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石蒜科生物碱石蒜硷抑制登革热和兹卡病毒的复制。

Amaryllidaceae Alkaloid Cherylline Inhibits the Replication of Dengue and Zika Viruses.

机构信息

Department of Chemistry, Biochemistry, and Physics, Université du Québec à Trois-Rivièresgrid.265703.5, Trois-Rivières, Québec, Canada.

Laboratoire de Chimie Organique et Chimie Thérapeutique, Faculté de Médecine, de Pharmacie, et d'Odontologie de Dakar, Dakar, Senegal.

出版信息

Antimicrob Agents Chemother. 2021 Aug 17;65(9):e0039821. doi: 10.1128/AAC.00398-21.

Abstract

Dengue fever, caused by dengue virus (DENV), is the most prevalent arthropod-borne viral disease and is endemic in many tropical and subtropical parts of the world, with an increasing incidence in temperate regions. The closely related flavivirus Zika virus (ZIKV) can be transmitted vertically and causes congenital Zika syndrome and other birth defects. In adults, ZIKV is associated with Guillain-Barré syndrome. There are no approved antiviral therapies against either virus. Effective antiviral compounds are urgently needed. Amaryllidaceae alkaloids (AAs) are a specific class of nitrogen-containing compounds produced by plants of the Amaryllidaceae family with numerous biological activities. Recently, the AA lycorine was shown to present strong antiflaviviral properties. Previously, we demonstrated that Crinum jagus contained lycorine and several alkaloids of the cherylline, crinine, and galanthamine types with unknown antiviral potential. In this study, we explored their biological activities. We show that crude alkaloid extract inhibited DENV infection. Among the purified AAs, cherylline efficiently inhibited both DENV (50% effective concentration [EC], 8.8 μM) and ZIKV replication (EC, 20.3 μM) but had no effect on HIV-1 infection. Time-of-drug-addition and -removal experiments identified a postentry step as the one targeted by cherylline. Consistently, using subgenomic replicons and replication-defective genomes, we demonstrate that cherylline specifically hinders the viral RNA synthesis step but not viral translation. In conclusion, AAs are an underestimated source of antiflavivirus compounds, including the effective inhibitor cherylline, which could be optimized for new therapeutic approaches.

摘要

登革热是由登革病毒(DENV)引起的,是最常见的虫媒病毒病,在世界上许多热带和亚热带地区流行,并在温带地区发病率不断上升。密切相关的黄病毒寨卡病毒(ZIKV)可垂直传播,并导致先天性寨卡综合征和其他出生缺陷。在成人中,ZIKV 与格林-巴利综合征有关。目前还没有针对这两种病毒的批准抗病毒疗法。急需有效的抗病毒化合物。石蒜科生物碱(AAs)是一类由石蒜科植物产生的含氮化合物,具有多种生物活性。最近,AA 石蒜碱被证明具有很强的抗黄病毒特性。此前,我们证明了 Crinum jagus 含有石蒜碱和几种生物碱,属于石蒜碱、石蒜碱和加兰他敏型,具有未知的抗病毒潜力。在这项研究中,我们探讨了它们的生物学活性。我们表明粗生物碱提取物抑制 DENV 感染。在纯化的 AAs 中,石蒜碱能有效抑制 DENV(50%有效浓度[EC],8.8μM)和 ZIKV 复制(EC,20.3μM),但对 HIV-1 感染没有影响。加药和停药时间实验确定了一个感染后步骤是石蒜碱靶向的。一致地,使用亚基因组复制子和复制缺陷型基因组,我们证明石蒜碱特异性地阻碍病毒 RNA 合成步骤,但不影响病毒翻译。总之,AAs 是抗黄病毒化合物的一个被低估的来源,包括有效的抑制剂石蒜碱,它可以被优化用于新的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb73/8370201/625d3fb56f9c/aac.00398-21-f0001.jpg

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