TY - JOUR
T1 - Development of FGI-106 as a broad-spectrum therapeutic with activity against members of the family Bunyaviridae
AU - Smith, Darci R.
AU - Ogg, Monica
AU - Garrison, Aura
AU - Yunus, Abdul
AU - Honko, Anna
AU - Johnson, Josh
AU - Olinger, Gene
AU - Hensley, Lisa E.
AU - Kinch, Michael S.
PY - 2010/4/30
Y1 - 2010/4/30
N2 - The family Bunyaviridae is a diverse group of negative-strand RNA viruses that infect a wide range of arthropod vectors and animal hosts. Based on the continuing need for new therapeutics to treat bunyavirus infections, we evaluated the potential efficacy of FGI-106, a small-molecular compound that previously demonstrated activity against different RNA viruses. FGI-106 displayed substantial antiviral activity in cell-based assays of different bunyavirus family members, including Asian and South American hantaviruses (Hantaan virus and Andes virus), Crimean-Congo hemorrhagic fever virus, La Crosse virus, and Rift Valley fever virus. The pharmacokinetic profile of FGI-106 revealed sufficient exposure of the drug to critical target organs (lung, liver, kidney, and spleen), which are frequently the sites of bunyavirus replication. Consistent with these findings, FGI-106 treatment delivered via intraperitoneal injection prior to virus exposure was sufficient to delay the onset of Rift Valley fever virus infection in mouse-based models and to enhance survival in the face of an otherwise lethal infection. Altogether, these results suggest a potential opportunity for the use of FGI-106 to treat infections by members of the family Bunyaviridae.
AB - The family Bunyaviridae is a diverse group of negative-strand RNA viruses that infect a wide range of arthropod vectors and animal hosts. Based on the continuing need for new therapeutics to treat bunyavirus infections, we evaluated the potential efficacy of FGI-106, a small-molecular compound that previously demonstrated activity against different RNA viruses. FGI-106 displayed substantial antiviral activity in cell-based assays of different bunyavirus family members, including Asian and South American hantaviruses (Hantaan virus and Andes virus), Crimean-Congo hemorrhagic fever virus, La Crosse virus, and Rift Valley fever virus. The pharmacokinetic profile of FGI-106 revealed sufficient exposure of the drug to critical target organs (lung, liver, kidney, and spleen), which are frequently the sites of bunyavirus replication. Consistent with these findings, FGI-106 treatment delivered via intraperitoneal injection prior to virus exposure was sufficient to delay the onset of Rift Valley fever virus infection in mouse-based models and to enhance survival in the face of an otherwise lethal infection. Altogether, these results suggest a potential opportunity for the use of FGI-106 to treat infections by members of the family Bunyaviridae.
KW - Antiviral
KW - Bunyavirus
KW - Hantavirus
KW - Rift valley fever virus
KW - Therapeutic
UR - http://www.scopus.com/inward/record.url?scp=77953383259&partnerID=8YFLogxK
M3 - Review article
AN - SCOPUS:77953383259
SN - 1179-1624
VL - 2
SP - 9
EP - 20
JO - Virus Adaptation and Treatment
JF - Virus Adaptation and Treatment
IS - 1
ER -