The ESCRT-I Subunit Tsg101 Plays Novel Dual Roles in Entry and Replication of Classical Swine Fever Virus

• Published in: Journal of virology Vol. 95; no. 6
• Main Authors: Liu, Chun-Chun, Liu, Ya-Yun, Cheng, Yan, Zhang, Yun-Na, Zhang, Jin, Liang, Xiao-Dong, Gao, Ya, Chen, Huan, Baloch, Abdul Sattar, Yang, Qian, Go, Yun Young, Zhou, Bin
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 24.02.2021
• Subjects: Animals; Cell Line; Classical Swine Fever - metabolism; Classical Swine Fever - virology; Classical Swine Fever Virus - physiology; DNA-Binding Proteins - genetics; DNA-Binding Proteins - metabolism; Endoplasmic Reticulum - metabolism; Endoplasmic Reticulum - virology; Endosomal Sorting Complexes Required for Transport - genetics; Endosomal Sorting Complexes Required for Transport - metabolism; Endosomes - metabolism; Endosomes - virology; Host-Pathogen Interactions; Lysosomes - metabolism; Lysosomes - virology; RNA, Viral - metabolism; Swine; Transcription Factors - genetics; Transcription Factors - metabolism; Viral Nonstructural Proteins - metabolism; Viral Replication Compartments - metabolism; Virus Internalization; Virus Replication; Virus-Cell Interactions; replication; Tsg101; classical swine fever virus; entry; ESCRT
• ISSN: 0022-538X; 1098-5514
• DOI: 10.1128/JVI.01928-20

Classical swine fever (CSF), caused by classical swine fever virus (CSFV), is a highly contagious disease of swine with high morbidity and mortality that negatively affects the pig industry worldwide, in particular in China. Soon after the endocytosis of CSFV, the virus makes full use of the components of host cells to complete its life cycle. The endocytosis sorting complex required for transport (ESCRT) system is a central molecular machine for membrane protein sorting and scission in eukaryotic cells that plays an essential role in many physiological metabolic processes, including invasion and egress of envelope viruses. However, the molecular mechanism that ESCRT uses to regulate the replication of CSFV is unknown. In this study, we demonstrated that the ESCRT-I complex Tsg101 protein participates in clathrin-mediated endocytosis of CSFV and is also involved in CSFV trafficking. Tsg101 assists the virus in entering the host cell through the late endosome (Rab7 and Rab9) and finally reaching the lysosome (Lamp-1). Interestingly, Tsg101 is also involved in the viral replication process by interacting with nonstructural proteins 4B and 5B of CSFV. Finally, confocal microscopy showed that the replication complex of Tsg101 and double-stranded RNA (dsRNA) or NS4B and NS5B protein was close to the endoplasmic reticulum (ER), not the Golgi, in the cytoplasm. Collectively, our finding highlights that Tsg101 regulates the process of CSFV entry and replication, indicating that the ESCRT plays an important role in the life cycle of CSFV. Thus, ESCRT molecules could serve as therapeutic targets to combat CSFV infection. CSF, caused by CSFV, is a World Organization for Animal Health (OIE) notifiable disease and causes significant financial losses to the pig industry globally. The ESCRT machinery plays an important regulatory role in several members of the genera and within the family , such as hepatitis C virus, Japanese encephalitis virus, and dengue virus. Previous reports have shown that assembling and budding of these viruses require ESCRT. However, the role of ESCRT in infection remains to be elucidated. We determined the molecular mechanisms of the regulation of CSFV infection by the major subunit Tsg101 of ESCRT-I. Interestingly, Tsg101 plays an essential regulatory role in both clathrin-mediated endocytosis and genome replication of CSFV. Overall, the results of this study provide further insights into the molecular function of ESCRT-I complex protein Tsg101 during CSFV infection, which may serve as a molecular target for pestivirus inhibitors.