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评价抗生素多粘菌素 B 的抗隐球菌活性:体外和体内研究。

Evaluation of the anticryptococcal activity of the antibiotic polymyxin B in vitro and in vivo.

机构信息

Department of Biology, 3258 Texas A&M University, College Station, TX 77843-3258, USA.

出版信息

Int J Antimicrob Agents. 2013 Mar;41(3):250-4. doi: 10.1016/j.ijantimicag.2012.11.006. Epub 2013 Jan 10.

Abstract

Polymyxin B (PMB), a cationic lipid oligopeptide used to treat Gram-negative bacterial infections, was previously identified to possess broad-spectrum antifungal activity and to work synergistically with azole antifungals in vitro. Here we evaluated the efficacy of PMB against Cryptococcus neoformans in vitro and in vivo and explored the mechanism of the hypersensitivity of this fungus to this compound. Using comparative time-course assays, PMB was found to kill both proliferative and quiescent cryptococcal cells in vitro. Presence of the polysaccharide capsule, a characteristic feature of Cryptococcus, significantly enhances the susceptibility of this fungus to the fungicidal activity of PMB. Furthermore, PMB is able to reduce the tissue fungal burden both in intravenous and inhalation models of murine cryptococcosis at a level comparable with the commonly used antifungal fluconazole. These findings suggest that PMB could provide an additional option for treatment against systemic cryptococcosis.

摘要

多粘菌素 B(PMB)是一种阳离子脂质寡肽,用于治疗革兰氏阴性细菌感染,先前已被确定具有广谱抗真菌活性,并在体外与唑类抗真菌药协同作用。在这里,我们评估了 PMB 对新型隐球菌的体外和体内疗效,并探讨了这种真菌对该化合物过敏的机制。通过比较时间过程测定,发现 PMB 可杀死体外增殖和静止的隐球菌细胞。多糖荚膜的存在,隐球菌的一个特征,显著增强了这种真菌对 PMB 杀菌活性的敏感性。此外,PMB 能够降低静脉内和吸入性小鼠隐球菌病模型中的组织真菌负荷,水平可与常用的抗真菌药氟康唑相媲美。这些发现表明,PMB 可能为治疗全身性隐球菌病提供了另一种选择。

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