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Expression of Hemagglutinin-Neuraminidase and fusion epitopes of Newcastle Disease Virus in transgenic tobacco
Ghaffar Shahriari, Amir; Bagheri, Abdolreza; Bassami, Mohammad Reza; Malekzadeh-Shafaroudi, Saeid; Afsharifar, Alireza; Niazi, Ali.
Affiliation
  • Ghaffar Shahriari, Amir; Ferdowsi University of Mashhad. Department of Crop Biotechnology and Breeding. Mashhad. IR
  • Bagheri, Abdolreza; Ferdowsi University of Mashhad. Department of Crop Biotechnology and Breeding. Mashhad. IR
  • Bassami, Mohammad Reza; Ferdowsi University of Mashhad. Department of Crop Biotechnology and Breeding. Mashhad. IR
  • Malekzadeh-Shafaroudi, Saeid; Ferdowsi University of Mashhad. Department of Crop Biotechnology and Breeding. Mashhad. IR
  • Afsharifar, Alireza; Ferdowsi University of Mashhad. Department of Crop Biotechnology and Breeding. Mashhad. IR
  • Niazi, Ali; Ferdowsi University of Mashhad. Department of Crop Biotechnology and Breeding. Mashhad. IR
Electron. j. biotechnol ; Electron. j. biotechnol;19(4): 38-43, July 2016. ilus
Article in En | LILACS | ID: lil-793951
Responsible library: CL1.1
ABSTRACT

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.
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Full text: 1 Index: LILACS Main subject: Newcastle disease virus / Vaccines, Synthetic / HN Protein / Plants, Genetically Modified Language: En Journal: EJB / Electron. j. biotechnol / Electronic journal of biotechnology Journal subject: BIOTECNOLOGIA Year: 2016 Type: Article

Full text: 1 Index: LILACS Main subject: Newcastle disease virus / Vaccines, Synthetic / HN Protein / Plants, Genetically Modified Language: En Journal: EJB / Electron. j. biotechnol / Electronic journal of biotechnology Journal subject: BIOTECNOLOGIA Year: 2016 Type: Article