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TRIM21 inhibits porcine epidemic diarrhea virus proliferation by proteasomal degradation of the nucleocapsid protein
Tripartite motif protein 21 (TRIM21) is an E3 ubiquitin ligase and cytosolic antibody receptor of the TRIM family. Previous reports have indicated that TRIM21 plays an important role during viral infection. This study aimed at examining the role of TRIM21 in the replication of porcine epidemic diarr...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8074351/ https://www.ncbi.nlm.nih.gov/pubmed/33900472 http://dx.doi.org/10.1007/s00705-021-05080-4 |
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author | Wang, Hua Chen, Xiaoyong Kong, Ning Jiao, Yajuan Sun, Dage Dong, Sujie Qin, Wenzhen Zhai, Huanjie Yu, Lingxue Zheng, Hao Tong, Wu Yu, Hai Tong, Guangzhi Shan, Tongling |
author_facet | Wang, Hua Chen, Xiaoyong Kong, Ning Jiao, Yajuan Sun, Dage Dong, Sujie Qin, Wenzhen Zhai, Huanjie Yu, Lingxue Zheng, Hao Tong, Wu Yu, Hai Tong, Guangzhi Shan, Tongling |
author_sort | Wang, Hua |
collection | PubMed |
description | Tripartite motif protein 21 (TRIM21) is an E3 ubiquitin ligase and cytosolic antibody receptor of the TRIM family. Previous reports have indicated that TRIM21 plays an important role during viral infection. This study aimed at examining the role of TRIM21 in the replication of porcine epidemic diarrhea virus (PEDV) and showed that TRIM21 inhibits PEDV proliferation by targeting and degrading the nucleocapsid (N) protein through the proteasomal pathway. Furthermore, the endogenous expression of TRIM21 was found to be downregulated by PEDV infection in Vero and LLC-PK1 cells. Overexpression of TRIM21 inhibited PEDV replication, whereas knockdown of TRIM21 increased viral titers and N protein levels. TRIM21 was found to interact and colocalize with the N protein, and the TRIM21-mediated antiviral effect was dependent on its ubiquitin ligase activity, which engages in polyubiquitination and degradation of the N protein in a proteasome-dependent manner. Taken together, these findings provide information about the role of TRIM21 in PEDV proliferation and increase our understanding of host-virus interactions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00705-021-05080-4. |
format | Online Article Text |
id | pubmed-8074351 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-80743512021-04-26 TRIM21 inhibits porcine epidemic diarrhea virus proliferation by proteasomal degradation of the nucleocapsid protein Wang, Hua Chen, Xiaoyong Kong, Ning Jiao, Yajuan Sun, Dage Dong, Sujie Qin, Wenzhen Zhai, Huanjie Yu, Lingxue Zheng, Hao Tong, Wu Yu, Hai Tong, Guangzhi Shan, Tongling Arch Virol Original Article Tripartite motif protein 21 (TRIM21) is an E3 ubiquitin ligase and cytosolic antibody receptor of the TRIM family. Previous reports have indicated that TRIM21 plays an important role during viral infection. This study aimed at examining the role of TRIM21 in the replication of porcine epidemic diarrhea virus (PEDV) and showed that TRIM21 inhibits PEDV proliferation by targeting and degrading the nucleocapsid (N) protein through the proteasomal pathway. Furthermore, the endogenous expression of TRIM21 was found to be downregulated by PEDV infection in Vero and LLC-PK1 cells. Overexpression of TRIM21 inhibited PEDV replication, whereas knockdown of TRIM21 increased viral titers and N protein levels. TRIM21 was found to interact and colocalize with the N protein, and the TRIM21-mediated antiviral effect was dependent on its ubiquitin ligase activity, which engages in polyubiquitination and degradation of the N protein in a proteasome-dependent manner. Taken together, these findings provide information about the role of TRIM21 in PEDV proliferation and increase our understanding of host-virus interactions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00705-021-05080-4. Springer Vienna 2021-04-26 2021 /pmc/articles/PMC8074351/ /pubmed/33900472 http://dx.doi.org/10.1007/s00705-021-05080-4 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Article Wang, Hua Chen, Xiaoyong Kong, Ning Jiao, Yajuan Sun, Dage Dong, Sujie Qin, Wenzhen Zhai, Huanjie Yu, Lingxue Zheng, Hao Tong, Wu Yu, Hai Tong, Guangzhi Shan, Tongling TRIM21 inhibits porcine epidemic diarrhea virus proliferation by proteasomal degradation of the nucleocapsid protein |
title | TRIM21 inhibits porcine epidemic diarrhea virus proliferation by proteasomal degradation of the nucleocapsid protein |
title_full | TRIM21 inhibits porcine epidemic diarrhea virus proliferation by proteasomal degradation of the nucleocapsid protein |
title_fullStr | TRIM21 inhibits porcine epidemic diarrhea virus proliferation by proteasomal degradation of the nucleocapsid protein |
title_full_unstemmed | TRIM21 inhibits porcine epidemic diarrhea virus proliferation by proteasomal degradation of the nucleocapsid protein |
title_short | TRIM21 inhibits porcine epidemic diarrhea virus proliferation by proteasomal degradation of the nucleocapsid protein |
title_sort | trim21 inhibits porcine epidemic diarrhea virus proliferation by proteasomal degradation of the nucleocapsid protein |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8074351/ https://www.ncbi.nlm.nih.gov/pubmed/33900472 http://dx.doi.org/10.1007/s00705-021-05080-4 |
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