Department of Pharmacy, Singapore General Hospital, Singapore.
J Antibiot (Tokyo). 2009 Dec;62(12):675-9. doi: 10.1038/ja.2009.99. Epub 2009 Oct 30.
Outbreaks of carbapenem-resistant Acinetobacter species have emerged, especially in Singapore. Combination therapy may be the only viable option until new antibiotics are available. The objective of this study was to identify potential antimicrobial combinations against carbapenem-resistant Acinetobacter baumannii and Acinetobacter species in Singapore. From an ongoing surveillance program, two isolates of A. baumannii and an isolate of Acinetobacter species that were multidrug resistant were selected on the basis of their unique resistance mechanisms. The two A. baumannii isolates carried the carbapenemase bla(OXA-23)-like gene and the Acinetobacter species carried a metallo-beta-lactamase IMP-4 gene. Time-kill studies were conducted with approximately 10(5) CFU ml(-1) at baseline with 0.5 times minimum inhibitory concentrations (MICs) of polymyxin B and tigecycline, and at a maximally achievable clinical concentration of meropenem(64 microg ml(-1)) and rifampicin(2 microg ml(-1)), alone and in combinations. The MICs (microg ml(-1)) of Acinetobacter species A105, A. baumannii AB112 and A. baumannii AB8879 to polymyxin B/tigecycline/rifampicin/meropenem were found to be 1/0.5/4/64, 1/4/4/32 and 2/2/2/64, respectively. In time-kill studies, enhanced combined killing effects were observed in the tigecycline-rifampicin combination; the tigecycline-rifampicin and rifampicin-polymyxin B combination; and the rifampicin-polymyxin B combination for Acinetobacter species A105, A. baumannii AB112 and A. baumannii AB8879, respectively, with >5 log kill at 24 h suggesting synergism, with no regrowth observed at 72 h. These findings demonstrate that in vitro synergy of antibiotic combinations in carbapenem-resistant Acinetobacter species may be strain dependent. It may guide us in choosing a preemptive therapy for carbapenem-resistant Acinetobacter species infections and warrants further investigations.
耐碳青霉烯不动杆菌种的爆发已经出现,特别是在新加坡。在新的抗生素问世之前,联合治疗可能是唯一可行的选择。本研究的目的是确定针对新加坡耐碳青霉烯鲍曼不动杆菌和不动杆菌种的潜在抗菌组合。根据其独特的耐药机制,从正在进行的监测计划中选择了两株鲍曼不动杆菌和一株耐多药不动杆菌种的分离株。这两株鲍曼不动杆菌分离株携带碳青霉烯酶 bla(OXA-23)-like 基因,而不动杆菌种携带金属β-内酰胺酶 IMP-4 基因。采用时间杀伤研究,在基线时用大约 10(5) CFU ml(-1),用 0.5 倍最小抑菌浓度 (MIC) 的多粘菌素 B 和替加环素,以及在最大可达到的临床浓度美罗培南 (64 μg ml(-1)) 和利福平 (2 μg ml(-1)),单独和联合使用。不动杆菌种 A105、鲍曼不动杆菌 AB112 和鲍曼不动杆菌 AB8879 对多粘菌素 B/替加环素/利福平/美罗培南的 MIC(microg ml(-1))分别为 1/0.5/4/64、1/4/4/32 和 2/2/2/64。在时间杀伤研究中,替加环素-利福平组合、替加环素-利福平与多粘菌素 B 组合以及利福平-多粘菌素 B 组合对不动杆菌种 A105、鲍曼不动杆菌 AB112 和鲍曼不动杆菌 AB8879 均观察到增强的联合杀菌作用,24 小时时杀菌效果超过 5 个对数级,提示协同作用,72 小时时未观察到再生长。这些发现表明,耐碳青霉烯不动杆菌种中抗生素组合的体外协同作用可能取决于菌株。它可以指导我们选择针对耐碳青霉烯不动杆菌种感染的先发制人的治疗,并需要进一步研究。