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Antimicrobial Activity of Gallium Protoporphyrin IX against Acinetobacter baumannii Strains Displaying Different Antibiotic Resistance Phenotypes

机译:镓原卟啉IX对表现出不同抗药性表型的鲍曼不动杆菌菌株的抗菌活性

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摘要

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 19606T and ACICU MDR isolate after 24-h incubation. Recovery of ATCC 19606T 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 19606T 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.
机译:缺乏有效的,目前可用的抗生素以及抗生素开发的停滞对患有多重耐药性(MDR)鲍曼不动杆菌感染的患者的治疗提出了重大挑战。因此,必须评估新的治疗策略,以满足对这些通常威胁生命的感染的治疗需求。因此,我们检查了原卟啉IX(Ga-PPIX)对一系列鲍曼不动杆菌菌株的抗生素活性,包括非军事和军事菌株以及代表不同克隆谱系和分类为敏感或MDR的菌株。药敏试验表明,当在阳离子调节的Mueller-Hinton肉汤中以MIC为20μg/ ml进行培养时,Ga-PPIX会抑制所有待测菌株的生长。该浓度显着降低了细菌的活力,而40μg/ ml孵育24小时后杀死了鲍曼不动杆菌ATCC 19606 T 和ACICU MDR分离株的所有细胞。当向培养基中添加Ga-PPIX时,尤其是在40μg/ ml的浓度下,从感染的A549人肺泡上皮单层中回收ATCC 19606 T 和ACICU菌株的比例也降低。类似地,细菌与Ga-PPIX的共注射可提高感染ATCC 19606 T 或ACICU的加勒梅幼虫的存活率。仅当单层或幼虫分别暴露于比具有抗菌活性的浓度高16倍和1,250倍的浓度时,Ga-PPIX才具有细胞毒性。这些结果表明,Ga-PPIX可能是治疗顽固鲍曼不动杆菌感染的可行治疗选择,而与引起这些感染的菌株的耐药表型,克隆谱系,分离时间和分离地点及其铁吸收表型或铁的含量无关。媒体。

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