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Porcine transmissible gastroenteritis virus nonstructural protein 2 contributes to inflammation via NF-κB activation

Transmissible gastroenteritis virus (TGEV) infection causes acute enteritis in swine of all ages, and especially in suckling piglets. Small intestinal inflammation is considered a central event in the pathogenesis of TGEV infections, and nuclear factor-kappa B (NF-κB) is a key transcription factor i...

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Autores principales: Wang, Li, Qiao, Xinyuan, Zhang, Sijia, Qin, Yue, Guo, Tiantian, Hao, Zhenye, Sun, Li, Wang, Xiaona, Wang, Yanan, Jiang, Yanping, Tang, Lijie, Xu, Yigang, Li, Yijing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000202/
https://www.ncbi.nlm.nih.gov/pubmed/30322331
http://dx.doi.org/10.1080/21505594.2018.1536632
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author Wang, Li
Qiao, Xinyuan
Zhang, Sijia
Qin, Yue
Guo, Tiantian
Hao, Zhenye
Sun, Li
Wang, Xiaona
Wang, Yanan
Jiang, Yanping
Tang, Lijie
Xu, Yigang
Li, Yijing
author_facet Wang, Li
Qiao, Xinyuan
Zhang, Sijia
Qin, Yue
Guo, Tiantian
Hao, Zhenye
Sun, Li
Wang, Xiaona
Wang, Yanan
Jiang, Yanping
Tang, Lijie
Xu, Yigang
Li, Yijing
author_sort Wang, Li
collection PubMed
description Transmissible gastroenteritis virus (TGEV) infection causes acute enteritis in swine of all ages, and especially in suckling piglets. Small intestinal inflammation is considered a central event in the pathogenesis of TGEV infections, and nuclear factor-kappa B (NF-κB) is a key transcription factor in the inflammatory response. However, it is unclear whether NF-κB is crucial for inducing inflammation during a TGEV infection. Our results show that NF-κB was activated in swine testicular (ST) cells and intestinal epithelial cell lines J2 (IPEC-J2) cells infected with TGEV, which is consistent with the up-regulation of pro-inflammatory cytokines. Treatment of TGEV-infected ST cells and IPEC-J2 cells with the NF-κB-specific inhibitor caused the down-regulation of pro-inflammatory cytokine expression, but did not significantly affect TGEV replication. Individual TGEV protein screening results demonstrated that Nsp2 exhibited a high potential for activating NF-κB and enhancing the expression of pro-inflammatory cytokines. Functional domain analyzes indicated that the first 120 amino acid residues of Nsp2 were essential for NF-κB activation. Taken together, these data suggested that NF-κB activation was a major contributor to TGEV infection-induced inflammation, and that Nsp2 was the key viral protein involved in the regulation of inflammation, with amino acids 1–120 playing a critical role in activating NF-κB. Abbreviations: TCID50: 50% tissue culture infectious dose; DMEM: Dulbecco’s Modified Eagle Medium; eNOS: Endothelial nitric oxide synthase; FBS: fetal bovine serum; IFA: Indirect immunofluorescence; IκB: inhibitor of nuclear factor kappa-B; IL: interleukin; IPEC-J2: intestinal epithelial cell lines J2; IKK: IκB kinase; Luc: luciferase reporter gene; mAbs: monoclonal antibodies; MOI: multiple of infection; Nsp: nonstructural protein; NF-κB: nuclear factor-kappa ; ORFs: open reading frames; PBS: phosphate-buffered saline; p65 p-p65: phosphorylated; RT-PCR: reverse transcription PC; SeV: Sendai virus; ST: swine testicular; TGEV: Transmissible gastroenteritis virus; TNF-α: tumor necrosis factor α; UV-TGEV: Ultraviolet light-inactivated TGEV; ZnF: zinc finger
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spelling pubmed-70002022020-02-19 Porcine transmissible gastroenteritis virus nonstructural protein 2 contributes to inflammation via NF-κB activation Wang, Li Qiao, Xinyuan Zhang, Sijia Qin, Yue Guo, Tiantian Hao, Zhenye Sun, Li Wang, Xiaona Wang, Yanan Jiang, Yanping Tang, Lijie Xu, Yigang Li, Yijing Virulence Research Paper Transmissible gastroenteritis virus (TGEV) infection causes acute enteritis in swine of all ages, and especially in suckling piglets. Small intestinal inflammation is considered a central event in the pathogenesis of TGEV infections, and nuclear factor-kappa B (NF-κB) is a key transcription factor in the inflammatory response. However, it is unclear whether NF-κB is crucial for inducing inflammation during a TGEV infection. Our results show that NF-κB was activated in swine testicular (ST) cells and intestinal epithelial cell lines J2 (IPEC-J2) cells infected with TGEV, which is consistent with the up-regulation of pro-inflammatory cytokines. Treatment of TGEV-infected ST cells and IPEC-J2 cells with the NF-κB-specific inhibitor caused the down-regulation of pro-inflammatory cytokine expression, but did not significantly affect TGEV replication. Individual TGEV protein screening results demonstrated that Nsp2 exhibited a high potential for activating NF-κB and enhancing the expression of pro-inflammatory cytokines. Functional domain analyzes indicated that the first 120 amino acid residues of Nsp2 were essential for NF-κB activation. Taken together, these data suggested that NF-κB activation was a major contributor to TGEV infection-induced inflammation, and that Nsp2 was the key viral protein involved in the regulation of inflammation, with amino acids 1–120 playing a critical role in activating NF-κB. Abbreviations: TCID50: 50% tissue culture infectious dose; DMEM: Dulbecco’s Modified Eagle Medium; eNOS: Endothelial nitric oxide synthase; FBS: fetal bovine serum; IFA: Indirect immunofluorescence; IκB: inhibitor of nuclear factor kappa-B; IL: interleukin; IPEC-J2: intestinal epithelial cell lines J2; IKK: IκB kinase; Luc: luciferase reporter gene; mAbs: monoclonal antibodies; MOI: multiple of infection; Nsp: nonstructural protein; NF-κB: nuclear factor-kappa ; ORFs: open reading frames; PBS: phosphate-buffered saline; p65 p-p65: phosphorylated; RT-PCR: reverse transcription PC; SeV: Sendai virus; ST: swine testicular; TGEV: Transmissible gastroenteritis virus; TNF-α: tumor necrosis factor α; UV-TGEV: Ultraviolet light-inactivated TGEV; ZnF: zinc finger Taylor & Francis 2018-10-29 /pmc/articles/PMC7000202/ /pubmed/30322331 http://dx.doi.org/10.1080/21505594.2018.1536632 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Wang, Li
Qiao, Xinyuan
Zhang, Sijia
Qin, Yue
Guo, Tiantian
Hao, Zhenye
Sun, Li
Wang, Xiaona
Wang, Yanan
Jiang, Yanping
Tang, Lijie
Xu, Yigang
Li, Yijing
Porcine transmissible gastroenteritis virus nonstructural protein 2 contributes to inflammation via NF-κB activation
title Porcine transmissible gastroenteritis virus nonstructural protein 2 contributes to inflammation via NF-κB activation
title_full Porcine transmissible gastroenteritis virus nonstructural protein 2 contributes to inflammation via NF-κB activation
title_fullStr Porcine transmissible gastroenteritis virus nonstructural protein 2 contributes to inflammation via NF-κB activation
title_full_unstemmed Porcine transmissible gastroenteritis virus nonstructural protein 2 contributes to inflammation via NF-κB activation
title_short Porcine transmissible gastroenteritis virus nonstructural protein 2 contributes to inflammation via NF-κB activation
title_sort porcine transmissible gastroenteritis virus nonstructural protein 2 contributes to inflammation via nf-κb activation
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000202/
https://www.ncbi.nlm.nih.gov/pubmed/30322331
http://dx.doi.org/10.1080/21505594.2018.1536632
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