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Infectious cDNA clones of porcine reproductive and respiratory syndrome virus and their potential as vaccine vectors
Full-length infectious cDNA clones have recently become available for both European and North American genotypes of porcine reproductive and respiratory syndrome virus (PRRSV), and it is now possible to alter the PRRSV genome and create genetically defined mutant viruses. Among many possible applica...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112621/ https://www.ncbi.nlm.nih.gov/pubmed/15507301 http://dx.doi.org/10.1016/j.vetimm.2004.09.019 |
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author | Yoo, Dongwan Welch, Siao-Kun W. Lee, Changhee Calvert, Jay G. |
author_facet | Yoo, Dongwan Welch, Siao-Kun W. Lee, Changhee Calvert, Jay G. |
author_sort | Yoo, Dongwan |
collection | PubMed |
description | Full-length infectious cDNA clones have recently become available for both European and North American genotypes of porcine reproductive and respiratory syndrome virus (PRRSV), and it is now possible to alter the PRRSV genome and create genetically defined mutant viruses. Among many possible applications of the PRRSV infectious cDNA clones, development of genetically modified vaccines is of particular interest. Using infectious clones, the PRRSV genome has been manipulated by changing individual amino acids, deleting coding regions, inserting foreign sequences, and generating arterivirus chimeras. The limited available data suggest that all structural proteins of PRRSV are essential for replication of the virus, and that PRRSV infectivity is relatively intolerant of subtle changes within the structural proteins. The major tasks in PRRSV research are to identify virulence factors and pathogenic mechanisms, and to understand the structure–function relationships of individual viral proteins. Utilizing these infectious clones as tools, a new generation of safe and efficacious PRRS vaccines may be constructed. |
format | Online Article Text |
id | pubmed-7112621 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71126212020-04-02 Infectious cDNA clones of porcine reproductive and respiratory syndrome virus and their potential as vaccine vectors Yoo, Dongwan Welch, Siao-Kun W. Lee, Changhee Calvert, Jay G. Vet Immunol Immunopathol Article Full-length infectious cDNA clones have recently become available for both European and North American genotypes of porcine reproductive and respiratory syndrome virus (PRRSV), and it is now possible to alter the PRRSV genome and create genetically defined mutant viruses. Among many possible applications of the PRRSV infectious cDNA clones, development of genetically modified vaccines is of particular interest. Using infectious clones, the PRRSV genome has been manipulated by changing individual amino acids, deleting coding regions, inserting foreign sequences, and generating arterivirus chimeras. The limited available data suggest that all structural proteins of PRRSV are essential for replication of the virus, and that PRRSV infectivity is relatively intolerant of subtle changes within the structural proteins. The major tasks in PRRSV research are to identify virulence factors and pathogenic mechanisms, and to understand the structure–function relationships of individual viral proteins. Utilizing these infectious clones as tools, a new generation of safe and efficacious PRRS vaccines may be constructed. Elsevier B.V. 2004-12-08 2004-10-14 /pmc/articles/PMC7112621/ /pubmed/15507301 http://dx.doi.org/10.1016/j.vetimm.2004.09.019 Text en Copyright © 2004 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 Yoo, Dongwan Welch, Siao-Kun W. Lee, Changhee Calvert, Jay G. Infectious cDNA clones of porcine reproductive and respiratory syndrome virus and their potential as vaccine vectors |
title | Infectious cDNA clones of porcine reproductive and respiratory syndrome virus and their potential as vaccine vectors |
title_full | Infectious cDNA clones of porcine reproductive and respiratory syndrome virus and their potential as vaccine vectors |
title_fullStr | Infectious cDNA clones of porcine reproductive and respiratory syndrome virus and their potential as vaccine vectors |
title_full_unstemmed | Infectious cDNA clones of porcine reproductive and respiratory syndrome virus and their potential as vaccine vectors |
title_short | Infectious cDNA clones of porcine reproductive and respiratory syndrome virus and their potential as vaccine vectors |
title_sort | infectious cdna clones of porcine reproductive and respiratory syndrome virus and their potential as vaccine vectors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112621/ https://www.ncbi.nlm.nih.gov/pubmed/15507301 http://dx.doi.org/10.1016/j.vetimm.2004.09.019 |
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