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盐酸 CP100356,一种 P-糖蛋白抑制剂,抑制拉萨病毒进入:候选泛哺乳动物病毒进入抑制剂的意义。

CP100356 Hydrochloride, a P-Glycoprotein Inhibitor, Inhibits Lassa Virus Entry: Implication of a Candidate Pan-Mammarenavirus Entry Inhibitor.

机构信息

Laboratory of Ultrastructural Virology, Institute for Frontier Life and Medical Sciences, Kyoto University, Shogoin-Kawahara-cho 53, Sakyo-ku, Kyoto 606-8507, Japan.

Laboratory of Ultrastructural Virology, Graduate School of Biostudies, Kyoto University, 53 Shogoin Kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan.

出版信息

Viruses. 2021 Sep 3;13(9):1763. doi: 10.3390/v13091763.

Abstract

Lassa virus (LASV)-a member of the family -causes Lassa fever in humans and is endemic in West Africa. Currently, no approved drugs are available. We screened 2480 small compounds for their potential antiviral activity using pseudotyped vesicular stomatitis virus harboring the LASV glycoprotein (VSV-LASVGP) and a related prototypic arenavirus, lymphocytic choriomeningitis virus (LCMV). Follow-up studies confirmed that CP100356 hydrochloride (CP100356), a specific P-glycoprotein (P-gp) inhibitor, suppressed VSV-LASVGP, LCMV, and LASV infection with half maximal inhibitory concentrations of 0.52, 0.54, and 0.062 μM, respectively, without significant cytotoxicity. Although CP100356 did not block receptor binding at the cell surface, it inhibited low-pH-dependent membrane fusion mediated by arenavirus glycoproteins. P-gp downregulation did not cause a significant reduction in either VSV-LASVGP or LCMV infection, suggesting that P-gp itself is unlikely to be involved in arenavirus entry. Finally, our data also indicate that CP100356 inhibits the infection by other mammarenaviruses. Thus, our findings suggest that CP100356 can be considered as an effective virus entry inhibitor for LASV and other highly pathogenic mammarenaviruses.

摘要

拉沙病毒(LASV)是丝状病毒科的一员,可引起人类拉沙热,在西非流行。目前尚无批准的药物。我们使用携带 LASV 糖蛋白的假型水疱性口炎病毒(VSV-LASVGP)和相关的原型沙粒病毒,即淋巴细胞性脉络丛脑膜炎病毒(LCMV),对 2480 种小分子化合物进行了潜在抗病毒活性筛选。后续研究证实,CP100356 盐酸盐(CP100356)是一种特异性 P 糖蛋白(P-gp)抑制剂,对 VSV-LASVGP、LCMV 和 LASV 的半数最大抑制浓度分别为 0.52、0.54 和 0.062 μM,而无明显细胞毒性。尽管 CP100356 不能在细胞表面阻断受体结合,但它抑制了沙粒病毒糖蛋白介导的依赖低 pH 的膜融合。P-gp 下调并没有导致 VSV-LASVGP 或 LCMV 感染的显著减少,这表明 P-gp 本身不太可能参与沙粒病毒的进入。最后,我们的数据还表明 CP100356 抑制了其他哺乳动物沙粒病毒的感染。因此,我们的研究结果表明 CP100356 可被视为 LASV 和其他高致病性哺乳动物沙粒病毒的有效病毒进入抑制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21ba/8473031/d145a12e22b3/viruses-13-01763-g001.jpg

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