TY - JOUR
T1 - Development and characterization of a guinea pig-adapted Sudan virus
AU - Wong, Gary
AU - He, Shihua
AU - Wei, Haiyan
AU - Kroeker, Andrea
AU - Audet, Jonathan
AU - Leung, Anders
AU - Cutts, Todd
AU - Graham, Jill
AU - Kobasa, Darwyn
AU - Embury-Hyatt, Carissa
AU - Kobinger, Gary P.
AU - Qiu, Xiangguo
N1 - Publisher Copyright:
© 2015, American Society for Microbiology.
PY - 2016
Y1 - 2016
N2 - Infections with Sudan virus (SUDV), a member of the genus Ebolavirus, result in a severe hemorrhagic fever with a fatal outcome in over 50% of human cases. The paucity of prophylactics and therapeutics against SUDV is attributed to the lack of a small-animal model to screen promising compounds. By repeatedly passaging SUDV within the livers and spleens of guinea pigs in vivo, a guinea pig-adapted SUDV variant (SUDV-GA) uniformly lethal to these animals, with a 50% lethal dose (LD50) of 5.3×10-2 50% tissue culture infective doses (TCID50), was developed. Animals infected with SUDV-GA developed high viremia and died between 9 and 14 days postinfection. Several hallmarks of SUDV infection, including lymphadenopathy, increased liver enzyme activities, and coagulation abnormalities, were observed. Virological analyses and gross pathology, histopathology, and immunohistochemistry findings indicate that SUDV-GA replicates in the livers and spleens of infected animals similarly to SUDV infections in nonhuman primates. These developments will accelerate the development of specific medical countermeasures in preparation for a future disease outbreak due to SUDV.
AB - Infections with Sudan virus (SUDV), a member of the genus Ebolavirus, result in a severe hemorrhagic fever with a fatal outcome in over 50% of human cases. The paucity of prophylactics and therapeutics against SUDV is attributed to the lack of a small-animal model to screen promising compounds. By repeatedly passaging SUDV within the livers and spleens of guinea pigs in vivo, a guinea pig-adapted SUDV variant (SUDV-GA) uniformly lethal to these animals, with a 50% lethal dose (LD50) of 5.3×10-2 50% tissue culture infective doses (TCID50), was developed. Animals infected with SUDV-GA developed high viremia and died between 9 and 14 days postinfection. Several hallmarks of SUDV infection, including lymphadenopathy, increased liver enzyme activities, and coagulation abnormalities, were observed. Virological analyses and gross pathology, histopathology, and immunohistochemistry findings indicate that SUDV-GA replicates in the livers and spleens of infected animals similarly to SUDV infections in nonhuman primates. These developments will accelerate the development of specific medical countermeasures in preparation for a future disease outbreak due to SUDV.
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U2 - 10.1128/JVI.02331-15
DO - 10.1128/JVI.02331-15
M3 - Article
C2 - 26491156
AN - SCOPUS:84953896558
SN - 0022-538X
VL - 90
SP - 392
EP - 399
JO - Journal of virology
JF - Journal of virology
IS - 1
ER -