Occurrence of four mycotoxins in cereal and oil products in Yangtze Delta region of China and their food safety risks

A total of 76 cereal and oil products collected from Yangtze Delta region of China were analyzed for occurrences of aflatoxins (AFs), aflatoxin B₁ (AFB₁), ochratoxin A (OTA), deoxynivalenol (DON) and zearalenone (ZEN). The mycotoxins were determined by the standard detection procedures using immunoaffinity column clean-up coupled with fluorometer (or HPLC-UV). ZEN was the most prevalent toxin, with the incidence of 27.6% (range = 10.0–440.0 μg kg⁻¹), and 9.2% of the evaluated samples were contaminated with a concentration higher than that of the legislation limit of China (60 μg kg⁻¹). AFs and AFB₁ were detected in 14.5% of the samples analyzed, the concentrations ranging 1.1–35.0 μg kg⁻¹ for AFs, and 1.0–32.2 μg kg⁻¹ for AFB₁; 4.0% of the samples had the concentrations of AFs and AFB₁ higher than that of the corresponding legislation limits of China (5.0, 10.0 and 20.0 μg kg⁻¹ for different products). OTA was detected in 14.5% of the cereal and oil products collected; the concentrations ranged 0.51–16.2 μg kg⁻¹. Only 2 samples showed OTA levels higher than that of the legislation limit of China (5.0 μg kg⁻¹). DON was detected in 7.9% of the samples; the concentrations ranged 100–700 μg kg⁻¹, and none of the samples showed DON concentration higher than that of the legislation limit of China (1.0 mg kg⁻¹). A total of 15.8% cereal and oil products were contaminated with at least two mycotoxins (multiple contaminations with different combinations including AFs-ZEN, AFs-OTA-ZEN, OTA-ZEN, ZEN-DON, OTA-ZEN-DON). The dietary exposure assessment results indicated that AFs (AFB₁), OTA, DON and ZEN from cereal-based products represented a series health risk to both adults and children in Yangtze Delta region of China. This is the first report of safety evaluation associated with major mycotoxins for the area.     

A survey of mycotoxins in random street-vended snacks from Lagos,Nigeria, using QuEChERS-HPLC-MS/MS

A survey in African snacks was carried out in order to evaluate the intake of 23 mycotoxins. The African snack samples were purchased from street vendors within Lagos metropolis (Nigeria) and evaluated for the presence of 23 mycotoxins using a modified QuEChERS procedure coupled with liquid chromatography-triple quadrupole linear ion trap mass spectrometer. The snacks included akara, baked coconut, coconut candy, donkwa, groundnut cake (kulikuli), lafun, milk curd (wara), fresh and dried tiger-nuts, and yam flour. Only three mycotoxins were detected in 23.8% of the studied snacks, and at concentrations ranging from 6 to 54 μg kg⁻¹. The concentrations of aflatoxin B₁ (AFB₁) and AFB₂ reached 23 μg kg⁻¹ and 3 μg kg⁻¹, respectively. Moreover a sample of baked coconut contained α-zearalenol (α-ZOL), which was up to 54 μg kg⁻¹ in coconut candy. As considers prevalence, aflatoxins and α-ZOL were not detected in lafun and groundnut-based snacks (donkwa and kulikuli), whereas each of the three mycotoxins contaminated 12.5% (1/8) of the coconut-based samples. This is the first report of α-ZOL in cassava and coconut, and their products. AFB₁ and total aflatoxins (TAFs) concentrations exceeded the maximum allowable limit recommended by National Agency for Food and Drug Administration and Control Nigeria (NAFDAC) in one sample of baked coconut (AFB₁ = 23 μg kg⁻¹ and TAFs = 26 μg kg⁻¹) and donkwa (AFB₁ = 19 μg kg⁻¹ and TAFs = 21 μg kg⁻¹).     

Annual and regional variations of aflatoxin B1 levels seen in grains and feed coming from Croatian dairy farms over a 5-year period

The aim of the study was to investigate annual and regional differences in the level of aflatoxin B₁ (AFB₁) in grains and dairy cattle feed. Maize (n = 972), wheat (n = 201), barley (n = 147), oat (n = 136), grain mixtures (n = 168), and dairy cattle feed (n = 325) were sampled from 2009 to 2013 on different farms and in different farm factories situated in four Croatian regions. The samples were analysed for AFB₁ using the validated ELISA immunoassay. AFB₁ was determined in 16.4% of all investigated samples, among which maize was proven to be the most contaminated, with 21.7% of the samples recovered during 2013 harbouring AFB₁ in concentrations over the permissible ones. Levels higher than permitted were observed in 17.9% and 12.3% of grain mixtures and dairy cattle feed, respectively, whereas concentrations of AFB₁ determined in other crops throughout the investigated period met the stipulated requirements. The results revealed the AFB₁ occurrence to be significantly (p < 0.05) dependent on the cultivation region, with the highest levels generally found in maize harvested in 2013 and consequently in grain mixtures and cattle feed that can most likely be associated with climatic conditions as the most critical factor for mould formation, and thus also AFB₁ production.     

Multi-mycotoxins analysis in ginger and related products by UHPLC-FLR detection and LC-MS/MS confirmation

The aim of this study was to optimize and validate a powerful method for the simultaneous analysis of aflatoxins B₁ (AFB₁), B₂ (AFB₂), G₁ (AFG₁), G₂ (AFG₂) and ochratoxin A (OTA) in ginger and related products collected from local markets in Beijing, China. The optimized analytical procedure was based on immunoaffinity column (IAC) clean-up, followed by ultra-high performance liquid chromatography with fluorescence (UHPLC-FLR) detection. Limits of detection (LOD) and quantification (LOQ) for the five mycotoxins were 0.005–0.2 and 0.0125–0.5 μg kg⁻¹, respectively. The average recoveries ranged from 84.2 to 97.3% with relative standard deviations (RSDs) from 0.63 to 7.86% at three spiking levels. Good linearity was observed for the analytes with correlation coefficients all higher than 0.9995. The established method was applied to 30 samples of 10 different species of ginger and related products, and all positive samples were confirmed by liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS). The results showed that 5 samples of ginger products were contaminated with AFB₁ at 0.13–1.38 μg kg⁻¹, while 3 samples of ginger and 2 samples of ginger products were contaminated with OTA at 0.31–5.17 μg kg⁻¹. All the contamination levels were below the legally allowable limits.     

The in vitro ability of different Saccharomyces cerevisiae – Based products to bind aflatoxin B1

The purpose of this study was to evaluate the ability of Saccharomyces cerevisiae (SC) – based products from sugar cane fermentation (dried yeast – DY, autolyzed yeast – AY, cell wall – CW) and from beer fermentation (brewery dehydrated residue – BDR) to bind aflatoxin B₁ (AFB₁) in phosphate buffer saline (PBS) spiked with 0.5 μg AFB₁ mL⁻¹. All SC cells were heat-killed (121 ° C, 10 min) and then used for checking the effect of contact time (5, 10, 20 and 30 min) on toxin binding capacity. Compared to the CW and BDR treatments, DY and AY had higher (p < 0.05) capability to bind AFB₁ in PBS, although there were no differences (p > 0.05) among the contact times for any product evaluated. The mean percentages of AFB₁ bound by the DY were higher than AY, varying from 96.5% to 99.3% and from 90.4% to 97.5%, respectively, although the differences were not significant (p > 0.05). The SC-based products from sugar cane fermentation have a potential application for reducing levels of AFB₁ in contaminated food products. However, additional studies are needed to investigate the mechanisms involved in the removal process of toxin by SC and factors that affect toxin sequestration aiming the commercial application in food industry.     

Highly sensitive toxin microarray assay for aflatoxin B1 detection in cereals

We report a rapid, highly sensitive microarray method for quantitative aflatoxin B₁ (AFB₁) detection in cereal samples. Following optimisation using an indirect competitive immunoassay, optimised amounts of AFB₁-bovine serum albumin (AFB₁-BSA)-conjugate were contact-printed onto 16 isolated sub-arrays on multi-pad nitrocellulose coated slides subsequently used in competitive binding assays.The toxin microarray working range for AFB₁ was established in the range of 15 pg g⁻¹ to 3.04 ng g⁻¹, with a detection limit of 1 pg g⁻¹. To determine assay sensitivity in contaminated food models, wheat flour and barley grains samples were spiked with AFB₁ standard dilutions. Following extraction, the working ranges of 0.11–4.15 and 0.18–4.31 ng g⁻¹ were determined, with detection limits of 30 and 90 pg g⁻¹, respectively. The sensitivity of the developed assay is below the European commission limit set for AFB₁ detection and the assay procedure was completed in 3 h time. Good recoveries (98% ± 11%) obtained demonstrate the suitability of the proposed method for rapid and sensitive quantification of AFB₁ in contaminated cereal samples.     

Development and validation of an accurate and rapid LC-ESI-MS/MS method for the simultaneous quantification of aflatoxin B1, B2, G1 and G2 in lotus seeds

An accurate and rapid LC-ESI-MS/MS analytical method was developed and validated for the simultaneous determination of aflatoxin B₁, B₂, G₁ and G₂ in lotus seeds. The samples were firstly extracted with methanol-water solution (80:20, v/v), and then cleaned up by immunoaffinity columns. The mass spectrometer was operated in the positive ionization electrospray (ESI+) mode using multiple reaction monitoring (MRM) for analysis of four aflatoxins. The transitions of m/z 313 → 285 (AFB₁, CE 33 eV), m/z 315 → 259 (AFB₂, CE 37 eV), m/z 329 → 243 (AFG₁, CE 37 eV) and m/z 331 → 257 (AFG₂, CE 37 eV) were used to quantify these four aflatoxins, respectively. The limits of detection (LODs) of aflatoxin B₁, B₂, G₁ and G₂ were 0.007, 0.005, 0.003 and 0.005 μg kg^?1 based on a signal-to-noise ratio of 3:1, respectively. The limits of quantification (LOQs) of aflatoxin B₁, B₂, G₁ and G₂ were 0.02, 0.015, 0.01 and 0.015 μg kg^?1 based on a signal-to-noise ratio of 10:1, respectively. Recoveries for samples of spiked lotus seeds were all above 66% with relative standard deviation all below 15% for all compounds. Nineteen out of twenty batches of lotus seeds collected from different drug stores or markets in China were found to be contaminated with aflatoxins at different levels ranging from 0.02 to 688.4 μg kg^?1.     

Effect of ozone treatment on aflatoxin B1 and safety evaluation of ozonized corn

This paper studies the ozone treatment effect on degradation of aflatoxin B₁ (AFB₁) in corn with different moisture content (MC). The toxicity of the degradation products (DPs) of the ozone-treated AFB₁-Contaminated Corn (ACC) was also evaluated using the human hepatocellular carcinoma cell line (HepG2) as model cells. The degradation rate of AFB₁ in corn increases with ozone concentration and treatment time. The results showed that ACC with 13.47% MC was easier to be degraded by ozone than with 20.37% MC. Treated with 90 mg L⁻¹ ozone for 20 min and 40 min, AFB₁ in corn with 13.47% MC decreased from 83 μg kg⁻¹ to 18.12 μg kg⁻¹ and 9.9 μg kg⁻¹, respectively, well meeting the China National Standard of AFB₁ in corn (20 μg kg⁻¹). In order to evaluate the safety of ozone used on ACC, the impacts of AFB₁ as well as untreated and ozone-treated ACC with the same level of AFB₁ content on HepG2's survival rate, morphology, and apoptosis were studied. The results showed that ACC had high cell toxicity while the toxicity of ozone-treated ACC had no significant difference with that of the AFB₁-free culture solution. It is concluded that ozonation can quickly and effectively degrade AFB₁ in corn and diminish ACC's toxicity, and therefore, ozonation is expected to be an effective, fast, and safe method for AFB₁ degradation in ACC.     

Determination of aflatoxins in walnut sujuk and Turkish delight by HPLC-FLD method

This study aims to assess the risk of aflatoxins (AFs) in traditional confectionery products (walnut sujuk and Turkish delight) of Turkey. A high performance liquid chromatography coupled with fluorescence detection (HPLC-FLD) method was used for the determination of AFs. Evaluation of the method showed good selectivity, linearity, recovery and precision. The limit of quantification (LOQ) ranged from 0.106 to 0.374 μg kg⁻¹. The expanded measurement uncertainty was less than 40% for all target analytes. The validated method was successfully applied to the determination of AFs in 112 traditional confectionery products containing nuts (hazelnuts and walnuts). AFs were detected in 43.8% of walnuts and 60.9% of hazelnuts used as ingredients in walnut sujuk and Turkish delight and at levels ranging from 0.58 to 15.2 μg kg⁻¹ and 0.43–63.4 μg kg⁻¹, respectively. This means that AFs levels in walnut sujuk and Turkish delight were up to levels of 6.1 and 9.5 μg kg⁻¹, respectively. Six walnut samples and twenty-one hazelnut samples were above the EU maximum limits (MLs) of 2 and 5 μg kg⁻¹ for aflatoxin B₁ (AFB₁), respectively.     

Co-occurrence of aflatoxins and ochratoxin A in spices commercialized in Italy

A total of 130 spice samples coming from India, China, South America, USA, Northern Africa, Europe and Sub-Saharan Africa were collected in different stores of Northern Italy. They were analysed for aflatoxins (AFs: AFB₁, AFB₂, AFG₁, AFG₂) and ochratoxin A (OTA) content by liquid chromatography with mass spectroscopy and positive electrospray ionization (LC/ESI-MS/MS), and HPLC with fluorescence detector (FLD), respectively. The analysis showed that 20 (15.4%) and 31 (23.8%) out of 130 samples were contaminated with AFs and OTA, respectively. A low level of total AFs contamination was found in the positive samples, the average concentration was 0.64 ng g⁻¹, far below the maximum threshold admitted by the European legislation (5 ng g⁻¹ for AFB₁, and 10 ng g⁻¹ for total aflatoxins (AFB₁, AFB₂, AFG₁ and AFG₂). A higher incidence of OTA was found in chili (60.0%) more than in pepper (13.3%), ranging from 2.16 to 16.35 ng g⁻¹, and from 1.61 to 15.85 ng g⁻¹, respectively. Moreover, three spice samples (2.3%) contaminated by OTA trespassed the threshold admitted by the European Regulation (EC, 2010). The co-occurrence of OTA and AFs in spices was detected in 6 out of 130 samples (4.6%), ranging from 1.61 to 15.85 ng g⁻¹ and from 0.57 to 3.19 ng g⁻¹, respectively.     

Aflatoxin B1 and ochratoxin A in breakfast cereals from athens market: Occurrence and risk assessment

A method for aflatoxin B₁ (AFB₁) and ochratoxin A (OTA) determination in breakfast cereals is described using a simultaneous methanolic-aqueous extraction followed by immunoaffinity columns clean-up step and High Pressure Liquid Chromatography (HPLC) with Fluorescence Detector (FD). Recoveries were found to be 78% and 83% for AFB₁ and OTA, respectively, while the detection limit (DL) was 0.02 ng g^?1 for both mycotoxins. Both determinations were applied in fifty five samples of breakfast cereals purchased from Athens market. Results revealed the presence of AFB₁ in 56.3% of the samples examined (mean 1.42 ng AFB₁ g^?1). Seven samples (median 3.5 ng AFB₁ g^?1) were found to be contaminated at levels higher than the EU limit (2 g g^?1). OTA was detected in 60% of the samples (mean 0.18 ng g^?1). Nineteen samples were found to be contaminated by both mycotoxins. In addition in the present study the daily exposure to AFB₁ and OTA is discussed.     

Aflatoxin B1 production by Aspergillus parasiticus and strains of Aspergillus section Nigri in currants of Greek origin

Aflatoxin B₁ (AFB₁) mostly produced by Aspergillus flavus and Aspergillus parasiticus, is an extremely toxic and carcinogenic metabolite. Currants are used in the Mediterranean diet as a food with antioxidant properties. Four strains of Aspergillus section Nigri have been isolated from currants originated from Crete and Corinth. In this study AFB₁ production by A. parasiticus and the four strains of Aspergillus section Nigri in Cretan and Corinthian currants (Vitis vinifera L.) is investigated. AFB₁ determination was performed by HPLC–FID. Results revealed that the four strains Aspergillus section Nigri, as well as the aflatoxigenic strain A. parasiticus produced AFB₁ (0.0052–1.31 μg AFB₁ 15 g⁻¹, corresponding to 0.0003–0.087 μg AFB₁ g⁻¹) in both type of currants (Cretan and Corinthian) on the 12th day of observation. Moreover, AFB₁ production, by A. parasiticus in the synthetic Yeast Extract Sucrose (YES) medium was also studied. The ability of AFB₁ production has been affected by the special characteristics of each isolate and the currants substrate.     

Aflatoxin B1 decontamination by UV-mutated live and immobilized Aspergillus niger

The decontamination of Aflatoxin B₁ (AFB₁) by immobilized cells of a new mutant strain, prepared on a base of HSCAS (hydrated sodium calcium aluminosilicate), was studied. Novel strains were induced by UV irradiation, from which 50 were screened according to their degradation efficacy on AFB_1, compared with the wild strain (FS-Z1). The FS-UV1 strain exhibited highest degradation efficacy, which was confirmed by 18SrDNA to be Aspergillus niger. The results indicate that both immobilized cells and this mutant strain which are incubated for 48 h at 30 °C, would considerably remediate AFB₁ in nutrient broth culture, by 95.32% and 82.43%, respectively. By the application of samples of contaminated cottonseed meal, with results of 93.46%∼96.82%, the degradation rate was also validated. The results of Ames test indicate the mutagenic activity of treated AFB₁ is greatly abated, with treated controls. The Application of LC-q-TOFMS (liquid-chromatography, quadrupole, time-of-flight mass spectrometry) deduces the structure and molecular formulas of the degradation products. In the vivo study, the damages of photomicrographic evidence are decreased in kidney and liver and the serum biochemical parameters is improved, in response to preventative treatment with immobilized cells. This is the application of HSCAS-prepared, immobilized A. niger cells to degrade AFB₁ of contaminated samples. The investigation in this paper offers a novel path for economical, time-saving biodegradation of AFB₁ in foods and feeds.     

Multiple mycotoxin co-occurrence in maize grown in three agro-ecological zones of Tanzania

In this study, the co-occurrence of multiple mycotoxins in maize kernels collected from 300 households' stores in three agro-ecological zones in Tanzania was evaluated by using ultra high performance liquid chromatography/time-of-flight mass spectrometry (TOFMS) with a QuEChERS-based procedure as sample treatment. This method was validated for the analysis of the main eleven mycotoxins of health concern that can occur in maize: aflatoxin B₁ (AFB₁), aflatoxin B₂ (AFB₂), aflatoxin G₁ (AFG₁), aflatoxin G₂ (AFG₂), ochratoxin A (OTA), deoxynivalenol (DON), fumonisin B₁ (FB₁), fumonisin B₂ (FB₂), HT-2 toxin, T-2 toxin and zearalenone (ZEN). From each zone one major maize producing district for home consumption was chosen and 20 villages for each district were randomly selected for sampling. All mycotoxins of health concern, except for T-2 toxin, were detected in the maize samples. Particularly high levels of AFB₁ (50%; 3–1,081 μg kg⁻¹), FB₁ (73%; 16–18,184 μg kg⁻¹), FB₂ (48%; 178–38,217 μg kg⁻¹) and DON (63%; 68–2,196 μg kg⁻¹) were observed. Some samples exceeded the maximum limits set in Tanzania for aflatoxins or in European regulations for other mycotoxins in unprocessed maize. Eighty seven percent of samples were contaminated with more than one mycotoxin, with 45% of samples co-contaminated by carcinogenic mycotoxins, aflatoxins and fumonisins. Significant differences in contamination pattern were observed among the three agro-ecological zones. The high incidence and at high levels (for some) of these mycotoxins in maize may have serious implications on the health of the consumers since maize constitute the staple food of most Tanzanian population. Effective strategies targeting more than one mycotoxin are encouraged to reduce contamination of maize with mycotoxins.     

Effectiveness of pulsed light treatment for degradation and detoxification of aflatoxin B1 and B2 in rough rice and rice bran

Aflatoxins primarily accumulate in the hull and bran layers of rough rice making these by-products of rice milling unsuitable for animal feed or human consumption. Contaminated rough rice is also a potential source of aflatoxin exposure to workers handling the grain during post-harvest storage and processing. Currently, no technologies are available to remove or detoxify these toxic and mutagenic fungal metabolites from contaminated rough rice. Pulsed light (PL) is a novel technology with the potential to degrade and detoxify aflatoxins in foods and their processing by-products. Rough rice was inoculated with Aspergillus flavus to produce aflatoxin B₁ (AFB₁) and B₂ (AFB₂) contamination, followed by PL treatments of 0.52 J/cm²/pulse for various durations. A PL treatment time of 80 s reduced AFB₁ and AFB₂ in rough rice by 75.0% and 39.2%, respectively; while a treatment time of 15 s reduced AFB₁ and AFB₂ in rice bran by 90.3% and 86.7%, respectively. Since PL treatments result in the degradation of aflatoxins in situ, the toxicity and mutagenic activity of the residual by-products of AFB₁ and AFB₂ after PL treatment were evaluated. Toxicity was estimated using the brine shrimp (Artemia salina) lethality assay and mutagenicity measured by the fluctuation test with Salmonella typhimurum tester strains TA98 and TA100. The mutagenic activity of AFB₁ and AFB₂ was completely eliminated by PL treatment, while the toxicity of these two aflatoxins was significantly decreased. The obtained results suggest that PL technology has a promising potential to degrade, detoxify, and inactivate the mutagenic activity of aflatoxins in rough rice and rice bran.     

Aflatoxin and fumonisin contamination of yam flour from markets in Nigeria

The natural occurrence of aflatoxins (AFs) and fumonisins (FBs) in yam flour samples (n = 100) obtained in south-western Nigeria was evaluated. AFs were determined by HPLC with fluorescence detection and FBs by HPLC coupled with mass spectrometry. Aflatoxin B₁ (AFB₁) and aflatoxin G₁ (AFG₁) were found in 57% and 21% of flours from white yam with concentrations ranging from <0.02 (limit of detection, LOD) to 3.2 μg kg⁻¹ (mean = 0.4 μg kg⁻¹) and from <0.05 to 3.5 μg kg⁻¹, respectively. AFB₁ was the only aflatoxin detected in samples from water yam, contaminating 32% of the samples with values ranging from <LOD to 0.6 μg kg⁻¹ (mean = 0.1 μg kg⁻¹). Fumonisin B₁ was found in 32% of the white yam samples (<0.5 (LOD) to 91 μg kg⁻¹; mean = 5 μg kg⁻¹) and in 5% of water yam samples (<LOD to 2 μg kg⁻¹). AFs and FBs were significantly higher (P < 0.05) in white yam flours compared to water yam flours. Preparation of amala from naturally-contaminated yam flour resulted in reduction of AFB₁ and AFG₁ by 44% and 51% respectively. From this study, only 7% of the samples contained AFs above the European standard limits for cereals intended for direct human consumption, while all the FBs-positive samples were well below the limits. The occurrence of ochratoxin A, zearalenone and deoxynivalenol was also evaluated in 20 samples; these mycotoxins were never detected.     

Aflatoxin M1 in UHT milk consumed in Turkey and first assessment of its bioaccessibility using an in vitro digestion model

Contamination of milk and dairy products with aflatoxin M₁ (AFM₁) continues to receive increased attention because of its potential health hazard to humans. The first aim of this study was to know the occurrence and levels of AFM₁ in whole UHT milk from main processors in Turkey in order to make a preliminary exposure assessment. A total of 40 milk samples were analysed for AFM₁ using high performance liquid chromatography with fluorescence detection (HPLC-FD) after immunoaffinity column clean-up. Aflatoxin M₁ was detected in 20% of samples at levels ranging from <0.004 to 0.076 μg l⁻¹. Only two samples contained AFM₁ above the EU limit of  0.05 μg l⁻¹.The second aim of this study was to determine the bioaccessibility of AFM₁ from milk using an in vitro digestion model. The bioaccessibility of AFM₁ in spiked and naturally contaminated milk samples ranged from 80.5 to 83.8% and from 81.7 to 86.3%, respectively. No difference (P > 0.05) in AFM₁ bioaccessibility was found between spiked and naturally contaminated milk samples. This study also assessed the binding of AFM₁ by six probiotic bacteria under simulated gastrointestinal conditions. A 15.5–31.6% reduction in AFM₁ bioaccessibility was observed in the presence of probiotic bacteria. Based on the results obtained in the present study, the mean daily intake of AFM₁ through milk consumption was estimated as 0.008 ng kg⁻¹ b.w. day⁻¹ for Turkish adults.     

Aflatoxin contamination of dried red chilies: Contrasts between the United States and Nigeria,two markets differing in regulation enforcement

Dried red chilies are among the world’s most consumed spices. From farm to fork, chilies go through cropping, harvest, drying, processing and storage. Chilies are susceptible to infection by aflatoxin producing fungi and subsequent contamination by aflatoxins at every stage. Aflatoxins are highly regulated, hepatotoxic carcinogens produced by fungi in Aspergillus section Flavi. The current study examined prevalence of aflatoxin B₁ (AFB₁) in chilies from markets across the United States (US) and Nigeria, and determined predisposition of chilies to aflatoxins post-harvest. Aflatoxin B₁ was detected in 64% chilies from US markets (n = 169), and 93% of Nigerian chilies (n = 55) with a commercial lateral flow assay (Limit of Detection = 2 μg/kg). Two percent of US samples exceeded the aflatoxin regulatory limit of 20 μg/kg, while the highest concentration detected was 94.9 μg/kg. Aspergillus spp. could be recovered only from 40% of samples from the US, and aflatoxin levels did not correlate with quantities of Aspergillus section Flavi (Colony Forming Units g⁻¹), suggesting fungi associated with chilies in US markets were killed during processing. Both average AFB₁ concentrations and fungal quantities were significantly higher (p < 0.01) in Nigerian chilies. The most contaminated sample contained 156 μg/kg AFB₁. Aflatoxin concentrations in Nigerian chilies increased as an exponential function of the quantities of Aspergillus section Flavi (r² = 0.76). Results indicate that high rates of chili consumption may be associated with unacceptable aflatoxin exposure.     

Degradation of AFB1 in aqueous medium by electron beam irradiation: Kinetics,pathway and toxicology

The degradation study of aflatoxin B₁ (AFB₁) in aqueous medium was performed under electron beam irradiation (EBI) at various AFB₁ initial concentrations. It has been proven that the degradation of AFB₁ in the selected ranges of concentrations follows pseudo first-order reaction kinetics well (R² > 0.95). Five degradation products of AFB₁ in aqueous solution were identified by UPLC-Q-TOF/MS, and the possible degradation pathway was proposed. The Ames and cytotoxicity tests were employed to evaluate the toxicity of the AFB₁ degradation products in aqueous solution, and the results indicated that the mutagenicity and cytotoxicity of EBI treated samples decreased significantly compared with that of untreated samples, but were not completely disappeared. The study provided clues involving the application of EBI methods in AFB₁ decontamination.     

Mycotoxins occurrence in Argentina’s maize (Zea mays L.), from 1999 to 2010

The natural occurrence of mycotoxins in maize in Argentina, from 1999 to 2010 was analysed. Total aflatoxins, deoxynivalenol and zearalenone, were detected and quantified by TLC. Each aflatoxins and fumonisins was quantified by HPLC. A total of 3246 samples for freshly harvested (1655) and storage (1591) was obtained from different regions, from 1999 to 2010. Except for 2003 year in harvest, and for 2007 in storage, aflatoxins levels were low. Average values of aflatoxin B₁ for freshly harvested samples were between 0.38 and 2.54 μg kg⁻¹ and for storage samples were between 0.22 and 4.5 μg kg⁻¹. The average values and frequency of contamination for zearalenone and deoxynivalenol, were low for all years. The average zearalenone contamination in samples of freshly harvested, showed values from no detected up to 83 μg kg⁻¹, and in storage samples, from no detected to 17 μg kg⁻¹. The average deoxynivalenol contamination of freshly harvested, showed values from no detected up to 140 μg kg⁻¹, and for storage samples showed values from no detected to 14 μg kg⁻¹. The percentage of maize samples contaminated by fumonisins was between 90 and 100% for all years studied; the average levels were from 1773 to 9093 μg kg⁻¹ for freshly harvested maize and for storage from 2525 to 11,528 μg kg⁻¹.Co-occurrence of aflatoxins and fumonisin was the most frequent (8.4%), followed by zearalenone and fumonisins (2%).