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埃及伊蚊 Domino 直系同源蛋白 p400 调节抗病毒外源小干扰 RNA 通路活性和表达。

The Aedes aegypti Domino Ortholog p400 Regulates Antiviral Exogenous Small Interfering RNA Pathway Activity and Expression.

机构信息

MRC-University of Glasgow Centre for Virus Research, Glasgow, Scotland.

Usher Institute for Population Health Sciences & Informatics, University of Edinburgh, Edinburgh, United Kingdom.

出版信息

mSphere. 2020 Apr 8;5(2):e00081-20. doi: 10.1128/mSphere.00081-20.

Abstract

Arboviruses are pathogens of humans and animals. A better understanding of the interactions between these pathogens and the arthropod vectors, such as mosquitoes, that transmit them is necessary to develop novel control measures. A major antiviral pathway in the mosquito vector is the exogenous small interfering RNA (exo-siRNA) pathway, which is induced by arbovirus-derived double-stranded RNA in infected cells. Although recent work has shown the key role played by Argonaute-2 (Ago-2) and Dicer-2 (Dcr-2) in this pathway, the regulatory mechanisms that govern these pathways have not been studied in mosquitoes. Here, we show that the Domino ortholog p400 has antiviral activity against the alphavirus Semliki Forest virus () both in -derived cells and Antiviral activity of p400 was also demonstrated against chikungunya virus () and Bunyamwera virus (e) but not Zika virus (). p400 was found to be expressed across mosquito tissues and regulated but not transcript levels in mosquitoes. These findings provide novel insights into the regulation of an important aedine exo-siRNA pathway effector protein, Ago-2, by the Domino ortholog p400. They add functional insights to previous observations of this protein's antiviral and RNA interference regulatory activities in Female mosquitoes are vectors of human-infecting arthropod-borne viruses (arboviruses). In recent decades, the incidence of arthropod-borne viral infections has grown dramatically. Vector competence is influenced by many factors, including the mosquito's antiviral defenses. The exogenous small interfering RNA (siRNA) pathway is a major antiviral response restricting arboviruses in mosquitoes. While the roles of the effectors of this pathway, Argonaute-2 and Dicer-2 are well characterized, nothing is known about its regulation in mosquitoes. In this study, we demonstrate that p400, whose ortholog Domino in is a chromatin-remodeling ATPase member of the Tip60 complex, regulates siRNA pathway activity and controls expression levels. In addition, we found p400 to have antiviral activity against different arboviruses. Therefore, our study provides new insights into the regulation of the antiviral response in mosquitoes.

摘要

虫媒病毒是人类和动物的病原体。为了开发新的控制措施,有必要更好地了解这些病原体与传播它们的节肢动物媒介(如蚊子)之间的相互作用。蚊子中的主要抗病毒途径是外源性小干扰 RNA(exo-siRNA)途径,该途径由感染细胞中虫媒病毒衍生的双链 RNA 诱导。尽管最近的工作表明 Argonaute-2(Ago-2)和 Dicer-2(Dcr-2)在该途径中起着关键作用,但尚未在蚊子中研究调节这些途径的调控机制。在这里,我们表明 Domino 同源物 p400 对 alphavirus Semliki Forest 病毒(SFV)具有抗病毒活性,无论是在 -衍生细胞中还是在 p400 对基孔肯雅病毒(CHIKV)和 Bunyamwera 病毒(BUNV)也表现出抗病毒活性,但对寨卡病毒(ZIKV)没有活性。发现 p400 在蚊子组织中表达,并调节 但不调节 在 蚊子中的转录水平。这些发现为 Domino 同源物 p400 对重要的 Aedine exo-siRNA 途径效应蛋白 Ago-2 的调节提供了新的见解。它们为先前观察到该蛋白在 中的抗病毒和 RNA 干扰调节活性提供了功能上的见解。雌性 蚊子是感染人类的节肢动物传播病毒(arboviruses)的媒介。在过去的几十年中,节肢动物传播的病毒感染的发病率急剧上升。媒介能力受许多因素影响,包括蚊子的抗病毒防御能力。外源性小干扰 RNA(siRNA)途径是限制蚊子中 arboviruses 的主要抗病毒反应。尽管该途径的效应物 Argonaute-2 和 Dicer-2 的作用已得到很好的描述,但对其在蚊子中的调节却一无所知。在这项研究中,我们证明 p400,其在 中的直系同源物 Domino 是 Tip60 复合物的染色质重塑 ATP 酶成员,调节 siRNA 途径活性并控制 表达水平。此外,我们发现 p400 对不同的 arboviruses 具有抗病毒活性。因此,我们的研究为 蚊子中的抗病毒反应调节提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/681f/7142294/b3d00d8c5b4b/mSphere.00081-20-f0001.jpg

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