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荧光免疫层析法结合免疫磁珠分离技术快速检测单增李斯特菌
引用本文:张赛,何小维,刘晓云,彭运平,李文美.荧光免疫层析法结合免疫磁珠分离技术快速检测单增李斯特菌[J].现代食品科技,2014,30(11):229-234.
作者姓名:张赛  何小维  刘晓云  彭运平  李文美
作者单位:(1.华南理工大学轻工与食品学院,广东广州 510640) (2.广州万孚生物技术股份有限公司自检型快速诊断国家地方联合工程实验室,广东广州 510663);华南理工大学轻工与食品学院,广东广州 510640;(2.广州万孚生物技术股份有限公司自检型快速诊断国家地方联合工程实验室,广东广州 510663) (3.南方医科大学公共卫生与热带医学学院,广东广州 510515);广州万孚生物技术股份有限公司自检型快速诊断国家地方联合工程实验室,广东广州 510663;(1.华南理工大学轻工与食品学院,广东广州 510640) (2.广州万孚生物技术股份有限公司自检型快速诊断国家地方联合工程实验室,广东广州 510663)
基金项目:“十二五”国家科技支撑计划项目(2012BAK08B07);国家发改委创新平台建设资助项目(发改高技[2011]2041号)
摘    要:为建立单增李斯特菌简单快速、灵敏度高和特异性强的检测方法,本研究以抗单增李斯特菌单克隆抗体偶联磁珠制备免疫磁珠;以羧基荧光微球标记的抗单增李斯特菌多克隆抗体及鼠IgG为标记抗体,抗单增李斯特菌多克隆抗体和羊抗鼠二抗分别作为检测线和质控线制备荧光免疫层析试纸条。将免疫磁珠分离与荧光免疫层析法相结合应用于单增李斯特菌的现场快速检测中。结果表明:荧光免疫层析试纸条对纯培养单增李斯特菌的检测限为4×105CFU/mL,联合检测方法10倍、100倍浓缩时,检测限分别为4×104CFU/mL和1×104CFU/mL。联合检测体系特异性较好,与实验室保存的10株细菌无交叉反应。人工污染样本检测限为1×104CFU/mL,同纯培养物相比检测灵敏度并没有降低。本方法的建立对于食品中单增李斯特菌的现场快速检测具有重要意义。

关 键 词:单增李斯特菌  抗体  免疫磁珠  荧光免疫层析  快速检测
收稿时间:5/8/2014 12:00:00 AM

Rapid Detection of Listeria monocytogenes Using a Fluorescence Immunochromatographic Assay Combined with Immunomagnetic Bead Separation
ZHANG Sai,HE Xiao-wei,LIU Xiao-yun,PENG Yun-ping and LI Wen-mei.Rapid Detection of Listeria monocytogenes Using a Fluorescence Immunochromatographic Assay Combined with Immunomagnetic Bead Separation[J].Modern Food Science & Technology,2014,30(11):229-234.
Authors:ZHANG Sai  HE Xiao-wei  LIU Xiao-yun  PENG Yun-ping and LI Wen-mei
Affiliation:(1.College of Light Industry and Food Science, South China University of Technology, Guangzhou 510640, China) (2.National & Local United Engineering Lab of Rapid Diagnostic Test, Wondfo Biotech Co., Ltd., Guangzhou 5l0663, China);College of Light Industry and Food Science, South China University of Technology, Guangzhou 510640, China;(2.National & Local United Engineering Lab of Rapid Diagnostic Test, Wondfo Biotech Co., Ltd., Guangzhou 5l0663, China) (3.School of Public Health and Tropical Medicine, Southern Medical University, Guangzhou 510515, China);National & Local United Engineering Lab of Rapid Diagnostic Test, Wondfo Biotech Co., Ltd., Guangzhou 5l0663, China;(1.College of Light Industry and Food Science, South China University of Technology, Guangzhou 510640, China) (2.National & Local United Engineering Lab of Rapid Diagnostic Test, Wondfo Biotech Co., Ltd., Guangzhou 5l0663, China)
Abstract:In order to establish a simple, rapid, sensitive, and specific method to detect Listeria monocytogenes, in this study, immunomagnetic beads were prepared by coupling anti-L. monocytogenes monoclonal antibody with magnetic beads. The fluorescence immunochromatographic strips were composed of anti-L. monocytogenes polyclonal antibody and mouse IgG marked by fluorescent microspheres as the detection antibody, anti-L. monocytogenes polyclonal antibody as the test line, and the goat anti-mouse IgG secondary antibody as the control line. Immunomagnetic separation was combined with a fluorescence immunochromatographic assay, and this method was applied to rapidly detect L. monocytogenes. The results showed that the detection limit of fluorescence immunochromatographic strips for pure cultures was 4 × 105 CFU/mL. For the joint detection method using samples concentrated 10- and 100-fold, the detection limits of pure culture samples were 4 × 104 CFU/mL and 1 × 104 CFU/mL, respectively. The joint detection method showed good specificity, and no cross-reactivity of the 10 strains kept in the laboratory was observed. The detection limit of artificially contaminated samples was also 1 × 104 CFU/mL and was not reduced compared with pure cultures. This method is of great value for rapid on-site detection of L. monocytogenes in food products.
Keywords:Listeria monocytogenes  antibody  immunomagnetic beads  fluorescence immunochromatography  rapid detection
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