Burkholderia pseudomallei capsular polysaccharide conjugates provide protection against acute melioidosis

• Published in: Infection and immunity Vol. 82; no. 8; pp. 3206 - 3213
• Main Authors: Scott, Andrew E, Burtnick, Mary N, Stokes, Margaret G M, Whelan, Adam O, Williamson, E Diane, Atkins, Timothy P, Prior, Joann L, Brett, Paul J
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 01.08.2014
• Subjects: Animals; Antibodies, Bacterial - blood; Antigens, Bacterial - immunology; Bacterial Capsules - immunology; Bacterial Vaccines - administration & dosage; Bacterial Vaccines - immunology; Burkholderia pseudomallei; Burkholderia pseudomallei - immunology; Female; Immunoglobulin G - blood; Melioidosis - prevention & control; Mice; Mice, Inbred BALB C; Microbial Immunity and Vaccines; Survival Analysis; Vaccines, Conjugate - administration & dosage; Vaccines, Conjugate - immunology
• ISSN: 0019-9567; 1098-5522
• DOI: 10.1128/IAI.01847-14

Burkholderia pseudomallei, the etiologic agent of melioidosis, is a CDC tier 1 select agent that causes severe disease in both humans and animals. Diagnosis and treatment of melioidosis can be challenging, and in the absence of optimal chemotherapeutic intervention, acute disease is frequently fatal. Melioidosis is an emerging infectious disease for which there are currently no licensed vaccines. Due to the potential malicious use of B. pseudomallei as well as its impact on public health in regions where the disease is endemic, there is significant interest in developing vaccines for immunization against this disease. In the present study, type A O-polysaccharide (OPS) and manno-heptose capsular polysaccharide (CPS) antigens were isolated from nonpathogenic, select-agent-excluded strains of B. pseudomallei and covalently linked to carrier proteins. By using these conjugates (OPS2B1 and CPS2B1, respectively), it was shown that although high-titer IgG responses against the OPS or CPS component of the glycoconjugates could be raised in BALB/c mice, only those animals immunized with CPS2B1 were protected against intraperitoneal challenge with B. pseudomallei. Extending upon these studies, it was also demonstrated that when the mice were immunized with a combination of CPS2B1 and recombinant B. pseudomallei LolC, rather than with CPS2B1 or LolC individually, they exhibited higher survival rates when challenged with a lethal dose of B. pseudomallei. Collectively, these results suggest that CPS-based glycoconjugates are promising candidates for the development of subunit vaccines for immunization against melioidosis.