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Differential expression analysis and profiling of hepatic miRNA and isomiRNA in dengue hemorrhagic fever

Authors :
Layanna Freitas de Oliveira
Amanda Araújo Serrão de Andrade
Carla Pagliari
Leda Viegas de Carvalho
Taiana S. Silveira
Jedson Ferreira Cardoso
André Luiz Teles e Silva
Janaina Mota de Vasconcelos
Caroline Aquino Moreira-Nunes
Rommel Mario Rodríguez Burbano
Márcio Roberto Teixeira Nunes
Eduardo José Melo dos Santos
João Lídio da Silva Gonçalves Vianez Júnior
Source :
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Publication Year :
2021
Publisher :
Nature Portfolio, 2021.

Abstract

Abstract Dengue virus causes dengue hemorrhagic fever (DHF) and has been associated to fatal cases worldwide. The liver is one of the most important target tissues in severe cases, due to its intense viral replication and metabolic role. microRNAs role during infection is crucial to understand the regulatory mechanisms of DENV infection and can help in diagnostic and anti-viral therapies development. We sequenced the miRNome of six fatal cases and compared to five controls, to characterize the human microRNAs expression profile in the liver tissue during DHF. Eight microRNAs were differentially expressed, including miR-126-5p, a regulatory molecule of endothelial cells, miR-122-5p, a liver specific homeostasis regulator, and miR-146a-5p, an interferon-regulator. Enrichment analysis with predicted target genes of microRNAs revealed regulatory pathways of apoptosis, involving MAPK, RAS, CDK and FAS. Immune response pathways were related to NF- kB, CC and CX families, IL and TLR. This is the first description of the human microRNA and isomicroRNA profile in liver tissues from DHF cases. The results demonstrated the association of miR-126-5p, miR-122-5p and miR-146a-5p with DHF liver pathogenesis, involving endothelial repair and vascular permeability regulation, control of homeostasis and expression of inflammatory cytokines.

Subjects

Subjects :
Medicine
Science

Details

Language :
English
ISSN :
20452322
Volume :
11
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Scientific Reports
Publication Type :
Academic Journal
Accession number :
edsdoj.f566d1f7724ed99f9710ec7b9758a1
Document Type :
article
Full Text :
https://doi.org/10.1038/s41598-020-72892-w