Department of Pediatrics, Chang Gung Memorial Hospital, Keelung Branch, Keelung, Taiwan; Chang Gung University College of Medicine, Taoyuan, Taiwan; Molecular Infectious Disease Research Center, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
Chang Gung University College of Medicine, Taoyuan, Taiwan; Department of Laboratory Medicine, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
Int J Antimicrob Agents. 2014 Dec;44(6):541-5. doi: 10.1016/j.ijantimicag.2014.07.022. Epub 2014 Sep 16.
Pseudomonas aeruginosa isolates that were initially carbapenem-susceptible and later became selective carbapenem-resistant following antimicrobial therapy were identified from individual cases during the same hospitalisation. Cross-resistance to other β-lactams was not found and their susceptibilities remained identical in consecutive isolates. Real-time quantitative reverse transcription PCR was performed to investigate the role of OprD, an outer membrane protein regulating the entry of carbapenems, in the appearance of carbapenem-resistant-only P. aeruginosa (CROPA). Fifteen paired isolates of carbapenem-susceptible P. aeruginosa (CS-PA) and CROPA were identified. All of the cases had carbapenem exposure history within 1 month before the appearance of CROPA (mean 10 days). Reduced OprD expression was found in 93% (14/15) of the isolates, suggesting that oprD inactivation was the major contributor to selective carbapenem resistance. Of the 14 cases with CROPA due to oprD mutation, 71% (10/14) were persistent infection, as genotype analysis revealed that their paired strains were isogenic; 29% (4/14) represented re-infections as they were heterogenic, suggesting that oprD-deficient CROPA existed in the hospital and that carbapenem selective pressure promoted its spread to patients. We conclude that CROPA may occur soon after the use of carbapenems to treat CS-PA infections and that oprD mutation is the major mechanism of resistance in CROPA. Restriction of empirical use of carbapenems by antibiotic stewardship is important to halt the occurrence of CROPA.
从同一住院患者中鉴定出初始对碳青霉烯类敏感但随后在抗菌治疗后选择性碳青霉烯类耐药的铜绿假单胞菌分离株。未发现对其他β-内酰胺类药物的交叉耐药性,连续分离株的药敏性保持一致。进行实时定量逆转录 PCR 以研究外膜蛋白 OprD 在仅耐碳青霉烯类铜绿假单胞菌(CROPA)出现中的作用,该蛋白调节碳青霉烯类药物的进入。鉴定出 15 对碳青霉烯类敏感铜绿假单胞菌(CS-PA)和 CROPA 的配对分离株。所有病例在 CROPA 出现前 1 个月内均有碳青霉烯类药物暴露史(平均 10 天)。发现 93%(14/15)的分离株 OprD 表达减少,表明 oprD 失活是选择性碳青霉烯类耐药的主要原因。在由于 oprD 突变而导致的 14 例 CROPA 中,71%(10/14)为持续性感染,因为基因型分析显示其配对菌株是同系物;29%(4/14)为再感染,因为它们是异质的,这表明 oprD 缺陷型 CROPA 存在于医院中,碳青霉烯类选择性压力促进了其在患者中的传播。我们得出结论,CROPA 可能在使用碳青霉烯类治疗 CS-PA 感染后不久发生,并且 oprD 突变是 CROPA 耐药的主要机制。抗生素管理通过限制碳青霉烯类药物的经验性使用对于阻止 CROPA 的发生很重要。