海洋微生物培养液中提取的抗严重发热伴血小板减少综合征病毒多靶点化合物表面活性素的鉴定

IF 2 Q4 VIROLOGY
Shuzo Urata, Jun Takouda, Yoshihiro Watanabe, M. Sakaguchi, Yasuteru Sakurai, Y. Inahashi, M. Iwatsuki, J. Yasuda, Yoshimasa Tanaka, K. Takeda
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摘要

严重发热伴血小板减少综合征病毒(SFTSV)是一种蜱传病毒,2011年首次在中国发现,后来在其他亚洲国家报道。已经做出了重大努力来开发抗SFTSV的化合物;然而,目前还没有批准的针对SFTSV感染的疫苗或抗病毒药物。海洋生物提供了几乎无限的生物资源来生产用于治疗和控制疾病的治疗药物。在本研究中,我们旨在从日本长崎县海岸采集的海洋微生物培养液提取物中鉴定抗SFTSV的化合物。在80种提取物中,有两种显示出抗SFTSV的作用。其中一种表现出低细胞毒性,用于进一步表征。化学分析和抗SFTSV作用相结合,确定表面活性素是所选提取物的主要成分之一。我们的研究表明,从海洋微生物中鉴定出新的抗病毒化合物可以对抗感兴趣的病毒。进一步的分析表明,在低pH条件下,表面活性素影响病毒粒子膜的完整性,并抑制SFTSV感染诱导的膜融合。此外,表面活性素抑制病毒在细胞中复制的进入后步骤,这是表面活性素抗病毒作用的一种新模式。这些结果表明,表面活性素可以靶向细胞中SFTSV复制的多个步骤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of surfactin as an anti-severe fever with thrombocytopenia syndrome virus multi-target compound extracted from the culture broth of marine microbes
Severe fever with thrombocytopenia syndrome virus (SFTSV) is a tick-borne virus first identified in China in 2011 and later reported in other Asian countries. Significant efforts have been made to develop anti-SFTSV compounds; however, there are no approved vaccines or antivirals against SFTSV infections. Marine organisms provide nearly unlimited biological resources to produce therapeutic drugs for the treatment and control of disease. In this study, we aimed to identify anti-SFTSV chemical compounds from the culture broth extracts of marine microbes collected from the coasts of the Nagasaki Prefecture, Japan. Of the 80 extracts, two showed an anti-SFTSV effect. One of them, which exhibited low cell toxicity, was used for further characterization. Chemical analysis combined with the anti-SFTSV effect identified surfactin as one of the main components of the selected extract. Our study showed a proof-of-concept to identify novel antiviral compounds from marine microbes against the virus of interest. Further analysis showed that surfactin affected the integrity of the virion membrane and inhibited SFTSV infection-induced membrane fusion at low pH conditions. Furthermore, surfactin inhibits the post-entry step of viral replication in the cell, which is a novel mode of antiviral action of surfactin. These results indicate that surfactin can target multiple steps of SFTSV replication in cells.
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