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hnRNP K Degrades Viral Nucleocapsid Protein and Induces Type I IFN Production to Inhibit Porcine Epidemic Diarrhea Virus Replication

Wenzhen Qin, Ning Kong, Chunmei Wang, Sujie Dong, Huanjie Zhai, Xueying Zhai, Xinyu Yang, Chenqian Ye, Manqing Ye, Tong Wu, Changlong Liu, Lingxue Yu, Hao Zheng, Hai Yu, Daoliang Lan, Wen Zhang, Guangzhi Tong, Tongling Shan

2022Journal of Virology20 citationsDOIOpen Access PDF

Abstract

The spread of the highly virulent PEDV in many countries is still leading to several epidemic and endemic outbreaks. To elucidate effective antiviral mechanisms, it is important to study the relationship between host antiviral factors and the virus and to investigate the mechanisms underlying host immune response against PEDV infection. In the work, we detected hnRNP K as a new host restriction factor which can hinder PEDV replication through degrading the nucleocapsid protein based on E3 ubiquitin ligase MARCH8 and the cargo receptor NDP52. In addition, via the upregulation of MyD88 expression, hnRNP K could also activate the interferon (IFN) signaling pathway. This study describes a previously unknown antiviral function of hnRNP K and offers a new vision toward host antiviral factors that regulate innate immune response as well as a protein degradation pathway against PEDV infection.

Topics & Concepts

Porcine epidemic diarrhea virusBiologyVirologyViral replicationVirusCoronavirusUbiquitin ligaseInterferonViral structural proteinViral proteinViral entryUbiquitinGeneGeneticsDiseasePathologyInfectious disease (medical specialty)Coronavirus disease 2019 (COVID-19)MedicineAnimal Virus Infections StudiesViral Infections and Immunology ResearchViral gastroenteritis research and epidemiology
hnRNP K Degrades Viral Nucleocapsid Protein and Induces Type I IFN Production to Inhibit Porcine Epidemic Diarrhea Virus Replication | Litcius