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Paraoxonase-1 Facilitates PRRSV Replication by Interacting with Viral Nonstructural Protein-9 and Inhibiting Type I Interferon Pathway
Paraoxonase-1 (PON1), an esterase with specifically paraoxonase activity, has been proven to be involved in inflammation and infection. Porcine reproductive and respiratory syndrome virus (PRRSV) is still a major concern in pigs and causes severe economic losses to the swine industry worldwide. In t...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9230610/ https://www.ncbi.nlm.nih.gov/pubmed/35746674 http://dx.doi.org/10.3390/v14061203 |
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author | Zhang, Lin Pan, Yu Xu, Yunfei Zhang, Wenli Ma, Wenjie Ibrahim, Yassein M. Werid, Gebremeskel Mamu Zhang, He Xia, Changyou Wei, Ping Chen, Hongyan Wang, Yue |
author_facet | Zhang, Lin Pan, Yu Xu, Yunfei Zhang, Wenli Ma, Wenjie Ibrahim, Yassein M. Werid, Gebremeskel Mamu Zhang, He Xia, Changyou Wei, Ping Chen, Hongyan Wang, Yue |
author_sort | Zhang, Lin |
collection | PubMed |
description | Paraoxonase-1 (PON1), an esterase with specifically paraoxonase activity, has been proven to be involved in inflammation and infection. Porcine reproductive and respiratory syndrome virus (PRRSV) is still a major concern in pigs and causes severe economic losses to the swine industry worldwide. In this study, the role of PON1 was investigated in porcine alveolar macrophages (PAMs) during PRRSV infection. The results showed that PRRSV replication downregulated PON1, and the knockdown of PON1 significantly decreased PRRSV replication. Similarly, PON1 overexpression could enhance PRRSV replication. Interestingly, we observed that PON1 interacted with PRRSV nonstructural protein 9 (Nsp9), the RNA-dependent RNA polymerase, and the knockdown of PON1 lowered the RNA binding ability of Nsp9, suggesting that PON1 can facilitate Nsp9 function in viral replication. In addition, the knockdown of PON1 expression led to the amplification of type I interferon (IFN) genes and vice versa. In summary, our data demonstrate that PON1 facilitates PRRSV replication by interacting with Nsp9 and inhibiting the type I IFN signaling pathway. Hence, PON1 may be an additional component of the anti-PRRSV defenses. |
format | Online Article Text |
id | pubmed-9230610 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-92306102022-06-25 Paraoxonase-1 Facilitates PRRSV Replication by Interacting with Viral Nonstructural Protein-9 and Inhibiting Type I Interferon Pathway Zhang, Lin Pan, Yu Xu, Yunfei Zhang, Wenli Ma, Wenjie Ibrahim, Yassein M. Werid, Gebremeskel Mamu Zhang, He Xia, Changyou Wei, Ping Chen, Hongyan Wang, Yue Viruses Article Paraoxonase-1 (PON1), an esterase with specifically paraoxonase activity, has been proven to be involved in inflammation and infection. Porcine reproductive and respiratory syndrome virus (PRRSV) is still a major concern in pigs and causes severe economic losses to the swine industry worldwide. In this study, the role of PON1 was investigated in porcine alveolar macrophages (PAMs) during PRRSV infection. The results showed that PRRSV replication downregulated PON1, and the knockdown of PON1 significantly decreased PRRSV replication. Similarly, PON1 overexpression could enhance PRRSV replication. Interestingly, we observed that PON1 interacted with PRRSV nonstructural protein 9 (Nsp9), the RNA-dependent RNA polymerase, and the knockdown of PON1 lowered the RNA binding ability of Nsp9, suggesting that PON1 can facilitate Nsp9 function in viral replication. In addition, the knockdown of PON1 expression led to the amplification of type I interferon (IFN) genes and vice versa. In summary, our data demonstrate that PON1 facilitates PRRSV replication by interacting with Nsp9 and inhibiting the type I IFN signaling pathway. Hence, PON1 may be an additional component of the anti-PRRSV defenses. MDPI 2022-05-31 /pmc/articles/PMC9230610/ /pubmed/35746674 http://dx.doi.org/10.3390/v14061203 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhang, Lin Pan, Yu Xu, Yunfei Zhang, Wenli Ma, Wenjie Ibrahim, Yassein M. Werid, Gebremeskel Mamu Zhang, He Xia, Changyou Wei, Ping Chen, Hongyan Wang, Yue Paraoxonase-1 Facilitates PRRSV Replication by Interacting with Viral Nonstructural Protein-9 and Inhibiting Type I Interferon Pathway |
title | Paraoxonase-1 Facilitates PRRSV Replication by Interacting with Viral Nonstructural Protein-9 and Inhibiting Type I Interferon Pathway |
title_full | Paraoxonase-1 Facilitates PRRSV Replication by Interacting with Viral Nonstructural Protein-9 and Inhibiting Type I Interferon Pathway |
title_fullStr | Paraoxonase-1 Facilitates PRRSV Replication by Interacting with Viral Nonstructural Protein-9 and Inhibiting Type I Interferon Pathway |
title_full_unstemmed | Paraoxonase-1 Facilitates PRRSV Replication by Interacting with Viral Nonstructural Protein-9 and Inhibiting Type I Interferon Pathway |
title_short | Paraoxonase-1 Facilitates PRRSV Replication by Interacting with Viral Nonstructural Protein-9 and Inhibiting Type I Interferon Pathway |
title_sort | paraoxonase-1 facilitates prrsv replication by interacting with viral nonstructural protein-9 and inhibiting type i interferon pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9230610/ https://www.ncbi.nlm.nih.gov/pubmed/35746674 http://dx.doi.org/10.3390/v14061203 |
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