Characterization Of Pathogenesis Of And Immune Response To Burkholderia Pseudomallei K9243 Using Both Inhalational And Intraperitoneal Infection Models In BALB/c and C57BL/6 Mice

Burkholderia pseudomallei, the etiologic agent of melioidosis, is a gram negative bacterium designated as a Tier 1 threat. This bacterium is known to be endemic in Southeast Asia and Northern Australia and can infect humans and animals by several routes. Inhalational melioidosis has been associated...

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Main Authors: Cote,C K, Bearss,J J, Hunter,M, Dankmeyer,J L, Fritts,K A, Klimko,C P, Shoe,J L, Weaver,C H, Toothman,R G, Webster,W M, Fetterer,D, Bozue,J A, Worsham,P L, Welkos,S L, Amemiya,K, Quirk,A V
Format: Report
Language:English
Subjects:
bacterial infections
Burkholderia pseudomallei
Countermeasures
disease attributes
Gram negative bacteria
infection
Infectious diseases
inhalational immune response
intraperitoneal
melioidosis
mice
mouse
pathogenesis
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Summary:Burkholderia pseudomallei, the etiologic agent of melioidosis, is a gram negative bacterium designated as a Tier 1 threat. This bacterium is known to be endemic in Southeast Asia and Northern Australia and can infect humans and animals by several routes. Inhalational melioidosis has been associated with monsoonal rains in endemic areas and is also a significant concern in the biodefense community. There are currently no effective vaccines for B. pseudomallei and antibiotic treatment can be hampered by non-specific symptomology and also the high rate of naturally occurring antibiotic resistant strains. Well-characterized animal models will be essential when selecting novel medical countermeasures for evaluation prior to human clinical trials. Here, we further characterize differences between the responses of BALB/c and C57BL/6 mice when challenged with similarly low doses of a low-passage and well-defined stock of B. pseudomallei K96243 via either intraperitoneal or aerosol routes of exposure. Before challenge, mice were each implanted with a transponder to collect body temperature readings, and daily body weights were also recorded. Mice were euthanized on select days for pathological analyses and determination of the bacterial burden in selected tissues (blood, lungs, liver, and spleen). Additionally, spleen homogenate and sera samples were analyzed to better characterize the host immune response after infection with aerosolized bacteria. These clinical, pathological, and immunological data highlighted and confirmed important similarities and differences between these murine models and exposure routes. PLoS One , 12, 2, 01 Jan 0001, 01 Jan 0001,