Use of gaseous ozone to reduce aflatoxin B1 and microorganisms in poultry feed

This study was undertaken to evaluate the efficacy of gaseous ozone for the degradation of aflatoxin B₁ (AFB₁) and inactivation of indigenous microflora in poultry feed. Feed samples were treated with continuous stream of two different constant concentrations (2.8 and 5.3 mg/L) of ozone at room temperature up to 240 min. The initial AFB₁ level in artificially contaminated feed samples, determined as 32.8 μg/kg, decreased by 74.3 and 86.4% after 240 min of exposure at 2.8 and 5.3 mg/L, respectively. At the both ozone concentrations, 240 min exposure was reduced the aerobic plate and yeast and mold counts below the detection limit (<10 CFU/g) with a reduction more than 3.2 and 2.7 log, respectively. The thiobarbituric acid reactive substances (TBARS) assay indicated that no significant (P ≥ 0.05) increase occurred in the level of lipid oxidation in feed samples during 120 min ozonation at 2.8 mg/L. At the end of the 240 min of exposure at 2.8 and 5.3 mg/L, initial TBARS concentration, determined as 2.4 mg/kg, reached to 4.4 and 5.3 mg/kg with a significant (P < 0.05) increases, respectively. The results presented in this study suggested that significant (P < 0.05) reductions in the AFB₁ level and microbial population can be achieved in poultry feed by ozonation with an acceptable changes in lipid oxidation.     

Effectiveness of modified yeast cell wall extracts to reduce aflatoxin B1 absorption in dairy ewes

This study investigated the effect of a modified yeast cell wall extract preparation (YCW) on the excretion of aflatoxin B1 (AFB1) and aflatoxin M1 (AFM1) in feces, urine, and milk of dairy ewes fed an aflatoxin-contaminated diet. Sixteen ewes in mid-lactation were assigned to 4 treatment groups: control, AF (60 μg of AFB1/kg of feed), YCW (2 g/kg of feed), and AF+YCW. The trial consisted of a short-term (3-d) exposure period followed by a long-term (21-d) exposure period. At the end of each exposure period, milk, urine, and feces were collected over 72 h. The treatments did not affect feed intake, milk production, milk composition, or body weight. The presence of AFM1 was detected in all matrices, whereas AFB1 was only present in feces. Daily excretion was higher following long-term exposure and reached 26.9 μg of AFB1/d in feces, 37.2 μg of AFM1/d in feces, and 10.7 μg of AFM1/d in urine. Supplementation with YCW was effective in increasing aflatoxin excretion in feces in the long-term exposure (up to 156% increase). The effect was accompanied by a trend of decreasing urinary excretion of AFM1. In contrast, the addition of YCW to the contaminated diet did not affect the transfer of aflatoxins from feed to milk under the present experimental conditions with low-producing ewes. The transfer rates of AFM1 in milk ranged from 0.24 to 0.54%. In conclusion, feed supplementation with YCW reduced the absorption of AFB1 and increased the elimination of AFB1 and AFM1 in ewe feces. Yeast cell wall extract could be used to protect ruminants from chronic exposure to aflatoxins present in feeds.     

Human aflatoxin exposure in Kenya, 2007: a cross-sectional study

Aflatoxins contaminate approximately 25% of agricultural products worldwide. They can cause liver failure and liver cancer. Kenya has experienced multiple aflatoxicosis outbreaks in recent years, often resulting in fatalities. However, the full extent of aflatoxin exposure in Kenya has been unknown. Our objective was to quantify aflatoxin exposure across Kenya. We analysed aflatoxin levels in serum specimens from the 2007 Kenya AIDS Indicator Survey – a nationally representative, cross-sectional serosurvey. KAIS collected 15,853 blood specimens. Of the 3180 human immunodeficiency virus-negative specimens with ≥1 mL sera, we randomly selected 600 specimens stratified by province and sex. We analysed serum specimens for aflatoxin albumin adducts by using isotope dilution MS/MS to quantify aflatoxin B1-lysine, and normalised with serum albumin. Aflatoxin concentrations were then compared by demographic, socioeconomic and geographic characteristics. We detected serum aflatoxin B1-lysine in 78% of serum specimens (range = <LOD–211 pg/mg albumin, median = 1.78 pg/mg albumin). Aflatoxin exposure did not vary by sex, age group, marital status, religion or socioeconomic characteristics. Aflatoxin exposure varied by province (p < 0.05); it was highest in Eastern (median = 7.87 pg/mg albumin) and Coast (median = 3.70 pg/mg albumin) provinces and lowest in Nyanza (median = <LOD) and Rift Valley (median = 0.70 pg/mg albumin) provinces. Our findings suggest that aflatoxin exposure is a public health problem throughout Kenya, and it could be substantially impacting human health. Wide-scale, evidence-based interventions are urgently needed to decrease exposure and subsequent health effects.     

Biological reduction of aflatoxin B1 in yogurt by probiotic strains of Lactobacillus acidophilus and Lactobacillus rhamnosus

Food Science and Biotechnology - The present study was conducted to investigate the ability of two probiotic strains, L. acidophilus PTCC 1643 and L. rhamnosus PTCC 1637, to bind aflatoxin B1...     

Determination of aflatoxin B1 levels in peanut butter using an immunoaffinity column clean-up procedure: inter-laboratory study

Ten United Kingdom laboratories participated in an evaluation of an immunoaffinity column sample preparation procedure used to prepare aflatoxin B1 containing extracts obtained from peanut butters contaminated by aflatoxins. Each laboratory was sent seven randomly numbered samples of roasted peanut butter which included two sets of undisclosed triplicates. These two peanut butters were naturally contaminated with aflatoxin B1 at levels of about 12 and 35 micrograms/kg. The other sample was a nominal blank peanut butter containing approximately 2 micrograms/kg of aflatoxin B1 which was also employed by participants for recovery experiments. Participating laboratories were instructed to follow a protocol regarding the use of the immunoaffinity columns for extract preparation, but were allowed a free choice of instrumental technique for quantification of aflatoxin levels. Mean recovery for spikes was 72%. Coefficients of variation for the results from the 10 participants for the two contaminated roasted peanut butters were, respectively, 45% (on a mean of 13.6 micrograms/kg) and 36% (on a mean of 37.2 micrograms/kg).     

Binding of aflatoxin B1 to bifidobacteria in vitro

Aflatoxins are mycotoxins that cause health and economic problems when they contaminate food and feed. One potential method for reducing human health effects due to aflatoxin ingestion is to block uptake via binding by bacteria that either make up the normal gut flora or are present in fermented foods in our diet. These bacteria would bind aflatoxin and make it unavailable for absorption in the intestinal tract. Bifidobacteria comprise a large fraction of the normal gut flora, are thought to provide many probiotic effects and are increasingly used in fermented dairy products. These qualities targeted bifidobacteria for studies to determine if various strains of heat-killed bifidobacteria can bind aflatoxin B1 (AFB1) in vitro. The AFB1 binding affinities of various strains of bifidobacteria, Staphylococcus aureus, and Escherichia coli were quantitated utilizing enzyme-linked immunosorbent and [3H]AFB1 binding assays. The bacteria analyzed were found to bind significant quantities of AFB1 ranging from 25% to nearly 60% of the added toxin. The data also suggest that there are reproducible strain differences in AFB1 binding capacity.     

Exposure to aflatoxins in Japan: risk assessment for aflatoxin B1

The intake of total aflatoxins (AFT) and aflatoxin B₁ (AFB₁) from food in Japan was estimated from AFT and AFB₁ concentration and frequency data in 24 foods (884 samples) from a 3-year retail market survey from the summer of 2004 to the winter of 2006, and by food consumption data from the National Health and Nutrition Survey performed in 2005. The AFT and AFB₁ survey revealed that peanut, peanut products, cocoa, chocolate, pistachio, white pepper, red pepper, almond, job's tears, buckwheat and corn grits are considered to be contributors of AFT (or AFB₁) intake in Japan (maximum AFB₁ (AFT) levels ranged from 0.21 to 28.0 µg kg^?1 (from 0.21 to 9.0 µg kg^?1)) in AFT-contaminated food. A probabilistic approach using the Monte Carlo method was carried out to simulate an estimate of the AFT (or AFB₁) intake distributions in each age group in Japan. In this study, AFB₁ intake ranged from 0.003 to 0.004 ng kg^?1 body weight day^?1 (from lower to upper limits), and the potential risk for cancer using a formula devised by the Joint Food and Agricultural Organization/World Health Organization (FAO/WHO) Expert Committee on Food Additives (JECFA) was estimated at 0.00004–0.00005 person/year/100,000 persons, even though this was in the higher levels (95.0th percentile) of the consumer population. The results suggest that the current dietary intake of AFB₁ in Japan has no appreciable effect on health.     

细菌降解黄曲霉毒素B1的研究进展

黄曲霉毒素B1是目前已发现的黄曲霉毒素中毒性最强的一种,其具有强肝毒性、高致突变性和高致畸性。广泛存在于农产品及饲料食品中,对人类健康存在严重威胁,同时对粮食和畜牧业造成严重的经济损失。细菌降解黄曲霉毒素B1是一种有效、安全和环保的解毒方法,该文通过对黄曲霉毒素B1降解的影响因素、细菌胞外酶和胞内酶等对黄曲霉毒素B1的降解机理以及黄曲霉毒素B1降解菌活性产物的应用研究等方面对细菌降解黄曲霉毒素B1进行了论述,并对细菌降解黄曲霉毒素B1应用前景进行展望,为以后更进一步研究提供较为全面的资料。     

EC-collaborative study on the determination of aflatoxin B1 in animal feeding stuffs

A collaborative study was conducted to test a method, proposed in the European Community (EC) as a candidate-official method for the determination of aflatoxin B1 in compounded feeding stuffs. The study was undertaken on behalf of the European Commission's Community Bureau of Reference (BCR). It involved 25 laboratories from 11 EC countries. The method, based on chloroform extraction and Sep-Pak Florisil and C18 cartridge clean-up, offered either reverse-phase high performance liquid chromatography (HPLC) with iodine post-column derivatization, or two-dimensional thin-layer chromatography (TLC) as determinative steps. In the study, 22 laboratories applied HPLC, three laboratories applied TLC. The study involved six unknown samples. These consisted of blind duplicate samples of compounded feeding stuff, with target concentrations of aflatoxin B1 at less than 2, 8 and and 14 micrograms/kg. Statistical analysis of the HPLC data was carried out according to ISO 5725. For the less than 2 micrograms/kg sample, all reported aflatoxin concentrations were less than 2 micrograms/kg. At the 8 and 14 micrograms/kg level (pooled), repeatability (r) and reproducibility (R), expressed as ratios, were 1.4 and 1.7 respectively, and within-laboratory and between-laboratory coefficients of variation were 11% and 18% respectively. The study revealed that admittance of daylight in the laboratory caused losses of aflatoxin B1 and must be avoided. New glassware coming into contact with aqueous solutions containing aflatoxin B1 was found to be a potential cause of loss of aflatoxin B1. The method has been recommended to the European Commission to be considered for adoption in EC regulations.     

Transfer of aflatoxin B1 and fumonisin B1 from naturally contaminated raw materials to beer during an industrial brewing process

The aim of this research was to determine the fate of aflatoxins (AFs) and fumonisins (FBs) naturally occurring in raw materials (maize grit and malted barley) during four industrial brewing processes. The aflatoxin B₁ (AFB₁) level in raw materials varied from 0.31 to 14.85 µg kg^?1, while the fumonisin B₁ (FB₁) level (only in maize grit) varied from 1146 to 3194 µg kg^?1. The concentration in finished beer ranged from 0.0015 to 0.022 µg l^?1 for AFB₁ and from 37 to 89 µg l^?1 for FB₁; the other aflatoxins and fumonisin B₂ were not found in beer samples. The average percentage of toxins recovered in finished beer, referring to the amounts contained in raw materials, were 1.5% ± 0.8% for AFB₁ and 50.7% ± 4.7% for FB₁. These results were mainly due to the different solubility of the two mycotoxins during the mashing process. If raw materials comply with the limits fixed by European Commission Regulations, the contribution of a moderate daily consumption of beer to AFB₁ and FB₁ intake does not contribute significantly to the exposure of the consumer.     

Assessment of dietary exposure to aflatoxin B1 from corn arepas in Colombia

ABSTRACT

The aim of this research was to evaluate dietary exposure to aflatoxin B1 (AFB₁) in corn arepas in Colombia. In addition, in this study an assessment considering compliance to the maximum level of AFB₁ (4 µg kg^?1) for this food was conducted. AFB₁ concentration data in corn arepas were obtained from 168 samples. The samples were collected from factories in 16 departments in Colombia. AFB₁ was quantified by High-Performance Liquid Chromatography with a fluorescence detector. Consumption data and body weight (b.w.) were measured from the 2005 Colombian National Survey of Nutritional Status. Probabilistic estimates were made by Monte Carlo simulation of dietary exposure and margin of exposure (MOE) segmented by age group. The results showed that 27% of corn arepa samples were contaminated with AFB₁, with an average concentration of 15.1 µg kg^?1 and a maximum value of 111.1 µg kg^?1. The stochastic dietary exposure assessment showed that the age group most exposed was children between 4 and 8 years old (10.014 ng (kg b.w. day)^?1). In addition, the MOE values for all age groups were lower than 10,000, indicating a potential risk for consumers. However, in the scenario where AFB₁ concentration level complies with the maximum limit of 4 µg kg^?1 AFB₁, the level of concern could be reduced for the adult population between 14 and 64 years old because the MOE value is above 10,000.     

云南省部分食品黄曲霉毒素B1膳食暴露风险评估

目的评估云南省部分食品中黄曲霉毒素B1(aflatoxinB1,AFB1)膳食暴露风险。方法结合2012～2017年云南省部分地区市售大米及其制品、玉米及其制品等6类主要食品的黄曲霉毒素B1含量数据,以及本省营养监测消费量数据,采用点评估方法对云南省居民AFB1暴露水平进行评估。结果云南省全人群来源于6类食品的AFB1暴露量为1.02×10-3μg/kgbw,其中来源于大米的AFB1暴露量最高,占总暴露量的50.98%,其次是玉米及其制品,占18.63%。总暴露量为大城市贫困农村中小城市一般农村;云南省居民AFB1膳食暴露量对肝癌发病率的贡献为0.040/10万人;各地区居民暴露边界比(margin of exposure, MOE)值介于144.07～180.85之间。结论云南省AFB1污染状况相对良好,仍需持续关注; 6类食物中大米、玉米是云南省AFB1的主要暴露来源。     

Dietary mycotoxins binders: a strategy to reduce aflatoxin m1 residues and improve milk quality of lactating Beetal goats

Aflatoxin M1 (AFM1) is a metabolite of aflatoxin B1 (AFB1) and secreted in milk of animals that are kept on a moldy diet. AFB1 is produced by several toxigenic species of fungi. In this study, the comparative efficacy of two mycotoxin binders was evaluated in terms of reducing excretion of AFM1, total viable bacterial count and somatic cell count in milk obtained from goats fed with AFB1 contaminated diet. A total of 32 lactating Beetal goats were reared and divided into 4 equal groups: Animals of group A were kept as control, while those in groups B, C, and D were individually fed with AFB1 at 40 µg alone, 40 µg AFB1 along with mycotoxin binder Toxfin^® at 3 g kg^?1 of cotton seed cake, and 40 µg AFB1 along with mycotoxin binder Elitox^® at a dose rate of 1 g kg^?1 of cotton seed cake, respectively. Toxfin^® significantly decreased the excretion of AFM1 in goats’ milk by 49.57 % while Elitox^® non-significantly reduced the excretion of AFM1 in goats’ milk by 19.49 %. Total viable bacterial count in milk samples of group C and D, and somatic cell count in milk samples of group C did not reduce significantly. However, somatic cell count in milk samples of group D reduced significantly. We conclude that the addition of Toxfin^® in the moldy diet significantly reduce the excretion of AFM1 in animals’ milk and minimize the risk of mycotoxin toxicity to public health.     

Spontaneously fermented millet product as a natural probiotic treatment for diarrhoea in young children: an intervention study in Northern Ghana

Indigenous lactic acid fermented foods may have potential as probiotic treatment for diarrhoea, due to high levels of lactic acid bacteria. In this study the effect of a millet drink, spontaneously fermented by lactic acid bacteria, as a therapeutic agent among Ghanaian children with diarrhoea, was assessed. Children below 5 years of age coming to Northern Ghana health clinics for treatment of diarrhoea were randomised to two groups. Children of both groups received treatment for diarrhoea given at the local clinic. The intervention group in addition received up to 300 ml fermented millet drink (KSW) daily for 5 days after enrolment. The clinical outcome of diarrhoea and reported well-being were registered every day for the 5-day intervention and again 14 days after diagnosis. Among 184 children (mean age 17.4, standard deviation 11.3 months) included, no effects of the intervention were found with respect to stool frequency, stool consistency and duration of diarrhoea. However, KSW was associated with greater reported well-being 14 days after the start of the intervention (P = 0.02). The fact that no effect of KSW on diarrhoea was observed could be because many children had a mild form of diarrhoea, and many were treated with antibiotics. Either this could have affected the lactic acid bacteria, or the lactic acid bacteria in KSW had no probiotic effects. It is speculated that the effect after two weeks could be due to a preventing effect of KSW on antibiotic-associated diarrhoea which could help reducing persistent diarrhoea.     

Efficacy of Solis, NovasilPlus, and MTB-100 to reduce aflatoxin M1 levels in milk of early to mid lactation dairy cows fed aflatoxin B1

An experiment was conducted to determine the efficacy of 3 adsorbents, Solis (SO; Novus International Inc.), NovasilPlus (NOV; Engelhard Corp.), and MTB-100 (MTB; Alltech), in reducing aflatoxin (AF) M₁ concentrations in milk of dairy cows fed an AF-contaminated diet. Twelve early to mid lactation dairy cows averaging 163 d in milk were used in a 4 × 4 Latin square design with 3 replications. Cows were blocked by parity, body weight, and milk production and were provided ad libitum access to feed and water. Within each replicate, cows were randomly assigned to the 4 dietary treatments for 4 consecutive 7-d periods. Dietary treatments included AF [112 μg of AFB₁/kg of diet dry matter (DM)]; AF + 0.56% SO; AF + 0.56% NOV; and AF + 0.56% MTB. Milk samples were collected on d 6 and 7 of each of the experimental periods. Feed intake, milk production, milk fat percentage, milk protein percentage, and linear somatic cell scores were not affected by dietary treatments and averaged 22.20 kg/d of DM, 33.87 kg/d, 3.78%, 2.95%, and 1.60, respectively, across all treatments. Transfer rates of AF from feed to milk averaged 2.65, 1.48, 1.42, and 2.52% for cows fed AF, AF + SO, AF + NOV, and AF + MTB, respectively. Daily AFM₁ excretion in milk averaged 66, 37, 35, and 63 μg/d for cows fed AF, AF + SO, AF + NOV, and AF + MTB, respectively. The addition of SO and NOV to the AF diet resulted in a significant reduction in milk AFM₁ concentrations (SO, 45%; NOV, 48%) and AFM₁ excretion (SO, 44%; NOV, 46%). In contrast, MTB was not effective in reducing milk AFM₁ concentrations (4%), AFM₁ excretion (5%), or AF transfer from feed to milk (2.52%). Results indicated that SO and NOV at 0.56% of the diet were effective in reducing milk AFM₁ concentrations in cows consuming a total mixed ration containing 112 μg of AFB₁/kg of diet DM.     

Enzyme-linked immunosorbent (ELISA) determination of aflatoxin B1 in peanut butter: collaborative trial

Fourteen laboratories in the United Kingdom participated in a collaborative trial of a commercially available ELISA test kit for the determination of aflatoxin B1 in peanut butter. Each laboratory carried out six replicate analyses of each of six individual samples. Collaborators received a control, uncontaminated sample, together with samples prepared by blending naturally-contaminated and control material to give target levels of 8 micrograms/kg, 25 micrograms/kg and 75 micrograms/kg. Two of these samples (8 micrograms/kg and 25 micrograms/kg) were supplied as undisclosed duplicates. The repeatabilities of the assay ranged from 6.2 to 16.7 micrograms/kg. The reproducibilities for aflatoxin B1 concentrations in naturally-contaminated samples ranged from 3.6 to 18.7 micrograms/kg using uncontaminated peanut butter as a reference blank. Modifications to the format of the commercial kit were recommended as a result of the collaborative trial.     

Studies on damage to sunflower seeds: water activity, germination, acidity index and aflatoxin B1 presence

The significance of fungal contamination during the storage of sunflower seeds has been investigated. Samples were taken during 7 months at 45 day-intervals. Water activity, seed germination, presence of aflatoxin B1 and free fatty acids were monitored. It was demonstrated that water activity increased during storage, germinability decreased, the content of free fatty acid increased and so did the content of aflatoxin B1.