Current affiliation: National Emerging Infectious Diseases Laboratory, Department of Microbiology, Boston University School of Medicine, 620 Albany St, Boston, MA 02118, USA
Benjamin Klaffke
Texas Biomedical Research Institute, 8715 W. Military Dr., San Antonio, TX 78227, USA
Gloria F. Rodriguez
Texas Biomedical Research Institute, 8715 W. Military Dr., San Antonio, TX 78227, USA
Priscilla Escareno
Texas Biomedical Research Institute, 8715 W. Military Dr., San Antonio, TX 78227, USA
Carmen Bartley
Texas Biomedical Research Institute, 8715 W. Military Dr., San Antonio, TX 78227, USA
Anysha Ticer
Texas Biomedical Research Institute, 8715 W. Military Dr., San Antonio, TX 78227, USA
Elizabeth A. Clemmons
Texas Biomedical Research Institute, 8715 W. Military Dr., San Antonio, TX 78227, USA
John W. Dutton III
Texas Biomedical Research Institute, 8715 W. Military Dr., San Antonio, TX 78227, USA
Anthony Griffiths
Current affiliation: National Emerging Infectious Diseases Laboratory, Department of Microbiology, Boston University School of Medicine, 620 Albany St, Boston, MA 02118, USA
Gabe T. Meister
Battelle Biomedical Research Center (BBRC), 1425 Plain City Georgesville Road, West Jefferson, OH 43162, USA
Daniel C. Sanford
Battelle Biomedical Research Center (BBRC), 1425 Plain City Georgesville Road, West Jefferson, OH 43162, USA
Chris M. Cirimotich
Battelle Biomedical Research Center (BBRC), 1425 Plain City Georgesville Road, West Jefferson, OH 43162, USA
Ricardo Carrion
Texas Biomedical Research Institute, 8715 W. Military Dr., San Antonio, TX 78227, USA
The primary objective of this study was to characterize the disease course in cynomolgus macaques exposed to Sudan virus (SUDV), to determine if infection in this species is an appropriate model for the evaluation of filovirus countermeasures under the FDA Animal Rule. Sudan virus causes Sudan virus disease (SVD), with an average case fatality rate of approximately 50%, and while research is ongoing, presently there are no approved SUDV vaccines or therapies. Well characterized animal models are crucial for further developing and evaluating countermeasures for SUDV. Twenty (20) cynomolgus macaques were exposed intramuscularly to either SUDV or sterile phosphate-buffered saline; 10 SUDV-exposed animals were euthanized on schedule to characterize pathology at defined durations post-exposure and 8 SUDV-exposed animals were not part of the scheduled euthanasia cohort. Survival was assessed, along with clinical observations, body weights, body temperatures, hematology, clinical chemistry, coagulation, viral load (serum and tissues), macroscopic observations, and histopathology. There were statistically significant differences between SUDV-exposed animals and mock-exposed animals for 26 parameters, including telemetry body temperature, clinical chemistry parameters, hematology parameters, activated partial thromboplastin time, serum viremia, and biomarkers that characterize the disease course of SUDV in cynomolgus macaques.