Narciclasine inhibits vaccinia virus infection by activating the RhoA signaling pathway

IF 3 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Biosafety and Health Pub Date : 2024-12-01 DOI:10.1016/j.bsheal.2024.11.002
Ting Xu , Zhengyang Pan , Xue Li , Mengyang Zhao , Zichen Li , Leiliang Zhang
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Abstract

In 2022, a sharp rise in global cases of mpox virus (MPXV) led the World Health Organization (WHO) to declare it a public health emergency of international concern. However, progress in developing drugs targeting MPXV has been slow. Here, we investigate the natural alkaloid narciclasine as a potential inhibitor of poxviruses. Our investigation demonstrates that narciclasine at 40 nmol/L (nM) to 160 nM dosages effectively blocks vaccinia virus (VACV), a representative poxvirus. Specifically, narciclasine disrupts the production of extracellular enveloped virus (EEV), which is crucial for viral spread. Narciclasine’s antiviral impact is probably attributed to its activation of the RhoA signaling pathway. This study highlights narciclasine’s potential as a promising new therapeutic candidate against poxviruses, offering prospects for its development into a potent antiviral agent that is essential for combating emerging poxvirus outbreaks.
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水仙素通过激活RhoA信号通路抑制牛痘病毒感染
2022年,全球麻疹病毒病例急剧增加,世界卫生组织(世卫组织)宣布其为国际关注的突发公共卫生事件。然而,针对MPXV的药物开发进展缓慢。在这里,我们研究了天然生物碱水仙素作为痘病毒的潜在抑制剂。本研究表明,水仙素在40 ~ 160 nM剂量下能有效阻断痘病毒的代表——牛痘病毒(VACV)。具体来说,水仙环素破坏细胞外包膜病毒(EEV)的产生,这对病毒传播至关重要。水仙碱的抗病毒作用可能归因于其激活RhoA信号通路。本研究突出了水仙素作为一种有前途的新型痘病毒治疗候选药物的潜力,为其发展成为对抗新出现的痘病毒爆发所必需的强效抗病毒药物提供了前景。
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文献相关原料
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陶术
Narciclasine
索莱宝
Dimethylsulfoxide (DMSO)
索莱宝
DMSO
来源期刊
Biosafety and Health
Biosafety and Health Medicine-Infectious Diseases
CiteScore
7.60
自引率
0.00%
发文量
116
审稿时长
66 days
期刊最新文献
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