Natural History of Aerosol Exposure with Marburg Virus in Rhesus Macaques
Evan C Ewers1, William D Pratt2, Nancy A Twenhafel3,4
1Department of Medicine, Tripler Army Medical Center, Honolulu, HI 96859, USA. evan.c.ewers.mil@mail.mil.
Abstract:
Marburg virus causes severe and often lethal viral disease in humans, and there are currently no Food and Drug Administration (FDA) approved medical countermeasures. The sporadic occurrence of Marburg outbreaks does not allow for evaluation of countermeasures in humans, so therapeutic and vaccine candidates can only be approved through the FDA animal rule-a mechanism requiring well-characterized animal models in which efficacy would be evaluated. Here, we describe a natural history study where rhesus macaques were surgically implanted with telemetry devices and central venous catheters prior to aerosol exposure with Marburg-Angola virus, enabling continuous physiologic monitoring and blood sampling without anesthesia. After a three to four day incubation period, all animals developed fever, viremia, and lymphopenia before developing tachycardia, tachypnea, elevated liver enzymes, decreased liver function, azotemia, elevated D-dimer levels and elevated pro-inflammatory cytokines suggesting a systemic inflammatory response with organ failure. The final, terminal period began with the onset of sustained hypotension, dehydration progressed with signs of major organ hypoperfusion (hyperlactatemia, acute kidney injury, hypothermia), and ended with euthanasia or death. The most significant pathologic findings were marked infection of the respiratory lymphoid tissue with destruction of the tracheobronchial and mediastinal lymph nodes, and severe diffuse infection in the liver, and splenitis.
Insights
A study in rhesus macaques details the severe progression of Marburg virus disease. This research is crucial for developing medical countermeasures against this lethal hemorrhagic fever.
Area of Science:
- Virology
- Pathology
- Veterinary Medicine
Background:
- Marburg virus causes a severe, often fatal hemorrhagic fever in humans.
- No FDA-approved medical countermeasures currently exist for Marburg virus disease.
- The FDA animal rule necessitates well-characterized animal models for countermeasure approval.
Purpose of the Study:
- To describe the natural history of Marburg virus disease in a non-human primate model.
- To establish a well-characterized animal model for evaluating Marburg virus countermeasures.
Main Methods:
- Rhesus macaques were surgically implanted with telemetry devices and central venous catheters.
- Animals were exposed to Marburg-Angola virus via aerosol.
- Continuous physiologic monitoring and blood sampling were performed without anesthesia.
Main Results:
- A 3-4 day incubation period was followed by fever, viremia, and lymphopenia.
- Systemic inflammatory response with organ failure was indicated by tachycardia, tachypnea, elevated liver enzymes, azotemia, and increased pro-inflammatory cytokines.
- The terminal phase involved hypotension, dehydration, organ hypoperfusion, and significant pathology in lymphoid tissues, liver, and spleen.
Conclusions:
- Aerosolized Marburg-Angola virus infection in rhesus macaques recapitulates key features of human disease.
- This model provides a platform for the evaluation of potential Marburg virus therapeutics and vaccines.
- Understanding the disease progression is vital for developing effective medical countermeasures.
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