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赭曲霉毒素A和玉米赤霉烯酮-二联胶体金免疫层析试纸条的制备及应用
引用本文:章先,付子贤,周一钊,方维焕,宋厚辉.赭曲霉毒素A和玉米赤霉烯酮-二联胶体金免疫层析试纸条的制备及应用[J].微生物学通报,2019,46(5):1235-1245.
作者姓名:章先  付子贤  周一钊  方维焕  宋厚辉
作者单位:1 浙江农林大学动物科技学院 浙江 杭州 311300;2 动物健康检测互联网技术浙江省工程实验室 浙江 杭州 311300;3 中澳动物健康大数据分析联合实验室 浙江 杭州 311300;4 浙江大学动物科学学院 浙江 杭州 310058,1 浙江农林大学动物科技学院 浙江 杭州 311300;2 动物健康检测互联网技术浙江省工程实验室 浙江 杭州 311300;3 中澳动物健康大数据分析联合实验室 浙江 杭州 311300,1 浙江农林大学动物科技学院 浙江 杭州 311300;2 动物健康检测互联网技术浙江省工程实验室 浙江 杭州 311300;3 中澳动物健康大数据分析联合实验室 浙江 杭州 311300,1 浙江农林大学动物科技学院 浙江 杭州 311300;2 动物健康检测互联网技术浙江省工程实验室 浙江 杭州 311300;3 中澳动物健康大数据分析联合实验室 浙江 杭州 311300;4 浙江大学动物科学学院 浙江 杭州 310058,1 浙江农林大学动物科技学院 浙江 杭州 311300;2 动物健康检测互联网技术浙江省工程实验室 浙江 杭州 311300;3 中澳动物健康大数据分析联合实验室 浙江 杭州 311300
基金项目:浙江省自然科学基金(LQ17C170002);浙江农林大学人才项目(2016FR025);国家高技术研究发展计划(863计划) (2012AA101602)
摘    要:【背景】真菌毒素为真菌的有毒次级代谢产物,混合污染时毒性显著增强,可对人类和动物健康造成严重伤害。制备二联胶体金免疫层析试纸条,实现对常见真菌毒素混合污染的快速监测,具有重要意义。【目的】制备赭曲霉毒素A (Ochratoxin A,OTA)和玉米赤霉烯酮(Zeralenone,ZEN)金标单克隆抗体,基于免疫层析原理,采用竞争反应模式,建立二联胶体金免疫层析检测法用于污染样品中OTA和ZEN的同时快速检测。【方法】采用柠檬酸钠还原法制备胶体金颗粒,并标记获得两种真菌毒素金标单克隆抗体,通过优化相关条件,建立稳定的二联胶体金免疫层析检测方法,用于同时检测谷物和饲料样品中的OTA和ZEN。【结果】制备的OTA和ZEN二联胶体金试纸条对OTA和ZEN的检测限分别为0.625 ng/mL和1.25 ng/mL,且与谷物和饲料中其它真菌毒素(黄曲霉毒素B1、伏马毒素B1、桔青霉毒素、展青霉毒素和呕吐毒素)均无交叉反应,人工添加试验结果准确。对天然样本检测结果表明该方法与LC-MS/MS一致性良好。【结论】本研究制备的二联胶体金试纸条可用于实际样品中OTA和ZEN的同时快速筛查。

关 键 词:赭曲霉毒素A,玉米赤霉烯酮,胶体金,免疫检测

Dual flow immunochromatographic assay for simultaneous determination of ochratoxin A and zearalenone in cereal and feed samples
ZHANG Xian,FU Zi-Xian,ZHOU Yi-Zhao,FANG Wei-Huan and SONG Hou-Hui.Dual flow immunochromatographic assay for simultaneous determination of ochratoxin A and zearalenone in cereal and feed samples[J].Microbiology,2019,46(5):1235-1245.
Authors:ZHANG Xian  FU Zi-Xian  ZHOU Yi-Zhao  FANG Wei-Huan and SONG Hou-Hui
Institution:1 College of Animal Science and Technology, Zhejiang A&F University, Hangzhou, Zhejiang 311300, China;2 Zhejiang Provincial Engineering Laboratory for Animal Health Inspection and Internet Technology, Hangzhou, Zhejiang 311300, China;3 China-Australian Joint Laboratory for Animal Health Big Data Analytics, Hangzhou, Zhejiang 311300, China;4 College of Animal Sciences, Zhejiang University, Hangzhou, Zhejiang 310058, China,1 College of Animal Science and Technology, Zhejiang A&F University, Hangzhou, Zhejiang 311300, China;2 Zhejiang Provincial Engineering Laboratory for Animal Health Inspection and Internet Technology, Hangzhou, Zhejiang 311300, China;3 China-Australian Joint Laboratory for Animal Health Big Data Analytics, Hangzhou, Zhejiang 311300, China,1 College of Animal Science and Technology, Zhejiang A&F University, Hangzhou, Zhejiang 311300, China;2 Zhejiang Provincial Engineering Laboratory for Animal Health Inspection and Internet Technology, Hangzhou, Zhejiang 311300, China;3 China-Australian Joint Laboratory for Animal Health Big Data Analytics, Hangzhou, Zhejiang 311300, China,1 College of Animal Science and Technology, Zhejiang A&F University, Hangzhou, Zhejiang 311300, China;2 Zhejiang Provincial Engineering Laboratory for Animal Health Inspection and Internet Technology, Hangzhou, Zhejiang 311300, China;3 China-Australian Joint Laboratory for Animal Health Big Data Analytics, Hangzhou, Zhejiang 311300, China;4 College of Animal Sciences, Zhejiang University, Hangzhou, Zhejiang 310058, China and 1 College of Animal Science and Technology, Zhejiang A&F University, Hangzhou, Zhejiang 311300, China;2 Zhejiang Provincial Engineering Laboratory for Animal Health Inspection and Internet Technology, Hangzhou, Zhejiang 311300, China;3 China-Australian Joint Laboratory for Animal Health Big Data Analytics, Hangzhou, Zhejiang 311300, China
Abstract:Background] Mycotoxins produced by different species of fungi may coexist in single cereal or feed samples, which could become highly toxic for humans and animals. In this context, a dual flow immunochromatographic assay for rapid monitoring mixed mycotoxin contamination has become a necessity. Objective] Development of the colloidal gold dual immunoassay for simultaneous detection of ochratoxin A and zearalenone in cereal and feed samples. Methods] Mycotoxins monoclonal antibodies were labeled with colloidal gold nanoparticles. After optimizing the materials, reagents as well as the experimental conditions, a dual flow immunochromatographic assay was developed and tested for determining the ochratoxin A and zearalenone in cereal and feed samples. Results] The detection limit for ochratoxin A and zearalenone was 0.625 ng/mL and 1.25 ng/mL, respectively. Naturally contaminated cereal and feed samples were analyzed using both immunochromatographic assay and LC-MS/MS, and showed a good agreement between these two methods. Conclusion] This immunoassay could detect ochratoxin A and zearalenone in cereal and feed samples rapidly and accurately, more easily and at a lower cost.
Keywords:Ochratoxin A  Zeralenone  Colloidal gold nanoparticles  Immunoassay
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