Dual-specificity phosphatase 1 inhibits Singapore grouper iridovirus replication via regulating apoptosis in Epinephelus coioides

• Published in: Fish & shellfish immunology 2024-02, Vol.145, p.109313-109313, Article 109313
• Main Authors: He, Jia-Yang, Cai, Yi-Jie, Li, Yong-Xuan, Huang, Wei, Zhang, Yue, Liu, Ke-Jian, Sun, Zhuo, Dai, Li-Ling, Qi, Qi-Wei, Sun, Hong-Yan
• Format: Article
• Language: English
• ISSN: 1050-4648; 1095-9947
• DOI: 10.1016/j.fsi.2023.109313

The dual-specificity phosphatase (DUSP) family plays key roles in the maintenance of cellular homeostasis and apoptosis etc. In this study, the DUSP member DUSP1 of Epinephelus coioides was characterized: the length was 2371 bp including 281 bp 5' UTR, 911 bp 3' UTR, and a 1125 bp open reading frame encoding 374 amino acids. E. coioides DUSP1 has two conserved domains, a ROHD and DSPc along with a p38 MAPK phosphorylation site, localized at Ser308. E. coioides DUSP1 mRNA can be detected in all of the tissues examined, and the subcellular localization showed that DUSP1 was mainly distributed in the nucleus. Singapore grouper iridovirus (SGIV) infection could induce the differential expression of E. coioides DUSP1. Overexpression of DUSP1 could inhibit SGIV-induced cytopathic effect (CPE), the expressions of SGIV key genes, and the viral titers. Overexpression of DUSP1 could also regulate SGIV-induced apoptosis, and the expression of apoptosis-related factor caspase 3. The results would be helpful to further study the role of DUSP1 in viral infection.