食品科学 ›› 2023, Vol. 44 ›› Issue (4): 300-305.doi: 10.7506/spkx1002-6630-20220127-283

• 安全检测 • 上一篇    下一篇

基于多重连接探针扩增技术的食品中六重过敏原成分检测

王鸣秋,刘艳,李诗瑶,董婉婷,张涛,林津,朱必婷,张莉   

  1. (1.湖北省食品质量安全监督检验研究院 动物源性食品中重点化学危害物检测技术国家市场监管重点实验室,湖北省食品质量安全检测工程技术研究中心,湖北 武汉 430075;2.武汉软件工程职业学院,湖北 武汉 430205)
  • 发布日期:2023-03-01
  • 基金资助:
    国家市场监督管理总局科技计划项目(2020MK067);湖北省重点研发计划项目(2020BCA091)

Multiplex Ligation-Dependent Probe Amplification for Simultaneous Detection of Six Allergenic Ingredients in Foods

WANG Mingqiu, LIU Yan, LI Shiyao, DONG Wanting, ZHANG Tao, LIN Jin, ZHU Biting, ZHANG Li   

  1. (1. Key Laboratory of Detection Technology of Focus Chemical Hazards in Animal-derived Food for State Market Regulation, Hubei Provincial Engineering and Technology Research Center for Food Quality and Safety Test, Hubei Provincial Institute for Food Supervision and Test, Wuhan 430075, China; 2. Wuhan Vocational College of Software and Engineering, Wuhan 430205, China)
  • Published:2023-03-01

摘要: 基于多重连接探针扩增(multiplex ligation-dependent probe amplification,MLPA)技术建立了一种六重过敏原成分检测方法,可实现食品中大豆、芝麻、花生、杏仁、榛子和核桃6 种成分的同时检测。选取多拷贝ITS基因为靶标基因,设计并合成6 组特异性杂交探针。探针经杂交、连接和聚合酶链式反应得到扩增片段,经毛细管电泳分析扩增片段大小可明确区分6 种过敏原成分。该体系经20余种相关植物、动物及微生物DNA验证显示其特异性良好,经模拟参考样品验证其检出限为5 mg/kg。30 份不同种类市售食品MLPA检测结果表明,该方法性能满足实际样品的过敏原的多重检测。因此,本研究建立的基于MLPA技术的六重过敏原检测方法特异性强、灵敏度高,能够为食品过敏原评估、标识管理和风险控制提供技术支撑。

关键词: 多重连接探针扩增;食品过敏原;多重检测;检出限

Abstract: A multiplex ligation-dependent probe amplification (MLPA) technique was developed for simultaneous detection of six food allergens: soy, sesame, peanut, almond, hazelnut and walnut. Six pairs of species-specific MLPA probes targeting the internal transcribed spacer (ITS) sequences were designed and synthesized. The probes were hybridized with the target DNA, ligated and amplified by polymerase chain reaction (PCR) and the amplicons were detected using capillary electrophoresis, revealing that they could clearly discriminate the six food allergens. Good specificity of the MLPA system was observed for more than 20 plants, animals and bacteria. The limit of detection (LOD) of the assay was determined to be 5 mg/kg for model cookie spiked with different concentrations of the target species. The applicability of the MLPA assay was demonstrated through the analysis of 30 different commercial products, evidencing good performance in practical applications. Therefore, the MLPA technique is highly specific and sensitive and can provide technical support for the assessment, label management and risk control of food allergens.

Key words: multiplex ligation-dependent probe amplification; food allergen; multiple detection; limit of detection

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