Novel Dihydroorotate Dehydrogenase Inhibitors with Potent Interferon-Independent Antiviral Activity against Mammarenaviruses In Vitro

被引:9
|
作者
Kim, Yu-Jin [1 ]
Cubitt, Beatrice [1 ]
Cai, Yingyun [2 ]
Kuhn, Jens H. [2 ]
Vitt, Daniel [3 ]
Kohlhof, Hella [3 ]
de la Torre, Juan C. [1 ]
机构
[1] Scripps Res Inst, Dept Immunol & Microbiol, La Jolla, CA 92037 USA
[2] NIAID, Integrated Res Facil Ft Detrick IRF Frederick, NIH, B-8200 Res Plaza, Ft Detrick, MD 21702 USA
[3] Immun Therapeut, New York, NY 10036 USA
来源
VIRUSES-BASEL | 2020年 / 12卷 / 08期
关键词
mammarenavirus; DHODH; pyrimidine biosynthesis; interferon; antiviral; LYMPHOCYTIC CHORIOMENINGITIS VIRUS; LASSA FEVER; INFECTION; PATHOGEN; BINDING;
D O I
10.3390/v12080821
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Mammarenaviruses cause chronic infections in rodents, which are their predominant natural hosts. Human infection with some of these viruses causes high-consequence disease, posing significant issues in public health. Currently, no FDA-licensed mammarenavirus vaccines are available, and anti-mammarenavirus drugs are limited to an off-label use of ribavirin, which is only partially efficacious and associated with severe side effects. Dihydroorotate dehydrogenase (DHODH) inhibitors, which blockde novopyrimidine biosynthesis, have antiviral activity against viruses from different families, includingArenaviridae, the taxonomic home of mammarenaviruses. Here, we evaluate five novel DHODH inhibitors for their antiviral activity against mammarenaviruses. All tested DHODH inhibitors were potently active against lymphocytic choriomeningitis virus (LCMV) (half-maximal effective concentrations [EC50] in the low nanomolar range, selectivity index [SI] > 1000). The tested DHODH inhibitors did not affect virion cell entry or budding, but rather interfered with viral RNA synthesis. This interference resulted in a potent interferon-independent inhibition of mammarenavirus multiplication in vitro, including the highly virulent Lassa and Junin viruses.
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页数:19
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