Department of Microbiology, The Ohio State University, Columbus, OH 43210, USA.
Clin Infect Dis. 2012 Aug;55 Suppl 2(Suppl 2):S127-31. doi: 10.1093/cid/cis358.
Fidaxomicin was recently approved for the treatment of Clostridium difficile infection. It inhibits transcription by bacterial RNA polymerase. Because transcription is a multistep process, experiments were conducted in which fidaxomicin was added at different stages of transcriptional initiation to identify the blocked step. DNA footprinting experiments were also conducted to further elucidate the stage inhibited. Fidaxomicin blocks initiation only if added before the formation of the "open promoter complex," in which the template DNA strands have separated but RNA synthesis has not yet begun. Binding of fidaxomicin precludes the initial separation of DNA strands that is prerequisite to RNA synthesis. These studies show that it has a mechanism distinct from that of elongation inhibitors, such as streptolydigin, and from the transcription initiation inhibitors myxopyronin and the rifamycins.
非达霉素最近被批准用于治疗艰难梭菌感染。它通过抑制细菌 RNA 聚合酶的转录来发挥作用。由于转录是一个多步骤的过程,因此进行了实验,在这些实验中,非达霉素在转录起始的不同阶段添加,以确定受阻的步骤。还进行了 DNA 足迹实验以进一步阐明被抑制的阶段。只有在形成“开放启动子复合物”之前添加非达霉素,才能阻止转录起始,在“开放启动子复合物”中,模板 DNA 链已经分离,但 RNA 合成尚未开始。非达霉素的结合阻止了 RNA 合成所必需的 DNA 链的初始分离。这些研究表明,它的作用机制与伸长抑制剂(如链道霉素)以及转录起始抑制剂米诺环素和利福霉素不同。