Expression of chimeric HCV peptide in transgenic tobacco plants infected with recombinant alfalfa mosaic virus for development of a plant-derived vaccine against HCV

  • AK El Attar Plant Pathology Research Institute, Agriculture Research Center, Giza, Egypt and National Institutes of Health, Vaccine and Therapeutic Section, Oral Infection and Immunity Branch, NIDCR, Bethesda, MD, USA.
  • AM Shamloul Vaccine and Therapeutic Development Section, Fraunhofer Center for Molecular Biotechnology, Newark, DE, USA.
  • AA Shalaby Plant Pathology Research Institute, Agriculture Research Center, Giza, Egypt
  • BY Riad Faculty of Science, Cairo University, Giza, Egypt.
  • A Saad Faculty of Science, Cairo University, Giza, Egypt.
  • HM Mazyad Plant Pathology Research Institute, Agriculture Research Center, Giza, Egypt
  • JM Keith Plant Pathology Research Institute, Agriculture Research Center, Giza, Egypt
Keywords: Hepatitis C virus (HCV), transgenic tobacco plants (P12), consensus HCV HVR1 epitope (R9), and chimeric ALMV-RNA4

Abstract

Hepatitis C virus (HCV) is the major etiologic agent of blood transfusion–associated and sporadic non-A non-B hepatitis affecting more than 180 million worldwide. Vaccine development for HCV has been difficult and there is no vaccine or effective therapy against this virus. In this paper, we describe the development of an experimental plant-derived subunit vaccine against HCV. Our subunit vaccine originates from a consensus HCV-HVR1 epitope (R9) that antigenically mimics many natural HVR1 variants. This HVR1 sequence was cloned into the open reading frame of a plant virus, Alfalfa Mosaic Virus (ALMV) coat protein (CP). The chimeric ALMV RNA4 containing sequence-encoding R9 epitope was introduced into full-length infectious ALMV-RNA3 that was utilized as an expression vector. The recombinant chimeric protein is expressed in transgenic tobacco plants (P12) expressing ALMV RNA1 and 2. Plant–derived HVR1/ALMV-CP reacted with HVR1 and/or ALMV-CP specific monoclonal antibodies and immune sera from individuals infected with HCV. Using plant-virus based transient expression to produce this unique chimeric antigen will facilitate the development and production of an experimental HCV vaccine. A plant derived recombinant HCV vaccine can potentially reduce expenses normally associated with production and delivery of conventional vaccine.
Key Words: Hepatitis C virus (HCV), transgenic tobacco plants (P12), consensus HCV HVR1 epitope (R9), and chimeric ALMV-RNA4.
African Journal of Biotechnology Vol.3(11) 2004: 588-594
Published
2005-03-23
Section
Articles

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eISSN: 1684-5315