Interaction of SERINC5 and IFITM1/2/3 regulates the autophagy-apoptosis-immune network under CSFV infection

The host restriction factor serine incorporator 5 (SERINC5) plays a key role in inhibiting viral activity and has been shown to inhibit classical swine fever virus (CSFV) infection. However, the action of SERINC5 in the interaction between host cells and CSFV remains poorly understood. This study fo...

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Main Authors: Wenhui Li, Zilin Zhang, Liangliang Zhang, Qingfeng Zhou, Yuwan Li, Lin Yi, Hongxing Ding, Mingqiu Zhao, Jinding Chen, Shuangqi Fan
Format: Article
Language:English
Published: Taylor & Francis Group 2022-12-01
Series:Virulence
Subjects:
Online Access:https://www.tandfonline.com/doi/10.1080/21505594.2022.2127241
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author Wenhui Li
Zilin Zhang
Liangliang Zhang
Qingfeng Zhou
Yuwan Li
Lin Yi
Hongxing Ding
Mingqiu Zhao
Jinding Chen
Shuangqi Fan
author_facet Wenhui Li
Zilin Zhang
Liangliang Zhang
Qingfeng Zhou
Yuwan Li
Lin Yi
Hongxing Ding
Mingqiu Zhao
Jinding Chen
Shuangqi Fan
author_sort Wenhui Li
collection DOAJ
description The host restriction factor serine incorporator 5 (SERINC5) plays a key role in inhibiting viral activity and has been shown to inhibit classical swine fever virus (CSFV) infection. However, the action of SERINC5 in the interaction between host cells and CSFV remains poorly understood. This study found that SERINC5 represses CSFV-induced autophagy through MAPK1/3-mTOR and AKT-mTOR signalling pathways. Further research showed that SERINC5 promotes apoptosis by repressing autophagy. Likewise, it was demonstrated that SERINC5 interacting proteins IFITM1/2/3 inhibit CSFV replication and regulate autophagy in a lysosomal-associated membrane protein LAMP1-dependent manner. In addition, IFITM1/2/3 interference promotes the NF-κB signalling pathway for potential immunoregulation by inhibiting autophagy. Finally, the functional silencing of IFITM1/2/3 genes was demonstrated to enhance the inhibitory effect of SERINC5 on autophagy. Taken together, These data uncover a novel mechanism through SERINC5 and its interacting proteins IFITM1/2/3, which mediates CSFV replication, and provides new avenues for controlling CSFV.
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spelling doaj.art-99a0a270958d4b56a9935de6e5c0c7ff2022-12-22T03:54:47ZengTaylor & Francis GroupVirulence2150-55942150-56082022-12-011311720174010.1080/21505594.2022.2127241Interaction of SERINC5 and IFITM1/2/3 regulates the autophagy-apoptosis-immune network under CSFV infectionWenhui Li0Zilin Zhang1Liangliang Zhang2Qingfeng Zhou3Yuwan Li4Lin Yi5Hongxing Ding6Mingqiu Zhao7Jinding Chen8Shuangqi Fan9College of Veterinary Medicine, South China Agricultural University, Guangzhou, ChinaCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, ChinaCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, ChinaCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, ChinaCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, ChinaCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, ChinaCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, ChinaCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, ChinaCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, ChinaCollege of Veterinary Medicine, South China Agricultural University, Guangzhou, ChinaThe host restriction factor serine incorporator 5 (SERINC5) plays a key role in inhibiting viral activity and has been shown to inhibit classical swine fever virus (CSFV) infection. However, the action of SERINC5 in the interaction between host cells and CSFV remains poorly understood. This study found that SERINC5 represses CSFV-induced autophagy through MAPK1/3-mTOR and AKT-mTOR signalling pathways. Further research showed that SERINC5 promotes apoptosis by repressing autophagy. Likewise, it was demonstrated that SERINC5 interacting proteins IFITM1/2/3 inhibit CSFV replication and regulate autophagy in a lysosomal-associated membrane protein LAMP1-dependent manner. In addition, IFITM1/2/3 interference promotes the NF-κB signalling pathway for potential immunoregulation by inhibiting autophagy. Finally, the functional silencing of IFITM1/2/3 genes was demonstrated to enhance the inhibitory effect of SERINC5 on autophagy. Taken together, These data uncover a novel mechanism through SERINC5 and its interacting proteins IFITM1/2/3, which mediates CSFV replication, and provides new avenues for controlling CSFV.https://www.tandfonline.com/doi/10.1080/21505594.2022.2127241CSFVSERINC5IFITM1/2/3autophagyapoptosis
spellingShingle Wenhui Li
Zilin Zhang
Liangliang Zhang
Qingfeng Zhou
Yuwan Li
Lin Yi
Hongxing Ding
Mingqiu Zhao
Jinding Chen
Shuangqi Fan
Interaction of SERINC5 and IFITM1/2/3 regulates the autophagy-apoptosis-immune network under CSFV infection
Virulence
CSFV
SERINC5
IFITM1/2/3
autophagy
apoptosis
title Interaction of SERINC5 and IFITM1/2/3 regulates the autophagy-apoptosis-immune network under CSFV infection
title_full Interaction of SERINC5 and IFITM1/2/3 regulates the autophagy-apoptosis-immune network under CSFV infection
title_fullStr Interaction of SERINC5 and IFITM1/2/3 regulates the autophagy-apoptosis-immune network under CSFV infection
title_full_unstemmed Interaction of SERINC5 and IFITM1/2/3 regulates the autophagy-apoptosis-immune network under CSFV infection
title_short Interaction of SERINC5 and IFITM1/2/3 regulates the autophagy-apoptosis-immune network under CSFV infection
title_sort interaction of serinc5 and ifitm1 2 3 regulates the autophagy apoptosis immune network under csfv infection
topic CSFV
SERINC5
IFITM1/2/3
autophagy
apoptosis
url https://www.tandfonline.com/doi/10.1080/21505594.2022.2127241
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