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J Med Microbiol 53 (2004), 1177-1182; DOI: 10.1099/jmm.0.45766-0
© 2004 Society for General Microbiology
ISSN 0022-2615

Evaluation of lipopolysaccharide and capsular polysaccharide as subunit vaccines against experimental melioidosis

Michelle Nelson, Joann L Prior, M Stephen Lever, Helen E Jones, Timothy P Atkins and Richard W Titball

Defence Science and Technology Laboratory, Porton Down, Salisbury SP4 0JQ, UK

Correspondence Michelle Nelson mnelson{at}dstl.gov.uk

Received June 3, 2004
Accepted August 26, 2004

Burkholderia pseudomallei is the causative agent of melioidosis, which is a major cause of morbidity and mortality in endemic regions. Currently there is no human vaccine against melioidosis. In this study, LPS or capsular polysaccharide was used to immunize BALB/c mice. The different polysaccharide antigens induced antibody responses. Mice vaccinated with LPS developed predominantly IgM and IgG3 responses. Contrastingly, mice vaccinated with capsular polysaccharide developed a predominantly IgG2b response. After immunization, mice were challenged by the intra-peritoneal route and an increased mean time to death was observed compared with unvaccinated controls. Immunization with LPS provided an optimal protective response. Mice challenged by the aerosol route showed a small increase in the mean time to death compared with the unvaccinated controls. The passive transfer of antigen from immunized into naïve mice provided protection against a subsequent challenge. This study is the first time antigens protective by active immunization have been identified and suggests that polysaccharides have potential as vaccine candidates against melioidosis.


Abbreviations: i.p., intra-peritoneal; MLD, median lethal dose; MPL, monophosphoryl lipid A; MTTD, mean time to death; NCTC, National Collection of Type Cultures; RAS, Ribi Adjuvant system.




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