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LMBV-ICP46通过激活cGAS-STING-p53轴抑制病毒复制

邹悦 蔺凌云 郭琼瑶 姚嘉赟 沈锦玉 陶震 潘晓艺

中国水产科学2026,Vol.33Issue(7):67-80,14.
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中国水产科学2026,Vol.33Issue(7):67-80,14.DOI:10.12264/JFSC2025-0352

LMBV-ICP46通过激活cGAS-STING-p53轴抑制病毒复制

ICP46 of largemouth bass virus inhibits viral replication through activation of the cGAS-STING-p53 axis

邹悦 1蔺凌云 2郭琼瑶 2姚嘉赟 2沈锦玉 1陶震 3潘晓艺1

作者信息

  • 1. 浙江海洋大学水产学院,浙江 舟山 316022||浙江省淡水水产研究所(浙江省淡水渔业环境监测站),农业农村部淡水渔业健康养殖重点实验室,浙江省鱼类健康与营养重点实验室,浙江 湖州 313001
  • 2. 浙江省淡水水产研究所(浙江省淡水渔业环境监测站),农业农村部淡水渔业健康养殖重点实验室,浙江省鱼类健康与营养重点实验室,浙江 湖州 313001
  • 3. 浙江海洋大学水产学院,浙江 舟山 316022
  • 折叠

摘要

Abstract

Largemouth bass virus(LMBV)causes significant economic losses to the Micropterus salmoides aquaculture industry;however,the functions of many ranavirus immediate-early genes remain poorly understood.Cytosolic DNA sensing via the cGAS-STING axis is a key antiviral pathway that can also engage apoptosis to limit DNA virus replication.Defining how LMBV proteins interface with these defenses is important for understanding pathogenesis and control.This study aimed to characterize the immediate-early gene ICP46 of LMBV,determine its temporal expression and subcellular localization,and evaluate whether ICP46 modulates viral replication by regulating host cGAS-STING signaling and apoptosis-related responses in MSSC cells.MSSC cells were infected with LMBV and treated with cycloheximide(CHX)and cytosine arabinoside(Ara)to classify ICP46 as an immediate-early transcript by PCR-based temporal analysis.An EGFP-tagged expression plasmid(pEGFP-ICP46)was constructed to assess intracellular localization by confocal microscopy at different post-transfection times.ICP46 function was examined by(i)ectopic overexpression and(ii)siRNA-mediated knockdown followed by LMBV challenge.Viral replication was quantified by qPCR targeting the major capsid protein gene(MCP)and by viral copy-number calculation.Host responses were evaluated by qPCR of cGAS-STING pathway markers(STING,IRF3)and apoptosis-associated genes(p53,caspase-8,bcl-2,bcl-xL).These results identify LMBV ICP46 as an immediate-early protein that restricts,rather than enhances,viral replication.This contrasts with the reported pro-replication role of ICP46 previously reported in SGIV,highlighting functional diversification among ranavirus homologs.The reciprocal outcomes of overexpression and knockdown support a specific,gene-dependent phenotype.Mechanistically,ICP46 is associated with enhanced cGAS-STING-IRF3 signaling and a shift toward apoptosis,which potentially creates an antiviral cellular environment unfavorable for LMBV propagation.These findings provide novel insights into LMBV-host interactions and highlight ICP46 and its downstream pathways as potential targets for the development of antiviral strategies and rational disease control in largemouth bass aquaculture.

关键词

大口黑鲈蛙虹彩病毒/即刻早期蛋白ICP46/cGAS-STING通路/P53轴/细胞凋亡/病毒复制

Key words

largemouth bass virus/immediate early protein ICP46/cGAS-STING pathway/P53 axis/apoptosis/virus replication

分类

农业科技

引用本文复制引用

邹悦,蔺凌云,郭琼瑶,姚嘉赟,沈锦玉,陶震,潘晓艺..LMBV-ICP46通过激活cGAS-STING-p53轴抑制病毒复制[J].中国水产科学,2026,33(7):67-80,14.

基金项目

国家重点研发计划项目(2023YFD2400702) (2023YFD2400702)

湖州市公益应用研究项目(2023GZ45) (2023GZ45)

浙江省"三农九方"科技协作计划项目(2026SNJF043). (2026SNJF043)

中国水产科学

1005-8737

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