湖北农业科学 ›› 2025, Vol. 64 ›› Issue (9): 168-172.doi: 10.14088/j.cnki.issn0439-8114.2025.09.027

• 检测分析 • 上一篇    下一篇

食品中金黄色葡萄球菌的等温多自配引发扩增(IMSA)方法优化与应用

郭振1, 曾春梅1, 谢玉锋2,3, 李莎1, 吴观凤1, 张庆发4, 宋淑婷4   

  1. 1.江西煌上煌集团食品股份有限公司技术中心,南昌 330200;
    2.哈尔滨学院食品工程学院,哈尔滨 150086;
    3.酿酒生物技术及应用四川省重点实验室,四川 宜宾 643002;
    4.广州迪澳生物科技有限公司,广州 510700
  • 收稿日期:2025-01-17 出版日期:2025-09-25 发布日期:2025-10-28
  • 通讯作者: 曾春梅(1993-),女,江西赣州人,助理工程师,主要从事食品质量等研究工作,(电子信箱)zengcm901@126.com。
  • 作者简介:郭 振(1969-),男,江西南昌人,高级工程师,主要从事食品质量等研究工作,(电子信箱)nihme@foxmail.com。
  • 基金资助:
    四川省重点实验室基金项目(NJ2024-04)

Optimization and application of isothermal multiple self-matching-initiated amplification (IMSA)method for detection of Staphylococcus aureus in foods

GUO Zhen1, ZENG Chun-mei1, XIE Yu-feng2,3, LI Sha1, WU Guan-feng1, ZHANG Qing-fa4, SONG Shu-ting4   

  1. 1. Technology Center, Jiangxi Huangshanghuang Group Food Co., Ltd., Nanchang 330200, China;
    2. College of Food Engineering, Harbin University, Harbin 150086, China;
    3. Sichuan Provincial Key Laboratory of Brewing Biotechnology and Application, Yibin 643002, Sichuan, China;
    4. Guangzhou Deaou Bio-technology Co., Ltd., Guangzhou 510700, China
  • Received:2025-01-17 Published:2025-09-25 Online:2025-10-28

摘要: 基于nuc基因设计特异性引物,通过设置不同温度、孵育时间、酶用量等条件进行梯度试验,优化等温多自配引发扩增(Isothermal multiple self-matching-initiated amplification,IMSA)方法的反应体系,并对其特异性、灵敏度进行评估,同时与PCR方法对比。结果表明,IMSA方法的反应体系在63 ℃反应温度、45 min孵育时间、16 U/管 Bst DNA聚合酶、4.0 mmol/L Mg2+、2.0 mmol/L dNTPs和1.2 mol/L甜菜碱条件下可获得最佳扩增效率与特异性。在生鲜牛奶、肉制品和果蔬制品3类样品的检测中,IMSA方法与PCR方法的阳性符合率和阴性符合率均达100%,Kappa值均为1.00(P<0.01),表明2种检测方法对3类样品中金黄色葡萄球菌(Staphylococcus aureus)的检测结果完全一致。基于IMSA方法的金黄色葡萄球菌快速检测方法在食品检测中具有高特异性、高灵敏度和良好的实用性,为食品安全检测提供了一种高效、可靠的手段。

关键词: 食品, 金黄色葡萄球菌(Staphylococcus aureus), 等温多自配引发扩增(IMSA)方法, 优化, 应用

Abstract: Specific primers were designed based on the nuc gene, and the reaction system of the isothermal multiple self-matching-initiated amplification (IMSA) method was optimized through gradient experiments by setting different temperatures, incubation times, enzyme amounts, and other conditions; its specificity and sensitivity were evaluated and compared with the PCR method. The results showed that the reaction system of the IMSA method achieved optimal amplification efficiency and specificity under the conditions of 63 ℃ reaction temperature, 45 min incubation time, 16 U/reaction Bst DNA polymerase, 4.0 mmol/L Mg2+, 2.0 mmol/L dNTPs, and 1.2 mol/L betaine. In the detection of three types of samples (raw milk, meat products, and fruit and vegetable products), both the positive agreement rate and negative agreement rate between the IMSA method and the PCR method reached 100%, with Kappa values both being 1.00 (P<0.01), indicating that the detection results of Staphylococcus aureus in the three types of samples by the two methods were completely consistent. The rapid detection method for Staphylococcus aureus based on the IMSA method exhibited high specificity, high sensitivity, and good practicality in food testing, providing an efficient and reliable means for food safety detection.

Key words: food, Staphylococcus aureus, isothermal multiple self-matching-initiated amplification (IMSA)method, optimization, application

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