| Literature DB >> 17145938 |
Margaret G M Stokes1, Richard W Titball, Brendan N Neeson, James E Galen, Nicola J Walker, Anthony J Stagg, Dominic C Jenner, Joanne E Thwaite, James P Nataro, Leslie W J Baillie, Helen S Atkins.
Abstract
Bacillus anthracis is the causative agent of anthrax, a disease that affects wildlife, livestock, and humans. Protection against anthrax is primarily afforded by immunity to the B. anthracis protective antigen (PA), particularly PA domains 4 and 1. To further the development of an orally delivered human vaccine for mass vaccination against anthrax, we produced Salmonella enterica serovar Typhimurium expressing full-length PA, PA domains 1 and 4, or PA domain 4 using codon-optimized PA DNA fused to the S. enterica serovar Typhi ClyA and under the control of the ompC promoter. Oral immunization of A/J mice with Salmonella expressing full-length PA protected five of six mice against a challenge with 10(5) CFU of aerosolized B. anthracis STI spores, whereas Salmonella expressing PA domains 1 and 4 provided only 25% protection (two of eight mice), and Salmonella expressing PA domain 4 or a Salmonella-only control afforded no measurable protection. However, a purified recombinant fusion protein of domains 1 and 4 provided 100% protection, and purified recombinant 4 provided protection in three of eight immunized mice. Thus, we demonstrate for the first time the efficacy of an oral S. enterica-based vaccine against aerosolized B. anthracis spores.Entities:
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Year: 2006 PMID: 17145938 PMCID: PMC1865694 DOI: 10.1128/IAI.01242-06
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441