Mycotoxins are a group of structurally different secondary fungal metabolites that occur as contaminant of grains in worldwide crops (FAO). Species of fungi like Aspergillus, Fusarium, Penicillium, and Claviceps are everywhere in nature, and under ideal conditions, often infect economically important crops and forages during storage, transportation and processing.
However, several hundreds of mycotoxins can be associated with animal disorders. The most important to be mentioned are Aflatoxin, Vomitoxin, Ochratoxin, Zearalenone, Fumonisin and T-2 toxin. Raw materials are undoubtedly contaminated with different mould species and therefore will contain more than one of these mycotoxins, for example, the co-contamination with Zearalenone and Vomitoxin, very often in cereals (wheat, etc.) or with Aflatoxin and Fumonisin in corn. During feed processing, raw materials are mixed together which causes the proliferation of colonies by fungi and consequently a high level of mycotoxins. The combination of different mycotoxins produces a greater negative effect on health and productivity of animals than they individually do, because of their synergistic, additive or antagonistic characteristics. Poor livestock performance and/or diseases symptoms observed in commercial animals farms can also be considered to be a consequence of this interaction.The clinical response of animals is both dose- and time-dependent and can vary from acute to chronic. The reaction to known mycotoxins of clinical importance tends to be sub-acute or chronic and symptoms are often not noticeable.
Figure 1: Prevalence of mycotoxins, tested samples: cereals (corn, wheat, and barley), oil-seed products (sunflower, soybean) and feeds (by NUTRIAD). Possible measures taken by the livestock industry to protect animals from the toxic effects of mycotoxins include the use of microbial inactivation, mould inhibition, fermentation, physical separation, thermal inactivation, irradiation, ammonification, ozone degradation and adsorptions.
Unfortunately, most of these methods are costly, time-consuming, and only partially effective. The most promising and practical approach has been the addition of mycotoxic in-activators with multi-functional activity to contaminated feed in order to selectively bind, fixate or transform mycotoxins during the digestive process and to protect or regenerate vital organs, avoiding mycotoxins to become harmful to the animal.
The natural contamination of feed with several mycotoxins at relative low concentrations can disturb the digestibility of nutrients in the animal by reducing feed intake and growth which ,subsequently, increases the feed conversion ratio weakening the liver functionalities and causing organ injury and stress.
Reduced nutrient digestibility, increased hepatic mycotoxic levels and consequently declined animal performance.
The presence of different mycotoxins at relative low concentrations in broilers diets had affected the nutrient digestibility of the birds and as a consequence the zoo technical performance. This was demonstrated in a broiler trial at the All-Russian Scientific Research and Technological Institute of Poultry Breeding (GNU-VNITIP), Russia (2008) (See table 1), a completely randomized experimental design with three mycotoxins types (Ochratoxin A at 0.41 ppm, T2-toxin at 0.16 ppm and fumonisin B1 at 12.7 ppm) ,natural contaminants in feed and two levels of UNIKE resp. 0 and 1kg/ton.
Tabel 1
The effect on digestibility in broilers receiving diets free of mycotoxins (neg control) or containing mycotoxins (pos control) treated with 1.0 kg/ton UNIKE is shown here below. (Fig.:2 and 3).
Fig 2 and 3: Body weight and FCR at 35 days of the birds fed with mycotoxic free diet or Ochratoxin A at 0.41 ppm, T2-toxin and fumonisin B1contaminated diet with 0 or 1 kg/ton UNIKE ®. Further analysis demonstrated that a large part of the mycotoxins were available for absorption into the gastro intestinal tract (GIT) (up to 91.1% of T2-toxin, up to 54.4% of fumonisin B1 and up to 52.0% of ochratoxin A). Mycotoxins hepatic concentrations (fig.: 4 and 5) were high, the liver being the basic organ responsible for detoxification. Supplementation of UNIKE® to the mycotoxins contaminated feed led to a significant raise of mycotoxins excretion from the gastro-intestinal tract. As a result, the absolute content of toxic agents in the liver decreased by 22-42% (p£0.05-0.02).
Fig 4 and 5: Residual mycotoxin concentrations in the liver of birds fed with T2, OTA and FUM contaminated diets supplemented with 0 or 1 kg/ton UNIKE.
The impact of Aflatoxins and Fumonisins contaminated corn
A trial (LAMIC, Federal University of Santa Maria, department of preventive veterinarian medication, Brazil) was set up to investigate the efficacy of the mycotoxin in-activator UNIKE (based on botanicals, yeast and clay-minerals) in counteracting the toxic effects of aflatoxins and fumonisins in broilers. A randomized experimental design with two mycotoxins types (aflatoxins and fumonisins) and four levels of the mycotoxin in-activator were used. Three hundred day-old male Cob broilers were distributed into 5 treatments with 6 replicates of 10 birds. UNIKE was included at 0, 1.5, at 2.5 and at 5.0 kg/ton of feed, contaminated with aflatoxins (1.4 mg/kg) and fumonisins (25 mg/kg). The weight loss at 21 days of age was significantly lower in birds fed with the diet containing the mycotoxin in-activator (resp. 5.1 %, 7.4 % and 7.9 %) than in birds receiving the mycotoxin contaminated control diet(Fig.: 6).
Fig. 6: Average body weight of broilers at 21 days of age. Birds receiving Aflatoxin and fumonisin contaminated diets treated with 0 % (Control), 0.15 %, 0.25 % and 0.50 % UNIKE®. Birds receiving treated feed at 0.25 % and 0.50 % in the contaminated diets showed significant lower liver weight against those receiving the control diet (Fig.: 7).
Fig. 7: Relative liver weight of broilers at 21 days of age. Birds receiving Aflatoxin and fumonisin contaminated diets treated with 0 % (Control), 0.15 %, 0.25 % and 0.50 % UNIKE®. Higher liver weight is an indication of increased liver activity, which is observed in acute aflatoxicosis. (Fig.:8)
Fig. 8: Livers of broilers at 21 days of age. Birds receiving Aflatoxin and fumonisin contaminated diets treated with 0 % (Control), 0.15 %, 0.25 % and 0.50 % UNIKE®. Lipopolysaccharides potentiate the effects of T-2 toxin on oral lesions in broilers (Guaiume, 2005).
An experiment was conducted to investigate the efficacy of the mycotoxic in-activator UNIKE (based on botanicals, yeast and clay-minerals) in broilers (Cobb) challenged with E.coli lipopolysaccharide (LPS) raised from 0 to 21 days of age to counteract the toxic effects of T-2 toxin (T-2). (University of Missouri, Columbia, USA, 2007).
A 2 x 2 x 2 factorial arrangement of dietary treatments was used with 5 pens of 7 chicks (first 12 days) or 5 birds (12-21 days) assigned to each of the dietary treatments. Treatments included a basal diet supplemented with two levels of UNIKE® (0 or 0.3 %), two levels of T-2 (0 or 2.5 ppm) or two levels of LPS (0 or 150 mg/bird). The birds received a first LPS challenge at day 9 and a second at day 19. Creatine phosphokinase (CPK), an indicator for organ injury and stress, showed increased levels in
the blood plasma of birds receiving T2-toxin and LPS, whereas these blood plasma levels were reduced in birds receiving the diet addition of UNIKE at 3 kg/ton. (fig.: 9)
Fig.: 9: Effects of UNIKE® on serum chemistry parameters (CPK) of broiler chicks fed with T-2 toxin and challenged with E.coli lipopolysaccharid. The diet addition of T-2 decreased (p<0.05) feed intake (figure 8) and body weight gain (BWG) after the first and second challenge measured at 21 days. There was an additive T-2 + LPS interaction on BWG
(P< 0.05).(Fig.: 10)
Fig.: 10. Effects of UNIKE® on Performance (feed intake) of broiler chicks fed T-2 toxin and challenged with E.coli lipopolysaccharide. The T-2 diet addition increased (p< 0.05) the numbers of oral lesions, while the addition of UNIKE® decreased the severity of them by 39 %.
The effect of Zearalenone, DON, Aflatoxin, Fumonisin and T2-toxin in pigs’ diets
A trial with 20 weaned pigs (female) was set up in Spain, Zaragoza, to evaluate the zoo technical performance and health condition when offering diets without mycotoxins and with mycotoxins (596 ppb of Zearalenone, 1.56 ppm Vomitoxin (DON), 1 ppb Aflatoxin B1, 1.8 ppm of Fumonisin B1, 22.2 ppb of T2-toxin and the presence of Ochratoxin) where UNIKE® had been included at 0 and 1.5 kg/ton.
The pigs’ body weight was reduced in the group receiving contaminated feed with 39.7 % against those receiving the control diet. The inclusion of UNIKE® in the contaminated diet diminished the negative impact on body weight and feed efficiency significantly.
The alanine amino transferase (ALT) liver enzyme is an indication of hepato-cellular damage. The presence of mycotoxins in the diet has clearly an impact on the pigs (fig.:11). The diet inclusion of UNIKE® in contaminated feed prevented the liver cells from being damaged.
Fig.: 11. Alanine amino transferase enzyme level of the pigs receiving control diet or contaminated diet with 0 or 1.5 kg/ton UNIKE®
The estrogens level in the group receiving natural contaminated feed with UNIKE® remained higher over the whole trial period compared to the control group.
Conclusions
Feeds are obviously contaminated with different types of mycotoxins, which have an impact on nutrient digestion, animal performance and health, even at low concentrations. A multi-functional approach such as UNIKE is essential to counteract the negative influence of these so dissimilar noxious molecules and to reduce the interaction among themselves and with other molecules such as lipo-polysaccharides. Not only the discussed experiments, but also many years of practical experience indicate the necessity of specific concepts to neutralize the toxic effect of mycotoxins for preserving animal health and performance in today’s economic challenged environment.