microRNAs Control Antiviral Immune Response, Cell Death and Chemotaxis Pathways in Human Neuronal Precursor Cells (NPCs) during Zika Virus Infection

• Published in: International journal of molecular sciences Vol. 23; no. 18; p. 10282
• Main Authors: Polonio, Carolina M., da Silva, Patrick, Russo, Fabiele B., Hyppolito, Brendo R. N., Zanluqui, Nagela G., Benazzato, Cecília, Beltrão-Braga, Patrícia C. B., Muxel, Sandra M., Peron, Jean Pierre S.
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 07.09.2022; MDPI
• Subjects: Apoptosis; Brain; Cell death; Chemotaxis; Datasets; Disease transmission; Encephalitis; Fetuses; Gene expression; Genes; Guillain-Barre syndrome; Immune response; Immune system; Infections; inflammation; Microcephaly; Microencephaly; microRNA; MicroRNAs; miRNA; Morbidity; Neural networks; Neuronal-glial interactions; Neuropathogenesis; Pathogenesis; Post-transcription; Precursors; Public health; Viral infections; Viruses; West Nile virus; Zika virus; ZIKV; Africa
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms231810282

Viral infections have always been a serious burden to public health, increasing morbidity and mortality rates worldwide. Zika virus (ZIKV) is a flavivirus transmitted by the Aedes aegypti vector and the causative agent of severe fetal neuropathogenesis and microcephaly. The virus crosses the placenta and reaches the fetal brain, mainly causing the death of neuronal precursor cells (NPCs), glial inflammation, and subsequent tissue damage. Genetic differences, mainly related to the antiviral immune response and cell death pathways greatly influence the susceptibility to infection. These components are modulated by many factors, including microRNAs (miRNAs). MiRNAs are small noncoding RNAs that regulate post-transcriptionally the overall gene expression, including genes for the neurodevelopment and the formation of neural circuits. In this context, we investigated the pathways and target genes of miRNAs modulated in NPCs infected with ZIKV. We observed downregulation of miR-302b, miR-302c and miR-194, whereas miR-30c was upregulated in ZIKV infected human NPCs in vitro. The analysis of a public dataset of ZIKV-infected human NPCs evidenced 262 upregulated and 3 downregulated genes, of which 142 were the target of the aforementioned miRNAs. Further, we confirmed a correlation between miRNA and target genes affecting pathways related to antiviral immune response, cell death and immune cells chemotaxis, all of which could contribute to the establishment of microcephaly and brain lesions. Here, we suggest that miRNAs target gene expression in infected NPCs, directly contributing to the pathogenesis of fetal microcephaly.