fbpx

Mycotoxins in the European dairy sector: A guide

19-10-2010 | |
Mycotoxins in the European dairy sector: A guide

Apart from the threat to human health, mycotoxins are associated with economic losses for both crops and animals, including ruminants. Ruminants seem to be more resistant to mycotoxicosis than monogastrics, but clinical signs of acute mycotoxicosis such as reduced feed intake, decreased milk production, and liver damage have also been observed in cattle.

 

 

Fumonisins
Geographic distribution. Fumonisins can cause illness and poor performance of livestock all over the Europe (Germany, France, UK, Italy).

Source of contamination. The majority of fumonisin positive samples are found in cereals: corn and corn derived products, wheat, barley and oats. Silage and hay can be heavily contaminated with fumonisins due to bad storage condition that allow Fusarium mould to grow.
The fermentation process of DDGS production does not destroy mycotoxins, hence, this important raw material for the dairy sector can be a source of fumonisin contamination of feed.

Negative effects. Fumonisin B1 has been shown to be toxic to sheep, goats, beef cattle and dairy cattle. Because of greater production stress, dairy cattle may be more sensitive to fumonisin than beef cattle.

Fumonisins are water-soluble polar compounds, and their absorption from the gastrointestinal tract is very low (about 1%). Fumonisins are degraded by the rumen flora only to very minor extent, and thus seem to be absorbed in the small intestines of ruminants in the same ratio as in monogastric species. Smith and Thakur (1996) and Caloni et al. (2000) found that fumonisin B1 is eliminated from the body mainly unmetabolised.
Ingestion of feed containing 75 ppm fumonisin B1 daily for 14 days by Jersey cows increased serum cholesterol concentration and decreased feed intake and milk production (Richard et al., 1996). Holstein and Jersey dairy cattle fed diets containing 100 ppm fumonisin for approximately 7 days prior to calving and for 70 days thereafter demonstrated lower milk production (6 kg/cow/day), explained primarily by reduced feed consumption (Diaz et al., 2000). Fumonisin carryover from feed to milk is thought to be negligible (Scott et al., 1994).
The liver and the kidneys are the target organs for fumonisin toxicity in ruminants. Toxic threshold levels still need to be defined, but normally they exceed 10 ppm (up to 100 ppm per kg feed), reflecting again the very low bioavailability of fumonisins in comparison to other Fusarium toxins (Fink-Gremmels, 2005).

Carryover. Available data on carryover of fumonisins from animal feeds into milk indicate that transfer is limited and thus residues in animal tissues contribute insignificantly to total human exposure (Opinion of the Scientific Panel on Contaminants in Food Chain on a request from the Commission related to fumonisins as undesirable substances in animal feed).
Maximum limits in feed. The EU recommendation to the maximum limit in feed for adult ruminants is 50 ppm (Table 1).

 
Detoxification of mycotoxins
Many fungal species are capable of simultaneously producing several mycotoxins. Therefore, an individual grain may be naturally contaminated with more than one mycotoxin. Moreover the incorporation of numerous grain sources, which are each contaminated with a different mycotoxin, into a single feed may result in a diet that contains a number of different mycotoxins. Hence, poor livestock performance and/or disease syndromes, reported in commercial operations, may be due to additive, synergistic interactions between multiple mycotoxins.

Prevention of mould infection is the most desirable method of reducing mycotoxins in feeds, although contamination often is unavoidable, even with the best agricultural practices. Therefore, several strategies have been developed to reduce post harvest product contamination. Some of these methods involve early identification and segregation of grossly infected kernels to identify and to reject spoiled grains. Another strategy is the use of detoxifying agents, which prevent absorption of mycotoxins in animals. Many companies and researchers have tried to find means of detoxifying mycotoxin contaminated grains. Most of the treatments have been found to be either too expensive or to have side effects on the end products that reduce the benefits of detoxification. The addition of inorganic adsorbents, along with vitamins, proteins, and trace elements added to feed, have the most positive effects. The adsorbents bind and immobilize the toxins holding them in the intestinal tract, allowing them to be eliminated in urine and faeces.

Conclusions
Dairy farmers face some significant dilemmas. Diarrhoea, lowered feed consumption, mastitis, estrus errors, etc. may be a part of one or more mycotoxins impacts on the dairy animal. However, none of them are unique to fungal toxins and most may more often occur as a result of other factors. Similarly, if one takes the research on ruminal degradation of mycotoxins at first sight, it would seem that ruminants are uniquely protected against these fungal metabolites. How then, can it be that staggers, slobbers, abortion, loss of production can all be induced by a dietary application of certain toxins at levels consistent with what is found naturally under farm conditions?

Various mycotoxins appear to have considerable immunotoxic potential, depending on the level of exposure. The idea that mycotoxins can potentiate or antagonize the action of other mycotoxins is no longer a supposition. It has been proven extensively in the literature. We have little ability to predict what might happen when four or five or more toxins are present together in the animal’s ration. The effects of long-term feeding of mycotoxins at low levels also have not been well characterized.

Key conclusions
Ruminants seem to be more resistant to mycotoxicosis than monogastrics, but clinical signs of acute mycotoxicosis such as reduced feed intake, decreased milk production, and liver damage have also been observed in cattle

In Europe the different climatic conditions among the northern, middle and southern parts favours the development of different fungal species
The diet of a dairy cow generally includes both forages and concentrates, which can increase the probability of multiple mycotoxin contaminations
Prevention of mould infection is the most desirable method of reducing mycotoxins in feeds, although contamination often is unavoidable, even with the best agricultural practices. Therefore, the use of detoxifying agents, which prevent absorption of mycotoxins in animals can reduce post harvest product contamination

Abstract
The inclusion of numerous feedingstuffs of various geographical origins into a dairy cow feed may result in a number of different mycotoxins in a diet. A microbial population including bacteria, protozoa and fungi in the rumen seems to be effective in mycotoxin metabolism in this section of the cow digestive tract. However, mycotoxin metabolites produced in the rumen may be equally or even more toxic than the initial contaminant for the animal itself as well as for the milk consumers.
The article describes the negative effects of the main mycotoxins such as aflatoxins, fumonisins, zearalenone, Trichotecenes, ochratoxin A, citrinin, patulin and ergot alkaloids on a dairy cow performance. A unique summary of mycotoxins carryover from feed into milk is introduced together with European advisory levels of mycotoxins in feed for dairy cattle.
More and more often dairy cow nutritionist suspect moulds in the raw material such as silage, hay, grains are causing a mycotoxin challenge to the cows. The use of inorganic adsorbents has positive effects on a cow performance. They bind and immobilize the mycotoxins holding them in the intestinal tract, allowing them to be eliminated in urine and faeces. Kemin Europa N.V. already experienced the cows yield had risen by 2 litres per head per day within one week with clay-based mycotoxin adsorbent Toxfin®.
 
References:
Battacone, G., Nudda, A., Cannas, A., Cappio Borlino, A., Bomboi, G. and Pulina G. (2003). Excretion of aflatoxin M1 in milk of dairy ewes treated with different doses of aflatoxin B1. J. Dairy Sci. 86: 2667–2675
Böhm, J. and Razzazi-Fazeli, E. (2005). Effects of mycotoxins on domestic pet species. The mycotoxin blue book. pp. 77-92. Nottingham University Press, Nottingham, UK
Breitholtz-Emanuelsson, A., Olsen, M., Oskarsson, A., Palminger, I. and Hult K. (1993). Ochratoxin A in cow’s milk and in human milk with corresponding human blood samples. J. AOAC International. 76: 842-846.
Caloni, F., Spotti, M., Auerbach, H., Camp, H. O., Gremmels, J. F. and Pompa, G. (2000). In vitro metabolism of fumonisin B1 by ruminal microflora. Vet. Res. Com. 24: 379-387
Charmley, E., Trenholm, H. L., Thompsom, B. K., Vudathala, D., Nicholson, J. W. G., Prelusky, D. B. and Charmley, L. L. (1993). Influence of level of deoxynivalenol in the diet of dairy cows on feed intake, milk production, and its composition. J. Dairy Sci. 76: 3580-3587
Colak, H. (2007). Determination of aflatoxin M1 levels in Turkish white and Kashar cheeses made of experimentally contaminated raw milk. J. Food and Drug Analysis 15: 163-168
Coulombe, R. A. (1993). Biological action of mycotoxins. J. Dairy Sci. 76: 880-891
Cundliffe, E. and Davis, J. (1977). Inhibition of initiation, elongation and termination of eukaryotic protein synthesis by trichothecene fungal toxins. Antimicrob. Agents Chemother. 11: 491
Dänicke, S., Matthaus, K., Lebzien, P., Valenta, H., Stemme, K., Überschar, K.–H., Razzazi-Fazeli, E., Böhm, J. and Flachowsky, G. (2005). Effects of Fusarium toxin-contaminated wheat grain on nutrient turnover, microbial protein synthesis and metabolism of deoxynivalenol and zearalenone in the rumen of dairy cows. J. Anim. Physiol. and Anim. Nutr. 89: 303-315
Diaz, D. E., Hopkins, B. A., Leonard, L. M., Hagler Jr., W. M. and Whitlow, L. W. (2000). Effect of fumonisin on lactating dairy cattle. J. Dairy Sci. 83 (abstr.): 1171
Diekman, M. A. and Green, M. L. (1992). Mycotoxins and reproduction in domestic livestock. J. Anim. Sci. 70: 1615-1627
Dörr, J. A. (2003). Effects of mycotoxins on ruminal bacteria and animal performance. Tri-State Dairy Nutrition Conference, April 8-9, 2003, USA
Eriksen, G. S. and Pettersson, H. (2004). Toxicological evaluation of Trichothecenes in animal feed. Anim. Feed Sci. Tech., 114: 205-239
Fink-Gremmels, J. (2005). Mycotoxicoses in animal health. Dept. of Veterinary Pharmacology, Pharmacy and Toxicology, Faculty of Veterinary Medicine, Utrecht University, 3508 TD Utrecht, The Netherlands
Hsu, I. C., Smalley, C. B., Strong, F. M. and Ribelin, W. E. (1972). Identification of T-2 toxin in mouldy corn associated with a lethal toxicosis in dairy cattle. Appl. Microbiol. 24: 684-690
Ingalls, J. R. (1996). Influence of deoxynivalenol on feed consumption by dairy cows. Anim. Feed Sci. Tech. 60: 297-300.
Jouany, J.-P. and Diaz, D. E. (2005). Effects of mycotoxins in ruminants. The mycotoxin blue book. pp. 295-322. Nottingham University Press, Nottingham, UK
Kegl, T. and Vanyi, A. (1991). T-2 fusariotoxicosis in a cattle stock. Magyar Allatorvosok Lapja 46: 467-471
Kiessling, K. H., Pettersson, H., Sandholm, K. and Olsen, M. (1984). Metabolism of aflatoxin, ochratoxin, zearalenone, and three Trichothecenes by intact rumen fluid, rumen protozoa, and rumen bacteria. Appl. Environ. Microbiol. 47: 1070-1073
Kosuri, N. R., Grave, M. D., Yates, S. G., Tallent, W. H., Ellis, J. J., Wolff, I. A. and Nichols, R. E. (1970). Response of cattle to mycotoxins of Fusarium tricinctum isolated from corn and fescue. J. Am. Vet. Med. Assoc. 157: 938-940
Lanyasunya, T. P., Wamae, L. W., Musa, H. H., Olowofeso, O. and Lokwaleput, I. K. (2005). The risk of mycotoxins contamination of dairy feed and milk on smallholder dairy farms in Kenya. Pakistan J. Nutrition 4 (3): 162-169
Mantle, P .G. (1996). Detection of ergot (C/aviceps purpurea) in a dairy feed component by gas chromatography and mass spectrometry. J Dairy Sci. 79:1988-1991
Mirocha, C. J., Weaver, G., Gustafsson, B., Chi, M., Pathre, S. V., Robison, T. S. and Bates, F. (1978). Pharmacological and toxicological studies on zearalenone in food producing animals. Quarterly Report 11, Food and Drug Administration, Washington, DC, USA
Opinion of the Scientific Panel on Contaminants in Food Chain on a request from the Commission related to fumonisins as undesirable substances in animal feed. Request No. EFSA-Q-2003-040 (2005). The EFSA Journal 235: 1-32
Opinion of the Scientific Panel on Contaminants in Food Chain on a request from the Commission related to ochratoxin A (OTA) as undesirable substances in animal feed. Request No. EFSA-Q-2003-039 (2004). The EFSA Journal 101: 1-36
Petrie, L., Robb, J. and Stewart, A. F. (1977). The identification of T-2 toxin and its association with a haemorrhagic syndrome in cattle. Vet. Rec. 101: 326-326
Pettersson, H. (1998). Carryover of aflatoxin from feedingstuffs to milk. Department of Animal Nutrition and Management, Swedish University of Agricultural Sciences, Upsala, Sweden
Pier, A. C., Richard, I. L. and Cysewski, S. J. (1980). The implications of mycotoxins in animal disease. J. Am. Vet. Med. Assoc. 176: 719
Richard, J. L., Meerdink, G., Maragos, C. M., Tumbleson, M., Bordson, G., Rice, L. G. and Ross, P. F. (1996). Absence of detectable fumonisins in the milk of cows fed Fusarium proliferatum (matsushima) Nierenberg culture material. Mycopathologia 133: 123-126
Scott, P. M., Delgado, T., Prelusky, D. B., Trenholm, H. L. and Miller, J. D. (1994). Determination of fumonisin in milk. J. Environ. Sci. Health. B29: 989-998
Sharma R. P. (1993). lmmunotoxicity of mycotoxins. J. Dairy Sci. 76: 892-897
Seeling, K., Lebzien, P., Dänicke, S., Spilke, J., Sudekum, K.-H. and Flachowsky, G. (2006). Effects of level of feed intake and Fusarium toxin-contaminated wheat on rumen fermentation as well as on blood and milk parameters in cows. J. Anim. Physiol. and Anim. Nutr. 90: 103-115
Smith, T. K. and MacDonald, E. J. (1991). Effect of fusaric acid on brain regional neurochemistry and vomiting behavior in swine. J. Anim. Sci. 69: 2044-2049
Smith, J. S. and Thakur, R.A. (1996). Occurrence and fate of fumonisins in beef. Adv. Exp. Med. Biol. 392: 39-55
Tiemann, U., Viergutz, T., Jonas, L. and Schneider, F. (2003). Influence of the mycotoxins α- and β-zearalenol and deoxynivalenol on the cell cycle of cultured porcine endometrial cells. Reprod. Toxicol. 5506: 1-10
Trenholm, H. L., Hamilton, R. M. G., Friend, D. W., Thompson, B. K. and Hartin, K. E. (1984). Feeding trials with vomitoxin (deoxynivalenol)-contaminated wheat: Effects on swine, poutry and dairy cattle. J. Am. Vet. Med. Assoc. 185: 527-531
Ueno, Y. (1984). Toxicological features of T-2 and related Trichothecenes. Fund. Appl. Toxicol. 4: 124
Veldman A., Meijst, J. A. C., Borggereve, G. J. and Heeres-van der Tol, J. J. (1992). Carry-over of aflatoxin from cow’s food to milk. Anim. Prod. 55, 163-168
Weaver, G. A., Kurtz, H. J. and Behrens, J. C. (1986). Effect of zearalenone on the fertility of virgin dairy heifers. Am. J. Vet. Res. 47: 1395-1397
Weaver, G. A., Kurtz, H. J., Mirocha, C. J., Bates, F. Y., Behrens, J. C., Robison, T. S. and Swanson, S. P. (1980). The failure of T-2 mycotoxin to produce hemorrhaging in dairy cattle. Can. Vet. J. 21: 210-213
Whitlow, L. W. and Hagler, W. M. (2006). Mycotoxins: managing a unique obstacle to successful dairy production. Penn State Dairy Cattle Nutrition Workshop, 2006, USA
Whitlow, L. M., Nebel, R. L., Behlow, R. F., Hagler, W. M. and Brownie, C. F.-G. (1986). Mycotoxins in North Carolina dairy feeds – a survey of 100 dairy farms. J. Dairy Sci. 69 (Suppl. 1): 223 (Abstr.)

Join 26,000+ subscribers

Subscribe to our newsletter to stay updated about all the need-to-know content in the feed sector, three times a week.
Contributors
Contributors Global Feed Sector Authors