1. Background
Fusarium mycotoxins are secondary metabolites produced by fungi in the genus
Fusarium, which often occur as contaminants of corn and other grains that are used as a main source of feed for livestock and poultry [
1]. Among these, zearalenone (ZEA) is the most common
Fusarium toxin detected in corn–soybean meal diets that are used extensively for swine production, and has been reported to cause substantial economic losses to the pig industry every year [
2]. Its primary toxic effects on animals include damage to the reproductive organs and a reduction in reproductive capacity [
3,
4], oxidative stress [
5], endocrine disorders, cytotoxicity [
6], and immunotoxicity [
7]. ZEA can be converted to a range of different metabolites in animals, which affect the digestion and absorption of nutrients and reduce production performance, and swine appear to be particularly sensitive to this toxin.
Previous studies have concluded that the intestinal tract is the target organ of ZEA and that the toxin leads to pathological intestinal damage [
8]. It has been reported that ZEA may disrupt the activity of antioxidant enzymes through oxidative stress, thereby reducing the growth performance of animals [
3]. In addition, ZEA can also disrupt the activity of digestive enzymes, thus hindering the processes of digestion and absorption. Currently, however, there is little information available regarding the changes of disaccharidase activity in the small intestine of piglets attributable to ZEA, and the underlying mechanisms remain to be elucidated.
Previous toxicity studies have indicated that at concentrations of 2.5 and 40 μm, ZEA reduced the survival of jejunal epithelial cells in piglets [
9]. Furthermore, a study found that ZEA had adverse effects on the development of early porcine blastocysts [
10], which is consistent with the observations of Kouadio et al. [
11], who demonstrated that ZEA can cause lipid peroxidation and lead to cell death. Heat shock protein 70 (Hsp70) is a ubiquitous member of the heat shock protein family found in most types of animal cells, and has been found to play range of different physiological roles, such as enhancing immune function and as an antioxidant [
12]. Notably, it was found that Hsp70 may play a key role in defense against cellular oxidative stress induced by ZEA [
13]. Different stress can damage the gastrointestinal membrane of piglets and induce the expression of Hsp70. Previous study has also shown that overexpression of Hsp70 can reduce the damage of jejunum mucosa of weaned piglets induced by lipopolysaccharide [
14]. However, the Hsp70 expression and its location in the small intestine of piglet need to be further explored.
The European Commission has limited the ZEA concentration in piglet diets to 0.1 mg/kg [
15], while in China, the maximum ZEA in piglet diets is 0.15 mg/kg [
16]. However, a five-year investigation carried out by our team showed that the positive detection rate of ZEA was 69.15%, and the average value of ZEA was 0.97 mg/kg [
17]. Given that contamination of cereal feed with ZEA is an extremely common phenomenon, it is highly desirable to characterize the effects of this toxin and identify the underlying mechanisms. Therefore, in this study, we sought to examine the effects of 1.04 mg/kg ZEA on the growth performance of weaned gilts, as well as disaccharidase activity, antioxidative activity, and Hsp70 expression in the small intestine of these animals, thereby providing a scientific basis for guidance on the production of healthy pigs.
2. Materials and Methods
2.1. ZEA-Contaminated Diet and Mycotoxin Determination
The purified ZEA was dissolved in ethyl acetate and sprayed on talcum powder. ZEA premix (1000 mg/kg) was prepared, and the mixture was put into the fume hood for 12 h. The purpose was to evaporate the residual ethyl acetate. The 10 mg/kg ZEA corn premix was obtained by diluting ZEA premix (1000 mg/kg) with corn flour without toxins. Based on the above premix, 1.0 mg/kg ZEA feed was prepared. Before the implementation, a covered container was prepared for storing the experimental feed. In this paper, the amount of ZEA was based on the research results of other researchers such as Jiang et al. [
3], Chen et al. [
18], and Dai et al. [
4]. The nutritional components were analyzed at the beginning and after the experiment. Qingdao entry exit inspection and Quarantine Bureau was entrusted for toxin analysis. Levels of ZEA and aflatoxin (AFL) were quantified using liquid chromatography in conjunction with fluorescence detection, affinity column chromatography, and the external standard method, whereas high-performance liquid chromatography tandem mass spectrometry with fluorescence detection, affinity column chromatography, and the external standard method were used to quantify the levels of fumonisin (FUM) and deoxynivalenol (DON) [
19,
20]. The minimum detection concentration is 1.0 μg/kg for AFL, 0.01 mg/kg for ZEA, 0.05 mg/kg for DON, and 0.1 mg/kg for FUM.
2.2. Experimental Design, Animals, and Management
The use and prevention of this study met the requirements of “guidelines for the care and use of laboratory animals”, which was proposed by the national standards and ethics committee of the people’s Republic of China, and the approval number is GB/T 35892-2018. Twenty 42-day-old healthy gilts (Duroc × Landrace × Large White), with an average body weight of 12.84 ± 0.26 kg, were randomly divided into two treatment groups. Based on NRC (2012), piglets were fed with basal diet supplemented with 0 (control) or 1.0 (ZEA1.0) mg/kg for 35 days, with 0 and 1.04 mg/kg as the analyzed ZEA concentrations. No other toxins were found in the diet of the two groups.
Table 1 shows the nutritional levels and composition of the basic diet. In the course of the experiment, the animals were raised in the Institute of Animal Nutrition, Shandong Agricultural University. When raising piglets, the environment was controlled. All piglets were placed in different metabolic cages (0.48 m
2). Each cage had a feeder and a nipple water dispenser. In the first 7 days of the test, the ambient temperature was controlled at 30 °C, and after 7 days, the temperature was controlled at 26 °C to 28 °C, and 65% was relative humidity. When raising piglets, we should vaccinate them regularly, do a good job in routine management, and provide them with sufficient drinking water. The piglets were fed at 7:00 a.m., 1:00 p.m., and 7:00 p.m. respectively according to the feed intake during the pre-test period. A small amount of leftover feed in the trough was ensured at 7:00 a.m. on the following day, and the leftover feed was collected and weighed before refeeding.
2.3. Growth Performance Determination
Piglets were weighed individually before the morning feeding on two consecutive days at the beginning (40 and 41-day-old) and end (76 and 77-day-old) of the 35-day feeding period to determine the average daily gain (ADG). The average daily feed intake (ADFI) of different sows can be determined, and the feed efficiency can be calculated according to ADFI and ADG.
2.4. Small Intestine Sample Collection
At the end of the test, piglets were fasted for 12 h and euthanized by electrocution (head only). The abdomen was opened and intestinal samples were taken no more than 15 min. The distal duodenum, middle jejunum, and middle ileum (5–6 cm) were quickly washed with ice phosphate buffered saline (PBS, pH 7.4) and transferred to a 10 mL Eppendorf tube at −80 °C for the further analyses of disaccharidase and antioxidant enzyme activities, gene expression, and western blotting. A fourth sample (3–5 cm) from each intestinal region was rapidly fixed in Bouin’s solution for 24 to 48 h and dehydrated in a graded alcohol series for immunohistochemical analysis.
2.5. Disaccharidase Activity
The tissue samples were thawed, rinsed with ice deionized water, dried with filter paper, homogenized with 0.02 mmol/L Tris-HCl (pH 7.4) at 1:10 (mg/mL), and centrifuged (10,000× g) at 4 °C for 15 min. The supernatant was analyzed for protein content and enzyme activities. Disaccharidase activity within each intestinal sample was examined via a glucose oxidase–peroxidase coupled assay (with sucrose, maltose, and lactose used as substrates for sucrase, maltase, and lactase, respectively) using a commercial kit A082 (Nanjing Jiancheng Bioengineering Institute, Nanjing, China). Total intestinal protein content was determined using the Coomassie Brilliant Blue using a commercial kit A045-2 (Nanjing Jiancheng Bioengineering Institute). Enzyme-coupled assays were performed in triplicate to account for inter-assay variation.
2.6. Antioxidant Activity and Malondialdehyde Content
Intestinal samples were prepared as described in the previous section. The activity of catalase (CAT), glutathione peroxidase (GSH-Px), superoxide dismutase (SOD), and contents of malondialdehyde (MDA) in collected supernatants were determined using respective assay kits (A007, A005, A001, A001, and A003, Nanjing Jiancheng Bioengineering Institute). The activity of CAT was estimated based on the levels of H
2O
2 remaining after enzyme catalysis and determined according to the method described by Góth [
21]. The activity of GSH-Px, which catalyzes glutathione oxidation from the reduced tripeptide glutathione (GSH), was determined using the method described by Maral et al. [
22]. The activity of superoxide dismutase (SOD) was determined by the method of Ōyanagui [
23]. Malondialdehyde (MDA) content was quantified using the thiobarbituric acid-reactive (TBA) method described by Placer et al. [
24].
2.7. Immunohistochemistry
The small intestinal tissue fixed in Bouin’s solution were trimmed, dehydrated by gradient alcohol, transparented by xylene, and then embedded in paraffin. The wax blocks were continuously sliced with a thickness of 5 μm. Six consecutive slices treated with polylysine were selected for Hsp70 immunohistochemical staining. In order to obtain the antigen, the tissue sections were pretreated with sodium citrate buffer. The buffer concentration was 0.01 mol/L, pH was 6.0, and the treatment time was 20 min. In order to block the nonspecific binding, 10% normal goat serum (zsgb-bio, Beijing, China) was used to culture. In order to block the endogenous peroxidase activity, 10% hydrogen peroxide (H2O2) was used for 1.5 h. Then, the polyclonal antibody Hsp70 (1:50, bm0368, BIOSS, Beijing, China) was incubated with sections at 4 °C for 12 h. The samples were tested for immunohistochemical analysis using tissue staining SP Kit (spn-9001, zsgb-bio, Beijing, China); polink-2 plus Polymer horseradish peroxidase (HRP) rabbit or mouse primary antibody detection system (pv-9002, zsgb-bio, Beijing, China). The sections were soaked in diaminobenzidine tetrachloride, and the DAB Kit (pa110, Tiangen, Beijing, China) was used, and the time was no more than 3 min. The distribution of positive cells should be dehydrated and sealed, and observed by microscope.
2.8. Integrated Optical Density Measurement
Heat shock protein 70 (Hsp70) labeling was examined using a Nikon ELIPSE 80i microscope (Nikon, Tokyo, Japan). For each specimen, stained sections (10 stained sections per treatment) were randomly selected and photographed. The number of Hsp70 antigen and staining was detected and the image was analyzed. The software was Image Pro Plus 6.0 image analysis software (media controls, Silver Spring, MD, USA). These yielded values of the total cross-sectional integrated optical density (IOD) and single villus IOD (SIOD) of Hsp70 in the duodenum, jejunum, and ileum of weaned gilts [
25] were used to compare the amounts of staining of samples obtained from control and ZEA-treated gilts.
2.9. Total RNA Extraction, cDNA Preparation, and Quantitative Real-Time Reverse Transcription-Polymerase Chain Reaction (qRT-PCR)
The small intestine sample was taken out from −80 °C and cut into 50–100 mg. The total RNA was extracted with Trizol Kit (Invitrogen, Carlsbad, CA, USA). The purity of RNA was detected at the absorbance ratio of 260/280 nm. The ds-11 ultraviolet spectrophotometer (denovix, Wilmington, DE, USA) was used. If the ratio was between 1.8 and 2.0, it showed that the RNA had high purity. The specific primers for Hsp70 gene were designed by searching the gene sequence of GenBank. The software was primer6.0, and the primer synthesis was undertaken by Bioengineering Co., Ltd (Shanghai, China). The reference gene transcript was
GAPDH Gene. The target gene was normally expressed by using this method. The primer sequences and lengths of the amplified product are shown in
Table 2. Reverse transcription was carried out immediately after the determination of mass and concentration, and was performed according to the instructions of a PrimerScript@ RT Master Mix Perfect Real Time kit (DDR036A: TaKaRa, Dalian, China). The reaction system (20 μL) was prepared according to the instructions of a SYBR
®Premix Ex TaqTM Tli RNaseH Plus quantitative fluorescence quantitative kit (RR420A; TaKaRa, Dalian, China). For each sample, target and internal reference genes were analyzed in triplicate. The internal reference gene and target gene were divided into three parts. ABI 7500 (Applied Biosystems, Foster City, CA, USA) was used for amplification under the following conditions: initial denaturation at 95 °C for 30 s, 95 °C for 43 cycles, lasting for 5 s, 60 °C for 34 s, 95 °C for 15 s, °C for 60 s. The fluorescence information was detected at 60 ℃, and the relative mRNA level was determined by 2
−△△CT method [
26].
2.10. Western Blotting
Small intestine total protein was extracted according to the instructions of a commercial kit (Beyotime, Shanghai, China), and concentrations were determined using a BCA protein determination kit (Beyotime, Shanghai, China). Having established the concentration of each sample, the concentration of aliquots was adjusted to 60 μg, and these samples were electrophoretically separated on polyacrylamide gels, and subsequently transferred to solid-phase transfer membranes (Solarbio, Beijing, China). The membranes were incubated in 10% skimmed milk powder for 2 h, washed 3 times with Tris-buffered saline containing Tween (TBST) after incubation, and then incubated again with primary antibodies [polyclonal mouse anti-Hsp70, 1:300 (BIOSS); and monoclonal anti-actin, 1:1000 (Beyotime, Shanghai, China)], diluted with primary antibody dilution buffer (Beyotime, Shanghai, China), at 4 °C overnight. After washing with TBST, the membranes were incubated with anti-rabbit IgG and anti-mouse IgG antibodies (1:3000; Beyotime, Shanghai, China), and diluted with secondary antibody dilution buffer (Beyotime, Shanghai, China), at 37 °C for 2.5 h. Thereafter, the membranes were immersed in a high-sensitivity luminescence reagent (BeyoECL Plus; Beyotime, Shanghai, China), exposed to film using the FusionCapt Advance FX7 system (Beijing Oriental Science and Technology Development Co., Ltd., Beijing, China). The software for image analysis is IPP 6.0 (Media Cybernetics, Inc., Rockville, MD, USA).
2.11. Statistical Analysis
All data are expressed as the mean ± standard error (SE). To determine differences between groups, the data were evaluated to be normal distribution and variance homogeneity before t-test, and statistically analyzed using a two-sample pairwise t-test with SAS 9.2 statistical software (SAS Inst. Inc., Cary, NC, USA), with a p value < 0.05 being considered indicative of a significant difference.
4. Conclusions
Through this study, it can be clear that when the concentration meets the condition of 1.04 mg/kg, the expression of heat stress protein 70 and the content of malondialdehyde in duodenum, jejunum, and ileum of weaned piglets can be affected, and the intestinal tract of the body will be damaged and oxidative stress will occur. Therefore, it can be considered that ZEA can promote oxidative stress reaction. In order to further study the relationship between the two, more in vitro studies are needed to clarify the relationship between oxidative stress and intestinal injury in pigs.