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A Burkholderia pseudomallei outer membrane vesicle vaccine provides protection against lethal sepsis
Wildaliz Nieves1, Hailey Petersen, Barbara M Judy
1Department of Microbiology and Immunology, Tulane University School of Medicine, New Orleans, Louisiana, USA.
Abstract:
The environmental Gram-negative encapsulated bacillus Burkholderia pseudomallei is the causative agent of melioidosis, a disease associated with high morbidity and mortality rates in areas of Southeast Asia and northern Australia in which the disease is endemic. B. pseudomallei is also classified as a tier I select agent due to the high level of lethality of the bacterium and its innate resistance to antibiotics, as well as the lack of an effective vaccine. Gram-negative bacteria, including B. pseudomallei, secrete outer membrane vesicles (OMVs) which are enriched with multiple protein, lipid, and polysaccharide antigens. Previously, we demonstrated that immunization with multivalent B. pseudomallei-derived OMVs protects highly susceptible BALB/c mice against an otherwise lethal aerosol challenge. In this work, we evaluated the protective efficacy of OMV immunization against intraperitoneal challenge with a heterologous strain because systemic infection with phenotypically diverse environmental B. pseudomallei strains poses another hazard and a challenge to vaccine development. We demonstrated that B. pseudomallei OMVs derived from strain 1026b afforded significant protection against septicemic infection with B. pseudomallei strain K96243. OMV immunization induced robust OMV-, lipopolysaccharide-, and capsular polysaccharide-specific serum IgG (IgG1, IgG2a, and IgG3) and IgM antibody responses. OMV-immune serum promoted bacterial killing in vitro, and passive transfer of B. pseudomallei OMV immune sera protected naive mice against a subsequent challenge. These results indicate that OMV immunization provides antibody-mediated protection against acute, rapidly lethal sepsis in mice. B. pseudomallei-derived OMVs may represent an efficacious multivalent vaccine strategy against melioidosis.
Insights
Outer membrane vesicles (OMVs) from Burkholderia pseudomallei offer protection against melioidosis. Immunization with these OMVs generated antibodies and protected mice against lethal bacterial challenge, suggesting a potential vaccine strategy.
Area of Science:
- Microbiology
- Immunology
- Vaccine Development
Background:
- Burkholderia pseudomallei causes melioidosis, a severe disease endemic in Southeast Asia and Australia.
- B. pseudomallei is a tier I select agent due to high lethality, antibiotic resistance, and lack of a vaccine.
- Outer membrane vesicles (OMVs) from Gram-negative bacteria contain antigens and can be used for immunization.
Purpose of the Study:
- To evaluate the protective efficacy of B. pseudomallei-derived OMVs against a heterologous strain challenge.
- To assess the antibody responses induced by OMV immunization.
- To determine if OMV immunization provides protection against lethal sepsis.
Main Methods:
- Mice were immunized with B. pseudomallei strain 1026b-derived OMVs.
- Immunized mice were challenged intraperitoneally with B. pseudomallei strain K96243.
- Serum antibody levels (IgG, IgM) and bacterial killing in vitro were assessed.
- Passive transfer of immune serum was used to evaluate protection.
Main Results:
- OMV immunization significantly protected mice against lethal septicemic infection with a heterologous B. pseudomallei strain.
- Robust antibody responses (IgG, IgM) specific to OMVs, lipopolysaccharide, and capsular polysaccharide were induced.
- Immune serum promoted bacterial killing in vitro, and passive transfer of serum protected naive mice.
- OMV immunization conferred antibody-mediated protection against acute, lethal sepsis.
Conclusions:
- B. pseudomallei-derived OMVs provide significant protection against lethal sepsis caused by heterologous strains.
- OMV immunization induces protective antibody responses, suggesting a potential multivalent vaccine strategy for melioidosis.
- OMVs represent a promising platform for developing an effective vaccine against melioidosis.
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