Park Si-Hong, Kim Hyun-Joong, Kim Jae-Hwan, Kim Tae-Woon, Kim Hae-Yeong
Institute of Life Sciences & Resources, Graduate School of Biotechnology, Kyung Hee University, Suwon 449-701, Korea.
J Microbiol Biotechnol. 2007 Jul;17(7):1177-82.
Bacillus cereus group bacteria share a significant degree of genetic similarity. Thus, to differentiate and identify the Bacillus cereus group efficiently, a multiplex PCR method using the gyrB and groEL genes as diagnostic markers is suggested for simultaneous detection. The assay yielded a 400 bp amplicon for the groEL gene from all the B. cereus group bacteria, and a 253 bp amplicon from B. anthracis, 475 bp amplicon from B. cereus, 299 bp amplicon from B. thuringiensis, and 604 bp amplicon from B. mycoides for the gyrB gene. No nonspecific amplicons were observed with the DNA from 29 other pathogenic bacteria. The specificity and sensitivity of the B. cereus group identification using this multiplex PCR assay were evaluated with different kinds of food samples. In conclusion, the proposed multiplex PCR is a reliable, simple, rapid, and efficient method for the simultaneous identification of B. cereus group bacteria from food samples in a single tube.
蜡样芽孢杆菌群细菌具有高度的遗传相似性。因此,为了高效地区分和鉴定蜡样芽孢杆菌群,建议使用gyrB和groEL基因作为诊断标记的多重PCR方法进行同步检测。该检测方法从所有蜡样芽孢杆菌群细菌中扩增出了一条400 bp的groEL基因扩增子,从炭疽芽孢杆菌中扩增出了一条253 bp的扩增子,从蜡样芽孢杆菌中扩增出了一条475 bp的扩增子,从苏云金芽孢杆菌中扩增出了一条299 bp的扩增子,从蕈状芽孢杆菌中扩增出了一条604 bp的gyrB基因扩增子。未观察到来自其他29种病原菌的DNA产生非特异性扩增子。使用该多重PCR检测方法对蜡样芽孢杆菌群鉴定的特异性和灵敏度进行了不同种类食品样本的评估。总之,所提出的多重PCR是一种可靠、简单、快速且高效的方法,可在单管中同时从食品样本中鉴定蜡样芽孢杆菌群细菌。