Literature DB >> 16271808

A recombinant 63-kDa form of Bacillus anthracis protective antigen produced in the yeast Saccharomyces cerevisiae provides protection in rabbit and primate inhalational challenge models of anthrax infection.

Robert W Hepler1, Rosemarie Kelly, Tessie B McNeely, Hongxia Fan, Maria C Losada, Hugh A George, Andrea Woods, Leslie D Cope, Alka Bansal, James C Cook, Gina Zang, Steven L Cohen, Xiaorong Wei, Paul M Keller, Elizabeth Leffel, Joseph G Joyce, Louise Pitt, Loren D Schultz, Kathrin U Jansen, Myra Kurtz.   

Abstract

Infection by Bacillus anthracis is preventable by prophylactic vaccination with several naturally derived and recombinant vaccine preparations. Existing data suggests that protection is mediated by antibodies directed against the protective antigen (PA) component of the anthrax toxin complex. PA is an 83-kDa protein cleaved in vivo to yield a biologically active 63-kDa protein. In an effort to evaluate the potential of yeast as an expression system for the production of recombinant PA, and to determine if the yeast-purified rPA63 can protect from a lethal inhalational challenge, the sequence of the 63-kDa form of PA was codon-optimized and expressed in the yeast Saccharomyces cerevisiae. Highly purified rPA63 isolated from Saccharomyces under denaturing conditions demonstrated reduced biological activity in a macrophage-killing assay compared to non-denatured rPA83 purified from Escherichia coli. Rabbits and non-human primates (NHP) immunized with rPA63 and later challenged with a lethal dose of B. anthracis spores were generally protected from infection. These results indicate that epitopes present in the 63-kDa from of PA can protect rabbits and non-human primates from a lethal spore challenge, and further suggest that a fully functional rPA63 is not required in order to provide these epitopes.

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Year:  2005        PMID: 16271808     DOI: 10.1016/j.vaccine.2005.10.018

Source DB:  PubMed          Journal:  Vaccine        ISSN: 0264-410X            Impact factor:   3.641


  6 in total

1.  Expression of either lethal toxin or edema toxin by Bacillus anthracis is sufficient for virulence in a rabbit model of inhalational anthrax.

Authors:  Julie A Lovchik; Melissa Drysdale; Theresa M Koehler; Julie A Hutt; C Rick Lyons
Journal:  Infect Immun       Date:  2012-04-23       Impact factor: 3.441

Review 2.  Anthrax vaccination strategies.

Authors:  Robert J Cybulski; Patrick Sanz; Alison D O'Brien
Journal:  Mol Aspects Med       Date:  2009-09-01

3.  Detoxified lethal toxin as a potential mucosal vaccine against anthrax.

Authors:  Qingfu Xu; Mingtao Zeng
Journal:  Clin Vaccine Immunol       Date:  2008-02-06

4.  Protection Afforded by Fluoroquinolones in Animal Models of Respiratory Infections with Bacillus anthracis, Yersinia pestis, and Francisella tularensis.

Authors:  Johnny W Peterson; Scott T Moen; Daniel Healy; Jennifer E Pawlik; Joanna Taormina; Jason Hardcastle; John M Thomas; William S Lawrence; Cindy Ponce; Bagram M Chatuev; Bryan T Gnade; Sheri M Foltz; Stacy L Agar; Jian Sha; Gary R Klimpel; Michelle L Kirtley; Tonyia Eaves-Pyles; Ashok K Chopra
Journal:  Open Microbiol J       Date:  2010-06-03

5.  Production of Functionally Active and Immunogenic Non-Glycosylated Protective Antigen from Bacillus anthracis in Nicotiana benthamiana by Co-Expression with Peptide-N-Glycosidase F (PNGase F) of Flavobacterium meningosepticum.

Authors:  Tarlan Mamedov; Jessica A Chichester; R Mark Jones; Ananya Ghosh; Megan V Coffin; Kristina Herschbach; Alexey I Prokhnevsky; Stephen J Streatfield; Vidadi Yusibov
Journal:  PLoS One       Date:  2016-04-21       Impact factor: 3.240

Review 6.  Macaque models of human infectious disease.

Authors:  Murray B Gardner; Paul A Luciw
Journal:  ILAR J       Date:  2008
  6 in total

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