Suppr超能文献

新型抗真菌药物 F901318(奥利伏霉素)对烟曲霉生长和活力的影响。

Effect of the Novel Antifungal Drug F901318 (Olorofim) on Growth and Viability of Aspergillus fumigatus.

机构信息

F2G Ltd., Manchester, United Kingdom

Manchester Fungal Infection Group, Division of Infection, Immunity and Respiratory Medicine, University of Manchester, Manchester, United Kingdom.

出版信息

Antimicrob Agents Chemother. 2018 Jul 27;62(8). doi: 10.1128/AAC.00231-18. Print 2018 Aug.

Abstract

F901318 (olorofim) is a novel antifungal drug that is highly active against species. Belonging to a new class of antifungals called the orotomides, F901318 targets dihydroorotate dehydrogenase (DHODH) in the pyrimidine biosynthesis pathway. In this study, the antifungal effects of F901318 against were investigated. Live cell imaging revealed that, at a concentration of 0.1 μg/ml, F901318 completely inhibited germination, but conidia continued to expand by isotropic growth for >120 h. When this low F901318 concentration was applied to germlings or vegetative hyphae, their elongation was completely inhibited within 10 h. Staining with the fluorescent viability dye bis-(1,3-dibutylbarbituric acid) trimethine oxonol (DiBAC) showed that prolonged exposure to F901318 (>24 h) led to vegetative hyphal swelling and a decrease in hyphal viability through cell lysis. The time-dependent killing of F901318 was further confirmed by measuring the fungal biomass and growth rate in liquid culture. The ability of hyphal growth to recover in drug-free medium after 24 h of exposure to F901318 was strongly impaired compared to that of the untreated control. A longer treatment of 48 h further improved the antifungal effect of F901318. Together, the results of this study indicate that F901318 initially has a fungistatic effect on isolates by inhibiting germination and growth, but prolonged exposure is fungicidal through hyphal swelling followed by cell lysis.

摘要

F901318(奥利伏霉素)是一种新型抗真菌药物,对 种具有高度活性。属于一种称为奥托米德的新型抗真菌药物,F901318 靶向二氢乳清酸脱氢酶(DHODH)在嘧啶生物合成途径中。在这项研究中,研究了 F901318 对 的抗真菌作用。活细胞成像显示,在 0.1μg/ml 的浓度下,F901318 完全抑制了萌发,但孢子继续通过各向同性生长扩大超过 120 小时。当这种低浓度的 F901318 应用于发芽体或营养菌丝时,其伸长在 10 小时内完全被抑制。用荧光存活染料双-(1,3-二丁基巴比妥酸)三甲氧基氧杂蒽(DiBAC)染色表明,长时间暴露于 F901318(>24 小时)导致营养菌丝肿胀,并通过细胞裂解导致菌丝活力下降。通过在液体培养中测量真菌生物量和生长速率进一步证实了 F901318 的时间依赖性杀伤作用。与未处理的对照相比,在暴露于 F901318 24 小时后,在无药物的培养基中菌丝生长恢复的能力受到强烈损害。较长时间(48 小时)的处理进一步提高了 F901318 的抗真菌效果。总之,这项研究的结果表明,F901318 最初通过抑制萌发和生长对 分离株具有抑菌作用,但长时间暴露则通过菌丝肿胀继而细胞裂解产生杀菌作用。

相似文献

引用本文的文献

9
An update on the global treatment of invasive fungal infections.全球侵袭性真菌感染治疗的最新进展。
Future Microbiol. 2023 Nov;18(15):1095-1117. doi: 10.2217/fmb-2022-0269. Epub 2023 Sep 26.

本文引用的文献

5
The Fungal Cell Wall: Structure, Biosynthesis, and Function.真菌细胞壁:结构、生物合成与功能。
Microbiol Spectr. 2017 May;5(3). doi: 10.1128/microbiolspec.FUNK-0035-2016.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验