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Comparison of three non-human primate aerosol models for glanders, caused by Burkholderia mallei
David M Waag1, Taylor B Chance2, Sylvia R Trevino1
1Bacteriology Division, United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD, USA.
Abstract:
Burkholderia mallei is a gram-negative obligate animal pathogen that causes glanders, a highly contagious and potentially fatal disease of solipeds including horses, mules, and donkeys. Humans are also susceptible, and exposure can result in a wide range of clinical forms, i.e., subclinical infection, chronic forms with remission and exacerbation, or acute and potentially lethal septicemia and/or pneumonia. Due to intrinsic antibiotic resistance and the ability of the organisms to survive intracellularly, current treatment regimens are protracted and complicated; and no vaccine is available. As a consequence of these issues, and since B. mallei is infectious by the aerosol route, B. mallei is regarded as a major potential biothreat agent. To develop optimal medical countermeasures and diagnostic tests, well characterized animal models of human glanders are needed. The goal of this study was to perform a head-to-head comparison of models employing three commonly used nonhuman primate (NHP) species, the African green monkey (AGM), Rhesus macaque, and the Cynomolgus macaque. The natural history of infection and in vitro clinical, histopathological, immunochemical, and bacteriological parameters were examined. The AGMs were the most susceptible NHP to B. mallei; five of six expired within 14 days. Although none of the Rhesus or Cynomolgus macaques succumbed, the Rhesus monkeys exhibited abnormal signs and clinical findings associated with B. mallei infection; and the latter may be useful for modeling chronic B. mallei infection. Based on the disease progression observations, gross and histochemical pathology, and humoral and cellular immune response findings, the AGM appears to be the optimal model of acute, lethal glanders infection. AGM models of infection by B. pseudomallei, the etiologic agent of melioidosis, have been characterized recently. Thus, the selection of the AGM species provides the research community with a single NHP model for investigations on acute, severe, inhalational melioidosis and glanders.
Insights
African green monkeys (AGMs) are the optimal nonhuman primate model for acute glanders, a serious bacterial disease. Rhesus macaques may model chronic infection, aiding biodefense research.
Area of Science:
- * Infectious Diseases
- * Veterinary Pathology
- * Biodefense Research
Background:
- * *Burkholderia mallei* causes glanders, a contagious and potentially fatal disease in solipeds and humans.
- * Intrinsic antibiotic resistance and intracellular survival complicate treatment; no vaccine exists.
- * *B. mallei* is a potential biothreat agent due to aerosol transmission and severity.
Purpose of the Study:
- * To compare African green monkeys (AGMs), Rhesus macaques, and Cynomolgus macaques as models for *B. mallei* infection.
- * To identify the optimal nonhuman primate (NHP) model for studying acute and chronic glanders.
- * To inform the development of medical countermeasures and diagnostic tools.
Main Methods:
- * Head-to-head comparison of three NHP species infected with *B. mallei*.
- * Evaluation of clinical, histopathological, immunochemical, and bacteriological parameters.
- * Assessment of disease progression, pathology, and immune responses.
Main Results:
- * AGMs showed highest susceptibility, with 5/6 expiring within 14 days, indicating an optimal acute lethal model.
- * Rhesus macaques exhibited clinical signs but did not succumb, suggesting potential for chronic infection modeling.
- * Cynomolgus macaques showed less pronounced disease compared to AGMs and Rhesus macaques.
Conclusions:
- * The African green monkey is the preferred NHP model for acute, lethal glanders.
- * Rhesus macaques may serve as a model for chronic glanders.
- * AGMs provide a unified NHP model for both acute glanders and melioidosis research.
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