Based on epidemiological studies, Aspergillus candidus has been demonstrated as an emerging fungal agent of toenail onychomycosis. Here we report a case of a toenail infection caused by A. candidus in a healthy 60-year-old woman. Based on macroscopic and microscopic characteristics of the culture as well as nucleotide sequencing of 28S region, the causative agent was identified as A. candidus.

Recent investigations revealed the effects of herbal extracts on both fungal growth as well as aflatoxins production. In the present study, we tried to evaluate antifungal activity as well as antitoxin activity of Glycyrrhiza glabra (licorice) extract. Strain American Type Culture Collection 15517 of Aspergillus parasiticus was used to perform antifungal susceptibility test according to Clinical and Laboratory Standards Institute document M27-A3, and the rate of aflatoxin production was determined using high-performance liquid chromatography technique after exposure to different concentrations of licorice extract. Quantitative changes in the expression of the aflR gene were analyzed by measuring the cognate aflR mRNA level with quantitative real-time reverse-transcription polymerase chain reaction assay. Our obtained results demonstrated the inhibitory effect of licorice extract on Aspergillus parasiticus growth at 500 mg/mL of licorice extract. In addition, a significant decrease in aflatoxin production was revealed at the same concentration. However, the production of aflatoxin B1 was entirely inhibited in 10 g/mL of licorice extract. The level of aflR gene expression was significantly decreased after the exposure of fungal cells to 500 g/mL of licorice extract. Evaluation of the antifungal and antitoxin activity of licorice extract on Aspergillus parasiticus revealed its antifungal properties as well as its effective ability to decrease aflatoxin production.

Recent studies indicated the inhibitory effects of lactic acid bacteria (LAB) strains isolated from different origins on both fungal growth and aflatoxin production. This study aimed to investigate the inhibitory effect of Lactobacillus plantarum and L. delbrueckii subsp. Lactis on Aspergillus parasiticus ATCC15517 growth. Quantification of aflatoxin was performed using high‐performance liquid chromatography technique. Quantitative changes in the expression of the aflR gene were analyzed by measuring the cognate aflR mRNA level with quantitative real‐time reverse‐transcription polymerase chain reaction. Our results demonstrated the inhibitory effect of LAB on A. parasiticus growth at 2 × 103 cfu/ml of L. plantarum and L. delbrueckii subsp. Lactis. Aflatoxin G2 production was significantly inhibited to lower than level of detection. The level of aflR gene expression was considerably decreased after the exposure of fungal cells with used LABs. Assessment of the used LABs on A. parasiticus revealed antifungal properties and effective ability to decrease aflatoxin production. Practical applications Fungi spoilage is widespread among different types of food that may result in huge amounts of waste and economical lost. In addition, side effects raised by using chemical additives as preservative, are a serious source of health concern. Therefore, natural agents such as lactic acid bacteria which are also commonly used as probiotics in recent years, could play a good role as inhibitors of fungal growth as well as mycotoxin production both in food and feed. Different media like dairy foods and so on, can be formulated with Lactobacillus plantarum and L. delbrueckii subsp. Lactis, to prevent Aspergillus parasiticus growth and mycotoxin excretion. LAB can be added to processed food during inoculation step and even for protection, they can be capsulated with edible materials to improve their efficiency.

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Aflatoxin M1 is a derivate of aflatoxin B1 and an important contaminant of milk and dairy products. This systematic review and meta-analysis was conducted on relevant Persian and English original articles in national and international databases with no time limits until 1 January 2018. In total 605 articles were found among which 70 articles met the inclusion criteria for meta-analysis. The prevalence (95% confidence interval (CI)) and mean concentration (95% CI) of aflatoxin M1 was found to be 64% (53-75%) and 39.7 ng/l (31.9-47.4 ng/l) in raw milk, 95% (89-98%) and 62.3 ng/l (40.6-84 ng/l) in pasteurised milk, 71% (56-84%) and 60.1 ng/l (30.9-89.3 ng/l) in sterilised milk, 59% (20-93%) and 5.5 ng/l (3.3-7.7 ng/l) in breast milk and 72% (61-81%) and 82.3 ng/kg (63.7-100.9 ng/kg) in dairy products. In general, 9% (4-16%) of milks and 10% (4-17%) of dairy products had aflatoxin M1 in concentrations exceeding the permitted level of Iranian standards (500 ng/l). Based on the maximum permitted aflatoxin M1 concentration in standards of Europe (50 ng/l), these percentages increase to 25% (18-32%) for milks and 18% (9-29%) for dairy products. According to the results, further control and preventive measures should be applied on livestock feeds because decreased aflatoxin B1 contamination at this level results in decreased aflatoxin M1 in milk and dairy products.