Buchan Blake W, McLendon Molly K, Jones Bradley D
Department of Microbiology, University of Iowa School of Medicine, 51 Newton Road, Iowa City, IA 52242-1109, USA.
Appl Environ Microbiol. 2008 May;74(9):2637-45. doi: 10.1128/AEM.02882-07. Epub 2008 Mar 14.
Francisella tularensis is the etiologic agent of an intracellular systemic infection of the lymphatic system in humans called tularemia. The organism has become the subject of considerable research interest due to its classification as a category A select agent by the CDC. To aid genetic analysis of this pathogen, we have constructed a temperature-sensitive Tn5-based transposon delivery system that is capable of generating chromosomal reporter fusions with lacZ or luxCDABE, enabling us to monitor gene expression. Transposition is catalyzed by the hyperactive Tn5 transposase, whose expression is driven by the Francisella groES promoter. When high-temperature selection (42 degrees C) is applied to a bacterial culture carrying the transposon delivery plasmid, approximately 0.1% of the population is recovered with Tn5 insertions in the chromosome. Nucleotide sequence analysis of a sample of mutants revealed that the insertions occur randomly throughout the chromosome. The kanamycin-selectable marker of the transposon is also flanked by FLP recombination target sequences that allow deletion of the antibiotic resistance gene when desired. This system has been used to generate transposon mutant libraries for the F. tularensis live vaccine strain as well as two different virulent F. tularensis strains. Chromosomal reporters delivered with the transposon were used to identify genes upregulated by growth in Chamberlain's defined medium. Genes in the fsl operon, reported to be involved in iron acquisition, as well as genes in the igl gene cluster were among those identified by the screen. Further experiments implicate the ferric uptake regulator (Fur) protein in the negative regulation of fsl but not igl reporters, which occurs in an iron-dependent manner. Our results indicate that we have created a valuable new transposon that can be used to identify and characterize virulence genes in F. tularensis strains.
土拉弗朗西斯菌是人类一种称为兔热病的淋巴系统细胞内系统性感染的病原体。由于被美国疾病控制与预防中心(CDC)列为A类选择生物制剂,该生物体已成为大量研究关注的对象。为了辅助对这种病原体进行遗传分析,我们构建了一种基于温度敏感型Tn5的转座子递送系统,该系统能够产生与lacZ或luxCDABE的染色体报告基因融合体,使我们能够监测基因表达。转座由高活性Tn5转座酶催化,其表达由土拉弗朗西斯菌groES启动子驱动。当对携带转座子递送质粒的细菌培养物进行高温选择(42℃)时,约0.1%的群体可回收得到染色体上有Tn5插入的菌株。对突变体样本的核苷酸序列分析表明,插入在整个染色体上随机发生。转座子的卡那霉素选择标记也侧翼有FLP重组靶序列,允许在需要时删除抗生素抗性基因。该系统已用于为土拉弗朗西斯菌活疫苗株以及两种不同的土拉弗朗西斯菌强毒株构建转座子突变体文库。随转座子递送的染色体报告基因用于鉴定在张伯伦限定培养基中生长上调的基因。据报道参与铁摄取的fsl操纵子中的基因以及igl基因簇中的基因是通过筛选鉴定出的基因之一。进一步的实验表明,铁摄取调节蛋白(Fur)对fsl报告基因有负调控作用,但对igl报告基因没有,这种调控以铁依赖的方式发生。我们的结果表明,我们创建了一种有价值的新型转座子,可用于鉴定和表征土拉弗朗西斯菌菌株中的毒力基因。