PRRSV Non-Structural Proteins Orchestrate Porcine E3 Ubiquitin Ligase RNF122 to Promote PRRSV Proliferation

• Published in: Viruses Vol. 14; no. 2; p. 424
• Main Authors: Sun, Ruiqi, Guo, Yanyu, Li, Xiaoyang, Li, Ruiqiao, Shi, Jingxuan, Tan, Zheng, Zhang, Lilin, Zhang, Lei, Han, Jun, Huang, Jinhai
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 18.02.2022; MDPI
• Subjects: Alternative splicing; Animals; Antiviral agents; Cell Line; Cloning; Drug development; E2F protein; Genomes; Hogs; Immunoregulation; Immunosuppressive agents; Interferon Type I - metabolism; Interferon-Induced Helicase, IFIH1 - metabolism; Mammals; Monoclonal antibodies; nsp; nsp1; nsp4; NSP4 protein; Plasmids; Porcine Reproductive and Respiratory Syndrome - metabolism; Porcine Reproductive and Respiratory Syndrome - virology; porcine reproductive and respiratory syndrome virus (PRRSV); Porcine respiratory and reproductive syndrome virus - metabolism; Proteins; RNF122; Signal Transduction; Structural proteins; Swine; Thermal cycling; Transcription Factors; Ubiquitin; Ubiquitin-protein ligase; Ubiquitin-Protein Ligases - metabolism; Ubiquitination; Viral Nonstructural Proteins - chemistry; Viral Nonstructural Proteins - metabolism; Virus Replication - physiology; Viruses; α-Interferon; United States > US; China; nsp; nsp4; nsp1; ubiquitination; RNF122; porcine reproductive and respiratory syndrome virus (PRRSV)
• ISSN: 1999-4915; 1999-4915
• DOI: 10.3390/v14020424

Ubiquitination plays a major role in immune regulation after viral infection. An alternatively spliced porcine E3 ubiquitin ligase RNF122 promoted PRRSV infection and upregulated in PRRSV-infected PAM cells was identified. We characterized the core promoter of RNF122, located between -550 to -470 bp upstream of the transcription start site (TSS), which displayed significant differential transcriptional activities in regulating the transcription and expression of RNF122. The transcription factor HLTF was inhibited by nsp1α and nsp7 of PRRSV, and the transcription factor E2F complex regulated by nsp9. Together, they modulated the transcription and expression of RNF122. RNF122 could mediate K63-linked ubiquitination to raise stability of PRRSV nsp4 protein and thus promote virus replication. Moreover, RNF122 also performed K27-linked and K48-linked ubiquitination of MDA5 to degrade MDA5 and inhibit IFN production, ultimately promoted virus proliferation. In this study, we illustrate a new immune escape mechanism of PRRSV that enhances self-stability and function of viral nsp4, thus, regulating RNF122 expression to antagonize IFNα/β production. The present study broadens our knowledge of PRRSV-coding protein modulating transcription, expression and modification of host protein to counteract innate immune signaling, and may provide novel insights for the development of antiviral drugs.