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Generation and characterization of a recombinant Newcastle disease virus expressing the red fluorescent protein for use in co-infection studies

BACKGROUND: Many viruses have evolved multiple strategies to prevent super infection of host cells by more than one virion. This phenomenon, known as super infection exclusion, may play an important role on virus evolution because it can affect the frequency of reassortment and/or recombination. New...

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Autores principales: Li, Jinnan, Hu, Haixia, Yu, Qingzhong, Diel, Diego G, Li, De-shan, Miller, Patti J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502164/
https://www.ncbi.nlm.nih.gov/pubmed/23034005
http://dx.doi.org/10.1186/1743-422X-9-227
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author Li, Jinnan
Hu, Haixia
Yu, Qingzhong
Diel, Diego G
Li, De-shan
Miller, Patti J
author_facet Li, Jinnan
Hu, Haixia
Yu, Qingzhong
Diel, Diego G
Li, De-shan
Miller, Patti J
author_sort Li, Jinnan
collection PubMed
description BACKGROUND: Many viruses have evolved multiple strategies to prevent super infection of host cells by more than one virion. This phenomenon, known as super infection exclusion, may play an important role on virus evolution because it can affect the frequency of reassortment and/or recombination. Newcastle disease virus (NDV), a negative sense single-stranded RNA virus, is characterized by its continuous evolutionary dynamics and by a low frequency of recombination events. However, the mechanisms that contribute to the low recombination rates on NDV are still not completely understood. METHODS: In this study we assessed the ability of two NDV strains (LaSota and B1) to super infect host cells in vitro. We generated a recombinant NDV strain LaSota expressing the red fluorescent protein (RFP) and used it in co-infection assays with a related NDV strain B1 expressing the green fluorescent protein (GFP). DF-1 cells were inoculated with both viruses at the same time or at different intervals between primary infection and super infection. RESULTS: When both viruses were inoculated at the same time point, a 27% co-infection rate was observed, whereas when they were inoculated at different time points the super infection rates decreased to levels as low as 1.4%. CONCLUSIONS: These results indicate that although different NDV strains can co-infect host cells in vitro, the super infection rates are low, specially as the time between the primary infection and super infection increases. These results confirm the occurrence of super infection exclusion between different strains of NDV.
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spelling pubmed-35021642012-11-21 Generation and characterization of a recombinant Newcastle disease virus expressing the red fluorescent protein for use in co-infection studies Li, Jinnan Hu, Haixia Yu, Qingzhong Diel, Diego G Li, De-shan Miller, Patti J Virol J Research BACKGROUND: Many viruses have evolved multiple strategies to prevent super infection of host cells by more than one virion. This phenomenon, known as super infection exclusion, may play an important role on virus evolution because it can affect the frequency of reassortment and/or recombination. Newcastle disease virus (NDV), a negative sense single-stranded RNA virus, is characterized by its continuous evolutionary dynamics and by a low frequency of recombination events. However, the mechanisms that contribute to the low recombination rates on NDV are still not completely understood. METHODS: In this study we assessed the ability of two NDV strains (LaSota and B1) to super infect host cells in vitro. We generated a recombinant NDV strain LaSota expressing the red fluorescent protein (RFP) and used it in co-infection assays with a related NDV strain B1 expressing the green fluorescent protein (GFP). DF-1 cells were inoculated with both viruses at the same time or at different intervals between primary infection and super infection. RESULTS: When both viruses were inoculated at the same time point, a 27% co-infection rate was observed, whereas when they were inoculated at different time points the super infection rates decreased to levels as low as 1.4%. CONCLUSIONS: These results indicate that although different NDV strains can co-infect host cells in vitro, the super infection rates are low, specially as the time between the primary infection and super infection increases. These results confirm the occurrence of super infection exclusion between different strains of NDV. BioMed Central 2012-10-03 /pmc/articles/PMC3502164/ /pubmed/23034005 http://dx.doi.org/10.1186/1743-422X-9-227 Text en Copyright ©2012 Li 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 Research
Li, Jinnan
Hu, Haixia
Yu, Qingzhong
Diel, Diego G
Li, De-shan
Miller, Patti J
Generation and characterization of a recombinant Newcastle disease virus expressing the red fluorescent protein for use in co-infection studies
title Generation and characterization of a recombinant Newcastle disease virus expressing the red fluorescent protein for use in co-infection studies
title_full Generation and characterization of a recombinant Newcastle disease virus expressing the red fluorescent protein for use in co-infection studies
title_fullStr Generation and characterization of a recombinant Newcastle disease virus expressing the red fluorescent protein for use in co-infection studies
title_full_unstemmed Generation and characterization of a recombinant Newcastle disease virus expressing the red fluorescent protein for use in co-infection studies
title_short Generation and characterization of a recombinant Newcastle disease virus expressing the red fluorescent protein for use in co-infection studies
title_sort generation and characterization of a recombinant newcastle disease virus expressing the red fluorescent protein for use in co-infection studies
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502164/
https://www.ncbi.nlm.nih.gov/pubmed/23034005
http://dx.doi.org/10.1186/1743-422X-9-227
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