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不动杆菌属的研究进展:抗菌药物耐药机制及米诺环素和其他治疗选择的体外最新活性。

Update on Acinetobacter species: mechanisms of antimicrobial resistance and contemporary in vitro activity of minocycline and other treatment options.

机构信息

JMI Laboratories, North Liberty, Iowa.

出版信息

Clin Infect Dis. 2014 Dec 1;59 Suppl 6:S367-73. doi: 10.1093/cid/ciu706.

Abstract

Among Acinetobacter species, A. baumannii and other closely related species are commonly implicated in nosocomial infections. These organisms are usually multidrug resistant (MDR), and therapeutic options to treat A. baumannii infections are very limited. Clinicians have been resorting to older antimicrobial agents to treat infections caused by MDR A. baumannii, and some of these agents have documented toxicity and/or are not optimized for the infection type to be treated. Recent clinical experience supported by antimicrobial susceptibility data suggests that minocycline has greater activity than other tetracyclines and glycylcyclines against various MDR pathogens that have limited therapeutic options available, including Acinetobacter species. An intravenous formulation of minocycline has recently become available for clinical use, and in contrast to most older tetracyclines, minocycline has high activity against Acinetobacter species. In this report, we summarized some of the characteristics of the tetracycline class, and quantified the minocycline activity against contemporary (2007-2011) isolates and its potential therapeutic role against a collection of 5477 A. baumannii and other relevant gram-negative organisms when compared directly with tetracycline, doxycycline, and other broad-spectrum antimicrobial agents. Acinetobacter baumannii strains were highly resistant to all agents tested, with the exception of minocycline (79.1% susceptible) and colistin (98.8% susceptible). Minocycline (minimum inhibitory concentration that inhibits 50% and 90% of the isolates [MIC(50/90)]: 1/8 µg/mL) displayed greater activity than doxycycline (MIC(50/90): 2/>8 µg/mL) and tetracycline hydrochloride (HCL) (only 30.2% susceptible) against A. baumannii isolates, and was significantly more active than other tetracyclines against Burkholderia cepacia, Escherichia coli, Serratia marcescens, and Stenotrophomonas maltophilia isolates. In vitro susceptibility testing using tetracycline HCL as a surrogate for the susceptibility other tetracyclines fails to detect minocycline-susceptible isolates and the potential utility of minocycline for the treatment of many MDR A. baumannii infections and other difficult-to-treat species, where there are often limited choices of antimicrobials.

摘要

在不动杆菌属中,鲍曼不动杆菌和其他密切相关的物种通常与医院获得性感染有关。这些生物体通常是多药耐药(MDR)的,治疗鲍曼不动杆菌感染的治疗选择非常有限。临床医生一直在诉诸于较老的抗菌药物来治疗由 MDR 鲍曼不动杆菌引起的感染,并且其中一些药物已经证明具有毒性和/或不适用于要治疗的感染类型。最近的临床经验支持抗菌药物敏感性数据表明,米诺环素对各种 MDR 病原体的活性大于其他四环素类和甘氨酰环素,这些病原体的治疗选择有限,包括不动杆菌属。米诺环素的静脉制剂最近已可用于临床,与大多数较老的四环素类药物不同,米诺环素对不动杆菌属具有很高的活性。在本报告中,我们总结了四环素类的一些特征,并量化了米诺环素对当代(2007-2011 年)分离株的活性及其与四环素、多西环素和其他广谱抗菌药物直接比较时对 5477 株鲍曼不动杆菌和其他相关革兰氏阴性菌的潜在治疗作用。除米诺环素(79.1%敏感)和粘菌素(98.8%敏感)外,鲍曼不动杆菌菌株对所有测试的药物均具有高度耐药性。米诺环素(抑制 50%和 90%分离株的最小抑菌浓度[MIC(50/90)]:1/8 µg/mL)对鲍曼不动杆菌分离株的活性大于多西环素(MIC(50/90):2/>8 µg/mL)和盐酸四环素(仅 30.2%敏感),并且对铜绿假单胞菌、大肠杆菌、粘质沙雷氏菌和嗜麦芽窄食单胞菌分离株的活性明显大于其他四环素类药物。使用四环素盐酸盐作为其他四环素类药物敏感性的替代物进行体外药敏试验不能检测到米诺环素敏感的分离株,并且米诺环素在治疗许多 MDR 鲍曼不动杆菌感染和其他难以治疗的物种中的潜在用途,这些物种通常对抗微生物药物的选择有限。

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