宿主限制性因子APOBEC3G和IFITM3可抑制Chandipura病毒在Vero细胞中的复制

Dibyakanti Mandal
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引用次数: 0

摘要

昌迪普拉病毒(CHPV)是印度次大陆和一些西非国家的一种新发病原体。该病毒在幼儿中引起发烧、脑炎和死亡,迄今尚无疫苗或药物可用于治疗CHPV感染。本研究旨在研究干扰素诱导蛋白、人APOBEC3G (hA3G)和IFITM3是否能抑制CHPV复制,这两种蛋白被称为抗病毒宿主因子。用空斑法测定病毒的感染性,结果显示hA3G和IFITM3显著抑制了Vero E6细胞中的CHPV复制(分别为90 %和75 %)。Western blotting结果显示,上清液中的CHPV N蛋白水平与斑块分析一致。进一步分析感染CHPV和转染hA3G的细胞上清液,发现hA3G未掺入CHPV病毒颗粒中。病毒RNA序列分析表明,hA3G在病毒转录/复制过程中不会引起CHPV基因组的诱导突变。这是首次报道宿主因子介导的CHPV限制,本研究值得进一步深入研究,以了解这些因子对CHPV和其他负链RNA病毒的抑制机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chandipura virus replication in Vero cells is inhibited by host restriction factors APOBEC3G and IFITM3
Chandipura virus (CHPV) is an emerging pathogen of Indian subcontinent and in some West African countries. The virus causes fever, encephalitis and death among young children and there is no vaccine or drug available till date to treat CHPV infection. The present study aims to investigate if CHPV replication is inhibited by interferon induced proteins, human APOBEC3G (hA3G) and IFITM3, which are known as antiviral host factors. Virus infectivity was determined by plaque assays and results showed that CHPV replication in Vero E6 cells was significantly inhibited by both hA3G and IFITM3 (90 % and 75 % respectively). Western blotting results showed that CHPV N proteins levels in the supernatants are in agreement with the plaque assays. Further analysis of CHPV infected and hA3G transfected cell supernatants showed that hA3G was not incorporated into CHPV virus particles. Analysis of virus RNA sequences indicated that hA3G does not cause induced mutation of CHPV genome during virus transcription/replication. This is the first report about the host factor mediated restrictions of CHPV and the present study warrant further in-depth studies to understand the mechanisms of inhibition of CHPV and other negative stranded RNA viruses by these factors.
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