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阻断Wee1激酶诱导有丝分裂灾难以抑制猪圆环病毒2型复制

张二伟 颜焰 周继勇 吴威

浙江大学学报(农业与生命科学版)2026,Vol.52Issue(4):621-632,12.
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浙江大学学报(农业与生命科学版)2026,Vol.52Issue(4):621-632,12.DOI:10.3785/j.issn.1008-9209.2026.01.291

阻断Wee1激酶诱导有丝分裂灾难以抑制猪圆环病毒2型复制

Wee1 inhibition induces mitotic catastrophe to suppress porcine circovirus type 2 replication

张二伟 1颜焰 1周继勇 1吴威1

作者信息

  • 1. 浙江大学动物医学中心/农业农村部动物病毒学重点实验室,浙江 杭州 310058
  • 折叠

摘要

Abstract

Porcine circovirus type 2(PCV2)is the primary pathogen of porcine circovirus-associated diseases,posing a serious threat to the global swine industry.This study aimed to evaluate the effect of targeting the host cell cycle regulator Wee1 kinase on PCV2 replication.Using an in vitro infection model,we systematically analyzed the impact of PCV2 infection on the host DNA damage response(DDR)and cell cycle progression through a chromosome spread assay,indirect immunofluorescence assay,and Western blotting analyses,and assessed the antiviral activity of the Wee1 inhibitor MK-1775.The results showed that PCV2 infection significantly activated host DDR,with 84%of infected cells exhibiting γ-H2AX positivity,and induced cell cycle arrest in the S phase.Further analysis revealed that MK-1775 treatment triggered mitotic catastrophe in approximately 60%of infected cells,accompanied by a significant reduction in the PCV2 infection rate and viral protein expression levels.These findings indicate that PCV2 replication relies on host cell cycle regulation,and that Wee1 inhibition effectively suppresses viral replication by disrupting cell cycle checkpoints and inducing mitotic catastrophe.Thus,targeting the host cell cycle regulator Wee1 may represent a potential strategy for intervening in PCV2 infection.

关键词

猪圆环病毒2型/DNA损伤应答/细胞周期阻滞/Wee1抑制剂/有丝分裂灾难

Key words

porcine circovirus type 2/DNA damage response/cell cycle arrest/Wee1 inhibitor/mitotic catastrophe

分类

农业科技

引用本文复制引用

张二伟,颜焰,周继勇,吴威..阻断Wee1激酶诱导有丝分裂灾难以抑制猪圆环病毒2型复制[J].浙江大学学报(农业与生命科学版),2026,52(4):621-632,12.

基金项目

国家自然科学基金重大项目(32192454) (32192454)

杭州城西科创大走廊创新发展专项. ()

浙江大学学报(农业与生命科学版)

1008-9209

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