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      https://www.ias.ac.in/article/fulltext/jbsc/034/01/0045-0058

    • Keywords

       

      Cattle; foot-and-mouth disease virus; full-length infectious cDNA clone; guinea pigs; in vitro transcribed RNA; transfection; vaccine

    • Abstract

       

      Foot-and-mouth disease virus (FMDV) serotype O is the most predominant among the endemic serotypes in India. A stable, full-length cDNA clone of FMDV type O1BFS 1860 preceded by a bacteriophage T7 polymerase promoter was assembled in a plasmid vector pGEMR-7Zf(–). An ∼8.2 kb PCR product was amplified from the cDNA clone and a full-length RNA was generated from it by in vitro transcription. Transfection of BHK-21 cells with the in vitro transcripts resulted in the production of infectious recombinant FMDV particles as evidenced by cytopathic effects (CPE). Further, characterization of the recombinant virus by immunofluorescence, microneutralization test (MNT), antigen ELISA, RT-PCR, plaque assay and electron microscopy revealed similarity to the parental strain. The immunogenicity of an oil-adjuvant vaccine prepared using the inactivated recombinant virus was tested in guinea pigs and cattle. Neutralizing antibodies were produced in both vaccinated guinea pigs and cattle. Vaccinated animals were protected on challenge. The results demonstrated that the recombinant virus was as stable and effective as the parental strain for the preparation of inactivated vaccine, suggesting the potential application of this strategy to make genetically engineered FMDV vaccines.

    • Author Affiliations

       

      M Hema1 2 D Chandran1 S B Nagendrakumar1 M Madhanmohan1 V A Srinivasan1

      1. Indian Immunologicals Limited, Rakshapuram, Gachibowli, Hyderabad 500 032, India
      2. Department of Biotechnology, Sri Padmavathi Mahila Viswavidyalayam (Women's University), Tirupati 517 502, India
    • Dates

       
  • Journal of Biosciences | News

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