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一种用于鉴定和区分炭疽杆菌强毒株的多重实时 PCR 方法。

A multiplex real-time PCR for identifying and differentiating B. anthracis virulent types.

机构信息

National Institute for Public Health and the Environment, Centre for infectious Disease Control, Laboratory for Zoonoses and Environmental Microbiology, Antonie van Leeuwenhoeklaan 9, PO Box 1, Bilthoven, The Netherlands.

出版信息

Int J Food Microbiol. 2011 Mar 1;145 Suppl 1:S137-44. doi: 10.1016/j.ijfoodmicro.2010.07.039. Epub 2010 Aug 10.

Abstract

Bacillus anthracis is closely related to the endospore forming bacteria Bacillus cereus and Bacillus thuringiensis. For accurate detection of the life threatening pathogen B. anthracis, it is essential to distinguish between these three species. Here we present a novel multiplex real-time PCR for simultaneous specific identification of B. anthracis and discrimination of different B. anthracis virulence types. Specific B. anthracis markers were selected by whole genome comparison and different sets of primers and probes with optimal characteristic for multiplex detection of the B. anthracis chromosome, the B. anthracis pXO1 and pXO2 plasmids and an internal control (IC) were designed. The primer sets were evaluated using a panel of B. anthracis strains and exclusivity was tested using genetically closely related B. cereus strains. The robustness of final primer design was evaluated by laboratories in three different countries using five different real-time PCR thermocyclers. Testing of a panel of more than 20 anthrax strains originating from different locations around the globe, including the recent Swedish anthrax outbreak strain, showed that all strains were detected correctly.

摘要

炭疽芽孢杆菌与产芽孢细菌蜡样芽孢杆菌和苏云金芽孢杆菌密切相关。为了准确检测具有生命威胁的病原体炭疽芽孢杆菌,区分这三种细菌至关重要。在此,我们提出了一种新型多重实时 PCR 方法,可同时特异性鉴定炭疽芽孢杆菌并区分不同的炭疽芽孢杆菌毒力类型。通过全基因组比较选择了特定的炭疽芽孢杆菌标记物,并设计了不同的引物和探针组,以优化多重检测炭疽芽孢杆菌染色体、炭疽芽孢杆菌 pXO1 和 pXO2 质粒以及内部对照 (IC) 的特性。使用一组炭疽芽孢杆菌菌株评估了引物组的特异性,并用遗传上密切相关的蜡样芽孢杆菌菌株进行了排他性测试。通过三个不同国家的实验室使用五台不同的实时 PCR 热循环仪评估了最终引物设计的稳健性。对来自全球不同地区的 20 多种炭疽菌株的测试,包括最近的瑞典炭疽爆发菌株,表明所有菌株均被正确检测到。

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