An Autographa californica multiple nucleopolyhedrovirus-encoded microRNA, AcMNPV-miR-5, downregulates the expression of viral gene ac66.

IF 4.3 4区 医学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Tingkai Teng, Zhuowen Duan, Ang Li, Jinwen Wang
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引用次数: 0

Abstract

Four Autographa californica multiple nucleopolyhedrovirus (AcMNPV)-encoded microRNAs (miRNAs) have been characterized previously. Here, we report the fifth AcMNPV-encoded miRNA, AcMNPV-miR-5 (Ac-miR-5), which downregulates the viral gene ac66. Target genes were predicted through sequence analysis and validated using luciferase reporter assays. The regulatory effects of Ac-miR-5 on ac66 expression were assessed by reverse transcription quantitative PCR and Western blot. The impact of Ac-miR-5 overexpression on virus infection was analysed by TCID50 assay and quantitative real-time PCR in Sf9 cells. The results showed that Ac-miR-5 downregulates ac66 at both the mRNA and protein levels. Meanwhile, the budded virion production and DNA replication were decreased. Furthermore, microscopy revealed a decrease in the number of polyhedra formed. These findings suggest that Ac-miR-5 overexpression restricts viral load, potentially contributing to the establishment of a stable viral infection within the host cell.

加州签名虫多核多角体病毒编码的microRNA AcMNPV-miR-5下调病毒基因ac66的表达。
四种加州签名虫多核多角体病毒(AcMNPV)编码的microRNAs (miRNAs)已经被鉴定。在这里,我们报道了第五个acmnpv编码的miRNA, AcMNPV-miR-5 (Ac-miR-5),它下调了病毒基因ac66。通过序列分析预测靶基因,并使用荧光素酶报告基因检测进行验证。通过反转录定量PCR和Western blot检测Ac-miR-5对ac66表达的调控作用。在Sf9细胞中采用TCID50和实时荧光定量PCR分析Ac-miR-5过表达对病毒感染的影响。结果表明,Ac-miR-5在mRNA和蛋白水平上均下调ac66。同时出芽病毒粒子产量和DNA复制减少。此外,显微镜显示多面体形成的数量减少。这些发现表明,Ac-miR-5过表达限制了病毒载量,可能有助于在宿主细胞内建立稳定的病毒感染。
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来源期刊
Journal of General Virology
Journal of General Virology 医学-病毒学
CiteScore
7.70
自引率
2.60%
发文量
91
审稿时长
3 months
期刊介绍: JOURNAL OF GENERAL VIROLOGY (JGV), a journal of the Society for General Microbiology (SGM), publishes high-calibre research papers with high production standards, giving the journal a worldwide reputation for excellence and attracting an eminent audience.
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