Arivett Brock A, Fiester Steven E, Ohneck Emily J, Penwell William F, Kaufman Cynthia M, Relich Ryan F, Actis Luis A
Department of Microbiology, Miami University, Oxford, Ohio, USA.
Division of Clinical Microbiology, Indiana University Health Pathology Laboratory, Indianapolis, Indiana, USA.
Antimicrob Agents Chemother. 2015 Dec;59(12):7657-65. doi: 10.1128/AAC.01472-15. Epub 2015 Sep 28.
A paucity of effective, currently available antibiotics and a lull in antibiotic development pose significant challenges for treatment of patients with multidrug-resistant (MDR) Acinetobacter baumannii infections. Thus, novel therapeutic strategies must be evaluated to meet the demands of treatment of these often life-threatening infections. Accordingly, we examined the antibiotic activity of gallium protoporphyrin IX (Ga-PPIX) against a collection of A. baumannii strains, including nonmilitary and military strains and strains representing different clonal lineages and isolates classified as susceptible or MDR. Susceptibility testing demonstrated that Ga-PPIX inhibits the growth of all tested strains when cultured in cation-adjusted Mueller-Hinton broth, with a MIC of 20 μg/ml. This concentration significantly reduced bacterial viability, while 40 μg/ml killed all cells of the A. baumannii ATCC 19606(T) and ACICU MDR isolate after 24-h incubation. Recovery of ATCC 19606(T) and ACICU strains from infected A549 human alveolar epithelial monolayers was also decreased when the medium was supplemented with Ga-PPIX, particularly at a 40-μg/ml concentration. Similarly, the coinjection of bacteria with Ga-PPIX increased the survival of Galleria mellonella larvae infected with ATCC 19606(T) or ACICU. Ga-PPIX was cytotoxic only when monolayers or larvae were exposed to concentrations 16-fold and 1,250-fold higher than those showing antibacterial activity, respectively. These results indicate that Ga-PPIX could be a viable therapeutic option for treatment of recalcitrant A. baumannii infections regardless of the resistance phenotype, clone lineage, time and site of isolation of strains causing these infections and their iron uptake phenotypes or the iron content of the media.
目前有效的抗生素匮乏,且抗生素研发陷入停滞,这给耐多药鲍曼不动杆菌感染患者的治疗带来了重大挑战。因此,必须评估新的治疗策略,以满足这些往往危及生命的感染的治疗需求。相应地,我们检测了原卟啉IX镓(Ga-PPIX)对一系列鲍曼不动杆菌菌株的抗菌活性,这些菌株包括非军事和军事菌株、代表不同克隆谱系的菌株以及被分类为敏感或耐多药的分离株。药敏试验表明,当在阳离子调整的 Mueller-Hinton 肉汤中培养时,Ga-PPIX 可抑制所有测试菌株的生长,最低抑菌浓度(MIC)为 20 μg/ml。该浓度显著降低了细菌活力,而 40 μg/ml 的浓度在孵育 24 小时后杀死了鲍曼不动杆菌 ATCC 19606(T) 和 ACICU 耐多药分离株的所有细胞。当培养基中添加 Ga-PPIX 时,尤其是在 40 μg/ml 的浓度下,从感染的 A549 人肺泡上皮单层中回收的 ATCC 19606(T) 和 ACICU 菌株也减少了。同样,将细菌与 Ga-PPIX 共同注射可提高感染 ATCC 19606(T) 或 ACICU 的大蜡螟幼虫的存活率。仅当单层或幼虫分别暴露于比显示抗菌活性的浓度高 16 倍和 1250 倍的浓度时,Ga-PPIX 才具有细胞毒性。这些结果表明,无论导致这些感染的菌株的耐药表型、克隆谱系、分离时间和地点以及它们的铁摄取表型或培养基的铁含量如何,Ga-PPIX 都可能是治疗顽固性鲍曼不动杆菌感染的可行治疗选择。