Harnessing endogenous miRNA targeting ZIKV: A cutting-edge strategy to inhibit virus infection
Year: 2025
Type: article
Abstract: Emerging RNA virus outbreaks, including Zika virus, highlight the urgent need for novel antiviral strategies. Zika virus, a positive-strand RNA virus, causes congenital Zika syndrome, and to date, there are no approved vaccines or antiviral treatments. In this context, microRNAs are small non-coding RNAs that regulate gene expression and show potential as antiviral agents due to their ability to target viral RNA, making them a promising therapeutic approach against Zika syndrome. In this study, we identified endogenous microRNAs that interact with the virus genome using computational algorithms and overexpressed them in VERO cells. Twelve microRNAs reduced viral cytopathic effects by more than 50% in cells infected with a Brazilian Zika virus strain. Additionally, we used a computational platform to select pharmacological compounds capable of modulating endogenous microRNAs in human cells, achieving over 90% inhibition of Zika virus activity. These findings offer a promising path through drug repurposing for antiviral therapy by modulating endogenous microRNAs, with potential applications for other positive-strand RNA viruses.
Authors: Rhubia S.M. Rosa, Soledad Palameta, Jessica M. Toscaro, Michael E. Miller, Paulo S. Lopes-de-Oliveira, Marcio C. Bajgelman
Language: English
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $3,900
Funders: Fundação de Amparo à Pesquisa do Estado de São Paulo, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Ministério da Ciência, Tecnologia e Inovação, Conselho Nacional de Desenvolvimento Científico e Tecnológico, Centro Nacional de Pesquisa em Energia e Materiais, Ministério da Ciência, Tecnologia, Inovações e Comunicações, Laboratório Nacional de Biociências
Awards: Exploring therapeutic benefit of immunomodulatory vaccines derived from genetically modified human cells, to potentiate antitumor response in triple negative breast cancer model, G400555021, G4462329558, Development of a Treg Immunotherapy approach based on chimeric aptamers to potentiate antitumor vaccines
OpenAlex ID: W4410352138
