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Nucleotide-binding oligomerization domain-like receptor X1 restricts porcine reproductive and respiratory syndrome virus-2 replication by interacting with viral Nsp9

Porcine reproductive and respiratory syndrome virus (PRRSV) causes one of the most economically important diseases of swine worldwide. Current antiviral strategies provide only limited protection. Nucleotide-binding oligomerization domain-like receptor (NLR) X1 is unique among NLR proteins in its fu...

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Autores principales: Jing, Huiyuan, Song, Tao, Cao, Sufang, Sun, Yanting, Wang, Jinhe, Dong, Wang, Zhang, Yan, Ding, Zhen, Wang, Ting, Xing, Zhao, Bao, Wenqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114581/
https://www.ncbi.nlm.nih.gov/pubmed/31132368
http://dx.doi.org/10.1016/j.virusres.2019.05.011
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author Jing, Huiyuan
Song, Tao
Cao, Sufang
Sun, Yanting
Wang, Jinhe
Dong, Wang
Zhang, Yan
Ding, Zhen
Wang, Ting
Xing, Zhao
Bao, Wenqi
author_facet Jing, Huiyuan
Song, Tao
Cao, Sufang
Sun, Yanting
Wang, Jinhe
Dong, Wang
Zhang, Yan
Ding, Zhen
Wang, Ting
Xing, Zhao
Bao, Wenqi
author_sort Jing, Huiyuan
collection PubMed
description Porcine reproductive and respiratory syndrome virus (PRRSV) causes one of the most economically important diseases of swine worldwide. Current antiviral strategies provide only limited protection. Nucleotide-binding oligomerization domain-like receptor (NLR) X1 is unique among NLR proteins in its functions as a pro-viral or antiviral factor to different viral infections. To date, the impact of NLRX1 on PRRSV infection remains unclear. In this study, we found that PRRSV infection promoted the expression of NLRX1 gene. In turn, ectopic expression of NLRX1 inhibited PRRSV replication in Marc-145 cells, whereas knockdown of NLRX1 enhanced PRRSV propagation in porcine alveolar macrophages (PAMs). Mechanistically, NLRX1 was revealed to impair intracellular viral subgenomic RNAs accumulation. Finally, Mutagenic analyses indicated that the LRR (leucine-rich repeats) domain of NLRX1 interacted with PRRSV Nonstructural Protein 9 (Nsp9) RdRp (RNA-dependent RNA Polymerase) domain and was necessary for antiviral activity. Thus, our study establishes the role of NLRX1 as a new host restriction factor in PRRSV infection.
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spelling pubmed-71145812020-04-02 Nucleotide-binding oligomerization domain-like receptor X1 restricts porcine reproductive and respiratory syndrome virus-2 replication by interacting with viral Nsp9 Jing, Huiyuan Song, Tao Cao, Sufang Sun, Yanting Wang, Jinhe Dong, Wang Zhang, Yan Ding, Zhen Wang, Ting Xing, Zhao Bao, Wenqi Virus Res Article Porcine reproductive and respiratory syndrome virus (PRRSV) causes one of the most economically important diseases of swine worldwide. Current antiviral strategies provide only limited protection. Nucleotide-binding oligomerization domain-like receptor (NLR) X1 is unique among NLR proteins in its functions as a pro-viral or antiviral factor to different viral infections. To date, the impact of NLRX1 on PRRSV infection remains unclear. In this study, we found that PRRSV infection promoted the expression of NLRX1 gene. In turn, ectopic expression of NLRX1 inhibited PRRSV replication in Marc-145 cells, whereas knockdown of NLRX1 enhanced PRRSV propagation in porcine alveolar macrophages (PAMs). Mechanistically, NLRX1 was revealed to impair intracellular viral subgenomic RNAs accumulation. Finally, Mutagenic analyses indicated that the LRR (leucine-rich repeats) domain of NLRX1 interacted with PRRSV Nonstructural Protein 9 (Nsp9) RdRp (RNA-dependent RNA Polymerase) domain and was necessary for antiviral activity. Thus, our study establishes the role of NLRX1 as a new host restriction factor in PRRSV infection. Elsevier B.V. 2019-07-15 2019-05-24 /pmc/articles/PMC7114581/ /pubmed/31132368 http://dx.doi.org/10.1016/j.virusres.2019.05.011 Text en © 2019 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Jing, Huiyuan
Song, Tao
Cao, Sufang
Sun, Yanting
Wang, Jinhe
Dong, Wang
Zhang, Yan
Ding, Zhen
Wang, Ting
Xing, Zhao
Bao, Wenqi
Nucleotide-binding oligomerization domain-like receptor X1 restricts porcine reproductive and respiratory syndrome virus-2 replication by interacting with viral Nsp9
title Nucleotide-binding oligomerization domain-like receptor X1 restricts porcine reproductive and respiratory syndrome virus-2 replication by interacting with viral Nsp9
title_full Nucleotide-binding oligomerization domain-like receptor X1 restricts porcine reproductive and respiratory syndrome virus-2 replication by interacting with viral Nsp9
title_fullStr Nucleotide-binding oligomerization domain-like receptor X1 restricts porcine reproductive and respiratory syndrome virus-2 replication by interacting with viral Nsp9
title_full_unstemmed Nucleotide-binding oligomerization domain-like receptor X1 restricts porcine reproductive and respiratory syndrome virus-2 replication by interacting with viral Nsp9
title_short Nucleotide-binding oligomerization domain-like receptor X1 restricts porcine reproductive and respiratory syndrome virus-2 replication by interacting with viral Nsp9
title_sort nucleotide-binding oligomerization domain-like receptor x1 restricts porcine reproductive and respiratory syndrome virus-2 replication by interacting with viral nsp9
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114581/
https://www.ncbi.nlm.nih.gov/pubmed/31132368
http://dx.doi.org/10.1016/j.virusres.2019.05.011
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