环肽天然产物激发的自由生活变形虫的抑制剂

IF 3.6 2区 生物学 Q2 CHEMISTRY, MEDICINAL
Chenyang Lu, Samantha Nelson, Gabriela Coy, Chris Neumann, Elizabeth I. Parkinson* and Christopher A. Rice*, 
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引用次数: 0

摘要

Balamuthia mandrillaris是一种致病的自由生活阿米巴原虫(pFLA),可引起中枢神经系统(CNS)感染,称为Balamuthia阿米巴脑炎(BAE),以及皮肤和全身疾病。由于缺乏有效的治疗,感染山魈的患者死亡率很高。通常建议使用非优化的抗菌药物方案;然而,它的抗寄生虫活性很差,并可能引起各种严重的副作用。环状肽具有广谱的抗菌活性,但其抗阿米巴活性尚未得到充分的研究。在这项研究中,我们评估了抗b。从不同细菌物种的约500个生物合成基因簇中提取的合成天然产物激发环肽(SNaPP)对山毛线虫的影响。预测天然产物-43 (pNP-43;从SNaPP文库中鉴定的BICyP1及其衍生物对mandrillaris滋养虫具有明显的抑制作用,其中5个pNPs的ic50≤5 μM。此外,所有命中的天然产物激发肽对人类红细胞(rbc)和永生化的人类癌细胞的溶血和细胞毒性作用很小或没有。我们的研究首次证明了抗b。环肽的作用,为药物开发提供了一个有希望的新方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cyclic Peptide Natural Product Inspired Inhibitors of the Free-Living Amoeba Balamuthia mandrillaris

Balamuthia mandrillaris is a pathogenic free-living amoeba (pFLA) that can cause infection of the central nervous system (CNS), called Balamuthia amoebic encephalitis (BAE), as well as cutaneous and systemic diseases. Patients infected with B. mandrillaris have a high mortality rate due to a lack of effective treatments. A nonoptimized antimicrobial drug regimen is typically recommended; however, it has poor antiparasitic activity and can cause various and severe side effects. Cyclic peptides exhibit a broad spectrum of antimicrobial activities but are underexplored for their antiamoebic activity. In this study, we evaluated the anti-B. mandrillaris effect of Synthetic Natural Product Inspired Cyclic Peptides (SNaPP) mined from ∼500 biosynthetic gene clusters of various bacterial species. The predicted natural product-43 (pNP-43; BICyP1), identified from the SNaPP library, and its derivates displayed a significant inhibition against B. mandrillaris trophozoites, with five pNPs having IC50s ≤ 5 μM. Furthermore, all hit natural product inspired peptides demonstrated minimal to no hemolytic and cytotoxic effects on human red blood cells (RBCs) and immortalized human carcinoma cells, respectfully. Our study is the first to demonstrate the anti-B. mandrillaris effects of cyclic peptides, offering a promising new direction for drug development.

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来源期刊
CiteScore
9.10
自引率
5.90%
发文量
294
审稿时长
2.3 months
期刊介绍: The Journal of Natural Products invites and publishes papers that make substantial and scholarly contributions to the area of natural products research. Contributions may relate to the chemistry and/or biochemistry of naturally occurring compounds or the biology of living systems from which they are obtained. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin. When new compounds are reported, manuscripts describing their biological activity are much preferred. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.
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