Findlay Jacqueline, Moreno Hector, Greub Gilbert, Le Terrier Christophe, Bouvier Maxime, Nordmann Patrice
Medical and Molecular Microbiology, Faculty of Science and Medicine, University of Fribourg, 1700 Fribourg, Switzerland.
Institute of Microbiology, University Hospital Centre and University of Lausanne, 1011 Lausanne, Switzerland.
FEMS Microbiol Lett. 2025 Jan 10;372. doi: 10.1093/femsle/fnaf052.
The treatment of infections caused by MBL-producing Pseudomonas aeruginosa, including IMP-producers, can be challenging since MBLs confer resistance to most clinically available ß-lactams, leaving few viable options. Thiol-containing compounds, such as meso-dimercaptosuccinic acid (DMSA), have been suggested as inhibitors of MBLs, and particularly have been proposed to exert effective activity against IMP-1 enzymes. In this context, we sought to determine the activity of DMSA, in combination with carbapenems or cephalosporins, against diverse MBL and carbapenemase variants, particularly focussing on IMP variants. In recombinant strains producing either IMP-1, IMP-10, or IMP-13, both with and without a functional OprD, synergy was observed with ceftazidime (CAZ), cefepime (FEP), and meropenem. Negligible changes were observed for other MBLs and no effect was observed in stains producing KPC-2. Testing of the CAZ/DMSA and FEP/DMSA combinations against clinical IMP-producing P. aeruginosa isolates resulted in fractional inhibitory concentration indexes indicating synergy. Enzymatic assays showed a significantly increased inhibitory activity of DMSA against the IMP variants, compared to the other enzymes tested. These findings highlight a possible role of DMSA or DMSA-like compounds to be developed for the treatment of infections caused by IMP-producing P. aeruginosa.
由产金属β-内酰胺酶(MBL)的铜绿假单胞菌引起的感染,包括产IMP酶的菌株,其治疗颇具挑战性,因为MBL可使细菌对大多数临床可用的β-内酰胺类抗生素产生耐药性,从而使可行的治疗选择寥寥无几。含硫醇的化合物,如内消旋二巯基琥珀酸(DMSA),已被认为是MBL的抑制剂,尤其被提议对IMP-1酶具有有效活性。在此背景下,我们试图确定DMSA与碳青霉烯类或头孢菌素类联合使用时,对多种MBL和碳青霉烯酶变体的活性,特别关注IMP变体。在产生IMP-1、IMP-10或IMP-13的重组菌株中,无论有无功能性外膜孔蛋白D(OprD),均观察到与头孢他啶(CAZ)、头孢吡肟(FEP)和美罗培南有协同作用。对于其他MBL,观察到的变化可忽略不计,而在产KPC-2的菌株中未观察到任何影响。对临床产IMP的铜绿假单胞菌分离株进行CAZ/DMSA和FEP/DMSA组合测试,结果显示部分抑菌浓度指数表明存在协同作用。酶活性测定表明,与其他测试酶相比,DMSA对IMP变体的抑制活性显著增加。这些发现凸显了DMSA或类似DMSA的化合物在开发用于治疗产IMP的铜绿假单胞菌引起的感染方面可能发挥的作用。