Hu Xiaomin, Hansen Bjarne Munk, Hendriksen Niels Bohse, Yuan Zhiming
Wuhan Institute of Virology, Chinese Academy of Science, Wuhan 430071, China.
Biochem Biophys Res Commun. 2006 Nov 3;349(4):1214-9. doi: 10.1016/j.bbrc.2006.08.125. Epub 2006 Aug 31.
The presence of one of the anthrax virulence plasmid pXO1 conserved fragments was analyzed in 24 Bacillus cereus and B. thuringiensis strains, including 6 B. thuringiensis subspecies, by polymerase chain reactions. Twelve out of 24 strains showed PCR-positive for an ORF101 homologous sequence. Two pXO1-ORF101-like fragments from a B. cereus B-4ac and a commercial B. thuringiensis kurstaki HD1 were cloned, sequenced and expressed in Escherichia coli. Toxicity assays revealed that the product encoded by the pXO1-ORF101-like fragment had no impact on either Vero cells or Chinese Hamster Ovary cells, suggesting that this fragment probably not contribute to enterotoxic activity. Sequence alignment of the pXO1-ORF101 from three Bacillus anthracis and ORF101-like fragments from other 12 B. cereus group isolates indicated high identity (more than 90%) and the presence of subgroup- and strain-specific SNPs among these fragments.
通过聚合酶链反应,对24株蜡样芽孢杆菌和苏云金芽孢杆菌菌株(包括6个苏云金芽孢杆菌亚种)进行分析,检测其中一个炭疽毒力质粒pXO1保守片段的存在情况。24株菌株中有12株对ORF101同源序列呈PCR阳性。从蜡样芽孢杆菌B-4ac和商业苏云金芽孢杆菌库斯塔克HD1中克隆了两个pXO1-ORF101样片段,进行测序并在大肠杆菌中表达。毒性试验表明,pXO1-ORF101样片段编码的产物对Vero细胞或中国仓鼠卵巢细胞均无影响,这表明该片段可能对肠毒素活性没有贡献。对来自三株炭疽芽孢杆菌的pXO1-ORF101和来自其他12株蜡样芽孢杆菌属分离株的ORF101样片段进行序列比对,结果显示这些片段具有高度同一性(超过90%),并且在这些片段中存在亚组和菌株特异性单核苷酸多态性。