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超级细菌NDM-1基因高通量微球悬浮芯片检测方法的建立

Establishment of detecting method of NDM-1 gene by microsphere suspension array

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【作者】 张云霞郝杰吴兴海杨伟克梁炜陈长法曹际娟

【Author】 Zhang Yunxia1, Hao jie1, Wu Xinghai2+, Yang Weike1, Liang Wei2, Chen Changfa1, Cao Jijuan3(1 Qingdao Exit-Entry Inspection and Quarantine Bureau, Qingdao 266002, China;2 Shandong Exit-Entry Inspection and Quarantine Bureau, Qingdao 266002, China;3 Liao Ning Exit-Entry Inspection and Quarantine Bureau, Dalian 116000,China)

【机构】 青岛出入境检验检疫局山东出入境检验检疫局辽宁出入境检验检疫局技术中心

【摘要】 本研究以建立微球体悬浮芯片检测方法为目的,选择三种超级细菌NDM-1基因(metallo-beta-lactamase 1 gene)为目的基因,设计并合成标记特异性探针,与荧光编码微球偶联后与细菌NDM-1基因的PCR产物杂交反应,用微球悬浮芯片检测仪检测荧光信号,建立可快速检测该种基因的微球体悬浮芯片检测方法。特异性和灵敏度检测结果表明:该方法对NDM-1基因检测具有特异性,最低检测限可达10fg/μL,灵敏度高于普通PCR技术,提示微球体悬浮芯片是一种针对NDM-1的快速、灵敏、便捷的新型核酸检测技术。

【Abstract】 In this paper, a new method, which based on liquid chip to detect NDM-1 (metallo-beta-lactamase 1 gene) sample was established. A highly specific probe was synthesized and marked by biotin to target the NDM-1, coupled with fluorescent coded microspheres, and then hybridized with the PCR product of NDM-1 gene. Hybridization fluorescence signal was detected through microsphere suspension array (MSA). Specific and sensitivity were tested which were compared with PCR method. The result shows that the sensitivity of MSA was 10 fg/μl of vector DNA, which was higher than the result of PCR method. Detecting NDM-1 with MSA is specific and sensitive method.

【基金】 山东检验检疫局科技专项:食品中超级细菌耐药基因NDM-1基因多重复合痕量检测体系的建立(SK2008-19)
  • 【文献出处】 食品安全质量检测学报 ,Journal of Food Safety & Quality , 编辑部邮箱 ,2011年03期
  • 【分类号】TS207.4;R155
  • 【下载频次】135
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