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A Mechanism Underlying Attenuation of Recombinant Influenza A Viruses Carrying Reporter Genes
Influenza A viruses (IAV) carrying reporter genes provide a powerful tool to study viral infection and pathogenesis in vivo, however, incorporating a non-essential gene into the IAV genome often results in virus attenuation and genetic instability. Very few studies have systematically compared diffe...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316390/ https://www.ncbi.nlm.nih.gov/pubmed/30513620 http://dx.doi.org/10.3390/v10120679 |
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author | Zhao, Xiujuan Wang, Lin Cui, Qinghua Li, Ping Wang, Yanyan Zhang, Yingying Yang, Yong Rong, Lijun Du, Ruikun |
author_facet | Zhao, Xiujuan Wang, Lin Cui, Qinghua Li, Ping Wang, Yanyan Zhang, Yingying Yang, Yong Rong, Lijun Du, Ruikun |
author_sort | Zhao, Xiujuan |
collection | PubMed |
description | Influenza A viruses (IAV) carrying reporter genes provide a powerful tool to study viral infection and pathogenesis in vivo, however, incorporating a non-essential gene into the IAV genome often results in virus attenuation and genetic instability. Very few studies have systematically compared different reporter IAVs, and most optimization attempts seem to lack authentic directions. In this study, we evaluated the ratio of genome copies to the number of infectious unit of two reporter IAVs, PR8-NS1-Gluc and PR8-PB2-Gluc. As a result, PR8-NS1-Gluc and PR8-PB2-Gluc produced 41.4 and 3.8 genomes containing noninfectious particles respectively for every such particle produced by parental PR8 virus. RdRp assay demonstrated that modification of segment NS by inserting reporter genes can interfere with the replication competitive property of the corresponding vRNAs, and the balance of the 8 segments of the reporter IAVs were drastically impaired in infected cells. As a consequence, large amounts of NS-null noninfectious particles were produced during the PR8-NS1-Gluc packaging. In summary, we unravel a mechanism underlying attenuation of reporter IAVs, which suggests a new approach to restore infectivity and virulence by introducing extra mutations compensating for the impaired replication property of corresponding segments. |
format | Online Article Text |
id | pubmed-6316390 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63163902019-01-10 A Mechanism Underlying Attenuation of Recombinant Influenza A Viruses Carrying Reporter Genes Zhao, Xiujuan Wang, Lin Cui, Qinghua Li, Ping Wang, Yanyan Zhang, Yingying Yang, Yong Rong, Lijun Du, Ruikun Viruses Article Influenza A viruses (IAV) carrying reporter genes provide a powerful tool to study viral infection and pathogenesis in vivo, however, incorporating a non-essential gene into the IAV genome often results in virus attenuation and genetic instability. Very few studies have systematically compared different reporter IAVs, and most optimization attempts seem to lack authentic directions. In this study, we evaluated the ratio of genome copies to the number of infectious unit of two reporter IAVs, PR8-NS1-Gluc and PR8-PB2-Gluc. As a result, PR8-NS1-Gluc and PR8-PB2-Gluc produced 41.4 and 3.8 genomes containing noninfectious particles respectively for every such particle produced by parental PR8 virus. RdRp assay demonstrated that modification of segment NS by inserting reporter genes can interfere with the replication competitive property of the corresponding vRNAs, and the balance of the 8 segments of the reporter IAVs were drastically impaired in infected cells. As a consequence, large amounts of NS-null noninfectious particles were produced during the PR8-NS1-Gluc packaging. In summary, we unravel a mechanism underlying attenuation of reporter IAVs, which suggests a new approach to restore infectivity and virulence by introducing extra mutations compensating for the impaired replication property of corresponding segments. MDPI 2018-11-30 /pmc/articles/PMC6316390/ /pubmed/30513620 http://dx.doi.org/10.3390/v10120679 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhao, Xiujuan Wang, Lin Cui, Qinghua Li, Ping Wang, Yanyan Zhang, Yingying Yang, Yong Rong, Lijun Du, Ruikun A Mechanism Underlying Attenuation of Recombinant Influenza A Viruses Carrying Reporter Genes |
title | A Mechanism Underlying Attenuation of Recombinant Influenza A Viruses Carrying Reporter Genes |
title_full | A Mechanism Underlying Attenuation of Recombinant Influenza A Viruses Carrying Reporter Genes |
title_fullStr | A Mechanism Underlying Attenuation of Recombinant Influenza A Viruses Carrying Reporter Genes |
title_full_unstemmed | A Mechanism Underlying Attenuation of Recombinant Influenza A Viruses Carrying Reporter Genes |
title_short | A Mechanism Underlying Attenuation of Recombinant Influenza A Viruses Carrying Reporter Genes |
title_sort | mechanism underlying attenuation of recombinant influenza a viruses carrying reporter genes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316390/ https://www.ncbi.nlm.nih.gov/pubmed/30513620 http://dx.doi.org/10.3390/v10120679 |
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