Aerosol Exposure to the Angola Strain of Marburg Virus Causes Lethal Viral Hemorrhagic Fever in Cynomolgus Macaques

• Published in: Veterinary pathology Vol. 47; no. 5; pp. 831 - 851
• Main Authors: Alves, D. A., Glynn, A. R., Steele, K. E., Lackemeyer, M. G., Garza, N. L., Buck, J. G., Mech, C., Reed, D. S.
• Format: Journal Article
• Language: English
• Published: Los Angeles, CA SAGE Publications 01.09.2010
• Subjects: Animals; Blood Cell Count; Blood Pressure - immunology; Body Temperature - immunology; Cynomolgus; Cytokines - analysis; Disease Models, Animal; Female; Filovirus; Heart Rate - immunology; Humans; Immunohistochemistry; Inhalation Exposure - adverse effects; Liver - pathology; Liver - virology; Lung - pathology; Lung - virology; Lymph Nodes - pathology; Lymph Nodes - virology; Macaca; Macaca fascicularis; Male; Marburg virus; Marburg Virus Disease - immunology; Marburg Virus Disease - pathology; Marburg Virus Disease - virology; Marburgvirus - immunology; Spleen - pathology; Spleen - virology; Viremia - immunology; Viremia - pathology; Viremia - virology; nonhuman primate; Marburg virus; animal model; aerosol
• ISSN: 0300-9858; 1544-2217
• DOI: 10.1177/0300985810378597

Cynomolgus macaques were exposed to the Angola strain of Lake Victoria Marburg virus (MARV) by aerosol to examine disease course and lethality. Macaques became febrile 4 to 7 days postexposure; the peak febrile response was delayed 1 to 2 days in animals that received a lower dose; viremia coincided with the onset of fever. All 6 macaques succumbed to the infection, with the 3 macaques in the low-dose group becoming moribund on day 9, a day later than the macaques in the high-dose group. Gross pathologic lesions included maculopapular cutaneous rash; pulmonary congestion and edema; pericardial effusion; enlarged, congested, and/or hemorrhagic lymphoid tissues; enlarged friable fatty liver; and pyloric and duodenal congestion and/or hemorrhage. Fibrinous interstitial pneumonia was the most consistent pulmonary change. Lymphocytolysis and lymphoid depletion, as confirmed by TUNEL (terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick end labeling), were observed in the mediastinal lymph nodes and spleen. MARV antigen was detected in the lungs, mediastinal lymph nodes, spleen, and liver of all animals examined. In infected macaques, nuclear expression of interleukin-33 was lost in pulmonary arteriolar and mediastinal lymph node high endothelial venule endothelial cells; interleukin-33-positive fibroblastic reticular cells in the mediastinal lymph node were consistently negative for MARV antigen. These macaques exhibited a number of features similar to those of human filovirus infections; as such, this model of aerosolized MARV-Angola might be useful in developing medical countermeasures under the Animal Rule.