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探讨蜱传黄病毒与硬蜱之间的二元蛋白-蛋白相互作用。

Exploration of binary protein-protein interactions between tick-borne flaviviruses and Ixodes ricinus.

机构信息

UMR 1161 Virologie Laboratoire de Santé Animale, ANSES, INRAE, Ecole Nationale Vétérinaire d'Alfort, Paris-Est Sup, Maisons-Alfort, France.

Department of Infection Biology and Microbiomes, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.

出版信息

Parasit Vectors. 2021 Mar 6;14(1):144. doi: 10.1186/s13071-021-04651-3.

Abstract

BACKGROUND

Louping ill virus (LIV) and tick-borne encephalitis virus (TBEV) are tick-borne flaviviruses that are both transmitted by the major European tick, Ixodes ricinus. Despite the importance of I. ricinus as an arthropod vector, its capacity to acquire and subsequently transmit viruses, known as vector competence, is poorly understood. At the molecular scale, vector competence is governed in part by binary interactions established between viral and cellular proteins within infected tick cells.

METHODS

To investigate virus-vector protein-protein interactions (PPIs), the entire set of open reading frames for LIV and TBEV was screened against an I. ricinus cDNA library established from three embryonic tick cell lines using yeast two-hybrid methodology (Y2H). PPIs revealed for each viral bait were retested in yeast by applying a gap repair (GR) strategy, and notably against the cognate protein of both viruses, to determine whether the PPIs were specific for a single virus or common to both. The interacting tick proteins were identified by automatic BLASTX, and in silico analyses were performed to expose the biological processes targeted by LIV and TBEV.

RESULTS

For each virus, we identified 24 different PPIs involving six viral proteins and 22 unique tick proteins, with all PPIs being common to both viruses. According to our data, several viral proteins (pM, M, NS2A, NS4A, 2K and NS5) target multiple tick protein modules implicated in critical biological pathways. Of note, the NS5 and pM viral proteins establish PPI with several tumor necrosis factor (TNF) receptor-associated factor (TRAF) proteins, which are essential adaptor proteins at the nexus of multiple signal transduction pathways.

CONCLUSION

We provide the first description of the TBEV/LIV-I. ricinus PPI network, and indeed of any PPI network involving a tick-borne virus and its tick vector. While further investigation will be needed to elucidate the role of each tick protein in the replication cycle of tick-borne flaviviruses, our study provides a foundation for understanding the vector competence of I. ricinus at the molecular level. Indeed, certain PPIs may represent molecular determinants of vector competence of I. ricinus for TBEV and LIV, and potentially for other tick-borne flaviviruses.

摘要

背景

鹿病毒性脑炎病毒(LIV)和蜱传脑炎病毒(TBEV)是两种通过主要的欧洲蜱,蓖子硬蜱传播的蜱传黄病毒。尽管蓖子硬蜱作为节肢动物传播媒介非常重要,但它获取和随后传播病毒的能力,即媒介能力,知之甚少。在分子水平上,媒介能力部分由感染蜱细胞中病毒和细胞蛋白之间建立的二元相互作用决定。

方法

为了研究病毒-媒介蛋白-蛋白相互作用(PPIs),使用酵母双杂交法(Y2H)筛选了来自三个胚胎蜱细胞系的 cDNA 文库,对 LIV 和 TBEV 的整套开放阅读框进行了筛选。针对每个病毒诱饵发现的 PPIs,通过缺口修复(GR)策略在酵母中进行了重新测试,特别是针对两种病毒的同源蛋白,以确定 PPIs是针对单一病毒还是两种病毒共有的。通过自动 BLASTX 鉴定相互作用的蜱蛋白,并进行了计算机分析,以暴露 LIV 和 TBEV 靶向的生物学过程。

结果

对于每种病毒,我们鉴定了涉及六种病毒蛋白和 22 种独特蜱蛋白的 24 种不同的 PPIs,所有的 PPIs 对两种病毒都是共同的。根据我们的数据,几种病毒蛋白(pM、M、NS2A、NS4A、2K 和 NS5)靶向多个涉及关键生物学途径的蜱蛋白模块。值得注意的是,NS5 和 pM 病毒蛋白与几种肿瘤坏死因子(TNF)受体相关因子(TRAF)蛋白建立了 PPI,TRAF 蛋白是多种信号转导途径的关键衔接蛋白。

结论

我们首次描述了 TBEV/LIV-I. ricinus 的 PPI 网络,实际上也是描述了任何涉及蜱传病毒及其蜱媒介的 PPI 网络。虽然需要进一步研究来阐明每个蜱蛋白在蜱传黄病毒复制周期中的作用,但我们的研究为在分子水平上理解蓖子硬蜱的媒介能力提供了基础。事实上,某些 PPI 可能是蓖子硬蜱对 TBEV 和 LIV 以及潜在其他蜱传黄病毒的媒介能力的分子决定因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9283/7937244/028ffeb805c9/13071_2021_4651_Fig1_HTML.jpg

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