1. Introduction
The health condition of piglets is highly unstable at weaning because of the stress of changing feed form, separation from the mother sow, and changes in the physical environment [
1,
2,
3]. These stressors may cause dysbiosis due to sudden microbial changes in the intestine [
1,
4]. Postweaning intestinal microbiota dysbiosis is associated with some unstable situations including enteric infectious pathogens growth, leaky gut, and incomplete intestinal integrity [
4]. Besides, in hot seasons, weanling pigs are under the negative influence of high temperatures, which may enhance the adverse effects of weaning stress. The low recovery rate of heat-stressed weanling piglets is mainly due to the increased oxidative damage [
5]. These critical conditions impair the immune system function and intestinal mucosal development, making the piglets susceptible to oxidative stress and microbial infection.
Supplementation of pharmacological doses of ZnO (2500 mg/kg or over) in the piglet diet is a common practice among feed mills and farmers to control the adverse effects of postweaning diarrhea and increase growth performance. There is evidence that high doses of dietary ZnO controlled pathogen growth in the intestine [
6]. Besides, dietary supplementation with high doses of ZnO increases the absorption rate that can enhance the antioxidant status [
7]. However, feeding high doses of ZnO results in substantial quantities of Zn excretion, and causes environmental concerns [
6]. The use of pharmacological doses of ZnO will be banned in June 2022 in the European Union [
8], and much lower ZnO concentrations will be allowed to be used in order to reduce Zn excretion.
It is well documented that the infectious morbidity attenuates by
l-arginine (Arg) as an immune–nutrient factor [
9,
10]. The protective role of Arg is related to the intestinal mucosa integration and the increase in the recovery rate of the intestinal barrier [
9,
11]. The nutritional requirement of Arg is highly dependent on environmental and physiological conditions. Therefore, stressors such as microbial change, heat stress, and sepsis dramatically increase the Arg requirements [
10,
12,
13]. Arginine plays a crucial role in the production of polyamine and NO, which are strong anti-stress and vasodilator factors in mammals [
2]. In addition, Arg facilitates the provision of cellular signaling, intestinal recovery, and immunity factors [
10,
14]. Therefore, it can be hypothesized that the use of dietary Arg levels in higher doses than the recommended requirement may decrease the ZnO requirement during the stressful condition. Little information is available on the role of Arg and ZnO on oxidative damage of weanling piglets during a high ambient environment, in particular, that of immunity status, intestinal integrity, and growth performance. In this study, high dietary Arg (1.6% of the diet) and different levels of ZnO are applied to evaluate their effects on growth performance, immune status, intestinal microbiota, and morphology of pigs.
2. Material and Methods
The project underwent proper ethical standards and the experiments (KW-170519-1) were approved by the Institutional Animal Care and Use Committee of Kangwon National University, Chuncheon, Republic of Korea.
2.1. Animals and Experimental Design
A total of 180 weaned pigs (28-day-old; Landrace × Yorkshire × Duroc; initial body weight (BW): 10.45 ± 0.03 kg) of mixed sex were randomly allotted to six treatments with 6 replicate pens in each treatment and 5 pigs per pen. The dietary treatments were Con (1.1% Arg); P-Zn (1.1% Arg + 2500 mg Zn as ZnO/kg diet); ARG (1.6% Arg); ZnArg1 (500 mg of Zn as ZnO/kg diet + 1.6% Arg); ZnArg2 (1000 mg of Zn as ZnO/kg diet + 1.6% Arg); ZnArg3 (2500 mg of Zn as ZnO/kg diet + 1.6% Arg). All the piglets were clinically healthy at the beginning of the trial. All diets (
Table 1) met or exceeded the nutrient requirements according to the National Research Council (NRC) [
15] containing 19% crude protein, 0.85% calcium, 0.68% phosphorus, 1.2% SID (standardized ileal digestibility) Lys, 0.39% SID Met, and 0.73% SID Met + Cys. The treatment diets were fed in a meal form in 2 phases (day 0 to 7, phase Ⅰ; and day 8 to 14, phase Ⅱ). This experiment was conducted at the facility of Kangwon National University farm and the piglets were housed in slotted and concrete floor pens with a pen size of 1.90 m × 3.0 m. All pens were equipped with a self-feeder and nipple drinker to allow ad libitum access to feed and water. Individual weanling piglet weight and feed intake from each pen were recorded at the beginning and the end of every phase to determine average daily gain (ADG), average daily feed intake (ADFI), and gain to feed ratio (G:F). All pigs were subjected to a constant room temperature of 35 °C for 10 h (07:00–17:00). The average relative humidity of the room was in the range of 43% to 59%, which indicates temperature and humidity index between 83.4 and 86.6 at the heat stress period. The rectal temperature was measured at days 1, 7, and 14 of the experiment using a digital thermometer (MSR, Measure Technology Co., Ltd.; Taipei, Taiwan). The pigs were sacrificed by electrocution followed by exsanguination.
2.2. Chemical Analysis
Diet samples were analyzed in triplicate for crude protein (Method 990.03), calcium, and phosphorus (method 985.01), and ether extract (method 920.39), according to Association of Official Analytical Chemists [
16]. Gross energy of diets was measured by a bomb calorimeter (Model 1261, Parr Instrument Co., Moline, IL, USA). Amino acid composition of feed samples was analyzed by High Performance Liquid Chromatography (Waters 486, Waters Corp., Milford, MA, USA) after acid hydrolysis [
17]. The methionine and cysteine were determined following oxidation with performic acid [
18].
2.3. Microbial Analyses
To study the effects of dietary treatments on small intestinal microbiota, representative piglets from each group (2 piglets per replicate; one male and one female) reflecting the average BW of the pen were selected at days 7 and 14. The digesta from the ileum was collected in sterile plastic bottles for microbial analysis. The samples collected for microbial analysis were placed on ice and immediately sent to the laboratory for analysis. The ileal digesta samples (one gram) were mixed with 9 mL peptone broth (1%) and the homogenized (Becton, Dickinson and, Franklin Lakes, NJ, USA). In the next step, serially 10-fold dilutions in the pellets were used for Viable counts of bacteria. To determine the total anaerobic bacteria (Tryptic soy agar), Lactobacillus spp. (using MRS agar + 0.200 g/L NaN3 + 0.500 g/L l-cystine hydrochloride monohydrate), Bifidobacterium spp. (MRS-NPNL: MRS agar + nalidixic acid, paromomycin + neomycin sulphate + lithium chloride), Clostridium spp. (TSC agar) and coliforms (violet red bile agar) were used. The gas pack anaerobic system (BBL, No. 260678, Difco, Detroit, MI, USA) was used for preparing anaerobic conditions. The tryptic soy agar, MRS agar, and violet red bile agar were purchased from Difco Laboratories (Detroit, MI, USA), and TSC agar (CM0589) was purchased from Oxoid (Hampshire, UK). The bacterial concentrations were transformed (log) before statistical analysis.
2.4. Small Intestinal Morphology
The sacrificed pigs (two pigs per pen) were subjected to morphological tests at day 14. The intestinal morphology test was performed according to the procedure described by Hosseindoust et al. [
19]. Five-centimeter cross-sectional segments were taken from the duodenum (approximately 10 cm from the pylorus), jejunum (at 50% of the total intestinal length), and ileum (at 75% of the total intestinal length). In short, for each intestinal sample, three cross-sections were prepared after staining with azure A and eosin using standard paraffin-embedding procedures. A total of 10 intact, well-oriented crypt-villus units were selected in triplicate for each intestinal cross-section. The measurement of villus height was performed from the tip of the villi to the villus–crypt junction, while the crypt depth was defined as the depth of the invagination between adjacent villi, and villus width was measured till the mid of the villus. All morphological measurements (villus height and crypt depth) were performed in 10-μm increments using an image processing and analysis system (Optimus software version 6.5, Media Cybergenetics, North Reading, MA, USA).
2.5. RNA Extraction and Real-Time PCR of Organ Samples
The sacrificed pigs (two pigs per pen, one male and one female) were subjected to gene expression analysis at day 14. Total RNA was isolated from the Jejunum (50 mg; from the middle jejunum segment), liver (50 mg; from the liver left lateral lobe), and muscle (50 mg; from the longissimus dorsi muscle close to the fourth rib) samples using Trizol reagent (Invitrogen, Carlsbad, CA, USA) according to the manufacturer’s instruction. Extracted RNA was quantified to 1 μg/μL and cDNA synthesis was conducted using the Improm-II Reverse transcription system (Promega, Fitchburg, MA, USA) and PCR was performed using Mx3000P real-time PCR (Stratagen, Redmond, WA, USA). The results were expressed as a relative expression by using the delta-delta method. The primers of interleukin-4 (IL-4), interleukin-6 (IL-6), interferon-γ (IFNγ), heat shock protein-27 (HSP27), toll-like receptor-4 (TLR4), and tumor necrosis factor-α (TNF-α) were presented in
Table 2. In this process, β-actin was introduced to adjust the quantity of input cDNA to maintain the role in internal control [
20]. A total of 20 μL reaction system included 10 μL SYBR Premix Ex Taq, 0.8 μL of forward and reverse primer (10 μM), 0.4 μL ROX Reference Dye II (50×), 2.0 μL cDNA template, and 6 μL dd H
2O. Cycling conditions were as follows: 30 s at 95 °C, 40 cycles of denaturation step at 95 °C for 3 s, 60 °C annealing step for 34 s and a 72 °C extension step for 15 s.
2.6. Blood Parameters
The blood samples were collected from 2 piglets per pen on the last day of each phase. Five milliliters of ethylenediaminetetraacetic acid (EDTA) treated (Becton Dickinson, Franklin Lakes, NJ, USA) and not-treated blood samples were collected from the jugular vein and stored on ice for immediate hematological analysis. The EDTA-treated blood was diluted by Natt-Herrick solution and mixed for 15 min for white blood cells (WBC), red blood cells (RBC), lymphocytes, and monocytes analyses using Hemavet Multispecies Hematology Systems (Scientific Inc., Oxford, CT, USA). The rest of the blood samples were centrifuged at 1500 rpm for 20 min in a centrifuge, and plasma was separated and used for cortisol analysis. Cortisol was analyzed using an ELISA kit (ADI-900-70; Enzo Life Sciences, Farmingdale, NY, USA).
2.7. Statistical Analysis
The data were analyzed as a completely randomized design using the GLM procedure of SAS (version 9.4, 1996, SAS Inst. Inc., Cary, NC, USA). The initial body weight was used as a covariate for growth performance but was removed from the model when not significant. Each piglet was an experimental unit for growth performance, feed intake, microbial test, intestinal morphology, blood parameters, and gene expression analyses. The Tukey means comparison test was applied for treatment means separation by at p < 0.05 statistical level. Probability level of less than 0.1 was considered a tendency.
4. Discussion
The supplementation of pharmacological doses of ZnO is routinely considered in weaned pigs’ diets to alleviate diarrhea incidence and reduce growth depression during the weaning period [
6,
21]. In our study, the response to ADG and ADFI in pigs fed the ZnArg3 diet was increased relative to the pigs fed the Con diet, however, there were no differences between the ARG and ZnArg3 treatments. Compromising the growth performance in pigs fed the Con diet could be resulting from the insufficient nutrients intake, as shown by the significantly reduced ADFI in the Con treatment. The finding that supplementing 2500 mg/kg of Zn as ZnO showed no growth benefit compared with pigs fed 500 or 1000 mg/kg ZnO was in contrast to a previous study, which reported a significant difference between 2500 mg/kg ZnO and levels less than 1000 mg/kg [
22]. It is believed that the lower doses of ZnO (below 1000 mg/kg) are not effective in the performance of weaned pigs [
6,
23]. The literature shows that the pharmacological dose of ZnO (2500 mg/kg or above) increases ADG and ADFI due to controlling the population of
Escherichia coli,
clostridium, and incidence of diarrhea [
9,
24]. Pigs fed the ZnArg3 diet were less under stress due to the lower gene expression of HSP27, which can be responsible for higher ADFI. In addition, our results showed that the ADG and ADFI of pigs in ZnArg1 treatments were comparable with pigs in ZnArg3 treatment. It may be postulated that the positive anti-stress effects of dietary Arg may be responsible for insignificant differences between ZnArg3 and ZnArg1 treatments. Anti-stress effects of Arg may have a complementary role for the pharmacological dose of ZnO in case of decreasing stress, as Arg activates the production of nitric oxide and peroxynitrite [
25]. However, our results rejected the hypothesis of the direct effects of Arg in eliminating pathogens [
26] due to the lack of difference in the number of coliforms and clostridia in the ARG treatment, and only the pharmacological dose of ZnO (2500 mg/kg) showed a definite effect in controlling
Clostridium spp. The decreased villus height in pigs fed the Con diet may be another reason for the lower growth performance, which may be related to the anti-pathogenic properties of ZnO.
During weaning stress, the manipulation of microbial population in order to control opportunistic pathogens becomes a priority. Moreover, it is widely accepted that intestinal mucosal integrity is generally associated with gut microbiota. This interaction might be of importance when animals have to struggle with the change of diet form and facing a severe change in the microbial biomass and composition in the intestine. Although in the current study the absorption of Zn and the concentration of ZnO in the digesta were not studied, the microbiota composition in different phases was evaluated. A lower number of
Clostridium spp. was detected in pigs fed the ZnArg3 diet compared with pigs fed the Con diet, however, the lower ZnO supplementations (ZnArg1 and ZnArg2) did not show a significant effect on
Clostridium spp. colonization. Hosseindoust et al. [
24] and Liu et al. [
7] reported that the antimicrobial activity of ZnO against coliforms makes it an ideal candidate to control the microbiota, however, they did not report any change in the number of
Clostridium spp. In another study, the population of coliforms and
Clostridium spp. was linearly decreased in the ileum and colon of weaned pigs when the dose of ZnO increased from 500 mg/kg to 2500 mg/kg [
6]. It is reasonable to speculate that influences on the intestinal microbiota might not be modified by ZnO with lower doses than the pharmacological one. Additionally, the supplementation with 1.6% Arg did not modify the microbial population. This result disagrees with the report of Ren et al. [
27], who supplemented a high dose of Arg containing 0.93%
l-arginine gram into the diet of mice to manipulate the microbial change in favor of beneficial bacteria including
Lactobacillus spp. It is crucial to investigate which ratio of Arg and ZnO will influence the weaned pig’s microbiota and immune status.
In the present study, a severe decrease in villus height in the duodenum occurred in pigs fed the Con diet compared with pigs fed ZnArg1 and ZnArg3. Intriguingly, the villus height in the jejunum and ileum remained unchanged. Kim et al. [
6] reported a greater villus height in the duodenum and ileum of weaned pigs by the supplementation of a pharmacological dose of ZnO into the diet. The reduced villus crypt structure alteration including villus height and crypt depth, crypt hyperplasia, and generally intestinal structural injury occurs mostly during the weaning [
28]. The villus height was not improved in pigs fed ARG diet. The role of different doses of Arg on intestinal morphology should be further studied since the weaning time is the most critical period.
The mRNA expression levels of HSP27 in the livers were remarkably decreased in pigs fed P-Zn, ZnArg1, ZnArg2, and ZnArg3 diets compared with the Con treatment. The positive correlation between HSP expression and stress was previously reported in other studies [
2,
4,
13]. The low gene expression of HSP27 in the liver and a tendency for lower blood cortisol in the ZnArg2 and ZnArg3 treatments may indicate a lower stress level compared with the Con treatment. Arg is reported to be an anti-stress or immunomodulatory factor by the activation of ornithine decarboxylase and generating polyamines [
10]. In addition, to our knowledge, there is no report related to the influence of dietary Arg on the TLR gene expression in weanling pigs during heat stress. In this study, a high level (1.6% of diet) of dietary Arg increased the gene expression of TLR4 in the jejunum and liver. These findings may be explained by the result of a microbial test wherein dietary Arg showed significantly higher
Clostridium spp. population compared with ZnO-supplemented treatments in the small intestine. A lower number of
Clostridium spp. was detected in pigs fed the ZnArg3 diet compared with pigs fed the Con diet, which might have caused a decrease in TLR4 expression in the jejunum. The pathogenic microbes are recognized by the innate immune system through the stimulation of TLRs. The TLR4 is a type of pattern recognition receptors in epithelial cells that have been identified as the main pathway on the innate immune system for recognition of lipopolysaccharide (LPS), a component of the bacterial cell wall [
29]. The over-expression of the TLR signaling pathway may be responsible for the stress-induced suppression of the immune system. Interestingly, our result supports the hypothesis that cytokines production increases through TLR4 signaling among ZnO-supplemented treatments by increasing the gene expression of IL-4 in the jejunum and IL-4 and TNF-α in the liver. Dietary ZnO beneficially affected the bacterial communities and mRNA expression of inflammatory cytokines and TLR4.
A large body of evidence has shown the upregulation of pro-inflammatory cytokine gene expression within a short time of weaning [
28,
30,
31]. In the present study, the expression of TNF-α was decreased in the jejunum of pigs fed P-Zn, ZnArg1, ZnArg2, and ZnArg3 diets. Intestinal inflammation occurs in pigs after weaning [
23]. The high inflammation induces an elevated specific secretion of cytokines from intestinal lymphocytes [
32]. The current study showed a lower expression of IL-4 in the jejunum and a lower count of lymphocytes in pigs fed ZnArg1, ZnArg2, and ZnArg3 diets. IL-4 is known as a B lymphocyte growth promoter and can linearly modulate the production and development of B and T lymphocytes [
33]. In contrast, Han et al. [
10] reported that the content of IL-2 and IFNγ in the serum was increased in cyclophosphamide-challenged weaned piglets. The over-production of TNF-α and IL-6 compromise the intestinal epithelial permeability, resulting in increased pathologic opening in the tight junction [
22]. The extra-cellular pathogens, such as intestinal microbes, secrete IL-4, IL-10, and IL-13 to activate the immune system and produce strong antibody-mediated responses [
34]. In agreement, it has long been known that the IL-6 concentration increases in stressful conditions and during acute inflammation [
35]. The increased gene expressions of TNF-α, IL-6, and IFNγ were noticed in salmonella-challenged pigs [
36]. It has been reported that lactic acid bacteria downregulate the gene expression of inflammatory cytokines [
37]. In addition, the higher number of eosinophils in pigs fed the Con diet may be responsible for higher gene expression of cytokines. It has been reported that the eosinophils increase the gene expression of IL-1, IL-4, IL-6, and TNF-α [
38]. As the increase in pro-inflammatory cytokines adversely affects the development of intestinal epithelium, controlling the concentration of intestinal inflammatory cytokines and intestinal integrity is crucial to alleviate intestinal disorders at the weaning time.