Increased viperin expression induced by avian infectious bronchitis virus inhibits viral replication by restricting cholesterol synthesis: an in vitro study

• Published in: Veterinary research (Paris) 2024-09, Vol.55 (1), p.116-14, Article 116
• Main Authors: Zhang, Yu, Zhang, Tao-Ni, Lu, Yan-Peng, Ren, Li-Na, Chen, Sheng-Ting, Liu, Ling, Wei, Lan-Ping, Chen, Ji-Ming, Huang, Jian-Ni, Mo, Mei-Lan
• Format: Article
• Language: English
• Subjects: Animals; Antiviral agents; Bronchitis; Chickens; Cholesterol; Cholesterol - metabolism; Coronavirus Infections - veterinary; Coronavirus Infections - virology; Cyclodextrins; Genetic aspects; Health aspects; Infectious bronchitis virus; Infectious bronchitis virus - physiology; Life Sciences; Poultry Diseases - virology; Poultry industry; viperin; Virus Replication
• ISSN: 1297-9716; 0928-4249; 1297-9716
• DOI: 10.1186/s13567-024-01368-w

With the emergence of new variant strains resulting from high mutation rates and genome recombination, avian infectious bronchitis virus (IBV) has caused significant economic losses to the poultry industry worldwide. Little is known about the underlying mechanisms of IBV-host interactions, particularly how IBV utilizes host metabolic pathways for efficient viral replication and transmission. In the present study, the effects of the cell membrane, viral envelope membrane, and viperin-mediated cholesterol synthesis on IBV replication were explored. Our results revealed significant increase in cholesterol levels and the expression of viperin after IBV infection. Acute cholesterol depletion in the cell membrane and viral envelope membrane by treating cells with methyl-β-cyclodextrin (MβCD) obviously inhibited IBV replication; thereafter, replenishment of the cell membrane with cholesterol successfully restored viral replication, and direct addition of exogenous cholesterol to the cell membrane significantly promoted IBV infection during the early stages of infection. In addition, overexpression of viperin effectively suppressed cholesterol synthesis, as well as IBV replication, whereas knockdown of viperin (gene silencing with siRNA targeting viperin, siViperin) significantly increased IBV replication and cholesterol levels, whereas supplementation with exogenous cholesterol to viperin-transfected cells markedly restored viral replication. In conclusion, the increase in viperin induced by IBV infection plays an important role in IBV replication by affecting cholesterol production, providing a theoretical basis for understanding the pathogenesis of IBV and discovering new potential antiviral targets.