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EVALUATION OF IMMUNOGENICITY OF TRANSGENIC CHLOROPLAST DERIVED PROTECTIVE ANTIGEN OF BACILLUS ANTHRACIS

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  • Additional Information
    • Contributors:
      Koya, Vijay (Author); Daniell, Henry (Committee Chair); University of Central Florida (Degree Grantor)
    • Publication Information:
      University of Central Florida
    • Collection:
      UCF Digital Collections (University of Central Florida)
    • Abstract:
      Anthrax, a fatal bacterial infection is caused by Bacillus anthracis, a gram-positive, spore forming, capsulated, rod shaped organism. Centers for Disease Control (CDC) lists anthrax as Category A biological agent due to its severity of impact on human health, high mortality rate, acuteness of the disease and potential for delivery as a biological weapon. The currently available human vaccine in the United States (AVA anthrax vaccine adsorbed) is prepared from Alum adsorbed formalin treated supernatant culture of toxigenic, non-encapsulated strain of Bacillus anthracis with the principle component being protective antigen (PA83). Evaluation of anthrax vaccine given to nearly 400,000 US military personnel by Vaccine Adverse Event Reporting System (VAERS) showed adverse effects such as flu-like symptoms, local pain, large degree of inflammation, edema, malaise, rash, arthralgia, and headache following vaccination. All the adverse reactions are attributed to the composition of vaccine components. These vaccine preparations contain trace contaminants of lethal and edema factors that contribute to the adverse side effects. Also, the current method of vaccine manufacture has limited production capacity.The production of PA83, in plants through chloroplast genetic engineering might eliminate the concerns of adverse side effects and the levels of expression would ensure the availability of vaccine for the human population in an environmentally friendly approach. The primary concern is whether the PA83 purified from transgenic chloroplasts is as immunogenic as the PA83 in the AVA. For this, PA83 has been expressed in transgenic chloroplasts of Nicotiana tabacum var. petit Havana, by inserting the pag (2205 bp) with the N-terminal 6X histidine tag, into the chloroplast genome by homologous recombination. Chloroplast integration of the pag was confirmed by PCR and Southern analysis. The PA83 protein was detected in transgenic chloroplasts by immunoblot analysis using anti-PA83 antibodies. Maximum expression levels of PA83 ...
    • Relation:
      CFE0000298; ucf:46213; http://purl.flvc.org/ucf/fd/CFE0000298
    • Online Access:
      http://purl.flvc.org/ucf/fd/CFE0000298
    • Rights:
      campus 2006-01-31
    • Accession Number:
      edsbas.6E7FC086