Marinho Mikaela Dos Santos, Zhang Ya-Nan, Cassani Natasha Marques, Santos Igor Andrade, Costa Oliveira Ana Laura, Dos Santos Pereira Anna Karla, Corbi Pedro Paulo, Zhang Bo, Jardim Ana Carolina Gomes
Laboratory of Antiviral Research, Institute of Biomedical Science, Federal University of Uberlândia (UFU), Uberlândia, MG, Brazil.
Key Laboratory of Virology and Biosafety, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, 430071, China.
Heliyon. 2024 Jul 2;10(13):e33885. doi: 10.1016/j.heliyon.2024.e33885. eCollection 2024 Jul 15.
Arboviruses are etiological agents in an extensive group of emerging diseases with great clinical relevance in Brazil, due to the wide distribution of their vectors and the favorable environmental conditions. Among them, the Mayaro virus (MAYV) has drawn attention since its emergence as the etiologic agent of Mayaro fever, a highly debilitating disease. To study viral replication and identify new drug candidates, traditional antiviral assays based on viral antigens and/or plaque assays have been demonstrating low throughput, making it difficult to carry out larger-scale assays. Therefore, we developed and characterized two DNA-launched infectious clones reporter viruses based on the MAYV strain BeAr 20290 containing the reporter genes of and designated as MAYV- and MAYV-, respectively. The viruses replicated efficiently with similar properties to the parental wild-type MAYV, and luminescence expression levels reflected viral replication. Reporter genes were also preserved during passage in cell culture, remaining stably expressed for one round of passage for MAYV- and three rounds for MAYV- Employing the infectious clone, we described the effect of Rimantadine, an FDA-approved Alzheimer's drug, as a repurposing agent for MAYV but with a broad-spectrum activity against Zika virus infection. Additionally, we validated MAYV- as a tool for antiviral drug screening using the compound EIDD-2749 (4'-Fluorouridine), which acts as an inhibitor of alphavirus RNA-dependent RNA polymerase.
虫媒病毒是巴西一组广泛的新兴疾病的病原体,因其传播媒介分布广泛且环境条件适宜而具有重大临床意义。其中,马亚罗病毒(MAYV)自作为马亚罗热的病原体出现以来就备受关注,马亚罗热是一种使人极度虚弱的疾病。为了研究病毒复制并确定新的候选药物,基于病毒抗原和/或蚀斑试验的传统抗病毒检测方法显示通量较低,难以进行大规模检测。因此,我们开发并鉴定了两种基于MAYV毒株BeAr 20290的DNA启动感染性克隆报告病毒,分别含有 和 的报告基因,命名为MAYV- 和MAYV- 。这些病毒能高效复制,其特性与亲本野生型MAYV相似,发光表达水平反映了病毒复制情况。报告基因在细胞培养传代过程中也得以保留,MAYV- 在一轮传代中保持稳定表达,MAYV- 在三轮传代中保持稳定表达。利用该感染性克隆,我们描述了一种美国食品药品监督管理局(FDA)批准用于治疗阿尔茨海默病的药物金刚烷胺作为MAYV的一种重新利用药物的效果,它对寨卡病毒感染具有广谱活性。此外,我们验证了MAYV- 作为一种抗病毒药物筛选工具的作用,使用了化合物EIDD-2749(4'-氟尿苷),它可作为甲病毒RNA依赖性RNA聚合酶的抑制剂。