用于检测丝状病毒VP35蛋白对I型干扰素反应抑制作用的测定方法。

Assays to Measure Suppression of Type I Interferon Responses by Filovirus VP35 Proteins.

作者信息

Luthra Priya, Basler Christopher F

机构信息

Center for Microbial Pathogenesis, Institute for Biomedical Sciences, Georgia State University, Atlanta, GA, USA.

出版信息

Methods Mol Biol. 2017;1628:133-142. doi: 10.1007/978-1-4939-7116-9_10.

Abstract

Innate immunity is the first line of defense against virus infections and is marked by production of type I interferons (IFN), a family of cytokines that includes IFN-β and several IFN-αs. For the filoviruses and many other RNA viruses that replicate in the cytoplasm, the RIG-I-like pattern recognition receptors (RLRs) are potential triggers of IFN production. To counteract such innate antiviral responses, many viruses encode proteins that antagonize RLR signaling. Ebola virus (EBOV) and other filoviruses produce VP35 proteins that block IFN induction via RLR signaling. We describe here cell-based reporter gene assays that quantify the IFN-antagonist function of filovirus VP35 proteins by assessing activation of the IFN-β promoter.

摘要

天然免疫是抵御病毒感染的第一道防线,其特征是产生I型干扰素(IFN),这是一类细胞因子,包括IFN-β和几种IFN-α。对于在细胞质中复制的丝状病毒和许多其他RNA病毒,视黄酸诱导基因I样模式识别受体(RLR)是IFN产生的潜在触发因素。为了对抗这种天然抗病毒反应,许多病毒编码拮抗RLR信号传导的蛋白质。埃博拉病毒(EBOV)和其他丝状病毒产生VP35蛋白,通过RLR信号传导阻断IFN诱导。我们在此描述基于细胞的报告基因测定法,该方法通过评估IFN-β启动子的激活来量化丝状病毒VP35蛋白的IFN拮抗剂功能。

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