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优化的选择性增菌培养基对李斯特菌 p60 蛋白作为抗原在特异性夹心 ELISA 中表达的影响。

Effect of the optimized selective enrichment medium on the expression of the p60 protein used as Listeria monocytogenes antigen in specific sandwich ELISA.

机构信息

INRS-Institut Armand-Frappier, Research Laboratories in Sciences Applied to Food, Canadian Irradiation Centre, 531 boulevard des Prairies, Laval, Quebec, H7V 1B7, Canada.

Institute of Food Science -CNR, Laboratory for Molecular Sensing, Via Roma, 64 111, 83100, Avellino, Italy.

出版信息

Res Microbiol. 2019 Jun-Aug;170(4-5):182-191. doi: 10.1016/j.resmic.2019.03.004. Epub 2019 Apr 3.

DOI:10.1016/j.resmic.2019.03.004
PMID:30953690
Abstract

This paper presents the effects of the composition of different media (i.e., Tryptic soy broth (TSB), Brain heart infusion (BHI), Listeria enrichment broth (LEB), Fraser broth (FB) and University of Vermont medium (UVM)) on the detection of a short peptide fragment PepD specific to the p60 protein (p60) of L. monocytogenes by a monoclonal antibody (anti-PepD mAb). Expression of the p60 obtained was demonstrated to be proportional to the cellular growth of Listeria monocytogenes regardless of the tested growth medium. However, the early growth of L. monocytogenes and the expression of the p60 were negatively affected by the presence of selective agents present in LEB, FB and UVM. Among those three selective enrichment media commonly used for L. monocytogenes, LEB allowed a better expression of L. monocytogenes p60 after an incubation period of 18 h. Optimization of the LEB revealed that the dextrose concentration was the critical factor for improving the expression of p60 and promotes the early expression of p60. Moreover, an optimal dextrose concentration of 0.5% (w/v) in LEB, coupled with anti-PepD mAb immobilized to solid support, reduced the detection of p60 from 18 h to 9 h for an initial concentration of L. monocytogenes of 10 CFU/ml.

摘要

本文研究了不同培养基(即胰蛋白胨大豆肉汤(TSB)、脑心浸液(BHI)、李斯特菌增菌肉汤(LEB)、弗氏肉汤(FB)和佛蒙特大学培养基(UVM))的组成对单克隆抗体(抗 PepD mAb)检测短肽片段 PepD (特异性针对李斯特菌 p60 蛋白(p60)的影响。结果表明,无论使用何种测试生长培养基,p60 的表达都与李斯特菌的细胞生长成正比。然而,LEB、FB 和 UVM 中存在的选择性试剂会对李斯特菌的早期生长和 p60 的表达产生负面影响。在这三种常用的李斯特菌选择性增菌培养基中,LEB 允许在孵育 18 小时后更好地表达李斯特菌 p60。LEB 的优化结果表明,葡萄糖浓度是提高 p60 表达和促进 p60 早期表达的关键因素。此外,在 LEB 中葡萄糖浓度优化至 0.5%(w/v),并将抗 PepD mAb 固定在固体载体上,可将 p60 的检测时间从 18 小时缩短至 9 小时,对于初始浓度为 10 CFU/ml 的李斯特菌。

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