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Humanized Exposures of Cefiderocol a Siderophore Cephalosporin Display Sustained in vivo Activity against Siderophore-Resistant Pseudomonas aeruginosa

机译:头孢洛尔一种铁载体头孢菌素的人源化暴露显示出抗铁载体耐铜绿假单胞菌的体内活性持续。

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摘要

We evaluated the in vivo efficacy of humanized exposures of cefiderocol, a novel siderophore cephalosporin, against a test panel of P. aeruginosa (PSA) previously shown to develop resistance to 2 preclinical candidate siderophores (MB-1 and SMC-3176). In the thigh infection model, the PSA bacterial density in untreated controls grew from 5.54 ± 0.23 to 8.68 ± 0.57 log10 CFU over 24 h. The humanized cefiderocol exposure resulted in >1 log10 CFU reduction in all 8 isolates, while MB-1 and SMC-3176 exhibited variable activity similar to that previously reported. Humanized exposures of cefepime and levofloxacin, acting as positive antimicrobial controls displayed activity consistent with that of the bacterial phenotypic susceptibility profiles. Cefiderocol manifested in vivo efficacy against all PSA isolates including those resistant to cefepime and levofloxacin in contrast to its predecessor siderophore compounds. These preclinical data are supportive of further evaluation of cefiderocol in the treatment of P. aeruginosa.
机译:我们评估了铜绿假单胞菌(PSA)的测试小组对新型药性头孢铁菌头孢德罗醇的人源化暴露的体内疗效,铜绿假单胞菌(PSA)先前显示出对2种临床前候选铁载体(MB-1和SMC-3176)具有抗性。在大腿感染模型中,未经治疗的对照组的PSA细菌密度在24小时内从5.54±0.23增加到8.68±0.57 log10 CFU。人源化的头孢地洛尔暴露导致所有8个分离株的CFU降低> 1 log10,而MB-1和SMC-3176表现出的可变活性与先前报道的相似。头孢吡肟和左氧氟沙星的人源化暴露(作为阳性抗菌控制)显示出与细菌表型药敏谱一致的活性。头孢地洛尔显示出对所有PSA分离物的体内功效,包括对头孢吡肟和左氧氟沙星有抗性的PSA分离物,与其先前的铁载体化合物相反。这些临床前数据支持进一步评估头孢地洛在铜绿假单胞菌治疗中的作用。

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