Department of Chemistry, Middle Tennessee State University, Murfreesboro, Tennessee.
Department of Biology, Middle Tennessee State University, Murfreesboro, Tennessee.
Biopolymers. 2019 Jun;110(6):e23276. doi: 10.1002/bip.23276. Epub 2019 Apr 2.
Cryptococcus neoformans is a fungal pathogen that causes cryptococcal meningitis in immunocompromised individuals. Existing antifungal treatment plans have high mammalian toxicity and increasing drug resistance, demonstrating the dire need for new, nontoxic therapeutics. Antimicrobial peptoids are one alternative to combat this issue. Our lab has recently identified a tripeptoid, AEC5, with promising efficacy and selectivity against C. neoformans. Here, we report studies into the broad-spectrum efficacy, killing kinetics, mechanism of action, in vivo half-life, and subchronic toxicity of this compound. Most notably, these studies have demonstrated that AEC5 rapidly reduces fungal burden, killing all viable fungi within 3 hours. Additionally, AEC5 has an in vivo half-life of 20+ hours and no observable in vivo toxicity following 28 days of daily injections. This research represents an important step in the characterization of AEC5 as a practical treatment option against C. neoformans infections.
新型隐球菌是一种真菌病原体,可导致免疫功能低下个体发生隐球菌性脑膜炎。现有的抗真菌治疗方案具有较高的哺乳动物毒性和不断增加的耐药性,这迫切需要开发新的、无毒的治疗方法。抗菌肽是解决这一问题的一种替代方法。我们实验室最近发现了一种三肽,AEC5,对新型隐球菌具有有前景的疗效和选择性。在这里,我们报告了这项化合物的广谱疗效、杀菌动力学、作用机制、体内半衰期和亚慢性毒性研究。值得注意的是,这些研究表明 AEC5 能迅速降低真菌负荷,在 3 小时内杀死所有存活的真菌。此外,AEC5 的体内半衰期超过 20 小时,并且在 28 天的每日注射后没有观察到体内毒性。这项研究代表了将 AEC5 作为一种针对新型隐球菌感染的实用治疗选择进行特征描述的重要一步。