vertebrates (Additional file 7: Fig. S3, Additional file 8: Fig. S4). To investigate the conservations within the members of GPR family, we pairwise aligned the sequences of encoded GPR members, but no similarity above 30% was received between any pair of GPR members. The same results were received from the comparisons of HDAC members.
Related KEGG pathways of differentially expressed GPRs and HDACs
In the epithelium growth network, the upregulated expressions of GPR1, 89A, and 155 were correlated to the upregulated expressions of regulator complex protein (LAMTOR3), mitogen-activated protein kinase kinase kinase 11 (MAP3K11), and ETS domain-containing protein (ELK1), all of which were located on mitogen-activated protein kinase (MAPK) signaling pathway and related to cell proliferation and differentiation. ELK1 was also on the insulin and oxytocin signaling pathway in the regulation of cell proliferation and differentiation. Moreover, the increased expression of GPR1 was associated with the decreased expression of acid ceramidase (ASAH1), which was on the sphingolipid signaling pathway regulating cell apoptosis, survival, and proliferation. As for HDACs, the upregulation of HDAC 4, 5, 6, and 10 was correlated to the downregulation of five neighbors that regulated the cell apoptosis, survival, proliferation, and differentiation via modulation of 14 signaling pathways.
In the epithelium metabolism network, the upregulation of GPR1, 87, and 89A expression was correlated to the upregulation of nicotinamide adenine dinucleotide dehydrogenase subunits 2, 4, and 4L (ND2, 4, 4L), H+ transporting adenosine triphosphate synthase (ATP5H), and nicotinamide adenine dinucleotide dehydrogenase 1 alpha subcomplex 4 (NDUFA4). The downregulation of HDAC1 expression was correlated to the upregulation of ND6 expression. All of these enzymes were related to the oxidative phosphorylation of energy metabolism. The increased expression of GPR1 and decreased expression of HDAC1 were associated with the increased expression of microsomal glutathione S-transferase 3 (MGST3) and monoamine oxidase A (MAOA). These two kinds of enzymes modulated the xenobiotic biodegradation and metabolism of the rumen epithelium. On the contrary, the decreased expressions of protein O-mannosyltransferase 2 (POMT2), RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyl transferase (RFNG), xylosyltransferase 2 (XYLT2), and mannosidase alpha class 2C member 1 (MAN2C1) were associated with the increased expression of GPR87, HDAC4, and HDAC5. All of these enzymes regulate glycan biosynthesis and metabolism in the rumen epithelium. In addition, the metabolism of other amino acids can be regulated by GPR1-MGST3 and HDAC10-methionyl-tRNA synthetase 2 (MARS2) pathways. Lipid metabolism can be regulated by GPR1-N-acylsphingosine amidohydrolase 1 (ASAH1), GPR-ectonucleotide pyrophosphatase 2 (ENPP2), GPR87-propanoyl-CoA C-acyltransferase (SCP2), HDAC1-peroxisomal multifunctional enzyme type 2 (HSD17B4), and HDAC10-sphingosine kinase 2 (SPHK2) pathways. Carbohydrate metabolism might be regulated by the GPR89A-phosphatidylinositol-4-phosphate 3-kinase C2 domain-containing gamma polypeptide (PIK3C2G), HDAC4-phospholipase C, gamma 1 (PLCG1), and HDAC1-2,3-bisphosphoglycerate mutase (BPGM) pathways. Amino acid metabolism might be modulated by the HDAC1-MAOA and HDAC1-BPGM pathways. The metabolism of cofactors and vitamins might be modulated by GPR155-molybdenum cofactor biosynthesis protein 1 gene (LOC102170834) pathway.
Relationships of GPR and HDAC expression, molar proportions of individual SCFAs, and relative abundance of bacterial genera
The present study revealed that the MC diet promoted the upregulation of the concentrations of acetate, butyrate, and total SCFA from 2 to 5 h after feeding and the concentration of propionate at 5 h after feeding. Moreover, NMDS and ANOSIM analyses indicated that the changes of ruminal SCFA concentrations were associated with the compositional changes of ruminal microbiota. Phylogenetic analysis of detectable OTUs showed that the relative abundance of five prokaryotic families, namely the Prophyromonadacea, Synergistaceae, Ruminococcaceae, Veillonellaceae, and Verrucomicrobia subdivision 5, were increased significantly in the MC group. Among these taxa promoted by the MC diet, members of the Ruminococcaceae are the important contributors to cellulose degradation . Members of the Veillonellaceae and Prophyromonadacea are capable of utilizing lactate and converting it largely to acetate and propionate . Members of the Synergistaceae are able to ferment amino acids and peptides to produce acetate in animal gut . A recent study of the first cultured representative of Verrucomicrobia subdivision 5 indicated that this strain of the taxon could ferment monosaccharide to produce acetate and lactate . Therefore, we inferred that the bacterial increasing mainly involved the species responsible for decreasing the concentration of lactate in the rumen. Accumulation of lactate in the rumen is a major reason of subacute ruminal acidosis (SARA), characterized by low feed intake and chronic inflammation . Therefore, such reshaping of the microbial community may play important roles in maintaining the stable pH of the rumen during the period of relatively high SCFA concentrations. In addition, the expansion also involved the cellulose-degrading bacteria indicating that the increased dietary NFC in the MC group promoted cellulose degradation by the microbes. This is supported by a previous study in which the positive correlation of the dietary starch and the rate of cellulose degradation were detected . However, the majority of OTUs detected in our investigation have unknown functions, making the interpretation of microbial reshaping associated with SCFA profiles difficult. We can only speculate that the increased butyrate was converted from the acetate by specific microbes via the acetate CoA-transferase pathway, since the expansion of A-producing bacteria and the synergetic upregulation of ruminal butyrate and acetate concentrations were observed.
Broad effects of SCFAs on the physiological processes of ruminal epithelium have been reported. However, little is known concerning the mechanisms related to this SCFA-mediated regulation in the rumen. In present study, we observed the specific expression of the members of the GPR and HDAC families in the rumen epithelium. However, the previously reported GPRs (GPR4, GPR41/FFAR3, GPR43/FFAR2), whose expressions were detected by quantitative PCRs in rumen epithelium [5, 28], were little expressed in the present study. The disturbances of unmapped reads in transcriptome assembling and an overestimation of isoform expressions in quantitative PCRs might be the reasons for the inconsistent results. Since the highly conserved sequences of these genes within vertebrates, our results indicate the possibility that commensal bacteria regulate the epithelium physiology via metabolite-mediated GPR and HDAC pathways in the rumen. Furthermore, our data suggest the GPR87 and HDAC1 play more important roles in the ruminal epithelium than other members of the respective families.
According to our epithelium growth network, in the MC group, GPR1, 89A, and 155 might promote cell proliferation and differentiation via the MAPK, sphingolipid, insulin, and oxytocin signaling pathways. Also in MC group, HDAC 4, 5, 6, and 10 may suppress cell apoptosis, survival, proliferation, and differentiation by suppressing the expression of genes located on 14 signaling pathways. Among them, nuclear factor kappa B signaling has been established to control the expression of cyclin D1 via the modulation of the production of pro-inflammatory cytokines in mice [34, 35]. WNT signaling has been shown to regulate cell differentiation and apoptosis in a dose-dependent manner in human, i.e., low-intensity signaling leads to controlled self-renewal, moderate-intensity signaling promotes uncontrolled cell proliferation, and high-intensity signaling leads to apoptosis [36, 37]. Calcium signaling has also been demonstrated to regulate the cell cycle by decreasing intracellular cyclic adenosine monophosphate (cAMP) in human . Taken together, these data suggest that, in an environment with relatively high SCFA concentrations, GPRs promote cell proliferation and differentiation via the promotion of the expressions of related genes. However, at the same time, HDACs might suppress cell proliferation, differentiation, and survival by suppressing the expression of another set of related genes. Interestingly, the sphingolipid signaling pathway, which is related to cell apoptosis, might be suppressed by both HDAC10 and GPR1 in the MC group. These results suggest that epithelium homeostasis is maintained by GPR and HDAC co-regulation mechanisms.
Our analysis of the epithelium metabolism network has revealed that, in the MC group, the changed expressions of GPR1, 87, 89A, and HDAC1 possibly enhance energy metabolism by promoting the expressions of seven genes related to mitochondrial respiratory chain function. The decreased expression of HDAC1 might enhance glycolysis by promoting the expression of BPGM, a crucial enzyme in the regulation of hemoglobin-associated oxygen. Moreover, the decreased expression of HDAC1 might enhance amino acid metabolism by promoting the expression of MAOA, the enzyme catalyzing the oxidative deamination of monoamines. The enhanced capability of amino acid metabolism by the epithelium might increase ketone synthesis, providing more energy for the animal. In addition, the suppression of glycosaminoglycan biosynthesis and glycan degradation by HDAC5 possibly increases the amount of glycan entering the blood. Promotion of primary bile acid biosynthesis by GPR87 and HDAC1 probably enhances glucose metabolism and energy expenditure via the bile acid signaling pathway . All the abovementioned changes in the epithelium metabolism of the MC group will improve energy supplements for the animal. Additionally, in the MC group, the enhancement of exogenous toxin degradation by GPR1 and HDAC1 benefits the animal health. Suppression of O-glycan biosynthesis by GPR87 and HDAC5 might inhibit the activation of T lymphocytes . Suppression of sphingolipid metabolism by GPR1 and HDAC10 possibly promotes the stability of membrane structure and cell-to-cell recognition [41, 42]. Enhancing the ether lipid metabolism by GPR1 can increase the activity of the potassium channel , maintaining the stability of the rumen ecosystem. So far, GPRs have been reported to regulate host metabolism via the modulation of hormone secretion, sympathetic activity, and immunity responses [9, 44, 45]. Our results suggest that the regulation of GPRs and HDACs in epithelium metabolism have major effects via the modulation of the expression of related enzymes. Furthermore, we have found that the regulation of GPRs and HDACs, induced by relatively high SCFA concentrations, will benefit animal growth and health.
Studies in humans have shown that gut microbe-derived butyrate was the most potent inhibitor of HDACs, with a maximum efficiency of approximately 80% inhibition of HDAC1/2 . In present study, the highly negative correlation between the molar proportion of butyrate and the expression of HDAC1, revealed by CCA analysis, suggested that, in the goat rumen, microbiota-derived butyrate was also the most powerful inhibitor of HDAC1 in epithelium. In addition, the study of Kimura et al.  revealed that ffar2-deficient and ffar2-overexpressing mice exhibited different phenotypes (obesity or leanness, respectively) in comparison with wild-type mice. However, these mice lost the corresponding phenotypes when grown under germ-free conditions or when treated with antibiotics suggesting that the activation of GPRs might be dependent on the existence of gut microbes. In our CCA analysis, a high correlation existed between the relative abundance of Clostridium_IV and the expressions of GPR1. Members of Clostridium_IV are well known to be the major butyrate-producing bacteria in the animal gut . A previous study has shown that the depletion of butyrate-producing bacteria is a common feature in patients suffering from inflammatory bowel diseases (IBD) and colorectal cancer (CRC) . Despite limitations, we speculate that butyrate-producing bacteria play an important role in the promotion of epithelium growth and metabolism via the modulation of the expression of GPR1. Unfortunately, most of the significantly correlated species cannot as yet be cultured, and we cannot infer their roles in these regulation networks. Further studies are required for the identification of their functions and significance in the animal gut.
Our results indicate that SCFA-mediated GPR and HDAC co-regulation networks exist in the rumen epithelium, allowing the animals to receive signaling from their resident microbiota, sensitively and accurately. These networks regulate a variety of physiological processes in the epithelium, especially growth and metabolism, and play important roles in the maintenance of epithelial integrity and the promotion of animal growth. Moreover, these networks are important mechanisms for commensal bacteria to improve their co-habiting conditions by the modulation of epithelium physiology. By understanding these reciprocal mechanisms between the host and microbiota, coupled with the corresponding modulation factors in the diet, we will be able to improve animal production in healthy and sustainable ways.
This work was supported by the Project Grant Natural Science Foundation of Jiangsu Province (BK20150654), the Chinese National “973” Project (2011CB100801), the Independent Innovation Project of Nanjing Agriculture University (KYZZ01628), and the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD).
Availability of data and materials
The meta-genome and transcriptome data are available in the NCBI under BioProject PRJNA335777.
HS analyzed the data and wrote the paper. ZL designed the research. ZL and ZC performed the experiments. ZS edited the version of the paper to be published. All authors approved the final manuscript.
This study was approved by the Animal Care and Use Committee of Nanjing Agricultural University, in compliance with the Regulations for the Administration of Affairs Concerning Experimental Animals (approved by the State Council of China on October 31, 1988, and promulgated by Decree No. 2 of the State Science and Technology Commission on November 14, 1988.) .
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The authors declare that they have no competing interests.
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