Inactivation of aflatoxigenic fungi (Aspergillus spp.) on granular food model,maize, in an atmospheric pressure fluidized bed plasma system

Atmospheric plasma provides the advantages of high microbial inactivation that can be performed under ambient conditions; therefore, it is regarded as a potential alternative to traditional food preservation methods. The present work presents the results of a critical study conducted on the efficiency of a non-thermal atmospheric pressure fluidized bed plasma (APFBP) system used for decontamination of maize. Maize grains that were artificially contaminated with Aspergillus flavus and Aspergillus parasiticus spores were treated in APFBP system for 1–5 min at two differently designed fluidized bed reactors with air and nitrogen. Results indicate maximum significant reductions of 5.48 and 5.20 log (cfu/g) in Aspergillus flavus and A. parasiticus after 5 min air plasma treatment. The native microbial flora of the maize grains decreased to more than 3 log after 3 min APFBP treatment, and no viable cells were counted. During the storage of plasma treated maize samples at 25 °C for 30 days, the Aspergillus spp. spores log reduction was maintained with no occurrence of re-growth. Overall, this study shows that plasma treatment has a fungicidal effect on A. flavus and A. parasiticus spores associated with alterations in spore surface morphology and loss of spore integrity. APFBP can inactivate aflatoxigenic spores on maize grains and could be optimized to improve the safety and quality of produce.     

Biological activities of Boswellia sacra extracts on the growth and aflatoxins secretion of two aflatoxigenic species of Aspergillus species

Aflatoxins are the most serious carcinogenic, hepatotoxic, teratogenic and mutagenic secondary metabolites which adversely affect human and animal health. This study was designed to evaluate the in vitro inhibitory effect of different concentrations of Boswellia sacra resin (2.5, 5, 7.5 and 10 g/100 ml), leaf extract (5, 7.5, 10, 12.5 and 15 ml/100 ml), and essential oil (1, 2, 3, and 4 ml/100 ml) on the growth and aflatoxins production by two species of Aspergilli, namely Aspergillus flavus (SQU21) and Aspergillus parasiticus (CBS921.7). Resin of B. sacra caused 57.9–92.1% inhibition of aflatoxin secretion by A. flavus and 43.6–95.7% for A. parasiticus. However, the mycelial dry weights were significantly increased by 20.9–52.7% for A. flavus, and 8.9–68.5% for A. parasiticus. The leaf extract of B. sacra apparently enhanced aflatoxins production by 20–50%, and mycelial dry weight by 25.5–29.1% for A. flavus and A. parasiticus. The essential oil of B. sacra at different concentrations similarly inhibited the fungal growth and aflatoxins production by 45.8–83.7% for A. flavus and 41.3–83.5% for A. parasiticus which indicates the antifungal activity of this oil. None of the B. sacra extracts detoxified pure aqueous aflatoxin B₁. We have concluded that B. sacra resin and essential oil possess biological activity against biochemical synthesis and metabolic pathway of aflatoxin production of the two Aspergillus species. Therefore, the resin and essential oil of B. sacra can be recommended as safe plant based bioreservatives to enhance shelf life of food and feed products with reference to adverse effect of physical and synthetic chemical preservatives and their antimicrobial and aflatoxins inhibition activity.     

Aflatoxigenic fungi and aflatoxins occurrence in sultanas and dried figs commercialized in Brazil

The presence of aflatoxins, Aspergillus flavus and Aspergillus parasiticus in dried fruits was investigated. A total of 62 dried fruit samples were analyzed (24 black sultanas, 19 white sultanas and 19 dried figs). A total of 10 A. flavus isolates were found, nine in one white sultana sample (corresponding to 18% infection) and one isolate in dried figs (2%), and all of them were aflatoxin B₁ and B₂ producers. A. parasiticus was not found. Aflatoxins were detected in 3 of 19 (16%) white sultana samples analyzed and, the limits were not higher than 2.0 μg/kg. In dried figs 11 of 19 (58%) samples were contaminated with aflatoxins and, with exception of one sample that was contaminated with 1500 μg/kg of B₁ aflatoxin, the others had less than 2.0 μg/kg. Neither aflatoxigenic or aflatoxins contaminated black sultanas.     

Inactivation of Aspergillus flavus spores by curcumin-mediated photosensitization

Minimizing fungal infection is essential to the control of mycotoxin contamination of foods and feeds but many potential control methods are not without their own safety concerns for the consumers. Photodynamic inactivation is a novel light-based approach which offers a promising alternative to conventional methods for the control of mycotoxigenic fungi. This study describes the use of curcumin to inactivate spores of Aspergillus flavus, one of the major aflatoxin producing fungi in foods and feeds. Curcumin is a natural polyphenolic compound from the spice turmeric (Curcuma longa). In this study the plant has shown to be an effective photosensitiser when combined with visible light (420 nm). The experiment was conducted in in vitro and in vivo where A. flavus spores were treated with different photosensitiser concentration and light dose both in buffer solution and on maize kernels. Comparison of fungal load from treated and untreated samples was determined, and reductions of fungal spore counts of up to 3 log CFU ml⁻¹ in suspension and 2 log CFU g⁻¹ in maize kernels were obtained using optimal dye concentrations and light dose combinations. The results in this study indicate that curcumin-mediated photosensitization is a potentially effective method to decontaminate A. flavus spores in foods and feeds.     

Effect of Hibiscus sabdariffa extract and Nigella sativa oil on the growth and aflatoxin B1 production of Aspergillus flavus and Aspergillus parasiticus strains

This study was undertaken to evaluate the inhibitory effect of Hibiscus sabdariffa calyx extract at concentrations of 5, 7.5, 10 and 12.5 g/100 ml and Nigella sativa oil at concentrations of 1, 2 and 3 ml/100 ml on the growth and aflatoxin B₁ production by Aspergillus parasiticus (CBS 921.7) and Aspergillus flavus (SQU 21) strains. The inhibition of aflatoxin B₁ production by the different concentrations of H. sabdariffa calyx ranged between 91.5-97.9% and 87.1-93.3% for A. flavus and A. parasiticus strains, respectively, whereas the inhibition by different concentrations of N. sativa oil ranged between 47.9 and 58.3% for A. flavus and 32-48% for A. parasiticus strains. The different concentrations of H. sabdariffa calyx and N. sativa oil had no significant effect on the growth of either Aspergillus species. Neither H. sabdariffa calyx nor N. sativa oil detoxified pure aqueous aflatoxin. Our results suggest that H. sabdariffa calyx and N. sativa oil extracted from seeds had metabolic effects on aflatoxin biosynthesis pathway of both Aspergillus species and can be used as an effective biocontrol and non-toxic biopreservatives in food industry against aflatoxin contamination.     

Mycological quality and mycotoxin contamination of Sri Lankan peppers (Piper nigrum L.) and subsequent exposure assessment

The aim of the study was to characterize the toxigenic moulds and to screen different mycotoxins in peppers (Piper nigrum L.) of Sri Lankan origin. Aspergillus flavus, Aspergillus parasiticus, Aspergillus niger and Penicillium spp. were found to be the most dominant fungi. Characterization of the moulds was carried out in A. flavus and parasiticus agar (AFPA) and malt extract agar (MEA) in 77 black pepper (BP) and 11 white pepper (WP) samples. In total, 73% of the BP and 64% of the WP samples were contaminated with A. flavus and/or A. parasiticus (AfAp). A BP sample with water activity (a_w) 0.70 recorded the highest count of AfAp (4.3*10⁴ CFU/g). Moreover, 75% of the BP samples exceeded the safe a_w limit (0.65) set by the European Spice Association (ESA). The frequency of occurrence of A. niger in BP was 62% with counts up to 1.3*10³ CFU/g. Penicillium spp. were found in 61% and 55% of the BP and WP samples, respectively. In BP 94% of the samples had a Penicillium contamination below 10³ CFU/g. Other Aspergillus spp, found in peppers included, Aspergillus terrus, Aspergillus tamarii, Aspergillus candidus, Aspergillus penicilloides, Aspergillus sydowii and Aspergillus fumigatus. Mould counts in BP (10²–10⁴ CFU/g) were significantly higher than that of WP (<10² CFU/g). Apart from the occurrence of “classical mycotoxins” of spices, aflatoxins (<LOQ-18 μg/kg) and ochratoxin A (<LOQ-79 μg/kg), other toxins including fumonisin B1 (<LOQ-135 μg/kg), sterigmatocystin (<LOQ-49 μg/kg) and citrinin (<LOQ-112 μg/kg) were detected in peppers. In total, 63% of the BP samples were contaminated with at least one mycotoxin. Mycotoxin contamination in WP was significantly less compared to BP. The exposure to aflatoxins and ochratoxin A by consuming pepper remains harmless considering the existing pepper dietary intake data of the Sri Lankan population.     

The potential of some spice essential oils in the control of A. parasiticus CFR 223 and aflatoxin production

Essential oils of sweet basil (Ocimum basilicum), cassia (Cinnamomum cassia), coriander (Coriandrum sativum) and bay leaf (Laurus nobilis) at 1–5% (v/v) concentration in palm kernel broth inoculated with spore suspension (10⁶/ml) of Aspergillus parasiticus CFR 223 were evaluated for their potential in the control of aflatoxigenic fungus A. parasiticus CFR 223 and aflatoxin production. Healthy sorghum grains (120/treatment) immersed in the oils and distributed in three petri dishes with wet cotton wool were also inoculated with spore suspension (10⁶/ml) of A. parasiticus CFR 223 and assayed for grain protection. Sweet basil oil at optimal protective dosage of 5% (v/v) was fungistatic on A. parasiticus CFR 223 and aflatoxins produced in vitro and on fungal development on sorghum grains (P ⩽ 0.05) with a residual effect that lasted for 32 days. In contrast, oils of cassia and bay leaf stimulated the mycelia growth of the fungus in vitro but reduced the aflatoxin concentration (B₁ + G₁) of the fungus by 97.92% and 55.21% respectively, while coriander oil did not have any effect on both the mycelia growth and aflatoxin content of the fungus. The combination of cassia and sweet basil oils at half their optimal protective dosages (2.5% v/v) completely inhibited the growth of the fungus. The feasibility of implementing the results of this study to control aflatoxins was examined by the addition of whole and ground dry basil leaves at 5% and 10% (w/w), respectively, to 10 g sorghum, groundnut, maize and melon seed after 35 days storage period. It was found that the addition of whole and ground basil leaves markedly reduced aflatoxin contamination; however, 10% (w/w) of whole leaves was more effective as the reduction in aflatoxin was between 89.05% and 91%.The findings showed that aflatoxins can be controlled by co-storing whole sweet basil leaves with aflatoxin infected foods. The economic value of the study lies in the simplified technique for control of aflatoxin contamination in agricultural products and the benefits derivable from the use of local resources.     

Reference organism selection for microwave atmospheric pressure plasma jet treatment of young coconut liquid endosperm

This study identified a reference organism for the establishment of microwave atmospheric pressure plasma jet treatment of young coconut liquid endosperm. Three different, predominant spoilage bacteria were isolated from spoiled liquid endosperm and identified through 16S rDNA sequencing, prior to propagation and eventual challenge studies. Basic Local Alignment Search Tool comparisons revealed that the isolated spoilage bacteria were Klebsiella sp., Staphylococcus sp., and Kluyvera sp (%Identity 97.34–97.82%). The isolates were propagated to mid-stationary growth phase (17 h) and thereafter suspended in liquid endosperm. The inactivation rates of the spoilage isolates in liquid endosperm subjected to plasma jet at 450 and 650 W input power settings were determined and compared to those of pathogens Escherichia coli O157:H7, Salmonella enterica, and Listeria monocytogenes. Inactivation rates of all test organisms at 450 W (2.76–5.98 min) were significantly less (p < 0.05) than those at 650 W (1.86–3.11 min). In both power settings, S. enterica exhibited the significantly (p < 0.05) greatest resistance towards plasma treatment, while Staphylococcus sp. exhibited the least. Heat penetration studies in both power settings revealed that the temperature of the liquid endosperm did not significantly increase and did not reach bactericidal ranges (<30 °C) during plasma jet treatment, hence the observed inactivation were attributed to antimicrobial species generated by the plasma. Optical emission spectroscopy revealed that these antimicrobial species included atomic oxygen (777.41 and 844.67 nm) and ultraviolet radiation (200–280 nm). Thus, this study determined S. enterica as an appropriate target organism for the establishment of plasma jet process for coconut liquid endosperm, the inactivation rate of which shall be soon established in higher scale treatment process.     

Aflatoxin-producing Aspergillus spp. and aflatoxin levels in stored cassava chips as affected by processing practices

Cassava chips (cassava balls, and cassava pellets) are derived cassava products traditionally produced by farmers in sub-Saharan Africa following fermentation, and drying of fresh roots of cassava, and are widely consumed in Cameroon. Once produced, this food commodity can be stored for more than two months and contaminated by a wide array of harmful microbes. In order to assess persistence of toxigenic fungi in cassava chips, aflatoxin-producing fungi (Aspergillus flavus, Aspergillus nomius, and Aspergillus parasiticus) and aflatoxins were contrasted at regular intervals in home-stored cassava chips collected in two locations of southern Cameroon throughout a two-month monitoring period. Three hundred and forty-six isolates of aflatoxin-producing fungi were found to be associated with all samples. A. flavus contaminated more samples in both types of chips (267 isolates in 53 samples), followed by A. nomius (58 isolates in 15 samples), whereas A. parasiticus was rarest. A direct competitive Enzyme-linked immunosorbent assay (ELISA)-based method was implemented to quantify the content in aflatoxins. Eighteen of the samples contained some aflatoxins at detectable levels whereas 54 did not. The levels of aflatoxin ranged between 5.2 and 14.5 ppb. The distribution of aflatoxin in positive samples depended on 8 parameters including pH, moisture content, storage duration, types of chips, level of contamination by aflatoxin-producing fungi, processing practices and storage facilities. From analysis of variance results, only pH (p < 0.01), duration of storage (p < 0.01), population of aflatoxin-producing species (0.0001) and the chip type (p < 0.05) were significantly related to aflatoxin in positive samples. A stepwise regression analysis (forward selection procedure) indicated that aflatoxin levels were significantly (p < 0.01) correlated with processing practices, storage facilities, and storage duration of the chips.     

Detection of potentially mycotoxigenic Aspergillus species in Capsicum powder by a highly sensitive PCR-based detection method

The objective of this study was to gain information about the toxigenic Aspergillus species present in a wide survey of retail samples of paprika and chilli collected in Spain. Detection of these mycotoxigenic species was performed with an optimized protocol for paprika and chilli which includes a set of species-specific PCR assays. Occurrence of toxigenic Aspergillus species was higher in paprika than in chilli samples (83.9% and 64.5%, respectively). Paprika showed also the highest percentage of co-occurrence of two or more different species (43.6%) in comparison with chilli (35.5%). The most common aspergilli were Aspergillus niger aggregate (67.7%), followed by Aspergillus flavus (49.5%). Aspergillus carbonarius, Aspergillus parasiticus and Aspergillus steynii were detected at lower frequency (1.1%). The high co-occurrence of Aspergillus species able to produce ochratoxin A and aflatoxins, particularly in paprika, suggested the need of a more efficient control during processing and storage to reduce fungal contamination, and additional legislation to consider the simultaneous presence of both toxins in these matrices.     

Chemical composition and antiaflatoxigenic activity of Carum carvi L., Thymus vulgaris and Citrus aurantifolia essential oils

In order to find out plants useful to controlling aflatoxins (AFs) production, the essential oils (EOs) from 12 medicinal plants prepared by hydrodistillation were studied with special reference to the inhibition of Aspergillus parasiticus growth and AFs production. The toxigenic fungus was cultured in presence of various oils in 6-well microplates using a microbioassay technique. The mycelial mass was estimated as an index of fungal growth, while the aflatoxins B₁ (AFB₁) and G₁ (AFG₁) were measured by high performance liquid chromatography (HPLC). Among plants tested, Thymus vulgari and Citrus aurantifolia were found to inhibit both A. parasiticus and AF production. The EOs from Mentha spicata L., Foeniculum miller, Azadirachta indica A. Juss, Conium maculatum and Artemisia dracunculus were only inhibited fungal growth, while Carum carvi L. effectively inhibited AF production without any obvious effect on fungal growth. The other plants including Ferula gummosa, Citrus sinensis, Mentha longifolia and Eucalyptus camaldulensis had no effect on A. parasiticus growth and AF production at all concentrations used. The IC₅₀ values of T. vulgaris, C. aurantifolia and C. carvi for AF inhibition were reported as 93.5, 285.6, and 621.9 μg/ml for AFB₁, while they were calculated as 11.7, 50.1, and 56.0 μg/ml for AFG₁. These results indicate that the EOs of some medicinal plants may be considered as potential candidates to protect foods and feeds from toxigenic fungus growth and subsequent AF contamination.     

High pressure processing pretreatment enhanced the thermosonication inactivation of Alicyclobacillus acidoterrestris spores in orange juice

The spoilage of high acid fruit juices and nectars by Alicyclobacillus acidoterrestris is a major concern to juice manufacturers around the world since it is difficult to detect. In this study, thermosonication (ultrasound and heat, TS) and thermal inactivation of A. acidoterrestris spores in pretreated orange juice were carried out and resistance parameters were estimated. First, the effect of TS acoustic energy density (AED, 0.3–20.2 W/mL) on the inactivation at 75 °C was investigated. Then, the influence of TS temperature (70–78 °C) on the spore inactivation (AED = 20.2 W/mL) was studied. Next, we explored the effect of high pressure processing (HPP) pretreatment of juice on the 20.2 W/mL TS inactivation at the best temperature (78 °C). Lastly, the thermal inactivation of spores in juice heat shocked + 1 min sonicated vs. untreated juice was also investigated.Results of TS showed higher spore inactivation for higher AED (D_75°C-value of 49 min for 20.2 W/mL vs. 217 min for 0.33 W/mL). Lower D-values were obtained at higher temperatures (D_78°C-value of 28 min vs. D_70°C-value of 139 min at 20.2 W/mL). The TS D_78°C-value (at 20.2 W/mL) decreased further from 28 min to 14 min when the orange juice was previously submitted to 600 MPa for 15 min. Thermal treatment alone at 78 °C resulted in almost no spore inactivation, whereas the heat shock + ultrasound pretreatment of juice enhanced the thermal inactivation of spores (D_85°C-value decreased from 69 to 29 min). To conclude, HPP-assisted TS provided the best method for spore inactivation, indicating the benefit of high pressure and power ultrasound technology in addition to heat. TS required at least 8 °C lower temperatures than thermal treatments to achieve the same spore inactivation, which could enhance juice quality and energy savings.     

Mycoflora and absence of aflatoxin contamination of commercialized cassava chips in Benin, West Africa

Studies conducted in Benin, in which the main staple foods are maize, cassava, groundnuts and yams, showed high levels of aflatoxin residues in blood of the exposed population. The natural contamination with fungi and aflatoxins in cassava chips sold at markets in Benin, West Africa was investigated. A total of sixty samples were sampled from open markets in 11 districts of 3 agroecological zones and analyzed for the presence of mycoflora and aflatoxin B₁, B₂, G₁ and G₂. Fourteen genera of fungi were associated with marketed dried cassava chips. Within these, twenty- two isolates were identified to species level, whereas four were identified only to genus. The dominating fungal species isolated were Rhizopus oryzae, Nigrospora oryzae, Chrysonilia sitophila, Cladosporium resinae, Cladosporium herbarum, Apergillus niger and Aspergillus flavus. Fifty-four out of sixty samples were contaminated with A. flavus. The rate of occurrence in CFU/g of A. flavus fungi was lower than for all other fungal species together. Aflatoxin was not detected in any of the samples analyzed using HPLC with post-column photochemical derivatization and fluorescence detection. The limit of detection (LOD) was 0.1 μg/kg. Results from this study suggest cassava chips are unlikely to be a source of aflatoxin in Benin, and that other staples such as maize and groundnuts are more important in aflatoxin exposure. Therefore it can be speculated that staples like maize and groundnut are more important in aflatoxin exposure.     

Effect of water activity and temperature on the growth of Aspergillus flavus,the expression of aflatoxin biosynthetic genes and aflatoxin production in shelled peanuts

The contamination of peanuts with Aspergillus flavus and subsequent aflatoxins is considered to be one of the most serious safety problems in the world. Water activity (a_w) and temperature are limiting factors for fungal growth and aflatoxins production during storage. To optimize the practical storage parameter, the effect of a_w (0.85–0.99) and temperature (15–42 °C) on fungal growth, aflatoxin production and the expression of aflatoxin biosynthetic and regulatory genes in shelled peanuts was investigated. A. flavus grew at a lower rate when temperature ≤20 °C or a_w ≤ 0.85. For the growth of A. flavus in shelled peanuts, the optimum conditions were a_w was 0.98, and the optimum temperature was 37 °C. The maximum amount of AFB₁ in peanuts was obtained at 28 °C and a_w 0.96. Real-time analysis showed that 16 of 25 genes had highest expression levels at 28 °C under a_w 0.92, while 9 genes had highest expression levels at 37 °C under a_w 0.92. Compared with 37 °C, all aflatoxin biosynthetic pathway genes were down-regulated at 42 °C. All the pathway genes and laeA were up-expressed at a_w of 0.96 under 28 °C, compared to a_w 0.99. Furthermore, there was a good positive correlation between the ratio of aflS/aflR and AFB₁ production. The expression of laeA was also positively correlated with AFB₁ production while the expression of brlA was correlated with the A. flavus growth. The results of this study suggest that AFB₁ production in peanut kernels can occur over a wider range of a_w × temperatures levels compared to formula media and peanut media. Previous studies have showed that AFB₁ could not be produced on formula media at 37 °C without the expression of most aflatoxin structural genes. But, in the un-autoclaved shelled peanuts, high concentration of AFB₁ was produced at 37 °C with up-regulation of some aflatoxin biosynthetic genes. From a food safety point of view, the results can be used to optimize certain food technological processes and develop prevention strategies to control such carcinogenic natural metabolites in grains (such as peanuts, maize and rice) and derived products.     

Effects of high pressure processing on immunoreactivity and microbiological safety of crushed peanuts

Peanuts are a common economical food source consumed worldwide but exist health concern of food allergy and are particularly susceptible to infection by the mold fungus Aspergillus flavus during storage, accumulating highly toxic substance aflatoxin. In this study, the effect of high pressure treatments on peanut immunoreactivity, peanut amino acid composition, A. flavus growth and aflatoxin contents on crushed peanuts was evaluated. Results showed that immunoreactivity of peanuts treated with 600 MPa and 800 MPa for 10 min was significantly lower (P < 0.05) than those of the control group by 69.2 ± 5.3% and 73.3 ± 1.9%, respectively. High pressure treatment at 800 MPa decreased total essential amino acid content as well as two nutritional indexes, the chemical score and the essential amino acid index, by 32.4 ± 2.1% and 31.1 ± 3.2%, respectively. The growth of aflatoxigenic fungi was inhibited in peanuts with aflatoxin accumulation that were subjected to different levels of pressure treatments during 30 days of storage. Peanuts treated with 600 MPa and 800 MPa had considerably lower aflatoxin levels, 0.26 μg/g and 0.22 μg/g in wet basis, respectively, than the control peanut aflatoxin level (9.08 μg/g) on day 30. Results were demonstrated that high pressure treatment had a significant inhibitory effect on A. flavus growth in peanuts and this contributes to reduction of aflatoxin production and accumulation instead of directly destroy aflatoxin. Taken together, the findings of this study indicated that high pressure treatment could preserve peanut quality by reducing food immunoreactivity and by eliminating A. flavus in peanuts.     

In vitro antifungal activity of lactic acid bacteria against mycotoxigenic fungi and their application in loaf bread shelf life improvement

Food spoilage caused by mycotoxigenic fungi represents an important food safety problem. Lactic acid bacteria (LAB) are used as starter cultures in a larger number of food products. In this study, 16 strains of LAB were cultivated in MRS broth under anaerobiosis. Then, cell free supernatants were obtained by centrifugation and their antifungal activity against Aspergillus parasiticus and Penicillium expansum was tested using the disc-diffusion method. Furthermore, the LABs that showed in vitro antifungal activity were used in bread fermentation with yeast in order to study fungal growth inhibition and aflatoxin (AF) reduction in processed bread previously inoculated with A. parasiticus. The compounds present in the fermented medium of six LAB strains induced inhibition of P. expansum growth, whereas five probiotic strains produced antifungal compounds against A. parasiticus. The analysis by liquid chromatography coupled to mass spectrometry in tandem showed a reduction of the AF content in bread samples fermented with yeast and LABs. The reduction of AFs ranged from 84.1 to 99.9%. Moreover, bread sample studies showed a shelf life increase of about 3–4 days.     

Combined antibacterial activity of green tea extract with atmospheric radio-frequency plasma against pathogens on fresh-cut dragon fruit

The objective of this research was to observe the combined effect of green tea extract (at a tea: water; g ml⁻¹, ratio of 2.5–10.0%) and cold plasma (20 W and 40 W) against bacteria pathogens (Escherichia coli, Salmonella typhimurium, and Listeria monocytogenes) that can be found on the fresh-cut dragon fruit. The change in pathogens after plasma treatment of a fresh-cut dragon fruit treated with green tea at 4 ± 1 °C was also investigated. Dragon fruit's nutritional value, mineral, total phenolic content, and sensory within and without plasma and green tea was determined. It was found that atmospheric radio-frequency (RF) plasma at 40 W could extend the protection against all pathogen growth on the surface of fresh-cut dragon fruit treated with at a 5.0% of green tea to at least 15 days. Without the plasma treatment, green tea of 2.5–10.0% could not inhibit all bacterial growth. In addition, higher values of total phenolic content, crude protein, crude fat and crude fibre were observed in the fresh-cut dragon fruit with green tea after the plasma (p < 0.05) treatment; however, no change was found (p > 0.05) regarding the minerals Fe, Cu, and Mn and the sensory test. The research indicated that green tea extract and atmospheric RF plasma in combination could protect against the growth of pathogens on fresh-cut dragon fruit and extend its shelf-life.     

Gaseous allyl isothiocyanate to inhibit the production of aflatoxins,beauvericin and enniatins by Aspergillus parasiticus and Fusarium poae in wheat flour

There is a growing concern about the presence of mycotoxins in foods, since up to 25% of cereals and cereal foods are contaminated with these compounds. Moreover, the general public is against the use of synthetic preservatives in foods and the use of natural antimicrobials in foods is a current trend. Allyl isothiocyanate (AITC) is a volatile antimicrobial derived from oriental and black mustard. The objective of this work was to evaluate the capacity of gaseous AITC in inhibiting the production of mycotoxins by Aspergillus parasiticus (aflatoxin producer) and Fusarium poae (beauvercin and enniatin producer) in wheat flour. Petri dish lids filled with 2 g of wheat flour were inoculated with 10⁴ conidia/g of A. parasiticus or F. poae and placed in a 1 L mason jar. AITC was added at 0.1, 1 or 10 µL/L in the gaseous phase. Jars were hermetically closed and kept at 23 °C for 30 d. Mycotoxins were identified and quantified by LC-MS/MS. Even 0.1 µL/L of AITC was able to produce 6.9–23% reduction of mycotoxin production. In general, synthesis of aflatoxins and beauvericin was more affected than enniatins. The use of AITC at 10 µL/L completely inhibited the production of all mycotoxins for 30 d. AITC at low doses could be added to flour packages in order to inhibit the production of potentially dangerous mycotoxins.     

Effect of low-dose microwave radiation on Aspergillus parasiticus

The effect of low-dose microwave radiation (LDMR; 2.45 GHz, 1.5 W/g) on biochemical characteristics and mortality of Aspergillus parasiticus was investigated and compared to the effects of conventional heating treatment (water bath), in order to provide a theoretical basis for microwave control of mildew in rice and other food products. The effects of LT50 (52 ± 2 °C) and LT100 (72 ± 2 °C) with microwave treatment on A. parasiticus were both lower than those (62 ± 2 °C and 92 ± 2 °C, respectively) with conductive heating. LDMR and conventional heating treatment both caused increased cell membrane permeability, and thus an increase in electrolyte, Ca²⁺, protein and DNA leakage, and the surface of mycelia appeared rough and swollen. LDMR was more effective in disrupting the cell membrane and causing DNA damage than conductional heating. The severity of DNA injury increased with the rise in temperature. The mechanism causing death of the mold evidently differed between LDMR and conventional heating treatment. LDMR led to the death of A. parasiticus mainly through the increased Ca²⁺ permeability and DNA degradation, and conventional heating treatment induced death mainly by augmenting electrolyte permeability and DNA concentration.     

Comparative study of the simultaneous action of three essential oils on Aspergillus flavus and Sitophilus zeamais Motsch

Maize is among the most important produced and consumed crops in Cameroon. However, the availability of this cereal is limited by post-harvest losses, especially in the course of storage. Therefore, there is an urgent need to overcome this phenomenon through the use of efficient, cheap methods. To this effect, the simultaneous action of three essential oils, obtained by hydrodistillation from leaves of Ocimum gratissimum and Lippia rugosa and fruits of Xylopia aethiopica, on Aspergillus flavus and Sitophilus zeamais was investigated using a 2⁴ factorial design. The three essential oils and the storage time were considered as factors. The results revealed that low volume (60 μl/200 g grain) for O. gratissimum and high volume for L. rugosa (310 μl/200 g grain) and X. aethiopica (250 μl/200 g grain) showed the most important efficiencies against A. flavus and S. zeamais in a 2 weeks storage. Hence, the rate of mortality for S. zeamais was 92% and 89%, respectively, in samples of maize infested by S. zeamais and samples of maize infested by S. zeamais and A. flavus. Ninety five percent of A. flavus conidia were inhibited in samples of maize infested by A. flavus and samples of maize infested by S. zeamais and A. flavus.