Expression of Hemagglutinin-Neuraminidase and fusion epitopes of Newcastle Disease Virus in transgenic tobacco

Background: Newcastle disease is an important avian infectious disease that brings about vast economic damage for poultry industry. Transgenic plants represent a cost-effective system for the production of therapeutic proteins and are widely used for the production of poultry vaccines. In an attempt...

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Autores principales: Ghaffar Shahriari,Amir, Bagheri,Abdolreza, Bassami,Mohammad Reza, Malekzadeh-Shafaroudi,Saeid, Afsharifar,Alireza, Niazi,Ali
Lenguaje:English
Publicado: Pontificia Universidad Católica de Valparaíso 2016
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-34582016000400006
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spelling oai:scielo:S0717-345820160004000062016-09-13Expression of Hemagglutinin-Neuraminidase and fusion epitopes of Newcastle Disease Virus in transgenic tobaccoGhaffar Shahriari,AmirBagheri,AbdolrezaBassami,Mohammad RezaMalekzadeh-Shafaroudi,SaeidAfsharifar,AlirezaNiazi,Ali Agrobacterium tumefaciens ELISA Recombinant vaccine Transgenic plants Background: Newcastle disease is an important avian infectious disease that brings about vast economic damage for poultry industry. Transgenic plants represent a cost-effective system for the production of therapeutic proteins and are widely used for the production of poultry vaccines. In an attempt to develop a recombinant vaccine, a plant expression binary vector pBI121, containing the genes encoding Hemagglutinin-Neuraminidase (HN) and Fusion (F) epitopes of Newcastle Disease Virus (NDV) under the control of CaMV35S promoter and NOS terminator was constructed and introduced into the tobacco ( Nicotiana tabacum) plant by Agrobacterium-mediated transformation. Results: Putative transgenic plants were screened in a selection medium containing 50 mg/L kanamycin and 30 mg/L meropenem. Integration of the foreign gene in plant genome was confirmed by PCR. Expression of foreign gene was analyzed at transcription level by RT-PCR and at translation level by means of dot blotting and ELISA. All analyses confirmed the expression of recombinant protein. Conclusion: Developments in genetic engineering have led to plant-based systems for recombinant vaccine production. In this research, tobacco plant was used to express F and HN epitopes of NDV. Our results indicate that for the production of recombinant vaccine, it is a novel strategy to use concatenated epitopes without their genetic fusion onto larger scaffold structure such as viral coat protein.info:eu-repo/semantics/openAccessPontificia Universidad Católica de ValparaísoElectronic Journal of Biotechnology v.19 n.4 20162016-07-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-34582016000400006en10.1016/j.ejbt.2016.05.003
institution Scielo Chile
collection Scielo Chile
language English
topic Agrobacterium tumefaciens
ELISA
Recombinant vaccine
Transgenic plants
spellingShingle Agrobacterium tumefaciens
ELISA
Recombinant vaccine
Transgenic plants
Ghaffar Shahriari,Amir
Bagheri,Abdolreza
Bassami,Mohammad Reza
Malekzadeh-Shafaroudi,Saeid
Afsharifar,Alireza
Niazi,Ali
Expression of Hemagglutinin-Neuraminidase and fusion epitopes of Newcastle Disease Virus in transgenic tobacco
description Background: Newcastle disease is an important avian infectious disease that brings about vast economic damage for poultry industry. Transgenic plants represent a cost-effective system for the production of therapeutic proteins and are widely used for the production of poultry vaccines. In an attempt to develop a recombinant vaccine, a plant expression binary vector pBI121, containing the genes encoding Hemagglutinin-Neuraminidase (HN) and Fusion (F) epitopes of Newcastle Disease Virus (NDV) under the control of CaMV35S promoter and NOS terminator was constructed and introduced into the tobacco ( Nicotiana tabacum) plant by Agrobacterium-mediated transformation. Results: Putative transgenic plants were screened in a selection medium containing 50 mg/L kanamycin and 30 mg/L meropenem. Integration of the foreign gene in plant genome was confirmed by PCR. Expression of foreign gene was analyzed at transcription level by RT-PCR and at translation level by means of dot blotting and ELISA. All analyses confirmed the expression of recombinant protein. Conclusion: Developments in genetic engineering have led to plant-based systems for recombinant vaccine production. In this research, tobacco plant was used to express F and HN epitopes of NDV. Our results indicate that for the production of recombinant vaccine, it is a novel strategy to use concatenated epitopes without their genetic fusion onto larger scaffold structure such as viral coat protein.
author Ghaffar Shahriari,Amir
Bagheri,Abdolreza
Bassami,Mohammad Reza
Malekzadeh-Shafaroudi,Saeid
Afsharifar,Alireza
Niazi,Ali
author_facet Ghaffar Shahriari,Amir
Bagheri,Abdolreza
Bassami,Mohammad Reza
Malekzadeh-Shafaroudi,Saeid
Afsharifar,Alireza
Niazi,Ali
author_sort Ghaffar Shahriari,Amir
title Expression of Hemagglutinin-Neuraminidase and fusion epitopes of Newcastle Disease Virus in transgenic tobacco
title_short Expression of Hemagglutinin-Neuraminidase and fusion epitopes of Newcastle Disease Virus in transgenic tobacco
title_full Expression of Hemagglutinin-Neuraminidase and fusion epitopes of Newcastle Disease Virus in transgenic tobacco
title_fullStr Expression of Hemagglutinin-Neuraminidase and fusion epitopes of Newcastle Disease Virus in transgenic tobacco
title_full_unstemmed Expression of Hemagglutinin-Neuraminidase and fusion epitopes of Newcastle Disease Virus in transgenic tobacco
title_sort expression of hemagglutinin-neuraminidase and fusion epitopes of newcastle disease virus in transgenic tobacco
publisher Pontificia Universidad Católica de Valparaíso
publishDate 2016
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-34582016000400006
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