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进口唑和伊维菌素抑制经典核输入途径抑制轮状病毒复制。

Suppression of classical nuclear import pathway by importazole and ivermectin inhibits rotavirus replication.

机构信息

Division of Virology, ICMR-National Institute of Cholera and Enteric Diseases, P-33, C.I.T. Road, Scheme-XM, Beliaghata, 700010, Kolkata, West Bengal, India.

Division of Bacteriology, ICMR-National Institute of Cholera and Enteric Diseases, Kolkata, West Bengal, India.

出版信息

J Antimicrob Chemother. 2022 Nov 28;77(12):3443-3455. doi: 10.1093/jac/dkac339.

Abstract

BACKGROUND

Rotavirus is the foremost cause of acute gastroenteritis among infants in resource-poor countries, causing severe morbidity and mortality. The currently available rotavirus vaccines are effective in reducing severity of the disease but not the infection rates, thus antivirals as an adjunct therapy are needed to reduce the morbidity in children. Viruses rely on host cellular machinery for nearly every step of the replication cycle. Therefore, targeting host factors that are indispensable for virus replication could be a promising strategy.

OBJECTIVES

To assess the therapeutic potential of ivermectin and importazole against rotaviruses.

METHODS

Antirotaviral activity of importazole and ivermectin was measured against various rotavirus strains (RV-SA11, RV-Wa, RV-A5-13, RV-EW) in vitro and in vivo by quantifying viral protein expression by western blot, analysing viroplasm formation by confocal microscopy, and measuring virus yield by plaque assay.

RESULTS

Importin-β1 and Ran were found to be induced during rotavirus infection. Knocking down importin-β1 severely impaired rotavirus replication, suggesting a critical role for importin-β1 in the rotavirus life cycle. In vitro studies revealed that treatment of ivermectin and importazole resulted in reduced synthesis of viral proteins, diminished production of infectious virus particles, and decrease in viroplasm-positive cells. Mechanistic study proved that both drugs perform antirotavirus activity by inhibiting the function of importin-β1. In vivo investigations in mice also confirmed the antirotavirus potential of importazole and ivermectin at non-toxic doses. Treatments of rotavirus-infected mice with either drug resulted in diminished shedding of viral particles in the stool sample, reduced expression of viral protein in the small intestine and restoration of damaged intestinal villi comapared to untreated infected mice.

CONCLUSIONS

The study highlights the potential of importazole and ivermectin as antirotavirus therapeutics.

摘要

背景

轮状病毒是资源匮乏国家婴幼儿急性肠胃炎的首要病因,可导致严重的发病率和死亡率。目前可用的轮状病毒疫苗可有效降低疾病的严重程度,但不能降低感染率,因此需要抗病毒药物作为辅助治疗来降低儿童的发病率。病毒依赖宿主细胞机制完成复制周期的几乎每一步。因此,针对对病毒复制必不可少的宿主因素可能是一种有前途的策略。

目的

评估伊维菌素和依氟鸟氨酸治疗轮状病毒的潜力。

方法

通过western blot 定量检测病毒蛋白表达、通过共聚焦显微镜分析类核形成以及通过噬斑试验测量病毒产量,在体外和体内评估依氟鸟氨酸和伊维菌素对各种轮状病毒株(RV-SA11、RV-Wa、RV-A5-13、RV-EW)的抗病毒活性。

结果

发现轮状病毒感染过程中诱导了 importin-β1 和 Ran 的表达。敲低 importin-β1 严重损害了轮状病毒的复制,表明 importin-β1 在轮状病毒生命周期中起着关键作用。体外研究表明,伊维菌素和依氟鸟氨酸的治疗导致病毒蛋白合成减少、感染性病毒颗粒产生减少以及类核阳性细胞减少。机制研究证明,这两种药物通过抑制 importin-β1 的功能发挥抗轮状病毒活性。在小鼠体内研究也证实了依氟鸟氨酸和伊维菌素在非毒性剂量下的抗轮状病毒潜力。与未感染的对照相比,用药物治疗感染轮状病毒的小鼠可减少粪便样本中病毒颗粒的脱落、小肠中病毒蛋白的表达以及受损的肠绒毛的恢复。

结论

该研究强调了依氟鸟氨酸和伊维菌素作为抗轮状病毒治疗药物的潜力。

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