Park Hee Soo, Yoon Yu Min, Jung Sung Ji, Yun I Na Rae, Kim Cheol Min, Kim Jeong Mi, Kwak Jin-Hwan
School of Life and Food Sciences, Handong Global University, Seoul, South Korea.
Int J Antimicrob Agents. 2007 Nov;30(5):446-51. doi: 10.1016/j.ijantimicag.2007.07.006. Epub 2007 Aug 27.
CG400462, a novel FabI inhibitor, has a potent antibacterial activity against staphylococci. The minimal inhibitory concentration at which 90% of bacterial strains tested were inhibited (MIC(90)) of CG400462 was 0.5 microg/mL against 238 strains of Staphylococcus aureus and 1.0 microg/mL against 51 strains of coagulase-negative staphylococci, irrespective of whether the strains were methicillin-susceptible or -resistant. CG400462 was also effective by subcutaneous administration against systemic infections in mice. In time-kill studies, CG400462 at concentrations of 1x, 2x and 4x MIC had a bacteriostatic activity over 24h. Genetic approaches have confirmed that the mode of action of CG400462 is via inhibition of FabI, which is involved in the biosynthesis of fatty acids in bacteria. Study of the resistance mechanism of S. aureus showed that CG400462-resistant mutants had an alteration in FabI of Met99-->Thr or Tyr147-->His.
新型FabI抑制剂CG400462对葡萄球菌具有强大的抗菌活性。CG400462对238株金黄色葡萄球菌的90%受试菌株被抑制时的最低抑菌浓度(MIC90)为0.5微克/毫升,对51株凝固酶阴性葡萄球菌的MIC90为1.0微克/毫升,无论这些菌株对甲氧西林敏感还是耐药。CG400462经皮下给药对小鼠全身感染也有效。在时间-杀菌研究中,浓度为1倍、2倍和4倍MIC的CG400462在24小时内具有抑菌活性。遗传学方法已证实CG400462的作用方式是通过抑制FabI,FabI参与细菌脂肪酸的生物合成。对金黄色葡萄球菌耐药机制的研究表明,对CG400462耐药的突变体在FabI中存在Met99→Thr或Tyr147→His的改变。