Okechukwu Viola O, Kappo Abidemi P, Njobeh Patrick B, Mamo Messai A
Department of Biochemistry, Auckland Park Kingsway Campus, University of Johannesburg, South Africa.
Department of Food and Biotechnology, PO Box 17011, Doornfontein Campus, University of Johannesburg, South Africa.
Food Chem (Oxf). 2024 Feb 27;8:100197. doi: 10.1016/j.fochms.2024.100197. eCollection 2024 Jul 30.
This study identified and monitored the levels of aflatoxins (B and B) produced by isolate VKMN22 (OP355447) in maize samples sourced from a local shop in Johannesburg, South Africa. Maize samples underwent controlled incubation after initial rinsing, and isolates were identified through morphological and molecular methods. In another experiment, autoclaved maize grains were intentionally re-inoculated with the identified fungal isolate using spore suspension (106 spore/mL), after which 1 g of the contaminated maize sample was inoculated on PDA media and cultured for seven days. The aflatoxin concentrations in the contaminated maize inoculated on culture media was monitored over seven weeks and then measured using liquid chromatography-mass spectroscopy (LC-MS). Results confirmed the successful isolation of strain VKMN22 with accession number OP355447, which consistently produced higher levels of AFB compared to AFB. AF concentrations increased from week one to five, then declined in week six and seven. AFB levels ranged from 594.3 to 9295.33 µg/kg (week 1-5) and then reduced from 5719.67 to 2005 µg/kg in week six and seven), while AFB levels ranged from 4.92 to 901.67 µg/kg (weeks 1-5) and then degraded to 184 µg/kg in week six then 55.33 µg/kg (weeks 6-7). Levene's tests confirmed significantly higher mean concentrations of AFB compared to AFB (p ≤ 0.005). The study emphasizes the importance of consistent biomonitoring for a dynamic understanding of AF contamination, informing accurate prevention and control strategies in agricultural commodities thereby safeguarding food safety.
本研究鉴定并监测了分离株VKMN22(OP355447)在从南非约翰内斯堡一家当地商店采购的玉米样品中产生的黄曲霉毒素(B1和B2)水平。玉米样品在初步冲洗后进行受控培养,并通过形态学和分子方法鉴定分离株。在另一个实验中,使用孢子悬浮液(106个孢子/毫升)将已鉴定的真菌分离株有意重新接种到经高压灭菌的玉米粒上,之后将1克受污染的玉米样品接种到PDA培养基上并培养7天。对接种在培养基上的受污染玉米中的黄曲霉毒素浓度进行了7周的监测,然后使用液相色谱 - 质谱联用仪(LC - MS)进行测量。结果证实成功分离出保藏编号为OP355447的菌株VKMN22,与黄曲霉毒素B2相比,该菌株始终产生更高水平的黄曲霉毒素B1。黄曲霉毒素B1浓度从第1周增加到第5周,然后在第6周和第7周下降。黄曲霉毒素B1水平在第1 - 5周为594.3至9295.33微克/千克,然后在第6周和第7周从5719.67降至2005微克/千克,而黄曲霉毒素B2水平在第1 - 5周为4.92至901.67微克/千克,然后在第6周降至184微克/千克,在第6 - 7周降至55.33微克/千克。Levene检验证实黄曲霉毒素B1的平均浓度显著高于黄曲霉毒素B2(p≤0.005)。该研究强调了持续生物监测对于动态了解黄曲霉毒素污染的重要性,为农产品中准确的预防和控制策略提供依据,从而保障食品安全。