Wagner P L, Neely M N, Zhang X, Acheson D W, Waldor M K, Friedman D I
Division of Geographic Medicine and Infectious Diseases, Tufts University School of Medicine, Boston, Massachusetts 02111, USA.
J Bacteriol. 2001 Mar;183(6):2081-5. doi: 10.1128/JB.183.6.2081-2085.2001.
Shiga toxins (Stxs), encoded by the stxA and stxB genes, are important contributors to the virulence of Escherichia coli O157:H7 and other Stx-producing E. coli (STEC) strains. The stxA and stxB genes in STEC strains are located on the genomes of resident prophages of the lambda family immediately downstream of the phage late promoters (p(R')). The phage-encoded Q proteins modify RNA polymerase initiating transcription at the cognate p(R') promoter which creates transcription complexes that transcend a transcription terminator immediately downstream of p(R') as well as terminator kilobases distal to p(R'). To test if this Q-directed processive transcription plays a role in stx(2)AB expression, we constructed a mutant prophage in an O157:H7 clinical isolate from which p(R') and part of Q were deleted but which has an intact pStx, the previously described stx(2)AB-associated promoter. We report that production of significant levels of Stx2 in this O157:H7 isolate depends on the p(R') promoter. Since transcription initiating at p(R') ultimately requires activation of the phage lytic cascade, expression of stx(2)AB in STEC depends primarily on prophage induction. By showing this central role for the prophage in stx(2)AB expression, our findings contradict the prevailing assumption that phages serve merely as agents for virulence gene transfer.
由stx A和stx B基因编码的志贺毒素(Stxs)是大肠杆菌O157:H7及其他产志贺毒素大肠杆菌(STEC)菌株毒力的重要贡献因素。STEC菌株中的stx A和stx B基因位于λ家族常驻原噬菌体的基因组上,紧挨着噬菌体晚期启动子(p(R'))的下游。噬菌体编码的Q蛋白修饰在同源p(R')启动子处起始转录的RNA聚合酶,从而形成转录复合物,该复合物能跨越p(R')下游紧邻的转录终止子以及p(R')下游数千碱基处的终止子。为了测试这种由Q引导的持续性转录是否在stx(2)AB表达中起作用,我们在一株O157:H7临床分离株中构建了一个突变原噬菌体,其中删除了p(R')和部分Q,但保留了完整的pStx,即先前描述的与stx(2)AB相关的启动子。我们报告称,该O157:H7分离株中产生显著水平的Stx2依赖于p(R')启动子。由于在p(R')处起始的转录最终需要噬菌体裂解级联反应的激活,因此STEC中stx(2)AB的表达主要依赖于原噬菌体诱导。通过证明原噬菌体在stx(2)AB表达中的这一核心作用,我们的发现与噬菌体仅作为毒力基因转移媒介的普遍假设相矛盾。