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Coronavirus Porcine Epidemic Diarrhea Virus Nucleocapsid Protein Interacts with p53 To Induce Cell Cycle Arrest in S-Phase and Promotes Viral Replication

Mingjun Su, Da Shi, Xiaoxu Xing, Shanshan Qi, Dan Yang, Jiyu Zhang, Yuru Han, Qinghe Zhu, Haibo Sun, Xiaoran Wang, Haoyang Wu, Meijiao Wang, Wei Shan, Chunqiu Li, Donghua Guo, Li Feng, Dongbo Sun

2021Journal of Virology70 citationsDOIOpen Access PDF

Abstract

Many viruses subvert the host cell cycle to create a cellular environment that promotes viral growth. PEDV, an emerging and reemerging coronavirus, has led to substantial economic loss in the global swine industry. Our study is the first to demonstrate that PEDV N-induced cell cycle arrest during the S-phase promotes viral replication. We identified a novel mechanism of PEDV N-induced S-phase arrest, where the binding of PEDV N protein to p53 maintains consistently high levels of p53 expression in the nucleus to mediate S-phase arrest by activating the p53-DREAM pathway. Furthermore, a small molecular compound, hyperoside, targeted the PEDV N protein, interfering with the interaction between the N protein and p53 and, importantly, inhibited PEDV replication by antagonizing cell cycle arrest. This study reveals a new mechanism of PEDV-host interaction and also provides a novel antiviral strategy for PEDV. These data provide a foundation for further research into coronavirus-host interactions.

Topics & Concepts

BiologyPorcine epidemic diarrhea virusViral replicationViral life cycleVero cellCoronavirusVirologyViral structural proteinViral entryViral proteinCell biologyCell cycle checkpointCell cycleVirusCellGeneticsMedicineInfectious disease (medical specialty)DiseaseCoronavirus disease 2019 (COVID-19)PathologyAnimal Virus Infections StudiesVirus-based gene therapy researchViral gastroenteritis research and epidemiology
Coronavirus Porcine Epidemic Diarrhea Virus Nucleocapsid Protein Interacts with p53 To Induce Cell Cycle Arrest in S-Phase and Promotes Viral Replication | Litcius