Dietary Enteromorpha Polysaccharides Supplementation Improves Breast Muscle Yield and Is Associated With Modification of mRNA Transcriptome in Broiler Chickens

Introduction

The antibiotics growth-promoters (AGP) have been widely used in poultry production to maintain high productivity and improve economic efficiency. However, abuse of AGP might bring antibiotic resistance in poultry and antibiotic residues in poultry products, leading to food safety and public health concerns (1, 2). Therefore, the search for in-feed antibiotic substitutes has become a research focus in recent years. Natural bioactive compounds possess several beneficial biological activities and maybe potential substitutes for antibiotics (3–5). Natural polysaccharides exert many functional benefits and improve broiler's growth performance and gut health (6–8). Thus, the natural polysaccharides can be used as growth promoters in broilers. The marine environment has rich sources of natural polysaccharides, and marine-derived polysaccharides have been confirmed to exert various biological functions, such as anti-oxidant, and anti-inflammatory responses (9). For instance, chitosan and chito-oligosaccharides improved the carcass traits, immunity, and anti-oxidant effects in broilers (10–13) and promoted beneficial gut microbiota while modulating metabolic pathways (8). However, to the best of our knowledge, there is no report evaluating the effects of dietary seaweed polysaccharides on carcass traits and ts he mRNA transcriptome of broilers.

Carcass traits are indicators of differences in the amount of nutrients deposited in tissues (14). Slaughter and whole net carcass yield can measure the performance of meat yield (15, 16). Meanwhile, the breast and leg muscle percentage can determine the meat yield of broilers (17). Therefore, the improvement of breast muscle yield is considered to be significant in the poultry industry. Knowing the mechanism associated with it will further help to develop a nutrition program. RNA-Sequencing (RNA-Seq) analysis has emerged as a powerful technology for transcriptome analysis to detect the whole transcriptional level of species (18). New transcripts could be found in the structure and expression level of the enriched single-chain mRNA by RNA-Seq. Also, the expression level of the low abundance gene was verified using RNA-Seq with desired results (19). At present, the RNA-Seq technique is of great significance to explore gene expression and regulation mechanisms at the transcriptional level and is widely used in life sciences research (20).

Enteromorpha is one of the largest green seaweeds, widely distributed in various sea. It contains abundant polysaccharides and has been confirmed to exert several biological functions, such as antitumor, antioxidation, and antiviral activities (21). Dietary inclusion of Enteromorpha polysaccharides (EP) enhanced the growth performance, antioxidation, and immunity in broilers (22). We conducted series of studies to evaluate different roles of dietary EP in various parameters of broilers. Dietary supplementation of EP improved the anti-oxidant performance in laying hens (9) and growth performance and intestinal barrier function in broilers (23). Similarly, our previous study found that the supplementation of EP mitigated AFB₁-induced toxicological effect of broilers (24). Also, it has been reported that natural dietary polysaccharides could improve the carcass traits in broilers (25, 26). However, to date, the effects of dietary EP on carcass traits of broilers, especially the underlying molecular mechanism, are unknown. Hence, the present study was conducted to evaluate the effect of dietary supplementation with graded levels of EP on carcass traits in broilers and to explore the molecular mechanism of mRNA transcriptome by using the RNA-Seq technique.

Materials and Methods

Source of EP

The EP were extracted from the Enteromorpha by Qingdao Haida Biotechnology Co., Ltd. (Qingdao, Shandong, China), with ≥ 48% purity and a molecular weight of 4,929 Da. The EP are water-soluble sulfated polysaccharides obtained from the natural green alga Enteromorpha by enzymatic extraction, purification, concentration, and spray drying. Briefly, after crushing the algae, the algal powders are soaked in water. Then the water extracts of the algae are subjected to stepwise enzymatic treatment with pectinase, cellulase, and papain. Then the enzymes are inactivated, centrifugal concentrated, precipitated with ethanol, and finally spray dried to obtain the EP used in this study. Based on the analysis by high-performance liquid chromatography (HPLC), the polysaccharides were mainly consisting of rhamnose (Rha), glucuronic acid (GlcA), glucose (Glc), galactose (Gal), and xylose (Xyl) monosaccharides. The molar percentage of monosaccharides in the EP were as follows: Rha 40.6%, GlcA 9.3%, Glc 38.2%, Gal 5.6%, and Xyl 6.3%.

Experimental Design, Birds, and Diets

A total of 396 1-day-old male Arbor Acres broiler chicks (initial body weight 44.65 ± 0.56 g) were obtained from a commercial hatchery (Nanning, Guangxi, China). The chicks were randomly allocated to 1 of 6 dietary treatments (6 replicates per treatment, with 11 broilers per cage), and the study was conducted for 35 day. Dietary treatments were as follows: basal diets supplemented with EP at 0 (CON), 1000 (EP_1000), 2500 (EP_2500), 4000 (EP_4000), 5500 (EP_5500), and 7000 (EP_7000) mg/kg of feed. The mash form basal diet was formulated (Table 1) to meet or exceed the nutrient requirements of broiler chickens (27) in two phases-starter (1–21 day) and finisher (22–35 day). The broilers were grown in a temperature-controlled room at 33 ± 1°C for the first 3 day and then gradually reduced by 3°C per week until reaching 24°C and maintaining humidity 65% for the rest of the study period. The birds had free access to feed and water all the time during the study period.

TABLE 1

Table 1. Basal diet composition (as-fed basis).

Carcass Traits Determination

At the end of the feeding trial, all birds were fasted for 12 h, and six birds (one bird from each replicate cage) were randomly selected from each treatment. Then the birds were weighed and slaughtered. The defeathered carcass, including the head and feet, was weighed as the carcass weight. The carcass was then eviscerated manually and weighed as the semi-eviscerated weight, which was measured as the carcass weight after removed the esophagus, trachea, spleen, gastrointestinal tract, crop, gallbladder, pancreas, and gonads. Eviscerated weight was measured as the semi-eviscerated weight after removed the head, feet, liver, heart, glandular stomach, gizzard, and abdominal fat. Finally, the carcass, semi-eviscerated carcass, eviscerated carcass, breast muscle, leg muscle, and abdominal fat yield was calculated as a percentage of live body weight. The detailed determination of carcass characteristics was done as follows.

Carcass yield (%) = (carcass weight/live body weight) × 100%;

Semi-eviscerated carcass yield (%) = (semi-eviscerated weight/live body weight) × 100%;

Eviscerated carcass yield (%) = (eviscerated weight/live body weight) × 100%;

Breast muscle yield (%) = (breast muscle weight on both sides/live body weight) × 100%;

Leg muscle yield (%) = (leg muscle weight on both sides/live body weight) × 100%;

Abdominal fat yield (%) = (abdominal fat weight/live body weight) × 100%.

Transcriptome Analysis

Based on the carcass traits data (Table 3), six breast muscle samples with significant differences between two treatments (CON and EP_7000 groups, three samples in each group) were randomly selected and sent for RNA-Seq analysis (Shanghai Majorbio Biological Co., Ltd., Shanghai, China). Total RNA was isolated from the breast muscle samples using TRIzol Reagent (Invitrogen, Carlsbad, CA, USA) according to the manufacturer's recommendations. For each of samples, 10 μg of RNA was used for RNA-seq library preparation by using the stranded Total RNA kit (Illumina TruSeq^®) followed by the kit's directions. The mRNA isolated from total RNA is used for the analysis of transcription information. Then, randomly interrupt the mRNA, add fragmentation buffer to break it into small fragments of about 300 bp. A six-base-pair random hexamer was added, and the mRNA was used as a template to reversely synthesize a single-strand cDNA, which was then synthesized into a two-stranded stable structure. After purification and enrichment, all libraries were sequenced using an Illumina HiSeq 2000 (Illumina, San Diego, CA, USA). After obtaining the Read Counts of the transcript, analyze the expression difference of the transcript between samples for the multi-sample project. The differentially expressed genes (DEGs) among different groups were analyzed using EdgeR software (Majorbio, Shanghai, China), p-values were adjusted (padj) using the Benjamini-Hochberg approach for controlling the false discovery rate. The GOATOOLS were used to perform Gene Ontology (GO) enrichment analysis on the transcripts in the gene set. When the corrected p < 0.05, the GO function is considered to be significantly enriched. The R Programming Language was used to write a script to perform Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis on the transcripts in the gene set. When the p < 0.05, it is considered that the KEGG pathway is significantly enriched.

Six DEGs were selected to verify the RNA-Seq results by using quantitative real- time PCR (qPCR). The description of the specific primers used for qPCR are presented in Table 2 (Primer Express 3.0 software, Applied Biosystems, Foster City, CA, USA). Primers were developed by Sangon Biotech Co., Ltd. (Shanghai, China), and the β-actin was used as the reference gene. The qPCR reactions were performed with a CFX-96 Real-Time PCR Detection System (BioRad, Hercules, CA, USA). It was carried out in a total volume of 20 μl, including 10 μL SYBR^® Premix Ex Taq II (Tli RNaseH Plus), 2 μl cDNA template, 1 μl of each primer (forward and reverse primers), and 6 μl DEPC treated water. The DEPC treated water for the replacement of cDNA template was used as a negative control. The PCR program was as follows: 95°C for 30 s, followed by 40 cycles of 95°C for 10 s, 30 s under T_m temperature, and 72°C for 15 s. Each sample was tested in triplicate. The relative mRNA expression levels of the six target genes were calculated using the 2^−ΔΔCt method.

TABLE 2

Table 2. Description of primers used in qPCR verification.

Statistical Analysis

The carcass data were statistically analyzed using general linear model procedures of SAS (SAS V9.2, SAS Institute Inc., Cary, NC, USA) with a pen as experimental unit. Orthogonal polynomial contrasts of the carcass data were used to test the linear, quadratic, and cubic effects of the increasing levels of dietary EP. The DEGs analysis of transcriptome was done using EdgeR software (Majorbio, Shanghai, China), genes enrichment pathway was analyzed using GOATOOLS software (GO analysis, Majorbio, Shanghai, China) and Majorbio software (KEGG analysis, Majorbio, Shanghai, China). The probability value of <0.05 was considered to be statistically significant, and 0.05 ≤ p < 0.10 was considered as a tendency.

Results

Carcass Traits

As shown in Table 3, graded dietary levels of EP supplementation had no significant effects on carcass, semi-eviscerated carcass, eviscerated carcass, leg muscle, and abdominal fat yield (p > 0.05). However, broilers in EP_7000 group had a significantly higher breast muscle yield than the CON group (p < 0.05).

TABLE 3

Table 3. Effects of dietary supplementation of Enteromorpha polysaccharides (EP) on carcass traits of broilers on d 35.

Transcriptome Analysis

The results of DEGs are presented in Figure 1 and Supplementary Table 1, and the selected DEGs (top 30 upregulated and 30 down-regulated genes) are presented in Tables 4, 5. Between the CON and EP_7000 groups, a total of 154 genes (p-adjust < 0.05) were differentially expressed. Among the identified 154 DEGs, 112 genes were significantly upregulated, and 42 genes were significantly down-regulated by EP_7000 supplementation. The six selected DEGs showed a consistent expression trend between the RNA-Seq and qPCR, suggesting that the results of RNA-Seq are reliable (Figure 2).

FIGURE 1

Figure 1. Volcano plot of differentially expressed genes of broiler fed with control and EP_7000 supplemented diets. CON, dietary supplementation of Enteromorpha polysaccharides (EP) at 0 mg/kg; EP_7000, dietary supplementation of Enteromorpha polysaccharides (EP) at 7000 mg/kg; nosig, no significant.

TABLE 4

Table 4. The 30 most upregulated differentially expressed genes in the broiler chickens fed Enteromorpha polysaccharides compared to control group^a.

TABLE 5

Table 5. The 30 most down-regulated differentially expressed genes in the broiler chickens fed Enteromorpha polysaccharides compared to control group^a.

FIGURE 2

Figure 2. Validation of RNA-Seq results by qPCR. CON, dietary supplementation of Enteromorpha polysaccharides (EP) at 0 mg/kg; EP_7000, dietary supplementation of Enteromorpha polysaccharides (EP) at 7000 mg/kg.

As described in Table 6 and Figure 3, 16 GO terms (p-corrected < 0.05) were significantly enriched. In GO enrichment analysis, the DEGs were divided into three main function groups, including biological processes, molecular functions, and cellular components. The result showed that the 16 terms significantly enriched the biological processes of the DEGs expressed in breast muscle. These were: immune system process, positive regulation of immune system process, immune response, negative regulation of leukocyte apoptotic process, positive regulation of cytokine production, positive regulation of macromolecule biosynthetic process, antigen processing and presentation, positive regulation of transcription, DNA-templated, positive regulation of nucleic acid-templated transcription, positive regulation of RNA biosynthetic process, positive regulation of RNA metabolic process, and regulation of MyD88-dependent toll-like receptors (TLRs) signaling pathway.

TABLE 6

Table 6. The GO enrichment analysis between CON and EP_7000 groups of broiler chickens^a.

FIGURE 3

Figure 3. Gene ontology (GO) enrichment analysis between CON and EP_7000 treatment group of broilers. CON, dietary supplementation of Enteromorpha polysaccharides (EP) at 0 mg/kg; EP_7000, dietary supplementation of Enteromorpha polysaccharides (EP) at 7,000 mg/kg.

In addition, using KEGG enrichment analysis, the functions of transcripts and controls were mapped to pathways. As described in Table 7 and Figure 4, the KEGG pathway analysis (p-corrected < 0.05) showed that three pathways were significantly enriched and were associated with disease-related pathways, including Herpes simplex infection, Influenza A, and Cell adhesion molecules.

TABLE 7

Table 7. The KEGG enrichment analysis between CON and EP_7000 groups of broiler chickens^a.

FIGURE 4

Figure 4. Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis between CON and EP_7000 treatment group of broilers. CON, dietary supplementation of Enteromorpha polysaccharides (EP) at 0 mg/kg; EP_7000, dietary supplementation of Enteromorpha polysaccharides (EP) at 7000 mg/kg.

Discussion

Natural polysaccharides are widely used as functional feed additives in broiler nutrition, which can be used as immunomodulators to replace antibiotic growth promoters in food animals (28, 29). The present study's findings indicated that dietary supplementation of EP_7000 significantly improves breast muscle yield. Consistent with our results, Ou Yang et al. (24) observed that the inclusion of natural polysaccharides (1.0 and 1.5%) improved the breast muscle yield of broilers and suggested that it may be related to the ability of the polysaccharides to increase protein metabolism and decrease fat metabolism. Sun et al. (25) also found that the dietary supplementation of Astragalus polysaccharides (500 mg/kg) improved the breast muscle yield in broilers. Several possible mechanisms could explain the beneficial effects of these natural polysaccharides on breast muscle yield in broilers, including enhancement of the protein metabolism and resistibility. In addition, it may be related to the fact that natural polysaccharides significantly increased the absorption of nutrients from the intestine of broilers, which helps in improving the growth of broilers, thereby promoting breast muscle growth (22).

On the other hand, it may be that the natural polysaccharides could enhance the immunity and disease resistance of broilers, thus improving the growth and meat yield (22). However, the results of this study are in disagreement with the findings of Li et al. (29). They observed no significant differences in the breast muscle yield of broilers after feeding chitosan with different molecular weights. Also, Chen et al. (30) reported that the dietary inclusion of low molecular weight chitosan (< 2,374 Da) had no significant effects on breast muscle yield in broilers. The reasons for these inconsistent findings may be due to the different structures of polysaccharides and the age and feeding environment of broilers. It may also be associated with the purity and quantity of polysaccharides used in the diet. Also, the results of this study showed that the dietary EP at the supplemental level of 1,000, 2,500, 4,000, and 5,000 mg/kg had no significant effect on breast muscle yield, indicating that the supplemental dose of EP at 7,000 mg/kg is more effective, and the effect of dietary EP on carcass traits is dose dependent. However, the specific reason needs to be further investigated.

The mRNA transcriptome analysis was conducted to explore the potential molecular mechanism of dietary EP to increase the breast muscle yield in the present study. The results of transcriptome analysis showed that a total of 154 DEGs were identified between the CON and EP_7000 groups. The GO enrichment analysis of DEGs found that DEGs were mainly enriched in the immune-related signaling pathways. These genes enable the immune system to calibrate when the body is invaded by potential threats. Some genes activate and accelerate the production of cytokines and the apoptosis of white blood cells. Furthermore, it can modulate the expression of the MyD88-dependent TLRs signaling pathway. Similarly, Wang et al. (31) demonstrated that the dietary Astragalus polysaccharides enhanced the intestinal mucosa immunity of broilers by regulating immune-related signaling pathways (TLRs). Lycium barbarum polysaccharides were also reported to affect the TLRs-mediated signaling pathway, thereby improving the immune function and alleviating liver injury induced by carbon tetrachloride in mice (32). Also, Liu et al. (33) suggested that the Astragalus polysaccharides could enhance the immune function of mice by modulating TLRs/NF-κB signaling pathway. Li et al. (34) reported that the Astragalus polysaccharides exerted anti-inflammatory effects in LPS-infected Caco2 cells, also related to the TLRs-mediated immune signaling pathway. Similarly, Chen et al. (35) found that the natural polysaccharides (extracted from mulberry leaf) elevated the immunity by upregulating TLR7 levels in broilers.

Additionally, other genes are significantly enriched in biological processes related to cell and nucleic acid transcription regulation and macromolecular biosynthesis. These genes can activate or increase the frequency of RNA biosynthetic and nucleic acid-templated transcription (36). Moreover, it can improve the chemical reactions and pathways of macromolecules and the frequency of the RNA biosynthesis process. It is possible to promote RNA biosynthesis, accelerate the process of RNA transcription and metabolism and then through the positive regulation of macromolecular biosynthesis of breast muscle (37), thus promoting the development of breast muscle and increase the breast muscle yield in broilers. Meanwhile, the KEGG enrichment analysis results showed that the DEGs are enriched in signaling pathways related to viral infectious diseases and cell adhesion molecules. Cell adhesion molecules play an essential role in cell growth, development and differentiation, maintenance of normal tissue structure, inflammatory response, and immune response (38, 39). These immunity and cell adhesion-related signaling pathways may activate innate immunity and promote muscle cell development, thereby improving the muscle growth of broilers. In addition to the immunity and cell adhesion-related signaling pathways, it is worth noting that the Lipin1, Sestrin1 (SESN1) and fibroblast growth factor receptor 2 (FGFR2) genes of the DEGs are associated with protein synthesis and lipid metabolic process, which also contribute to the muscle growth. As known, the Lipin1 gene has an important regulatory role in lipolysis and reducing fat accumulation (40). The regulation of Lipin1 gene expression in lipid metabolism is accompanied by alteration of the protein synthesis process (41). Recently, Li et al. (41) confirmed that higher Lipin1 gene expression is beneficial to promote muscle development of broiler chickens. The SESN1 gene encodes Sestrin protein required for normal lifespan and its function in muscle cells to prevent muscle degeneration over a lifetime (42). A previous study reported that the SESN1 gene is involved in muscle development in chickens (43). Furthermore, the FGFR2-mediated cell proliferation and differentiation processes also play a crucial role in the regulation of muscle development, and the function of FGFRs in myogenesis and reduction of lipid deposition has been investigated both in vitro and in vivo (44). It has been suggested that FGF is a strong inhibitor of cell differentiation (45). The present study's findings showed that the inclusion of dietary EP improved the breast muscle yield which was related to the down-regulation of FGFR2 gene expression. Similar to our observations, Zheng et al. (45) found that the expression of FGFR2 negatively correlated with the muscle growth and development in broilers. Cui et al. (46) demonstrated that FGF7 and FGFR1 genes had down-regulation effects on breast muscle weight of broiler chickens. Therefore, in this study, dietary EP supplementation upregulated the expression of Lipin1 and SESN1 genes. In contrast, down-regulated expression of the FGFR2 gene might result in higher protein synthesis and lower lipid deposition, thus promoting muscle development. However, further verification studies are necessary to confirm these propositions.

Conclusions

The results of this study suggest that the dietary supplementation of Enteromorpha polysaccharides at 7,000 mg/kg could promote the breast muscle yield of broilers. Further, the RNA-Seq analysis results showed that the differentially expressed genes were mainly enriched in immune-related signaling pathways, macromolecule biosynthetic, DNA-templated, RNA biosynthetic, protein synthesis, and lipid metabolic processes of broilers. Thus, the findings of the present study provided new insights for the dietary application of Enteromorpha polysaccharides as growth promoters and immune stimulants in broiler chickens.

Data Availability Statement

The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found here: https://www.ncbi.nlm.nih.gov/sra/PRJNA701498, PRJNA701498.

Ethics Statement

The animal study was reviewed and approved by Animal Care Committee, Guangdong Ocean University.

Author Contributions

W-CL, RJ, and BB: conceptualization, writing-review and editing. YZ and YG: analysis. YZ, S-JQ, and YG: data curation. YZ: writing-original draft preparation. W-CL and RJ: supervision. W-CL: project administration, methodology, and funding acquisition. All authors contributed to the article and approved the submitted version.

Funding

The present study was funded by the National Nature Science Foundation of China (32002196), Natural Science Foundation of Guangdong Province (2018A030307023), Talent Research Start-up Project of Guangdong Ocean University (R18007), South China Sea Scholar of Guangdong Ocean University (573118025), Innovative Strong School Engineering Youth Talent Project (2017KQNCX090) of Department of Education in Guangdong Province.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fvets.2021.663988/full#supplementary-material

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