1. Introduction
Tannic acid (TAN) is a natural polyphenolic compound found in plants, capable of forming stable complexes with dietary proteins through hydrogen bonding in the rumen’s optimal pH range of 6.0–7.0 [
1,
2]. This property allows TAN to protect vegetable proteins from degradation by rumen proteases. However, as tannin–protein complexes pass into the abomasum, the lower pH (2.5–3.5) dissociates these complexes, resulting in reduced protein degradation by rumen microbes [
3]. As a result, a larger amount of protein could pass through the rumen undigested and be subsequently digested and absorbed in the small intestine, improving dietary protein utilization [
2]. Additionally, TAN exhibited inhibitory effects on rumen microorganisms, including methane-producing bacteria, leading to reduced fiber digestibility and methane production [
1,
4,
5]. A meta-analysis conducted by Jayanegara et al. [
6] also concluded that increased TAN content in the diet correlated with decreased methane emissions. In vitro fermentation studies by Wisam et al. [
7] demonstrated that TAN addition had no effect on rumen fermentation pH, NH
3-N, acetic acid to propionic acid ratio, or total volatile fatty acids, but resulted in reduced methane production.
Due to its polyphenolic and flavonoid structure, TAN exhibits potential antioxidant activity [
8], as demonstrated by chemical and cellular antioxidant experiments [
9]. Anthocyanins, a type of TAN, have shown an oxygen radical absorbance capacity of approximately 4500 μmol Trolox equivalents/mmol (oxygen radical absorbance capacity), indicating that other types of TAN might possess similar effects [
10]. Furthermore, a previous study indicated that TAN could dose-dependently restore superoxide dismutase activity in thioacetamide-treated rats [
11]. Calis et al. [
12] also reported that TAN reduced malondialdehyde level in rat brain tissue homogenates and increased SOD activity in blood hemolysis, thereby alleviating oxidative stress in rats subjected to sodium glutamate monohydrate treatment. These findings suggest that TAN might have the potential to serve as an antioxidant additive in ruminant diets [
13].
Oxidative stress in beef cattle, mainly induced by factors such as diet composition [
14,
15], rearing environment [
16], and transportation [
17], might be experienced throughout their growth and development, which could highly impair the growth performance and meat quality of beef cattle [
14]. Current research on TAN in ruminants mainly focuses on methane (CH
4) emission [
5] and nitrogen utilization [
5,
18]. However, there is still a lack of clear understanding regarding the effects of TAN on the antioxidant capacity and health of beef cattle. Therefore, the purpose of this study was conducted to comprehensively investigate the effects of TAN on in vitro gas production, antioxidant, immune, and anti-inflammatory capabilities, and rumen fermentation of beef cattle through in vitro and in vivo experiments. The aim is to gain insight into the role of TAN in promoting performance in beef cattle and provide a scientific basis for its application in the diet.
2. Materials and Methods
The experiments were approved by the Animal Care and Use Committee of China Agricultural University (approval number AW71012022-1-3) and were carried out at the Beef Cattle Research Station of China Agricultural University in Beijing. The product (Silvafeed Bypro) used in this study was supplied by Silvateam S.p.a, Italy, and its composition included chestnut tannin extract and quebracho tannin extract.
2.1. In Vitro Culture Procedure
The in vitro fermentation was conducted following the method of Menke et al. [
19]. Fresh rumen fluid was collected 2 h before the morning feeding from 3 Angus cattle (460 ± 48 kg) with permanent rumen fistulas. The rumen fluid was then filtered through four layers of gauze and mixed with artificial saliva in a 1:2 volume ratio with CO
2 continuously introduced to maintain an anaerobic environment. Substrates (Formulation as
Table S1) with or without 0.15% TAN (dry matter basis, DM) weighing 220 mg were placed in 6 incubation tubes (D-89173, Haberle Labortechnik, Lonsee, Germany), with 3 replicates per treatment, 1 culture tube per replicate. A total of 30 mL of inoculum was injected into each tube using a Varispenser (Eppendorf AG, Hamburg, Germany). The incubation tubes were then quickly transferred into a water bath shaker (Jie Cheng Experimental Apparatus, Shanghai, China) maintained at 39 °C. The cumulative gas production was manually recorded at 0, 2, 4, 6, 8, 10, 12, 18, 24, 30, 36, 42, 48, 60, 72, 84, and 96 h during the incubation. Three gas samples were collected from each tube after incubating for 96 h, and the CH
4 and CO
2 production in each injection was determined by gas chromatography (TP-2060F, Beijing Beifen Tianpu Analytical Instrument Co., Ltd., Beijing, China). Fermentation fluid was sampled from each tube and then centrifuged at 8000×
g for 15 min at 4 °C, and the supernatant was put into 2.0 mL sterilized cryopreservation tubes (NEST Biotechnology Co., Ltd., Wuxi, China) and quickly stored in liquid nitrogen for subsequent sequencing microbial composition analysis.
2.2. Animals, Design and Management
A total of 19 beef cattle (550 ± 27.5 kg) aged 19 to 20 months were randomly divided into 2 treatments, with 10 replicates in the control group (CON, basal diet) and 9 replicates in the TAN group (the basal diet supplemented with TAN at 0.20% DM), replicate with 1 cattle and raised individually. The period lasted for 65 d, conducted in the last 2 months of fattening of cattle until the slaughter, divided into the early stage (d 0–31) and the late stage (d 31–65). The basal diet for the experiment was shown in
Table 1. The method of adding TAN to the diet was based on previous studies [
1,
13]. Briefly, TAN substituted for corn in the basal diet and was provided in powdered form. Initially, TAN was pre-mixed with cornmeal, then mixed using a feed mixer (Tiejia Agricultural Machinery Co., Ltd.; Dezhou, China), and the diets were fed twice a day, at 7:00 and 15:00, respectively, as the form of total mixed rations (TMR). The remaining feed from the previous day was removed at 6:30. During the experiment period, the beef cattle were ensured ad libitum feeding.
2.3. Sample Collecion
At the beginning, midpoint, and termination of the experiment, the individual weights of the cattle were measured for three consecutive mornings before feeding, from which the ADG was subsequently calculated. Cattle (n = 5) with body weights close to the mean in each group were selected for further study analysis of nutrient digestibility, blood, rumen fluid, and meat samples.
TMR and fresh fecal samples (300 g each) from each treatment group were collected over three consecutive days at the end of the experiment. These samples were amalgamated, and a 300 g subsample was taken for drying—the subsample was dried at 55 °C for 72 h and subsequently ground to a 2 mm size using a Wiley mill (Arthur H. Thomas Co., Philadelphia, PA, USA). This ground sample was then set aside in the refrigerator at 4 °C for further nutritional analysis.
Approximately 5 mL of blood was collected from the cattle via the tail vein using heparinized tubes before morning feeding on d 66. The collected blood samples were immediately centrifuged at 3000× g for 15 min at 4 °C to obtain serum and then stored in a −80 °C refrigerator. The samples of ruminal fluid were also collected 3 h after morning feeding on d 66 by aspiration using an esophagogastric tube. During rumen fluid extraction, the initial 200 mL was discarded. The remaining fluid was then filtered through four layers of sterile gauze. Subsequently, this filtered rumen fluid was aliquoted into three 2.0 mL sterile storage tubes (NEST Biotech Co. Ltd., Wuxi, China) and was cryopreserved in liquid nitrogen for future analysis. On the 67th day, the cattle were transported to a commercial slaughterhouse for humane slaughtering. Pertinent data including pre-slaughter weight, hot carcass weight, net meat weight, and bone weight were documented. Concurrently, samples were extracted from the longest dorsal muscle for meat quality assessment. Post-slaughter, liver tissue samples were promptly harvested from the median lobe, minced, and stored in 2.00 mL sterile storage tubes (manufacturer: Naisite Biotech Co. Ltd., Nanjing, China). These samples were then rapidly immersed in liquid nitrogen in preparation for subsequent sequencing analysis.
2.4. Chemical Analysis
2.4.1. Nutrient Digestibility
Comprehensive evaluations were performed on the principal nutritional components within the TMR and fecal samples. By employing the methods stipulated by AOAC [
20], the contents of dry matter (DM), crude ash (Ash), crude protein (CP), and ether extract (EE) were quantified. The content of organic matter (OM) was derived by subtracting the ash content from the total. The levels of neutral detergent fiber (NDF) and acid detergent fiber (ADF) were determined in accordance with the methodologies presented by Van Soest et al. [
20]. For the assessment of nutrient digestibility, the acid-insoluble ash method introduced by VanKeulen and Young [
21] was adopted. The formula for this measurement was:
In this equation, Ad (g/kg) and Af (g/kg) denote the acid-insoluble ash content in the feed and feces, respectively, while Nd (g/kg) and Nf (g/kg) correspond to the nutrient contents in the feed and feces, respectively.
2.4.2. Serum and Liver Biochemical Indicators
Serum and liver biochemical indicators, including total antioxidant capacity (T-AOC), superoxide dismutase (SOD), malondialdehyde (MDA), glucose (Glu), insulin (INS), total cholesterol (TC), triglyceride (TG), total protein (TP), albumin (ALB), and blood urea nitrogen (BUN) were analyzed using the commercial kits according to the instructions (Nanjing Jiancheng Bioengineering Research Institute, Nanjing, China) by a CLS880 fully automatic biochemical analyzer (Zecen Biotech, Taizhou, China). Serum and liver immunoglobulin A (IgA), immunoglobulin G (IgG), tumor necrosis factor-α (TNF-α), interleukin-10 (IL-10), heat shock protein 70 (HSP-70), and insulin-like growth factor-1 (IGF-1) were quantified using the method of enzyme-linked immunosorbent assay, which was performed following the instructions provided with the kit (Jiangsu Enzyme Industrial Co., Ltd., Taizhou, China).
2.4.3. Rumen Fermentation Parameters
The concentration of ammonia nitrogen was determined following the method delineated by Broderick and Kang [
22], and the subsequent quantification was carried out using a Shimadzu UV-1700 spectrophotometer (Shimadzu Corporation, Kyoto, Japan). The volatile fatty acids (VFA) were quantified utilizing a GC-8600 high-performance gas chromatograph (Beifen-Ruili Instrument Technology Co., Ltd., Beijing, China).
2.5. Meat Quality Analysis
The pH value was gauged 45 min post-slaughter using a Cyberscan pH310 pH meter (EUTECH, Singapore). Chromaticity values, including luminosity (L*), redness (a*), and yellowness (b*), were tested using a chromameter manufactured by Shanghai Precision Scientific Instrument Co., Shanghai, China. Each sample underwent triplicate measurements at a consistent site to ascertain an average value. Uniformly shaped samples of the longissimus dorsi were vacuum-sealed, minimizing meat–bag wall contact, and subsequently suspended in a refrigeration setting at 4 °C for 24 h. Drip loss was calculated based on the subsequent formula:
2.6. Rumen Microbiota Analysis
DNA extraction and PCR amplification: Total DNA of bacteria and methanogens was extracted using the E.Z.N.A.® Soil DNA Kit (Omega Bio-tek, Norcross, GA, USA) and its quality confirmed by 1% agarose gel electrophoresis. PCR amplification of the 16S rRNA gene was performed using primers 338F (5′-ACTCCTACGGGAGGCAGCAG-3′) and 806R (5′-GGACTACHVGGGTWTCTAAT-3′) or MLfF (5′-GGTGGTGTMGGATTCACACARTAYGCWACAGC-3′) and MLrR (5′-TTCATTGCRTAGTTWGGRTAGTT-3′) for bacteria and methanogens, respectively. The amplification procedure consisted of an initial denaturation at 95 °C for 3 min, followed by 27 cycles of denaturation at 95 °C for 30 s, annealing at 55 °C for 30 s, extension at 72 °C for 30 s, and a final extension at 72 °C for 10 min. The PCR reaction was carried out using an ABI GeneAmp® 9700 thermal cycler.
Illumina Miseq sequencing and data process: PCR products from the same sample were pooled, purified, and quantified. Library construction was carried out using the NEXTFLEX Rapid DNA-Seq Kit, including adapter linking, screening for self-ligated fragments, PCR amplification, and magnetic bead recovery. Sequencing was performed on the Illumina Miseq PE300/NovaSeq PE250 platform (Shanghai Meiji Biomedical Technology Co., Ltd., Shanghai, China). Quality control and read merging were conducted using fastp [
23] (
https://github.com/OpenGene/fastp, accessed on 11 June 2023) and FLASH [
24] (
http://www.cbcb.umd.edu/software/flash, accessed on 15 June 2023) software. The sequences were clustered into operational taxonomic units (OTUs) based on a similarity threshold of 97% [
25], and chimeric sequences were removed. The RDP classifier [
26] (
http://rdp.cme.msu.edu/, version 2.2, accessed on 20 June 2023) was employed for species classification annotation of each sequence, using the Silva 16S rRNA database (v138) with a comparison threshold set at 70%.
2.7. Statistical Analysis
Based on the formula proposed by Ørskov and McDonald [
27], the kinetic parameters of cumulative gas production were determined. The equation utilized was: Y = X × (1 − e
−ct). In this context, Y signifies the gas volume (mL) produced per 0.2 g DM substrate at time t; X denotes the asymptotic gas production from 0.2 g DM substrate (mL); and c represents the hourly rate of gas generation.
The data except microbiota were organized and analyzed using the SAS 9.4 (SAS Institute Inc., Cary, NC, USA) through unpaired Student’s t-test. Utilizing the Kruskal–Wallis rank sum test, the Linear Discriminant Analysis Effect Size (LEfSe) was employed to assess variations in microbial community abundance within fecal samples. A significant distinction in effect size is denoted by an LDA score (threshold ≥ 2.50). A p < 0.05 was considered indicative of significant differences between treatments. Differences of 0.05 ≤ p ≤ 0.10 were considered a tendency.
4. Discussion
An interesting observation of the in vitro experiment was that the TAN led to opposite changes in the rate and asymptotic gas production. TAN decreased the gas production rate but increased the cumulative gas production. Similar to our findings, Getachew et al. [
28] found that adding TAN to alfalfa during a 72 h fermentation resulted in increased gas production and decreased rate, suggesting that rumen microbes could degrade TAN or be able to tolerate the effects of TAN. Conversely, Geerkens et al. [
29] found that the inclusion of 167 mg/g gallic acid, a form of TAN, hindered in vitro rumen fermentation and suppressed gas production over a brief 24 h incubation period. Those results suggest that the impact of TAN on fermentation might be influenced by the length of fermentation, substrate, and the type of TAN used. For example, Deshpande and Salunkhe [
30] reported that two types of TAN have different binding abilities to different types of starch. Our study also found that TAN tended to reduce methane production and suppressed the relative abundance of
Methanosphaera and
Methanobacteriaceae in the fermentation fluid. Numerous studies have demonstrated the methane-reducing effects of TAN in ruminants [
31,
32], which might be mainly due to the ability of TAN to inhibit methane production by binding to microbial cell proteins and enzymes, thereby inhibiting rumen methanogenic microorganisms.
Our study found that the addition of TAN in the diet improved the ADG of beef cattle. However, Tabke et al. [
33] had different results; they reported that although TAN (30 or 60 g DM/steer daily, which was calculated to be approximately 0.30% or 0.60% of DM intake) numerically increased the ADG and carcass weight of beef cattle, the difference was not significant. Cattle from the current study were intact males, whereas Tabke et al. [
33] fed castrated and implanted. Additionally, our experiment was relatively shorter (65 vs. 156 d) and started with a higher initial body weight (550 vs. 349 kg), which could also contribute to the differences between our study and Tabke et al. [
33]. Interestingly, another study conducted by Barajas et al. [
34] reported that the duration of TAN feeding also had different effects on the growth performance of beef cattle. They observed that feeding TAN for 100 d increased the ADG by 0.155 kg/d and resulted in a final carcass weight increase of 10.9 kg compared to the control group. However, when fed for 68 d, adding TAN in the diet led to a similar ADG but a reduction in DM intake by 0.62 kg/d, resulting in an increased feed conversion ratio by 0.015. Our results also found that the TAN group had an average increase of 10 kg in carcass weight per head and significantly improved dressing percent (+1.30%) and net meat percentage (+1.60%). The findings above indicate that the effects of dietary TAN on the growth and slaughter performance of beef cattle might be influenced by the duration and dosage of feeding and the growth stage of the cattle. Research has found that excessive dietary TAN could potentially reduce feed intake and even lead to toxicity in ruminants [
35]. However, the lack of dry matter intake data in our research posed certain constraints in elucidating the effect of TAN on the ADG of fattening cattle. Future studies should consider incorporating dry matter intake to provide a more comprehensive evaluation of the impact of TAN on the ADG of beef cattle. In our research, the observed absence of adverse effects of TAN on growth and slaughter performance might be attributed to the conservative TAN dosage used and the fact that we fed cattle in the later stage of fattening with larger body weights.
Nutrient digestibility is a primary indicator for measuring the feed efficiency and growth performance of beef cattle [
36]. Our research demonstrated that 0.20% of TAN in the diet did not affect the digestibility of CP and other nutrients of beef cattle, which was different from Yang et al. [
5], who found that adding 0.65%, 1.3%, and 2.6% TAN in diet reduced CP digestibility of beef cattle, and 2.6% TAN even reduced DM and OM digestibility. Similarly, Zhou et al. [
2] observed a decrease in DM, OM, and CP digestibility in beef cattle fed with 1.69% TAN. The decline in nutrient digestibility due to dietary TAN might be attributed to incomplete digestion and degradation of TAN-bound components, such as CP, minerals, and polysaccharides (cellulose, hemicellulose, pectin, starch) in the rumen [
29,
30]. However, a study conducted on sheep indicated that adding 1 and 2 g/kg of European chestnut extract (a hydrolysable form of TAN) to the diet had no effect on CP, OM, NDF, and ADF digestibility [
37]. Overall, the impact of TAN on digestibility might be influenced by the dosage of supplementation and feeding conditions. Further research into the relationship between TAN and dietary components might reveal greater potential for understanding the effects of TAN on nutrient digestibility in beef cattle.
MDA, a product of lipid peroxidation, is frequently employed as a marker for oxidative stress in ruminants [
38,
39]. In this study, we found that diet TAN reduced the content of liver MDA in beef cattle, indicating that TAN improved the endogenous antioxidant status of beef cattle. Our finding was consistent with the results reported by Liu et al. [
40], who found that adding chestnut tannins (10 g/kg, DM basis) in the diet reduced MDA concentrations in the plasma and liver of lactating cows, thereby improving the antioxidant status. Those results might be attributed to the ability of TAN to inhibit the formation of superoxide in the body and lipid peroxidation [
41]. The chemical structure of tannin, including the O-dihydroxy structure in the B ring and the galloyl groups, might be involved in the activity of inhibiting lipid peroxidation, suggesting that they are important determinants for radical scavenging and antioxidative potential [
42]. Previous studies have shown that supplementing TAN in the diet can enhance antioxidant capacity in the plasma or liver of dairy cows [
43] and goats [
44]. While past research has seldom reported on the ability of dietary TAN to mitigate lipid peroxidation in the liver of beef cattle, our study presents a novel finding in this regard. The potential of TAN to inhibit liver lipid peroxidation in beef cattle may be attributed to its gallic acid composition. This component can scavenge free radicals and bolster endogenous antioxidant defense mechanisms against them [
43].
Blood glucose levels are influenced by transient shifts in insulin and glucagon concentrations, which react to the body’s nutrient requirements and availability [
45,
46]. In our study, beef cattle from the TAN group exhibited elevated blood glucose levels, which was constant with the finding of Reynolds et al. [
47], indicating that diet TAN might influence the glucose metabolism of ruminants. Previous research has indicated that persimmon tannins can positively impact glucose metabolism in mice [
48]. Additionally, hydrolyzed tannin extracts at a concentration of 1 μg/mL notably enhanced glucose transport in a pig intestinal cell model [
49]. For ruminants, glucose is primarily sourced from propionate via gluconeogenesis in the liver [
42]. This implies that TAN might boost the absorption and use of propionate generated in the rumen, subsequently enhancing hepatic gluconeogenesis. However, since our study lacked feed intake data and other metrics pertinent to glucose metabolism, this hypothesis warrants further investigation in future research. Dietary TAN could be metabolized by microorganisms in the rumen, releasing phenolic compounds such as gallic acid, pyrogallol, and resorcinol [
50,
51], and excessive degradation products of TAN might exceed the detoxification capacity of the liver [
52], leading to symptoms of toxicity in ruminants [
53]. It is worth noting that the TAN added in our experiment had no adverse effects on the immune, inflammatory, and biochemical parameters (BUN, TC, TG, TP, and ALB) in the serum and liver of beef cattle. This might be attributed to the relatively low feeding dose of TAN used in our experiment, approximately 0.036 g/kg body weight, which was much lower than the maximum recommended dose (<0.40 g/kg body weight daily) by Murdiati et al. [
52].
The ruminal NH
3-N had no significant change in our study, indicating that dietary TAN had less effect on rumen protein degradation. Similarly, Liu et al. [
9] reported that adding 1.00% of chestnut tannin in the diet of Alcott sheep had no effect on ruminal NH
3-N concentration, but a significant reduction was observed when the supplementation level was increased to 3.00%. This indicated that the protein-binding capacities of TAN might vary with different dosages or sources. Consistent with our findings, Aboagye et al. [
54] reported that adding 0.25% and 1.50% chestnut tannin in the diet of beef cattle had no significant effect on the rumen T-VFA and the ratio of acetate to propionate. However, Pineiro-Vazquez et al. [
4] reported that adding 1.00%, 2.00%, 3.00%, and 4.00% quebracho tannin in diet increased propionate and decreased the acetate-to-propionate ratio of beef cattle. Compared to the current study, Pieiro-Vazquez et al. [
4] used heifers with an average weight of 295 kg, while our study used the beef cattle of the later finishing stage with an average weight of 550 kg. This difference in animal sex and growth stage might be the main reason for the observed discrepancies between the two studies. Moreover, our study indicates that incorporating TAN into the diet could potentially enhance the glucose metabolism capacity of beef cattle, which was substantiated by the elevated glucose concentrations observed in the serum of the TAN group. This heightened glucose metabolism might accelerate the absorption rate of propionate in the rumen [
49], potentially explaining why there was not a significant uptick in the propionate concentration within the TAN group.
Higher Sobs, Chao, and Ace indices were observed in the TAN group, indicating that the addition of TAN in the diet increased the ruminal microbial diversity of beef cattle. Higher diversity of microbiota was generally associated with greater contributions to the health of the host [
55], suggesting that the inclusion of TAN in the diet might help reduce the risk of diseases in beef cattle.
Prevotella was one of the most abundant microbial genera in the rumen and played a crucial role in the digestion and utilization of substances such as starch, hemicellulose, pectin, and protein [
56]. A study reported that feeding chestnut tannin-rich pine bark to sheep reduced the relative abundance of rumen
Prevotella [
57], which was also approved in the in vitro fermentation experiment [
58]. TAN exerted strong inhibitory effects on the abundance of
Prevotella, which might subsequently inhibit fiber degradation [
59]. Consistent with previous research, we also observed a significant decrease in the relative abundance of
Prevotella of the TAN group in both in vitro and in vivo experiments.
Succiniclasticum played an important role in generating propionate from succinate [
60], while
Ruminococcaceae was considered highly specialized in degrading complex plant materials into VFA [
61]. We observed an increase in the relative abundance of
Succiniclasticum and
Ruminococcaceae in response to TAN addition; however, the concentration of rumen VFA remained unaffected, which suggested that besides
Succiniclasticum and
Ruminococcaceae, other rumen bacteria might also play a crucial role in the formation of VFA. Nonetheless, dietary TA has been evidenced to instigate shifts in the rumen microbiota, exhibiting beneficial modulatory attributes [
62]. The interaction of TAN with ruminal microbes, culminating in a reduction of methane and ammonia production and biohydrogenation of lipids in the rumen, stands pivotal in enhancing the growth performance of ruminants [
1,
63,
64].