Cargando…

Proteomic Investigation Reveals Eukaryotic Translation Initiation Factor 5A Involvement in Porcine Reproductive and Respiratory Syndrome Virus Infection in vitro

Porcine reproductive and respiratory syndrome virus (PRRSV), one of the most serious animal pathogens in the world, has caused enormous global swine industry losses. An in-depth investigation of the PRRSV-host interaction would be beneficial for preventing and controlling PRRSV infections and transm...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Huawei, Wan, Bo, Jiang, Dawei, Ji, Pengchao, Zhao, Mengmeng, Li, Xinfeng, Li, Rui, Qiao, Songlin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043857/
https://www.ncbi.nlm.nih.gov/pubmed/35498732
http://dx.doi.org/10.3389/fvets.2022.861137
_version_ 1784694976841515008
author Li, Huawei
Wan, Bo
Jiang, Dawei
Ji, Pengchao
Zhao, Mengmeng
Li, Xinfeng
Li, Rui
Qiao, Songlin
author_facet Li, Huawei
Wan, Bo
Jiang, Dawei
Ji, Pengchao
Zhao, Mengmeng
Li, Xinfeng
Li, Rui
Qiao, Songlin
author_sort Li, Huawei
collection PubMed
description Porcine reproductive and respiratory syndrome virus (PRRSV), one of the most serious animal pathogens in the world, has caused enormous global swine industry losses. An in-depth investigation of the PRRSV-host interaction would be beneficial for preventing and controlling PRRSV infections and transmission. In this study, we performed label-free quantitative proteomic assays to investigate proteome dynamics of porcine alveolar macrophages (PAMs) during infection with highly pathogenic PRRSV (HP-PRRSV) strain HN07-1. Analysis of the results led to identification of 269 significantly differentially expressed host cellular proteins, of which levels of proteins belonging to the eukaryotic translation initiation factor (eIF) family were found to be decreased in abundance in HP-PRRSV-infected PAMs. Furthermore, knockdown of eIF5A expression was demonstrated to markedly suppress HP-PRRSV propagation, as reflected by reduced progeny virus titers in vitro. These results highlight the importance of eIF5A in PRRSV infection, while also demonstrating that PAMs down-regulate eIF5A expression as a host cell antiviral strategy. Results of the current study deepen our understanding of PRRSV pathogenesis and provide novel insights to guide development of effective strategies to combat the virus.
format Online
Article
Text
id pubmed-9043857
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-90438572022-04-28 Proteomic Investigation Reveals Eukaryotic Translation Initiation Factor 5A Involvement in Porcine Reproductive and Respiratory Syndrome Virus Infection in vitro Li, Huawei Wan, Bo Jiang, Dawei Ji, Pengchao Zhao, Mengmeng Li, Xinfeng Li, Rui Qiao, Songlin Front Vet Sci Veterinary Science Porcine reproductive and respiratory syndrome virus (PRRSV), one of the most serious animal pathogens in the world, has caused enormous global swine industry losses. An in-depth investigation of the PRRSV-host interaction would be beneficial for preventing and controlling PRRSV infections and transmission. In this study, we performed label-free quantitative proteomic assays to investigate proteome dynamics of porcine alveolar macrophages (PAMs) during infection with highly pathogenic PRRSV (HP-PRRSV) strain HN07-1. Analysis of the results led to identification of 269 significantly differentially expressed host cellular proteins, of which levels of proteins belonging to the eukaryotic translation initiation factor (eIF) family were found to be decreased in abundance in HP-PRRSV-infected PAMs. Furthermore, knockdown of eIF5A expression was demonstrated to markedly suppress HP-PRRSV propagation, as reflected by reduced progeny virus titers in vitro. These results highlight the importance of eIF5A in PRRSV infection, while also demonstrating that PAMs down-regulate eIF5A expression as a host cell antiviral strategy. Results of the current study deepen our understanding of PRRSV pathogenesis and provide novel insights to guide development of effective strategies to combat the virus. Frontiers Media S.A. 2022-04-13 /pmc/articles/PMC9043857/ /pubmed/35498732 http://dx.doi.org/10.3389/fvets.2022.861137 Text en Copyright © 2022 Li, Wan, Jiang, Ji, Zhao, Li, Li and Qiao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Veterinary Science
Li, Huawei
Wan, Bo
Jiang, Dawei
Ji, Pengchao
Zhao, Mengmeng
Li, Xinfeng
Li, Rui
Qiao, Songlin
Proteomic Investigation Reveals Eukaryotic Translation Initiation Factor 5A Involvement in Porcine Reproductive and Respiratory Syndrome Virus Infection in vitro
title Proteomic Investigation Reveals Eukaryotic Translation Initiation Factor 5A Involvement in Porcine Reproductive and Respiratory Syndrome Virus Infection in vitro
title_full Proteomic Investigation Reveals Eukaryotic Translation Initiation Factor 5A Involvement in Porcine Reproductive and Respiratory Syndrome Virus Infection in vitro
title_fullStr Proteomic Investigation Reveals Eukaryotic Translation Initiation Factor 5A Involvement in Porcine Reproductive and Respiratory Syndrome Virus Infection in vitro
title_full_unstemmed Proteomic Investigation Reveals Eukaryotic Translation Initiation Factor 5A Involvement in Porcine Reproductive and Respiratory Syndrome Virus Infection in vitro
title_short Proteomic Investigation Reveals Eukaryotic Translation Initiation Factor 5A Involvement in Porcine Reproductive and Respiratory Syndrome Virus Infection in vitro
title_sort proteomic investigation reveals eukaryotic translation initiation factor 5a involvement in porcine reproductive and respiratory syndrome virus infection in vitro
topic Veterinary Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043857/
https://www.ncbi.nlm.nih.gov/pubmed/35498732
http://dx.doi.org/10.3389/fvets.2022.861137
work_keys_str_mv AT lihuawei proteomicinvestigationrevealseukaryotictranslationinitiationfactor5ainvolvementinporcinereproductiveandrespiratorysyndromevirusinfectioninvitro
AT wanbo proteomicinvestigationrevealseukaryotictranslationinitiationfactor5ainvolvementinporcinereproductiveandrespiratorysyndromevirusinfectioninvitro
AT jiangdawei proteomicinvestigationrevealseukaryotictranslationinitiationfactor5ainvolvementinporcinereproductiveandrespiratorysyndromevirusinfectioninvitro
AT jipengchao proteomicinvestigationrevealseukaryotictranslationinitiationfactor5ainvolvementinporcinereproductiveandrespiratorysyndromevirusinfectioninvitro
AT zhaomengmeng proteomicinvestigationrevealseukaryotictranslationinitiationfactor5ainvolvementinporcinereproductiveandrespiratorysyndromevirusinfectioninvitro
AT lixinfeng proteomicinvestigationrevealseukaryotictranslationinitiationfactor5ainvolvementinporcinereproductiveandrespiratorysyndromevirusinfectioninvitro
AT lirui proteomicinvestigationrevealseukaryotictranslationinitiationfactor5ainvolvementinporcinereproductiveandrespiratorysyndromevirusinfectioninvitro
AT qiaosonglin proteomicinvestigationrevealseukaryotictranslationinitiationfactor5ainvolvementinporcinereproductiveandrespiratorysyndromevirusinfectioninvitro