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用于检测致病性副溶血性弧菌菌株的多重实时聚合酶链反应检测法

Multiplex real-time PCR assay for detection of pathogenic Vibrio parahaemolyticus strains.

作者信息

He Peiyan, Chen Zhongwen, Luo Jianyong, Wang Henghui, Yan Yong, Chen Lixia, Gao Wenjie

机构信息

Jiaxing Center for Disease Control and Prevention, No. 486, Wen Qiao Road, Jiaxing, Zhejiang 314050, China.

Jiaxing Center for Disease Control and Prevention, No. 486, Wen Qiao Road, Jiaxing, Zhejiang 314050, China.

出版信息

Mol Cell Probes. 2014 Oct-Dec;28(5-6):246-50. doi: 10.1016/j.mcp.2014.06.001. Epub 2014 Jun 9.

Abstract

Foodborne disease caused by pathogenic Vibrio parahaemolyticus has become a serious public health problem in many countries. Rapid diagnosis and the identification of pathogenic V. parahaemolyticus are very important in the context of public health. In this study, an EvaGreen-based multiplex real-time PCR assay was established for the detection of pathogenic V. parahaemolyticus. This assay targeted three genetic markers of V. parahaemolyticus (species-specific gene toxR and virulence genes tdh and trh). The assay could unambiguously identify pathogenic V. parahaemolyticus with a minimum detection limit of 1.4 pg genomic DNA per reaction (concentration giving a positive multiplex real-time PCR result in 95% of samples). The specificity of the assay was evaluated using 72 strains of V. parahaemolyticus and other bacteria. A validation of the assay with clinical samples confirmed its sensitivity and specificity. Our data suggest the newly established multiplex real-time PCR assay is practical, cost-effective, specific, sensitive and capable of high-throughput detection of pathogenic V. parahaemolyticus.

摘要

由致病性副溶血性弧菌引起的食源性疾病已成为许多国家严重的公共卫生问题。在公共卫生背景下,快速诊断和鉴定致病性副溶血性弧菌非常重要。在本研究中,建立了一种基于 EvaGreen 的多重实时 PCR 检测方法,用于检测致病性副溶血性弧菌。该检测方法针对副溶血性弧菌的三个基因标记(种特异性基因 toxR 和毒力基因 tdh 及 trh)。该检测方法能够明确鉴定致病性副溶血性弧菌,每个反应的最低检测限为 1.4 pg 基因组 DNA(在 95%的样本中产生多重实时 PCR 阳性结果的浓度)。使用 72 株副溶血性弧菌和其他细菌评估了该检测方法的特异性。用临床样本对该检测方法进行验证,证实了其敏感性和特异性。我们的数据表明,新建立的多重实时 PCR 检测方法实用、经济高效、特异且灵敏,能够高通量检测致病性副溶血性弧菌。

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