Tyler Jessica S, Mills Melissa J, Friedman David I
Department of Microbiology and Immunology, University of Michigan, Ann Arbor, MI 48103, USA.
J Bacteriol. 2004 Nov;186(22):7670-9. doi: 10.1128/JB.186.22.7670-7679.2004.
The genes encoding Shiga toxin (Stx), the major virulence factor of Shiga toxin-producing Escherichia coli, are carried in the genomes of bacteriophages that belong to the lambdoid family of phages. Previous studies demonstrated that induction of prophages encoding stx significantly enhances the production and/or release of Stx from the bacterium. Therefore, factors that regulate the switch between lysogeny and lytic growth, e.g., repressor, operator sites, and associated phage promoters, play important roles in regulating the production and/or release of Stx. We report the results of genetic and biochemical studies characterizing these elements of the Stx-encoding bacteriophage 933W. Like lambda, 933W has three operator repeats in the right operator region (OR), but unlike lambda and all other studied lambdoid phages, which have three operator repeats in the left operator region (OL), 933W only has two operator repeats in OL. As was observed with lambda, the 933W OR and OL regions regulate transcription from the early PR and PL promoters, respectively. A lysogen carrying a 933W derivative encoding a noncleavable repressor fails to produce Stx, unlike a lysogen carrying a 933W derivative encoding a cleavable repressor. This finding provides direct evidence that measurable expression of the stx genes encoded by a 933W prophage requires induction of that prophage with the concomitant initiation of phage gene expression.
编码志贺毒素(Stx)的基因是产志贺毒素大肠杆菌的主要毒力因子,它存在于属于λ样噬菌体家族的噬菌体基因组中。先前的研究表明,诱导编码stx的原噬菌体可显著提高细菌中Stx的产生和/或释放。因此,调节溶原性和裂解生长之间转换的因素,如阻遏物、操纵位点和相关的噬菌体启动子,在调节Stx的产生和/或释放中起着重要作用。我们报告了对编码Stx的噬菌体933W这些元件进行遗传和生化研究的结果。与λ噬菌体一样,933W在右侧操纵区(OR)有三个操纵子重复序列,但与λ噬菌体以及所有其他已研究的λ样噬菌体不同,它们在左侧操纵区(OL)有三个操纵子重复序列,933W在OL区只有两个操纵子重复序列。正如在λ噬菌体中观察到的那样,933W的OR区和OL区分别调节早期PR和PL启动子的转录。与携带编码可裂解阻遏物的933W衍生物的溶原菌不同,携带编码不可裂解阻遏物的933W衍生物的溶原菌不能产生Stx。这一发现提供了直接证据,即933W原噬菌体编码的stx基因的可测量表达需要该原噬菌体的诱导以及噬菌体基因表达的同时启动。