Nutrition Notes Mold and Mycotoxins The following information was derived from an Ohio State University (OSU) website that is a cooperative effort among numerous land grant universities. Table 1 summarizes the main mycotoxins that affect livestock production. Species, mycotoxin, upper limit of safety and their effects are noted. Also included in this OSU document are preventative practices pre-harvest and post-harvest, as well as steps and methods for testing. MOLDY GRAINS, MYCOTOXINS AND FEEDING PROBLEMS Preventive Practices Prevention is the best method to control mold growth and possible toxin formation. The following practices can help minimize mold growth and subsequent toxin production in storage: Pre-harvest: Clean inside and outside of grain bins and dryers. Prior to storage, check the condition of the bin for possible water leaks, and clean it properly by removing dust, dirt, leftover grain and other foreign material. Crop rotation in many regions or tillage can reduce the risk of Gibberella ear rot in corn and Fusarium head blight of wheat. These practices have little effect on other corn ear rots. Some corn hybrids are more resistant to ear rots than others, but overall, resistance to ear rots is not widely available. Some Bt hybrids, those that produce BT in the kernels, have less ear rot due to insect control resulting in less toxin problems. Control of second generation European corn borers and other insect pests of corn ears can greatly reduce infection by Fusarium and Aspergillus. Few wheat varieties have high levels of resistance to Fusarium head blight (scab). Plant moderately resistant varieties when available. Planting several varieties that differ in maturity will reduce the risk of disease to the whole crop. As with any crop pest, early detection through scouting and early harvest can reduce serious losses and avoid crises. Decisions on handling moldy grain should be made before it is harvested. After harvest, spoilage can occur quickly if delays result from indecision. If extensive ear rot development is observed (10% or more of the ears with more than 10-20% mold), the field should be harvested as soon as moisture content reaches a level that can be harvested. Even if some drying costs are incurred, this will be less expensive than loss of crop value due to mycotoxins and resulting feeding problems. Post-harvest: The crops should be allowed to mature in the field to the following moisture contents: shelled corn, 23-25%; ear corn, 20-25%; small grain, 12-17%; and soybeans, 11-15%. Harvesting equipment should be adjusted to minimize damage to seeds or kernels and allow for maximum cleaning. Cracked or broken seeds or kernels are more susceptible to mold invasion. Upon storage, dry the grain to 13-14%, if possible, within 48 hours. Long-term storage can be achieved at a uniform moisture of 18% for ear corn; 13% for sorghum, wheat and shelled corn; and 11% for soybeans. After drying, store under cool temperatures (36-44° F). Every few weeks check the condition of the grain for temperature, wet spots and insects. Testing for Mycotoxins: The presence of a fungus known to produce toxins is not proof that the grain contains injurious levels of toxin. It may be a good investment to collect a representative sample and send it to a laboratory for chemical analysis. The first step in mycotoxin determination is sampling of the grain. Particular attention should be given to the sampling procedure because sampling error will be the greatest source of variation in the analytical procedure. This variation is primarily due to the uneven distribution of the mycotoxin contaminated kernels within a lot of grain or feed. The ideal sampling procedure should assure the highest probability of detecting mycotoxins even when contamination is low. One method of sampling grain is to use a probe sampler. Since mold growth usually occurs in spots in the grain lot, best sampling is done on recently blended lots of grain. Another method is to collect small samples from the moving stream of grain as it is moved in or out of the bins. With both sampling methods, the collected grain is pooled into a large aggregate sample that represents the lot. For shelled corn, it is recommended that the aggregate sample be about 10 pounds. The aggregate sample should be coarsely ground. Most analytical procedures need only about 25 grams (0.9 ounces) of ground corn, so it is important that the aggregate sample be thoroughly mixed after grinding. A one or two pound sub-sample is then taken and it is more finely ground. From this sub-sample a final sample is taken for analysis. A number of commercial, university and government laboratories perform mycotoxin analyses for a fee. Contact the lab to determine the proper way to obtain and ship the sample. Blending is not an approved practice by the FDA for interstate commerce. Blending is a practice intended to reduce toxins to acceptable levels in small lots only for on-farm use. If the mycotoxin in the contaminated feed is known, it may be a good idea to channel the feed to animals that are more tolerant. ZEARALENONE Table 1: Mycotoxins Reported Detrimental Feed Concentrations (ppm=parts per million) Swine Concentration Duration Effect Prepubertal gilts 1-5 ppm 3-7 days Hyperestrogenism, prolapse Sexually mature open gifts 3-10 ppm Mid-cycle (day 11-14) Anestrus, pseudopregnancy Bred sows 15-3 ppm 1st trimester Early embryonic death, small litters Juvenile boars 10-50 ppm Indefinite Reduced libido, small testicles Mature boars 200 ppm Indefinite No effect Cattle Concentration Duration Effect Virgin heifers 12 ppm Open Heifers Reduced conception Dairy Cows 50 ppm Open cows Reduced conception DEOXYNIVALENOL (vomitoxin, DON) Swine Concentration Duration Effect Feeder pigs 1-3 ppm 1-5 days Reduced feed intake Feeder pigs 5-10 ppm 1-5 days 50% reduction in feed intake, vomiting Feeder pigs 10-40 ppm 1-5 days Complete feed refusal, vomiting Sows 3-5 ppm Gestation, lactaction Lower fetal weights, or no effect Cattle Concentration Duration Effect Feeder Cattle 10 ppm Indefinite No effect Dairy Cows 6 ppm 6 weeks No effect or slightly reduced feed intake Dairy Cows 12 ppm 10 weeks No effect on milk production Poultry Concentration Duration Effect Broilers and turkey poults 50 ppm Indefinite No effect FUMONISINS (FB1 and/or FB2) Horses Concentration Duration Effect All classes All classes >10 ppm Liver damage, leucoencephalomalacia, death Swine Concentration Duration Effect All classes and ages >25 ppm 30 days Reduced gain and feed efficiency, mild liver damage All classes and ages >50 ppm 10 days Reduced gain and feed efficiency, moderate liver damage All classes and ages >100 ppm 5 days Severe pulmonary edema, death Cattle and Sheep Concentration Duration Effect All classes and ages > 100 ppm 30 days Slightly reduced gain, mild liver damage All classes and ages > 200 ppm 14 days Reduced feed intake and gain, moderate liver damage Turkeys Concentration Duration Effect All classes and ages >100 ppm 7-21 days Reduced feed intake, liver damage, diarrhea, rickets, tibial lesions Chickens Concentration Duration Effect All classes and ages > 200 ppm 7-21 days Reduced feed intake, liver damage, diarrhea, rickets, tibial lesions FDA’s guidance level for total fumonisins in corn and corn by-products (not to exceed 20% of the diet) used for equine and rabbit feed products is 5 ppm (1 ppm in finished feed). AFLATOXINS (ppb=parts per billion) Swine Concentration Effect All classes and ages 200 ppb Slow growth, reduced feed efficiency All classes and ages 400 ppb Liver damage and immune suppression Feeder Cattle Concentration Effect All classes and ages 400 ppb Tissue residues All classes and ages 700 ppb Mild liver damage, reduced growth and feed efficiency All classes and ages 1000 ppb Moderate liver damage and weight loss All classes and ages 2000 ppb Severe liver damage, jaundice, death Diary Cows Concentration Effect Lactating cows 20 ppb Detectable aflatoxin in milk Lactating cows 1500 ppb Decreased milk production Poultry Concentration Effect Broiler chicks 210 ppb No effect Turkeys 250 ppb Reduced growth Broiler chicks 420 ppb Lose weight, moderate liver damage after 3 weeks Horses Concentration Effect All classes and ages 400 ppb Liver damage and immune suppression Munkvold, G., Osweiler, G., Hartwig, N. 1997 Iowa State University Ext. 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