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

机译:新型二氢脱氢酶抑制剂具有强大的干扰素无抗病毒活性对哺乳动物抗病毒活性的体外体外

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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 block de novo pyrimidine biosynthesis, have antiviral activity against viruses from different families, including Arenaviridae, 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 Junín viruses.
机译:哺乳动系统毒剂导致啮齿动物的慢性感染,这是他们主要的天然宿主。人类感染与其中一些病毒导致高后疾病,在公共卫生方面造成了重大问题。目前,没有FDA持牌哺乳动物疫苗疫苗,抗哺乳动物病毒药物仅限于利巴韦林的偏离标签使用,这仅是部分有效和与严重的副作用相关。二氢脱氢酶(DHODH)抑制剂,其嵌入Novo嘧啶生物合成,对来自不同家庭的病毒的抗病毒活性,包括哺乳动物病毒的分类物系。在这里,我们评估五种新的Dhodh抑制剂,以针对哺乳动物捕杀剂的抗病毒活性。所有测试的Dhodh抑制剂都是效果抗淋巴细胞脉络膜炎病毒(LCMV)(半最大有效浓度[EC50]在低纳米摩尔范围内,选择性指数[Si]> 1000)。测试的Dhodh抑制剂没有影响病毒虫细胞进入或萌芽,而是干扰病毒RNA合成。这种干扰导致有效的干扰素无关抑制哺乳动物血管血清倍增,包括高毒性的兰萨和junín病毒。

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