Ochratoxin A: its impact on poultry gut health and microbiota, an overview

Abstract

Ochratoxin A (OTA) is a widespread mycotoxin, that has strong thermal stability, and is difficult to remove from feed. OTA is nephrotoxic, hepatotoxic, teratogenic, immunotoxic, and enterotoxic to several species of animals. The gut is the first defense barrier against various types of mycotoxins present in feed that enter the body, and it is closely connected to other tissues through enterohepatic circulation. Compared with mammals, poultry is more sensitive to OTA and has a lower absorption rate. Therefore, the gut is an important target tissue for OTA in poultry. This review comprehensively discusses the role of OTA in gut health and the gut microbiota of poultry, focusing on the effect of OTA on digestive and absorptive processes, intestinal barrier integrity, intestinal histomorphology, gut immunity, and gut microbiota. According to the studies described to date, OTA can affect gut dysbiosis, including increasing gut permeability, immunity, and bacterial translocation, and can eventually lead to gut and other organ injury. Although there are many studies investigating the effects of OTA on the gut health of poultry, further studies are needed to better characterize the underlying mechanisms of action and develop preventative or therapeutic interventions for mycotoxicosis in poultry.

Graphical abstract

Introduction

Mycotoxins, which have a low molecular mass (∼ 700 Da), are secondary metabolites produced by fungal genera (e.g., Aspergillus, Penicillium, and Fusarium) and are the most common natural food contaminants in components of human and animal diets, such as cereals and animal forages (Wild and Gong, 2010; Manizan et al., 2018). Fungal proliferation and production of mycotoxins arise naturally due to environmental factors, such as tropical conditions (Mohd-Redzwan et al., 2013), the warming earth (Medina et al., 2015), and downstream processing (Khazaeli et al., 2014). According to a survey, 25% of the world's crops, such as nuts, grains, and rice, are contaminated by molds and fungi (Pandya and Arade, 2016). The detection rates of aflatoxin B1, deoxynivalenol, zearalenone, and fumonisin in layer feed were 83.16, 93.68, 94.74, and 100%, respectively, and those in meat-type poultry feed were 89, 96, 85, and 94.74% in Southwest China (Li, 2016). Due to the ubiquitous nature of fungi, mycotoxins have been increasingly attracting the concern of health organizations where their occurrence in foods cannot be ignored and already poses a risk to consumers (Jahanian, 2016). When animals consume mycotoxin-contaminated diets, intestinal epithelial cells (IECs) are completely exposed to the contaminated feed, the epithelial cells of the esophagus and gastrointestinal tract (GIT) can be damaged, easily leading to gastrointestinal dysfunction, intestinal microbial imbalance, malnutrition, diarrhea, vomiting, and intestinal inflammation, and ultimately decreased growth performance (Zhang, 2018; Ruan et al., 2019; Wang et al., 2019).

Ochratoxins are a group of secondary metabolites produced by fungi of 2 genera: Penicillium and Aspergillus (Ringot et al., 2006). Ochratoxin A (OTA) is the most common and toxic ochratoxin (Liuzzi et al., 2016). It has been shown to be nephrotoxic, hepatotoxic, teratogenic, and immunotoxic to poultry (Hassan et al., 2012b; Hameed et al., 2017; Bhatti et al., 2019; Wang et al., 2019). Mycotoxin uptake and subsequent tissue distribution are mediated by the GIT. When mycotoxins are introduced into organisms via food or feed, they first interact with the GIT (Assunção et al., 2016). There is an increasing awareness of the deleterious effects of mycotoxins within the GIT. A healthy intestinal tract guarantees the welfare and health of both people and animals. Rapidly dividing and activated cells and tissues with a high protein turnover are predominant in the gut epithelium. Intestinal cells and tissues could become a main target of mycotoxins as many of these metabolites are inhibitors of protein synthesis. The absorption of OTA starts from the stomach and mainly occurs in the proximal jejunum (Grenier and Applegate, 2013). The absorption rate of OTA was low in poultry (Galtier et al., 1981), and the unabsorbed OTA could reach the hindgut to interact with the intestinal microbiota. Considering this background, the current review aims to provide a summary of the available evidence regarding the effects of OTA on intestinal health and microbiota in poultry.

OTA

Ochratoxin is mainly produced by Aspergillus and Penicillium. OTA (C₂₀H₁₈ClNO₆; molecular weight: 403.8) is a white, tasteless, and heat-stable crystalline solid preparation (melting point, 168°C–173°C) with poor water solubility (Pohland et al., 1982). OTA does not completely disappear during baking (Vidal et al., 2015); furthermore, OTA can resist 3 h of autoclaving at 121°C (Trivedi et al., 1992), and even at 250°C, it is only partially degraded (Boudra et al., 1995). During coffee roasting, OTA is only partially decomposed (Blanc et al., 1998; Gerrit et al., 2001). A structural analysis of OTA showed that OTA is a secondary metabolite derived from polyketide, which contains a dihydrocoumarin moiety coupled to a l-β-phenylalanine through an amide bond. The metabolite is derived from the shikimic acid pathway. The specific structure of OTA is shown in Figure 1 (André and Ali, 2010). OTA is a weak acid and has a strong capacity to bind with proteins. Once it enters the blood stream, approximately 99% of OTA binds to serum albumin. This binding contributes to the passive absorption of OTA in the nonionic form (Chu, 1971, 1974; Galtier et al., 1981; Hagelberg et al., 2010). After conjugated OTA reaches the hindgut, it is released by intestinal microorganisms, and a second peak appears in the intestinal contents, which is absorbed by the intestine again (Kumagai et al., 1985; Plestina, 1988; Roth et al., 1988; Sreemannarayana et al., 1988). Therefore, OTA may affect the intestinal microbiota, and OTA toxicity in the intestinal tract may be stronger than that in other tissues.

Figure 1.

Chemical structure of ochratoxin A (André and Ali, 2010).

Prevalence of OTA

As one of the most common toxins in food or feed, OTA is widely found in cereals (Mario et al., 2009), coffee, wine, dried fruits, nuts (Fink-Gremmels, 2005; Gagliano et al., 2006), herbal medicines (tangerine seeds, 92.3 μg/kg; Trichosanthis Semen, 6.05 ng/g; milk thistle, 10 μg/kg (Shim et al., 2014; Veprikova et al., 2015; Chen et al., 2015), food coloring agents (1.16–32.00 μg/kg), plant food supplements (1.16–20.03 μg/kg) (Solfrizzo et al., 2015), bottled water (0.2 ng/L) (Mata et al., 2015), and fresh sweet peppers (29.5 μg/kg) (Gambacorta et al., 2018). Among 87 human milk samples, 84 (96.6%) samples were positive for OTA at a mean level of 24.57 ± 13.6 ng/L, and 14 (16%) were positive samples with the maximum limit of 40 ng/L for ochratoxin (Parvin et al., 2014). An investigation showed that the probability of OTA detection in fresh sweet peppers was 51%, and the average content of OTA was 29.5 μg/kg (Gambacorta et al., 2018). The wide occurrence of OTA and its high thermal stability make the eradication of OTA from the food chain very difficult (Frantisek et al., 2016). OTA is also found in feed and feedstuffs. A study showed that OTA in mixed feed and feedstuffs used in some laying hens was found to be positive in 64 of the 89 samples analyzed (Gumus et al., 2018). In another study from South America published by Magnoli et al. (2007), OTA was present at a mean level of 25 to 30 μg/kg in poultry feedstuffs. Mycotoxins may remain in the tissues and eggs of poultry-fed moldy feed. Among 115 chicken meat and 80 egg samples, 41% of meat samples (average content of OTA was 1.41 ± 0.70 μg/kg), and 35% of the egg samples were positive for OTA (average content of OTA was 1.17 ± 0.42 μg/kg) (Iqbal et al., 2014), and the residues of OTA in eggs consistently increased with time and reached a maximum (7.396 ± 1.03 ng/g) at day 21 of toxin feeding with 5 mg of OTA/kg of feed (Hassan et al., 2012a). The OTA residue in eggs may harm the offspring, which was confirmed by Hassan et al. (2012b). After 2 wk of OTA administration in ducks (235 μg/kg body weight), the OTA residue concentrations in the kidney, cecum, liver, pectoral muscle, duodenum, jejunum, ileum, and leg muscle were 1.59, 0.94, 0.92, 0.54, 0.42, 0.41, 0.32, and 0.20 ng/kg, respectively (Wang et al., 2019). According to the these results, OTA residues were quite high in the intestine, especially in the cecum. These findings partly explain the enterotoxicity of OTA.

Limitation of OTA in Feed

Due to its toxic properties, OTA is subject to legal regulation at both the national and international level. However, to date, only a nonbinding recommendation exists for OTA levels in cereal feed and feed for poultry in the European Union (Commission Recommendation 2006/576/EC of 17 August 2006 on the presence of OTA in products intended for animal feeding, see Table 1) (European Union, 2006), and the limit for OTA in poultry feed is 0.10 mg/kg.

Table 1.

Guidance values for ochratoxin A under Commission Recommendation 2006/576/EC as in force.

Feed	Guidance value in mg/kg relative to feedstuffs with a moisture content of 12%
Feed materials—cereals and cereal products Complementary and complete feedstuffs	0.25
Complementary and complete feedstuffs for pigs	0.05
Complementary and complete feedstuffs for poultry	0.10

Sensitivity of Animals to OTA

Different animals have different sensitivities to OTA. Normally, young animals are more sensitive to OTA than mature ones due to the incomplete development of organs (Sherif et al., 2009; Adetunji et al., 2017). A study has shown that when 1-day-old ducks were fed OTA for 6 d, the median lethal dose (LD50) of the ducks was 0.5 mg/kg body weight (Van Der Merwe et al., 1965), while when 1-day-old Babcock B-300 cockerels were fed OTA for 7 d, the LD50 was 3.3 mg/kg body weight (Peckham et al., 1971). The comparative acute and oral toxicity of OTA for 3-day-old avian species is presented. The 7-day LD50 values for White Leghorns, turkeys, and Japanese quail were 3.4 ± 0.19, 5.9 ± 0.72, and 16.5 ± 0.56 mg/kg body weight, respectively (Prior et al., 1976). The LD50 for rats was 22 mg/kg for males and 20 mg/kg for females (Purchase et al., 1968). From these results, compared with mammals, poultry are considered to be more sensitive to OTA. Therefore, researchers should determine the effect of OTA on poultry health, especially on intestinal health, and pay attention to the contamination of OTA in poultry feed and feedstuff.

GIT

The GIT is responsible for food ingestion, digestion, energy and nutrient absorption, immune responses, and elimination of waste products (feces) (Pietro et al., 2017). GIT is a muscular tube forming a continuous passage that is lined by a mucous membrane consisting of 4 layers. All segments of the GIT are divided into 4 layers: the mucosa (epithelium, lamina propria, and muscular mucosa), the submucosa, the muscularis propria (inner circular muscle layer, intermuscular space, and outer longitudinal muscle layer), and the serosa (Jaladanki and Wang, 2016). The entire mucosa rests on the submucosa, beneath which is the muscularis propria. The outermost layer is named the serosa. The complex infoldings at the mucosal layer form an immense surface area for most efficient nutrient absorption. The submucosa contains arteries, veins, inflammatory cells, lymphatics, autonomic nerve fibers, and ganglion cells. The muscularis mucosa is a thin layer of smooth muscle that forms the basis of the peristalsis. The serosa is made of connective tissue that contains blood vessels, nerves, and fat. The innermost epithelial layer of the mucosa is of vital importance for intestinal barrier function. The intestinal epithelium is one layer of thin cells lining the gut lumen. The epithelium contains enterocytes, enteroendocrine, and goblet cells at villi, whereas Paneth cells are located under crypts (Fink et al., 2016). The epithelium serves as a barrier to block the entry of harmful agents such as pathogens, toxins, and foreign antigens. In addition, it plays an important role in nutrient absorption, including that of electrolytes, dietary nutrients, and water via its selective permeable membrane (Constantinescu and Chou, 2016). Each IEC is connected by desmosomes, tight junctions (TJs), and adherent junctions. The adherent junctions and desmosomes are responsible for the mechanical linkage of adjacent cells. TJs control the intercellular space and regulate selective paracellular ionic solute transport (Capaldo et al., 2014).

Modulation of Digestive and Absorptive Processes by OTA

The absorption of OTA starts from the stomach, and occurs mainly in the proximal jejunum. It enters IECs by passive diffusion, mainly by nonionic absorption, and enters the blood circulation to reach all tissues and organs of the body (Grenier and Applegate, 2013). The effect of mycotoxins on nutrient and energy digestibility has been documented. OTA in combination with aflatoxin had a more pronounced effect on the metabolizable energy content of the diet than the toxin in feed alone, and this reduction occurred through a significant increase in the maintenance energy requirement of hens (Verma et al., 2007). Razafimanjato et al. (2010) found that OTA inhibited the absorption of glutamate by decreasing the expression of glutamate/aspartate transporter and glutamate transporter at the cell surface. Feeding meat ducks with OTA-contaminated diets decreased the content of alanine, leucine, and glutamate in plasma, downregulated the expression of sodium-dependent glutamate transporter 1 mRNA in the jejunum, and decreased the mRNA expression of cationic amino acid transporter 1, excitatory amino acid transporter 4, and peptide transporter (Ruan, 2018). These results indicated the necessity for considering not only the OTA contamination in evaluating their effect on poultry health and performance, but also the possible physicochemical alterations of feedstuffs due to the OTA contamination. More studies should focus on the effect of OTA on nutrient digestibility and nutrient requirements of animals under mycotoxin contamination.

OTA Destroys Intestinal Barrier Integrity

IECs have 2 crucial but conflicting functions. On one hand, they transport nutrients and fluids; on the other hand, they restrict the access of luminal antigens to the internal milieu. They form a monolayer that constitutes a dynamic and selective barrier and mediates the transport of molecules in 2 ways: either across the cells (i.e., the transcellular pathway) or between the cells (i.e., the paracellular pathway) (Grenier and Applegate, 2013). When OTA are introduced into organisms from food, they first interact with the GIT. The TJs in the intestinal epithelium are important barriers for maintaining intestinal epithelial permeability, which is greatly assisted by TJ proteins that prevent harmful substances from entering the body and maintain the structural integrity of TJs (Buckley and Turner, 2018). Many studies have shown that OTA can destroy intestinal barrier integrity by suppressing TJ proteins, such as occludin, zonula occludens-1, and claudin-1, in poultry (Ruan et al., 2019; Wang et al., 2019; Yang et al., 2020). The increase in intestinal permeability, in turn, promotes the translocation of bacteria (Kelly et al., 2015). Together, OTA could destroy TJs, such as downregulating the expression of TJ genes and proteins and increasing the serum lipopolysaccharide content, thus increasing the gut permeability. The increased gut permeability may subsequently enable the translocation of harmful stressors, particular bacteria (commensals and pathogens), from the gut lumen to the internal environment and eventually cause harm to animals.

OTA Damages the Intestinal Histomorphology

The intestine is the largest mucosal tissue, and plays an important role in immune homeostasis. Mucus secretion by goblet cells is significant for the maintenance of mucosal homeostasis, which helps to maintain intestinal homeostasis (Johansson and Hansson, 2016; McGuckin and Hasnain, 2017). Although the kidney is the main target for OTA-induced toxicity, histological abnormalities and lesions of the GIT have been reported. In chickens, a decrease in villus height was observed in combination with an increase in necrosis and apoptosis of IECs with prismatic epithelium and alterations of brush border (Solcan et al., 2015). Ducks fed a diet containing 2 mg/kg OTA showed villous blunting and epithelial denudation along with a related decrease in villous height and increase in the depth of crypts (Figure 2A, Ruan, 2018). Similar studies have confirmed this result by Tong et al. (2020) (Figure 2B) and Malekinezhad et al. (2020) (Figure 2C). They reported that OTA decreased the villus height/crypt depth ratio and goblet cells of duodenum, jejunum, and ileum, and the cecum was inflated and bleeding, and a small amount of intestinal mucosa was detached in broilers. Alteration of intestinal histomorphology could reduce nutrient absorption, and the decrease in goblet cells rendered the gut vulnerable to infection. OTA exerts its effect on the gut via reduction of nutrient absorption, disruption of intestinal permeability, and modulation of the immune system.

Figure 2.

OTA damages the intestinal histomorphology. (A) Ducks fed diets with different doses of OTA showed villous blunting and epithelial denudation in the jejunum, compared with the controls (magnification, 200×; scale bar, 200 μm; Ruan, 2018). (B) Detection of pathological changes in duodenum, jejunum, and ileum tissue (magnification, 5×; scale bar, 500 μm). The arrows “→” indicate a intestinal pathological damage or breakage of broiler chickens received 50 µg of OTA/kg body weight/day for 21 d (Tong et al., 2020). (C) Histological structures of the ileum at 42 d of age (magnification, 5×): negative control diet with normal epithelial cells in the apical region of villi; (D) diet contaminated with OTA; the villus height was decreased and the apical region of epithelial cells was shedding (Malekinezhad et al., 2020). Abbreviation: OTA, ochratoxin A.

OTA and Gut Immunity

The first expression of OTA toxicity is immunosuppression, which may become clinically apparent before nephropathy is manifested (Aleo et al., 1991). The gut is the first defense barrier against various types of contamination in food (Grenier and Oswald, 2011); therefore, compared with other tissues, it is exposed to mycotoxins at higher concentrations upon ingestion of contaminated food (Marie-Caroline et al., 2016). Furthermore, immune cells of the gut-associated lymphoid tissue are more numerous than those of other secondary lymphoid tissues contained in the whole body, and the intestine plays an important role in immunity in the host (Castro and Arntzen, 1993). Seven-day-old male broiler chickens (Ross 308) were administered 20 and 50 μg/kg body weight OTA by gavage. After 14 d of exposure, OTA reduced the lymphocyte population in the intestinal epithelium and the lamina propria, and increased the CD4+ and CD8+ values in both the duodenum and jejunum after 28 d of administration (Solcan et al., 2015). OTA is a fungal metabolite with immunomodulatory effects. A study has suggested that OTA induces the secretion of proinflammatory cytokines, such as IL-1β and tumor necrosis factor α, in the jejunum of Pekin ducklings; moreover, OTA reduces the production of the anti-inflammatory factor IL-10 and decreases the IgA content in the jejunum (Ruan, 2018). A similar result was confirmed by Tong et al. (2020), who demonstrated that 1-day-old broiler chickens fed 50 μg of OTA/kg body weight show upregulated mRNA expression of IL-1β and tumor necrosis factor α and induced the phosphorylation of nuclear factor κB. The OTA group had a severely congested lamina propria of the intestine, in filtrated lymphocytes; several necrotic epithelial cells; and the intestinal villi were short, thick, and edematous at various degrees. The effect of OTA on gut immunity is summarized in Table 2. These results suggested that OTA is cytotoxic to the intestinal epithelium and mucosa-associated lymphoid tissue, altering the intestinal barrier and increasing susceptibility to various associated diseases.

Table 2.

OTA and gut health (absorption, barrier integrity, and immunity).

Gut function	Subjects	Dose	Time	Results	Reference
Absorption	HT-29-D4 cells	100 μmol	48 h	Na+-dependent glucose absorption was inhibited by 60 ± 4%	Maresca et al., (2001)
	Cortical astrocytes	10 μmol	72 h	OTA could inhibit the absorption of glutamate by decreasing the expression of GLAST and GLT-1 at the cell surface	Razafimanjato et al., (2010)
	1-day-old ducklings	2 mg/kg diet	21 d	OTA downregulated the expression of SGLT1, CAT1, EAAT, and PepT1 mRNA in jejunum, and decreased the expression	Ruan (2018)
Barrier integrity	1-day-old ducklings	2 mg/kg diet	21 d	OTA decrease the expression of occludin and tight junction protein 1 at the level of transcription and protein in jejunum	Ruan et al., (2019)
	7-day-old ducklings	235 μg/kg body weight	14 d	OTA decreased the expression of occludin and tight junction protein 1 at the level of transcription and protein in cecum, and increased the serum LPS content	Wang et al., (2019)
	1-day-old white feather broilers	50 μg/kg body weight	21 d	OTA decreased expressions of claudin-1, occludin and ZO-1 at the mRNA level, and decreased the expression of claudin-1 at the protein level	Yang et al., (2020)
Immunity	Male broiler chickens (Ross 308)	20 and 50 μg/kg body weight	28 d	OTA reduced the lymphocyte population in the intestinal epithelium and the lamina propria, and increased the CD4+ and CD8+ values in both the duodenum and jejunum after 28 d of administration	Solcan et al., (2015)
	Ducklings	2 mg/kg diet	21 d	OTA induced the secretion of IL-1β and TNF-α in the jejunum and decreased the IgA content in the jejunum	Ruan (2018)
	1-day-old broiler chickens	50 μg of OTA/kg body weight/d	21 d	OTA could upregulate the mRNA expression of IL-1β, TNF-α and induce phosphorylation of NF-κB	Tong et al., (2020)

Abbreviations: CAT1, cationic amino acid transporter 1; EAAT, excitatory amino acid transporter; GLAST, glutamate/aspartate transporter; GLT-1, glutamate transporter 1; LPS, lipopolysaccharide; NF-κB, nuclear factor κB; OTA, ochratoxin A; PepT1, peptide transporter 1; SGLT1, sodium-dependent glutamate transporter 1; TNF, tumor necrosis factor; ZO-1, zonula occludens 1.

Gut Microbiota

The gut microbiota represents an ensemble of microorganisms including bacteria, viruses, and fungi, that are harbored within the GIT of living organisms. The gut microbiota is found in virtually every metazoan, from invertebrates to vertebrates, and it affects numerous physiological functions of the intestine (Lee and Hase, 2014; Subramanian et al., 2014; Ren et al., 2016; Thaiss et al., 2016). The gut microbiota is linked to the pathogenesis of various diseases through the activity of the microbiome or its metabolic products (Louis et al., 2014; Qin et al., 2014; Anhê et al., 2015; Ponziani et al., 2019).

Composition and Functions of the Gut Microbiota

The composition of the gut microbiota varies significantly with the relative ratios of dominant phyla, genera, and species. In particular, stable and healthy gut microbiota is generally indicated by a rich diversity of gut bacteria (Mosca et al., 2016). The majority of the gut microbiota is composed of strict anaerobes, which dominate the facultative anaerobes and aerobes by 2 to 3 orders of magnitude (Gordon and Dubos, 1970; Savage, 1970; Harris et al., 1976). Adult poultry intestinal microbiota are dominated by 2 phyla, Bacteroidetes and Firmicutes, whereas the Actinobacteria (including Bifidobacterium spp.), Proteobacteria (including Escherichia coli and Enterobacteriaceae family members), and Verrucomicrobia (including Akkermansia muciniphila) phyla are present only in minor proportions (Wang et al., 2017; Zhai et al., 2020). The concentration and microbial diversity of the gut microbiota increase from the duodenum to distal colon segments. At the population level, the microbiota is generally stable and selected by evolution (Ochman et al., 2010; Jalanka-Tuovinen et al., 2011). However, commensal microbiota can be qualitatively and quantitatively modulated by the environment (Huttenhower et al., 2012). Diet plays an important role in shaping the gut microbiota (Salonen et al., 2014; Frese et al., 2015). Moreover, genetic background, diseases such as inflammatory bowel disease (Zhang et al., 2017), nonalcoholic fatty liver (Roy et al., 2012), obesity (Kallus and Brandt, 2012), and type 1 diabetes (Vaarala et al., 2008), genetic background (Goodrich et al., 2016), the mental health condition (stress) of the host (Karl et al., 2017), sports (García et al., 2014), and mycotoxin (Piotrowska et al., 2014; Wang et al., 2015) can also alter the composition and proportion of the gut microbiota.

Impact of OTA on the Gut Microbiota

The gut microbiota represents an important bridge between environmental substances and host metabolism. Findings showed that the gut microbiota, particularly in animals, has profound interactions upon the ingestion of mycotoxins. Indeed, the absorption rate of OTA varies from animals to humans (e.g., 66% in pigs, 56% in rabbits, and 40% in chickens [Galtier et al., 1981]). This indicates that most OTA are not absorbed, and thus reach the hindgut and interact with the intestinal microbiota, especially in poultry, which presents a low absorption rate. However, few studies have focused on the interaction between OTA and the gut microbiota. Evidence of disturbance to gut microbiota modulation induced by OTA has been summarized inTable 3.

Table 3.

Ochratoxin A and gut microbiota.

Subjects	Dose	Time	Results	Reference
1-day-old broilers	50 μg/kg body wight	21 d	OTA decreased the richness and diversity of cecum microbiota	Yang et al., (2020)
7-day-old ducklings	235 μg/kg body wight	14 d	OTA decreased the richness and diversity of cecum microbiota and increased the relative abundance of cecum Bacteroides	Wang et al., (2019)
1-day-old ducklings	2 mg/kg diet	21 d	OTA increased the relative abundance of cecum Bacteroides and decreased the butyric acid producing bacteria	Zhai et al., (2020)

Abbreviation: OTA, ochratoxin A.

The fate of OTA during colon digestion was investigated using a dynamic simulator of the human gut (Ouethrani et al., 2013). In previous research, gut microbiota degradation of OTA and microbiota diversity alteration were observed only in the descending colon after 1 wk of exposure to OTA, and OTA caused a specific, but lasting, loss of the beneficial species Lactobacillus reuteri (Ouethrani et al., 2013). Studies in broilers and ducks suggested that OTA decreased the richness and diversity of the cecum microbiota and induced intestinal TJ injury (Wang et al., 2019; Yang et al., 2020). Our latest research confirmed these results, which increased the relative abundance of cecum Bacteroides, in ducks fed OTA-contaminated diets (Zhai et al., 2020). Although Bacteroides (gram-negative bacteria) is often associated with leanness and other desirable health traits (Turnbaugh et al., 2006; Ridaura et al., 2013), some of its strains (e.g., Bacteroides fragilis, Bacteroides vulgatus, and Bacteroides dorei) have been linked to abdominal infections, metabolic disease, and inflammation (De Palma et al., 2010; Davis-Richardson et al., 2014). This outcome may further suggest that OTA may cause negative effects on host health via gut microbiota modulation. Moreover, the elevated bacterial strains may have some tolerance to OTA and may be able to degrade or absorb OTA. However, few studies have reported effects of OTA on gut microbiota and microbiota metabolites, especially with chronic exposure at safe doses. Therefore, this area of research needs to be addressed further. Moreover, evaluating the variations in microbial functions such as signal transduction and metabolism by transcriptomics and/or metabolomics might provide great opportunities to assess the impact of OTA on gut health and the development of bacteria and metabolites regulating OTA-induced intestinal injury.

Conclusion

All of the issues raised herein indicate the necessity for determining the deleterious effects of ingested OTA on the epithelium, mucosa, and microbiota of poultry. The gut microbiota can vary within the same species; thus, different results regarding OTA can be observed, as discussed in this article. However, a common consequence is that OTA disrupts the TJs and the gut microbiota balance and thereby dysregulates intestinal functions and impairs local immune response, which may eventually result in systemic toxicity that leads to chronic mycotoxicosis, such as liver inflammation. It will be interesting to study if the pathogenesis of OTA-induced disease in other organs (e.g., brain and kidney injury) depends on the intestinal microbiota.

Although there are many studies on the effects of OTA on the gut health of poultry, the types of gut microbes or metabolites affected by OTA and thus the harm they cause to gut health are not known. Whether there is a maternal effect of OTA on gut health has not been studied. In addition, the effects of chronic exposure to a safe OTA dose in poultry should not be underestimated. This review highlights the important role of the gut microbiota in OTA-induced gut injury in poultry, which may open a new path to novel preventative or therapeutic interventions for mycotoxicosis, such as regulating the intestinal microbiota and improving the intestinal barrier with probiotics.

Disclosures

The authors declare no conflict of interest.