PCNA promotes PRRSV replication by increasing the synthesis of viral genome

被引:2
作者
Wang, Qiumei [1 ]
Yi, Heyou [1 ]
Guo, Yanchen [1 ]
Sun, Yankuo [1 ,2 ,3 ]
Yu, Zhiqing [4 ]
Lu, Lechen [1 ]
Ye, Ruirui [1 ]
Xie, Ermin [1 ]
Wu, Qianwen [1 ]
Qiu, Yingwu [1 ]
Quan, Weipeng [1 ]
Zhang, Guihong [1 ,2 ,3 ]
Wang, Heng [1 ,2 ,3 ]
机构
[1] South China Agr Univ, Coll Vet Med, Guangdong Prov Key Lab Zoonosis Prevent & Control, Guangzhou 510462, Peoples R China
[2] Guangdong Lab Lingnan Modern Agr, Maoming Branch, Maoming 525000, Peoples R China
[3] South China Agr Univ, Natl Engn Res Ctr Breeding Swine Ind, Guangzhou 510642, Peoples R China
[4] Zhong mu Inst China Anim Husb Ind Co Ltd, Key Lab Vet Bioprod & Chem Med, Engn & Technol Res Ctr Beijing Vet Peptide Vaccine, Minist Agr, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
PRRSV; PCNA; Nuclear translocation; RNA synthesis; RESPIRATORY SYNDROME VIRUS; PROTEIN-PROTEIN INTERACTIONS; NUCLEOCAPSID PROTEIN; PORCINE; IDENTIFICATION;
D O I
10.1016/j.vetmic.2023.109741
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Porcine reproductive and respiratory syndrome virus (PRRSV) is an RNA virus belonging to the Arteriviridae family. Currently, the strain has undergone numerous mutations, bringing massive losses to the swine industry worldwide. Despite several studies had been conducted on PRRSV, the molecular mechanisms by which it causes infection remain unclear. Proliferating cell nuclear antigen (PCNA) is a sign of DNA damage and it participates in DNA replication and repair. Therefore, in this study, we investigated the potential role of PCNA in PRRSV infection. We observed that PCNA expression was stable after PRRSV infection in vitro; however, PCNA was translocated from the nucleus to the cytoplasm. Notably, we found the redistribution of PCNA from the nucleus to the cytoplasm in cells transfected with the N protein. PCNA silencing inhibited PRRSV replication and the synthesis of PRRSV shorter subgenomic RNA (sgmRNA) and genomic RNA (gRNA), while PCNA overexpression promoted virus replication and PRRSV shorter sgmRNA and gRNA synthesis. By performing immunoprecipita-tion and immunofluorescence colocalization, we confirmed that PCNA interacted with replication-related pro-teins, namely NSP9, NSP12, and N, but not with NSP10 and NSP11. Domain III of the N protein (41-72 aa) interacted with the IDCL domain of PCNA (118-135 aa). Therefore, we propose cytoplasmic transport of PCNA and its subsequent influence on PRRSV RNA synthesis could be a viral strategy for manipulating cell function, thus PCNA is a potential target to prevent and control PRRSV infection.
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页数:10
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