Biodesign Center for Health Through Microbiomes, Arizona State University, Tempe, AZ 85281, USA.
School for Engineering of Matter, Transport, and Energy, Arizona State University, Tempe, AZ 85281, USA.
Toxins (Basel). 2024 Jul 25;16(8):329. doi: 10.3390/toxins16080329.
Food crops around the world are commonly contaminated with , which can produce the carcinogenic mycotoxin aflatoxin B1 (AFB1). The objective of this study is to test an X-ray irradiation sterilization method for studying AFB1 in contaminated maize samples in the laboratory. Maize that had been naturally contaminated with 300 ppb AFB1 by the growth of aflatoxigenic was ground and then irradiated at 0.0, 1.0, 1.5, 2.0, 2.5, and 3.0 kGy. was quantified by dilution plating on potato dextrose agar (PDA) and modified Rose Bengal media (MDRB) for viability and qPCR for gene presence. AFB1 was quantified by HPLC and ELISA. viability, but not gene copies, significantly decreased with increasing doses of radiation (PDA: < 0.001; MDRB: < 0.001; qPCR: = 0.026). AFB1 concentration did not significantly change with increasing doses of radiation (HPLC: = 0.153; ELISA: = 0.567). Our results imply that X-ray irradiation is an effective means of reducing viable without affecting AFB1 concentrations. Reducing the hazard of fungal spores and halting AFB1 production at the targeted dose are important steps to safely and reproducibly move forward research on the global mycotoxin challenge.
全世界的粮食作物通常都受到 的污染, 能产生致癌的真菌毒素黄曲霉毒素 B1(AFB1)。本研究的目的是测试一种 X 射线辐照灭菌方法,用于在实验室研究受污染玉米样本中的 AFB1。用产黄曲霉的 自然污染的玉米,在 0.0、1.0、1.5、2.0、2.5 和 3.0 kGy 下辐照后研磨。通过在土豆葡萄糖琼脂(PDA)和改良玫瑰红孟加拉培养基(MDRB)上稀释平板进行活力测定,以及 qPCR 检测基因存在情况来定量 。通过 HPLC 和 ELISA 定量 AFB1。随着辐射剂量的增加, 活力显著降低,但基因拷贝数没有显著变化(PDA:<0.001;MDRB:<0.001;qPCR:=0.026)。随着辐射剂量的增加,AFB1 浓度没有显著变化(HPLC:=0.153;ELISA:=0.567)。我们的结果表明,X 射线辐照是一种减少存活 的有效手段,而不会影响 AFB1 浓度。减少真菌孢子的危害并在目标剂量下停止 AFB1 的产生,是安全且可重复地推进全球真菌毒素挑战研究的重要步骤。