Livermore David M, Warner Marina, Mushtaq Shazad, Woodford Neil
Antimicrobial Resistance and Healthcare Associated Infections Reference Unit, Public Health England, London, United Kingdom Norwich Medical School, University of East Anglia, Norwich, Norfolk, United Kingdom
Antimicrobial Resistance and Healthcare Associated Infections Reference Unit, Public Health England, London, United Kingdom.
Antimicrob Agents Chemother. 2015 Nov 9;60(1):554-60. doi: 10.1128/AAC.02184-15. Print 2016 Jan.
OP0595 is a novel diazabicyclooctane which, like avibactam, inhibits class A and C β-lactamases. In addition, unlike avibactam, it has antibacterial activity, with MICs of 0.5 to 4 μg/ml for most members of the family Enterobacteriaceae, owing to inhibition of PBP2; moreover, it acts synergistically with PBP3-active β-lactams independently of β-lactamase inhibition, via an "enhancer effect." Enterobacteriaceae mutants stably resistant to 16 μg/ml OP0595 were selected on agar at frequencies of approximately 10(-7). Unsurprisingly, OP0595 continued to potentiate substrate β-lactams against mutants derived from Enterobacteriaceae with OP0595-inhibited class A and C β-lactamases. Weaker potentiation of partners, especially aztreonam, cefepime, and piperacillin--less so meropenem--remained frequent for OP0595-resistant Enterobacteriaceae mutants lacking β-lactamases or with OP0595-resistant metallo-β-lactamases (MBLs), indicating that the enhancer effect is substantially retained even when antibiotic activity is lost.
OP0595是一种新型二氮杂双环辛烷,与阿维巴坦一样,可抑制A类和C类β-内酰胺酶。此外,与阿维巴坦不同的是,它具有抗菌活性,对大多数肠杆菌科细菌的最低抑菌浓度(MIC)为0.5至4μg/ml,这是由于其对青霉素结合蛋白2(PBP2)的抑制作用;此外,它通过“增强子效应”与PBP3活性β-内酰胺协同作用,而与β-内酰胺酶抑制无关。在琼脂平板上以约10^(-7)的频率筛选出对16μg/ml OP0595稳定耐药的肠杆菌科突变体。不出所料,OP0595继续增强底物β-内酰胺对来自肠杆菌科且其A类和C类β-内酰胺酶被OP0595抑制的突变体的作用。对于缺乏β-内酰胺酶或具有对OP0595耐药的金属β-内酰胺酶(MBL)的OP0595耐药肠杆菌科突变体,其对搭档药物(尤其是氨曲南、头孢吡肟和哌拉西林,美罗培南的情况稍弱)的增强作用仍然常见,这表明即使抗生素活性丧失,增强子效应仍基本保留。