Akoachere Monique, Squires Raynal C, Nour Adel M, Angelov Ludmyl, Brojatsch Jürgen, Abel-Santos Ernesto
Department of Chemistry, University of Nevada-Las Vegas, Las Vegas, Nevada 89154, USA.
J Biol Chem. 2007 Apr 20;282(16):12112-8. doi: 10.1074/jbc.M611432200. Epub 2007 Feb 12.
Germination of Bacillus anthracis spores into the vegetative form is an essential step in anthrax pathogenicity. This process can be triggered in vitro by the common germinants inosine and alanine. Kinetic analysis of B. anthracis spore germination revealed synergy and a sequential mechanism between inosine and alanine binding to their cognate receptors. Because inosine is a critical germinant in vitro, we screened inosine analogs for the ability to block in vitro germination of B. anthracis spores. Seven analogs efficiently blocked this process in vitro. This led to the identification of 6-thioguanosine, which also efficiently blocked spore germination in macrophages and prevented killing of these cells mediated by B. anthracis spores. 6-Thioguanosine shows potential as an anti-anthrax therapeutic agent.
炭疽芽孢杆菌孢子萌发为营养体形式是炭疽病致病性的一个关键步骤。此过程在体外可由常见萌发剂肌苷和丙氨酸触发。炭疽芽孢杆菌孢子萌发的动力学分析揭示了肌苷和丙氨酸与其同源受体结合之间的协同作用及顺序机制。由于肌苷在体外是一种关键的萌发剂,我们筛选了肌苷类似物阻断炭疽芽孢杆菌孢子体外萌发的能力。七种类似物在体外有效阻断了这一过程。这导致了6-硫代鸟苷的鉴定,其也能有效阻断巨噬细胞中的孢子萌发,并防止炭疽芽孢杆菌孢子介导的这些细胞的杀伤。6-硫代鸟苷显示出作为抗炭疽治疗剂的潜力。