Rocio Virus Encephalitis: In Silico Evidence for Drug Repurposing

被引:1
|
作者
Sagini, Joao Pedro [1 ]
Arantes, Pablo Ricardo [2 ]
Pedebos, Conrado [3 ]
Ligabue-Braun, Rodrigo [1 ,4 ]
机构
[1] Fed Univ Hlth Sci Porto Alegre UFCSPA, Grad Program Biol Sci PPGBio, Sarmento Leite 245, BR-90050170 Porto Alegre, Brazil
[2] Univ Calif Riverside, Dept Bioengn, Riverside, CA 92521 USA
[3] Univ Oxford, Dept Biochem, Oxford OX1 3QU, England
[4] Fed Univ Hlth Sci Porto Alegre UFCSPA, Dept Pharmacosci, Sarmento Leite 245, BR-90050170 Porto Alegre, Brazil
来源
MACROMOL | 2022年 / 2卷 / 01期
关键词
drug repurposing; emergent infection; molecular docking; rocio virus; NS1; ARBOVIRUS DISEASE; BRAZIL; EMERGENCE; DYNAMICS; MODEL; EPIDEMIC;
D O I
10.3390/macromol2010006
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Arboviral diseases have a high incidence in Brazil and constitute a serious public health problem. Rocio virus (ROCV) is an arbovirus belonging to the family Flaviviridae. It was responsible for the emergence of an outbreak of encephalitis on the Sao Paulo state coast in the late 1970s. Although no recent case of this virus has been reported, data suggest the circulation of ROCV throughout the Brazilian territory. Given these indications and the strong presence of fundamental factors for the resurgence of emerging diseases in Brazil, we conducted this study using virtual screenings to identify targets and therapeutic molecules that could be redirected to fight infections related to ROCV. Herein, we demonstrated that the National List of Essential Medicines of the Brazilian Unified Health System (SUS) has several molecules that could be redirected to combat this flavivirus, namely simeprevir, daclatasvir, iloprost, and itraconazole. Among them, itraconazole was found to be an interesting candidate since it interacts with both structural and nonstructural proteins of this virus and it is a strong binder to the NS1 protein, as confirmed by molecular simulations.
引用
收藏
页码:100 / 112
页数:13
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