Lee Seongyeon, Lee Taegum, Kim Mi Kyoung, Ahn Joong Hoon, Jeong Seri, Park Ki-Ho, Chong Youhoon
Department of Bioscience and Biotechnology, Bio/Molecular Informatics Center, Konkuk University, Hwayang-dong, Gwangjin-gu, Seoul 143-701, Republic of Korea.
Department of Laboratory Medicine, Hallym University College of Medicine, Chuncheon 24252, Republic of Korea.
Antibiotics (Basel). 2024 Dec 10;13(12):1202. doi: 10.3390/antibiotics13121202.
Previously, we reported that 3--alkyl difluoroquercetins (di-F-Q) potentiates the antimicrobial activity of aztreonam (ATM) against metallo-β-lactamase (MBL)-producing through simultaneous inhibition of MBLs and efflux pumps. However, the ATM-potentiating activity of the 3--alkyl di-F-Q was observed only at high and potentially toxic concentrations (32 mg/L). As both MBLs and efflux pumps reside in the periplasm of Gram-negative bacteria, their inhibitors should accumulate in the periplasmic space. However, the outer membrane porins, the major entry pathway in Gram-negative bacteria, allow the passive diffusion of hydrophilic polar molecules across the outer membrane. Thus, we reasoned that the introduction of a polar substituent at 7-OH position of 3--alkyl di-F-Q would enhance its periplasmic concentration to result in potentiation of ATM at lower concentrations. The title compound exhibited inhibitory activity against NDM-1 as well as the efflux pump of , which resulted in synergistical potentiation of ATM. A combination of ATM (8 mg/L) and (8 mg/L) inhibited 80% of the ATM-resistant CPPA, while ATM alone did not show any inhibition. In addition, only 4 mg/L of was needed to reduce the MIC of ATM four-fold in ATM-resistant CPPA (n = 15). The time-kill data further supported the effectiveness of the combined treatment of ATM with , and the combination of ATM (1xMIC) with 8 mg/L of showed bactericidal effects in every bacterial strain tested (PA-002, , PA-003, , PA-014, , and PA-017, ) by reducing the bacterial loads by 5.1 log8.9 log. The title compound exhibited inhibitory activity against NDM-1 as well as the efflux pump of , and the combined inhibitory activity resulted in synergistical potentiation of ATM. It should be noted that most CPPA isolates tested were sensitized to 8 mg/L of ATM upon combination with 48 mg/L of .
此前,我们报道了3-烷基二氟槲皮素(di-F-Q)通过同时抑制金属β-内酰胺酶(MBL)和外排泵,增强了氨曲南(ATM)对产MBL细菌的抗菌活性。然而,3-烷基二氟喹啉的ATM增强活性仅在高浓度且可能有毒的浓度(32mg/L)下才观察到。由于MBL和外排泵都存在于革兰氏阴性菌的周质中,它们的抑制剂应该在周质空间中积累。然而,外膜孔蛋白是革兰氏阴性菌的主要进入途径,它允许亲水性极性分子被动扩散穿过外膜。因此,我们推测在3-烷基二氟喹啉的7-OH位置引入极性取代基会提高其在周质中的浓度,从而在较低浓度下增强ATM的活性。标题化合物对NDM-1以及[具体细菌名称]的外排泵具有抑制活性,这导致了ATM的协同增强作用。ATM(8mg/L)和[标题化合物名称](8mg/L)的组合抑制了80%的耐ATM的[具体细菌名称],而单独的ATM没有显示出任何抑制作用。此外,在耐ATM的[具体细菌名称](n = 15)中,仅需4mg/L的[标题化合物名称]就能将ATM的最低抑菌浓度降低四倍。时间-杀菌数据进一步支持了ATM与[标题化合物名称]联合治疗的有效性,并且ATM(1xMIC)与8mg/L的[标题化合物名称]的组合在测试的每种细菌菌株(PA - 002、[具体细菌名称]、PA - 003、[具体细菌名称]、PA - 014、[具体细菌名称]和PA - 017、[具体细菌名称])中都显示出杀菌作用,使细菌载量降低了5.1 log至8.9 log。标题化合物对NDM-1以及[具体细菌名称]的外排泵具有抑制活性,并且联合抑制活性导致了ATM的协同增强作用。应该注意的是,大多数测试的[具体细菌名称]分离株在与4至8mg/L的[标题化合物名称]联合使用时对8mg/L的ATM敏感。