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Use of a novel cell-based fusion reporter assay to explore the host range of human respiratory syncytial virus F protein
Human respiratory syncytial virus (HRSV) is an important respiratory pathogen primarily affecting infants, young children, transplant recipients and the elderly. The F protein is the only virion envelope protein necessary and sufficient for virus replication and fusion of the viral envelope membrane...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1190219/ https://www.ncbi.nlm.nih.gov/pubmed/16014172 http://dx.doi.org/10.1186/1743-422X-2-54 |
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author | Branigan, Patrick J Liu, Changbao Day, Nicole D Gutshall, Lester L Sarisky, Robert T Del Vecchio, Alfred M |
author_facet | Branigan, Patrick J Liu, Changbao Day, Nicole D Gutshall, Lester L Sarisky, Robert T Del Vecchio, Alfred M |
author_sort | Branigan, Patrick J |
collection | PubMed |
description | Human respiratory syncytial virus (HRSV) is an important respiratory pathogen primarily affecting infants, young children, transplant recipients and the elderly. The F protein is the only virion envelope protein necessary and sufficient for virus replication and fusion of the viral envelope membrane with the target host cell. During natural infection, HRSV replication is limited to respiratory epithelial cells with disseminated infection rarely, if ever, occurring even in immunocompromised patients. However, in vitro infection of multiple human and non-human cell types other than those of pulmonary tract origin has been reported. To better define host cell surface molecules that mediate viral entry and dissect the factors controlling permissivity for HRSV, we explored the host range of HRSV F protein mediated fusion. Using a novel recombinant reporter gene based fusion assay, HRSV F protein was shown to mediate fusion with cells derived from a wide range of vertebrate species including human, feline, equine, canine, bat, rodent, avian, porcine and even amphibian (Xenopus). That finding was extended using a recombinant HRSV engineered to express green fluorescent protein (GFP), to confirm that viral mRNA expression is limited in several cell types. These findings suggest that HRSV F protein interacts with either highly conserved host cell surface molecules or can use multiple mechanisms to enter cells, and that the primary determinants of HRSV host range are at steps post-entry. |
format | Text |
id | pubmed-1190219 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-11902192005-08-25 Use of a novel cell-based fusion reporter assay to explore the host range of human respiratory syncytial virus F protein Branigan, Patrick J Liu, Changbao Day, Nicole D Gutshall, Lester L Sarisky, Robert T Del Vecchio, Alfred M Virol J Methodology Human respiratory syncytial virus (HRSV) is an important respiratory pathogen primarily affecting infants, young children, transplant recipients and the elderly. The F protein is the only virion envelope protein necessary and sufficient for virus replication and fusion of the viral envelope membrane with the target host cell. During natural infection, HRSV replication is limited to respiratory epithelial cells with disseminated infection rarely, if ever, occurring even in immunocompromised patients. However, in vitro infection of multiple human and non-human cell types other than those of pulmonary tract origin has been reported. To better define host cell surface molecules that mediate viral entry and dissect the factors controlling permissivity for HRSV, we explored the host range of HRSV F protein mediated fusion. Using a novel recombinant reporter gene based fusion assay, HRSV F protein was shown to mediate fusion with cells derived from a wide range of vertebrate species including human, feline, equine, canine, bat, rodent, avian, porcine and even amphibian (Xenopus). That finding was extended using a recombinant HRSV engineered to express green fluorescent protein (GFP), to confirm that viral mRNA expression is limited in several cell types. These findings suggest that HRSV F protein interacts with either highly conserved host cell surface molecules or can use multiple mechanisms to enter cells, and that the primary determinants of HRSV host range are at steps post-entry. BioMed Central 2005-07-13 /pmc/articles/PMC1190219/ /pubmed/16014172 http://dx.doi.org/10.1186/1743-422X-2-54 Text en Copyright © 2005 Branigan et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Branigan, Patrick J Liu, Changbao Day, Nicole D Gutshall, Lester L Sarisky, Robert T Del Vecchio, Alfred M Use of a novel cell-based fusion reporter assay to explore the host range of human respiratory syncytial virus F protein |
title | Use of a novel cell-based fusion reporter assay to explore the host range of human respiratory syncytial virus F protein |
title_full | Use of a novel cell-based fusion reporter assay to explore the host range of human respiratory syncytial virus F protein |
title_fullStr | Use of a novel cell-based fusion reporter assay to explore the host range of human respiratory syncytial virus F protein |
title_full_unstemmed | Use of a novel cell-based fusion reporter assay to explore the host range of human respiratory syncytial virus F protein |
title_short | Use of a novel cell-based fusion reporter assay to explore the host range of human respiratory syncytial virus F protein |
title_sort | use of a novel cell-based fusion reporter assay to explore the host range of human respiratory syncytial virus f protein |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1190219/ https://www.ncbi.nlm.nih.gov/pubmed/16014172 http://dx.doi.org/10.1186/1743-422X-2-54 |
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