Kim Kijeong, Seo Juwon, Wheeler Katherine, Park Chulmin, Kim Daewhan, Park Seungjoon, Kim Wonyong, Chung Sang-In, Leighton Terrance
Department of Microbiology, College of Medicine, Chung-Ang Univerisity, 221, Heuksuk-dong, Dongjak-gu, Seoul 156-756, South Korea.
FEMS Immunol Med Microbiol. 2005 Feb 1;43(2):301-10. doi: 10.1016/j.femsim.2004.10.005.
Bacillus anthracis has four plasmid possible virulence genotypes: pXO1+/pXO2+, pXO1+/pXO2-, pXO1-/pXO2+ or pXO1-/pXO2-. Due to the lack of a specific chromosomal marker for B. anthracis, differentiation of the pXO1-/pXO2- form of B. anthracis from closely related Bacillus cereus group species is difficult. In this study, we evaluate the ability of sspE, pXO1 and pXO2 primers to discriminate individual B. anthracis and the B. cereus group genotypes using multiplex real-time PCR and melting curve analysis. Optimal conditions for successful multiplex assays have been established. Purified DNAs from 38 bacterial strains including 11 strains of B. anthracis and 18 B. cereus group strains were analyzed. Nine of the B. cereus group near-neighbor strains were shown by multilocus sequence typing to be phylogenetically proximate to the B. anthracis clade. We have demonstrated that the four plasmid genotypes of B. anthracis and B. cereus group near-neighbors were differentially and simultaneously discriminated by this assay.
pXO1+/pXO2+、pXO1+/pXO2-、pXO1-/pXO2+或pXO1-/pXO2-。由于缺乏炭疽芽孢杆菌特异性的染色体标记,很难将炭疽芽孢杆菌的pXO1-/pXO2-形式与密切相关的蜡样芽孢杆菌群物种区分开来。在本研究中,我们使用多重实时PCR和熔解曲线分析评估了sspE、pXO1和pXO2引物区分单个炭疽芽孢杆菌和蜡样芽孢杆菌群基因型的能力。已建立了成功进行多重检测的最佳条件。对来自38株细菌的纯化DNA进行了分析,其中包括11株炭疽芽孢杆菌和18株蜡样芽孢杆菌群菌株。多位点序列分型显示,9株蜡样芽孢杆菌群近邻菌株在系统发育上与炭疽芽孢杆菌进化枝接近。我们已经证明,通过该检测可以同时区分炭疽芽孢杆菌的四种质粒基因型和蜡样芽孢杆菌群近邻菌株。