Occurrence of mycotoxins in feed ingredients and complete feeds obtained from the Beijing region of China
- Xiaoying Li†1,
- Lihong Zhao†1,
- Yu Fan1,
- Yaxiong Jia2,
- Lei Sun3,
- Shanshan Ma1,
- Cheng Ji1,
- Qiugang Ma1 and
- Jianyun Zhang1Email author
© Li et al.; licensee BioMed Central Ltd. 2014
Received: 7 January 2014
Accepted: 16 July 2014
Published: 22 July 2014
The current study was carried out to provide a reference for the control of mycotoxin contamination in feed ingredients and complete feeds for swine.
A total of 55 feed ingredients, including 14 corn, 13 wheat bran, 11 soybean meal and 17 dried distillers grains with solubles (DDGS) as well as 76 complete swine feeds including 7 creep feeds, 14 starter feeds, 14 grower feeds, 18 grower-finisher feeds, 10 gestating sow feeds, and 13 lactating sow feeds were randomly collected from 15 swine farms located in the Beijing region of China from July to August 2011. Immunoaffinity clean-up, using High-Performance Liquid Chromatography (HPLC) in combination with UV or Fluorescence Detection, was used for quantitative analysis of aflatoxin B1 (AFB1), deoxynivalenol (DON), zearalenone (ZEA) and ochratoxin A (OTA) in the ingredients and complete feeds.
DON and ZEA were the most prevalent mycotoxins found. DON was detected at percentages of 93, 92, 54, 100 and 97% with a mean level of 1.01, 0.44, 0.05, 1.36 and 0.65 ppm in the samples of corn, wheat bran, soybean meal, DDGS and complete feeds, respectively. The detected percentages of ZEA were 100, 100, 54, 100 and 100 with mean levels of 109.1, 14.9, 9.2, 882.7 and 58.9 ppb in the same samples. In the wheat bran and soybean meal samples, the content of all four mycotoxins were below the maximum limits set by Chinese regulations while the percentage of samples that exceeded regulatory limits were 7, 57 and 7% for corn, and 7, 14 and 3% for the complete feeds for AFB1, DON and OTA respectively. DDGS showed the most serious mycotoxin contamination and the percentage of samples that exceeded regulatory limits were 6, 88 and 41%, for AFB1, DON and ZEA, respectively.
This paper is the first to present data on the natural occurrence of AFB1, DON, ZEA and OTA in ingredients and complete feeds obtained from swine farms in China’s Beijing region. The data shows that feed ingredients and complete swine feeds obtained from these farms are most often contaminated with DON followed by contamination with AFB1 and ZEA.
KeywordsAflatoxinB1 Beijing region Deoxynivalenol Ochratoxin A Swine feeds Zearalenone
Mycotoxins are a large group of fungal metabolites found worldwide in cereal grains and other feed products. Mycotoxins pose a severe threat to humans and as well as causing huge economic losses in the feed and food industries . Aflatoxin, deoxynivalenol (DON), zearalenone (ZEA) and ochratoxin A (OTA) are considered the most economically important mycotoxins in terms of their prevalence and their negative effects on animal performance [2, 3]. Pigs are particularly susceptible to mycotoxins, suffering a variety of chronic or acute syndromes depending on the amount of contaminants they consume .
Aflatoxins are the most potent of the known mutagenic and carcinogenic natural substances produced by Aspergillus spp. . There are six types of aflatoxins that frequently contaminate feeds and foods, including B1, B2, G1 and G2. Aflatoxin B1 (AFB1) has long been considered one of the most poisonous carcinogens . A potent hepatocarcinogenic and hepatotoxic mycotoxin , it has been placed in Group ΙA by the International Agency for Research on Cancer IARC: .
DON is one of the most frequently detected trichothecene contaminants in cereals . The ingestion of feeds contaminated with DON leads to feed refusal and weight loss, decreases nutritional efficiency and causes lesions in the gastrointestinal tract, vomiting, bloody diarrhea and severe dermatitis accompanied by hemorrhaging and immune dysregulation. Swine are typically the most sensitive of the susceptible species in that they exhibit the most severe symptoms of acute DON toxicity [10, 11].
ZEA is a non-steroidal estrogenic toxin produced by certain Fusarium species . ZEA can competitively bind to estrogen receptors leading to reproductive disorders and estrogenic dysfunction in humans and animals (especially in breeding animals), impairing fertility and increasing the frequency of stillbirths along with reducing sperm quality [12, 13]. Swine are the animal species most severely affected by ZEA [14, 15].
OTA, produced by the Penicillium verrucosum fungus and various species of Aspergillus is a nephrotoxic mycotoxin that causes renal toxicity and possesses carcinogenic, teratogenic immunotoxic and possibly neurotoxic properties . This toxin has been classified by the IARC as a possible human carcinogen . Research on the effects of this mycotoxin in swine has revealed that it causes changes in renal function .
China faces a feed shortage. The feed that is available is frequently contaminated with mycotoxins . Furthermore, the high prices and scarcity of protein sources for animal feeds have led to the use of alternative protein sources such as distillers dried grains with solubles (DDGS). However, the supplementation of animal diets with DDGS must be carefully monitored for the presence of toxic compounds such as mycotoxins, especially AFB1, DON, ZEA and OTA .
Although Beijing is one of the largest cities in China, there has been little research conducted on the presence of the mycotoxins AFB1, DON, ZEA and OTA in the Beijing region. As the surveys that have been done have been limited and because more thorough research is very much necessary, the current study investigated the occurrence of four major mycotoxins in feed ingredients (corn, wheat bran, soybean meal and DDGS) and complete swine feeds for various stages of growth on a variety of swine farms in China’s Beijing region.
Sample collection and preparation
The protocol for the experiment was reviewed and approved by the Institutional Animal Care and Use Committee at China Agricultural University.
A total of 131 samples including 55 feed ingredients and 76 complete swine feeds were randomly sampled from 15 swine farms in the Beijing region from July through August 2011. The samples included 16 samples of corn, 13 samples of wheat bran, 12 samples of soybean meal, and 17 DDGS samples. The swine complete feeds included creep feeds (n = 7), starter feeds (n = 14), grower feeds (n = 14), grower-finisher feeds (n = 18), gestating sow feeds (n = 10) and lactating sow feeds (n = 13). The sampling was undertaken in accordance with European Regulation No. 401/2006 . All samples were ground, mixed and stored at 4°C prior to analysis.
Methods of analysis for mycotoxins
Samples were analyzed according to the methods of the AOAC . Briefly, 25 g of ground feed was extracted with 100 mL of methanol:water (80:20, v/v), blended at high speed for 3 min and then filtered through a sheet of Waterman Filter Paper No. 4. The extract was diluted with a phosphate-buffered saline solution (PBS, pH 7.40), mixed well and filtered through microfiber filter paper. The immunoaffinity column (AokinImmunoClean CF AFLA, Aokin AG, Berlin, Germany) was conditioned with 1 mL of sodium azide, and 10 mL of the diluted filtrate was passed through the column at a flow rate of 1 mL/min. The column was then washed with 10 mL of a methanol:water solution (10:90, v/v) at a flow rate of 3 mL/min. The retained chemicals were then eluted with 1 mL of methanol at a flow rate of 1 mL/min. Subsequently, 20 μL of the clear eluate was injected directly into an HPLC system. If the eluate was found not to be clear, it was passed through an organic filter unit (0.45 μm) before injection. The mobile phase utilized a methanol:water solution (50:50, v/v) with the flow rate set at 1 mL/min. Post-column derivatization was performed with a photochemical reactor (AURA, Los Angeles, CA). A C18 column (4.6 mm × 150 mm, 5 μm, Dikma, Beijing, China) was employed with the LOD set at 0.03 ppb and the LOQ at 0.1 ppb. A fluorescence detector (SHIMADZU, Kyoto, Japan) was set for excitation and emission wavelengths of 360 and 440 nm, respectively. The retention time was 16.5 min.
Samples were analyzed according to the method of GB/T 23503–2009. Briefly, 25 g of ground feed was extracted with 100 mL of a solution of methanol:water (60:40, v/v), blended at high speed for 3 min and then filtered through a sheet of Waterman Filter Paper No. 4. The extract was diluted with a phosphate-buffered saline solution (PBS, pH 7.4), mixed well and filtered through microfiber filter paper. The immunoaffinity column (AokinImmunoClean CF DON, Aokin AG, Berlin. Germany) was conditioned with 1 mL of sodium azide, and 10 mL of the diluted filtrate was passed through the column by gravity at a flow rate of 1 mL/min. The column was then washed with a 10 mL solution of methanol:water (10:90, v/v) at a flow rate of 3 mL/min. The bound compounds were then eluted with 3 mL of methanol at a flow rate of 1 mL/min. The purified samples were dried under a stream of nitrogen gas at 50°C. For the mobile phase, the residue was dissolved in 200 μL after evaporation. Subsequently, 20 μL of the eluate was injected into an HPLC system. The mobile phase utilized a methanol: water solution (30: 70, v/v)with the flow rate set at 1 mL/min. A C18 column (4.6 mm × 150 mm, 5 μm, Agilent, Santa Clara, CA) was employed with the LOD set at 0.02 ppm and the LOQ at 0.06 ppm. The absorption UV wavelength (SHIMADZU, Kyoto, Japan) was set at 218 nm. The retention time was 5.6 min.
Samples were analyzed according to the certified Chinese GB/T 23504–2009 method. Briefly, 25 g of feed was extracted with 100 mL of a methanol:water solution (60:40, v/v), blended at high speed for 3 min and then filtered through a sheet of Waterman Filter Paper No. 4. The extract was diluted with a phosphate-buffered saline solution (PBS, pH 7.40), mixed well and filtered through microfiber filter paper. The immunoaffinity column (AokinImmunoClean CF ZEA, Aokin AG, Berlin, Germany) was conditioned with 1 mL of sodium azide, and 10 mL of the diluted filtrate were passed through the column by gravity at a flow rate of 1 mL/min. The column was then washed with 10 mL of a methanol:water solution (10:90, v/v) at a flow rate of 3 mL/min. The bound chemicals were then eluted with 3 mL of methanol at a flow rate of 1 mL/min. Subsequently, 20 μL of the clear eluate was injected directly into an HPLC system. If the eluate was found not to be clear, it was passed through an organic filter unit (0.45 μm) before injection. The mobile phase utilized an acetonitrile:water:methanol solution (46: 46: 8, v/v/v with the flow rate set at 1 mL/min. A C18 column (4.6 mm × 150 mm, 5 μm, Dikma, Beijing, China) was employed with the LOD set at 1.5 ppb and the LOQ at 4 ppb. A fluorescence detector (SHIMADZU, Kyoto, Japan) was set for excitation and emission wavelengths of 274 and 440 nm, respectively. The retention time was 7.3 min.
Samples were analyzed according to the methods of the AOAC . Briefly, 25 g of feed was extracted with 100 mL of a methanol:water solution (60:40, v/v), blended at high speed for 3 min and then filtered through a sheet of Waterman Filter Paper No. 4. The extract was diluted with a phosphate-buffered saline solution (PBS, pH 7.4), mixed well and filtered through microfiber filter paper. The immunoaffinity column (AokinImmunoClean CF OTA, Aokin AG, Berlin, Germany) was conditioned with 1 mL of sodium azide, and 10 mL of the diluted filtrate was passed through the column by gravity at a flow rate of 1 mL/min. The column was then washed with 10 mL of a methanol:water solution (10:90, v/v) at a flow rate of 3 mL/min. The bound compounds were then eluted with 3 mL of methanol at a flow rate of 1 mL/min, after which 20 μL of the clear eluate was injected directly into an HPLC system. If the eluate was found not to be clear, it was passed through an organic filter unit (0.45 μm) before injection. The mobile phase utilized an acetonitrile:water:glacial acetic acid solution (99: 99: 2, v/v/v) with the flow rate set at 0.9 mL/min. A C18 column (4.6 mm × 150 mm, 5 μm, Dikma, Beijing, China) was employed with the LOD set at 0.035 ppb and the LOQ at 0.117 ppb. A fluorescence detector was set for excitation and emission wavelengths of 333 and 477 nm, respectively. The retention time was 11.4 min.
Validation of analytical methods
The analytical methods used were evaluated for linearity, recovery and reproducibility. Standard curves were generated by comparing the linear regressions of peak regions against concentrations. The recovery (precision) of mycotoxins was determined by spiking blank samples (corn, wheat bran, soybean meal, DDGS and complete feeds) with known levels of AFB1, DON, ZEA or OTA standards dissolved during the mobile phase. The spiked concentrations of AFB1, DON, ZEA and OTA were evaluated at high, intermediate and low levels for each standard mycotoxin concentration. Each sample was analyzed after being allowed to stand for 2 h to allow solvent equilibration between the analytes and the matrix. The reproducibility of the method was established by injecting five replicates of the same standard solution on the same day and over five different days.
The data were analyzed using MS Excel, expressed as average contents, detection rates and the percentage of samples that exceeded regulatory limits.
Results and discussion
Performance of the analytical methods
The standard curves for AFB1, DON, ZEN and OTA produced from three determinations of five concentration levels were linear with correlation coefficients (R2) ranging from 0.9990 to 0.9999. Both the intra-day and inter-day precision measurements showed relative standard deviations below 15%. The determination of recoveries in the blank samples spiked with AFB1, DON, ZEN and OTA were 80.3 to 85.0, 84.1 to 89.8, 86.6 to 90.4 and 87.3 to 90.8, respectively. Therefore, the performances of the employed analytical methods were shown to be satisfactory for the study’s purposes. The analytical methods were validated for all feed samples and met the performance criteria set by European Regulation No. 401/2006  for mycotoxin analysis.
The occurrence of mycotoxins in feed ingredients and complete feeds
Occurrence of mycotoxins in feed ingredients and complete swine feeds 1,2
Total samples, n
Detection rates, %
Percentage of samples over the maximum limits, %1,2
Gestating sow feed
Lactation sow feed
Corn is an energy ingredient frequently used in animal feeds in China. The results showed that corn is frequently contaminated with AFB1, DON, ZEA and OTA. The percentages of samples in which AFB1 exceeded regulatory limits were similar to those in corn samples surveyed by Rodrigues and Naehrer in North, South-East and South Asia and in Oceania . The results also showed that corn samples were contaminated with DON at an average value of 1.01 ppm while the highest value detected was 2.13 ppm which agrees with the maximum value in corn reported by Rodriguez and Naehrer . The average content of ZEA in corn was similar to the 121 ppb reported by the two researchers in China . It was similar to the concentrations of DON (93.20%) and ZEA (96.60%) in corn as reported by Guan et al. . The average values and concentrations of OTA in the samples that exceeded regulatory limits was in agreement with survey results that have shown lower contamination levels of OTA than other mycotoxins in corn [5, 23].
The occurrence of mycotoxin contamination with DDGS is summarized in Table 1. The results showed that 6% of the DDGS contained concentrations of AFB1 that exceeded regulatory limits, with an average content of 9.8 ppb. Approximately 88% of the samples contained concentrations of DON that exceeded regulatory limits with an average content of 1.4 ppm. The ZEA contamination levels in the DDGS samples ranged from 49 to 2,958 ppb. We found that 41% of the samples contained concentrations of ZEA that exceeded regulatory limits, with an average content of 883 ppb. However, the OTA content in the DDGS samples did not exceed the standard limits. These samples had an average OTA content of 23 ppb.
The occurrence of mycotoxins in DDGS used as an ingredient in pig diets has rarely been studied. Four mycotoxins were found to be prevalent in the DDGS samples used in our study. Contamination with DON and ZEN was particularly serious. The percentage of samples containing concentrations of DON that exceeded regulatory limits and the average content of DON detected in these samples were similar to the concentrations of DON that have been found in distillers dried grains with solubles sourced worldwide . These results may be explained by the fact that mycotoxins in DDGS (constituting the remaining portions within the final by-product) are up to three times more concentrated than in corn grain . Furthermore, if improperly stored, DDGS are easily contaminated with more mycotoxins due to their high moisture content. In addition, grains are damaged during the process of DDGS production, which can easily cause the production of more mycotoxins. Moreover, in our study, the DDGS were obtained from the regions lying along the middle and lower reaches of the Yangtze River (in Henan, Sichuan and Anhui provinces) which are characterized by a moist climate which may contribute to the contamination of corn with mycotoxins [25, 26]. What is more, this study has shown that multiple mycotoxins coexist in most feeds and feedstuffs [27, 28]. About 29% (5/17) of the DDGS samples used in this study were co-contaminated with DON and ZEN at levels of 1 ppm and 500 ppb, respectively, which exceeds Chinese regulatory limits for feedstuffs. The simultaneous occurrence of contamination by various kinds of mycotoxins leads not only to immune suppression in animals, but also lowered efficiency in animal production .
Wheat bran and soybean meal
The occurrence of mycotoxin contamination in wheat bran and soybean meal is summarized in Table 1. The detection rate of AFB1, DON, ZEA and OTA was 46, 92, 100 and 77% in wheat bran, and 36, 54, 54 and 64% in soybean meal, respectively.
Maximum limit regulations for mycotoxins in feedstuffs in China 1,2
Maximum limit, ppb
Starter pig feed
Grower pig feed
Swine complete feed
Swine complete feed
The occurrence of mycotoxin contamination in complete swine feed is summarized in Table 1. The incidences of the four investigated mycotoxins ranged from 57 to 100% in complete feeds obtained from swine farms. The detection rate of AFB1 in the samples of creep feed, starter pig feed, grower pig feed, grower-finisher pig feed, gestating sow feed and lactating sow feed were 57, 71, 57, 67, 70 and 69%, respectively, with mean concentrations of 0.54, 0.51, 0.31, 4.33, 0.25 and 9.55 ppb, respectively. In addition, the percentage of grower-finisher pig feed and lactating sow feed that contained concentrations of AFB1 that exceeded regulatory limits was 11 and 23%, respectively.
The detection rate of DON was also very high, with percentages in creep feed, starter pig feed, grower pig feed, grower-finisher pig feed, gestating sow feed and lactating sow feed of 86, 100, 100, 100, 94, 100 and 100%, with average concentrations of 0.28, 0.85, 0.62, 0.58, 0.82 and 0.62 ppm, respectively. The percentage of samples with DON concentrations exceeding regulatory limits in complete feeds for the various stages of pig growth was 0, 14, 14, 22, 10 and 23%, respectively. The highest concentration of DON was detected in starter pig feeds (2.31 ppm). Moreover, although high incidences of ZEA and OTA (86 to 100%) were found in swine feeds, the mean concentrations were low (that is, they did not exceed the maximum limits set in China), except for the concentrations of OTA found in gestating sow feed.
Although the levels of ZEA and OTA detected in our study did not seem to have any clear clinical effects, there may well be chronic accumulated carry-over effects on animal products over a long period of feed consumption . In contrast, AFB1 and DON were found in a high percentage of samples in concentrations that exceeded regulatory limits for swine feeds, which could have clinical effects on gilt and sow health. The fact that AFB1 was found at concentrations exceeding regulations in feeds for lactating sows could be of importance in terms of animal’s health. Indeed, it could lead to the excretion of AFM1 and to an exposure of piglets to that toxin, since young animals are more sensitive to AFB1 than adults. Concentrations as low as 1 ppm may cause loss of appetite, vomiting, low feed efficiency and a reduction in body weight gain [23, 30]. Therefore, the high incidence of mycotoxins found in complete feed samples obtained from swine farms highlights the need for surveillance and prevention.
The natural occurrence of mycotoxins has been reported in a variety of foods and feeds in many countries . The maximum admissible levels of these four mycotoxins in feed ingredients and swine complete feeds vary from one country to another with legislation prescribing mandatory upper limits that often take the form of product standards . The United States’ Food and Drug Administration has set a maximum permissible level of 20 ppb for total aflatoxins in all foodstuffs, while in China, the legal limit for AFB1 contamination in corn is 50 ppb. The wide variations in standards have resulted in conflicting perceptions regarding safe levels among the various national agencies. The regulatory limits of the four mycotoxins in this study is higher than the maximum limits set by the Chinese regulation (Table 2).
Pigs are among the most sensitive species to all of these toxins . This is also one of the most frequently exposed species due to its diet based mainly on cereals. The regulation is presented as a consequence of pigs sensitivity (in EU, limits for pigs feeds are often lower than those for other species).
The toxicology of mycotoxins and the incidence of mycotoxin contamination have aroused public awareness. Health authorities need to take action to mitigate the serious negative effects they can have on humans and animals in China. The reduction of mycotoxin contamination will require an integrated understanding of agronomy, fungal ecology, harvesting methods, storage conditions, feed processing and detoxification strategies [33, 34]. Effective control strategies have been implemented based on the establishment of the Hazard Analysis and Critical Control Point (HACCP). This approach can minimize mycotoxin contamination in the food chain through appropriate management of products .
Because mycotoxins are stable chemicals, physical and chemical degradation methods are limited in their effectiveness and include disadvantages such as loss of product nutrition, organoleptic qualities, undesirable health effects and high equipment cost . These disadvantages have encouraged the development of promising biodegradation methods by which mycotoxins may be detoxified [37, 38]. Further periodic investigations of feed ingredients and complete feed samples from various regions in China taken during all seasons are ongoing.
This paper is the first to present data on the natural occurrence of AFB1, DON, ZEA and OTA in feed ingredients and swine complete feeds obtained from livestock farms in China’s Beijing region. The results of this study should serve as a significant reference for feed manufacturers, animal farms and Chinese regulatory authorities for the future consideration of feed and food safety issues. Periodic surveillance and monitoring of the occurrence of mycotoxins in feed ingredients and in animals are very important for minimizing animal and human health risks.
The content of all four mycotoxins were below the maximum limits set by Chinese regulations in the wheat bran and soybean meal samples while the percentage of samples that exceeded regulatory limits were 7, 57 and 7% for corn, and 7, 14 and 3% for the complete feeds for AFB1, DON and OTA respectively. DDGS exhibited the most serious mycotoxin contamination and the percentage of samples that exceeded regulatory limits were 6, 88 and 41%, for AFB1, DON and ZEA, respectively.
This study was supported by the Introduction of International Advanced Agriculture Science and Technology Project (948 Project) (Grant No. 2013-Z20), the Program of Beijing Municipal Bureau of Agriculture (Grant No. 20120633), and National Key Technology Research and Development Program of the Ministry of Science and Technology of China (Grant No. 2011BAD26B04).
- Sundstol EG, Pettersson H, Lundh T: Comparative cytotoxicity of deoxynivalenol, nivalenol, their acetylated derivatives and de-epoxy metabolites. Food Chem Toxicol. 2004, 42: 619-624. 10.1016/j.fct.2003.11.006.View ArticleGoogle Scholar
- Lawlor PG, Lynch PB: Mycotoxins in pig feeds. 1: Source of toxins, prevention and management of mycotoxicosis. Irish Vet J. 2001, 54: 117-120.Google Scholar
- Miller JD: Fungi and mycotoxins in grain: implications for stored product research. J Stored Prod Res. 1995, 31: 1-16. 10.1016/0022-474X(94)00039-V.View ArticleGoogle Scholar
- Chayto AC, Hansen JA, Eric Van Heugten M, Todd S, Sung Woo K: Occurrence and decontamination of mycotoxins in swine feed. Asian-Aust J Anim Sci. 2011, 5: 723-738.View ArticleGoogle Scholar
- Kumagai S, Nakajima M, Tabata S, Ishikuro E, Tanaka T, Norizuki H, Itoh Y, Aoyama K, Fujita K, Kai S, Sato T, Saito S, Yoshiike N, Sugita-Konishi Y: Aflatoxin and ochratoxin A contamination of retail foods and intake of these mycotoxins in Japan. Food Add Contam Part A Chem Anal Control Expo Risk Assess. 2008, 25: 1101-1106. 10.1080/02652030802226187.View ArticleGoogle Scholar
- EFSA: Definition and description of emerging risks within the EFSA’ s mandate. 2007, Italy: European Food Safety AuthorityGoogle Scholar
- Tulayakul P, Sakuda S, Dong KS, Kumagai S: Comparative activities of glutathione-S-transferase and dialdehyde reductase toward aflatoxin B1 in livers of experimental and farm animals. Toxicology. 2005, 46: 204-209.Google Scholar
- IARC: Monograph on the evaluation of carcinogenic risk to humans: Some traditional herbal medicines some mycotoxins, naphthalene and styrene. 2002, Lyon, France, 82: 1-556.Google Scholar
- Jelinek CF, Pohland AE, Wood GE: Worldwide occurrence of mycotoxins in foods and feeds: An update. J Assoc Offic Anal Chem. 1989, 72: 223-230.Google Scholar
- Pestka JJ: Deoxynivalenol: toxicity, mechanisms and animal health risks. Anim Feed Sci Technol. 2007, 137: 283-298. 10.1016/j.anifeedsci.2007.06.006.View ArticleGoogle Scholar
- Wu F: Measuring the economic impacts of Fusarium toxins in animal feeds. Anim Feed Sci Technol. 2007, 137: 363-374. 10.1016/j.anifeedsci.2007.06.010.View ArticleGoogle Scholar
- Zinedine A, Soriano JM, Molto JC, Manes J: Review on the toxicity, occurrence, metabolism, detoxification, regulations and intake of zearalenone: An oestrogenic mycotoxin. Food Chem Toxicol. 2007, 45: 1-18. 10.1016/j.fct.2006.07.030.View ArticlePubMedGoogle Scholar
- Borutova R, Aragon YA, Hrer NAK, Berthiller F: Co-occurrence and statistical correlations between mycotoxins in feedstuffs collected in the Asia–Oceania in 2010. Anim Feed Sci Technol. 2012, 178: 190-197. 10.1016/j.anifeedsci.2012.09.015.View ArticleGoogle Scholar
- CAST: Mycotoxins: Risks in plant, animal, and human systems. 2003, Ames, IA: Council for Agric Sci Technol Task Force. Report No. 139Google Scholar
- Richard JL: Some major mycotoxins and their mycotoxicoses: An overview. Int J Food Microbiol. 2007, 119: 3-10. 10.1016/j.ijfoodmicro.2007.07.019.View ArticlePubMedGoogle Scholar
- Krogh P: Ochratoxins. Mycotoxins in Human and Animal Health. Edited by: Rodricks JV, Hesseltine CW, Mehlman MA. 1977, Park Forest South, IL: Pathotox Publishers, Inc, 489-498.Google Scholar
- Guan S, Gong M, Yin Y, Huang R, Ruan Z, Zhou T, Xie M: Occurrence of mycotoxins in feeds and feed ingredients in China. J Food Agric Environ. 2011, 9: 163-167.Google Scholar
- Rodrigues I, Chin LJ: A comprehensive survey on the occurrence of mycotoxins in maize dried distillers’ grain and solubles sourced worldwide. World Mycotoxin J. 2012, 5: 83-88. 10.3920/WMJ2011.1308.View ArticleGoogle Scholar
- European Commission: Commission regulation (EC) no. 401/2006 of 23 February 2006 laying down the methods of sampling and analysis for the official control of the levels of mycotoxins in foodstuffs. Offic J European Union. 2006, L70: 12-34.Google Scholar
- AOAC: Official Methods of Analysis. 18th ed. AOAC Official Method 999.07 – Aflatoxin B1 and total aflatoxins in peanut butter, pistachio paste, fig paste and paprika powder – immunoaffinity column liquid chromatography with post-column derivatisation first action 2008. 2008, Arlington, Virginia: Assoc Offic Anat ChemGoogle Scholar
- AOAC: Official Methods of Analysis. Determination of ochratoxin A in wine and beer. 2001, Arlington, Virginia: Assoc Offic Anal ChemGoogle Scholar
- Rodrigues I, Naehrer K: A three-year survey on the worldwide occurrence of mycotoxins in feedstuffs and feed. Toxins (Basel). 2012, 4: 663-675. 10.3390/toxins4090663.View ArticleGoogle Scholar
- Van Egmond HP, Schothorst RC, Jonker MA: Regulations relating to mycotoxins in food: Perspectives in a global and European context. Anal Bioanal Chem. 2007, 389: 147-157. 10.1007/s00216-007-1317-9.View ArticlePubMedGoogle Scholar
- Wu F, Munkvold GP: Mycotoxins in ethanol co-products: Modeling economic impacts on the livestock industry and management strategies. J Agric Food Chem. 2008, 56: 3900-3911. 10.1021/jf072697e.View ArticlePubMedGoogle Scholar
- Cui L, Selvaraj JN, Xing F, Zhao Y, Zhou L, Liu Y: A minor survey of deoxynivalenol in Fusarium infected wheat from Yangtze–Huaihe river basin region in China. Food Control. 2013, 30: 469-473. 10.1016/j.foodcont.2012.08.011.View ArticleGoogle Scholar
- Wang X, Liu X, Liu J, Wang G, Wan K: Contamination level of T-2 and HT-2 toxin in cereal crops from Aba area in Sichuan Province, China. Bull Environ Contam Toxicol. 2012, 88: 396-400. 10.1007/s00128-011-0478-6.View ArticlePubMedGoogle Scholar
- Binder EM, Tan LM, Chin LJ, Handl J, Richard J: Worldwide occurrence of mycotoxins in commodities, feeds and feed ingredients. Anim Feed Sci Technol. 2007, 137: 265-282. 10.1016/j.anifeedsci.2007.06.005.View ArticleGoogle Scholar
- Monbaliu S, Van Poucke C, Detavernier C, Dumoulin F, Van De Velde M, Schoeters E, Van Dyck S, Averkieva O, Van Peteghem C, De Saeger S: Occurrence of mycotoxins in feed as analyzed by a multi-mycotoxin LC-MS/MS method. J Agric Food Chem. 2009, 58: 66-71.View ArticleGoogle Scholar
- Speijers GJA, Speijers MHM: Combined toxic effects of mycotoxins. Toxicol Letters. 2004, 153: 91-98. 10.1016/j.toxlet.2004.04.046.View ArticleGoogle Scholar
- Eriksen GS, Pettersson H: Toxicological evaluation of trichothecenes in animal feed. Anim Feed Sci Technol. 2004, 114: 205-239. 10.1016/j.anifeedsci.2003.08.008.View ArticleGoogle Scholar
- Gutema T, Munimbazi C, Bullerman LB: Occurrence of fumonisins and moniliformin in corn and corn-based food products of U.S. origin. J Food Prot. 2000, 63: 1732-1737.PubMedGoogle Scholar
- Afsah-Hejri L, Jinap S, Arzandeh S, Mirhosseini H: Optimization of HPLC conditions for quantitative analysis of aflatoxins in contaminated peanut. Food Control. 2011, 22: 381-388. 10.1016/j.foodcont.2010.09.007.View ArticleGoogle Scholar
- Bryden WL: Mycotoxin contamination of the feed supply chain: Implications for animal productivity and feed security. Anim Feed Sci Techno. 2012, 173: 134-158. 10.1016/j.anifeedsci.2011.12.014.View ArticleGoogle Scholar
- Ma QG, Gao X, Zhou T, Zhao LH, Fan Y, Li XY, Lei YP, Ji C, Zhang JY: Protective effect of Bacillus subtilis ANSB060 on egg quality, biochemical and histopathological changes in layers exposed to aflatoxin B1. Poult Sci. 2012, 91: 2852-2857. 10.3382/ps.2012-02474.View ArticlePubMedGoogle Scholar
- Scudamore KA: Control of mycotoxins: Secondary processing. Mycotoxins in Food: Detection and Control. Edited by: Magan N, Olsen M. 2004, Cambridge CB1 6AH, England: Woodhead Publishing Ltd, 174-189. ISBN 1 85573 733 7Google Scholar
- Teniola OD, Addo PA, Brost IM, Rber PFA, Jany KD, Alberts JF, Van Zyl WH, Steyn PS, Holzapfel WH: Degradation of aflatoxin B1 by cell-free extracts of Rhodococcus erythropolis and Mycobacterium fluoranthenivorans sp. nov. DSM44556 T. Intern J Food Microbiol. 2005, 105: 111-117. 10.1016/j.ijfoodmicro.2005.05.004.View ArticleGoogle Scholar
- Guan S, He J, Young JC, Zhu H, Li XZ, Ji C, Zhou T: Transformation of trichothecene mycotoxins by microorganisms from fish digesta. Aquaculture. 2009, 290: 290-295. 10.1016/j.aquaculture.2009.02.037.View ArticleGoogle Scholar
- Zhao LH, Guan S, Gao X, Ma QG, Lei YP, Bai XM, Ji C: Preparation, purification and characteristics of an aflatoxin degradation enzyme from Myxococcus fulvus ANSM068. J Appl Microbiol. 2011, 110: 147-155. 10.1111/j.1365-2672.2010.04867.x.View ArticlePubMedGoogle Scholar
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