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从绞碎牛肉中免疫磁珠分离肠出血性大肠杆菌O157:H7并通过基质辅助激光解吸/电离飞行时间质谱和数据库检索进行鉴定。

Immunomagnetic isolation of enterohemorrhagic Escherichia coli O157:H7 from ground beef and identification by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry and database searches.

作者信息

Ochoa Mariela L, Harrington Peter B

机构信息

Center for Intelligent Chemical Instrumentation, Department of Chemistry and Biochemistry, Clippinger Laboratories, Ohio University, Athens, OH 45701-2979, USA.

出版信息

Anal Chem. 2005 Aug 15;77(16):5258-67. doi: 10.1021/ac0502596.

DOI:10.1021/ac0502596
PMID:16097767
Abstract

A rapid (25 min) and facile method was developed for the isolation and identification of the enterohemorrhagic Escherichia coli (serotype O157:H7) in ground beef. The isolation method employed microscopic magnetic beads coated with antibodies covalently bonded to the surface that were specific to antigens of serotype O157. This selective preconcentration step was necessary because direct matrix-assisted laser desorption/ionization (MALDI) MS analysis of bacteria was not amenable, serving to isolate the bacteria from meat components and other nontarget bacteria. The immunomagnetic separation increased the sensitivity of the method and permitted the detection of bacteria in meat. MALDI time-of-flight MS furnished bacterial mass spectra that were useful for organism identification. Molecular weight database searches using the Expert Protein Analysis System proved useful for confirmation of the organism's identity. Bacterial biomarkers from direct MALDI analysis of pure bacterial suspensions were consistently present in bacterial suspensions of buffer/tryptic soy broth (positive controls) and meat extract samples. The detection limits were 2 x 10(6) cells/mL for the experimental approach used herein. Cross-reactivity studies performed on three nontarget bacterial strains revealed that the immunomagnetic beads are specific only to E. coli strain serotype O157:H7, and there is no cross-reactivity with the other relatively innocuous strains studied.

摘要

开发了一种快速(25分钟)且简便的方法,用于分离和鉴定绞碎牛肉中的肠出血性大肠杆菌(血清型O157:H7)。该分离方法采用了表面共价结合有针对O157血清型抗原的抗体的微观磁珠。这一选择性预浓缩步骤是必要的,因为对细菌进行直接基质辅助激光解吸/电离(MALDI)质谱分析并不适用,其作用是从肉类成分和其他非目标细菌中分离出细菌。免疫磁分离提高了该方法的灵敏度,并能够检测肉类中的细菌。MALDI飞行时间质谱提供了有助于鉴定微生物的细菌质谱。使用专家蛋白质分析系统进行分子量数据库搜索被证明有助于确认微生物的身份。来自纯细菌悬液直接MALDI分析的细菌生物标志物始终存在于缓冲液/胰蛋白胨大豆肉汤(阳性对照)和肉提取物样品的细菌悬液中。本文所采用的实验方法的检测限为2×10⁶个细胞/毫升。对三种非目标细菌菌株进行的交叉反应研究表明,免疫磁珠仅对大肠杆菌O157:H7血清型菌株具有特异性,与所研究的其他相对无害的菌株无交叉反应。

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