MicroRNA miR-155 inhibits cyprinid herpesvirus 3 replication via regulating AMPK-MAVS-IFN axis
Chi Zhang, Qing Wang, An-qi Liu, Chu Zhang, Lan-Hao Liu, Long-Feng Lu, Jiagang Tu, Yong-An Zhang
Journal:DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY
IF:3.64
DOI:10.1016/j.dci.2021.104335
PMID:34929233
Published:2021-12-17
research field:分子生物学鱼类病理学免疫学微生物学病毒学
Abstract
Since emerged in the late 1990s, cyprinid herpesvirus 3 (CyHV-3) has caused huge economic losses in common and koi carp culture worldwide. Accumulating evidences suggest that teleost fish microRNA (miRNA), a class of non-coding RNA of ∼22 nucleotides, can participate in many cellular processes, especially in host antiviral defenses. However, the roles of miRNAs in CyHV-3 infection are still unclear. Here, using high-throughput miRNA sequencing and quantitative real-time PCR (qRT-PCR) verification, we found that miR-155 was significantly upregulated in common carp brain (CCB) cells upon CyHV-3 infection. Overexpression of miR-155 effectively inhibited CyHV-3 replication in CCB cells and promoted type I interferon (IFN–I) expression. Further study revealed that miR-155 targeted the 3′ untranslated region (UTR) of the mRNA of 5′AMP-activated protein kinase (AMPK), and that AMPK could interact with and degrade the mitochondrial antiviral signaling protein (MAVS), resulting in the reduction of interferon (IFN) expression. Collectively, our results show that miR-155, induced by CyHV-3 infection, exhibits anti -CyHV-3 activity via regulating AMPK-MAVS-IFN axis, which will help design anti -CyHV-3 drugs.
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