Stress, Nutrition, and Intestinal Immune Responses in Pigs — A Review

Article information

Asian-Australas J Anim Sci. 2016;29(8):1075-1082

Publication date (electronic) : 2016 May 12

doi : https://doi.org/10.5713/ajas.16.0118

In Kyu Lee ¹, Yoon Chul Kye ¹, Girak Kim ¹, Han Wool Kim ¹, Min Jeong Gu ¹, Johnny Umboh ², Kartini Maaruf ², Sung Woo Kim ³^,, Cheol-Heui Yun ¹^,⁴^,⁵^,

¹Department of Agricultural Biotechnology and Research Institute of Agriculture and Life Sciences, Seoul National University, Seoul 08826, Korea

²Faculty of Animal Science, Sam Ratulangi University, Manado Jl Kampus Selatan, Manado 95115, Indonesia

³Department of Animal Science, North Carolina State University, Raleigh NC 27695, USA

⁴Institutes of Green Bio Science and Technology, Seoul National University, Pyeongchang 25354, Korea

⁵Biomodulation major and Center for Food and Bioconvergence, Seoul National University, Seoul 08826, Korea

^*Corresponding Authors: Sung Woo Kim. Tel: +1-919-513-1494, Fax: +1-919-515-6884, E-mail: sungwoo_kim@ncsu.edu/Cheol-Heui Yun. Tel: +82-2-880-4802, Fax: +82-2-873-2271, E-mail: cyun@snu.ac.kr

Received 2016 February 14; Revised 2016 March 29; Accepted 2016 April 22.

Abstract

Modern livestock production became highly intensive and large scaled to increase production efficiency. This production environment could add stressors affecting the health and growth of animals. Major stressors can include environment (air quality and temperature), nutrition, and infection. These stressors can reduce growth performance and alter immune systems at systemic and local levels including the gastrointestinal tract. Heat stress increases the permeability, oxidative stress, and inflammatory responses in the gut. Nutritional stress from fasting, antinutritional compounds, and toxins induces the leakage and destruction of the tight junction proteins in the gut. Fasting is shown to suppress pro-inflammatory cytokines, whereas deoxynivalenol increases the recruitment of intestinal pro-inflammatory cytokines and the level of lymphocytes in the gut. Pathogenic and viral infections such as Enterotoxigenic E. coli (ETEC) and porcine epidemic diarrhea virus can lead to loosening the intestinal epithelial barrier. On the other hand, supplementation of Lactobacillus or Saccharaomyces reduced infectious stress by ETEC. It was noted that major stressors altered the permeability of intestinal barriers and profiles of genes and proteins of pro-inflammatory cytokines and chemokines in mucosal system in pigs. However, it is not sufficient to fully explain the mechanism of the gut immune system in pigs under stress conditions. Correlation and interaction of gut and systemic immune system under major stressors should be better defined to overcome aforementioned obstacles.

Keywords: Nutrition; Stress; Gut Immunity; Pigs

INTRODUCTION

Intestinal mucosa acts primarily as a barrier between inner part of the body and external environment. In livestock animals and humans, large quantities of various food antigens digested and absorbed are immunologically tolerable in general at intestinal mucosa. Morphology and characteristics of intestinal mucosa together with intestinal immune cells are constantly changing dependent on the food composition. A large number of pathogens, entering the body through the intestinal mucosa, are rapidly eliminated by protective mucosal immune responses. Otherwise, the intestine is normally home to many different commensal bacteria, continuously exposed to food proteins. As a result, the intestinal immune system must be able to discriminate harmless antigens from harmful ones (Wilson et al., 1996).

Status of porcine intestinal immune system is immature at birth, which develops further during perinatal period and then reaches to adult values between 5 and 7 weeks of life. Gut epithelial cells communicate with intestinal innate immune system, forming a functional barrier to antigens from diet and pathogens. Toll-like receptors (TLRs) are emerging as a functionally important class of membrane and cytosolic receptors with key roles in recognition of pathogens for innate immune modulation. Induction of adaptive immune responses begins with processing and presentation of antigen by specialized antigen presenting cells (Lee et al., 2014), in the organized tissues of the Peyer’s patches or mesenteric lymph nodes in the intestine (Gebert et al., 1996). One of the most important parts of adaptive intestinal immunity would be IgA responses, which require interactions between T and B lymphocytes (Cheon et al., 2014) within gut-associated lymphoid tissues.

Livestock are exposed to various stressors including diet, temperature, weaning and infection. Abrupt changes of these stress factors influence animal health negatively, resulting in lower productivity. Such stressors often challenge homeostasis of animals by inducing systemic or local inflammatory responses coincident with neuro-endocrine alteration. Considering the fact that gastrointestinal tract is tightly controlled by a reciprocal circuit composed of the immune system and neuro-endocrine system (Kayama and Takeda, 2012; Hayes et al., 2014), reducing stress would significantly improve gut homeostatic balance of livestock.

Gut immunity is surely one of the most crucial factors in domestic animals that is largely responsible for growth performance and host health. This article will discuss the impacts of stress on gut health and immune status of pigs.

GUT IMMUNITY IN PIGS UNDER VARIOUS STRESSORS

Heat stress

Climate change caused by global warming has forced high ambient temperatures in not only tropical regions, but also temperate regions. Heat stress (HS), therefore, is becoming a critical stress factor for health in the swine industry (Upadhyay, 2011). HS has affected an economic loss over 300 million USD per year in USA, and billions of dollars on a global scale (St-Pierre et al., 2003). It is, therefore, important to understand how HS is involving animal growth performance and health status in respect to nutritional and immune correlation, respectively.

It has been shown that destruction of tight junction (TJ) proteins, such as claudin 1/3 and occludin, caused an increase of the permeability of porcine gut epithelial cells (Gu et al., 2014). Interestingly, however, HS induced increase of the gut permeability without changing the expression of the TJ proteins while there was up-regulation of GLUT-2 (Pearce et al., 2013). It is to note that activation of SGLT 1, NA⁺ and glucose co-transporter causes an increase in the permeability (Turner et al., 1997). Thus, the expression change of glucose transporter on epithelial cells in porcine by HS is directly associated with the permeability. Although, HS increased the permeability and the concentration of endotoxins in blood was increased over three times, inflammatory cytokines, such as interleukin (IL)-1β, IL-8 and tumor necrosis factor (TNF)-α, were not up-regulated (Pearce et al., 2013). Since it is well established that endotoxin (lipopolysaccharide, LPS) is strong inducer of the inflammatory cytokines this study left scope for discovering how this occurs. It is probable that either HS caused immune suppression in the animal (Meng et al., 2013) or LPS was not as high as it appeared due to i) a technical error, ii) structural differences (Trent et al., 2006), iii) differential composition (Im et al., 2015; Lam et al., 2011) or iv) binding proteins of LPS (Lam et al., 2011; Im et al., 2015). It could well be that HS together with LPS does not induce all pro-inflammatory cytokines and perhaps are linked with specific cytokines such as IL-17 and/or transforming growth factor-β (TGF-β) which are in relation with regulatory T (Treg) and Th17 T cells. For example, the colonization of probiotics, such as Lactobacillus rhamnosus strain GG and Bifidobacterium lactis Bb12, in gnotobiotic pigs impacted to stable the balance of TGF-β and IL-17 after rotavirus challenge (Chattha et al., 2013). It has been also suggested that heat shock protein 70 (Pearce et al., 2014) and myeloperoxidase activity as the activation marker of neutrophils (Pearce et al., 2013) were increased under HS in porcine gut. This indirectly suggests that unlike the previous report by the same group, HS induces the inflammatory responses in intestine of pigs.

Taken together, HS induces alteration of barrier function coincident with gut inflammation in pigs. It appears that the influence of HS together with the solution to overcome the effects of HS on pigs’ immune system in relation to systemic and local inflammation should be further investigated.

Nutritional stress

Growth performance is the most critical factor for producers in the pig industry. Therefore, nutritional stress would be the greatest, if not the only, concern for them (Shen et al., 2014; Zhao et al., 2014). In general, fasting negatively impacts porcine gut health in terms of physiology and immunology. Deprivation of feed and/or water for 24 hrs raised the level of cortisol in blood, and suppressed TNF-α expression in jejunum of weaned pigs. Interestingly, there were no disruption of the TJ proteins, including claudin-1, occludin and zonula occludens protein-1 (ZO-1) in jejunum and ileum (Horn et al., 2014). Lacking glycine reduced the cell proliferation and protein synthesis, while apoptosis was increased in porcine gut epithelial cells. Coincidently, activation of both Akt and mammalian target of rapamycin (m-TOR) was reduced (Wang et al., 2014).

Mycotoxin is one of the major factors to contaminate animal feed causing nutritional stress (Weaver et al., 2014a). Deoxynivalenol (DON) disrupted the expression of the TJ proteins such as ZO-1, occludin and claudin-3, and permeability of porcine gut epithelial cells within 48 hrs (Gu et al., 2014; 2016). DON stimulated pro-inflammatory cytokines like TNF-α, IL-6, and IL-1β expression in jejunum and ileum (Bracarense et al., 2012) and increased the number of lymphocytes (Wu et al., 2015). It is apparent that TLR2 ligand can prevent the damage of porcine gut epithelial cells treated with DON (Gu et al., 2016). Fumonisin B1 (FB1) increased the permeability in porcine jejunum at over 10 days post stimulation (Bouhet et al., 2004) whilst DON took only 2 days to reach the similar level of the permeability (Gu et al., 2014). FB1 appeared to down-regulate the expression of IL-8 without changing other inflammatory cytokines, IL-6, IL-1β, IL-12p40, and TNF-α (Bouhet et al., 2006). It is likely that FB1 has relatively weak immunological effects on porcine gut epithelial cells when compared to those of DON. Chronic feeding with the combination of aflatoxin and DON for 33 to 42 days increased the number of monocytes and white blood cells coincident with high concentration of TNF-α in blood while a single treatment did not show such an impact (Chaytor et al., 2011; Weaver et al., 2013). It was noted that a combination of DON and zearalenone feeding for a long time increased twice the level of 8-hydroxy-deoxyguanosine indicating oxidative stress, together with DNA oxidative damage (Weaver et al., 2014b). For inflammatory cytokines including IL-12/IL-23p40 and IL-1β, and vasoactive intestinal peptides were increased in ileum Peyer’s patches after 42 days feeding of zearalenone (0.1 mg/kg) to pigs (Obremski et al., 2015a). While feeding of zearalenone (0.1 mg/kg) to pigs for 28 days induced a reduction of CD21⁺ B cells while increasing interferon (IFN)-γ concentration in ileocecal lymph nodes (Obremski et al., 2015b) suggesting that it may alter B cell responses. In addition, T-2 toxin reduced viability of intestinal epithelial cells in pigs infected with Salmonella Typhimurium. Although T-2 toxin did not alter the integrity of porcine gut epithelial cells, it increased translocation of bacteria (Verbrugghe et al., 2012). Chronic exposure of T-2 toxin at low dose by feeding for 21 days decreased the proportion of CD21⁺ B cells gradually from ileal Peyer’s patches. Besides, gene expression profiles of cytokines in T cells, such as IL-2, IL-4, and IFN-γ were not changed under the same condition (Obremski et al., 2013).

Conclusively, nutritional deficiency or ingestion with contaminated feed induces the change of intestinal pro-inflammatory cytokines and modulates barrier function in pigs. The immunological mechanism by which nutritional stress induces the modulation of gut immune system resulting in weak host response is yet to be defined.

Infectious stress

Enteric and respiratory infections are the most frequent and recurrent diseases in swine industry. Especially, enteric infection is one of major stressors causing low productivity in farm animals since it is known to suppress the feed conversion efficiency (Kiarie et al., 2011; Yang et al., 2014). Unlike other type of stressors, infectious stress is not easy to control and often causes long-term economic loss. Once there is an outbreak, transmission within and between the batches of animals occurs very fast because most modern animal farms have adopted intensive rearing system. At the same time, it is difficult to clear the pathogens completely from the site and region of the outbreak without a mass slaughter operation.

Most enteric pathogens come into contact with the animal from drinking water, feeds, or feces from other infected animals. After gaining access to the gut of the target animal, enteric pathogens generally disrupt the homeostasis of the epithelial barrier. Some pathogens including Escherichia coli induce intestinal damage through osmotic stress causing secretory diarrhea while others cause diarrhea by up-regulating pro-inflammatory cytokines, producing so called inflammatory diarrhea (Fairbrother et al., 2005). Enteric pathogens are known to suppress feed intake and feed conversion, which causes unnecessary energy loss for activating immune system. The main causes of enteric diseases in the swine industry are: E. coli, porcine epidemic diarrhea virus (PEDV), porcine delta coronavirus (PDCoV), and transmissible gastroenteritis coronavirus (TGEV).

E. coli is gram-negative, enteric bacteria composed of several strains, although some are pathogenic most are commensal. Pathogenic E. coli, also called enterotoxigenic E. coli (ETEC), has been known to cause diarrhea accompanied by dehydration, inhibition of the feed conversion and growth performance. It was also reported that ETEC shortened the length of villus and the depth of crypt of small intestine. It also inhibited the expression of TJ of intestinal epithelial cells by loosening the epithelial barrier. Supplementation of Lactobacillus plantarum (Yang et al., 2014), Saccharaomyces cerevisiae boulardii (Collier et al., 2011), chitosan (Xiao et al., 2013) or vasoactive intestinal peptide (Xu et al., 2014) has been reported to alleviate the infection stress of ETEC.

PEDV is an enteric coronavirus which had been prevalent only in East Asia, but there have been frequent outbreaks in America since 2013. Once PEDV appears, animal farms seem to suffer chronically because no strategy or treatment is available, even antibiotics have no effect (Song and Park, 2012). It was suggested that PEDV changed the microfilaments inside the epithelial cells followed by increase of permeability of the epithelial barrier through TLR 2, 3, and 9 (Cao et al., 2015). Not only epithelial cells but also the immune cells could be targeted by this virus since most immune cells are expressing TLRs. B cells located in mucosal tissues such as duodenum lamina propria produced much more IgG and IgA than those in systemic lymphoid tissues, spleen and blood (de Arriba et al., 2002). In pigs infected with PEDV, monocyte-derived dendritic cells produced a large amount of pro-inflammatory cytokines including IL-12 coincident with enhancing T-cell proliferation when co-cultured (Gao et al., 2015).

PDCoV and TGEV are less prevalent than E. coli or PEDV but they are still critical enteric coronaviruses in swine industry. PDCoV was once detected in Hong Kong (2009) and USA (2014). The pathology of PDCoV includes dehydration, loss of body weight but with less severe symptoms compared to other pathogens (Chen et al., 2015). However, it is important to note that PDCoV showed synergic pathology when co-infected with PEDV. TGEV was often reported in Asia and America causing vomiting and even death in piglets, when severe. It is assumed that this virus is derived from the same ancestor as porcine respiratory coronavirus which infects respiratory tracts (Kim et al., 2000).

In conclusion, infectious stress causes persistent economic loss of swine industry, especially with chronic infection. Research may have been biased to the treatment and eradication of the pathogens using treatment like antibiotics or vaccines. However, how to increase the disease tolerance in domestic animals against infection is not well understood. It is time to extend our effort to understand infectious stress affecting animal health and growth performance.

CONCLUSION

Various stressors are threatening the health and, at the same time, suppressing the growth performance in farm animals. The present paper focused on major stress factors, including thermal, nutritional and infectious, in relation to gut immunity in pigs. Numerous studies focusing on stresses in conjunction with porcine gut examined TJ proteins for the permeability, pro-inflammatory cytokines and/or gene profiles (Table 1). However, we do not know enough today to fully explain the precise mechanism of the gut immune system in pigs under stress conditions. In addition, the pig’s immune system cannot be directly extrapolated from that of humans and mice, for instance, CD4⁺CD8⁺ T cells in peripheral immune system (Cheon et al., 2014). In the near future, studies are expected to define i) the identification and the function of immune cells like innate lymphoid cells in intestine, ii) the immunological interaction between immune cells and gut epithelial cells under major stresses, iii) the alteration of intestinal immune system by major stresses to systemic immune responses and iv) gut health leading host immune system under multi-stress condition in pigs.

Table 1

i) The impact of major stresses on gut immunity

ACKNOWLEDGMENTS

This work was supported by a grant from the Next-Generation BioGreen 21 Program (PJ01112401), Rural Development Administration, and Korea Institute of Planning and Evaluation for Technology in Food, Agriculture, Forestry and Fisheries (IPET) through (Agricultural Microbiome R&D Program) the Strategic Initiative for Microbiomes in Agriculture and Food, funded by Ministry of Agriculture, Food and Rural Affairs (MAFRA), 916004-2, Republic of Korea. This work was also partially supported by a grant from North Carolina Agricultural Foundation (660101), Raleigh, USA.

Notes

CONFLICT OF INTEREST

We certify that there is no conflict of interest with any financial organization regarding the material discussed in the manuscript.

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Table 1

i) The impact of major stresses on gut immunity

Stressor	Condition	Sample	Change	Reference
Heat	35°C for 24 hrs	Ileum	GLUT2 (1.5 times), HSP70 (2 times) and HIF-1α (1.5 times) were upregulated Myeloperoxidase activity was increased by 4 U/mg	(Pearce et al., 2013)
		Ileum and colon	The permeability measured by using TER and FITC-dextran transport was increased
		Serum	Endotoxin was increased by more than 3 times
	37°C for 6 hrs	Ileum	Mucin 2 was increased by 0.35 ng/mL at 6 hrs post heat stress Villi height was deceased by 181 μm at 6 hrs post heat stress	(Pearce et al., 2014)
		Colon	HSP70 was increased more than twice at 2 hrs post heat stress The permeability measured by TER, FITC-dextran transport was increased at 2 hrs post heat stress
		Serum	LBP was decreased at 2 hrs post heat stress Endotoxin showed the tendency for a linear increase over time

ii)

Stressor	Condition	Sample	Change	Reference
Nutrition	Feed deprivation for 24 hrs	Jejunum	Gene expression of TNF-α was decreased by 4 times	(Horn et al., 2014)
	Feed deprivation for 24 hrs	Serum	Cortisol was increased by 14 ng/mL	(Horn et al., 2014)
	Glycine depletion	IPEC-1	Apoptosis was increased by more than 10% Activation of Art and m-TOR was reduced by more than half	(Wang et al., 2014)
	180 μg/kg of AF and 900 μg/kg of DON for 33 d	Serum	WBC increased from 18.4 to 23.4×10³×10³/μL TNFα increased from 299 to 335 pg/mL Feed intake reduced from 1.04 to 0.88 kg/d ADG was reduced from 0.52 to 0.41 kg/d	(Chaytor et al., 2011)
	150 μg/kg of AF and 1,100 μg/kg of DON for 42 d	Serum	Basophil increased from 0.09 to 0.16×10³/μL Monocyte increased from 0.97 to 1.43×10³/μL IgG increased from 10.5 to 15.1 mg/mL IgM increased from 3.02 to 4.39 mg/mL	(Weaver et al., 2013)
	2 μg/mL of DON for 48 hrs	IPEC-J2	ZO-1, occludin and claudin-3 were decreased Permeability was increased	(Gu et al., 2014)
	2.8 mg of DON/kg feed for 35 d	Jejunum	Lesion score was increased by 6 times Villi was flattened coincident with decreased villi height Number of goblet cells (3 cells in 1.5 mm²) and lymphocytes (10 cells in 1.5 mm²) were decreased Gene expression of IL-1β (1.78 times), IL-6 (2.17 times), MIP-1β (1.42 times), IL-2 (1.8 times) and IL-12p40 (1.71 times) was increased	(Bracarense et al., 2012)
	2.8 mg of DON/kg feed for 35 d	Ileum	Lesion score was increased by 6 times Gene expression of IL-1β (2 times), TNF-α (1.49 times) and IL-6 (2.13 times) was increased E-cadherin and occludin were decreased by more than half	(Bracarense et al., 2012)
	5.9 mg of FB (4.1 mg FB1 +1.8 mg FB2)/kg feed for 35 d	Jejunum	Lesion score was increased by 4 times The numbers of eosinophils (5 cells in 1.5 mm² ) and plasma cells (18 cells in 1.5 mm²) were increased Gene expression of IFN-γ (1.43 times) and IL-10 (1.51 times) was increased
	5.9 mg of FB (4.1 mg FB1 +1.8 mg FB2)/kg feed for 35 d	Ileum	Lesion score was increased by 4 times Gene expression of IL-1β (1.73 times) and TNF-α (1.42 tiems) were increased Gene expression of occludin was decreased by half
	0.5 mg of FB1/kg of body weight/day for 7 d	Ileum	Gene expression of IL-8 was decreased	(Bouhet et al., 2006)
	0–100 μM (0 to 72.2 mg/L) of FB1 for 4 d	IPEC-1	IL-8 was decreased in a dose-dependent manner
	0–500 μM FB1 for 28 d	IPEC-1	The integrity measured by TER was decreased at 10 days post treatment	(Bouhet et al., 2004)
	0.1 mg/kg of zearalenone for 42 d	Ileum Peyer’s patches	Inflammatory cytokines, including IL-12/IL-23p40 and IL-1β, and vasoactive intestinal peptide were up-regulated significantly	(Obremski et al., 2015a)
	0.1 mg/kg of zearalenone for 28 d	Ileocecal lymph nodes	CD21⁺ B cells were reduced but, IFN-γ concentration was increased significantly	(Obremski et al., 2015b)
	2.5 ng/mL of T-2 toxin for 24 hrs	IPEC-J2	Viability of intestinal epithelial cells was reduced in half under Salmonella Typhimurium infection condition	(Verbrugghe et al., 2012)
	1 ng/mL of T-2 toxin for 30 min		Translocation of Salmonella Typhimurium was significantly increased
	0.2 mg/kg of T-2 toxin for 21 d	Ileal Peyer’s patches	CD21⁺ B cells were reduced by about 19%	(Obremski et al., 2013)

iii)

Stressor	Condition	Sample	Change	Reference
Infection	ETEC K88 strain 1×10⁸ cfu for 3 d	Duodenum	Villi height was decreased by 180 μm	(Yang et al., 2014)
	ETEC K88 strain 1×10⁸ cfu for 3 d	Jejunum	Villi height was decreased by 200 μm Occludin was decreased by more than half Gene expression of ZO-1 were decreased by more than half	(Yang et al., 2014)
	Transfection to express PEDV E protein	IECs	NF-κB activity was increased by twice IL-8 was up-regulated ER stress was increased (GRP78, as a marker for ER stress, was increased by 6 times)	(Xu et al., 2013a)
	Transfection to express PEDV N protein	IECs	S phase in cell cycle was increased NF-κB activity was increased by 3 times ER stress was increased (GRP78 was increased by 7 times) IL-8 was up-regulated by 100 pg/mL	(Xu et al., 2013b)
	Orally inoculation with PEDV for 32 d	Feces	PEDV was peaked at 5 dpi and eliminated at 8 dpi	(de Arriba et al., 2002)
		Serum	PEDV specific IgG titer was increased gradually until 32 dpi PEDV specific IgA titer was increased until 21 dpi
		Duodenum	Over 4 (per 5×10⁵ MNC) PEDV specific IgM ASC was exited at 4 dpi Over 20 (per 5×10⁵ MNC) PEDV specific IgG ASC was exited at 21 dpi and decreased to over 5 (per 5×10⁵ MNC) PEDV specific IgG ASC at 25 dpi Over 3 (per 5×10⁵ MNC) PEDV specific IgA ASC was exited at 7 dpi and decreased to over 2 (per 5×10⁵ MNC) PEDV specific IgA ASC at 21 dpi
		Ileum	Over 3.5 (per 5×10⁵ MNC) PEDV specific IgM ASC was exited at 4 dpi Over 10 (per 5×10⁵ MNC) PEDV specific IgG ASC was exited at 25 dpi
		MLN	Over 2 (per 5×10⁵ MNC) PEDV specific IgM ASC was exited at 7 dpi
	PEDV 1 MOI infection for 2 hrs and then washed out, cultured 24 hrs	Mo-DCs	Immature DCs were infected preferentially than mature DCs Infected mature DCs decreased the expression of SWC3a⁺CD1a⁺, SWC3a⁺CD80/86⁺ and SWC3a⁺SLA-II-DR⁺ compared mature DCs The concentration of IL-10, IL-12 and IFN-γ from infected DC were decreased by comparing mature DCs	(Gao et al., 2015)
	10 mL of PDCoV 3×10³ TCID50/mL orally for 4 d	Middle jejunum	Villus height was decreased by 250 μm Crypt depth was increased by 20 μm	(Chen et al., 2015)
		Distal jejunum	Villus height was decreased by 250 μm Crypt depth was increased by 30 μm
		Ileum	Villus height was decreased by 180 μm Crypt depth was increased by 40 μm

hrs, hours; GLUT2, glucose transporter 2; HSP70, heat shock protein 70; HIF-1α, hypoxia-inducible factor 1-alpha; TER, transepithelial electrical resistance; FITC, fluorescein isothiocyanate; LBP, LPS binding protein; TNF-α, tumor necrosis factor-α; DON, deoxynivalenol; m-TOR, mammalian target of rapamycin; WBC, white blood cell; ADG, average daily gain; TER, transepithelial electrical resistance; ZO-1, zonula occludens protein-1; FB, fumonisin B; PEDV, porcine epidemic diarrhea virus; IECs, porcine small intestinal epithelial cells; GRP78, glucose regulated protein 78; dpi, days post inoculation; MNC, mononuclear cells; ASC, antibody secreting cells; MLN, mesenteric lymph nodes; MOI, multiplicity of infection; Mo-DCs, monocyte-derive dendritic cells; PDCoV, porcine deltacoronavirus.