Otitiglycomycins A and B: Glycolipids from the Strain Nocardia otitidiscavarum 20S-13 with Antiviral Activity against Zika Virus.

IF 3.6 2区 生物学 Q2 CHEMISTRY, MEDICINAL Journal of Natural Products Pub Date : 2025-02-28 Epub Date: 2025-02-03 DOI:10.1021/acs.jnatprod.4c01302
Phuong-Y Mai, Élodie Marguerite, Jamal Ouazzani, Philippe Lopes, Pascal Retailleau, Jean-François Gallard, Xavier Moppert, Bernard Costa, Géraldine Le Goff, Chaker El Kalamouni, Erwan Poupon, Mehdi A Beniddir
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Abstract

The Zika virus (ZIKV), an emerging orthoflavivirus, presents a significant public health threat due to its rapid dissemination and association with severe neurological complications. The urgent need for effective antiviral agents has driven research into novel bioactive compounds derived from unique natural sources. Microorganisms inhabiting extreme environments are particularly promising for such discoveries due to their potential to produce unique metabolites. In this study, we explored microorganisms from the underexplored French Polynesian microbial mats known as "Kopara" to identify new bioactive natural products. Using a molecular networking-based dereplication strategy, we investigated various culture and extraction techniques of the strain Nocardia otitidiscaviarum 20-S13, leading to the discovery of two novel glycoglycerolipids, otitiglycomycins A and B (1 and 2). Structure elucidation of these compounds was achieved through NMR spectroscopy, X-ray crystallography, and TDDFT-specific rotation prediction. We found that otitiglycomycin A (1), but not otitiglycomycin B (2), suppresses ZIKV infection at non cytotoxic concentrations without effects on cell viability. Time-of-drug addition assays along with virus inactivation and binding assays demonstrated that 1 neutralizes ZIKV infectivity by preventing the virus from attaching to the host cell membrane.

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抗寨卡病毒Nocardia otitidiscavarum 20S-13的糖脂素A和B。
寨卡病毒(ZIKV)是一种新出现的正黄病毒,由于其传播迅速并与严重的神经系统并发症相关,对公共卫生构成重大威胁。对有效抗病毒药物的迫切需求推动了从独特天然来源提取的新型生物活性化合物的研究。生活在极端环境中的微生物由于有可能产生独特的代谢物,因此对这些发现特别有希望。在这项研究中,我们探索了未被开发的法属波利尼西亚微生物垫“Kopara”中的微生物,以鉴定新的生物活性天然产物。使用基于分子网络的反复制策略,我们研究了菌株Nocardia otitidiscaviarum 20-S13的各种培养和提取技术,从而发现了两种新的糖甘油脂,otitiglycomycin a和B(1和2)。这些化合物的结构通过NMR波谱,x射线晶体学和tddft特异性旋转预测来实现。我们发现奥titiglycomycin A(1),而不是奥titiglycomycin B(2),在非细胞毒性浓度下抑制ZIKV感染,而不影响细胞活力。药物时间添加试验以及病毒灭活和结合试验表明,1通过阻止病毒附着在宿主细胞膜上来中和寨卡病毒的传染性。
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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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